WO2000004372A1 - Sensor arrays for the measurement and identification of multiple analytes in solutions - Google Patents
Sensor arrays for the measurement and identification of multiple analytes in solutions Download PDFInfo
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- WO2000004372A1 WO2000004372A1 PCT/US1999/016162 US9916162W WO0004372A1 WO 2000004372 A1 WO2000004372 A1 WO 2000004372A1 US 9916162 W US9916162 W US 9916162W WO 0004372 A1 WO0004372 A1 WO 0004372A1
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- CFSFEIZUJGTCRB-UHFFFAOYSA-N CC1CC(C2)C2C1 Chemical compound CC1CC(C2)C2C1 CFSFEIZUJGTCRB-UHFFFAOYSA-N 0.000 description 1
Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00277—Apparatus
- B01J2219/00279—Features relating to reactor vessels
- B01J2219/00306—Reactor vessels in a multiple arrangement
- B01J2219/00313—Reactor vessels in a multiple arrangement the reactor vessels being formed by arrays of wells in blocks
- B01J2219/00315—Microtiter plates
- B01J2219/00317—Microwell devices, i.e. having large numbers of wells
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00583—Features relative to the processes being carried out
- B01J2219/00603—Making arrays on substantially continuous surfaces
- B01J2219/00646—Making arrays on substantially continuous surfaces the compounds being bound to beads immobilised on the solid supports
- B01J2219/00648—Making arrays on substantially continuous surfaces the compounds being bound to beads immobilised on the solid supports by the use of solid beads
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00583—Features relative to the processes being carried out
- B01J2219/00603—Making arrays on substantially continuous surfaces
- B01J2219/00659—Two-dimensional arrays
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- C—CHEMISTRY; METALLURGY
- C40—COMBINATORIAL TECHNOLOGY
- C40B—COMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
- C40B60/00—Apparatus specially adapted for use in combinatorial chemistry or with libraries
- C40B60/14—Apparatus specially adapted for use in combinatorial chemistry or with libraries for creating libraries
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/808—Optical sensing apparatus
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/973—Simultaneous determination of more than one analyte
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/80—Fluorescent dyes, e.g. rhodamine
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/805—Optical property
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/807—Apparatus included in process claim, e.g. physical support structures
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/807—Apparatus included in process claim, e.g. physical support structures
- Y10S436/809—Multifield plates or multicontainer arrays
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
Definitions
- TITLE SENSOR ARRAYS FOR THE MEASUREMENT AND IDENTIFICATION OF MULTIPLE ANALYTES IN SOLUTIONS
- the present invention relates to a method and device for the detection of analytes in a fluid. More particularly, the invention relates to the development of a sensor array system capable of discriminating mixtures of analytes, toxins, and/or bacteria in medical, food/beverage, and environmental solutions.
- Array based sensors displaying the capacity to sense and identify complex vapors have been demonstrated recently using a number of distinct transduction schemes.
- functional sensors based on Surface Acoustic Wave (SAW), tin oxide (Sn0 2 ) sensors, conductive organic polymers, and carbon black polymer composites have been fashioned.
- SAW Surface Acoustic Wave
- tin oxide sensors for example, is described in U.S. Patent No. 5,654,497 to Hoffheins et al.
- These sensors display the capacity to identify and discriminate between a variety of organic vapors by virtue of small site-to-site differences in response characteristics. Pattern recognition of the overall fingerprint response for the array serves as the basis for an olfaction-like detection of the vapor phase analyte species.
- the electromc nose can be used only for the identification of volatile reagents. For many environmental, military, medical, and commercial applications, the identification and quantification of analytes present in liquid or solid-phase samples is necessary. Moreover, the electromc nose systems are expensive
- the Aromascan system costs about $50,000/un ⁇ t
- bulky > lft ⁇
- the functional elements for the currently available electromc nose are composed of conductive polymer systems which possess little chemical selectivity for many of the analytes which are of interest to the military and civilian cornmunities.
- LATs latex agglutination tests
- Commercially available LATs for more than 60 analytes are used routinely for the detection of infectious diseases, illegal drugs, and early pregnancy tests.
- the vast majonty of these types of sensors operate on the principle of agglutination of latex particles (polymer microspheres) which occurs when the antibody-denvatized microspheres become effectively "cross-linked" by a foreign antigen resulting in the attachment to, or the inability to pass through a filter.
- the dye-doped microspheres are then detected colo ⁇ met ⁇ cally upon removal of the antigen carrying solution.
- the LATs lack the ability to be utilized for multiple, real time analyte detection schemes as the nature of the response intrinsically depends on a cooperative effect of the entire collection of microspheres.
- array sensors that have shown great analytical promise are those based on the "DNA on a chip” technology. These devices possess a high density of DNA hyb ⁇ dizahon sites that are affixed in a two-dimensional pattern on a planar substrate. To generate nucleotide sequence information, a pattern is created from unknown DNA fragments binding to va ⁇ ous hyb ⁇ drzation sites. Both radiochermcal and optical methods have provided excellent detection limits for analysis of limited quantities of DNA. (Sampson, D. I.;
- a system of analyzing fluid samples using an a ⁇ ay formed of heterogeneous, semi-selective thin films which function as sensing receptor units is desc ⁇ bed m
- U.S. Patent No. 5,512,490 to Walt et al. which is incorporated by reference as if set forth herein.
- These sensor probes appear to be designed with the goal of obtaining unique, continuous, and reproducible responses from small localized regions of dye-doped polymer
- the polymer appears to serve as a solid support for mdicator molecules that provide information about test solutions through changes in optical properties.
- a method of rapid sample analysis for use m the diagnostic microbiology field is also desirable.
- the techniques now used for rapid microbiology diagnostics detect either antigens or nucleic acids. Rapid antigen testing is based on the use of antibodies to recognize either the smgle cell orgamsm or the presence of infected cell mate ⁇ al. Inherent to this approach is the need to obtain and characterize the binding of the antibody to unique structures on the orgamsm bemg tested. Smce the identification and isolation of the approp ⁇ ate antibodies is time consuming, these techniques are limited to a smgle agent per testing module and there is no opportunity to evaluate the amount of agent present.
- nucleic acids The alternative to antigen detection is the detection of nucleic acids.
- An approach for diagnostic testing with nucleic acids uses hybridization to target unique regions of the target orgamsm. These techniques require fewer organisms (10 3 to 10 5 ), but require about five hours to complete. As with antibody-antigen reactions this approach has not been developed for the simultaneous detection of multiple analytes. The most recent improvement m the detection of microorganisms has been the use of nucleic acid amplification. Nucleic acid amplification tests have been developed that generate both qualitative and quantitative data. However, the current limitations of these testing methods are related to delays caused by specimen preparation, amplification, and detection. Currently, the standard assays require about five hours to complete. The ability to complete much faster detection for a va ⁇ ety of microorganisms would be of tremendous importance to military intelligence, national safety, medical, environmental, and food areas.
- sensing system be adaptable to the simultaneous detection of a va ⁇ ety of analytes to improve throughput during vanous chemical and biological analytical procedures
- the system may be used for either liquid or gaseous fluids
- the system m some embodiments, may generate patterns that are diagnostic for both the individual analytes and mixtures of the analytes
- the system m some embodiments, is made of a plurality of chemically sensitive particles, formed in an ordered a ⁇ ay, capable of simultaneously detecting many different kmds of analytes rapidly
- An aspect of the system is that the array may be formed using a microfab ⁇ cation process, thus allowing the system to be manufactured m an inexpensive manner
- the system in some embodiments, includes a light source, a sensor array, and a detector
- the sensor a ⁇ ay, m is formed of a supporting member which is configured to hold a va ⁇ ety of chemically sensitive particles (herem referred to as "particles") m an ordered a ⁇ ay.
- the particles are, in some embodiments, elements which will create a detectable signal in the presence of an analyte.
- the particles may produce optical (e.g., absorbance or reflectance) or fluorescence/phosphorescent signals upon exposure to an analyte
- particles include, but are not limited to functionalized polyme ⁇ c beads, agarous beads, dextrose beads, polyacrylamide beads, control pore glass beads, metal oxides particles (e.g., silicon dioxide (S ⁇ 0 2 ) or alummum oxides (A1 2 0 3 )), polymer thin films, metal quantum particles (e g , silver, gold, platinum, etc.), and semiconductor quantum particles (e.g., Si, Ge, GaAs, etc.).
- a detector e.g., a charge-coupled device "CCD" in one embodiment is positioned below the sensor array to allow for the data acquisition. In another embodiment, the detector may be positioned above the sensor a ⁇ ay to allow for data acquisition from reflectance of the light off of the particles
- Light ongmating from the light source may pass through the sensor a ⁇ ay and out through the bottom side of the sensor a ⁇ ay
- Light modulated by the particles may pass through the sensor array and onto the proximally spaced detector
- Evaluation of the optical changes may be completed by visual inspection or by use of a CCD detector by itself or in combmation with an optical microscope.
- a microprocessor may be coupled to the CCD detector or the microscope.
- a fluid delivery system may be coupled to the supporting member of the sensor array. The fluid delivery system, m some embodiments, is configured to introduce samples into and out of the sensor array.
- the senor a ⁇ ay system mcludes an a ⁇ ay of particles
- the particles may mclude a receptor molecule coupled to a polyme ⁇ c bead
- the receptors m some embodiments, are chosen for interacting with analytes This interaction may take the form of a binding/association of the receptors with the analytes.
- the supporting member may be made of any matenal capable of supporting the particles, while allowing the passage of the approp ⁇ ate wavelengths of light.
- the supporting member may mclude a plurality of cavities. The cavities may be formed such that at least one particle is substantially contained within the cavity
- the optical detector may be integrated within the bottom of the supporting member, rather than usmg a separate detecting device.
- the optical detectors may be coupled to a microprocessor to allow evaluation of fluids without the use of separate detecting components
- a fluid delivery system may also be incorporated mto the supporting member. Integration of detectors and a fluid delivery system mto the supporting member may allow the formation of a compact and portable analyte sensing system
- a high sensitivity CCD array may be used to measure changes m optical characte ⁇ stics which occur upon bmdmg of the biological/chemical agents
- the CCD a ⁇ ays may be interfaced with filters, light sources, fluid delivery and micromachrned particle receptacles, so as to create a functional sensor array
- Data acquisition and handling may be performed with existing CCD technology
- CCD detectors may be configured to measure white light, ultraviolet light or fluorescence
- Other detectors such as photomultiplier tubes, charge induction devices, photo diodes, photodiode a ⁇ ays, and microchannel plates may also be used
- a particle in some embodiments, possess both the ability to bind the analyte of mterest and to create a modulated signal
- the particle may mclude receptor molecules which posses the ability to bmd the analyte of mterest and to create a modulated signal
- the particle may mclude receptor molecules and indicators
- the receptor molecule may posses the ability to bmd to an analyte o f mterest Upon bmdmg the analyte of mterest, the receptor molecule may cause the mdicator molecule to produce the modulated signal.
- the receptor molecules may be naturally occurring or synthetic receptors formed by rational design or combrnatonal methods Some examples of natural receptors mclude, but are not limited to, DNA, RNA, proteins, enzymes, obgopeptides, antigens, and antibodies. Either natural or synthetic receptors may be chosen for then: ability to bmd to the analyte molecules m a specific manner
- a naturally occurring or synthetic receptor is bound to a polyme ⁇ c bead m order to create the particle
- the particle in some embodiments, is capable of both bmdmg the analyte(s) of mterest and creating a detectable signal In some embodiments, the particle will create an optical signal when bound to an analyte of mterest.
- a va ⁇ ety of natural and synthetic receptors may be used.
- the synthetic receptors may come from a va ⁇ ety of classes including, but not limited to, polynucleotides (e g , aptamers), peptides (e g., enzymes and antibodies), synthetic receptors, polymenc unnatural biopolymers (e.g., polythioureas, polygua diniums), and imprinted polymers
- Polynucleotides are relatively small fragments of DNA which may be de ⁇ ved by sequentially building the DNA sequence
- Peptides include natural peptides such as antibodies or enzymes or may be synthesized from ammo acids
- Unnatural biopolymers are chemical structure which are based on natural biopolymers, but which are built from unnatural linking units
- polythioureas and polyguamdmiums have a structure similar to peptides, but may be synthesized from diamines (i.e., compounds which mclude at least two amine
- a large number of chemical/biological agents of mterest to the military and civilian communities may be sensed readily by the desc ⁇ bed array sensors Bacte ⁇ a may also be detected usmg a similar system
- Bacte ⁇ a may also be detected usmg a similar system
- the cell surface of one bactena may be differentiated from other bacte ⁇ a, or genomic mate ⁇ al may be detected usmg ohgonucleic receptors
- One method of accomplishmg this differentiation is to target cell surface ohgosaccha ⁇ des (l e , sugar residues)
- the use of synthetic receptors which are specific for ohgosacchandes may be used to determine the presence of specific bactena by analyzing for cell surface ohgosacchandes BRIEF DESCRIPTION OF THE DRAWINGS
- FIG. 1 depicts a schematic of an analyte detection system
- FIG. 2 depicts a particle disposed in a cavity
- FIG 3 depicts a sensor array
- FIG 4A-F depicts the formation of a Fabry-Perot cavity on the back of a sensor a ⁇ ay
- FIG. 5 depicts the chemical constituents of a particle
- FIG 6 depicts the chemical formulas of some receptor compounds
- FIG. 7 depicts a plot of the absorbance of green light vs. concentration of calcium (Ca +2 ) for a particle which mcludes an o-cresolphthalein complexone receptor,
- FIG 8 depicts a schematic view of the transfer of energy from a first mdicator to a second mdicator m the presence of an analyte
- FIG. 9 depicts a schematic of the interaction of a sugar molecule with a boromc acid based receptor.
- FIG. 10 depicts va ⁇ ous synthetic receptors
- FIG 11 depicts a synthetic pathway for the synthesis of polythioureas
- FIG. 12 depicts a synthetic pathway for the synthesis of polyguamdmiums
- FIG. 13 depicts a synthetic pathway for the synthesis of diamines from ammo acids
- FIG. 14 depicts fluorescent diamino monomers
- FIG. 15 depicts a plot of counts/sec. (i.e., intensity) vs. time as the pH of a solution su ⁇ ound g a particle coupled to o-cresolphthalein is cycled from acidic to basic conditions;
- FIG. 16 depicts the color responses of a va ⁇ ety of sensing particles to solutions of Ca +2 and va ⁇ ous pH levels
- FIG. 17 depicts an analyte detection system which mcludes a sensor a ⁇ ay disposed within a chamber;
- FIG. 18 depicts an integrated analyte detection system
- FIG. 19 depicts a cross-sectional view of a cavity covered by a mesh cover
- FIG. 20 depicts a top view of a cavity covered by a mesh cover
- FIG. 21 A-G depicts a cross-sectional view of a senes of processmg steps for the formation of a sensor array which mcludes a removable top and bottom cover
- FIG. 22A-G depicts a cross-sectional view of a senes of processmg steps for the formation of a sensor a ⁇ ay which mcludes a removable top and a stationary bottom cover;
- FIG. 23 A-G depicts a cross-sectional view of a senes of processmg steps for the formation of a sensor a ⁇ ay which mcludes a removable top
- FIG. 24A-D depicts a cross-sectional view of a senes of processmg steps for the formation of a silicon based sensor a ⁇ ay which mcludes a top and bottom cover with openings aligned with the cavity;
- FIG. 25A-D depicts a cross-sectional view of a senes of processmg steps for the formation of a photoresist based sensor a ⁇ ay which mcludes a top and bottom cover with openings aligned with the cavity
- FIG. 26A-E depicts a cross-sectional view of a senes of processmg steps for the formation of a plastic based sensor array which mcludes a top and bottom cover with openings aligned with the cavity;
- FIG. 27A-D depicts a cross-sectional view of a senes of processmg steps for the formation of a silicon based sensor a ⁇ ay which mcludes a top cover with openings aligned with the cavity and a tapered cavity
- FIG. 28 A-E depicts a cross-sectional view of a senes of processmg steps for the formation of a photoresist based sensor a ⁇ ay which mcludes a top cover with openmgs aligned with the cavity and a tapered cavity;
- FIG. 29A-E depicts a cross-sectional view of a senes of processmg steps for the formation of a photoresist based sensor a ⁇ ay which includes a top cover with openmgs aligned with the cavity and a bottom cover;
- FIG. 30A-D depicts a cross-sectional view of a senes of processmg steps for the formation of a plastic based sensor a ⁇ ay which mcludes a top cover with openmgs aligned with the cavity and a bottom cover;
- FIG. 31 depicts a cross-sectional view of a schematic of a micropump
- FIG. 32 depicts a top view of an electrohydrodynamic pump
- FIG. 33 depicts a cross-sectional view of a sensor a ⁇ ay which mcludes a micropump;
- FIG. 34 depicts a cross-sectional view of a sensor a ⁇ ay which mcludes a micropump and channels which are coupled to the cavities;
- FIG. 35 depicts a cross-sectional view of a sensor a ⁇ ay which mcludes multiple micropumps each micropump bemg coupled to a cavity;
- FIG. 36 depicts a top view of a sensor a ⁇ ay which mcludes multiple electrohydrodynamic pumps
- FIG. 37 depicts a cross-sectional view of a sensor a ⁇ ay which mcludes a system for delivering a reagent from a reagent particle to a sensmg cavity.
- the system may be used for either liquid or gaseous fluids.
- the system may generate patterns that are diagnostic for both mdividual analytes and mixtures of the analytes.
- the system m some embodiments, is made of a combination of chemically sensitive particles, formed in an ordered array, capable of simultaneously detecting many different lands of analytes rapidly.
- An aspect of the system is that the a ⁇ ay may be formed usmg a microfab ⁇ cation process, thus allowing the system to be manufactured in an inexpensive manner.
- FIG. 1 is an embodiment of a system for detecting analytes m a fluid.
- the system m some embodiments, mcludes a light source 110, a sensor array 120 and a detector 130.
- the light source 110 may be a white light source or light emitting diodes (LED)
- LED light emitting diodes
- light source 110 may be a blue light emitting diode (LED) for use m systems relymg on changes m fluorescence signals.
- colo ⁇ met ⁇ c e.g., absorbance
- a white light source may be used.
- the sensor a ⁇ ay 120 is formed of a supporting member which is configured to hold a va ⁇ ety of particles 124.
- a detecting device 130 may be positioned below the sensor a ⁇ ay to allow for data acquisition. In another embodiment, the detecting device 130 may be positioned above the sensor a ⁇ ay.
- Light originating from the light source 110 passes through the sensor a ⁇ ay 120 and out through the bottom side of the sensor a ⁇ ay.
- the supporting member and the particles together in some embodiments, provide an assembly whose optical properties are well matched for spectral analyses. Thus, light modulated by the particles may pass through the sensor a ⁇ ay and onto the proximally spaced detector 130.
- Evaluation of the optical changes may be completed by visual inspection (e.g., with a microscope) or by use of a microprocessor 140 coupled to the detector.
- a filter 135 may be placed between supporting member 120 and detector 130 to remove the excitation wavelength.
- a fluid delivery system 160 may be coupled to the supporting member.
- the fluid delivery system 160 may be configured to introduce samples into and out of the sensor a ⁇ ay.
- the sensor a ⁇ ay system includes an a ⁇ ay of particles. Upon the surface and within the interior region of the particles are, in some embodiments, located a variety of receptors for interacting with analytes.
- the supporting member in some embodiments, is used to localize these particles as well as to serve as a microenvironment in which the chemical assays can be performed.
- the particles used for analysis are about 0.05 - 500 microns in diameter, and may actually change size (e.g., swell or shrink) when the chemical environment changes.
- these changes occur when the a ⁇ ay system is exposed to the fluid stream which includes the analytes.
- a fluid stream which comprises a non-polar solvent may cause non-polar particles to change in volume when the particles are exposed to the solvent.
- the supporting member consist of an array of cavities which serve as micro test- tubes.
- the supporting member may be made of any material capable of supporting the particles, while allowing the passage of the appropriate wavelength of light.
- the supporting member is also made of a material substantially impervious to the fluid in which the analyte is present.
- a variety of materials may be used including plastics, glass, silicon based materials (e.g., silicon, silicon dioxide, silicon nitride, etc.) and metals.
- the supporting member includes a plurality of cavities. The cavities may be formed such that at least one particle is substantially contained within the cavity. Alternatively, a plurality of particles may be contained within a single cavity.
- the supporting member may consist of a strip of plastic which is substantially transparent to the wavelength of light necessary for detection.
- a series of cavities may be formed within the strip.
- the cavities may be configured to hold at least one particle.
- the particles may be contained within the strip by a transparent cover which is configured to allow passage of the analyte containing fluid into the cavities.
- the supporting member may be formed using a silicon wafer as depicted in FIG. 2.
- the silicon wafer 210 may include a substantially transparent layer 220 formed on the bottom surface of the wafer.
- the cavities 230 are formed by an anisotropic etch process of the silicon wafer. In one embodiment, anisotropic etching of the silicon wafer is accomplished using a wet hydroxide etch. Photolithographic techniques may be used to define the locations of the cavities.
- the cavities may be formed such that the sidewalls of the cavities are substantially tapered at an angle of between about 50 to 60 degrees. Formation of such angled cavities may be accomplished by wet anisotropic etching of ⁇ 100> silicon.
- ⁇ 100> silicon refers to the crystal orientation of the silicon wafer.
- Other types of silicon e.g., ⁇ 110> and ⁇ 111> silicon
- ⁇ 111> silicon may lead to sidewalls formed at about 90 degrees
- the angled sides of the cavities m some embodiments, serve as "mirror layers" which may improve the light collection efficiency of the cavities
- the etch process may be controlled so that the formed cavities extend through the silicon wafer to the upper surface of transparent layer 220 While depicted as pyramidal, the cavities may be formed m a number of shapes including but not limited to, sphencal, oval, cubic, or rectangular
- An advantage to usmg a silicon wafer for the support member is that the silicon matenal is substantially opaque to the light produced from the light source Thus, the light may be inhibited from passing from one cavity to adjacent cavities In this manner, light from one cavity may be inhibited from influencing the spectroscopic changes produced m an adjacent cavity
- the silicon wafer has an area of approximately 1 c ⁇ r to about 100 cm 2 and mcludes about 10' to about 10 6 cavities In an embodiment, about 100 cavities are formed m a ten by ten matrix The center to center distance between the cavities, in some embodiments, is about 500 microns Each of the cavities may mclude at least one particle
- the transparent layer 220 may serve as a window, allowmg light of a va ⁇ ety of wavelengths to pass through the cavities 230 and to the detector Additionally, the transparent layer may serve as a platform onto which the mdividual particles 235 may be positioned
- the transparent layer may be formed of silicon dioxide (S ⁇ 0 2 ), silicon mt ⁇ de (S ⁇ 3 N 4 ) or silicon dioxide/silicon nitnde multi-layer stacks
- the transparent layer m some embodiments, is deposited onto the silicon wafer p ⁇ or to the formation of the cavities
- the cavities 230 may be sized to substantially contam a particle 235
- the cavities are, m some embodiments, larger than a particle
- the cavities are, in some embodiments, sized to allow facile placement and removal of the particle within the cavities
- the cavity may be substantially larger than the particle, thus allowmg the particle to swell durmg use
- a particle may have a size as depicted m FIG 2 by particle 235.
- a fluid e g , a solvent
- contact with a fluid may cause the particle to swell, for example, to a size depicted as circle 236
- the cavity is sized to allow such swelling of the particle during use
- a particle may be positioned at the bottom of a cavity usmg, e g , a micromampulator After a particle has been placed within the cavity, a transparent cover plate 240 may be placed on top of the supporting member to keep the particle in place
- the particles When forming an a ⁇ ay which mcludes a plurality of particles, the particles may be placed m the a ⁇ ay m an ordered fashion usmg the micromampulator In this manner, a ordered a ⁇ ay havmg a predefined configuration of particles may be formed Alternatively, the particles may be randomly placed within the cavities The a ⁇ ay may subsequently undergo a calibration test to determine the identity of the particle at any specified location m the supporting member
- the transparent cover plate 240 in some embodiments, is coupled to the upper surface of the silicon wafer 220 such that the particles are inhibited from becoming dislodged from the cavity
- the transparent cover plate in some embodiments, is positioned a fixed distance above the silicon wafer, as depicted in FIG 2, to keep the particle m place, while allowmg the entrance of fluids mto the cavities
- the transparent cover plate m some embodiments, is positioned at a distance above the substrate which is substantially less than a width of the particle
- the transparent cover plate may be made of any matenal which is substantially transparent to the wavelength of light bemg utilized by the detector
- the transparent cover plate may be made of plastic, glass, quartz, or silicon dioxide/silicon mtnde
- the transparent cover plate 240 is a thin sheet of glass (e.g , a microscope slide cover shp).
- the slide may be positioned a fixed distance above the silicon wafer.
- Support structures 241 (See FIG. 2) may be placed upon the silicon wafer 210 to position the transparent cover plate 240.
- the support structures may be formed from a polymer or a silicon based matenal.
- a polymenc substrate is coupled to the silicon wafer to form the support structures 241 for the transparent cover plate 240
- a plastic mate ⁇ al with an adhesive backmg e.g., cellophane tape
- the support structures inhibit the transparent cover sheet from contacting the silicon wafer 200. In this manner, a channel is formed between the silicon wafer and the transparent cover plate which allow the fluid to pass mto the cavity, while inhibiting displacement of the particle by the fluid.
- the transparent cover plate 240 may be fastened to the upper surface of the silicon wafer, as depicted m FIG 3
- the fluid may be inhibited from entering the cavities 230 by the transparent cover plate 240
- a number of channels 250 may be formed m the silicon wafer
- the channels are onented to allow passage of the fluid mto substantially all of the cavities When contacted with the fluid, the particles may swell to a size which may plug the channels.
- the channels may be formed near the upper portion of the cavities, as depicted m FIG 3
- the channels, m one embodiment, are formed usmg standard photolithographic masking to define the regions where the trenches are to be formed, followed by the use of standard etching techniques.
- a depth of the cavity may be such that the particle resides substantially below the position of the channel. In this way, the pluggmg of the channels due to swelling of the particle may be prevented.
- the inner surfaces of the cavities may be coated with a matenal to aid the positioning of the particles within the cavities.
- a thin layer of gold or silver may be used to line the inner surface of the cavities
- the gold or silver layer may act as an anchoring surface to anchor particles (e.g., via alkylthiol bondmg)
- the gold or silver layer may also mcrease the reflectivity of the inner surface of the cavities The increased reflectance of the surface may enhance the analyte detection sensitivity of the system
- polymer layers and self-assembled monolayers formed upon the inner surface of the cavities may be used to control the particle adhesion interactions Additional chemical anchoring methods may be used for silicon surfaces such as those based on siloxane type reagents, which may be attached to Si-OH functionalities.
- monome ⁇ c and polymenc reagents attached to an rntenor region of the cavities can be used to alter the local wetting characte ⁇ stics of the cavities.
- This type of methodology can be used to anchor the particles as well as to alter the fluid delivery characte ⁇ stics of the cavity.
- amplification of the signals for the analytes may be accomplished with this type of strategy by causmg preconcentration of appropnate analytes in the approp ⁇ ate type of chemical environment
- the optical detector may be integrated within the bottom transparent layer 220 of the supportmg member, rather than usmg a separate detectmg device
- the optical detectors may be formed usmg a semiconductor-based photodetector 255
- the optical detectors may be coupled to a microprocessor to allow evaluation of fluids without the use of separate detecting components.
- the fluid delivery system may also be incorporated mto the supportmg member
- Micro-pumps and micro-valves may also be incorporated mto the silicon wafer to aid passage of the fluid through the cavities
- Integration of detectors and a fluid delivery system mto the supporting member may allow the formation of a compact and portable analyte sensmg system
- Optical filters may also be mtegrated mto the bottom membrane of the cavities These filters may prevent short wavelength excitation from producmg "false" signals m the optical detection system (e g , a CCD detector a ⁇ ay) during fluorescence measurements
- a sensmg cavity may be formed on the bottom surface of the support substrate
- An example of a sensmg cavity that may be used is a Fabry-Perot type cavity Fabry-Perot cavity-based sensors may be used to detect changes m optical path length mduced by either a change m the refractive mdex or a change m physical length of the cavity Us
- the barner layer 262 a/b is composed of a stack of dielectric mate ⁇ als As depicted in FIG 4A, the barner layer 262 a/b is composed of a stack of dielectnc matenals which mcludes a silicon mtnde layer 271 a/b and a sihcon dioxide layer 272a/b Both layers may be deposited usmg a low pressure chemical vapor deposition ("LPCVD") process Silicon mtnde may be deposited usmg an LPCVD reactor by reaction of ammonia (NH 3 ) and dichlorosilane (S ⁇ Cl 2 H 2 ) at a gas flow rate of about 3 5 1 , a temperature of about 800 DC, and a pressure of about 220 mTo ⁇ The silicon mtnde layer 271 a/b is deposited to a thickness m the range from about 100 A to about 500 A, preferably from 200 A to about 400 A, and more preferably of about 300 A Sihcon dioxide is may be deposited
- a bottom diaphragm layer 264a/b is deposited upon the barner layer 262a/b on both sides of the supporting member 260
- the bottom diaphragm layer 264a/b may be composed of sihcon mtnde, silicon dioxide, or sihcon oxynitnde
- the bottom diaphragm layer 264 a/b is composed of a stack of dielectnc matenals
- the bottom diaphragm layer 264a/b is composed of a stack of dielectnc matenals which mcludes a pair of silicon mtnde layers 273a/b and 275a/b surrounding a silicon dioxide layer 274ab All of the layers may be deposited usmg an LPCVD process
- the silicon mtnde layers 273a/b and 275a/b have a thickness in the range from about 500 A to about 1000 A, preferably from 700 A to about 800 A, and more preferably of about 750 A
- a cavity which will hold the particle may now be formed m the supporting member 260
- the bottom diaphragm layer 264b and the barner layer 262b formed on the back side 261 of the sihcon supportmg member 260 are patterned and etched usmg standard photolithographic techniques.
- the layers are subjected to a plasma etch process.
- the plasma etchmg of silicon dioxide and silicon mtnde may be performed usmg a mixture of carbontetrafluo ⁇ de (CF 4 ) and oxygen (0 2 ).
- the patterned back side layers 262b and 264b may be used as a mask for anisotropic etchmg of the silicon supporting member 260
- the silicon supporting member 260 in one embodiment, is amsotropically etched with a 40% potassium hydroxide ("KOH") solution at 80 DC to form the cavity
- KOH potassium hydroxide
- the etch is stopped when the front side silicon mtnde layer 271a is reached, as depicted in FIG 4B.
- the sihcon mtnde layer 271a inhibits etchmg of the mam barner layer 272a during this etch process.
- the cavity 267 may be formed extending through the supporting member 260. After formation of the cavity, the remaining portions of the back side barner layer 262b and the diaphragm layer 264b may be removed.
- Etch wmdows 266 are formed through the bottom diaphragm layer 264a on the front side of the wafer.
- a masking layer (not shown) is formed over the bottom diaphragm layer 264a and patterned usmg standard photolithographic techniques. Usmg the masking layer, etch wmdows 266 may be formed usmg a plasma etch.
- the plasma etchmg of silicon dioxide and sihcon mtnde may be performed usmg a mixture of carbontetrafluonde (CF 4 ) and oxygen (0 2 )
- the etchmg is continued through the bottom diaphragm layer 264a and partially mto the barner layer 262a In one embodiment, the etchmg is stopped at approximately half the thickness of the barner layer 262a.
- the etch wmdows 266 will extend through the bottom diaphragm layer 264a, communicating with the cavity 267
- stopp g the etchmg at a midpoint of the barner layer
- voids or discontinuities may be reduced smce the bottom diaphragm is still continuous due to the remaining barner layer.
- a sacnficial spacer layer 268a/b is deposited upon the bottom diaphragm layer 264a and within cavity 267, as depicted in FIG. 4C.
- the spacer layer may be formed from LPCVD polysihcon.
- the front side deposited spacer layer 268a will also at least partially fill the etch wmdows 266
- Polysihcon may be deposited usmg an LPCVD reactor usmg silane (S ⁇ H 4 ) at a temperature of about 650 DC.
- the spacer layer 268a/b is deposited to a thickness in the range from about 4000 A to about 10,000 A, preferably from 6000 A to about 8000 A, and more preferably of about 7000 A
- the prefe ⁇ ed thickness of the spacer layer 268a is dependent on the desned thickness of the internal air cavity of the Fabry-Perot detector.
- a spacer layer havmg a thickness of about 7000 A would be formed.
- a maskmg layer for etchmg the spacer layer 268a (not shown) is used to define the etch regions of the spacer layer 268a.
- the etchmg may be performed usmg a composition of mt ⁇ c acid (HN0 3 ), water, and hydrogen fluonde (HF) m a ratio of 25 : 13 : 1 , respectively, by volume
- the lateral size of the subsequently formed cavity is determined by the masking pattern used to define the etch regions of the spacer layer 268a.
- the top diaphragm layer 270a b is formed.
- the top diaphragm 270a/b m one embodiment, is deposited upon the spacer layer 268a/b on both sides of the supporting member.
- the top diaphragm 270a/b may be composed of silicon mtnde, silicon dioxide, or silicon oxymt ⁇ de.
- the top diaphragm 270a/b is composed of a stack of dielectnc matenals. As depicted m FIG.
- the top diaphragm 270a/b is composed of a stack of dielectnc materials which mcludes a pair of silicon mtnde layers 283a/b and 285a/b su ⁇ ounding a silicon dioxide layer 284a/b. All of the layers may be deposited usmg an LPCVD process.
- the silicon mtnde layers 283a/b and 285a/b have a thickness in the range from about 1000 A to about 2000 A, preferably from 1200 A to about 1700 A, and more preferably of about 1500 A
- the silicon dioxide layer 284a/b has a thickness m the range from about 5000 A to about 15,500 A, preferably from 7500 A to about 12,000 A, and more preferably of about 10,500 A
- top diaphragm 270a/b After depositing the top diaphragm 270a/b, all of the layers stacked on the bottom face of the supporting member (e.g., layers 268b, 283b, 284b, and 285b) are removed by multiple wet and plasma etchmg steps, as depicted m FIG. 4D. After these layers are removed, the now exposed portions of the barner layer 262a are also removed. This exposes the spacer layer 268a which is present in the etch wmdows 266. The spacer layer 268 may be removed from between the top diaphragm 270a and the bottom diaphragm 264a by a wet etch usmg a KOH solution, as depicted in FIG. 4D.
- the cavity 286 of the Fabry-Perot sensor may be filled with a sensmg substrate 290, as depicted in FIG. 4E.
- the sensmg substrate may be dissolved m a solvent. A solution of the sensmg substrate is applied to the supporting member 260.
- the solution is beheved to rapidly enter the cavity 286 through the etched wmdows 266 m the bottom diaphragm 264a, aided m part by capillary action.
- a thin film of the sensmg substrate 290 coats the inner walls of the cavity 286, as well as the outer surface of the bottom diaphragm 264a.
- the thickness of the sensmg substrate may be vaned.
- the sensmg substrate 290 is poly(3-dodecylth ⁇ ophene) whose optical properties change m response to changes m oxidation states.
- the sensmg substrate poly(3-dodecylth ⁇ ophene) may be dissolved m a solvent such as chloroform or xylene.
- a concentration of about 0.1 g of poly(3- dodecylth ⁇ ophene)/mL is used.
- Application of the solution of poly(3-dodecylth ⁇ ophene) to the supporting member causes a thm film of poly(3-dodecylth ⁇ ophene) to be formed on the inner surface of the cavity
- the sensmg substrate when deposited within a cavity of a Fabry-Perot type detector, may cause stress m the top diaphragm of the detector. It is believed that when a sensmg polymer coats a planar top diaphragm, extra residual stress on the top diaphragm causes the diaphragm to become deflected toward the bottom diaphragm. If the deflection becomes to severe, sticking between the top and bottom diaphragms may occur. In one embodiment, this stress may be relieved by the use of supporting members 292 formed within the cavity 286, as depicted m FIG. 4F. The supporting members 292 may be formed without any extra processmg steps to the above descnbed process flow.
- supporting members may be accomplished by deliberately leavmg a portion of the spacer layer within the cavity This may be accomplished by underetching the spacer layer (e.g., terminating the etch process before the entire etch process is finished). The remaining spacer will behave as a support member to reduce the deflection of the top diaphragm member.
- the size and shape of the support members may be adjusted by altering the etch time of the spacer layer, or adjusting the shape of the etch wmdows 266.
- a high sensitivity CCD a ⁇ ay may be used to measure changes m optical charactenstics which occur upon bmdmg of the biological/chemical agents.
- the CCD arrays may be interfaced with filters, light sources, fluid delivery and micromachrned particle receptacles, so as to create a functional sensor a ⁇ ay.
- Data acquisition and handlmg may be performed with existing CCD technology.
- Data streams e.g., red, green, blue for colorrmetnc assays; gray intensity for fluorescence assays
- Cu ⁇ ent CCDs may allow for read-out rates of 10 pixels per second
- the entire a ⁇ ay of particles may be evaluated hundreds of times per second allowing for studies of the dynamics of the vanous host-guest interaction rates as well as the analyte/polymer diffusional characte ⁇ stics.
- CCD detectors may be configured to measure white hght, ultraviolet light or fluorescence
- Other detectors such as photomultipher tubes, charge induction devices, photodiode, photodiode arrays, and microchannel plates may also be used
- the detector is depicted as bemg positioned under the supporting member, the detector may also be positioned above the supporting member
- the detector typically includes a sensmg element for detecting the spectroscopic events and a component for displaying the detected events
- the display component may be physically separated from the sensmg element
- the sensmg element may be positioned above or below the sensor a ⁇ ay while the display component is positioned close to a user
- a CCD detector may be used to record color changes of the chemical sensitive particles during analysis
- a CCD detector 130 may be placed beneath the supporting member 120
- the light transmitted through the cavities is captured and analyzed by the CCD detector
- the light is broken down mto three color components, red, green and blue
- each color is recorded usmg 8 bits of data.
- the data for each of the colors will appear as a value between 0 and 255.
- the color of each chemical sensitive element may be represented as a red, blue and green value.
- a blank particle e., a particle which does not mclude a receptor
- a typical blank particle when broken down mto the red, green and blue components, it is found that a typical blank particle exhibits a red value of about 253, a green value of about 250, and a blue value of about 222 This signifies that a blank particle does not significantly absorb red, green or blue light
- the particle When a particle with a receptor is scanned, the particle may exhibit a color change, due to absorbance by the receptor
- the particle shows a strong absorbance of blue light
- the CCD detector values for the 5-carboxyfluorescern particle exhibits a red value of about 254, a green value of about 218, and a blue value of about 57
- the decrease m transmittance of blue hght is believed to be due to the absorbance of blue light by the 5-carboxyfluorescern In this manner, the color changes of a particle may be quantitatively characterized
- the particles may absorb a portion of the light as the light illuminates the particles The light then reaches the detector, reduced m intensity by the absorbance of the particles
- the detector may be configure to measure the reduction m hght intensity (i.e., the absorbance) due to the particles
- the detector may be placed above the supporting member
- the detector may be configured to measure the amount of light reflected off of the particles
- the absorbance of light by the particles is manifested by a reduction m the amount of light bemg reflected from the cavity.
- the light source m either embodiment may be a white light source or a fluorescent light source CHEMICALLY SENSITIVE PARTICLES
- a particle in some embodiments, possess both the ability to bmd the analyte of mterest and to create a modulated signal
- the particle may include receptor molecules which posses the ability to bmd the analyte of mterest and to create a modulated signal
- the particle may mclude receptor molecules and indicators.
- the receptor molecule may posses the ability to bmd to an analyte o f mterest.
- the receptor molecule may cause the mdicator molecule to produce the modulated signal.
- the receptor molecules may be naturally occurring or synthetic receptors formed by rational design or combmato ⁇ al methods.
- natural receptors include, but are not limited to, DNA, RNA, proteins, enzymes, obgopeptides, antigens, and antibodies. Either natural or synthetic receptors may be chosen for their ability to bmd to the analyte molecules m a specific manner.
- the forces which dnve association/recognition between molecules m include the hydrophobic effect, anion-cation attraction, and hydrogen bondmg. The relative strengths of these forces depend upon factors such as the solvent dielectnc properties, the shape of the host molecule, and how it complements the guest. Upon host-guest association, attractive mteractions occur and the molecules stick together. The most widely used analogy for this chemical interaction is that of a "lock and key" The fit of the key molecule (the guest) mto the lock (the host) is a molecular recognition event.
- a naturally occurring or synthetic receptor may be bound to a polymenc resm m order to create the particle
- the polymeric resm may be made from a va ⁇ ety of polymers mcludmg, but not limited to, agarous, dextrose, acrylamide, control pore glass beads, polystyrene-polyethylene glycol resm, polystyrene-divinyl benzene resm, formylpolystyrene resm, t ⁇ tyl-polystyrene resm, acetyl polystyrene resm, chloroacetyl polystyrene resin, aminomethyl polystyrene-divmylbenzene resm, carboxypolystyrene resin, chloromethylated polystyrene- divinylbenzene resm, hydroxymethyl polystyrene-divmylbenzene resm
- polystyrene-divmyl benzene resm will swell within non-polar solvents, but does not significantly swell within polar solvents.
- polystyrene-divmyl benzene resm may be used for the analysis of analytes within non-polar solvents
- polystyrene-polyethylene glycol resm will swell with polar solvents such as water.
- Polystyrene-polyethylene glycol resm may be useful for the analysis of aqueous fluids.
- a polystyrene-polyethylene glycol-divmyl benzene mate ⁇ al is used to form the polyme ⁇ c resm
- the polystyrene-polyethylene glycol-divmyl benzene resm is formed from a mixture of polystyrene 375, divmyl benzene 380 and polystyrene-polyethylene glycol 385, see FIG 5.
- the polyethylene glycol portion of the polystyrene-polyethylene glycol 385, m one embodiment, may be terminated with an amine.
- the amine serves as a chemical handle to anchor both receptors and mdicator dyes
- Other chemical functional groups may be positioned at the terminal end of the polyethylene glycol to allow approp ⁇ ate couplmg of the polyme ⁇ c resm to the receptor molecules or indicators
- the chemically sensitive particle in one embodiment, is capable of both bmdmg the analyte(s) of mterest and creating a detectable signal In one embodiment, the particle will create an optical signal when bound to an analyte of mterest.
- a polyme ⁇ c bound receptors offer advantages both m terms of cost and configurability Instead of having to synthesize or attach a receptor drrecdy to a supporting member, the polyme ⁇ c bound receptors may be synthesized en masse and distnubbed to multiple different supporting members This allows the cost of the sensor a ⁇ ay, a major hurdle to the development of mass-produced environmental probes and medical diagnostics, to be reduced Additionally, sensor a ⁇ ays which mcorporate polyme ⁇ c bound receptors may be reconfigured much more quickly than a ⁇ ay systems m which the receptor is attached directly tot he supporting member For example, if a new vanant of a pathogen or a pathogen that contains a genetically engme
- a receptor which is sensitive to presence of metal cations is bound to a polyme ⁇ c particle to create a particle
- the receptor m this case is typically sensitive to the concentration of one or more metal cations present m a fluid solution
- colored molecules which will bmd cations may be used to determine the presence of a metal cation m a fluid solution
- Examples of receptors which may be used to momtor the presence of cations m a fluid sample m include alizarin complexone and o-cresolphthalein complexone, see FIG 6
- Each of these receptors undergoes significant color changes as the concentration of a specific metal ion m the fluid is altered
- Alizarin complexone is particularly sensitive to lanthanum ions In the absence of lanthanum, alizarin complexone will exhibit a yellow color As the concentration of lanthanum is increased, alizarin complexone will change to a red color o-Cresolphthalem complexone is particularly sensitive to calcium ions In the absence of calcium, o
- a graph of the absorbance of green light vs. concentration of calcium (Ca +2 ) is depicted for a particle which includes an o-cresolphthalein complexone receptor.
- concentration of calcium increases in a linear manner up to a concentration of about 0.0006 M.
- concentration of 0.0006 M is the solubility limit of calcium in the fluid, thus no significant change in absorbance is noted after this point.
- concentration of calcium is determined by measuring the absorbance of the fluid sample.
- a detectable signal may be caused by the altering of the physical properties of an indicator ligand bound to the receptor or the polymeric resin.
- two different indicators are attached to a receptor or the polymeric resin. When an analyte is captured by the receptor, the physical distance between the two indicators may be altered such that a change in the spectroscopic properties of the indicators is produced.
- a variety of fluorescent and phosphorescent indicators may be used for this sensing scheme. This process, known as Forster energy transfer, is extremely sensitive to small changes in the distance between the indicator molecules.
- a first fluorescent indicator 320 e.g., a fluorescein derivative
- a second fluorescent indictor 330 e.g., a rhodamine derivative
- first fluorescent indicator 320 e.g., a fluorescein derivative
- second fluorescent indictor 330 e.g., a rhodamine derivative
- first fluorescent indicator 320 e.g., a fluorescein derivative
- second fluorescent indictor 330 e.g., a rhodamine derivative
- This change in intermolecular distance may allow the excited first indicator 320 to transfer a portion of its fluorescent energy 325 to the second fluorescent indicator 330.
- This transfer in energy may be measured by either a drop in energy of the fluorescence of the first indicator molecule 320, or the detection of increased fluorescence 314 by the second mdicator molecule 330.
- the first and second fluorescent indicators may initially be positioned such that short wavelength excitation, may cause fluorescence of both the first and second fluorescent indicators, as described above. After binding of analyte 350 to the receptor, a structural change in the receptor molecule may cause the first and second fluorescent indicators to move further apart. This change in intermolecular distance may inhibit the transfer of fluorescent energy from the first indicator 320 to the second fluorescent indicator 330.
- This change in the transfer of energy may be measured by either a drop in energy of the fluorescence of the second indicator molecule 330, or the detection of increased fluorescence by the first indicator molecule 320.
- an indicator ligand may be preloaded onto the receptor. An analyte may then displace the indicator ligand to produce a change in the spectroscopic properties of the particles. In this case, the initial background absorbance is relatively large and decreases when the analyte is present.
- the indicator ligand in one embodiment, has a variety of spectroscopic properties which may be measured. These spectroscopic properties include, but are not limited to, ultraviolet absorption, visible absorption, infrared absorption, fluorescence, and magnetic resonance.
- the indicator is a dye having either a strong fluorescence, a strong ultraviolet absorption, a strong visible absorption, or a combination of these physical properties.
- indicators include, but are not limited to, carboxyfluorescein, ethidium bromide, 7-dimethylamino-4- methylcoumarin, 7-diemyla ⁇ nino-4-methylcoumarin, eosin, erythrosin, fluorescein, Oregon Green 488, pyrene, Rhodamine Red, tettame yhhodamine, Texas Red, Methyl Violet, Crystal Violet, Ethyl Violet, Malachite green, Methyl Green, Alizarin Red S, Methyl Red, Neutral Red, o-cresolsulfonephthalern, o-cresolphthalem, phenolphthalein, Acndme Orange, 5-naphthol, couma ⁇ n, and ⁇ -naphthionic acid.
- the receptor and mdicator When the mdicator is mixed with the receptor, the receptor and mdicator mteract with each other such that the above mentioned spectroscopic properties of the indicator, as well as other spectroscopic properties may be altered.
- the nature of this mteraction may be a bmdmg mteraction, wherein the mdicator and receptor are attracted to each other with a sufficient force to allow the newly formed receptor-indicator complex to function as a smgle unit
- the bmdmg of the mdicator and receptor to each other may take the form of a covalent bond, an ionic bond, a hydrogen bond, a van der Waals mteraction, or a combination of these bonds.
- the mdicator may be chosen such that the bmdmg strength of the mdicator to the receptor is less than the bindmg strength of the analyte to the receptor.
- the bmdmg of the mdicator with the receptor may be disrupted, releasmg the mdicator from the receptor.
- the physical properties of the mdicator may be altered from those it exhibited when bound to the receptor.
- the mdicator may revert back to its o ⁇ gmal structure, thus regammg its ongrnal physical properties.
- the fluorescence of the particle may be strong before treatment with an analyte containing fluid.
- the fluorescent mdicator may be released Release of the mdicator may cause a decrease m the fluorescence of the particle, smce the particle now has less mdicator molecules associated with it.
- a boronic acid substituted resm 505 as a particle.
- the boronic acid substituted resm 505 is treated with a sugar 510 which is tagged with an mdicator (e.g., resorufin) as depicted m FIG. 9.
- the sugar 510 bmds to the boronic acid receptor 500 imparting a color change to the boronic substituted resm 505 (yellow for the resorufin tagged sugar).
- the tagged sugar 510 may be displaced, causmg a decrease in the amount of color produced by the boromc acid substituted resm 505. This decrease may be qualitatively or, with the use of a detector (e.g., a CCD detector), quantitatively momtored.
- a detector e.g., a CCD detector
- a designed synthetic receptor may be used.
- a polycarboxylic acid receptor may be attached to a polymenc resm. The polycarboxylic receptors are discussed in U.S. patent application senal no. 08/950,712 which is incorporated herem by reference.
- the analyte molecules m the fluid may be pretreated with an mdicator ligand. Pretreatment may mvolve covalent attachment of an mdicator ligand to the analyte molecule.
- the fluid may be passed over the sensmg particles. Interaction of the receptors on the sensmg particles with the analytes may remove the analytes from the solution. Smce the analytes mclude an mdicator, the spectroscopic properties of the mdicator may be passed onto the particle.
- the presence and concentration of an analyte may be determined For example, the analytes within a fluid may be de ⁇ vatized with a fluorescent tag before introducing the stream to the particles. As analyte molecules are adsorbed by the particles, the fluorescence of the particles may mcrease. The presence of a fluorescent signal may be used to determine the presence of a specific analyte. Additionally, the strength of the fluorescence may be used to determine the amount of analyte within the stream.
- RECEPTORS RECEPTORS
- a vanety of natural and synthetic receptors may be used.
- the synthetic receptors may come from a vanety of classes mcludmg, but not limited to, polynucleotides (e.g., aptamers), peptides (e.g., enzymes and antibodies), synthetic receptors, polymenc unnatural biopolymers (e.g., polythioureas, polyguamdmiums), and imprinted polymers., some of which are generally depicted m FIG. 10.
- Natural based synthetic receptors mclude receptors which are structurally similar to naturally occurring molecules. Polynucleotides are relatively small fragments of DNA which may be de ⁇ ved by sequentially building the DNA sequence. Peptides may be synthesized from ammo acids.
- Unnatural biopolymers are chemical structure which are based on natural biopolymers, but which are built from unnatural linking units
- Unnatural biopolymers such as polythioureas and polyguamdmiums may be synthesized from diammes (I e , compounds which mclude at least two amine functional groups) These molecules are structurally similar to naturally occurring receptors, (e.g., peptides). Some diammes may, m turn, be synthesized from amino acids The use of ammo acids as the building blocks for these compounds allow a wide va ⁇ ety of molecular recognition units to be devised.
- the twenty natural ammo acids have side chams that possess hydrophobic residues, cationic and anionic residues, as well as hydrogen bonding groups. These side chams may provide a good chemical match to bmd a large number of targets, from small molecules to large ohgosacchandes Ammo acid based peptides, polythioureas, and polyguamdmiums are depicted m FIG. 10
- Removal of the protecting group is followed by couplmg of the ⁇ gid spacer 410 to the resulting amine 405 usmg diisopropylcarbodiimide (DIC) and 1-hydroxybenzotnazole hydrate (HOBT)
- the spacer group may inhibit formation of a thiazolone by reaction of the first ammo acids with subsequently formed thioureas
- another tBoc deprotection is performed to remove the spacer protecting group, givmg the amine 415
- monomer may be added incrementally to the growmg cham, each time followed by a tBoc deprotection.
- a denvative of the diamine 420 e.g , an lsothiocyanate
- amine 415 gives the mono-thiourea 425.
- a second thiourea substituent is also depicted.
- a solution of benzyhsothiocyanate or acetic anhydride may be added to cap any remaining amines on the growmg oligomers
- thioureas groups may be formed to produce a synthetic polythiourea receptor.
- polyguamdmiums may be accomplished as depicted m FIG. 12.
- the couplmg of a thiourea with a terminal amine m the presence of Mukaryama's reagent may be utilized
- the couplmg of the first thiourea diamine 430 with an ammo group of a polymenc particle gives the mono-guanidrnium 434
- Couplmg of the resulting mono-guanidinium with a second thiourea diamine 436 gives a di-guanidinium 438.
- Further couplmg may create a tn-guanidrnium 440.
- Between 1 to 20 guanidinium groups may be formed to produce a synthetic polyguanidinium receptor
- the above descnbed methods for making polythioureas and polyguamdmiums are based on the incorporation of diammes (l e , molecules which mclude at least two amine functional groups) mto the ohgomenc receptor.
- the method may be general for any compound having at least two amino groups.
- the diamine may be derived from amino acids.
- a method for forming diamines from amino acids is shown in FIG. 13.
- Treatment of a protected amino acid 450 with borane-THF reduces the carboxylic acid portion of the amino acid to the primary alcohol 452.
- the primary alcohol is treated with phmalimide under Mitsunobu conditions (PPh 3 /DEAD).
- the resulting compound 454 is treated with aqueous methylamine to form the desired monoprotected diamine 456.
- the process may be accomplished such that the enantiomeric purity of the starting amino acid is maintained. Any natural or synthetic amino acid may be used in the above described method.
- the three coupling strategies used to form the respective functional groups may be completely compatible with each other.
- the capability to mix linking groups (amides, thioureas, and guanidiniums) as well as the side chains (hydrophobic, cationic, anionic, and hydrogen bonding) may allow the creation of a diversity in the oligomers that is beyond the diversity of receptors typically found with natural biological receptors.
- these synthetic schemes may be used to build combinatorial libraries of particles for use in the sensor a ⁇ ay.
- the indicator ligand may be incorporated into synthetic receptors during the synthesis of the receptors.
- the ligand may be incorporated into a monomeric unit, such as a diamine, that is used during the synthesis of the receptor.
- the indicator may be covalently attached to the receptor in a controlled position.
- the positioning of the indicator ligand within the receptor may be controlled. This control may be difficult to achieve after synthesis of the receptor is completed.
- a fluorescent group may be incorporated into a mamine monomer for use in the synthetic sequences.
- Examples of monomeric units which may be used for the synthesis of a receptor are depicted in FIG. 14.
- the depicted monomers include fluorescent indicator groups.
- the interaction of the receptor with the analyte may induce changes in the spectroscopic properties of the molecule.
- hydrogen bonding or ionic substituents on the fluorescent monomer involved in analyte binding have the capacity to change the electron density and/or rigidity of the fluorescent ring system, thereby causing observable changes in the spectroscopic properties of the indicator.
- fluorescent indicators such changes may be exhibited as changes in the fluorescence quantum yield, maximum excitation wavelength, and/or maximum emission wavelength.
- two fluorescent monomers for signaling may be used for the synthesis of the receptor.
- compound 470 a derivative of fluorescein
- compound 475 a derivative of rhodamine
- FIG. 14 may both be incorporated into a synthetic receptor.
- Compound 470 contains a common colorimetric/fluorescent probe that will, in some embodiments, send out a modulated signal upon analyte binding. The modulation may be due to resonance energy transfer to compound 475.
- structural changes in the receptor may alter the distance between monomeric units 470 and 475.
- a large number of chemical/biological agents of interest to the military and civilian communities may be sensed readily by the described a ⁇ ay sensors including both small and medium size molecules.
- nerve gases typically produce phosphate structures upon hydrolysis in water.
- the presence of molecules which contain phosphate functional groups may be detected using polyguanidiniums.
- Nerve gases which have contaminated water sources may be detected by the use of the polyguanidinium receptors described above.
- bacteria may be detected as whole entities, as found in ground water, aerosols, or blood.
- the cell surface of one bacteria may be differentiated from other bacteria.
- One method of accomplishing this differentiation is to target cell surface oligosaccharides (i.e. sugar residues).
- Each bacterial class gram negative, gram positive, etc.
- the oligosaccharide which is the code that is read by other cells giving an identification of the cell, is part of the cell-cell recognition and communication process.
- the use of synthetic receptors which are specific for oligosaccharides may be used to determine the presence of specific bacteria by analyzing for the cell surface oligosaccharides.
- the senor a ⁇ ay may be used to optimize which receptor molecules should be used for a specific analyte.
- An a ⁇ ay of receptors may be placed within the cavities of the supporting member and a stream containing an analyte may be passed over the a ⁇ ay.
- the reaction of each portion of the sensing a ⁇ ay to the known analyte may be analyzed and the optimal receptor determined by determining which particle, and therefore which receptor, exhibits the strongest reaction toward the analyte. In this manner, a large number of potential receptors may be rapidly scanned.
- the optimal receptor may then be incorporated into a system used for the detection of the specific analyte in a mixture of analytes.
- the above descnbed sensor a ⁇ ay system offers a number of distinct advantages over exiting technologies
- One advantage is that "real time" detection of analytes may be performed
- Another advantage is that the simultaneous detection of multiple analytes may be realized
- the sensor a ⁇ ay system allows the use of synthetic reagents as well as biologically produced reagents
- Synthetic reagents typically have supe ⁇ or sensitivity and specificity toward analytes when compared to the biological reagents
- the sensor a ⁇ ay system may be readily modified by simply changing the particles which are placed within the sensor a ⁇ ay This lnterchangability may also reduce production costs
- FIG 15 Shown in FIG 15 is the magnitude of the optical signal transmitted through a smgle polymer particle de ⁇ vatized with o-cresolphthalem
- a filter is used to focus the analysis on those wavelengths which the dye absorbs most strongly (I e , about 550 nm)
- Data is provided for the particle as the pH is cycled between acid and basic environments In acidic media (I e , at times of 100-150 seconds and 180-210 seconds), the particle is clear and the system yields large signals (up to greater than 300,000 counts) at the optical detector
- the solution was made basic
- the particle turns purple m color and the transmitted green light is greatly diminished. Large signal reductions are recorded under such circumstances
- the evolution of the signal changes show that the response time is quite rapid, on the order of 10 seconds Furthermore, the behavior is highly reproducible
- PEG-PS polyethylene glycol-polystyrene
- the PEG-PS resm particles were obtamed from Novabiochem Corp , La Jolla, Ca The particles have an average diameter of about 130 ⁇ m when dry and about 250 ⁇ m when wet
- the indicator ligands of fluorescein, o-cresolphthalem complexone, and alizarin complexone were each attached to PEG-PS resm particles usmg a dicyclohexylcarbodnmide (DCC) couplmg between a terminal resm bound amine and a carboxylic acid on the mdicator ligand
- DCC dicyclohexylcarbodnmide
- the true power of the desc ⁇ bed bead sensor a ⁇ ay occurs when simultaneous evaluation of multiple chemically distinct bead structures is completed
- a demonstration of the capacity of five different beads is provided m FIG 16
- blank, alizarin, o-cresol phthalein, fluorescein, and al ⁇ za ⁇ n-Ce3+ complex de ⁇ vatized beads serve as a mat ⁇ x for subtle differentiation of chemical environments
- the blank bead is simply a polystyrene sphere with no chemical de ⁇ va ⁇ zation
- the bead de ⁇ vatized with o-cresolphthalem responds to Ca+2 at pHs values around 100
- the bmdmg of calcium is noted from the large green color attenuation noted for this dye while exposed to the cation
- the fluorescein denva ⁇ zed bead acts as a pH sensor At pHs below 74 it is light yellow, but at higher pHs it turns dark orange Interesting, the ahza ⁇ n complexone plays three distinct roles First,
- a series of receptors were prepared with functionalities that associate strongly with sugar molecules, as depicted in FIG. 9.
- a boronic acid sugar receptor 500 was utilized to demonstrate the functionality of a new type of sensing scheme in which competitive displacement of a resorufin derivatized galactose sugar molecule was used to assess the presence (or lack thereof) of other sugar molecules.
- the boromc acid receptor 500 was formed via a substitution reaction of a benzylic bromide.
- the boronic acid receptor was attached to a polyethylene glycol-polystyrene ("PEG-PS”) resin particle at the "R" position. Initially, the boronic acid derivatized particle was loaded with resorufin derivatized galactose 510.
- PEG-PS polyethylene glycol-polystyrene
- the resorufin derivatized galactose molecules 510 are displaced from the particle receptor sites.
- Visual inspection of the optical photographs taken before and after exposure to the sugar solution show that the boron substituted resin is capable of sequestering sugar molecules from an aqueous solution.
- the subsequent exposure of the colored particles to a solution of a non-tagged sugar e.g., glucose
- a non-tagged sugar e.g., glucose
- Displacement of this molecule leads to a change in the color of the particle.
- the sugar sensor turns from dark orange to yellow in solutions containing glucose.
- the particles were also tested in conditions of varying pH. It was noted that the color of the particles changes from dark orange to yellow as the pH is varied from low pH to high pH.
- the system includes a light source 512, a sensor a ⁇ ay 522, a chamber 550 for supporting the sensor a ⁇ ay and a detector 530.
- the sensor a ⁇ ay 522 may include a supporting member which is configured to hold a variety of particles.
- light originating from the light source 512 passes through the sensor array 522 and out through the bottom side of the sensor a ⁇ ay. Light modulated by the particles may be detected by a proximally spaced detector 530.
- the detector may be positioned above the sensor a ⁇ ay for reflectance measurements. Evaluation of the optical changes may be completed by visual inspection (e.g., by eye, or with the aid of a microscope) or by use of a microprocessor 540 coupled to the detector.
- the sensor array 522 is positioned within a chamber 550.
- the chamber 550 may be configured to allow a fluid stream to pass through the chamber such that the fluid stream interacts with the sensor array 522.
- the chamber may be constructed of glass (e.g, borosihcate glass or quartz) or a plastic mate ⁇ al which is transparent to a portion of the light from the light source.
- plastic matenals which may be used to form the chamber mclude, but are not limited to, acrylic resins, polycarbonates, polyester resins, polyethylenes, polyimides, polyvinyl polymers (e g , polyvinyl chlonde, polyvinyl acetate, polyvinyl dichlonde, polyvinyl fluonde, etc.), polystyrenes, polypropylenes, polytetrafluoroethylenes, and polyurethanes
- a Sykes-Moore chamber which is commercially available from Bellco Glass, Inc , m New Jersey Chamber 550, m one embodiment, mcludes a fluid mlet port 552 and a fluid outlet port 554.
- the fluid inlet 552 and outlet 554 ports are configured to allow a fluid stream to pass mto the mtenor 556 of the chamber during use
- the inlet and oudet ports may be configured to allow facile placement of a conduit for transferring the fluid to the chamber.
- the ports may be hollow conduits.
- the hollow conduits may be configured to have an outer diameter which is substantially equal to the inner diameter of a tube for transferring the fluid to or away from the chamber. For example, if a plastic or rubber tube is used for the transfer of the fluid, the internal diameter of the plastic tube is substantially equal to the outer diameter of the inlet and outlet ports.
- the inlet and oudet ports may be Luer lock style connectors.
- the inlet and outlet ports are female Luer lock connectors.
- the use of female Luer lock connectors will allow the fluid to be introduced via a syringe.
- syringes mclude a male Luer lock connector at the dispensing end of the syringe.
- Luer lock connectors may allow samples to be transfe ⁇ ed directly from a syringe to the chamber 550.
- Luer lock connectors may also allow plastic or rubber tubing to be connected to the chamber usmg Luer lock tubing connectors.
- the chamber may be configured to allow the passage of a fluid sample to be substantially confined to the mtenor 556 of the chamber. By confining the fluid to a small mtenor volume, the amount of fluid required for an analysis may be minimized
- the mtenor volume may be specifically modified for the desired application. For example, for the analysis of small volumes of fluid samples, the chamber may be designed to have a small mtenor chamber, thus reducmg the amount of fluid needed to fill the chamber. For larger samples, a larger mtenor chamber may be used. Larger chambers may allow a faster throughput of the fluid during use
- a system for detecting analytes in a fluid mcludes a light source 512, a sensor a ⁇ ay 522, a chamber 550 for supporting the sensor a ⁇ ay and a detector 530, all enclosed within a detection system enclosure 560.
- the sensor a ⁇ ay 522 is preferably formed of a supporting member which is configured to hold a va ⁇ ety of particles.
- an analyte detection system m a smgle enclosure may allow the formation of a portable detection system.
- a small controller 570 may be coupled to the analyte detection system.
- the controller 570 may be configured to mteract with the detector and display the results from the analysis.
- the controller mcludes a display device 572 for displaying information to a user.
- the controller may also mclude mput devices 574 (e.g., buttons) to allow the user to control the operation of the analyte detection system.
- the controller may control the operation of the light source 512 and the operation of the detector 530.
- the detection system enclosure 560 may be interchangeable with the controller. Coupling members 576 and 578 may be used to remove the detection system enclosure 560 from the controller 570. A second detection system enclosure may be readily coupled to the controller using coupling members 576 and 578. In this manner, a variety of different types of analytes may be detecting using a variety of different detection system enclosures.
- Each of the detection system enclosures may include different sensor arrays mounted within their chambers. Instead of having to exchange the sensor array for different types of analysis, the entire detection system enclosure may be exchanged. This may prove advantageous, when a variety of detection schemes are used. For example a first detection system enclosure may be configured for white light applications.
- the first detection system enclosure may include a white light source, a sensor that includes particles that produce a visible light response in the presence of an analyte, and a detector sensitive to white light.
- a second detection system enclosure may be configured for fluorescent applications, including a fluorescent light source, a sensor array which includes particles which produce a fluorescent response on the presence of an analyte, and a fluorescent detector.
- the second detection system enclosure may also include other components necessary for producing a proper detection system.
- the second detection system may also include a filter for preventing short wavelength excitation from producing "false" signals in the optical detection system during fluorescence measurements.
- a user need only select the proper detection system enclosure for the detection of the desired analyte. Since each detection system enclosure includes many of the required components, a user does not have to make light source selections, sensor array selections or detector arrangement selections to produce a viable detection system.
- the individual components of the system may be interchangeable.
- the system may include coupling members 573 and 575 that allow the light source and the detector, respectively, to be removed from the chamber 550.
- This may allow a more modular design of the system. For example, an analysis may be first performed with a white light source to give data co ⁇ esponding to an absorbance/reflectance analysis. After this analysis is performed the light source may be changed to a ultraviolet Ught source to allow ultraviolet analysis of the particles. Since the particles have already been treated with the fluid, the analysis may be preformed without further treatment of the particles with a fluid. In this manner a variety of tests may be performed using a single sensor array.
- the supporting member is made of any material capable of supporting the particles, while allowing the passage of the appropriate wavelength of light.
- the supporting member may also be made of a material substantially impervious to the fluid in which the analyte is present.
- materials may be used including plastics (e.g., photoresist materials, acrylic polymers, carbonate polymers, etc.), glass, silicon based materials (e.g., silicon, silicon dioxide, silicon nitride, etc.) and metals.
- the supporting member includes a plurality of cavities. The cavities are preferably formed such that at least one particle is substantially contained within the cavity. Alternatively, a plurality of particles may be contained within a single cavity.
- the particles are preferably held within cavities formed in a supporting member by the use of a transmission electron microscope ("TEM") grid.
- TEM transmission electron microscope
- a cavity 580 is formed in a supporting member 582.
- a TEM grid 586 may be placed atop the supporting member 582 and secured into position.
- TEM grids and adhesives for securing TEM grids to a support are commercially available from Ted Pella, Inc., Redding, CA.
- the TEM grid 586 may be made from a number of materials including, but not limited to, copper, nickel, gold, silver, aluminum, molybdenum, titanium, nylon, beryllium, carbon, and beryllium-copper.
- the mesh structure of the TEM grid may allow solution access as well as optical access to the particles that are placed in the cavities.
- FIG. 20 further depicts a top view of a sensor a ⁇ ay with a TEM grid 586 formed upon the upper surface of the supportmg member 582.
- the TEM grid 586 may be placed on the upper surface of the supporting member, trapping particles 584 within the cavities 580.
- the openings 588 in the TEM grid 586 may be sized to hold the particles 584 within the cavities 580, while allowing fluid and optical access to cavities 580.
- a sensor array in another embodiment, includes a supporting member configured to support the particles, while allowing the passage of the appropriate wavelength of light to the particle.
- the supporting member in one embodiment, includes a plurality of cavities. The cavities may be formed such that at least one particle is substantially contained within the cavity.
- the supporting member may be configured to substantially inhibit the displacement of the particles from the cavities during use.
- the supporting member may also be configured to allow the passage of the fluid through cavities, e.g., the fluid may flow from the top surface of the supporting member, past the particle, and out the bottom surface of the supporting member. This may increase the contact time between the particle and the fluid.
- Figures 21 A-G depict a sequence of processing steps for the formation of a sihcon based supporting member which includes a removable top cover and bottom cover.
- the removable top cover may be configured to allow fluids to pass through the top cover and into the cavity.
- the removable bottom cover may also be configured to allow the fluid to pass through the bottom cover and out of the cavity.
- a series of layers may be deposited upon both sides of a sihcon substrate 610.
- First removable layers 612 may be deposited upon the silicon substrate.
- the removable layers 612 may be sihcon dioxide, silicon nitride, or photoresist material. In one embodiment, a layer of silicon dioxide 612 is deposited upon both surfaces of the silicon substrate 610.
- covers 614 may be formed.
- covers 614 are formed from a material that differs from the material used to form the removable layers 612 and which is substantially transparent to the light source of a detection system.
- the removable layers 612 are formed from silicon dioxide, the cover may be formed from silicon nitride.
- Second removable layers 616 may be formed upon the covers 614.
- Second removable layers 616 may be formed from a material that differs from the material used to form the covers 614.
- Second removable layers 616 may be formed from a material similar to the material used to form the first removable layers 612.
- first and second removable layers 612 and 616 are formed from silicon dioxide and covers 614 are formed from sihcon nitride.
- the layers are patterned and etched using standard photolithographic techniques. In one embodiment, the remaining portions of the layers are substantially aligned in the position where the cavities are to be formed in the silicon substrate 610.
- spacer structures may be formed on the sidewalls of the first removable layers 612, the covers 614, and the second removable layers 616, as depicted in FIG. 21B.
- the spacer structures may be formed from the same material used to form the second removable layers 616.
- depositing a spacer layer of the appropriate material and subjecting the material to an anisotropic etch may form the spacer structures.
- An anisotropic etch such as a plasma etch, employs both physical and chemical removal mechanisms. Ions are typically bombarded at an angle substantially perpendicular to the semiconductor substrate upper surface. This causes substantially horizontal surfaces to be removed faster than substantially vertical surfaces.
- the spacer layers are preferably removed such that the only regions of the spacer layers that remain may be those regions near substantially vertical surfaces, e.g., spacer structures 618.
- cover support structures 620 may be formed.
- the cover support structures may be initially formed by depositing a support structure layer upon the second removable layer 616 and spacer structures 618.
- the support structure layer is then patterned and etched, using standard photolithography, to form the support structures 620.
- the support structures are formed from a material that differs from the removable layers material.
- the removable layers may be formed from silicon dioxide while the support structures and covers may be formed from silicon nitride.
- the second removable layers 616 and an upper portion of the spacer structures 618 are preferably removed using a wet etch process. Removal of the second removable layers leaves the top surface of the covers 614 exposed. This allows the covers to be patterned and etched such that openings 622 are formed extending through the covers. These openings 622 may be formed in the covers 614 to allow the passage of fluid through the cover layers. In one embodiment, the openings 622 are formed to allow fluid to pass through, while inhibiting displacement of the particles from the subsequently formed cavities.
- the remainder of the first removable layers 612 and the remainder of the spacer structures 618 may be removed using a wet etch.
- the removal of the removable layers and the spacer structures creates "floating" covers 614, as depicted in FIG. 21E.
- the covers 614 may be held in proximity to the silicon substrate 610 by the support structures 620.
- the covers 614 may now be removed by sliding the covers away from the support structures 620. In this manner removable covers 614 may be formed.
- cavities 640 may be formed in the silicon substrate 610, as depicted in FIG. 2 IF.
- the cavities 640 may be formed by, initially patterning and etching a photoresist material 641 to form a masking layer. After the photoresist material 641 is patterned, the cavities 640 may be etched into the sihcon substrate 610 using a hydroxide etch, as described previously.
- FIGS. 22 A-G depict a series of processing steps for the formation of a silicon based supporting member which includes a removable top cover and a secured bottom layer.
- the removable top cover is preferably configured to allow fluids to pass through the top cover and into the cavity. As depicted in FIG.
- a series of layers may be deposited upon both sides of a silicon substrate 610.
- a first removable layer 612 may be deposited upon the upper face 611 of the silicon substrate 610.
- the removable layer 612 may be silicon dioxide, silicon nitride, or photoresist material.
- a layer of silicon dioxide 612 is deposited upon the silicon substrate 610.
- a cover 614 may be formed upon the removable layer 612 of the silicon substrate 610.
- the cover 614 is formed from a material that differs from the material used to form the removable layer 612 and is substantially transparent to the light source of a detection system. For example, if the removable layer 612 is formed from silicon dioxide, the cover layer 614 may be formed from sihcon nitride.
- a bottom layer 615 is formed on the bottom surface 613 of the silicon substrate 610.
- the bottom layer 615 is formed from a material that is substantially transparent to the light source of a detection system.
- a second removable layer 616 may be formed upon the cover 614.
- Second removable layer 616 may be formed from a material that differs from the material used to form the cover layer 614.
- Second removable layer 616 may be formed from a material similar to the material used to form the first removable layer 612.
- first and second removable layers 612 and 616 are formed from silicon dioxide and cover 614 is formed from silicon nitride.
- the layers formed on the upper surface 611 of the sihcon substrate may be patterned and etched using standard photolithographic techniques. In one embodiment, the remaining portions of the layers formed on the upper surface are substantially aligned in the position where the cavities are to be formed in the silicon substrate 610.
- spacer structures may be formed on the side walls of the first removable layer 612, the cover 614, and the second removable layer 616, as depicted in FIG. 22B.
- the spacer structures may be formed from the same material used to form the second removable layer 616.
- the spacer structures may be formed by depositing a spacer layer of the appropriate material and subjecting the spacer layer to an anisotropic etch. During this etching procedure the spacer layer is preferably removed such that the only regions of the spacer layer which remain may be those regions near substantially vertical surfaces, e.g., spacer structures 618.
- cover support structures 620 may be formed upon the removable layer 616 and the spacer structures 618.
- the cover support structures 620 may be formed by depositing a support structure layer upon the second removable layer 616 and spacer structures 618.
- the support structure layer is then patterned and etched, using standard photolithography, to form the support structures 620.
- the support structures are formed from a material that differs from the removable layer materials.
- the removable layers may be formed from sihcon dioxide while the support structures and cover may be formed from sihcon nitride.
- the second removable layer 616 and an upper portion of the spacer structures 618 may be removed using a wet etch process. Removal of the second removable layer leaves the top surface of the cover 614 exposed. This allows the cover 614 to be patterned and etched such that openings 622 are formed extending through the cover 614. These openings 622 may be formed in the cover 614 to allow the passage of fluid through the cover. In one embodiment, the openings 622 are formed to allow fluid to pass through, while inhibiting displacement of the particle from a cavity.
- the bottom layer 615 may also be similarly patterned and etched such that openings 623 may be formed extending thorough the bottom layer 615.
- the first removable layer 612 and the remainder of the spacer structures 618 may be removed using a wet etch.
- the removal of the removable layers and the spacer structures creates a "floating" cover 614, as depicted in FIG. 22E.
- the cover 614 may be held in proximity to the sihcon substrate 610 by the support structures 620.
- the cover 614 may now be removed by sliding the cover 614 away from the support structures 620. In this manner a removable cover 614 may be formed.
- cavities 640 may be formed in the silicon substrate 610, as depicted in FIG. 22F.
- the cavities 640 may be formed by, initially patterning and etching a photoresist material 641 to form a masking layer. After the photoresist material 614 is patterned, the cavities 640 may be etched into the silicon substrate 610 using a hydroxide etch, as described previously.
- the photoresist material may be removed and particles 642 may be placed within the cavities, as depicted in FIG. 22G.
- the particles 642 may be inhibited from being displaced from the cavity 640 by placing cover 614 back onto the upper face 611 of the sihcon substrate 610.
- the bottom layer 615 may also aid in inhibiting the particle 642 from being displaced from the cavity 640. Openings 622 in cover 614 and openings 623 in bottom layer 615 may allow fluid to pass through the cavity during use.
- a sensor array may be formed using a supporting member and a removable cover.
- FIGS. 23 A-G depict a series of processing steps for the formation of a silicon based supporting member which includes a removable cover.
- the removable cover is preferably configured to allow fluids to pass through the cover and into the cavity.
- a series of layers may be deposited upon the upper surface 611 of a silicon substrate 610.
- a first removable layer 612 may be deposited upon the upper face 611 of the silicon substrate 610.
- the removable layer 612 may be sihcon dioxide, silicon nitride, or photoresist material.
- a layer of silicon dioxide 612 is deposited upon the silicon substrate 610.
- a cover 614 may be formed upon the removable layer 612.
- the cover is formed from a material which differs from the material used to form the removable layer 612 and which is substantially transparent to the light source of a detection system.
- the removable layer 612 is formed from sihcon dioxide
- the cover 614 may be formed from silicon nitride.
- a second removable layer 616 may be formed upon the cover 614.
- Second removable layer 616 may be formed from a material that differs from the material used to form the cover 614.
- Second removable layer 616 may be formed from a material similar to the material used to form the first removable layer 612.
- first and second removable layers 612 and 616 are formed from silicon dioxide and cover 614 is formed from silicon nitride.
- the layers formed on the upper surface 611 of the sihcon substrate may be patterned and etched using standard photolithographic techniques. In one embodiment, the remaining portions of the layers formed on the upper surface are substantially aligned in the position where the cavities are to be formed in the silicon substrate 610.
- spacer structures 618 may be formed on the side walls of the first removable layer 612, the cover layer 614, and the second removable layer 616, as depicted in FIG. 23B.
- the spacer structures 618 may be formed from the same material used to form the second removable layer 616.
- the spacers may be formed by depositing a spacer layer of the appropriate material upon the second removable layer and subjecting the material to an anisotropic etch. During this etching procedure the spacer layer is preferably removed such that the only regions of the spacer layer which remain may be those regions near substantially vertical surfaces, e.g., spacer structures 618.
- cover support structures 620 may be formed upon the removable layer 616 and the spacer structures 618.
- the cover support structure may be formed by initially depositing a support structure layer upon the second removable layer 616 and spacer structures 618.
- the support structure layer is then patterned and etched, using standard photolithography, to form the support structures 620.
- the support structures 620 are formed from a material that differs from the removable layer materials.
- the removable layers may be formed from sihcon dioxide while the support structure and cover layer may be formed from sihcon nitride. Turning to FIG.
- the second removable layer 616 and an upper portion of the spacer structures 618 may be removed usmg a wet etch process Removal of the second removable layer leaves the top surface of the cover 614 exposed This allows the cover 614 to be patterned and etched such that openmgs 622 are formed extendmg through the cover 614 These openmgs 622 may be formed m the cover 614 to allow the passage of flmd through the cover 614
- the remainder of the first removable layer 612 and the remainder of the spacer structures 618 may be removed usmg a wet etch
- the removal of the removable layers and the spacer structures creates a "floating" cover 614, as depicted in FIG. 23E
- the cover 614 is preferably held in proximity to the sihcon substrate 610 by the support structures 620.
- the cover 614 may now be removed by sliding the cover 614 away from the support structures 620 In this manner a removable cover 614 may be formed
- cavities 640 may be formed m the silicon substrate 610, as depicted in FIG. 23F
- the cavities 640 may be formed by initially depositing and patterning a photoresist mate ⁇ al 641 upon the silicon support 610
- the cavities 640 may be etched mto the sihcon substrate 610 usmg a hydroxide etch, as desc ⁇ bed previously
- the etchmg of the cavities may be accomphshed such that a bottom width of the cavity 643 is less than a width of a particle 642.
- the width of the bottom of the cavity may be controlled by varying the etch time.
- the photoresist mate ⁇ al may be removed and particles 642 may be placed within the cavities, as depicted m FIG.23G
- the particles 642 may be inhibited from bemg displaced from the cavity 640 by placing cover 614 back onto the upper face 611 of the sihcon substrate 610
- the na ⁇ ow bottom portion of the cavity may also aid m inhibiting the particle 642 from bemg displaced from the cavity 640
- Figures 24A-d depict a sequence of processmg steps for the formation of a sihcon based supporting member which mcludes a top partial cover and a bottom partial cover
- the top partial cover and bottom partial covers are, m one embodiment, configured to allow fluids to pass mto the cavity and out through the bottom of the cavity.
- a bottom layer 712 may be deposited onto the bottom surface of a sihcon substrate 710.
- the bottom layer 712 may be sihcon dioxide, silicon mtnde, or photoresist mate ⁇ al
- a layer of silicon mtnde 712 is deposited upon the silicon substrate 710.
- openmgs 714 are formed through the bottom layer as depicted m FIG 24A. Openmgs 714, in one embodiment, are substantially aligned with the position of the cavities to be subsequently formed.
- the openmgs 714 may have a width that is substantially less than a width of a particle. Thus a particle will be inhibited from passmg through the openmgs 714.
- Cavities 716 may be formed m the sihcon substrate 710, as depicted m FIG.24B
- the cavities 716 may be formed by initially depositing and patterning a photoresist layer upon the sihcon substrate 710 After the photoresist mate ⁇ al is patterned, cavities 716 may be etched mto the silicon substrate 710 usmg a number of etchmg techniques, including wet and plasma etches
- the width of the cavities 716 is preferably greater than the width of a particle, thus allowmg a particle to be placed within each of the cavities.
- the cavities 716, m one embodiment, are preferably formed such that the cavities are substantially aligned over the openings 714 formed in the bottom layer.
- particles 718 may be inserted into the cavities 716, as depicted in FIG. 24C.
- the etched bottom layer 712 may serve as a support for the particles 718.
- the openings 714 in the bottom layer 712 may allow fluid to pass through the bottom layer during use.
- a top layer 720 may be placed upon the upper surface 717 of the sihcon substrate.
- the top layer 720 is formed from a material is substantially transparent to the Ught source of a detection system.
- the top layer may be formed from siUcon nitride, sihcon dioxide or photoresist material. In one embodiment, a sheet of photoresist material is used.
- openings 719 may be formed in the top layer to aUow the passage of the fluid into the cavities.
- the openings may be initially formed by exposing the photoresist material to the appropriate wavelength and pattern of light. If the top layer is compose of siUcon dioxide or silicon nitride the top layer 720 may be developed by forming a photoresist layer upon the top layer, developing the photoresist, and using the photoresist to etch the underlying top layer.
- Similar sensor a ⁇ ays may be produced using materials other than siUcon for the supporting member.
- the supporting member may be composed of photoresist material.
- sheets of photoresist film may be used to form the supporting member.
- Photoresist film sheets are commercially available from E. I. du Pont de Nemours and Company, Wilmington, DE under the commercial name RISTON. The sheets come in a variety of sizes, the most common having a thickness ranging from about 1 mil. (25 ⁇ m) to about 2 mil. (50 ⁇ m).
- a first photoresist layer 722 is developed and etched such that openings 724 are formed.
- the openings may be formed proximate the location of the subsequently formed cavities.
- the openings have a width that is substantially smaUer than a width of the particle.
- the openings may inhibit displacement of the particle from a cavity.
- a main layer 726 is formed upon the bottom layer.
- the main layer 720 is preferably formed from a photoresist film that has a thickness substantially greater than a typical width of a particle.
- a main layer may be composed of a 50 ⁇ m photoresist material.
- the photoresist layer may be composed of a multitude of photoresist layers placed upon each other until the desired thickness is achieved, as will be depicted in later embodiments.
- the main photoresist layer may be patterned and etched to form the cavities 728, as depicted in FIG. 25B.
- the cavities in one embodiment, are substantially aligned above the previously formed openings 724.
- Cavities 728 in one embodiment, have a width which is greater than a width of a particle.
- the photoresist material is substantially transparent to the light source used.
- the photoresist material used for the main supporting layer may be substantially transparent to the light used by the light source.
- the transparent nature of the supporting member may allow light from the cavity to migrate, through the supporting member, into a second cavity. This leakage of light from one cavity to the next may lead to detection problems. For example, if a first particle in a first cavity produces a fluorescent signal in response to an analyte, this signal may be transmitted through the supporting member and detected in a proximate cavity. This may lead to inaccurate readings for the proximately spaced cavities, especially if a particularly strong signal is produced by the interaction of the particle with an analyte.
- a substantially reflective layer 730 may be formed along the inner surface of the cavity.
- the reflective layer 730 is composed of a metal layer which is formed on the upper surface of the main layer and the inner surface of the cavity.
- the metal layer may be deposited using chemical vapor deposition or other known techniques for depositing thin metal layers.
- the presence of a reflective layer may inhibit "cross-talk" between the cavities.
- the first photoresist layer 722 may serve as a support for the particles 718.
- the particles may be inhibited from being displaced from the cavities by the first photoresist layer 722.
- the openings 724 in the first photoresist layer 722 may allow fluid to pass through the bottom layer during use.
- a top photoresist layer 732 may be placed upon the upper surface of the silicon substrate.
- openings 734 may be formed in the cover layer to allow the passage of the fluid into the cavities.
- the supporting member may be formed from a plastic substrate, as depicted in FIG. 26A-D.
- the plastic substrate is composed of a material which is substantially resistant to the fluid which includes the analyte.
- plastic materials which may be used to form the plastic substrate include, but are not limited to, acrylic resins, polycarbonates, polyester resins, polyethylenes, polyimides, polyvinyl polymers (e.g., polyvinyl chloride, polyvinyl acetate, polyvinyl dichloride, polyvinyl fluoride, etc.), polystyrenes, polypropylenes, polytetrafluoroethylenes, and polyurethanes.
- the plastic substrate may be substantially transparent or substantially opaque to the light produced by the Ught source.
- a series of cavities 742 may be formed in the plastic material.
- the cavities 740 may be formed by driUing (either mechanically or with a laser), transfer molding (e.g., forming the cavities when the plastic material is formed using appropriately shaped molds), or using a punching apparatus to punch cavities into the plastic material.
- the cavities 740 are formed such that a lower portion 743 of the cavities is substantially na ⁇ ower than an upper portion 744 of the cavities.
- the lower portion 743 of the cavities may have a width substantially less than a width of a particle.
- the lower portion 743 of the cavities 740 may inhibit the displacement of a particle from the cavity 740. While depicted as rectangular, with a na ⁇ ower rectangular opening at the bottom, it should be understood that the cavity may be formed in a number of shapes including but not limited to pyramidal, triangular, trapezoidal, and oval shapes. An example of a pyramidal cavity which is tapered such that the particle is inhibited from being displaced from the cavity is depicted in FIG. 25D.
- particles 718 may be inserted into the cavities 742, as depicted in FIG. 26B.
- the lower portion 743 of the cavities may serve as a support for the particles 718.
- the particles 718 may be inhibited from being displaced from the cavities 742 by the lower portion 743 of the cavity.
- a cover 744 may be placed upon the upper surface 745 of the plastic substrate 740, as depicted in FIG. 26C.
- the cover is formed from a film of photoresist material. After the cover 744 is placed on the plastic substrate 740, openings 739 may be formed in the cover layer to allow the passage of the fluid into the cavities.
- a substantially transparent plastic material may be used.
- a transparent supporting member may lead to "cross-talk" between the cavities.
- a substantially reflective layer 748 may be formed on the inner surface 746 of the cavity, as depicted in FIG. 26E.
- the reflective layer 748 is composed of a metal layer which is formed on the inner surface of the cavities 742.
- the metal layer may be deposited using chemical vapor deposition or other techniques for depositing thin metal layers.
- the presence of a reflective layer may inhibit cross-talk between the cavities.
- a silicon based supporting member for a sensing particle may be formed without a bottom layer.
- FIG. 27A-D depicts the formation of a supporting member from a silicon substrate.
- a photoresist layer 750 is formed upon an upper surface of a silicon substrate 752, as depicted in FIG. 27A.
- the photoresist layer 750 may be patterned and developed such that the regions of the silicon substrate in which the cavities will be formed are exposed.
- Cavities 754 may now be formed, as depicted in FIG. 27B, by subjecting the silicon substrate to an anisotropic etch.
- a potassium hydroxide etch is used to produced tapered cavities. The etching may be controlled such that the width of the bottom of the cavities 750 is less than a width of the particle.
- a particle 756 may be inserted into the cavities 754 as depicted in FIG. 27C. The particle 756 may be inhibited from passing out of the cavities 754 by the na ⁇ ower bottom portion of the cavities.
- a cover 758 may be formed upon the siUcon substrate 752, as depicted in FIG. 27D.
- the cover may be formed of any material substantially transparent to the light produced by the Ught source used for analysis. Openings 759 may be formed in the cover 758 to aUow the fluid to pass into the cavity from the top face of the supporting member 752. The openings 759 in the cover and the opening at the bottom of the cavities 754 together may allow fluid to pass through the cavity during use.
- a supporting member for a sensing particle may be formed from a plurality of layers of a photoresist material.
- the cavity may be tapered to inhibit the passage of the particle from the cavity, through the bottom of the supporting member.
- FIGS. 28A-E depict the formation of a supportmg member from a plurality of photoresist layers.
- a first photoresist layer 760 is developed and etched to form a series of openings 762 which are positioned at the bottom of subsequently formed cavities, as depicted in FIG. 28A.
- a second layer of photoresist material 764 may be formed upon the first photoresist layer 760.
- the second photoresist layer may be developed and etched to form openings substantially aligned with the openings of the first photoresist layer 760.
- the openings formed in the second photoresist layer 764 in one embodiment, are substantially larger than the layers formed in the first photoresist layer 760. In this manner, a tapered cavity may be formed while using multiple photoresist layers.
- additional layers of photoresist material 766 and 768 may be formed upon the second photoresist layer 764.
- the openings of the additional photoresist layers 766 and 768 may be progressively larger as each layer is added to the stack. In this manner, a tapered cavity may be formed.
- Additional layers of photoresist material may be added until the desired thickness of the supporting member is obtained.
- the thickness of the supporting member in one embodiment, is greater than a width of a particle. For example, if a layer of photoresist material has a thickness of about 25 ⁇ m and a particle has a width of about 100 ⁇ m, a supporting member may be formed from four or more layers of photoresist material.
- the cavity may be formed in a number of different shapes, including but not limited to, rectangular, circular, oval, triangular, and trapezoidal. Any of these shapes may be obtained by appropriate patterning and etching of the photoresist layers as they are formed.
- the photoresist material may be substantially transparent to the light produced by the light source.
- a substantially reflective layer 770 may be formed along the inner surface of the cavities 762, as depicted in FIG. 28D.
- the reflective layer is composed of a metal layer which is formed on the inner surface of the cavities 762. The metal layer may be deposited using chemical vapor deposition or other techniques for depositing thin metal layers. The presence of a reflective layer may inhibit "cross-talk" between the cavities.
- particles 772 may be inserted into the cavities 762, as depicted in FIG. 28D.
- the na ⁇ ow portions of the cavities 762 may serve as a support for the particles 772.
- the particles 772 may be inhibited from being displaced from the cavities 762 by the lower portion of the cavities.
- a cover 774 may be placed upon the upper surface of the top layer 776 of the supporting member, as depicted in FIG. 28E.
- the cover 774 is also formed from a film of photoresist material. After the cover layer is formed, openings 778 may be formed in the cover 774 to allow the passage of the fluid into the cavities.
- a supporting member for a sensing particle may be formed from photoresist material which includes a particle support layer.
- a first photoresist layer 780 is developed and etched to form a series of openings 782 which may become part of subsequently formed cavities.
- a cavity having the appropriate depth may be formed by forming multiple layers of a photoresist material, as described previously.
- a second photoresist layer 784 may be formed upon the first photoresist layer 780.
- the second photoresist layer 784 may be patterned to form openings substantially aligned with the openings of the first photoresist layer 782.
- the openings formed in the second photoresist layer 784 may be substantially equal in size to the previously formed openings. Alternatively, the openings may be variable in size to form different shaped cavities.
- a substantially reflective layer 786 may be formed along the inner surface of the cavities 782 and the upper surface of the second photoresist layer 784, as depicted in FIG. 29C.
- the reflective layer is composed of a metal layer.
- the metal layer may be deposited using chemical vapor deposition or other techniques for depositing thin metal layers. The presence of a reflective layer may inhibit "cross-talk" between the cavities.
- a particle support layer 788 may be formed on the bottom surface of the first photoresist layer 780, as depicted in FIG. 29D.
- the particle support layer 788 may be formed from photoresist material, silicon dioxide, silicon nitride, glass or a substantially transparent plastic material.
- the particle support layer 788 may serve as a support for the particles placed m the cavities 782.
- the pamcle support layer, m one embodiment, is formed from a matenal that is substantially transparent to the light produced by the hght source.
- the particle support layer 788 may serve as a support for the particles
- the particles 785 may be inhibited from bemg displaced from the cavities by the particle support layer 788
- a cover 787 may be placed upon the upper surface of the second photoresist layer 784, as depicted in FIG 29E
- the cover is also formed from a film of photoresist mate ⁇ al
- openmgs 789 may be formed m the cover 787 to aUow the passage of the fluid mto the cavities
- the fluid is inhibited from flowing through the supporting member. Instead, the fluid may flow mto and out of the cavities via the openmgs 789 formed m the cover 787
- a similar supporting member may be formed from a plastic mate ⁇ al, as depicted m FIGS. 30A-D
- the plastic matenal may be substantially resistant to the fluid which mcludes the analyte
- the plastic mate ⁇ al may be substantially transparent or substantially opaque to the light produced by the light source
- a senes of cavities 792 may be formed m the plastic substrate 790
- the cavities may be formed by d ⁇ lling (either mechanically or with a laser), transfer moldmg (e.g , forming the cavities when the plastic substrate is formed usmg appropnately shaped molds), or usmg a punching machine to form the cavities.
- the cavities extend through a portion of the plastic substrate, terminating proximate the bottom of the plastic substrate, without passmg through the plastic substrate.
- particles 795 may be inserted mto the cavities 792, as depicted m FIG. 30B.
- the bottom of the cavity may serve as a support for the particles 795
- a cover 794 may be placed upon the upper surface of the plastic substrate 790, as depicted m FIG. 30C.
- the cover may be formed from a film of photoresist mate ⁇ al.
- openmgs 796 may be formed m the cover to allow the passage of the fluid mto the cavities While depicted as rectangular, is should be understood that the cavities may be formed m a vanety of different shapes, including tnangular, pyramidal, pentagonal, polygonal, oval, or circular. It should also be understood that cavities havmg a va ⁇ ety of different shapes may be formed mto the same plastic substrate, as depicted m FIG. 30D
- a senes of channels may be formed m the supporting member interconnecting some of the cavities, as depicted m FIG. 3
- Pumps and valves may also be incorporated mto the supporting member to aid passage of the fluid through the cavities
- a schematic figure of a diaphragm pump 800 is depicted m FIG. 31
- Diaphragm pumps, m general, m clude a cavity 810, a flexible diaphragm 812, an mlet valve 814, and an outlet valve 816.
- the flexible diaphragm 812 durmg use, is deflected as shown by a ⁇ ows 818 to create a pumping force
- a ⁇ ows 818 As the diaphragm is deflected toward the cavity 810 it may cause the mlet valve 814 to close, the outlet valve 816 to open and any liquid which is m the cavity 810 will be forced toward the outlet 816.
- the outlet valve 816 As the diaphragm moves away from the cavity 810, the outlet valve 816 may be pulled to a closed position, and the mlet valve 814 may be opened, allowmg additional fluid to enter the cavity 810 In this manner a pump may be used to pump fluid through the cavities.
- the pump depicted m FIG 31 is a generalized version of a diaphragm based pump.
- the diaphragm 810 may be made from a piezoelectric material. This material will contract or expand when an appropriate voltage is applied to the diaphragm. Pumps using a piezoelectric diaphragms are described in U.S. Patent Nos. 4,344,743, 4,938,742, 5,611,676, 5,705,018, and 5,759,015, all of which are incorporated by reference.
- the diaphragm may be activated using a pneumatic system.
- an air system may be coupled to the diaphragm such that changes in air density about the diaphragm, induced by the pneumatic system, may cause the diaphragm to move toward and away from the cavity.
- a pneumatically controlled pump is described in United States Patent No. 5,499,909 which is incorporated by reference.
- the diaphragm may also be controlled using a heat activated material.
- the diaphragm may be formed from a temperature sensitive material.
- the diaphragm may be formed from a material which is configured to expand and contract in response to temperature changes.
- a pump system which relies on temperature activated diaphragm is described in United States Patent No. 5,288,214 which is incorporated by reference.
- FIG. 32 depicts a typical electrode based system.
- a series of electrodes 820 may be a ⁇ anged along a channel 822 which may lead to a cavity 824 which includes a particle 826. By varying the voltage in the electrodes 820 a current flow may be induced in the fluid within the channel 822.
- Examples of electrode based systems include, but are not limited to, electroosmosis systems, electrohydrodynamic systems, and combinations of electroosmosis and electrohydrodynamic systems.
- Electrohydrodynamic pumping of fluids is known and may be appUed to smaU capillary channels.
- electrodes are typically placed in contact with the fluid when a voltage is applied. The applied voltage may cause a transfer in charge either by transfer or removal of an electron to or from the fluid. This electron transfer typically induces liquid flow in the direction from the charging electrode to the oppositely charged electrode.
- Electrohydrodynamic pumps may be used for pumping fluids such as organic solvents.
- Electroosmosis is a process which involves applying a voltage to a fluid in a small space, such as a capillary channel, to cause the fluid to flow.
- a voltage to a fluid in a small space, such as a capillary channel.
- the surfaces of many solids, including quartz, glass and the like become variously charged, negatively or positively, in the presence of ionic materials, such as for example salts, acids or bases.
- the charged surfaces will attract oppositely charged (positive or negative) counterions in aqueous solutions.
- the application of a voltage to such a solution results in a migration of the counterions to the oppositely charged electrode, and moves the bulk of the fluid as well.
- the volume flow rate is proportional to the cu ⁇ ent, and the volume flow generated in the fluid is also proportional to the applied voltage.
- electroosmosis pumps and electrohydrodynamic pumps may be used. Wire electrodes may be inserted into the walls of a channel at preselected intervals to form alternating electroosmosis and electrohydrodynamic devices. Because electroosmosis and electrohydrodynamic pumps are both present, a plurality of different solutions, both polar and non-polar, may be pump along a single channel. Alternatively, a plurality of different solutions may be passed along a plurality of different channels connected to a cavity.
- a system which includes a combination of electroosmosis pumps and electrohydrodynamic pumps is described in United States Patent No. 5,632,876 which is incorporated by reference.
- a pump may be incorporated into a sensor array system, as depicted in FIG. 32.
- a sensor a ⁇ ay 830 includes at least one cavity 832 in which a particle 834 may be placed.
- the cavity 832 may be configured to allow fluid to pass through the cavity during use.
- a pump 836 may be incorporated onto a portion of the supporting member 838
- a channel 831 may be formed m the supporting member 838 couplmg the pump 836 to the cavity 832
- the channel 831 may be configured to allow the fluid to pass from the pump 836 to the cavity 832
- the pump 836 may be positioned away from the cavity 832 to allow light to be directed through the cavity durmg use
- the supporting member 838 and the pump 836 may be formed from a sihcon substrate, a plastic mate ⁇ al, or photoresist matenal
- the pump 836 may be configured to pump fluid to the cavity via the channel, as depicted by the a ⁇ ows m FIG 32 When the fluid reaches the cavity 832, the fluid may flow past the particle 834 and out through the bottom of the cavity
- An advantage of usmg pumps is that better flow through the channels may be achieved Typically, the channels and cavities may have a small volume The small volume of the cavity and channel tends to inhibit flow of the fluid through the cavity By
- a pump may be coupled to a supporting member for analyzing analytes m a flmd stream, as depicted in FIG 34
- a channel 842 may couple a pump 846 to multiple cavities 844 formed m a supporting member 840
- the cavities 842 may mclude sensmg particles 848
- the pump may be configured to create a flow of the fluid through the channel 842 to the cavities 848
- the cavities may inhibit the flow of the fluid through the cavities 844
- the fluid may flow mto the cavities 844 and past the particle 848 to create a flow of fluid through the sensor a ⁇ ay system In this manner a smgle pump may be used to pass the fluid to multiple cavities While a diaphragm pump system is depicted m FIG 33, it should be understood that electrode pumping systems may also be incorporated mto the supporting member to create similar fluid flows
- multiple pumps may be coupled to a supporting member of a sensor a ⁇ ay system
- the pumps may be coupled m senes with each other to pump flmd to each of the cavities.
- a first pump 852 and a second pump 854 may be coupled to a supporting member 850
- the first pump 852 may be coupled to a first cavity 856
- the first pump may be configured to transfer fluid to the first cavity 856 durmg use
- the cavity 856 may be configured to allow the fluid to pass through the cavity to a first cavity outlet channel 858
- a second pump 854 may also be coupled to the supporting member 850
- the second pump 854 may be coupled to a second cavity 860 and the first cavity outlet channel 858
- the second pump 854 may be configured to transfer fluid from the first cavity outlet channel 858 to the second cavity 860
- the pumps may be synchronized such that a steady flow of fluid through the cavities is obtamed Additional pumps may be coupled to the second cavity outlet channel 862 such that the fluid may be pumped
- multiple electrode based pumps may be incorporated mto the sensor a ⁇ ay system
- the pumps may be formed along the channels which couple the cavities
- a plurality of cavities 870 may be formed in a supportmg member 872 of a sensor array
- Channels 874 may also be formed the supporting member 872 interconnecting the cavities 870 with each other
- An inlet channel 876 and an outlet channel 877, which allow the fluid to pass mto and out of the sensor a ⁇ ay, respectively, may also be formed
- a senes of electrodes 878 may be positioned over the channels 874, 876, and 877
- the electrodes may be used to form an electroosmosis pumpmg system or an electrohydrodynamic pumping system
- the electrodes may be coupled to a controller 880 which may apply the approp ⁇ ate voltage to the appropnate electrodes to produce a flow of the fluid through the channels
- the pumps may be synchronized such that a steady flow of fluid through the cavities is obtamed
- the second pump may be stopped and the fluid may be introduced to the first cavity
- the first pump may be used to transfer the fluid to the first cavity.
- the second pump may remam off, thus inhibiting flow of fluid from the reservoir to the first cavity.
- the reagent solution may be added to the first cavity while the fluid is added to the first cavity
- both the first and second pumps may be operated substantially simultaneously.
- the reagent may be added after an analysis.
- a particle may mteract with an analyte such that a change m the receptors attached to the first particle occurs. This change may not, however produce a detectable signal.
- the reagent attached to the second bead may be used to produce a detectable signal when it interacts with the first particle, if a specific analyte is present.
- the fluid is introduced mto the cavity first. After the analyte has been given time to react with the particle, the reagent may be added to the first cavity.
- the mteraction of the reagent with the particle may produce a detectable signal
- an mdicator reagent may react with a particle which has been exposed to an analyte to produce a color change on the particle Particle which have not been exposed to the analyte may remain unchanged or show a different color change.
- a system for detecting analytes m a fluid may mclude a light source 110, a sensor a ⁇ ay 120 and a detector 130.
- the sensor a ⁇ ay 120 is preferably formed of a supporting member which is configured to hold a vanety of particles 124 m an ordered a ⁇ ay
- a high sensitivity CCD a ⁇ ay may be used to measure changes m optical characte ⁇ stics which occur upon bmdmg of the biological/chemical agents.
- Data acquisition and handling is preferably performed with existing CCD technology.
- colo ⁇ metnc analysis may be performed usmg a white light source and a color CCD detector.
- color CCD detectors are typically more expensive than gray scale CCD detectors.
- a gray scale CCD detector may be used to detect colo ⁇ metnc changes.
- a gray scale detector may be disposed below a sensor a ⁇ ay to measure the intensity of light bemg transmitted through the sensor a ⁇ ay.
- a senes of lights e g., light emitting diodes
- groups of three LED lights may be a ⁇ anged above each of the cavities of the a ⁇ ay. Each of these groups of LED lights may mclude a red, blue and a green light. Each of the lights may be operated individually such that one of the lights may be on while the other two lights are off.
- each of the lights is sequentiaUy tumed on and the gray scale detector is used to measure the intensity of the hght passmg through the sensor a ⁇ ay After information from each of the lights is collected, the information may be processed to denve the absorption changes of the particle
- the data collected by the gray scale detector may be recorded usmg 8 bits of data.
- the data will appear as a value between 0 and 255
- the color of each chemical sensitive element may be represented as a red, blue and green value.
- a blank particle i.e., a particle which does not mclude a receptor
- the CCD detector will record a value co ⁇ espondmg to the amount of light transmitted through the cavity. The intensity of the light may be compared to a blank particle, to determine the absorbance of a particle with respect to the LED light which is used.
- the red, green and blue components may be recorded individually without the use of a color CCD detector
- a blank particle exhibits an absorbance of about 253 when illuminated with a red LED, a value of about 250 when illuminated by a green LED, and a value of about 222 when illuminated with a blue LED
- the particle may exhibit a color change, due to absorbance by the receptor
- the gray scale CCD detector may detect a value of about 254
- the gray scale detector may detect a value of about 218
- a gray scale detector may detect a value of about 57
- a particle may be positioned at the bottom of a cavity usmg a micromampulator This allows the location of a particular particle to be precisely controlled durmg the production of the a ⁇ ay
- the use of a micromampulator may, however, be impractical for production of sensor a ⁇ ay systems
- An alternate method of placmg the particles mto the cavities may mvolve the use of a silk screen like process
- a senes of masking matenals may be placed on the upper surface of the sensor a ⁇ ay p ⁇ or to filling the cavities
- the masking matenals may be composed of glass, metal or plastic matenals
- a collection of particles may be placed upon the upper surface of the masking matenals and the particles may be moved across the surface When a cavity is encountered, a particle may drop mto the cavity if the cavity is unmasked
- the masking pattern may be
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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EP99938752A EP1097369A1 (en) | 1998-07-16 | 1999-07-16 | Sensor arrays for the measurement and identification of multiple analytes in solutions |
AU53165/99A AU770949B2 (en) | 1998-07-16 | 1999-07-16 | Sensor arrays for the measurement and identification of multiple analytes in solutions |
CA002337155A CA2337155A1 (en) | 1998-07-16 | 1999-07-16 | Sensor arrays for the measurement and identification of multiple analytes in solutions |
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US09/287,248 US6908770B1 (en) | 1998-07-16 | 1999-04-07 | Fluid based analysis of multiple analytes by a sensor array |
US09/287,248 | 1999-04-07 |
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WO2000004372A1 true WO2000004372A1 (en) | 2000-01-27 |
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PCT/US1999/016162 WO2000004372A1 (en) | 1998-07-16 | 1999-07-16 | Sensor arrays for the measurement and identification of multiple analytes in solutions |
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US (4) | US6908770B1 (en) |
EP (1) | EP1097369A1 (en) |
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WO (1) | WO2000004372A1 (en) |
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US6680206B1 (en) | 2004-01-20 |
US20050164320A1 (en) | 2005-07-28 |
EP1097369A1 (en) | 2001-05-09 |
AU770949B2 (en) | 2004-03-11 |
US7491552B2 (en) | 2009-02-17 |
AU5316599A (en) | 2000-02-07 |
US20090258791A1 (en) | 2009-10-15 |
US6908770B1 (en) | 2005-06-21 |
CA2337155A1 (en) | 2000-01-27 |
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