CA2697026A1 - Method of making a capillary channel - Google Patents
Method of making a capillary channel Download PDFInfo
- Publication number
- CA2697026A1 CA2697026A1 CA2697026A CA2697026A CA2697026A1 CA 2697026 A1 CA2697026 A1 CA 2697026A1 CA 2697026 A CA2697026 A CA 2697026A CA 2697026 A CA2697026 A CA 2697026A CA 2697026 A1 CA2697026 A1 CA 2697026A1
- Authority
- CA
- Canada
- Prior art keywords
- format
- insert
- carrier
- sensor
- making
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502707—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the manufacture of the container or its components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
- B29C45/14639—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles for obtaining an insulating effect, e.g. for electrical components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
- B29C45/14754—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles being in movable or releasable engagement with the coating, e.g. bearing assemblies
-
- 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
- G01N21/01—Arrangements or apparatus for facilitating the optical investigation
- G01N21/03—Cuvette constructions
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44704—Details; Accessories
- G01N27/44717—Arrangements for investigating the separated zones, e.g. localising zones
- G01N27/4473—Arrangements for investigating the separated zones, e.g. localising zones by electric means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
- B01L2200/12—Specific details about manufacturing devices
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/06—Auxiliary integrated devices, integrated components
- B01L2300/0627—Sensor or part of a sensor is integrated
- B01L2300/0645—Electrodes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
- B01L2300/0825—Test strips
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
- B01L2400/0406—Moving fluids with specific forces or mechanical means specific forces capillary forces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
- B29C45/14754—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles being in movable or releasable engagement with the coating, e.g. bearing assemblies
- B29C2045/1477—Removable inserts, e.g. the insert being peeled off after moulding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
- B29C45/14065—Positioning or centering articles in the mould
-
- 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
- G01N21/01—Arrangements or apparatus for facilitating the optical investigation
- G01N21/03—Cuvette constructions
- G01N2021/0346—Capillary cells; Microcells
Abstract
An optical reagent format with a precise capillary chan-nel is made by molding a format on a carrier of a precise pre-determined thickness. The carrier includes an insert at least a portion of which is molded in the format. Once the format is made, the insert is detached from the carrier and removed from the format leaving a precisely dimensioned capillary channel with an inlet and vent. A reagent may be applied in the capillary channel and the format used to measure the ana-lyte in a fluid such as blood.
An electrochemical sensor with a capillary channel is formed by placing a sacrificial insert and electrodes on a sensor base and applying plastic material. After the plastic material is cured, the sacrificial is removed leaving a capil-lary channel in the sensor. The inserts may be removed by a tool including a clamp for clamping and holding each insert stationary and a sliding block to which the sensor is secured.
An electrochemical sensor with a capillary channel is formed by placing a sacrificial insert and electrodes on a sensor base and applying plastic material. After the plastic material is cured, the sacrificial is removed leaving a capil-lary channel in the sensor. The inserts may be removed by a tool including a clamp for clamping and holding each insert stationary and a sliding block to which the sensor is secured.
Description
METHOD OF MAKING A CAPILLARY CHANNEL
Field of the Invention The present invention relates to precision capillary channels for sensors and the method of making them.
Background of the Invention Sensors are used for sampling a fluid, mixing the fluid with a reagent, and making an analysis of the mixed sample.
One form of sensor includes a capillary channel between two optical paths and a reagent in the channel. Another sensor is injection molded with a capillary channel between a base and lid. Electrodes and a reagent are located in the channel. A
test fluid is drawn in to the channel by capillary action and reacts with the reagent. In the first sensor, a light source is applied to one of the optical paths, and light from the light source is transmitted through the fluid in the channel and directed to a detector applied to the other optical path.
In the second sensor an electric current acrossed the elec-trodes is measured.
A significant problem in the fabrication of optical rea-gent sensor is the production of a pzecision optical path length. This has been achieved by producing an optically clear part having a cavity of a certain depth. The cavity is covered by an optically clear lid. The precise depth of the cavity is difficult to produce repeatedly, but even is the depth can be repeatedly produced, it is very difficult to at-tach a lid and control the path length due to the tolerances of the method of attachment. In addition, if the attachment uses adhesives, variations in adhesives adds to the toler-ances. Other types of attachment such as sonic welding each has their own variability.
Field of the Invention The present invention relates to precision capillary channels for sensors and the method of making them.
Background of the Invention Sensors are used for sampling a fluid, mixing the fluid with a reagent, and making an analysis of the mixed sample.
One form of sensor includes a capillary channel between two optical paths and a reagent in the channel. Another sensor is injection molded with a capillary channel between a base and lid. Electrodes and a reagent are located in the channel. A
test fluid is drawn in to the channel by capillary action and reacts with the reagent. In the first sensor, a light source is applied to one of the optical paths, and light from the light source is transmitted through the fluid in the channel and directed to a detector applied to the other optical path.
In the second sensor an electric current acrossed the elec-trodes is measured.
A significant problem in the fabrication of optical rea-gent sensor is the production of a pzecision optical path length. This has been achieved by producing an optically clear part having a cavity of a certain depth. The cavity is covered by an optically clear lid. The precise depth of the cavity is difficult to produce repeatedly, but even is the depth can be repeatedly produced, it is very difficult to at-tach a lid and control the path length due to the tolerances of the method of attachment. In addition, if the attachment uses adhesives, variations in adhesives adds to the toler-ances. Other types of attachment such as sonic welding each has their own variability.
The difficulty in repeatedly producing a cavity of a pre-cise depth is critical when producing an optical reagent sen-sor that is to be used in the transmission mode. In the transmission mode the path length in the capillary gap is di-rectly proportional to an analyte being tested. If an identi-cal analyte is measured in two sensors that have different path lengths, the results reported will be different due to the path lengths. There is a need for a method of making op-tical reagent sensors with precise capillary channels that can be reproduced without variances or tolerances.
Similarly, the formation of a capillary channel in an in-jection molded sensor is difficult to produce. The usual way to fabricate sensors of this type is to precision screen print active areas within a capillary area formed by a shaped top lid. It is desirable to reduce the cost and assembly required by this construction. Moreover, it is difficult to provide electrodes in a small molded capillary channel of less than .005 inch in height and it is desirable to provide a sensor of this size with molded electrodes so that such a sensor could be used for electrochemical analysis.
Summary of the Invention The present invention is directed to an optical reagent sensor and an electrochemical sensor and to a method for mak-ing an optical reagent sensor and an electrochemical sensor.
The optical reagent sensor includes a precision capillary channel with an inlet and a vent. To fabricate such a sensor, a carrier made of a material that is chemically etched, punched, die cut or otherwise formed to a predetermined con-figuration and with precision thickness is provided as an in-sert. An optical sensor is molded onto the carrier and once the molder material is cured, the insert is detached from the carrier and removed from the sensor leaving a precise capil-lary channel in the sensor. A reagent can be applied to the channel for a particular analyte to be tested. The sensor is used by drawing a test fluid into the capillary channel.
The electrochemical sensor of the present invention in-cludes individual electrodes or contacts molded into the sen-sor. This process includes placing a first electrode in a base mold and placing a sacrificial insert in the mold above the first electrode. A second electrode is then placed in the base mold over the insert. A top mold is placed on the base mold and plastic material is injected into the top and base molds. After curing, the sensor is removed from the mold and the sacrificial insert is removed leaving a capillary channel with the two contact/electrodes in the channel.
Since the force required to remove or insert from the fabricated sensor could be quite high, it is desirable to use a tool that clamps the insert securely in place while applying a force on the sensor. The tool includes a clamp for clamping the insert in a stationary position and a moveable block to which the sensor is secured. A drive mechanism is coupled to the block to move the block relative to the clamp thereby withdrawing the insert from the sensor.
Brief Description of the Drawings Other objects and advantages of the invention will become apparent upon reading the following detailed description and upon reference to the drawings in which:
FIG. 1 is a perspective view of a sensor format on a car-rier;
FIG. 2 is a perspective view of a chain of sensor formats on a carrier;
Similarly, the formation of a capillary channel in an in-jection molded sensor is difficult to produce. The usual way to fabricate sensors of this type is to precision screen print active areas within a capillary area formed by a shaped top lid. It is desirable to reduce the cost and assembly required by this construction. Moreover, it is difficult to provide electrodes in a small molded capillary channel of less than .005 inch in height and it is desirable to provide a sensor of this size with molded electrodes so that such a sensor could be used for electrochemical analysis.
Summary of the Invention The present invention is directed to an optical reagent sensor and an electrochemical sensor and to a method for mak-ing an optical reagent sensor and an electrochemical sensor.
The optical reagent sensor includes a precision capillary channel with an inlet and a vent. To fabricate such a sensor, a carrier made of a material that is chemically etched, punched, die cut or otherwise formed to a predetermined con-figuration and with precision thickness is provided as an in-sert. An optical sensor is molded onto the carrier and once the molder material is cured, the insert is detached from the carrier and removed from the sensor leaving a precise capil-lary channel in the sensor. A reagent can be applied to the channel for a particular analyte to be tested. The sensor is used by drawing a test fluid into the capillary channel.
The electrochemical sensor of the present invention in-cludes individual electrodes or contacts molded into the sen-sor. This process includes placing a first electrode in a base mold and placing a sacrificial insert in the mold above the first electrode. A second electrode is then placed in the base mold over the insert. A top mold is placed on the base mold and plastic material is injected into the top and base molds. After curing, the sensor is removed from the mold and the sacrificial insert is removed leaving a capillary channel with the two contact/electrodes in the channel.
Since the force required to remove or insert from the fabricated sensor could be quite high, it is desirable to use a tool that clamps the insert securely in place while applying a force on the sensor. The tool includes a clamp for clamping the insert in a stationary position and a moveable block to which the sensor is secured. A drive mechanism is coupled to the block to move the block relative to the clamp thereby withdrawing the insert from the sensor.
Brief Description of the Drawings Other objects and advantages of the invention will become apparent upon reading the following detailed description and upon reference to the drawings in which:
FIG. 1 is a perspective view of a sensor format on a car-rier;
FIG. 2 is a perspective view of a chain of sensor formats on a carrier;
FIG. 3 is an enlarged view of a sensor format removed from a carrier with a portion of the carrier between the legs of the format;
FIG. 4 is a reduced view of the sensor format illustrated in FIG. 3 with the portion of the carrier removed from between the legs of the format;
FIG. 5 is a perspective view of an alternative embodiment of the sensor format illustrated in FIGS. 1-4 on a carrier;
FIG. 6 is an enlarged view of the format illustrated in FIG. 5 with the carrier removed;
FIG. 7 is a perspective view of a bottom mold of a mold-ing tool for molding an electrochemical biosensor with a first contact positioned in the bottom mold;
FIG. 8 is a view similar to FIG. 7 with a sacrificial protective insert positioned in the bottom mold;
FIG. 9 is a view similar to FIG. 8 with a second contact positioned in the bottom mold;
FIG. 10 is a perspective view of the molding tool with a top mold placed on the bottom mold;
FIG. 11 is an enlarged perspective view of a molded elec-trochemical biosensor with a sacrificial insert in the biosen-sor;
FIG. 12 is a perspective view of a tool used to remove the inserts from the biosensors illustrated in FIGS. 1-11;
FIG. 13 is a perspective view of an optical sensor with an insert;
FIG. 14 is a view similar to FIG. 13 with the insert withdrawn; and FIG. 15 is a perspective view of the optical sensor of FIG. 13.
While the invention is susceptible to various modifica-tions and alternative forms, specific embodiments thereof have been shown by way of examples in the drawings and will herein be described in detail. It should be understood, however, that it is not intended to limit the invention to the particu-lar forms disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Detailed Description of the Preferred Embodiments Referring to FIGS. 1-4, the sensor format 10 of the pres-ent invention is illustrated. The format 10 is an optical pipe formed of light transmission material. A light source is applied to an end 12 of a first leg 14 of the format 10.
Light from the light source travels the length of the first leg 14 until it strikes a first end surface 16 that is at a 45 angle to the longitudinal axis of the first leg 14. The light is reflected by the end surface 16 through capillary gap 18. Light that is not absorbed by material in the gap 18 strikes a second end surface 20 which is at a 45 to a longi-tudinal axis of a second leg 22 of the format 10. This light is reflected the length of the second leg 22 to a detector po-sitioned at an end 24 of the second leg 22.
The format 10 is used in the transmission mode and the path length in the gap 18 is directly proportional to an ana-lyte being tested. If the same analyte is measured in two different formats that have different path lengths, the re-sults reported will be different due to the different path lengths. The format 10 of the present invention is made in a manner to insure a capillary gap 18 of a precise thickness for each format 10 to minimize or eliminate any differences re-ported due to different path lengths through the gap 18.
The format 10 is formed by injection molding over a sin-gle carrier 26 with an insert 28 or a multiple carrier 30 with multiple inserts 32. The single carrier 26 and the multiple carrier 30 are of a material, such as metal, that can be chemically etched, laser cut, mechanically punched, die cut or a similar fabrication process, to a known precise thickness and configuration required to form a precise capillary gap 18.
The thickness of the carriers 26 and 30 are dependent on the desired light path length of the gap 18. The carriers 26 and 30 can be formed of materials whose melt temperatures are above the melt temperature of the format material and the car-rier material must have sufficient tensile strength to allow removal of the inserts 28 and 32 from the format 10 after the format 10 has been molded.
To mold a format 10, the single carrier 26 and the multi-ple carrier 30 are positioned and secured in a molding tool by tractor feed or pin positions holes 34. Plastic material is injected into the molding tool and the formats 10 are formed on the single carrier 26 and the multiple carrier 30. Once the plastic material is cured and the carriers 26 and 30 re-moved from the molding tool, the inserts 28 and 32 are sepa-rated from the carriers 26 and 30, respectively, and removed from the formats 10 leaving a precise capillary gap 18. Each gap 18 is of the same size and thickness due to the precision thickness and dimension of the inserts 28 and 32. A reagent can be wicked into each gap 18 and dried. If the gap 18 must be sealed on the sides, lids (not shown) can be secured to the sides of the format 10 without being part of the optical path.
An extension 36 of each carrier 26 and 30 extends between the first leg 14 and the second leg 22 of each format 10 and provides an opaque light barrier between the legs 14 and 22 or light paths (FIG. 3). The extension 36 also provides struc-tural integrity to the legs 14 and 22 and the format 10. If a light barrier or structural integrity is not needed, the ex-tension 36 can be removed from between the legs 14 and 22 (FIG. 4).
A format 110 that requires sides to be sealed and pro-vides a direct optical read is shown in FIGS. 5 and 6. The format 110 is injection molded onto a carrier 112 in a manner similar to the molding of the reagent format 10 in FIGS. 1-4.
The carrier 112 is of the same material as the carriers 26 and 30 and fabricated in the same manner to a known precise thick-ness to form a precise capillary gap 114. The gap 114 is formed by an insert 116 that is part of the carrier 112.
The carrier 112 is positioned in a molding tool by trac-tor feed or pin position holes 118, and casting material is injected into the molding tool to form the formats 110. After the casting material has cured, the carrier 112 is removed from the molding tool and the inserts 116 are extracted from the formats 110 leaving the precise capillary gaps 114 of mi-cron sizes. There is an entrance or inlet 117 to each gap 114 and a vent formed by extensions 119 on carrier 112 on a side opposite the inlet 118. The gap 114 is enclosed on the sides 114A and 114B and sides or a lid is not required to form the gap 114.
The format 110 includes. a first cone 120 above the gap 114 and a second cone 122 below the gap. The shape of the cones 120 and 122 can be any shape such as square and need not be the truncated cone shape shown in the drawings. A light source is placed at an end 124 of the first cone 120 and a light or optical detector is placed at an end 126 of the sec-ond cone 122. Light from the light source travels through the first cone 120 to an analyte in the gap 114, and light passing through the gap 114 and the analyte passes along the second cone 122 to the optical detector for measurement of the ana-lyte or other specimen. The cones 120 and 122 isolate the op-tical components (light source and detector) from the gap 114 and the specimen in the gap to prevent contamination. If con-tamination is not an issue, the cones 120 and 122 can be eliminated.
Referring to FIGS. 7-11 an electrochemical sensor 210 is illustrated. The sensor 210 includes a first electrode 212 and a second electrode 214 molded into the sensor 210 (FIG.
11). The sensor 210 also includes a precise small capillary channel formed by a sacrificial insert 216.
The sensor 210 is injection molded in a molding tool 218 having a bottom mold 220 and a top mold 222 (FIG. 10). The bottom mold 220 (FIGS. 7-9) includes a cavity 224 in the shape of the sensor 210. A plurality of locator pins 226, 228, 230, 232, 234, 236, 238 and 240 are provided on the bottom mold for properly locating the first and second electrodes 212 and 215 and the sacrificial insert 216.
The first and second electrodes 212 and 214 are loaded in the bottom mold 220 by stacking them such that the sacrificial insert 216 extends between them. The first electrode 212 is loaded first by fitting holes in the first electrode 212 over locator pins 226, 228 and 230 (FIG. 7). The sacrificial in-sert 216 is loaded next by fitting holes 238 and 240 in the insert over locator pins 238 and 240 (FIG. 8). The sacrifi-cial insert 216 extends into the cavity 224 and over and on a forward end of the first electrode 212. The second electrode 214 is loaded in the bottom mold 220 onto locator pins 232, 234 and 236 with its forward end over and on the sacrificial insert 216 and over the forward end of the first electrode 212 (FIG. 9). The top mold 222 is then placed on the bottom mold 220 and compressed to provide compressive loading of both sides of the sacrificial insert 216. This compressive loading can be provided by raised portions in the bottom mold 220 and the top mold 222 that engage the sacrificial insert 216 be-tween them as the top mold 222 is mounted on the bottom mold 220.
Once the molding tool 218 is assembled (FIG. 10), plastic material is injected into the tool 218. Due to the compres-sive loading, the cavity 224 is filled with plastic material but since plastic can not flow into the stack of the forward ends of the first and second electrodes 212 and 214 and the insert 216, the plastic material does not flow between the forward ends of the electrodes 212 and 214 and the insert 216.
Once the plastic material has cured, the molding tool 218 is opened and the sensor 210 with the first electrode 212 and second electrode 214 and the insert 216 are removed. The in-sert 216 is then removed from the sensor 210 leaving a precise small capillary channel 242 (FIG. 11) with the first electrode 212 on the bottom of the channel 242 and the second electrode 214 on the top of the channel 242.
An optical version of the electrochemical sensor 210 is illustrated in FIGS. 13-15. In these FIGS. 13-15 there is il-lustrated an optical sensor 410. The optical sensor 410 is molded in a manner and tool similar to that for the sensor 210 except instead of electrodes 212, 214, the optical sensor 410 includes an access window 412 for source optics and an access window for detector optics directly below the access window 412. A capillary cavity or channel 414 is formed in the opti-cal sensor 410 between the access windows so that light from source optics directed into the access window 412 passes through a specimen in the capillary cavity or channel 414 and is read by detector optics positioned at the lower access win-dow.
A mold or tool that forms the optical sensor 410 includes inserts that are highly polished and extend into the mold. As plastic material is injected into the mold, the plastic mate-rial flows around the inserts to form the access windows.
Since the inserts are highly polished, the access windows are clear with little distortion.
The capillary cavity or channel 414 is formed by an in-sert 416 that may be made of stainless steel or similar mate-rial. The insert 416 is similar to the insert 216 in FIGS. 7-11 and includes fitting holes 438 and 440 that fit over loca-tor pins similar to pins 238 and 240 in a mold (FIG. 8).
Because the insert 416 is very thin and large pressures occur in the mold during molding of the optical sensor 410, an access hole 418 is formed in the optical sensor 410 by a por-tion of the mold that grips the insert 416 and holds it stable as plastic material flows around the insert 416. The optical sensor 410 also includes a hole 446 similar to the hole 346 in the sensor 210.
In each of the above described embodiments the insert 28 or 216 must be removed from the sensor 14 or 210, respec-tively, and the force required to do this could be quite high.
Therefore, it is desirable to have a tool that will hold the sensor 14 or 210 securely in place and supply sufficient force inline to the insert 28 or 216 to withdraw the insert 28 or 216 from the sensor 14 or 210. An insert removal tool or ex-tractor 300 to accomplish these objectives is illustrated in FIG. 12. The extractor 300 is secured to a base 312 and in-cludes a clamp 314. The clamp 314 may be a DeStaca clamp with a handle 316 pivotally mounted on a stand 318. The stand 318 is secured to the base 312. The handle 316 is coupled to a clamp head 320 by a linkage 322 such that rotating the handle 316 causes the clamp head 320 to move toward and away from the base 312.
The base 312 includes a cavity 324 in which is positioned a sliding block 326. A cover plate 328 is secured to the base 312 over a portion of the cavity 324. The cover plate 328 has a slot 330 through which extends a drive pin and bearing 332 that are attached to the sliding block 326. An extraction drive level 334 is pivotally mounted on the base 312 by a pin 336 and abuts the drive pin and bearing 332 such that as the extraction drive lever 334 is pivoted in a clockwise direction about the pin 336 as view in FIG. 12, the drive pin and bear-ing 332 are moved in the slot 330 moving the sliding block 326 out of the end of the cavity 324.
To remove an insert 28, 216 or 416 the sensor 14, 210 or 410 (in FIG. 12 sensor 210 is illustrated) is placed in the cavity 324 with the holes 238 and 240 (FIG. 11) in the sensor 216 placed over the pins 342 and 344 which are rigidly mounted on the base 312. A hole 346 (FIG. 11) in the sensor 210 is positioned over a sensor pin 348 on the sliding block 326.
Accordingly, the sensor 210 is secured to the sliding block 326 and the insert 216 is secured to the base 312. A force distribution block 340 is placed over the pins 342 and 344 and clamped down onto the insert 216 by the clamp 314.
The insert 216 is withdrawn from the sensor 210 by a force inline with the sensor 210 and insert 216 by pivoting the extraction drive lever 334 to move the sliding block 326 in the cavity 324. This action pulls the sensor 210 away from the insert 216 cleanly withdrawing the insert.
While the present invention has been described with ref-erence to one or more particular embodiments, those skilled in the art will recognize that many changes may be made thereto without departing from the spirit and scope of the present in-vention. Each of these embodiments and obvious variations thereof is contemplated as falling within the spirit and scope of the claimed invention.
FIG. 4 is a reduced view of the sensor format illustrated in FIG. 3 with the portion of the carrier removed from between the legs of the format;
FIG. 5 is a perspective view of an alternative embodiment of the sensor format illustrated in FIGS. 1-4 on a carrier;
FIG. 6 is an enlarged view of the format illustrated in FIG. 5 with the carrier removed;
FIG. 7 is a perspective view of a bottom mold of a mold-ing tool for molding an electrochemical biosensor with a first contact positioned in the bottom mold;
FIG. 8 is a view similar to FIG. 7 with a sacrificial protective insert positioned in the bottom mold;
FIG. 9 is a view similar to FIG. 8 with a second contact positioned in the bottom mold;
FIG. 10 is a perspective view of the molding tool with a top mold placed on the bottom mold;
FIG. 11 is an enlarged perspective view of a molded elec-trochemical biosensor with a sacrificial insert in the biosen-sor;
FIG. 12 is a perspective view of a tool used to remove the inserts from the biosensors illustrated in FIGS. 1-11;
FIG. 13 is a perspective view of an optical sensor with an insert;
FIG. 14 is a view similar to FIG. 13 with the insert withdrawn; and FIG. 15 is a perspective view of the optical sensor of FIG. 13.
While the invention is susceptible to various modifica-tions and alternative forms, specific embodiments thereof have been shown by way of examples in the drawings and will herein be described in detail. It should be understood, however, that it is not intended to limit the invention to the particu-lar forms disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Detailed Description of the Preferred Embodiments Referring to FIGS. 1-4, the sensor format 10 of the pres-ent invention is illustrated. The format 10 is an optical pipe formed of light transmission material. A light source is applied to an end 12 of a first leg 14 of the format 10.
Light from the light source travels the length of the first leg 14 until it strikes a first end surface 16 that is at a 45 angle to the longitudinal axis of the first leg 14. The light is reflected by the end surface 16 through capillary gap 18. Light that is not absorbed by material in the gap 18 strikes a second end surface 20 which is at a 45 to a longi-tudinal axis of a second leg 22 of the format 10. This light is reflected the length of the second leg 22 to a detector po-sitioned at an end 24 of the second leg 22.
The format 10 is used in the transmission mode and the path length in the gap 18 is directly proportional to an ana-lyte being tested. If the same analyte is measured in two different formats that have different path lengths, the re-sults reported will be different due to the different path lengths. The format 10 of the present invention is made in a manner to insure a capillary gap 18 of a precise thickness for each format 10 to minimize or eliminate any differences re-ported due to different path lengths through the gap 18.
The format 10 is formed by injection molding over a sin-gle carrier 26 with an insert 28 or a multiple carrier 30 with multiple inserts 32. The single carrier 26 and the multiple carrier 30 are of a material, such as metal, that can be chemically etched, laser cut, mechanically punched, die cut or a similar fabrication process, to a known precise thickness and configuration required to form a precise capillary gap 18.
The thickness of the carriers 26 and 30 are dependent on the desired light path length of the gap 18. The carriers 26 and 30 can be formed of materials whose melt temperatures are above the melt temperature of the format material and the car-rier material must have sufficient tensile strength to allow removal of the inserts 28 and 32 from the format 10 after the format 10 has been molded.
To mold a format 10, the single carrier 26 and the multi-ple carrier 30 are positioned and secured in a molding tool by tractor feed or pin positions holes 34. Plastic material is injected into the molding tool and the formats 10 are formed on the single carrier 26 and the multiple carrier 30. Once the plastic material is cured and the carriers 26 and 30 re-moved from the molding tool, the inserts 28 and 32 are sepa-rated from the carriers 26 and 30, respectively, and removed from the formats 10 leaving a precise capillary gap 18. Each gap 18 is of the same size and thickness due to the precision thickness and dimension of the inserts 28 and 32. A reagent can be wicked into each gap 18 and dried. If the gap 18 must be sealed on the sides, lids (not shown) can be secured to the sides of the format 10 without being part of the optical path.
An extension 36 of each carrier 26 and 30 extends between the first leg 14 and the second leg 22 of each format 10 and provides an opaque light barrier between the legs 14 and 22 or light paths (FIG. 3). The extension 36 also provides struc-tural integrity to the legs 14 and 22 and the format 10. If a light barrier or structural integrity is not needed, the ex-tension 36 can be removed from between the legs 14 and 22 (FIG. 4).
A format 110 that requires sides to be sealed and pro-vides a direct optical read is shown in FIGS. 5 and 6. The format 110 is injection molded onto a carrier 112 in a manner similar to the molding of the reagent format 10 in FIGS. 1-4.
The carrier 112 is of the same material as the carriers 26 and 30 and fabricated in the same manner to a known precise thick-ness to form a precise capillary gap 114. The gap 114 is formed by an insert 116 that is part of the carrier 112.
The carrier 112 is positioned in a molding tool by trac-tor feed or pin position holes 118, and casting material is injected into the molding tool to form the formats 110. After the casting material has cured, the carrier 112 is removed from the molding tool and the inserts 116 are extracted from the formats 110 leaving the precise capillary gaps 114 of mi-cron sizes. There is an entrance or inlet 117 to each gap 114 and a vent formed by extensions 119 on carrier 112 on a side opposite the inlet 118. The gap 114 is enclosed on the sides 114A and 114B and sides or a lid is not required to form the gap 114.
The format 110 includes. a first cone 120 above the gap 114 and a second cone 122 below the gap. The shape of the cones 120 and 122 can be any shape such as square and need not be the truncated cone shape shown in the drawings. A light source is placed at an end 124 of the first cone 120 and a light or optical detector is placed at an end 126 of the sec-ond cone 122. Light from the light source travels through the first cone 120 to an analyte in the gap 114, and light passing through the gap 114 and the analyte passes along the second cone 122 to the optical detector for measurement of the ana-lyte or other specimen. The cones 120 and 122 isolate the op-tical components (light source and detector) from the gap 114 and the specimen in the gap to prevent contamination. If con-tamination is not an issue, the cones 120 and 122 can be eliminated.
Referring to FIGS. 7-11 an electrochemical sensor 210 is illustrated. The sensor 210 includes a first electrode 212 and a second electrode 214 molded into the sensor 210 (FIG.
11). The sensor 210 also includes a precise small capillary channel formed by a sacrificial insert 216.
The sensor 210 is injection molded in a molding tool 218 having a bottom mold 220 and a top mold 222 (FIG. 10). The bottom mold 220 (FIGS. 7-9) includes a cavity 224 in the shape of the sensor 210. A plurality of locator pins 226, 228, 230, 232, 234, 236, 238 and 240 are provided on the bottom mold for properly locating the first and second electrodes 212 and 215 and the sacrificial insert 216.
The first and second electrodes 212 and 214 are loaded in the bottom mold 220 by stacking them such that the sacrificial insert 216 extends between them. The first electrode 212 is loaded first by fitting holes in the first electrode 212 over locator pins 226, 228 and 230 (FIG. 7). The sacrificial in-sert 216 is loaded next by fitting holes 238 and 240 in the insert over locator pins 238 and 240 (FIG. 8). The sacrifi-cial insert 216 extends into the cavity 224 and over and on a forward end of the first electrode 212. The second electrode 214 is loaded in the bottom mold 220 onto locator pins 232, 234 and 236 with its forward end over and on the sacrificial insert 216 and over the forward end of the first electrode 212 (FIG. 9). The top mold 222 is then placed on the bottom mold 220 and compressed to provide compressive loading of both sides of the sacrificial insert 216. This compressive loading can be provided by raised portions in the bottom mold 220 and the top mold 222 that engage the sacrificial insert 216 be-tween them as the top mold 222 is mounted on the bottom mold 220.
Once the molding tool 218 is assembled (FIG. 10), plastic material is injected into the tool 218. Due to the compres-sive loading, the cavity 224 is filled with plastic material but since plastic can not flow into the stack of the forward ends of the first and second electrodes 212 and 214 and the insert 216, the plastic material does not flow between the forward ends of the electrodes 212 and 214 and the insert 216.
Once the plastic material has cured, the molding tool 218 is opened and the sensor 210 with the first electrode 212 and second electrode 214 and the insert 216 are removed. The in-sert 216 is then removed from the sensor 210 leaving a precise small capillary channel 242 (FIG. 11) with the first electrode 212 on the bottom of the channel 242 and the second electrode 214 on the top of the channel 242.
An optical version of the electrochemical sensor 210 is illustrated in FIGS. 13-15. In these FIGS. 13-15 there is il-lustrated an optical sensor 410. The optical sensor 410 is molded in a manner and tool similar to that for the sensor 210 except instead of electrodes 212, 214, the optical sensor 410 includes an access window 412 for source optics and an access window for detector optics directly below the access window 412. A capillary cavity or channel 414 is formed in the opti-cal sensor 410 between the access windows so that light from source optics directed into the access window 412 passes through a specimen in the capillary cavity or channel 414 and is read by detector optics positioned at the lower access win-dow.
A mold or tool that forms the optical sensor 410 includes inserts that are highly polished and extend into the mold. As plastic material is injected into the mold, the plastic mate-rial flows around the inserts to form the access windows.
Since the inserts are highly polished, the access windows are clear with little distortion.
The capillary cavity or channel 414 is formed by an in-sert 416 that may be made of stainless steel or similar mate-rial. The insert 416 is similar to the insert 216 in FIGS. 7-11 and includes fitting holes 438 and 440 that fit over loca-tor pins similar to pins 238 and 240 in a mold (FIG. 8).
Because the insert 416 is very thin and large pressures occur in the mold during molding of the optical sensor 410, an access hole 418 is formed in the optical sensor 410 by a por-tion of the mold that grips the insert 416 and holds it stable as plastic material flows around the insert 416. The optical sensor 410 also includes a hole 446 similar to the hole 346 in the sensor 210.
In each of the above described embodiments the insert 28 or 216 must be removed from the sensor 14 or 210, respec-tively, and the force required to do this could be quite high.
Therefore, it is desirable to have a tool that will hold the sensor 14 or 210 securely in place and supply sufficient force inline to the insert 28 or 216 to withdraw the insert 28 or 216 from the sensor 14 or 210. An insert removal tool or ex-tractor 300 to accomplish these objectives is illustrated in FIG. 12. The extractor 300 is secured to a base 312 and in-cludes a clamp 314. The clamp 314 may be a DeStaca clamp with a handle 316 pivotally mounted on a stand 318. The stand 318 is secured to the base 312. The handle 316 is coupled to a clamp head 320 by a linkage 322 such that rotating the handle 316 causes the clamp head 320 to move toward and away from the base 312.
The base 312 includes a cavity 324 in which is positioned a sliding block 326. A cover plate 328 is secured to the base 312 over a portion of the cavity 324. The cover plate 328 has a slot 330 through which extends a drive pin and bearing 332 that are attached to the sliding block 326. An extraction drive level 334 is pivotally mounted on the base 312 by a pin 336 and abuts the drive pin and bearing 332 such that as the extraction drive lever 334 is pivoted in a clockwise direction about the pin 336 as view in FIG. 12, the drive pin and bear-ing 332 are moved in the slot 330 moving the sliding block 326 out of the end of the cavity 324.
To remove an insert 28, 216 or 416 the sensor 14, 210 or 410 (in FIG. 12 sensor 210 is illustrated) is placed in the cavity 324 with the holes 238 and 240 (FIG. 11) in the sensor 216 placed over the pins 342 and 344 which are rigidly mounted on the base 312. A hole 346 (FIG. 11) in the sensor 210 is positioned over a sensor pin 348 on the sliding block 326.
Accordingly, the sensor 210 is secured to the sliding block 326 and the insert 216 is secured to the base 312. A force distribution block 340 is placed over the pins 342 and 344 and clamped down onto the insert 216 by the clamp 314.
The insert 216 is withdrawn from the sensor 210 by a force inline with the sensor 210 and insert 216 by pivoting the extraction drive lever 334 to move the sliding block 326 in the cavity 324. This action pulls the sensor 210 away from the insert 216 cleanly withdrawing the insert.
While the present invention has been described with ref-erence to one or more particular embodiments, those skilled in the art will recognize that many changes may be made thereto without departing from the spirit and scope of the present in-vention. Each of these embodiments and obvious variations thereof is contemplated as falling within the spirit and scope of the claimed invention.
Claims (13)
1. A method of making an optical reagent format with a capillary gap, comprising:
providing a carrier with an insert, said carrier and insert being of a predetermined thickness;
placing said carrier in a mold;
molding a format onto said carrier and insert;
separating said insert from said carrier; and removing said insert from said format leaving a capillary gap in said format.
providing a carrier with an insert, said carrier and insert being of a predetermined thickness;
placing said carrier in a mold;
molding a format onto said carrier and insert;
separating said insert from said carrier; and removing said insert from said format leaving a capillary gap in said format.
2. The method of making an optical reagent format claimed in Claim 1 further comprising applying reagent in said capillary gap.
3. The method of making an optical reagent format claimed in Claim 1 said capillary gap having open sides, and sealing said open sides of said capillary gap.
4. The method of making an optical reagent format claimed in Claim 1 further comprising removing said format from said carrier.
5. The method of making an optical reagent format claimed in Claim 1 providing a plurality of carriers joined together and each including an insert, and molding a format onto each of said plurality of carriers and inserts.
6. The method of making an optical reagent format claimed in Claim 1 said format including a pair of legs, further comprising forming said capillary gap between a pair of legs of said format.
7. The method of making an optical reagent format claimed in Claim 1 wherein molding said format comprises molding a first format on an upper surface of said carrier and molding a second format on a lower surface of said carrier.
8. The method of making an optical reagent format claimed in Claim 7 wherein said first and second formats are of a conical configuration.
9. A method of making an optical reagent format with a capillary gap, comprising:
providing a carrier of predetermined thickness;
providing an insert on said carrier;
molding a format onto said carrier and said insert with a portion of said insert extending out of said format; and removing said insert from said format to provide a capillary channel with an inlet and a vent in said format formed by said insert.
providing a carrier of predetermined thickness;
providing an insert on said carrier;
molding a format onto said carrier and said insert with a portion of said insert extending out of said format; and removing said insert from said format to provide a capillary channel with an inlet and a vent in said format formed by said insert.
10. The method of making an optical reagent format claimed in Claim 9 comprising removing said carrier from said format.
11. The method of making an optical reagent format claimed in Claim 9 said insert comprising a material of a melt temperature higher than the melt temperature of the material of said format.
12. The method of making an optical reagent format claimed in Claim 9 comprising molding said format with a first leg for the application of a light source and a second leg for the application of a light detector, said capillary channel being between said first and second legs.
13. The method of making an optical reagent format claimed in Claim 9 comprising molding said format with a first conical member on a first side of said format and a second conical member on a second side of said format with said capillary channel between said first conical member and said second conical member.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25462600P | 2000-12-12 | 2000-12-12 | |
US60/254,626 | 2000-12-12 | ||
CA2364132A CA2364132C (en) | 2000-12-12 | 2001-11-27 | Method of making a capillary channel |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2364132A Division CA2364132C (en) | 2000-12-12 | 2001-11-27 | Method of making a capillary channel |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2697026A1 true CA2697026A1 (en) | 2002-06-12 |
Family
ID=22964991
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2364132A Expired - Fee Related CA2364132C (en) | 2000-12-12 | 2001-11-27 | Method of making a capillary channel |
CA2697026A Abandoned CA2697026A1 (en) | 2000-12-12 | 2001-11-27 | Method of making a capillary channel |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2364132A Expired - Fee Related CA2364132C (en) | 2000-12-12 | 2001-11-27 | Method of making a capillary channel |
Country Status (5)
Country | Link |
---|---|
US (4) | US6911130B2 (en) |
EP (1) | EP1215479A3 (en) |
JP (2) | JP3850722B2 (en) |
AU (1) | AU780801B2 (en) |
CA (2) | CA2364132C (en) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6036924A (en) | 1997-12-04 | 2000-03-14 | Hewlett-Packard Company | Cassette of lancet cartridges for sampling blood |
US6391005B1 (en) | 1998-03-30 | 2002-05-21 | Agilent Technologies, Inc. | Apparatus and method for penetration with shaft having a sensor for sensing penetration depth |
US8641644B2 (en) | 2000-11-21 | 2014-02-04 | Sanofi-Aventis Deutschland Gmbh | Blood testing apparatus having a rotatable cartridge with multiple lancing elements and testing means |
CA2364132C (en) | 2000-12-12 | 2010-06-01 | Bayer Corporation | Method of making a capillary channel |
US6572745B2 (en) * | 2001-03-23 | 2003-06-03 | Virotek, L.L.C. | Electrochemical sensor and method thereof |
US6576102B1 (en) * | 2001-03-23 | 2003-06-10 | Virotek, L.L.C. | Electrochemical sensor and method thereof |
US7122102B2 (en) | 2001-06-11 | 2006-10-17 | Bayer Healthcare Llc | Electrochemical sensor |
US8337419B2 (en) | 2002-04-19 | 2012-12-25 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US7981056B2 (en) | 2002-04-19 | 2011-07-19 | Pelikan Technologies, Inc. | Methods and apparatus for lancet actuation |
US9226699B2 (en) | 2002-04-19 | 2016-01-05 | Sanofi-Aventis Deutschland Gmbh | Body fluid sampling module with a continuous compression tissue interface surface |
CA2448902C (en) | 2001-06-12 | 2010-09-07 | Pelikan Technologies, Inc. | Self optimizing lancing device with adaptation means to temporal variations in cutaneous properties |
US9427532B2 (en) | 2001-06-12 | 2016-08-30 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US7025774B2 (en) | 2001-06-12 | 2006-04-11 | Pelikan Technologies, Inc. | Tissue penetration device |
AU2002344825A1 (en) | 2001-06-12 | 2002-12-23 | Pelikan Technologies, Inc. | Method and apparatus for improving success rate of blood yield from a fingerstick |
US9795747B2 (en) | 2010-06-02 | 2017-10-24 | Sanofi-Aventis Deutschland Gmbh | Methods and apparatus for lancet actuation |
ES2352998T3 (en) | 2001-06-12 | 2011-02-24 | Pelikan Technologies Inc. | LANCETA ELECTRIC ACTUATOR. |
WO2002100254A2 (en) | 2001-06-12 | 2002-12-19 | Pelikan Technologies, Inc. | Method and apparatus for lancet launching device integrated onto a blood-sampling cartridge |
CA2448905C (en) | 2001-06-12 | 2010-09-07 | Pelikan Technologies, Inc. | Blood sampling apparatus and method |
US7291117B2 (en) | 2002-04-19 | 2007-11-06 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7371247B2 (en) | 2002-04-19 | 2008-05-13 | Pelikan Technologies, Inc | Method and apparatus for penetrating tissue |
US7901362B2 (en) | 2002-04-19 | 2011-03-08 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US9795334B2 (en) | 2002-04-19 | 2017-10-24 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US7909778B2 (en) | 2002-04-19 | 2011-03-22 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7232451B2 (en) | 2002-04-19 | 2007-06-19 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7229458B2 (en) | 2002-04-19 | 2007-06-12 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7297122B2 (en) | 2002-04-19 | 2007-11-20 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US9314194B2 (en) | 2002-04-19 | 2016-04-19 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US7175642B2 (en) | 2002-04-19 | 2007-02-13 | Pelikan Technologies, Inc. | Methods and apparatus for lancet actuation |
US8360992B2 (en) | 2002-04-19 | 2013-01-29 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US7674232B2 (en) | 2002-04-19 | 2010-03-09 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7892183B2 (en) | 2002-04-19 | 2011-02-22 | Pelikan Technologies, Inc. | Method and apparatus for body fluid sampling and analyte sensing |
US8221334B2 (en) | 2002-04-19 | 2012-07-17 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US8372016B2 (en) | 2002-04-19 | 2013-02-12 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for body fluid sampling and analyte sensing |
US9248267B2 (en) | 2002-04-19 | 2016-02-02 | Sanofi-Aventis Deustchland Gmbh | Tissue penetration device |
US7547287B2 (en) | 2002-04-19 | 2009-06-16 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US8579831B2 (en) | 2002-04-19 | 2013-11-12 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US8702624B2 (en) | 2006-09-29 | 2014-04-22 | Sanofi-Aventis Deutschland Gmbh | Analyte measurement device with a single shot actuator |
US7976476B2 (en) | 2002-04-19 | 2011-07-12 | Pelikan Technologies, Inc. | Device and method for variable speed lancet |
US8784335B2 (en) | 2002-04-19 | 2014-07-22 | Sanofi-Aventis Deutschland Gmbh | Body fluid sampling device with a capacitive sensor |
US7713214B2 (en) | 2002-04-19 | 2010-05-11 | Pelikan Technologies, Inc. | Method and apparatus for a multi-use body fluid sampling device with optical analyte sensing |
US8267870B2 (en) | 2002-04-19 | 2012-09-18 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for body fluid sampling with hybrid actuation |
US7648468B2 (en) | 2002-04-19 | 2010-01-19 | Pelikon Technologies, Inc. | Method and apparatus for penetrating tissue |
US7491178B2 (en) | 2002-04-19 | 2009-02-17 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7331931B2 (en) | 2002-04-19 | 2008-02-19 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7717863B2 (en) | 2002-04-19 | 2010-05-18 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
CA2446328C (en) * | 2002-10-29 | 2013-12-31 | Bayer Healthcare Llc | Optical reagent format for small sample volumes |
US8574895B2 (en) | 2002-12-30 | 2013-11-05 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus using optical techniques to measure analyte levels |
EP2238892A3 (en) | 2003-05-30 | 2011-02-09 | Pelikan Technologies Inc. | Apparatus for body fluid sampling |
US7850621B2 (en) | 2003-06-06 | 2010-12-14 | Pelikan Technologies, Inc. | Method and apparatus for body fluid sampling and analyte sensing |
WO2006001797A1 (en) | 2004-06-14 | 2006-01-05 | Pelikan Technologies, Inc. | Low pain penetrating |
WO2005033659A2 (en) | 2003-09-29 | 2005-04-14 | Pelikan Technologies, Inc. | Method and apparatus for an improved sample capture device |
WO2005037095A1 (en) | 2003-10-14 | 2005-04-28 | Pelikan Technologies, Inc. | Method and apparatus for a variable user interface |
CA2542897A1 (en) | 2003-10-30 | 2005-05-12 | Bayer Healthcare Llc | Optical cuvette with platform-and-well construction |
RU2006118710A (en) * | 2003-10-30 | 2007-12-10 | Байер Хелткэр Ллс (Us) | FORMATS FOR OPTICAL ANALYSIS AND METHODS OF PRODUCING THEM |
US7822454B1 (en) | 2005-01-03 | 2010-10-26 | Pelikan Technologies, Inc. | Fluid sampling device with improved analyte detecting member configuration |
US8668656B2 (en) | 2003-12-31 | 2014-03-11 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for improving fluidic flow and sample capture |
EP1751546A2 (en) | 2004-05-20 | 2007-02-14 | Albatros Technologies GmbH & Co. KG | Printable hydrogel for biosensors |
US9775553B2 (en) | 2004-06-03 | 2017-10-03 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for a fluid sampling device |
WO2005120365A1 (en) | 2004-06-03 | 2005-12-22 | Pelikan Technologies, Inc. | Method and apparatus for a fluid sampling device |
EP1526372A3 (en) * | 2004-11-02 | 2005-05-04 | Agilent Technologies, Inc. | Microfluidic system with adjustment for an optical detection |
US8652831B2 (en) | 2004-12-30 | 2014-02-18 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for analyte measurement test time |
DE102007006195A1 (en) * | 2007-02-07 | 2008-08-14 | Infineon Technologies Ag | Contact element, contact unit, method for producing a contact unit and method for commissioning fine-pitch components |
DE102007048211B4 (en) * | 2007-10-08 | 2011-05-12 | Thomas Dr. Calabasas Sahiri | Method and device for producing a cuvette and cuvette produced therewith |
US9386944B2 (en) | 2008-04-11 | 2016-07-12 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for analyte detecting device |
US9375169B2 (en) | 2009-01-30 | 2016-06-28 | Sanofi-Aventis Deutschland Gmbh | Cam drive for managing disposable penetrating member actions with a single motor and motor and control system |
US8965476B2 (en) | 2010-04-16 | 2015-02-24 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
CN105277597B (en) * | 2014-07-17 | 2017-09-15 | 光宏精密股份有限公司 | Electrochemical sensing test piece electric-conductor method to set up |
WO2019150946A1 (en) | 2018-01-30 | 2019-08-08 | エンゼルプレイングカード株式会社 | Management system for table game, layout for gaming table, and gaming table |
CN113109915B (en) * | 2021-04-08 | 2022-04-22 | 北京大学 | Capillary channel preparation device |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB234220A (en) * | 1964-12-10 | 1925-05-28 | Stanley Joseph William Charlto | Improved means for measuring quantities or doses of granular or powdered materials |
US3749538A (en) * | 1971-04-20 | 1973-07-31 | V Rudnev | Apparatus for making hollow mould cores |
US3773646A (en) * | 1972-05-12 | 1973-11-20 | Electro Nucleonics | Electrophoresis test kits |
US4082512A (en) * | 1976-12-22 | 1978-04-04 | The Upjohn Company | Mixing head for a reaction injection molding machine |
NL8001420A (en) | 1980-03-10 | 1981-10-01 | Cordis Europ | ELECTRODE COMPOSITIVE COMPOSITE, FOR AN ELECTROCHEMICAL MEASUREMENT, IN PARTICULAR AN ISFET-CONSTRUCTED COMPOSITION, AND METHOD FOR MANUFACTURING THE ASSEMBLY. |
DE3312923A1 (en) * | 1983-04-11 | 1984-10-11 | Boehringer Mannheim Gmbh, 6800 Mannheim | ELECTRODE ARRANGEMENT FOR ELECTROCHEMICAL ANALYSIS OF ELECTROLYTIC COMPONENTS OF A LIQUID |
US4637693A (en) * | 1985-07-23 | 1987-01-20 | Icl Scientific Corp. | Microscope inspection slide |
US4654532A (en) * | 1985-09-09 | 1987-03-31 | Ord, Inc. | Apparatus for improving the numerical aperture at the input of a fiber optics device |
US4816123A (en) * | 1986-04-16 | 1989-03-28 | The Perkin-Elmer Corporation | Method of fabricating capillary electrophoresis separation channels |
JPS62273454A (en) * | 1986-04-28 | 1987-11-27 | アイ・シー・アイ・オーストラリヤ・リミテツド | Method and device for reaction |
CA1315181C (en) * | 1987-04-13 | 1993-03-30 | Joel M. Blatt | Test strip device with volume metering capillary gap |
US4797549A (en) * | 1987-11-09 | 1989-01-10 | General Motors Corporation | Optical sensor and method of making same |
US5710011A (en) | 1992-06-05 | 1998-01-20 | Medisense, Inc. | Mediators to oxidoreductase enzymes |
US5437999A (en) * | 1994-02-22 | 1995-08-01 | Boehringer Mannheim Corporation | Electrochemical sensor |
US5591139A (en) | 1994-06-06 | 1997-01-07 | The Regents Of The University Of California | IC-processed microneedles |
US5639428A (en) * | 1994-07-19 | 1997-06-17 | Becton Dickinson And Company | Method and apparatus for fully automated nucleic acid amplification, nucleic acid assay and immunoassay |
JP3370504B2 (en) | 1996-03-13 | 2003-01-27 | 松下電器産業株式会社 | Biosensor |
EP0907412B1 (en) * | 1996-06-28 | 2008-08-27 | Caliper Life Sciences, Inc. | High-throughput screening assay systems in microscale fluidic devices |
AT403962B (en) * | 1996-10-30 | 1998-07-27 | Avl Verbrennungskraft Messtech | DEVICE FOR CARRYING OUT ELECTROCHEMICAL AND / OR OPTICAL MEASURING PROCEDURES IN LIQUIDS |
US5759364A (en) | 1997-05-02 | 1998-06-02 | Bayer Corporation | Electrochemical biosensor |
US5798031A (en) * | 1997-05-12 | 1998-08-25 | Bayer Corporation | Electrochemical biosensor |
US5997817A (en) * | 1997-12-05 | 1999-12-07 | Roche Diagnostics Corporation | Electrochemical biosensor test strip |
US6153070A (en) * | 1998-05-07 | 2000-11-28 | Honeywell Inc | Sensor packaging using heat staking technique |
US6338790B1 (en) | 1998-10-08 | 2002-01-15 | Therasense, Inc. | Small volume in vitro analyte sensor with diffusible or non-leachable redox mediator |
MXPA01012959A (en) * | 1999-06-28 | 2002-07-30 | California Inst Of Techn | Microfabricated elastomeric valve and pump systems. |
US6547210B1 (en) | 2000-02-17 | 2003-04-15 | Wright Medical Technology, Inc. | Sacrificial insert for injection molding |
CA2364132C (en) | 2000-12-12 | 2010-06-01 | Bayer Corporation | Method of making a capillary channel |
US6576102B1 (en) | 2001-03-23 | 2003-06-10 | Virotek, L.L.C. | Electrochemical sensor and method thereof |
-
2001
- 2001-11-27 CA CA2364132A patent/CA2364132C/en not_active Expired - Fee Related
- 2001-11-27 CA CA2697026A patent/CA2697026A1/en not_active Abandoned
- 2001-11-30 AU AU95238/01A patent/AU780801B2/en not_active Ceased
- 2001-12-04 JP JP2001370285A patent/JP3850722B2/en not_active Expired - Fee Related
- 2001-12-07 US US10/010,233 patent/US6911130B2/en not_active Expired - Fee Related
- 2001-12-11 EP EP01129230A patent/EP1215479A3/en not_active Withdrawn
-
2004
- 2004-11-09 US US10/984,504 patent/US7550104B2/en not_active Expired - Fee Related
-
2006
- 2006-01-26 JP JP2006017360A patent/JP2006119155A/en active Pending
-
2007
- 2007-01-18 US US11/654,975 patent/US20070116604A1/en not_active Abandoned
- 2007-01-18 US US11/654,954 patent/US8298487B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
AU9523801A (en) | 2002-06-13 |
EP1215479A2 (en) | 2002-06-19 |
AU780801B2 (en) | 2005-04-21 |
US6911130B2 (en) | 2005-06-28 |
US20070116603A1 (en) | 2007-05-24 |
US7550104B2 (en) | 2009-06-23 |
JP3850722B2 (en) | 2006-11-29 |
JP2006119155A (en) | 2006-05-11 |
CA2364132A1 (en) | 2002-06-12 |
CA2364132C (en) | 2010-06-01 |
US8298487B2 (en) | 2012-10-30 |
US20070116604A1 (en) | 2007-05-24 |
US20050061668A1 (en) | 2005-03-24 |
EP1215479A3 (en) | 2003-10-08 |
US20020079218A1 (en) | 2002-06-27 |
JP2002257693A (en) | 2002-09-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2364132C (en) | Method of making a capillary channel | |
EP1096254B1 (en) | Capillary hematocrit separation structure and method | |
KR101295534B1 (en) | A cuvette and a method and shaping tool for manufacture thereof | |
AU776004B2 (en) | System and method for filling a substrate with a liquid sample | |
JP4142280B2 (en) | Apparatus for fluid analysis and controlled transport of fluids | |
US20070023287A1 (en) | Method of making an electrochemical sensor | |
US20020128593A1 (en) | Valve integrally associated with microfluidic liquid transport assembly | |
US5569607A (en) | Slide for the microscopic evaluation of liquid specimens | |
JP2006292742A (en) | Device having self-sealing fluid port | |
CN1898022B (en) | Cassette for handling and holding tissue samples during processing, embedding and microtome procedures, and methods therefor | |
US7586612B2 (en) | Photometric analysis of biological samples using in-plane detection | |
CN109425573B (en) | Solution detection device and detection method | |
US6607701B1 (en) | Production of microcuvettes | |
JPH11230895A (en) | Apparatus for measuring adhesion of resin-molded body | |
JP3525200B2 (en) | Liquid sample analyzer | |
JPH0430527Y2 (en) | ||
DE102020207021A1 (en) | Embossing device for producing a carrier element for an analysis device and method for producing a carrier element | |
JP3421451B2 (en) | Insert mold for dental root canal treatment instrument | |
JP2003172734A (en) | Probe for molten metal and manufacturing method therefor | |
JPH0891859A (en) | Forming device of glass cell | |
JP2002347053A (en) | Resin mold |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued |
Effective date: 20121127 |
|
FZDE | Discontinued |
Effective date: 20121127 |