CA2258898C - Microchip drug delivery devices - Google Patents

Abstract

Microchips are provided, which control both the rate and time of release of multiple chemical substances and which allow for the release of a wide variety of molecules in either a continuous or pulsatile manner. In all of the preferred embodiments, a material that is impermeable to the drugs or other molecules to be delivered and the surrounding fluids is used as the substrate. Reservoirs are etched into the substrate using either chemical (wet) etching or ion beam (dry) etching techniques well-known in the field of microfabrication.
Hundreds to thousands of reservoirs can be fabricated on a single microchip using these techniques. A release system, which includes the molecules to be delivered, is inserted into the reservoirs by injection, inkjet printing or spin coating methods. Exemplary release systems include polymers and polymeric matrices, non-polymeric matrices, and other excipients or diluents. The physical properties of the release system control the rate of release of the molecules. The reservoirs can contain multiple drugs or other molecules in variable dosages. The filled reservoirs can be capped with materials that either degrade, dissolve, or allow the molecules to diffuse passively out of the reservoir over time or materials that, upon application of an electric potential, oxidize to form soluble compounds or ions that dissolve into the surrounding fluids. Release from an active device can be controlled by a preprogrammed microprocessor, remote control, or by biosensors.

Description

MICROCHIP DRUG DELIVERY DEVICES
Background of the Invention This invention relates to miniaturized drug delivery devices and more particularly, to controlled time and rate release mufti-welled drug delivery devices.
Drug delivery is an important aspect of medical treatment. The efficacy of many drugs is directly related to the way in which they are administered. Some therapies require that the drug be repeatedly administered to the patient over a long period of time. This makes the selection of a proper drug delivery method problematic. Patients often forget, are unwilling, or are unable to take their medication. Drug delivery also becomes problematic when the drugs are too potent for systemic delivery. Therefore, attempts have been made to design and fabricate a delivery device which is capable of the controlled, pulsatile or continuous release of a wide variety of molecules including, but not limited to, drugs and other therapeutics.
Controlled release polymeric devices have been designed to provide drug release over a period of time via diffusion of the drug out of the polymer and/or degradation of the polymer over the desired time period following administration to the patient. However, these devices are relatively simple.
U.S. Patent No. 5,490,962 to Cima, et al. discloses the use of three dimensional printing methods to make more complex devices which provide release over a desired time frame, of one or more drugs.
Although the general procedure for making a complex device is described, specific designs are not detailed.
U.S. Patent No. 4,003,379 to Ellinwood describes an implantable electromechanically driven device that includes a flexible retractable walled container, which receives medication from a storage area via an inlet and then dispenses the medication into the body via an outlet. U.S.
Patent No. 4,146,029 and U.S. Patent No. 3,692,027 to Ellinwood _2_ disclose self powered medication systems that have programmable miniaturized dispensing means. U.S. Patent No. 4,360,019 to Jassawalla discloses an implantable infusion device that includes an actuating means for delivery of the drug through a catheter. The actuating means includes a solenoid driven miniature pump. All of these devices include miniature power-driven mechanical parts that are required to operate in the body, i.e., they must retract, dispense, or pump. These are complicated and subject to breakdown. Moreover, due to complexity and size restrictions, they are unsuitable to deliver more than a few drugs or drug mixtures at a time.
It is therefore an object of the present invention to provide a simple to use and manufacture, dependable, mufti-welled delivery device for drugs and other molecules which can operate for weeks or years at a time.
It is another object of the present invention to provide such a device that allows delivery of drugs or other molecules in either a pulsatile or continuous manner.
It is yet another object of the present invention to provide such a device that allows the delivery to be controlled either passively or actively.
It is also an object of the present invention to provide such a device that can hold many different drugs or other molecules of varying dosages and is small enough to be implanted, injected or swallowed, if desired.
Summary of the Invention In one aspect of the invention there is provided a microchip device for storage and release of molecules including a substrate and at least two reservoirs provided in the substrate. Molecules for release are provided in the reservoirs and reservoir caps are positioned over the molecules. Release of the molecules from the reservoir is controlled by the disintegration of the reservoir cap or diffusion of the molecules through the reservoir cap.

-2a-The invention also provides a microchip device for the storage and release of molecules including a substrate and at least two discrete reservoirs provided in spaced positions across at least one surface of the substrate. A
discrete release system is loaded in each of the two reservoirs and includes molecules dispersed in a degradable matrix material or in a non-degradable matrix material. Release of the molecules from each reservoir is controlled by the disintegration of the matrix material or diffusion of the molecules from the matrix material.
Microchips for delivery of a wide variety of molecules are provided.
Microchips are miniaturized devices constructed using methods commonly applied to the manufacture of integrated circuits such as ultraviolet (UV) photolithography, reactive ion etching, and electron beam evaporation. The microchips provide control over the rate the molecules WO 98!00107 PCT/CTS97/11589 are released as well as the time at which release begins. The time of release can be controlled passively or actively.
In the preferred embodiments, a material which is impermeable to the surrounding fluids arid to the molecules to be delivered is used as the substrate. Examples of substrate materials include ceramics, semiconductors such as silicon, and degradable and non-degradable polymers. Reservoirs are etched into the substrate using either chemical (wet) etching or ion (dry) etching techniques commonly used in microfabrication. Hundreds to thousands of reservoirs can be created in this manner and contained in a single microchip. Typically, a release system containing, encapsulating, or consisting of the molecule to be delivered is inserted into the reservoirs by injection, inkjet printing, or other means. The release system controls the rate of release of the molecule. The rate of release is a function of the composition and IS structure of the release system. The device design makes it possible to fill the reservoirs with a release system in solid, liquid, or gel form.
Each of the reservoirs of a single microchip can contain different molecules and/or different amounts and concentrations, which can be released independently.
In a preferred embodiment, the reservoir cap enables passive timed release, not requiring a power source, of molecules. The reservoirs are capped with materials that degrade or dissolve at a known rate or have a known permeability (diffusion constant) for the molecules to be delivered.
Therefore, the degradation, dissolution or diffusion characteristics of the cap material determine the time at which the release of molecules in a particular reservoir begins. In effect, the microchip provides dual control of the release of molecules by selection of the release system {rate ' controller) and selection of the cap material (time controller, and in some cases, rate controller).
In another preferred embodiment, the reservoir cap enables active timed release, requiring a power source, of molecules. In this embodiment, the reservoir caps consist of a thin film of conductive material that is deposited over the reservoir, patterned to a desired geometry, and serves as an anode. Cathodes are also fabricated on the device with their size and placement dependent on the device's application , and method of electric potential control. Conductive materials capable of dissolving into solution or forming soluble compounds or ions upon the .
application of an electric potential, including metals such as copper, gold, silver, and zinc and some polymers, are used in the active timed release device. When an electric potential is applied between an anode and cathode, the conductive material of the anode above the reservoir oxidizes to form soluble compounds or ions that dissolve into solution, exposing the release system containing the molecules to be delivered to the surrounding fluids. Alternatively, the application of an electric potential can be used to create changes in local pH near the anode reservoir cap to allow normally insoluble ions or oxidation products to become soluble.
This would allow the reservoir to dissolve and expose the release system to the surrounding fluids. In either case, the molecules to be delivered are released into the surrounding fluids by diffusion out of or by degradation or dissolution of the release system. The frequency of release is controlled by incorporation of a miniaturized power source and microprocessor onto the microchip. Activation of any reservoir can be achieved by preprogramming the microprocessor, by remote control, or by a signal from a biosensor.
Description of the Drawings Figure 1 depicts a typical fabrication scheme for a passive delivery device.
Figure 2 depicts a typical fabrication scheme for an active delivery device.
Figure 3 depicts a typical device control circuitry flowsheet.
Figure 4 depicts a passive delivery device.
Figure 5 depicts an active delivery device.

Figure 6 depicts an active device including insulator overlayers.
Figures 7a-i are schematic views of several configurations of passive delivery devices.
Figures 8a-c are schematic views of several configurations of v 5 active delivery devices.
Detailed Description Microchip devices have been provided which can accurately deliver drugs and other molecules at defined rates and times according to the needs of the patient or other experimental system. As used herein, a "microchip" is a miniaturized device fabricated using methods commonly applied to the manufacture of integrated circuits such as ultraviolet (UV) photolithography, reactive ion etching, and electron beam evaporation, as described, for example, by S. Wolf and R.N. Tauber, Silicon Processing for the VLSI Era, Volume I - Process Technoloy , Lattice Press, Sunset Beach, CA, 1986; and R.C. Jaeger, Introduction to Microelectronic Fabrication, Volume V in the Modular Series on Solid State Devices, Addison-Wesley, Reading, MA, 1988. The microchips provide control over the rate the molecules are released as well as the time at which release begins. The time of release can be controlled passively or actively. The microchip fabrication procedure allows the manufacture of devices with primary dimensions (length of a side if square or rectangular, or diameter if circular) ranging from a few millimeters to several centimeters. A typical device thickness is 300 Vim. However, the thickness of the device can vary from approximately 10 ~.m to several millimeters. Changing the device thickness affects the maximum number of reservoirs that may be incorporated onto a microchip and the volume of each reservoir. In vivo applications of the device would typically require devices having a primary dimension of 2 cm or smaller. Devices for in vivo applications are small enough to be swaIlored or implanted using minimally invasive procedures. Smaller in vivo devices {on the order of a millimeter) can be implanted using a catheter or other injectable means. Devices for in vitro applications have fewer size restrictions and, if necessary, can be made much larger than the dimension ranges for in vivo devices.
MATERIALS FOR DEVICE FABRICATION
Each device consists of a substrate, reservoirs, and a release system containing, enclosing, or layered with the molecules to be delivered. Devices which control the release time of the molecules may include reservoir caps. Active devices may include control circuitry and a power source.
IO The substrate The substrate contains the etched or machined reservoirs and serves as the support for the microchip. Any material which can serve as a support, is suitable for etching or machining, and is impermeable to the molecules to be delivered and to the surrounding fluids, for example, IS water, blood, electrolytes or other solutions, may be used as a substrate.
Biocompatibiiity of the substrate material is preferred, but not required.
For in vivo applications, non-biocompatible materials may be encapsulated in a biocompatible material, such as poly(ethyiene glycol) or polytetrafluoroethylene-like materials, before use. One example of a 20 strong, non-degradable, easily etched substrate that is impermeable to the molecules to be delivered and the surrounding fluids is silicon. In another embodiment, the substrate is made of a strong material that degrades or dissolves over a period of time into biocompatible components. This embodiment is preferred for in vivo applications where the device is 25 implanted and physical removal of the device at a Later time is not feasible or recommended, for example, brain implants. An example of a class of strong, biocompatible materials are the poly(anhydride-co-imides), discussed by K.E. Uhrich et al., "Synthesis and characterization of degradable poly(anhydride-co-imides)", Macromolecules, 1995, 28, 2184-30 93.

Release system The molecules to be delivered may be inserted into the reservoirs in their pure form, as a liquid solution or gel, or they may be encapsulated within or by a release system. As used herein, "release system" includes both the situation where the molecules are in pure form, as either a solid or liquid, or are in a matrix formed of degradable material or a material which releases incorporated molecules by diffusion out of or disintegration of the matrix. The molecules can be sometimes contained in a release system because the degradation, dissolution or diffusion properties of the release system provide a method for controlling the release rate of the molecules. The molecules can be homogeneously or heterogeneously distributed within the release system. Selection of the release system is dependent on the desired rate of release of the molecules. Both non-degradable and degradable release systems can be used for delivery of molecules. Suitable release systems include polymers and polymeric matrices, non-polymeric matrices, or inorganic and organic excipients and diluents such as, but not limited to, calcium carbonate and sugar. Release systems may be natural or synthetic, although synthetic release systems are preferred due to the better characterization of release profiles. The release system is selected based on the period over which release is desired, generally in the range of at least three to twelve months for in vivo applications. In contrast, release times as short as a few seconds may be desirable for some in vitro applications. In some cases, continuous (constant) release from a reservoir may be most useful. In other cases, a pulse (bulk) release from a reservoir may provide more effective results. Note that a single pulse from one reservoir can be transformed into pulsatile release by using multiple reservoirs. It is also - possible to incorporate several layers of a release system and other materials into a single reservoir to achieve pulsatile delivery from a single reservoir . Continuous release can be achieved by incorporating a release system that degrades, dissolves, or allows diffusion of molecules through WO 98/OO1U7 PCT/LTS97/ii589 _g_ it over an extended period of time. In addition, continuous release can be stimulated by releasing several pulses of molecules in quick succession.
The release system material can be selected so that molecules of various molecular weights are released from a reservoir by diffusion out or through the material or degradation of the material. Biodegradable polymers, bioerodible hydrogels, and protein delivery systems are preferred for release of molecules by diffusion, degradation, or dissolution. In general, these materials degrade or dissolve either by .
enzymatic hydrolysis or exposure to water in vivo or in vitro, or by surface or bulk erosion. Representative synthetic, biodegradable polymers include: poly(amides) such as poly(amino acids) and poly(peptides);
polyesters) such as poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic acid), and poly(caprolactone); poly(anhydrides};
poly(orthoesters); poly(carbonates); and chemical derivatives thereof (substitutions, additions of chemical groups, for example, alkyl, alkylene, hydroxylations, oxidations, and other modifications routinely made by those skilled in the art), copolymers and mixtures thereof.
Representative synthetic, non-degradable polymers include:
poly(ethers) such as polyethylene oxide), polyethylene glycol), and poly(tetramethylene oxide); vinyl polymers - poly(acrylates) and poly(methacrylates) such as methyl, ethyl, other alkyl, hydroxyethyl methacrylate, acrylic and methacrylic acids, and others such as polyvinyl alcohol), polyvinyl pyrolidone), and polyvinyl acetate}; poly(urethanes);
cellulose and its derivatives such as alkyl, hydroxyalkyI, ethers, esters, nitrocellulose, and various cellulose acetates; poiy(siloxanes); and any chemical derivatives thereof (substitutions, additions of chemical groups, for example, alkyl, alkylene, hydroxylations, oxidations, and other modifications routinely made by those skilled in the art), copolymers and mixtures thereof.

WO 98/00107 P'CT/US97/11589 Molecules to be released Any natural or synthetic, organic or inorganic molecule or mixture thereof can be delivered. In one embodiment, the microchip is used to deliver drugs systemically to a patient in need thereof. In another embodiment, the construction and placement of the microchip in a patient enables the localized release of drugs that may be too potent for systemic delivery. As used herein, drugs are organic or inorganic molecules, including proteins, nucleic acids, polysaccharides and synthetic organic molecules, having a bioactive effect, for example, anaesthetics, vaccines, I0 chemotherapeutic agents, hormones, metabolites, sugars, immunomodulators, antioxidants, ion channel regulators, and antibiotics.
The drugs can be in the form of a single drug or drug mixtures and can include pharmaceutically acceptable carriers. In another embodiment, molecules are released in vitro in any system where the controlled release IS of a small (milligram to nanogram) amount of one or more molecules is required, for example, in the fields of analytic chemistry or medical diagnostics. Molecules can be effective as pH buffering agents, diagnostic agents, and reagents in complex reactions such as the polymerase chain reaction or other nucleic acid amplification procedures.
20 Reservoir caps In the passive timed release drug delivery devices, the reservoir caps are formed from a material that degrades or dissolves over time, or does not degrade or dissolve but is permeable to the molecules to be delivered. These materials are preferably polymeric materials. Materials 25 can be selected for use as reservoir caps to give a variety of degradation rates or dissolution rates or permeabilities to enable the release of molecules from different reservoirs at different times and, in some cases, - different rates. To obtain different release times (amounts of release time delay), caps can be formed of different polymers, the same polymer with 30 different degrees of crosslinking, or a UV polymerizable polymer. In the latter case, varying the exposure of this polymer to UV light results in varying degrees of crosslinking and gives the cap material different WO 98/00107 I'CT/LTS97l11589 diffusion properties or degradation or dissolution rates. Another way to obtain different release times is by using one polymer, but varying the thickness of that polymer. Thicker films of some polymers result in , delayed release time. Any combination of polymer, degree of crosslinking, or polymer thickness can be modified to obtain a specific release time or rate. In one embodiment, the release system containing the molecules to be delivered is covered by a degradable cap material which is nearly impermeable to the molecules. The time of release of the molecules from the reservoir will be limited by the time necessary for the cap material to degrade or dissolve. in another embodiment, the cap material is non-degradable and is permeable to the molecules to be delivered. The physical properties of the material used, its degree of crosslinking, and its thickness will determine the time necessary for the molecules to diffuse through the cap material. If diffusion out of the release system is limiting, the cap material delays the onset of release. If diffusion through the cap material is Limiting, the cap material determines the release rate of the molecules in addition to delaying the onset of release.
In the active timed release devices, the reservoir caps consist of a thin film of conductive material that is deposited over the reservoir, patterned to a desired geometry, and serves as an anode. Cathodes are also fabricated on the device with their size and placement dependent on the device's application and method of electric potential control. The anode is defined as the electrode where oxidation occurs. Any conductive material capable of dissolving into solution or forming soluble ions or oxidation compounds upon application of an electric potential can be used for the fabrication of the anodes and cathodes. In addition, materials that normally form insoluble ions or oxidation products in response to an electric potential can be used if, for example, Local pH changes near the anode cause these oxidation products to become soluble. Examples of suitable reservoir cap materials include metals such as copper, gold, silver, and zinc, and some polymers, as described, for example, by LC.

Kwon et al. , "Electrically erodible polymer gel for controlled release of drugs", Nature, 1991, 354, 291-93; and Y.H. Bae et al., "Pulsatile drug release by electric stimulus", ACS Symposium Series, 1994, 545, 98-110.
Device packaging, control circuitry, and power source Microelectronic device packages are typically made of an insulating or dielectric material such as aluminum oxide or silicon nitride.
Their purpose is to allow all components of the device to be placed in close proximity and to facilitate the interconnection of components to power sources and to each other. For in vivo applications of the delivery device, the entire package, including all components (i.e. the device, the microprocessor, and the power source), are coated or encapsulated in a biocompatible material such as polyethylene glycol) or polytetrafluoroethylene-like materials. The materials requirements for in vitro applications may be less stringent and depend on the particular situation.
The control circuitry consists of a timer, a demultiplexer, a microprocessor, and a input source, for example, a memory source, a signal receiver, or a biosensor. The timer and demultiplexer circuitry can be designed and incorporated directly onto the surface of the microchip during electrode fabrication. The criteria for selection of a microprocessor are small size, low power requirement, and the ability to translate the output from memory sources, signal receivers, or biosensors into an address for the direction of power through the demultiplexer to a specific reservoir on the delivery device. Selection of a source of input to the microprocessor such as memory sources, signal receivers, or biosensors depends on the delivery device's particular application and whether device operation is preprogrammed, controlled by remote means, or controlled by feedback from its environment (i.e. biofeedback).
The criteria for selection of a power source are small size, sufficient power capacity, ability to be integrated into the control circuitry, the ability to be recharged, and the length of time before recharging is necessary. Several lithium-based, rechargeable microbatteries have been described by S.D. Jones and J.R. Akridge, "Development and performance of a rechargeable thin-film solid-state microbattery", Journal of Power Sources, 1995, 54, 63-67; and J.B.
Bates et al. , "New amorphous thin-film lithium electrolyte and rechargeable microbattery", IEEE 35'" International Power Sources Symposium, 1992, 337-39. These batteries are typically only ten microns thick and occupy 1 em2 of area. One or more of these batteries can be incorporated directly onto the delivery device.
METHODS OF DEVICE FABRICATION
Fabrication of the reservoirs Devices are manufactured using methods known to those skilled in the art, reviewed, for example, by Wolf et al. (1986); and Jaeger (1988);
Kwon et al. (1991).
In a preferred method of microchip manufacture, depicted in Figures i and 2, passive and active devices, respectively, fabrication begins by depositing and photolithographically patterning a material, typically an insulating or dielectric material, onto the substrate to serve as an etch mask during reservoir etching. Typical insulating materials for use as a mask include silicon nitride, silicon dioxide, and some polymers, such as polyimide. In a preferred embodiment, a thin film (approximately 1000-3000 ~) of amorphous silicon nitride (SiNx) is deposited on both sides of a silicon wafer 30/300 by Plasma Enhanced Chemical Vapor Deposition (PECVD). Alternatively, a low stress, silicon-rich nitride can be deposited in a Vertical Tube Reactor (VTR), or a stoichiometric, polycrystalline nitride can be deposited by Low Pressure Chemical Vapor Deposition (LPCVD). Reservoirs are patterned into the silicon nitride film on one side of the wafer 32/320 by ultraviolet photolithography and either plasma etching or a chemical etch consisting of hot phosphoric acid. The patterned silicon nitride serves as an etch mask for the chemical etching of the exposed silicon 34/340 by a concentrated potassium hydroxide solution (approximately 38.5 ~ wt. at a temperature of 80-85°C). Alternatively, the reservoirs can be etched into the substrate WO 98/00107 PCT/LTS9711i589 by dry etching techniques such as reactive ion etching or ion beam etching. These techniques are commonly used in the fabrication of microelectronic devices, as reviewed, for example, by Wolf et al. (1986) and Jaeger (1988). Use of these microfabrication techniques allows the incorporation of hundreds to thousands of reservoirs on a single microchip. In a passive device, the reservoirs may be as little as one ,um apart. In an active device, the distance between the reservoirs may be slightly larger (approximately 10-15 gum) due to the space occupied by the electrodes on or near each reservoir. Reservoirs can be made in nearly any shape and depth, and need not pass completely through the substrate.
In a preferred embodiment, the reservoirs etched into a {100) silicon substrate by potassium hydroxide are in the shape of a square pyramid having side walls sloped at 54° and pass completely through the substrate (approximately 300 ~.m) to the silicon nitride film on the other side of the substrate, forming a SiN4 membrane. {Here, the silicon nitride film serves as a potassium hydroxide etch stop. ) The pyramidal shape allows easy filling of the reservoirs through the large opening of the reservoir (approximately 500 ~,m by 500 ~,m) on the patterned side of the substrate, release through the small opening of the reservoir (approximately 30 lcm by 30 ,um) on the other side of the substrate, and provides a large cavity inside the device for storing the drugs or other molecules to be delivered.
Fabrication of passive timed release reservoir caps In the fabrication of passive timed release microchips, the reservoir cap material is injected with a micro-syringe 36a, printed with an inkjet printer cartridge, or spin coated 36b into a reservoir having the thin film of insulating mask material still present over the small opening of the reservoir. If injection or inkjet printing methods are used, cap formation is complete after the material is injected or printed into the reservoir 38a and does not require further. processing. If spin coating is used, the cap material is planarized by multiple spin coatings 36b. The surface of the film is then etched by a plasma, an ion beam, or chemical etchant until the desired cap thickness is obtained 38b. In a preferred embodiment, the insulating material used is silicon nitride and the cap material is printed into the reservoir with an inkget cartridge filled with a solution of the cap material.
Reservoir caps control the time at which molecules are released from the reservoirs. Each reservoir cap can be of a different thickness or have different physical properties to vary the time at which each release system containing the molecules is exposed to the surrounding fluids.
Injection, inkjet printing, and spin coating are the preferred methods of reservoir filling and any of these methods may be used to fill reservoirs, regardless of the reservoir's shape or size. However, injection and inkjet printing are the preferred methods of filling deep (greater than 10 p,m) reservoirs or reservoirs with large openings (greater than 100 hem) . For example, to obtain different cap thicknesses using injection, different amounts of cap material are injected or printed directly into each individual reservoir. Spin coating is the preferred method of filling shallow (less than 10 ,um) reservoirs, reservoirs that do not pass completely through the substrate, or reservoirs with small (less than 100 ~cm} openings. Variation in cap thickness or material by spin coating can be achieved by a repeated, step-wise process of spin coating, masking selected reservoirs, and etching. For example, to vary cap thickness with spin coating, the cap material is spin coated over the entire substrate.
Spin coating is repeated, if necessary, until the material is nearly planarized. A mask material such as photoresist is patterned to cover the cap material in all the reservoirs except one. Plasma, ion beam, or chemical etchant are used to etch the cap material in the exposed reservoir to the desired thickness. The photoresist is then removed from the substrate. The process is repeated as a new layer of photoresist is deposited and patterned to cover the cap material in all the reservoirs except one (the exposed reservoir is not the same one already etched to its desired thickness). Etching of the exposed cap material in this reservoir continues until the desired cap thickness is obtained. This process of depositing and patterning a mask material such as photoresist, etching, and mask removal can be repeated until each reservoir has its own unique cap thickness. The techniques, UV photolithography, plasma or ion beam etching, etc., are well known to those skilled in the field of microfabrication.
Although injection, inkjet printing and spin coating are the preferred methods of cap fabrication, it is understood that each reservoir can be capped individually by capillary action, by pulling or pushing the material into the reservoir using a vacuum or other pressure gradient, by melting the material into the reservoir, by centrifugation and related processes, by manually packing solids into the reservoir, or by any combination of these or similar reservoir filling techniques.
Once a cap fabrication method is selected, additional methods for controlling the time of release of molecules from a reservoir can be utilized. Two non-Limiting examples include either UV polymerizable polymers or the layering of release system and cap materials. First, if the reservoir caps are made of either an injected, inkjet printed or spin coated UV polymerizable polymer, each cap can be exposed to a different intensity of UV light to give varying degrees of crosslinking and therefore, different degradation or dissolution rates for degradable caps or different perrneabilities to the molecules for non-degradable caps.
Second, layers of cap material, both degradable and non-degradable, can be inserted between Layers of the release system containing the molecules to be delivered by injection, inkjet printing, spin coating, or selective crosslinking. These and other similar methods allow complex release profiles (i.e. pulsatile delivery at irregular time intervals} to be achieved from a single reservoir.
If desired, a passive timed release device can be fabricated without reservoir caps. The rate of release of the molecules is thus solely controlled by the physical and material properties of the release system containing the molecule to be delivered.

WO 98/001.07 PCT/U597/11589 Fabrication of active timed release reservoir caps In a preferred embodiment, photoresist is patterned in the form of electrodes on the surface of the substrate having the reservoirs covered by , the thin membrane of insulating or dielectric material. The photoresist is developed such that the area directly over the covered opening of the .
reservoir is left uncovered by photoresist and is in the shape of an anode.
A thin film of conductive material capable of dissolving into solution or forming soluble ions or oxidation compounds upon the application of an electric potential is deposited over the entire surface using deposition techniques such as chemical vapor deposition, electron or ion beam evaporation, sputtering, spin coating, and other techniques known in the art. Exemplary materials include metals such as copper, gold, silver, and zinc and some polymers, as disclosed by Kwon et al. (I991) and Bae et al. (1994). After film deposition, the photoresist is stripped from the substrate. This removes the deposited film, except in those areas not covered by photoresist (lift-off technique). This leaves conducting material on the surface of the substrate in the form of electrodes 360. An alternative method involves depositing the conductive material over the entire surface of the device, patterning photoresist on top of the conductive film using LTV or infrared (IR) photolithography, so that the photoresist lies over the reservoirs in the shape of anodes, and etching the unmasked conductive material using plasma, ion beam, or chemical etching techniques. The photoresist is then stripped, leaving conductive film anodes covering the reservoirs. Typical film thicknesses of the conductive material may range from 0.05 to several microns. The anode serves as the reservoir cap and the placement of the cathodes on the device is dependent upon the device's application and method of electric potential control.
An insulating or dielectric material such as silicon oxide (SiOX) or silicon nitride (SiNX) is deposited over the entire surface of the device by methods such as chemical vapor deposition (CVD), electron or ion beam evaporation, sputtering, or spin coating. Photoresist is patterned on top of the dielectric to protect it from etching except on the cathodes and the portions of the anodes directly over each reservoir 380. The dielectric material can be etched by plasma, ion beam, or chemical etching techniques. The purpose of this film is to protect the electrodes from corrosion, degradation, or dissolution in all areas where electrode film is not necessary for release.
The electrodes are positioned in such a way that when an electric between an anode and a cathode, the unprotected (not covered by dielectric) portion of the anode reservoir cap oxidizes to form soluble compounds or ions that dissolves into solution, exposing the release system containing the molecules to the surrounding fluids. The molecules are released from the reservoir at a rate dependent upon the degradation or dissolution rate of a degradable release system or the rate of diffusion of the molecules out of or through a non-degradable release system.
Removal of the insulator membrane (reservoir etch stop) The thin membrane of insulating or dielectric material covering the reservoir used as a mask and an etch stop during reservoir fabrication must be removed from the active timed release device before filling reservoir 400 and from the passive timed release device (if the reservoir extends completely through the substrate) after filling reservoir 44. The film may be removed in two ways. First, the film can be removed by an ion beam or reactive ion plasma. In a preferred embodiment, the silicon nitride film used as the insulating material can be removed by a reactive ion plasma composed of oxygen and fluorine containing gases such as CHF3 or CF4. Second, the film can be removed by chemical etching.
For example, buffered hydrofluoric acid (BHF or BOE) can be used to etch silicon dioxide and hot phosphoric acid can be used to etch silicon nitride.

WO 98!00107 PCT/US97/11589 Reservoir filling The release system containing the molecules for delivery is inserted into the large opening of the reservoir by injection, inkjet , printing or spin coating 40a/40b/400. Each reservoir can contain a different molecule and dosage. Similarly, the release kinetics of the molecule in each reservoir can be varied by the choice of the release system and cap materials. In addition, the mixing or layering of release system and cap materials in each reservoir can be used to tailor the release kinetics to the needs of a particular application.
The distribution over the microchip of reservoirs filled With the release system containing the molecules to be delivered can vary depending on the medical needs of the patient or other requirements of the system. For applications in drug delivery, for example, the drugs in each of the rows can differ from each other. One row may contain a hormone I5 and another row may contain a metabolite. Also, the release system can differ within each row to release a drug at a high rate from one reservoir and a slow rate from another reservoir. The dosages can also vary within each row. For those devices having deep (greater than 10 ,gym) reservoirs or reservoirs with large (greater than 100 /cm) openings, differences in reservoir loading can be achieved by injection or inkjet printing of different amounts of material directly into each reservoir. Variation between reservoirs is achieved in devices having shallow (less than 10 um) reservoirs, reservoirs that do not pass completely through the substrate, or reservoirs with small (less than 100 ~cm) openings by a repeated, step-wise process of masking selected reservoirs, spin coating, and etching, as described above regarding the fabrication by spin coating of passive timed release reservoir caps. Preferably, the release system and molecules to be delivered are mixed before application to the ' reservoirs. Although injection, inkjet printing and spin coating are the preferred methods of filling reservoirs, it is understood that each reservoir can be filled individually by capillary action, by pulling or pushing the material into the reservoir using a vacuum or other pressure gradient, by melting the material into the reservoir, by centrifugation and related processes, by manually packing solids into the reservoir, or by any combination of these or similar reservoir filling techniques.
Device packaging, control circuitry, and power source _ S The openings through which the reservoirs of passive and active devices are filled are sealed by wafer bonding or with a waterproof epoxy or other appropriate material impervious to the surrounding fluids 44/440.
For in vitro applications, the entire unit, except for the face of the device containing the reservoirs and electrodes, is encased in a material appropriate for the system. For in vivo applications, the unit would be encapsulated in a biocornpatibie material such as polyethylene glycol) or polytetrafluoroethylene.
The mechanism for release of molecules by the active timed release device does not depend on multiple parts fitted or glued together which must retract or dislodge. Control of the time of release of each reservoir can be achieved by a preprogrammed microprocessor, by remote control, by a signal from a biosensor, or by any combination of these methods, as shown schematically in Figure 3. First, a microprocessor is used in conjunction with a source of memory such as programmable read only memory (PROM), a timer, a demultiplexer, and a power source such as a microbattery, such as is described, for example, by Jones et al.
(1995) and Bates et al. (1992). The release pattern is written directly into the PROM by the user. The PROM sends these instructions to the microprocessor. When the time fox release has been reached as indicated by the timer, the microprocessor sends a signal corresponding to the address (location) of a particular reservoir to the demultiplexer. The demultiplexer sends an input, such as an electric potential, to the reservoir addressed by the microprocessor. A microbattery provides the power to operate the PROM, timer, and microprocessor, and provides the electric potential input that is directed to a particular reservoir by the demultiplexer. The manufacture, size, and location of each of these components is dependent upon the requirements of a particular application. In a preferred embodiment, the memory, timer, microprocessor, and demultiplexer circuitry is integrated directly onto the surface of the chip. The rnicrobattery is attached to the other side of the chip and is connected to the device circuitry by vias or thin Wires.
However, in some cases, it is possible to use separate, prefabricated, -component chips for memory, timing, processing, and demultipIexing.
These are attached to the backside of the miniaturized delivery device with the battery. The size and type of prefabricated chips used depends on the overall dimensions of the delivery device and the number of reservoirs. Second, activation of a particular reservoir by the application of an electric potential can be controlled externally by remote control.
Much of the circuitry used for remote control is the same as that used in the preprogrammed method. The main difference is that the PROM is replaced by a signal receiver. A signal such as radio waves, low power laser, or ultrasound is sent to the receiver by an external source, for example, computers or ultrasound generators. The signal is sent to the microprocessor where it is translated into a reservoir address. Power is then directed through the demultiplexer to the reservoir having the appropriate address. Third, a biosensor is integrated into the microchip to detect molecules in the surrounding fluids. When the concentration of the molecules reaches a certain level, the sensor sends a signal to the microprocessor to activate one or more reservoirs. The microprocessor directs power through the demultipIexer to the particular reservoir(s).
Electric Potential Control Methods The reservoir caps of an active device are anodes that oxidize to form soluble compounds and ions when a potential is applied between the anode and a cathode. For a given electrode material and electrolyte, there exists a range of electric potentiais over which these oxidation reactions are thermodynamically and kinetically favorable. In order to reproducibly oxidize and open the device's reservoir caps, the anode potential must be maintained in this potential range.

There exist two primary control methods for maintaining an electrode within a specific potential range. The first method is called potentiostatic control. As the name indicates, the potential is kept constant during reservoir activation. Control of the potential is typically r 5 accomplished by incorporating a third electrode into the system that has a known, constant potential, called a reference electrode. The reference electrode can take the form of an external probe whose tip is placed within one to three mm of the anode surface. The potential of the anode is measured and controlled with respect to the known potential of a IO reference electrode such as a saturated calomel electrode (SCE). In a preferred embodiment of potentiostatic control, a thin film reference electrode and potential feedback controller circuitry could be fabricated directly onto the surface of the microchip. For example, a microfabricated Ag/AgCI reference electrode integrated with a microchip 15 device would enable the device to maintain the anode potential of an activated reservoic within the oxidation regime until the reservoir was completely opened. The second method is called galvanostatic control.
As the name indicates, the current is kept constant during reservoir activation. One drawback to this method of control is that there is more 20 than one stable potential for a given current density. However, if the current density versus potential behavior is well characterized for the microchip device in a particular electrolyte system, the current density that will maintain the anode in teh oxidation regime will be known. In this case, the galvanostatic method of potential control would be 25 preferable to the potentiostatic control, because galvanostatic control does not require a reference electrode.
MICROCHIP APPLICATIONS
Passive and active microchip devices have numerous in vitro and in vivo applications. The microchip can be used in vitro to deliver small, 30 controlled amounts of chemical reagents or other molecules to solutions or reaction mixtures at precisely controlled times and rates. Analytical chemistry and medical diagnostics are examples of fields where the microchip delivery device can be used. The microchip can be used in vivo as a drug delivery device. The microchips can be implanted into a patient, either by surgical techniques or by injection, or can be swallowed. The microchips provide delivery of drugs to animals or persons who are unable to remember or be ambulatory enough to take -medication. The microchips further provide delivery of many different drugs at varying rates and at varying times of delivery.
The present invention will be further understood by reference to the following non-limiting examples.
Example 1: Microchip with passive timed drug release.
A passive timed release device, microchip 10 is shown in Figure 4. Microchip 10 is formed from substrate 14. Reservoirs I6 are etched into substrate 14. Positioned in reservoirs 16 is a release system containing molecules I8 for delivery. The reservoirs are capped with reservoir caps 12. The release system and the molecules for delivery 18 can vary between rows 20a, 20b, 20c, and within reservoirs of each row.
Microchip 10 can be inserted into solution for in vitro applications or be implanted in a selected part of the body or swallowed for in vivo applications and left to operate without requiring further attention. When exposed to the surrounding fluids, reservoir caps 12 will degrade, dissolve or become permeable to the release system containing molecules for delivery 18.
Figures 7a-i depict several additional possible configurations for passive delivery devices.
Example 2: Microchip with active controlled time release.
A drug delivery device that provides active timed release is shown as microchip 100 in Figure 5. Microchip 100 is similar to microchip 10 except that microchip 100 contains electrodes that provide for active timed release. Microchip 100 is formed from substrate 160, release system containing molecules 180 for delivery, anode reservoir caps 120, and cathodes 140. Preferably, microchip 100 further includes an input source, a microprocessor, a timer, a demultiplexer, and a power source (not shown). The power source provides energy to drive the reaction between selected anodes and cathodes. Upon application of a small potential between an anode and cathode, electrons pass from the anode to the cathode through the external circuit causing the anode material to oxidize and form soluble compounds or ions that dissolve into the surrounding fluids, exposing the release system containing the molecules for delivery 180 to the surrounding fluids. The microprocessor directs power to specific electrode pairs through a demultiplexer as directed by a PROM, remote control, or biosensor.
Figure 6 is a schematic of a second embodiment of a microchip 200 from from substrate 260 actively releasing drug 280 from the device upon application of an electric potential between an anode and cathode, which, unlike the device in Figure 5, includes an insulator overlayer.
Figures 8a-c depicts three additional possible configurations for active delivery devices.

Claims (38)

We claim:

1. A microchip device for the storage and release of molecules comprising:
a substrate;
at least two reservoirs provided in the substrate;
molecules for release, the molecules being provided in the at least two reservoirs; and reservoir caps positioned over the molecules, wherein release of the molecules from the reservoir is controlled by the disintegration of the reservoir cap or diffusion of the molecules through the reservoir cap.

2. The device of claim 1, wherein the reservoir cap is impermeable to the molecules and disintegration of the reservoir cap is actively controlled.

3. The device of claim 2, further comprising a cathode, a microprocessor, and a power source, wherein the reservoir cap is an anode, and wherein upon application of an electric potential between the cathode and the anode, the reservoir cap oxidizes, dissolves, and disintegrates to release the molecules.

4. The device of claim 2 or 3, wherein release of the molecules from one of the reservoirs is controlled by a signal from a biosensor, by remote control, or by a preprogrammed microprocessor.

5. The device of any one of claims 1-4, wherein the substrate comprises silicon.

6. The device of any one of claims 1-5, wherein the reservoir cap comprises a metal film.

7. The device of claim 1, wherein the disintegration of the reservoir cap is passively controlled.

8. The device of claim 7, wherein the release of the molecules from the reservoirs is controlled by the in vivo disintegration of the reservoir cap.

9. The device of claim 1 or 8, wherein the reservoir cap comprises a polymer.

10. The device of any one of claims 1-9, wherein the molecules for release are dispersed in a matrix material.

11. The device of claim 10, wherein the matrix material comprises a polymer.

12. The device of any one of claims 1-11, wherein the molecules for release comprise at least one drug.

13. A microchip device for the storage and release of molecules comprising:
a substrate;
at least two discrete reservoirs provided in spaced positions across at least one surface of the substrate; and a discrete release system loaded in each of the at least two reservoirs, the release system including molecules dispersed in a degradable matrix material or in a non-degradable matrix material, wherein release of the molecules from each reservoir is controlled by the disintegration of the matrix material or diffusion of the molecules from the matrix material.

14. The device of claim 13, wherein the molecules for release are drug molecules dispersed in a degradable matrix material and the release of the drug molecules from the reservoirs is controlled by the in vivo dissolution, enzymatic hydrolysis, or erosion of the matrix material.

15. The device of claim 14, wherein the matrix material comprises one or more hydrogels or biodegradable polymers.

16. The device of claim 15, wherein said one or more biodegradable polymers are selected from poly(amides), poly(esters), poly(anhydrides), poly(orthoesters), poly(carbonates), copolymers thereof, or mixtures thereof.

17. The device of claim 15, wherein said one or more biodegradable polymers are selected from poly(lactic acids), poly(glycolic acids), poly(lactic-co-glycolic acids), poly(caprolactones), or mixtures thereof.

18. The device of claim 13, wherein the molecules for release are drug molecules dispersed in a non-degradable matrix material and the release of the drug molecules from the reservoirs is controlled by the in vivo diffusion of the drug molecules from the matrix material.

19. The device of claim 18, wherein the matrix material comprises one or more hydrogels or synthetic polymers.

20. The device of claim 19, wherein said one or more synthetic polymers are selected from poly(ethers), poly(acrylates), poly(methacrylates), poly(vinyl pyrolidones), poly(vinyl acetates), poly(urethanes), celluloses, cellulose acetates, and poly(siloxanes).

21. The device of any one of claims 13-20, further comprising at least two discrete reservoir caps, each reservoir cap covering one of the at least two reservoirs, and further controlling release of the molecules from the reservoirs by the disintegration of the reservoir cap or diffusion of the molecules through the reservoir cap.

22. The device of any one of claims 1-12 and 21, wherein the reservoir cap is degradable and comprises a material that disintegrates in vivo by dissolution, enzymatic hydrolysis, or erosion.

23. The device of any one of claims 1-12 and 21, wherein the reservoir cap is non-degradable and permeable to the molecules.

24. The device of any one of claims 21-23, wherein one of the reservoir caps is formed of a first material and the other of the at least two reservoir caps is formed of a second material, wherein the first material has a different disintegration rate in vivo or different permeability to the molecules compared to the second material.

25. The device of any one of claims 21-24, wherein one of the reservoir caps has a first thickness and the other of the at least two reservoir caps has a second, greater thickness.

26. The device of any one of claims 21-25, wherein at least one of the discrete reservoir caps comprises one or more synthetic polymers.

27. The device of any one of claims 1-26, wherein the molecules comprise one or more therapeutic agents selected from anesthetics, chemotherapeutic agents, hormones, immunomodulators, ion channel regulators, and antibiotics.

28. The device of any one of claims 1-27, wherein the molecules comprise drug molecules and the dose of drug molecules in one of the at least two reservoirs is different from the dose of drug molecules in the other of the at least two reservoirs.

29. The device of any one of claims 1-28, wherein the kinetics of release of the molecules from one of the at least two reservoirs is different from the kinetics of release of the molecules from the other of the at least two reservoirs.

30. The device of any one of claims 1-29, wherein the molecules comprise drug molecules and a first drug is in one of the at least two reservoirs and a second, different drug is in the other of the at least two reservoirs.

31. The device of any one of claims 1-30, wherein at least one of the reservoirs comprises two or more layers of the release system.

32. The device of claim 31, wherein a first drug is contained in a first layer of the two or more layers, and a second drug is contained in a second layer of the two or more layers.

33. The device of any one of claims 1-32, wherein at least one of the reservoirs comprises:
at least two layers of a release system comprising a drug, and at least one layer of a degradable or soluble material which does not comprise any drug and which is disposed between the at least two layers of a release system comprising the drug.

34. The device of any one of claims 1-33, wherein release of the molecules from the device is in pulsatile manner.

35. The device of any one of claims 1-34, comprising at least two rows of the at least two reservoirs in an array in the device.

36. The device of claim 35, wherein release across the substrate surface differs in the type of molecules released or in the release kinetics.

37. The device of any one of claims 1-36, which is adapted for implantation into a patient.

38. The device of claim 1, which is made by a process comprising the steps of:

depositing and patterning a material on a substrate, the material being an etch mask;
etching a plurality of reservoirs in the substrate;
filling the reservoirs with a composition comprising the molecules for release;
and capping the reservoirs with a cap material which is selectively permeable to the molecules, a cap material which disintegrates to release the molecules, or a combination thereof.