Patent Application
20050230767
1. Field of the Invention
This invention relates generally to micro-fluidic biological micro-electro-mechanical systems (MEMS).
2. Description of Related Art
The use of micro-electro-mechanical systems (MEMS) in biological research is becoming increasingly common. Micro-devices allow for relatively easy observation and manipulation of individual cells, proteins, or other biological macromolecules. Sample sizes for such experiments may be reduced when using MEMS as compared to traditional techniques. J. D. Trumbull, et al., IEEE Transactions on Biomed. Eng. 47, 3 (2000). This allows biological systems to be studied at a new level of resolution while minimizing the materials required for an experiment.
Initially, microfluidic devices were used primarily for capillary electrophoresis. S. Jacobson, et al., Anal. Chem. 66 (1994) 1114; D. J. Harrison, et al., Anal. Chem. 64 (1992) 1926; Z. Liang, et al.; Anal. Chem. 68 (1996) 1040. Recently, there has been interest in incorporating a complete array of functional units, e.g., valves, pumps, reaction chambers, etc., onto a single chip to create a lab-on-a-chip (LOC). J. Voldman, et al., J. Microelectromech. Sys. 9 (2000) 295; I. Glasgow, et al., IEEE Transactions on Biomed. Eng. 48 (2001) 570; T. Fujii, Microelectronic Eng., 61-62 (2002) 907; A. Yamaguchi, et al., Analytical Chimica Acta., 468 (2002) 143; J. H. Kim, et al., Sensors and Actuators A. 95 (2002) 108; M. Krishnan, et al., Curr. Opinion Biotech. 12 (2001) 92; A. Hatch, et al., J. Microelectromech. Sys. 10 (2002) 215.
The ability to create MEMS and other devices such as biosensors and microarrays requires facile methods to precisely control surfaces. A variety of patterning techniques can be used to produce desired structures, while various methods have been investigated to control surface chemistries. For instance, microfabrication techniques are routinely applied to create patterned inorganic surfaces with nanometer to micrometer scale resolution. Xia, Y., et al., Angew. Chem, Int. Ed. Engl., 37, 550-575 (1998).
A variety of methods are presently available for fabrication of microfluidic devices. Channels can be micromachined into silicon using traditional microelectronics techniques. M. de Boer, et al., J. Microelectromech. Sys. 9, 94 (2000); G. Kovacs, et al., Proc. IEEE, 86, 1536 (1998); J. Bustillo, et al., Proc. IEEE, 86, 1552 (1998). Glass can be a substrate for biological applications, allowing for visual observation of activity inside the channel. C. H. Lin, et al. J. Micromech. Microeng., 11, 726 (2001). However, glass and silicon processing are expensive and time-consuming, and often require hazardous chemicals and expensive machinery.
Other drawbacks limit the effectiveness of conventional microfluidic devices. For example, current technology relies heavily on either manual alignment of bio-MEMS layers or complex and expensive thin film and lithographic processing techniques to ensure alignment. Current technology also relies on single-level microfluidic devices in which fluid insertion is carried out by microsyringes, exploiting capillary action and sometimes electrokinetics. In some cases, fluidic inputs and outputs have been construed by manual alignment of fluidic connections to the bioMEMS and subsequent hand-gluing of the seals. Neither of these approaches readily enables leak-tight fluidic sealing or direct integration of the inputs/outputs with the package level.
It is an object of the invention to provide a micro-electro-mechanical system (MEMS) device and method that permit easy alignment and reversible removal and attachment of layers.
Another object of the present invention is to provide a micro-electro-mechanical system (MEMS) device and method capable of fluid insertion and removal without requiring microsyringes or deconstruction of the system.
It is another object of the present invention to provide a micro-electro-mechanical system device and method that provide a fluid-tight seal around a microfluidic circuit comprising, for example, micro-channels and micro-reservoirs.
It is a further object of the present invention to provide a micro-electro-mechanical system device and method for controlling the deposition and conjugation of biomolecules, cells, and/or cellular species, onto an organic reactive layer, such as a polysaccharide mass.
To achieve one or more of the foregoing objects, and in accordance with the purposes of the invention as embodied and broadly described herein, an aspect of this invention provides a micro-electro-mechanical system (MEMS) device comprising a substrate, a patterned structure having a microchannel provided on the substrate, and an encapsulation membrane covering the microchannel. The encapsulation membrane is reversibly attachable and separable with respect to the patterned structure.
According to a second aspect of the invention, a micro-electro-mechanical system (MEMS) device is provided. The system comprises a substrate, a patterned structure on the substrate comprising SU-8 and having a microchannel, and a polydimethylsiloxane encapsulation membrane covering the microchannel.
A third aspect of the invention provides a micro-electro-mechanical system (MEMS) device, comprising a substrate, a patterned structure on the substrate having a microchannel, and an encapsulation membrane covering the microchannel. The patterned structure comprises an inlet reservoir and outlet reservoir connected via the microchannel. The encapsulation membrane comprises an inlet port in fluid communication with the inlet reservoir and an outlet port in fluid communication with the outlet reservoir for permitting introduction of fluid to the system and removal of fluid from the system without removal of the encapsulation membrane.
In accordance with a fourth aspect of the invention, there is provided a micro-electro-mechanical system (MEMS) device, comprising a substrate, a patterned structure on the substrate, and a compressible sealing layer. The patterned structure comprises a patterned layer having a microchannel, and a ridge protruding from the patterned layer and surrounding the microchannel. The compressible sealing layer covers the microchannel and is compressed against the ridge to provide a leak-tight seal.
A fifth aspect of the invention provides a micro-electro-mechanical system (MEMS) device comprising a substrate, a patterned ridge structure on the substrate, the patterned ridge structure forming and surrounding a microchannel, and a compressible sealing layer covering the microchannel and compressed against the ridge structure to provide a leak-tight seal.
According to another aspect of the invention, methods are provided for transporting fluids in the above-described MEMS devices.
According to another aspect of the invention, methods are provided for depositing biomolecules and/or cellular species in the microfluidic systems of the MEMS devices.
According to still another aspect of the invention, methods are provided for making the MEMS devices of the invention.
The accompanying drawings are incorporated in and constitute a part of the specification. The drawings, together with the general description given above and the detailed description of the certain preferred embodiments and methods given below, serve to explain the principles of the invention.
Reference will now be made in detail to the presently preferred embodiments and methods of the invention as illustrated in the accompanying drawings. It should be noted, however, that the invention in its broader aspects is not limited to the specific details, representative assemblies and methods, and illustrative examples shown and described in this section in connection with the preferred embodiments and methods. The invention according to its various aspects is particularly pointed out and distinctly claimed in the attached claims read in view of this specification, and appropriate equivalents.
It is to be noted that, as used in the specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise.
According to a first embodiment of the present invention illustrated in
MEMS device 100 and its various components will now be discussed in greater detail in connection with
The description below allows for synthesizing all-polymeric, microfluidic bio-MEMS devices. Polymer functional groups provide an interface between the inert, structural aspects of a device and the biological components in a MEMS device. Rather than simply housing reactants, polymer properties can be tailored to provide an environment in which to sustain biological species. However, it should be understood that the bioMEMS systems may comprise materials other than polymers. It also is to be understood that the following description of components and their characteristics and functions is presented by way of example, and not necessarily limitation.
Substrate
Substrate 102 in
Electrodes
Electrodes 104 in
The material or materials selected for the electrodes may be those upon which a reactive layer 126 (e.g., chitosan) may be deposited via electrochemical deposition. Suitable materials include but are not necessarily limited to metals (e.g., aluminum, chromium, cobalt, copper, gold, nickel, palladium, platinum, silver, tungsten, zinc), metal alloys, semiconductors, and conductive polymers (e.g., polypyrrole, etc.).
It is preferred that electrodes 104 comprise either a chemically inert metal (e.g., Au, Pt) or a conductive polymeric surface layer, and more preferably polypyrrole (PPy). Polypyrrole and other conductive polymers add utility to MEMS device 100 for use in biological experiments. Long-term compatibility of MEMS device 100 with mammalian cells is improved by using highly conducting polypyrrole instead of conductive materials such as gold. Further, polypyrrole is inexpensive and easy to use. For example, polypyrrole can be easily deposited electrochemically due to aqueous solubility and low oxidation potential of the monomer. Polypyrrole also can be solution cast. Anionic doping of polypyrrole enhances the conductivity as well as the hydrolytic stability of the film.
Polypyrrole can be deposited for use as an electrode such as 104 in
The thickness of polypyrrole film 142 is plotted as a function of deposition time in
Electrical conductivity of the PPy film was then calculated as the inverse of the resistivity of the sample using the following equation:
σ=1/ρ=L/RS
where σ, ρ, R, L and S are the conductivity, resistivity, resistance, length and cross section area of polypyrrole film 142 filled in trench 140, respectively. The average conductivity of polypyrrole film was determined to be 47±5 S/cm. This is higher than the 8.3 S/cm reported by Omastova et. al. for NaDBS doped polypyrrole films, but well within the range proposed by Gardner and Bartlett (10−5 to 102 S/cm) for polypyrrole films in general. The discrepancy is attributed to different preparation methods, doping levels, and evaluation techniques used for polypyrrole films.
It is to be understood that although the first embodiment described and illustrated herein includes electrodes, the invention in its broader aspects encompasses MEMS devices and methods without electrodes. For example, the MEMS device may be used to control flow of a fluid (i.e., a liquid and/or gas) through a micro-channel, without depositing a reactive layer (with or without conjugated molecules) over an electrode in the micro-channel.
Patterned Structure
First and second layers 108 and 110 of patterned structure 106 are preferably insulators made of a material capable of functioning as a photoresist for patterning. A photosensitive material suitable to be left in place after patterning and used for device structures is desirable because it simplifies the processing sequence. Preferably, SU-8, an epoxy resin, is the material of choice and acts as a negative photoresist during processing. When exposed to UV light, a Lewis acid catalyzes the hydroxyl coupling of the SU-8 epoxy rings, forming a solid, cross-linked polymer matrix. SU-8 is useful for microfluidics because it can produce well-defined, high aspect ratio structures. Complex multi-layer surfaces can be created in this manner. Other photoresist materials are suitable for combined patterning and subsequent use is known, generally referred to as photoimagable dielectrics.
Alternatively, one could use more conventional lithographic approaches, where a layer destined to serve as e.g. 108 is patterned and etched by a sacrificial photoresist layer.
A two-level SU-8 formation is used as patterned structure 106 of MEMS device 100. First patterned layer 108 forms the structural material for micro-channel 116 and reservoirs 112 and 114, while second patterned layer 110 is used to align encapsulating layer 118 with fluidic components in first patterned layer 108. Microchannel 116 and reservoirs 112 and 114 may be patterned using conventional techniques to process the SU-8 photoimagable dielectric, such as photolithographic-based processes. Processing of SU-8 usually involves only a contact aligner for lithography and a few solvents.
As referred to herein, micro-channel includes microfluidic structures capable of transporting or storing fluid. Micro-channel 116 is depicted in the figures as an elongated trench having parallel sides and a uniform width. It should be understood that the micro-channel may take other configurations, such as that of a pocket, groove, passage, mouth, etc., and other characteristics, such as non-linear (curved) or non-parallel sides. Microchannel dimensions for microfluidics are typically in the range of 10 to 500 microns in width and depth, with lengths, for example, from 100 to 5000 microns. However, the concepts and invention described herein apply to nanoscale regimes for nanofluidics, in which case one can expect widths and depths of about 0.005 microns (5 nm) to 0.010 microns (10 nm), and lengths of about 0.01 microns (10 nm). For the purposes of this disclosure, such nanoscale regimes may be considered micro-fluidics.
Although the embodiment illustrated in
In this regard, the terms pattern and patterned refer to the spatial localization of a material. The pattern may extend across the entire surface of patterned layer 108, or may be localized on a single surface portion. Multiple patterns may be present on a single surface. A pattern may comprise a repeating arrangement of objects or shapes, a non-repeating or random arrangement of objects or shapes, a particular defined shape, array, or the like. For example, the pattern may comprise a plurality of parallel lines spaced apart from one another by uniform or non-uniform intervals, cylindrical members, e.g., posts 120, etc.
Encapsulating Membrane
Encapsulation membrane (or layer) 118 in
As discussed in greater detail below in connection with
Alternatively, because PDMS thickness and patterning can be controlled by spin-casting, a PDMS encapsulation layer 118 can be created in one step to serve the function depicted in
Inlet and outlet ports 122 and 124 provide flow paths for the injection and removal of fluid to and from reservoirs 112 and 114, respectively. Inlet and outlet ports 122 and 124 are aligned with reservoirs 112 and 114, respectively, thereby allowing access to microchannel 116 even when microchannel 116 is covered by encapsulating membrane 118. Ports 122 and 124 then may serve to introduce fluid to and remove fluid from the microfluidic system in patterned structure 106. While ports 122 and 124 may alternatively be created using drilling techniques, the approach described herein creates posts 122 and 124 simultaneously with the alignment holes 120.
Four posts 110 of encapsulation membrane 118 align with holes 120 in encapsulating layer 118. Holes 120 may be formed in the same manner described above with regard to ports 122, 124. Encapsulating layer 118 simply ‘drops’ onto posts 108 when positioned correctly using surface tension, e.g., provided by drops of isopropanol. The alignment system created by the two-level SU-8 patterned structure 106 allows not only for simple channel encapsulation, but also for easy removal of encapsulating membrane 118. Removal of encapsulation membrane 118 allows a wafer of device 100 to be cleaned and reused after an experiment. Accordingly, components of device 100 can be recycled after cleaning, circumventing the need to spend a long time fabricating a separate MEMS device for each particular experiment. Encapsulating membrane 118 also is useful in preventing evaporation of aqueous solutions if maintained near atmospheric pressure so that pressure differentials between the encapsulated fluid and the outside are small.
The surface(s) of PDMS of encapsulation layer 118 can be oxidized by treatment with oxygen plasma. This creates —SiOH groups on the PDMS surface for adding other functional groups. Such oxidized PDMS is hydrophilic and easier to use for microfluidics, in comparison with the naturally hydrophobic character of PDMS. When brought into contact with glass, silicon, quartz, silicon nitride, polyethylene, polystyrene, glassy carbon, or even other oxidized PDMS, the oxidized PDMS can create an irreversible, covalent, siloxane bond, thereby permanently encapsulating the channel.
In the event that a removable membrane 118 is desired, covalent sealing techniques are not used, i.e., the PDMS is not oxidized. The strength of the seal provided by the surface energy of PDMS without covalent bonding is sufficient for most biological applications.
The bond strength between patterned structure 106 and encapsulating layer 118 is important for proper sealing of device 100. In the event encapsulation is to be reversible, low bond strength is desired. Still, the encapsulation should be strong enough to prevent water leakage under normal operating conditions. An estimate of the bond strength between PDMS and SU-8 was made using the ‘blister test’. A device suitable for carrying out the blister test is illustrated in
Using the test fixture of
γ=(0.088Pf2a4)/Etw3
in which Pf is the critical pressure for debonding; a is the radius of the hole; E is Young's modulus of PDMS (7.5×105 Pa) and tw is the thickness of PDMS.
With a 70 μm thick PDMS cover on a hole of radius 300 μm, the critical pressure for debonding was found to be 30.7 Torr above atmospheric pressure. Thus, the surface energy was calculated to be 0.047 J/m2±0.018 J/m2. This value is comparable with the values obtained for bonded hydrophilic silicon wafers. It is typical of surfaces bonded by Van der Waals forces in combination with weak chemical interactions (e.g., relatively weak hydrogen bonds). This surface energy is sufficient to prevent water leakage from the microfluidic channel of the device at the low pressures typically encountered during a biological experiment, yet sufficiently low to permit reversible removal and attachment of encapsulating membrane (PDMS) 118 to patterned structure (SU-8) 106.
Reactive Layer
MEMS device 100 is capable of using selective electrodeposition of a bio-polymer 126, such as chitosan, to successfully create an environment for complex biological experiments and biomolecular reactions within a microchannel composed of material such as SU-8 microchannel 1116. To accomplish such reactions a reactive layer 126 (
Reactive layer 126 preferably comprises an organic polymer and/or organic oligomer, especially those capable of controlled solubilization and insolubilization, such as via pH adjustment. For the purpose of describing the invention hereinafter, but not necessarily by limitation, the reactive layer will be exemplified as polysaccharide mass which can be solubilized under appropriate conditions in a liquid medium, preferably aqueous, and which can be subsequently deposited on an electrode. Other examples of reactive layers include proteins, such as polylysine.
The reactive layer of embodiments of the present invention preferably comprises or is derived from a composition comprising polysaccharides. As used herein, the term polysaccharide includes starches and polysugars, particularly polymers containing glucosamine residues. Ionizable polysaccharides include carboxymethylcellulose, chitosan, chitosan sulfate, pectin, alginate, glycosaminoglycans, ionizable agar, and carrageen. Other synthetic polymers include, for example, polymethacrylic acid, ligninsulfonates, polyvinylsulfonic acid, polyvinylphosphonic acid and polyethyleneimine; similar extracts of plants also may be used. Other suitable polysaccharides include gums from trees, pectins from fruits, starches from vegetables, and celluloses from woody fibers. Chitosan is the preferred ionizable polysaccharide of the present invention.
In preferred embodiments, the selective insolubilization and solubilization of the polysaccharides of the present invention is accomplished by modifying one or more of the polysaccharide ionizable group(s), which may be the same or different. At one or more range(s) of pH the polysaccharide will be soluble in an aqueous solvent (“solubilizing pH ranges”), whereas at one or more other pH values range(s), the polysaccharide will be insoluble (or less soluble), and thus be capable of forming an insoluble mass (e.g., hydrogel and/or compact film) deposited on a support. Suitable ionizable groups include those ionizable at low pH, e.g., capable of forming a positive charge (e.g., alkyl amine groups, primary, secondary or tertiary amine groups, guanidinium groups, imidazole groups, indole groups, purine groups, pyrimidine groups, pyrrole groups, etc.) and those that are ionizable at high pH, e.g., capable of forming a negative charge (e.g., alkoxide groups, carboxyl groups, hydroxy acid groups, phenolic groups, phosphate groups, sulfhydryl groups, etc.). Suitable groups may exhibit multiple pKs, which may be the same (e.g., polyacidic or polybasic) or different (e.g., zwitterionic). For selectively insolubilizable polysaccharides that are ionizable at low pH, amine groups are preferred; for selectively insolubilizable polysaccharides that are ionizable at high pH, carboxyl groups are preferred.
Chemical deposition of the selectively insolubilizable polysaccharide is preferably electrode selective, providing another degree of control over the process. Polysaccharides containing a group ionizable at a low pH, e.g., capable of forming a positive charge, are attracted to and deposit on the negative electrode (i.e., the cathode). Accordingly, for such polysaccharides the electrically conductive support (electrode 104 in
In contrast, a polysaccharide containing a group ionizable at a high pH, e.g., capable of forming a negative charge (e.g., alkoxide groups, carboxyl groups, carboxylate groups, hydroxy acid groups, phenolic groups, phosphate groups, sulfhydryl groups, etc.) is attracted in its soluble state to the positive electrode (i.e., the anode) and deposits on the positive electrode, but not the negative electrode. Accordingly, the electrically conductive support will be polarized to serve as the positive electrode for polysaccharides containing groups ionizable at a high pH.
Various aspects of the electrochemical cell, reaction conditions, and process parameters may be manipulated to control the chemical deposition on the electrically conductive support and the resulting properties and traits of the deposited polysaccharide mass. The physical state of the mass may be, for example, that of a solid compacted film, a semi-solid hydrogel, or a physical state between a compacted film and a hydrogel. Generally, reaction conditions and process parameters that have the greatest influence on physical state are the current density, pH, and deposition time. Other process conditions that may also influence the physical state of the deposition include the applied voltage, total ion concentration, polysaccharide concentration, temperature, and the like. Generally, high current densities and pH's relatively near the solubility limit are preferred for formation of hydrogels.
A preferred selectively insolubilizable polysaccharide is pH-responsive, nucleophilic chitosan, which is an amine-rich polysaccharide derived by deacetylation of chitin. Chitin is the second most abundant polysaccharide in nature and is found in crustaceans, insects, and fungi. Chitosan is also commercially available, such as from various suppliers (e.g., Aldrich, Sigma). The term chitosan includes chitosan polymers and oligomers with complete or substantially complete deacetylation, or chitosan with less than complete deacetylation. Chitosan also includes various derivatives of chitosan having the necessary solubility for this invention and at least a portion of the amino functional groups available for reaction.
Chitosan is water-soluble at low pH. At higher pH (>6.3), the amino group becomes deprotonated and the polymer precipitates out of solution. Chitosan can therefore be deposited from an aqueous solution under mildly acidic conditions. If a negative charge is induced on an electrode, deposition has been shown to occur on that electrode. This is understood from recognizing that the electrolysis of water which occurs at the negative electrode creates a locally high pH condition compared to the low pH bath, and when the negative electrode attracts the positively charges chitosan species near to it, these species precipitate out onto the electrode in the locally high pH region (where the chitosan is insoluble). Thus, chitosan selectively electrodeposits on cathodes while deposition fails to occur on unpolarized or positively charged surfaces. From a processing standpoint, its pH-dependent solubility makes chitosan an attractive polymer to use in a MEMS device.
The chitosan solution used to deposit chitosan onto the support may have a chitosan content of, for example, about 0.0001 to about 0.001 weight percent (grams chitosan/grams solution), about 0.001 to about 0.01 weight percent, about 0.01 to about 0.1 weight percent, about 0.1 to about 1 weight percent, about 1 to about 10 weight percent, about 10 to about 20 weight percent, and about 20 to about 30 weight percent. These ranges are provided only by way of example, and are not limiting. The range selected is dependent upon factors such as the amount of chitosan deposition desired.
The operational electrical circuit may be controlled by using a controlled constant voltage, a controlled constant current, or a mixture of the two as the deposition proceeds. Using constant voltage there is typically a large current and high deposition rate until an initial chitosan deposit is achieved, after which the current is reduced by the series resistance of the chitosan. Using constant current, the initial voltage is typically small but then increases rather quickly to a nearly constant value as the resistive chitosan deposit develops on the surface. The tendency of the depositing chitosan to form a solid compact film is increased with use of a pH of about 5 to about 5.5, a relatively low current density, e.g., about 0.1 to about 10 A/m2 (e.g., about 1 A/m2 to about 5 A/m2), and a relatively short deposition time, e.g., about 1 to about 10 minutes. For example, under typical conditions at a current density 2-5 A/m2, the voltage rises within 1 min to slightly over 2 V and remains nearly constant over a total deposition time of 5 min. The deposition process is more reproducible and controllable for constant current mode of electrodeposition of chitosan.
The thickness of the deposited chitosan hydrogel may range, for example, from about 0.01 micron to about 3 microns, although thicknesses outside this range may be achieved. The chitosan solution concentration, the voltage, and the time a current is applied to deposit chitosan on a substrate can be varied to control thickness.
It is to be understood that although the first embodiment described and illustrated herein includes a reactive film, the invention in its broader aspects encompasses MEMS devices and methods without reactive films and their conjugated molecules (discussed below). For example, the MEMS device may be used to control flow of a fluid (i.e., a liquid and/or gas) free of a reactive layer or its precursor through a micro-channel, without performing deposition of a reactive layer in the micro-channel.
Conjugated Molecules
Chitosan, a biocompatible, biodegradable amino-polysaccharide biopolymer, creates an environment that is biologically inert and flexible for sensing and manipulating macromolecules and organisms within a MEMS device. The chitosan amine functional groups are chemically at a broad range of pH environments. The nucleophilic properties of the amine group allow it to conjugate, such as by covalent coupling, to other molecules, including proteins, oligonucleotides, and even cells.
In the context of MEMS device 100, chitosan reactive layer 126 is able to anchor molecules such as proteins, nucleic acids, and cells to electrodes 104 on the bottom of microchannel 116. A mild, non-disruptive reaction environment can be created using chitosan, preserving biological activities and selectivities. This ability to easily anchor proteins to the MEMS device allows it to be used for biosensing applications by studying antigen-antibody interactions. Further, by controlling electrode placement and activation, it is possible to selectively control the spatial positioning of chitosan reactive layer(s) 126 and the conjugated molecules. Further, deposition controls provide flexibility in assigning different roles to reactive layers 126. For example, selective deposition allows some electrodes to be designated as sensing electrodes that hold reactant and/or record electrical activity, whereas other electrodes that are free of reactants can act as actuating electrodes for flow control. By playing different roles, these polymers are integrated to create smart sensors and actuators for biological applications.
Examples of molecules that may be bonded to the exposed portions of reactive layer 126 include biomolecular and/or cellular species (eukaryotic or prokaryotic). Examples of biomolecular species include proteins (especially enzymes, receptors, receptor ligands, and antibodies), nucleic acid molecules (especially DNA and RNA), antigens, polysaccharides, drugs (e.g., opiates, cannabinoids, etc.), etc. Examples of cellular species include whole cells (e.g., such as cultured or primary human, non-human mammalian, insect, yeast, fungal or other eukaryotic cells, or bacterial cells) or sub-cellular components thereof, viruses or sub-viral components thereof. As used herein, the terms sub-cellular and sub-viral components are intended to refer to membrane-associated proteins (especially enzymes, receptors, and receptor ligands), membrane-associated antigens, organelles, etc. The binding of such biomolecular and/or cellular species is particularly amenable for use in microfluidic systems. The reactive layer (e.g., polysaccharide mass) of the present invention may be modified to facilitate its ability to stably conjugate with other molecules. Additionally or alternatively, the other molecules may be modified to facilitate their ability to stably conjugate with the reactive layer (e.g., the polysaccharide mass).
Such modifications may include covalent cross-linking agents (e.g., dialdehydes (such as glutaldehyde, formaldehyde, glyoxal, etc.), anhydrides (such as succinimide, carbodiimide, dicyclohexylcarbodiimide, etc.), genipin, amino acids, etc.) or non-covalent crosslinking agents (such as tripolyphosphate (TPP), etc.). Such molecules may be nonspecifically divalent or multivalent, possessing two or more identical reactive groups that can be used to conjugate the polysaccharides of the reactive layer to other molecules (e.g., glutaraldehyde, lysine, arginine, glutamate, aspartate, polysaccharides, etc.) so as to provide “spacer” molecules that can address and diminish potential issues of steric interference. Alternatively, such molecules may comprise two or more different relevant reactive groups such that an orthogonal synthetic approach may be employed. Examples of such compounds include amino acids. The carboxyl group of such compounds can be conjugated to the amine group of, for example, chitosan, to yield a free, and more sterically accessible, amino group that can be conjugated to the carboxy group of a glutamate or aspartate residue of a protein. Likewise, the reactive layers of the present invention can be modified to contain chloromethylbenzyl or trialkylsulfoniumbenzyl groups that can then react with the carboxyl group of other molecules.
Modifications may optionally be conducted enzymatically. Any of a variety of enzymes may be used for this purpose. Such enzymes may be used to activate a chemical group of a protein or other ligand so as to facilitate its reaction with a chemical group of the reactive layer. For example, without wishing to be bound by theory, it is believed that such enzymes activate phenols (such as tyrosyl residues of proteins, such as green fluorescent protein (GFP)) to convert the phenols to quinones. The activated quinones can then react with nucleophilic substituents, such as nucleophilic substituents of chitosan. Such enzymes are readily available commercially, and are ubiquitous in natural sources. For example, tyrosinase enzymes, phenol oxidases, and polyphenol oxidases (also peroxidase enzymes and probably laccase enzymes) may be employed to react with the tyrosine residues of a protein so as to facilitate the covalent bonding of the tyrosine phenolic oxygen to an amine group of chitosan.
The specific activity of the enzyme used will determine how much of the enzyme should be added. As an illustration, for a mushroom tyrosinase enzyme, a convenient level is from about 1 to about 200 U/mL, preferably about 20 to about 100 U/mL, and most preferably about 60 U/mL. Higher amounts of enzyme content may result in depletion of the phenolic compound or molecular oxygen in the solution. The reaction is then allowed to proceed, conveniently with stirring overnight.
Owing to the flexibility of the chemistry involved, any of a wide variety of different compounds can be conjugated to the polymer. Such compounds particularly include proteins (especially enzymes, receptors, receptor ligands, or antibodies) and nucleic acid molecules (especially DNA or RNA).
For example, chitosan possesses amino groups that confer nucleophilic properties to the polymer. Specifically, the deprotonated amino groups have an unshared electron pair that can undergo reaction with a variety of electrophiles. As a result, various chemistries can be exploited to crosslink chitosan and to graft (or conjugate) substituents onto the polymer. The substituent may be coupled to the chitosan before and/or after the chitosan has been deposited onto the substrate. The substituent may comprise various molecules, such as labile biomolecules. Such biomolecules include, not necessarily by limitation, bound proteins, enzymes, polynucleotides, RNA, DNA, cells, and the like. The molecules are assembled on the polysaccharide template, which acts as an interface between the molecules and the inorganic substrate.
In one embodiment, the conjugated molecules of such surfaces or matrices will comprise one, two, three or more enzyme species. Significantly, by incubating such surfaces or matrices in contact with a fluidic layer (i.e., a surface or matrix that contains a flowing or flowable liquid or gas capable of transporting other molecules (e.g., nucleic acid molecules, proteins, enzymatic substrates and/or products, etc.)), multiple stepwise synthetic reactions can be made to occur, either sequentially or in parallel. Suitable enzyme species include: aminopeptidases, angiotensin converting enzymes, caspases, cathepsins, cholinesterases, collagenases, deaminases, endonucleases, endopeptidases, esterases, exonucleases, lipases, nucleotidases, phosphatases, proteases, restriction endonucleases, etc.
In another embodiment, the conjugated molecules of such surfaces or matrices will comprise one, two, three or more antibody species. As used herein, the term “antibodies” is intended to encompass not only conventional immunoglobulins, but also single chain antibodies, humanized antibodies, monoclonal antibodies etc. Significantly, by incubating such surfaces or matrices in contact with a fluidic layer containing antigens, multiple immunoassays can be simultaneously or sequentially conducted. Any of a wide variety of assay formats may be used in accordance with the methods of the present invention. They may be heterogeneous or homogeneous, and they may be sequential or simultaneous. They may be competitive or non-competitive. U.S. Pat. Nos. 5,563,036; 5,627,080; 5,633,141; 5,679,525; 5,691,147; 5,698,411; 5,747,352; 5,811,526; 5,851,778 and 5,976,822 illustrate several different assay formats and applications.
In another embodiment, the conjugated molecules of such surfaces or matrices will comprise one, two, three or more bound receptor molecule species or bound ligands of receptor molecules. Significantly, by incubating such surfaces or matrices in contact with a biological sample, multiple receptor/receptor ligand binding assays can be simultaneously or sequentially conducted. Suitable receptor species include: 5-hydroxytryptamine receptors, acetylcholine receptors, adenosine receptors, adrenoceptor receptors, adrenomedullin receptors, amylin receptors, amyloidreceptors, angiotensin receptors, atrial natriuretic peptide (ANP) receptors, bombesin receptors, bradykinin receptors, calcium-channel receptors, cannabinoid receptors, cgrp receptors, chemokine receptors, cholecystokinin and gastrin (CCK) receptors, corticotropin releasing factor (CRF) receptors, dopamine receptors, endothelin receptors, excitatory amino acid receptors, gaba receptors, galanin receptors, gastric inhibitory peptide (GIP) receptors, GDNF receptors, glucagon receptors, glucagon-like peptide receptors, glycoprotein hormones receptors, growth hormone secretagogue receptors, GTP-binding-protein receptors, hemotopoietin receptors, histamine receptors, imidazole receptors, integrin receptors, interleukin-1 receptors, melanin-concentrating hormone receptors, melanocortin receptors, melatonin receptors, metastin receptors, motilin receptors, neuromedin receptors, neuropeptide FF receptors, neuropeptide Y receptors, neurotensin receptors, opioid receptors, orexin receptors, P2 purinoceptor receptors, parathyroid hormone (PTH) receptors, phosphodiesterase enzyme, platelet activating factor (PAF) receptors, potassium-channel receptors, prolactin receptors, prostanoid receptors, retinoid receptors, selectin receptors, somatostatin receptors, steroid receptors, tachykinin receptors, tumour necrosis factor (TNF) receptors, tyrosine kinase receptors, urotensin II receptors, vasoactive intestinal peptide (VIP) receptors, vasopressin receptors, etc.
In another embodiment, the conjugated molecules of such surfaces or matrices will comprise one, two, three or more bound nucleic acid molecule species, which may be DNA or RNA or be composed of non-naturally occurring residues (e.g., PNA). Such nucleic acid molecules may have defined sequences (such as the sequences of genes or fragments thereof), or may be composed of random or pseudorandom oligonucleotides (i.e., nucleic acid molecules of 3-100 nucleotides in length) or polynucleotides (i.e, nucleic acid molecules greater than 100 nucleotides in length). Significantly, by incubating such surfaces or matrices in contact with a biological sample (or an extract thereof), multiple hybridization reactions involving nucleic acid molecules present in the sample can be simultaneously or sequentially conducted. Such hybridization reactions can be used in concert with nucleic acid amplification strategies (such as the polymerase chain reaction (PCR) (e.g., U.S. Pat. Nos. 4,683,202; 4,582,788; U.S. Pat. Nos. 4,683,194, 6,642,000, etc.)); ligase chain reaction (LCR), self-sustained sequence replication (3SR) (e.g., Guatelli et al., Proc. Natl. Acad. Sci. USA 87:1874-1878 (1990); PCT Publication. WO 88/10315), nucleic acid sequence based amplification (NASBA) (e.g., Kievits, J Virol Methods. 35:273-86 (1991)), strand displacement amplification (SDA) (e.g., U.S. Pat. No. 5,270,184), and amplification with Qβ replicase (Birkenmeyer et al., J. Virological Methods, 35:117-126 (1991); Landegren, Trends Genetics, 9:199-202 (1993); and rolling circle amplification (e.g., U.S. Pat. Nos. 5,854,033; 6,183,960; 5,354,668; 5,733,733)) to accomplish the amplification of the hybridized molecules, or their complements. The present invention permits hundreds, thousands, and tens of thousands of nucleic acid species to be deposited on to such surfaces or matrices.
Additionally, such hybridization reactions may be used to sequence the nucleic acid molecules present in the sample, or to assess the expression profile of the genes of cells present in the biological sample (or an extract thereof) (see, e.g., U.S. Pat. Nos. 6,632,606; 5,002,867; 5,202,231; 5,888,819; Lipshutz et al., Biotechniques, 9 (3):442-447 (1995) and Chee et al., Science, 274:610-614 (1996); DeRisi, J. et al. (1996) “U
In another embodiment, the conjugated molecules of such surfaces or matrices will comprise one, two, three or more non-ionizable polysaccharides or other polymer molecules. Thus, for example, the present invention permits one to accomplish the spatial and/or temporal selective deposition of polymers such as: aramids, celluloses, kevlars, nomex, nylons, poly(ether sulfone)s, poly(methyl methacrylate)s, poly(phenylene oxide)s, poly(phenylene sulfide)s, poly(vinyl acetate)s, poly(vinyl chloride)s, poly(vinyl) fluorides, poly(vinylidene chloride)s, poly(vinylidene fluoride)s, polyacrylonitriles, polybutadienes, polycarbonates, polychloroprene, polycyanoacrylates, polydicyclopentadienes, polyesters, polyethylenes, polyimides, polyisobutylenes, polyketones, polypropylenes, polystyrenes, polytetrafluoroethylenes, polyurethanes, polyvinylpyrrolidones, rayons, silicones, starches, etc.
System Fabrication
The method used for the fabrication of MEMS device 100 is shown in detail in
Chromium adhesion layer 160 and gold layer 162 were patterned using photolithography. A photoresist 164 (Shipley 1813) was applied on the gold layer 162 via conventional spin-coating techniques. A mask was placed over photoresist 164, and photoresist 164 was then patterned, for example, by exposure of the unmasked portions of photoresist 164 to UV light (
Silicon substrate 102 with metals 160 and 162 was then cleaned with piranha solution (3:1 ratio of H2SO4:H2O2) as a preparation for polypyrrole (PPy) deposition. Polypyrrole was then deposited electrochemically from an aqueous solution of 0.1 M pyrrole and 0.1 M sodium dodecyl benzene sulphonate (NaDBS). A constant potential of 0.55 V (versus Ag/AgCl) was applied until a PPy thickness of approximately 1-3 μm is reached. The PPy layer is represented by reference numeral 104 in
Microfluidic channel 116 containing polypyrrole electrodes 104 then was constructed using soft lithographic techniques. As shown in
The SU-8 substrate preparation process preferably comprises two baking steps. First, a pre-exposure bake helps to eliminate excess solvent from the photoresist matrix, increasing the resolution attainable with the negative photoresist. The post-exposure bake helps to complete the cross-linkage of the SU-8 chains, further solidifying the resulting structures. SU-8 also has a high coefficient of thermal expansion, allowing excess heat to crack the cross-linked structure. This presents a problem for bi-layer SU-8 structures because baking required for second layer 110 can crack first layer 108. To combat this problem, the post-exposure bake for first layer 108 is used as a pre-exposure bake for second layer 110. This reduces the total heat absorbed by first layer 108 and results in less cracking in the final structure.
To demonstrate the abilities of this embodiment of the invention, green fluorescent protein (GFP) was conjugated to the electrodeposited chitosan. GFP is a convenient model because the intact protein can be readily visualized under UV illumination. Prepared by well-established bioengineering methods, GFP was expressed in E. coli BL21 (Invitrogen) using a pTrcHisB (Invitrogen) expression vector. Cells were grown under standard fermentation conditions and the fusion protein was purified using immobilized metal affinity chromatography.
Glutaraldehyde was used to anchor the model protein, GFP, onto the selectively deposited chitosan on the PPy electrodes. Glutaraldehyde is a homo-bifunctional coupling agent that reacts with amines and is commonly used for coupling biopolymers (e.g. proteins and nucleic acids). In previous work, amine-terminated oligonucleotide probes were coupled to the glutaraldehyde-activated chitosan surface. This approach can be used to create biosensors based on nucleic acids. Glutaraldehdye can also be used to couple proteins to chitosan, although proteins are considerably more labile than nucleic acids.
After chitosan was selectively deposited, the wafer was immersed in glutaraldehyde solution (0.05%) for 30 minutes. After glutaraldehyde activation, the wafer was extensively washed with 0.1 M PBS (Dulbecco's Phosphate Buffered Saline, Sigma-Aldrich Chemicals) buffer and then immersed in a GFP solution (≈0.4 μg/ml) for 30 minutes. Two control experiments were performed at the same time. One control was a wafer with devices that lacked chitosan. The second control was a wafer in which chitosan was deposited onto the channel's electrodes, but the deposited chitosan was not activated with glutaraldehyde. Both controls were immersed in GFP solution for 30 minutes. All samples were extensively washed with PBS buffer before examination.
The bio-functionalized microfluidic channels were examined using a fluorescence stereomicroscope (MZFLIII, Leica) with a fluorescence filter set (GFP Plus) using an excitation filter at 480 nm (band width of 40 nm) and an emission barrier filter at 510 nm. Photomicrographs were prepared from the fluorescence microscope using a digital camera (Spot 32, Diagnostic Instruments).
After SU-8 processing, biopolymer (e.g., chitosan or a fluorescently-labeled chitosan derivative) layer 126 was electrodeposited (
Encapsulation membrane 118 (
The SU-8 template wafer was then washed with a 0.1 M solution of sodium dodecyl sulfate (SDS) and allowed to dry. Next, PDMS (Sylgard 184) was mixed in a 10:1 ratio with its curing agent. It was then poured onto the wafer and spun to a thickness of 70 μm, less than the height of the posts 172. After curing in a box furnace at 65° C. for 2 hours, PDMS encapsulation membrane 118 was then peeled from the master 170, giving a cover for microchannel 116. The PDMS cover was aligned onto the device using surface tension provided by drops of isopropanol. The alcohol was allowed to evaporate causing the PDMS to rest on the device. As shown in
A micro-electro-mechanical system (MEMS) device 200 according to a second embodiment of the invention is illustrated in
A patterned structure 206 is situated on substrate 202. Patterned structure 206 may comprise like materials (e.g., SU-8) and characteristics and may serve like functions as patterned structure 106 described above. Patterned structure 206 comprises a patterned layer 208 and a ridge (or “micro-knife edge”) 210. Patterned layer 208 defines a microchannel 216 aligned with at least one of the electrodes. Patterned layer 208 further defines an inlet/outlet reservoir 212. Ridge 210 is situated on the upper surface of patterned layer 208, and extends continuously around the peripheries of microchannel 216 and any related microfluidic structures (e.g., input/output reservoir 212) of the microfluidic circuit to form a continuous boundary.
Ridge 210 may be created with a rectangular cross-section as readily accomplished by conventional SU-8 lithographic processing. Alternatively, gray-scale lithography may be employed to tailor the vertical profile (3-D shape) of narrow ridge 210, i.e., micro knife edge, and thereby to optimize the efficacy and reliability of the seal. Gray scale lithography allows a rounded top to micro knife edge 210, or a sharper, roughly triangular top, where strongest contact with the flexible sealing layer occurs. Gray scale lithography is discussed in detail in B. Morgan, et al., “Compensated aspect ratio dependent etching (CARDE) using gray-scale technology,” Microelectronic Eng'g 77, 85-94 (2005), and C. Waits, “Investigation of gray-scale technology for large area 3D silicon MEMS structures”, J. Micromech. Microeng. 13, 170-177 (2003), the complete disclosures of which are incorporated herein by reference.
Generally, gray-scale lithography is a one-level process enabling the development of a pattern having gradient height profiles in a photoresist-masking layer. The photoresist is then used as a nested mask in dry anisotropic etching where the structure is transferred, typically into a silicon substrate, to a specified depth corresponding to the height of the desired final structure.
A reactive layer (not shown in
A compressible sealing layer 218 is situated over patterned structure 206 to cover microchannel 216. Sealing layer 218 may be made of the same materials (e.g., PDMS) and may be made using the same methods as described above in connection with membrane 118. An upper substrate layer 280 optionally is situated over sealing layer 218. Upper substrate layer 280 preferably is transparent, and may be made of, for example, a plexiglass wafer. Sealing layer 218 and upper substrate layer 280 have aligned input/output port 222 for permitting the introduction of fluid to and/or removal of fluid from reservoir 212.
A compressive force is shown applied to the upper surface of upper substrate layer 280 and the lower surface of lower substrate 202. When MEMS device 200 is placed under compression, sealing layer 218 is compressed against patterned structure 206, causing ridge 210 to apply stress to and deform sealing layer 218 at contact areas along ridge 210. The applied compressive force is preferably substantially uniform and sufficient to establish a substantially leak-tight seal around the periphery of microchannel 216 and any related microfluidic circuit structures, i.e., along the path of the ridge 210. Advantageously, the leak-tight seal is established without requiring the use of adhesives or elevated temperatures. Furthermore, it allows removal of sealing layer 218 for reuse or analysis of the microfluidic system.
It is to be understood that although the second embodiment has been described herein as including electrodes and a reactive layer, the invention in its broader aspects encompasses MEMS devices and methods without electrodes and/or reactive layers, which may be omitted from the second embodiment. For example, the MEMS device may be used to control flow of a fluid (i.e., a liquid and/or gas) through a micro-channel, without performing deposition of a reactive layer over an electrode in the micro-channel.
A third embodiment of the invention is illustrated in
A reactive layer (not shown in
Positioned below substrate 302 is a base frame 386 (e.g., polycarbonate). Situated on top of sealing layer 318 are, in order from lowest to highest, upper substrate layer 380 (e.g., PLEXIGLASS), gasket layer (e.g., PDMS) 382, and a cover frame 384 (e.g., polycarbonate). O-ring seal 388 is positioned along port 322 between gasket layer 382 and cover frame 384. Reference numeral 392 represents an input/output port connector flange for fluid transport. Port connector flange 392 may be coupled to, e.g., a valve pump. A clamp mechanism 390 maintains the package under compressive force, shown by the arrows in
Although not shown, gasket layer 382 optionally may be placed under further compression as follows. Threaded holes are drilled through cover frame 384, and screws are placed in the threaded holes and adjusted to further force and deflect cover frame 384 toward upper substrate layer 380. This makes it possible to tailor the stress distribution across the wafer and to improve the sealing at micro knife edge structure 310.
Base 386 may include a depression or other alignment device for reproducibly locating substrate 302 and the bioMEMS network (e.g., reservoir 312, channel 316) situated on the top of substrate 302. Using the polymeric bioMEMS designs described above, the bioMEMS circuit provides for fluidic and electrical inputs and outputs on the top of substrate 302, with fluidic seals to be completed when the sealing layer 318 (e.g., PDMS) is compressed, without or with micro knife edge structure 310 in
Sealing layer 318, gasket layer 382, and cover frame 384 collectively define input/output port 322. Although only a single port is illustrated in
It is to be understood that although the third embodiment has been described herein as including electrodes and a reactive layer, the invention in its broader aspects encompasses MEMS devices and methods without electrodes and/or reactive layers, which may be omitted from the third embodiment. For example, the MEMS device may be used to control flow of a fluid (i.e., a liquid and/or gas) through a micro-channel, without performing deposition of a reactive layer over an electrode in the micro-channel.
A micro-electro-mechanical system (MEMS) device 400 according to a fourth embodiment of the invention is illustrated in
A patterned ridge structure 416 is situated on substrate 402. The materials (e.g., SU-8) described above in connection with patterned structure 106 may be applied to patterned ridge structure (or “micro-knife edge”) 416. Notably, unlike patterned structure 206, structure 416 does not comprise a patterned layer (208 in
Gray-scale lithography may be employed to tailor the vertical profile (3-D shape) of narrow ridge member 410, i.e. micro knife edge, and thereby to optimize the efficacy and reliability of the seal. Gray scale lithography allows a rounded top to the micro knife edge, or a sharper, roughly triangular top, where strongest contact with the flexible sealing layer occurs. Other profiles are also possible.
A reactive layer (not shown in
A compressible sealing layer 418 is situated over patterned ridge structure 410 to cover microchannel 412. Sealing layer 418 may be made of the same materials (e.g., PDMS) and may be made using the same methods as described above in connection with membrane 118 and sealing layer 318. An upper substrate layer 480 optionally is situated over sealing layer 418. Upper substrate layer 480 preferably is transparent, and may be made of, for example, a plexiglass wafer. Sealing layer 418 and upper substrate layer 480 collectively define input/output port 422 for permitting the introduction of fluid to and/or removal of fluid from reservoir 412.
A compressive force is shown applied to the upper surface of upper substrate layer 480 and the lower surface of lower substrate 402. When MEMS device 400 is placed under compression, sealing layer 418 is compressed against patterned ridge structure 410, causing ridge 410 to apply stress to and deform sealing layer 418 at contact areas along ridge 410. The applied compressive force is preferably substantially uniform and sufficient to establish a substantially leak-tight seal around the periphery of microchannel 416 and any related microfluidic circuit structures, i.e., along the path of the ridge 410. Advantageously, the leak-tight seal is established without requiring the use of adhesives or elevated temperatures.
A first MEMS device 500a located on common substrate 502 comprises a first electrode 504a and a second electrode 505a. Preferably, one of the electrodes is an anode and the other a cathode. MEMS device 500a further comprises a continuous ridge structure 510a disposed on and protruding upward from common substrate 502. Ridge structure 510a defines a circular first reservoir 512a and a circular second reservoir 514a, one of which is designated an input reservoir and the other of which is designated an output reservoir. Each of reservoirs 512a and 514a has an opening, which is defined at its periphery by ridge structure 510a. Ridge structure 510a forms a continuous microchannel 516a that fluidly connects reservoirs 512a and 514a at their respective openings. In the illustrated embodiment, microchannel 516a begins at first reservoir 512a opening, extends radially inward to a first intermediate reservoir, changes direction to travel generally circumferentially yet in a straight path to pass over first electrode 504a and second electrode 505a until reaching a second intermediate reservoir, then extends radially outward until terminating at the opening of second reservoir 514a. Microchannel 516a thus places reservoirs 512a and 514a in fluid communication with one another. Microchannel 516a also allows for delivery of fluid to electrodes 504a and 505a. In this manner, a reactive layer or its precursor, with or without conjugated molecules, can be delivered to electrodes 504a, 505a for deposition. Also, conjugatable molecules may be delivered to a reactive layer deposited on electrodes 504a, 505a.
The remaining MEMS devices located on common substrate 502 are substantially identical in construction to device 500a discussed above. Reference numerals containing a suffix “b”, but otherwise using like numbers to those discussed above, represent like components and features of a second MEMS device 500b. The components (e.g., ridge structure 510a, etc.) of apparatus 598 are made of similar materials and serve similar functions to like components described above in connection other embodiments of the invention.
Methods of Operation
A non-exhaustive description of methods for operating the embodied MEMS devices will now be discussed with reference to
According to a first embodied deposition method, chitosan conjugated to a biocompatible molecule is dissolved into an aqueous solution at an acidic pH and introduced through inlet port 122 to inlet reservoir 112. Such motion may be accomplished by pressure-driven flow or through electrokinetic flow (e.g., electro-osmotic flow). The dissolved polymer with conjugated molecule travels along microchannel 116 and reaches the vicinity of cathode electrode 104. If negative voltage is applied to cathode electrode 104, the chitosan will deposit as the reactive layer on cathode electrode 104. The reactive layer may be maintained in an insolubilized state by maintaining the applied voltage. Alternatively, if the pH of the fluid in microchannel 116 is raised to basic levels, the insolubility of the chitosan reactive layer is improved, eventually reaching a state at which the voltage may be removed without solubilizing the chitosan.
If it is desired to remove the chitosan reactive layer, this can be subsequently accomplished by lowering or removing the applied negative voltage and changing the pH back to acidic levels. The dissolved chitosan with conjugated molecules then flow through microchannel to outlet reservoir 114, where the fluid may be removed through outlet port 124 using, e.g., pressure driven flows, pumps, etc.
According to a second embodied deposition method, chitosan without a conjugated molecule is dissolved into an aqueous solution at an acidic pH and introduced through inlet port 122 to inlet reservoir 112. The dissolved polymer is passed along microchannel 116 and deposited on cathode electrode 104. pH stabilization may be conducted as discussed above. The molecule to be conjugated (or conjugatable molecule) is then introduced in aqueous solution into the inlet port 122 to inlet reservoir 112, and likewise is passed to cathode electrode 104, where conjugation occurs.
According to a third embodied deposition method, prior to securing membrane 118 to patterned layer 106, chitosan without a conjugated molecule is electrodeposited on cathode electrode 104 of exposed microchannel 116. Encapsulating membrane 118 is then placed on patterned layer 106, and the conjugated molecule is introduced through inlet port 122 as discussed above.
According to a fourth embodied method, the MEMS devices described above are used to transport a fluid through a microchannel, preferably between reservoirs. The fluid may comprise a liquid (e.g., an aqueous solution) or gas. The fluid may contain or omit a solubilized reactive layer or reactive layer precursor. Optionally, gates and flow control devices may be arranged along the micro-channel and controlled using, for example, electrochemistry.
The bioMEMS packaging strategy embodied in this detailed description greatly facilitates the development and use of bioMEMS and microfluidic systems by providing robust means for generating leak-tight flow systems, versatile packaging and operation, and bioreaction processes. In this broader sense, and particularly for commercial biotechnology applications, bioMEMS fabrication and integration requires packaging that efficiently and easily accommodates inputs and outputs to the bioMEMS wafer, chip or device. A packaging design has been developed which accommodates not only the fluidic interconnects, but also electrical and ultimately optical interconnects to the bioMEMS wafer. Given the increasing complexity of bioMEMS wafers in terms of the number of inputs/outputs involved, such a packaging strategy is valuable.
Further, the construction of preferred embodiment permits the use of transparent materials over the microchannel. As a consequence, active areas are left accessible to a microscope for observation.
Advantageously, this invention facilitates the reuse of bioMEMS wafers or chips. After operation or testing of one bioMEMS wafer, the fluidic flow system can be used to blow out the microchannels, flow valves from the controller closed, and electrical power turned off. Then the top frame can be removed, the wafer removed, and a new wafer inserted. The top frame is then reattached, and operation of the new wafer is initiated. This strategy can be accomplished quickly to achieve rapid throughput of packages.
In particular, it should be noted that microfluidic devices and circuits may be of value in applications not involving electrical activation, reactive biopolymers, or biomolecules. The concepts and designs described herein and not directly related to electrical or biological functionality are equally applicable and valuable to other microfluidic systems and applications, including the fluidic sealing methods, the integration of fluidic inputs and outputs, the fabrication of microfluidic structures, etc.
A process flow for fabricating the SU-8 fluid flow wafer and PDMS gasket was carried out as follows.
Masks may be designed to create various geometries of microchannels and knife-edges. For example, the geometries may include 90-degree bends, curves, straight lines, etc. Channel size may be controlled over a broad range, and may be maintained uniform or varied, e.g., 30 microns to 750 microns. Similarly, micro-knife edge height and spacing from the channels could be controlled in a likewise manner. Using a WYCO NT1100 optical profiler (Veeco Instruments), channel depth was measured as 130 microns and micro-knife-edge height as 80 microns.
A completed microfluidic wafer with channels, micro-knife-edges, and gasket can then be clamped in the transparent packaging designed for simple fluid and electrical interfacing. So packaged, fluid can be pumped into and out of any selected inlet/outlet combination using an external peristaltic pump (Masterflex® L/S® variable-speed economy drive, Cole-Parmer Instrument Company) and valve manifold.
Fluid channels without micro-knife edges have been found to be leak-tight for continuous flow up to approximately five minutes at a flow rate of 1.0 mL/min. Small leaks have been found to occur after more than five minutes of flow, especially when fluid must be pumped upward (against gravity) for a long period of time. However, these leaks do not prevent fluid from continuing to flow through the channel and out the outlet, so experiments could continue in the channel being tested. (In contrast, when channels are sealed without micro-knife-edges, leaks occur immediately at the inlet and flow cannot be achieved through the channel at all.) This level of leak-tightness has been shown for channels with 90-degree bends and curves; for channels 500, 300, and 100 microns wide; and for micro-knife-edges 500 microns wide and 500 microns from the edge of the fluid.
The foregoing detailed description of the preferred embodiments of the invention has been provided for the purpose of explaining the principles of the invention and its practical application, thereby enabling others skilled in the art to understand the invention for various embodiments and with various modifications as are suited to the particular use contemplated. This description is not intended to be exhaustive or to limit the invention to the precise embodiments disclosed. Modifications and equivalents will be apparent to practitioners skilled in this art and are encompassed within the appended claims.
This application claims the benefit of priority of U.S. provisional application Ser. no. 60/527,394 filed in the U.S. Patent & Trademark Office on Dec. 5, 2003 entitled “Fabrication and Integration of Polymeric BioMEMS,” the complete disclosure of which is incorporated herein by reference. This application also claims the benefit of priority of U.S. provisional application Ser. No. 60/578,207 filed in the U.S. Patent & Trademark Office on Jun. 9, 2004 entitled “Micro-Knife-Edge Technique for Sealing of Microfluidic Systems,” the complete disclosure of which is incorporated herein by reference.
The U.S. Government has a paid-up license in this invention and the right in limited circumstances to require the patent owner to license others on reasonable terms as provided for by the terms of Grant No. DMR 4-32291 awarded by the National Science Foundation.
| Number | Date | Country | |
|---|---|---|---|
| 60527394 | Dec 2003 | US | |
| 60578207 | Jun 2004 | US |
