1. Field of the Invention
The present invention generally relates to microfluidic and nanofluidic analysis of particles. In particular, the present invention relates assaying particles based on their mobilization characteristics in applied mobilization fields.
2. Description of the Related Art
Separation by size or mass is a fundamental analytical and preparative technique in biology, medicine, chemistry, and industry. Conventional methods include gel electrophoresis, field-flow fractionation, sedimentation and size exclusion chromatography.
A few microfluidic and nanofluidic devices for separation and analysis of biomolecules and compounds have been developed. U.S. Pat. No. 5,427,663 discloses separating nucleic acid molecules using electric fields through an array of posts as sieving matrices. Chou et al. disclose sorting nucleic acid molecules according to their diffusion coefficients using an electric field which propels the molecules through gaps formed by an asymmetric array of objects. See Chou et al. (1999) PNAS USA 96:13762. Han & Craighead disclose separations using entropic traps consisting of a series of many narrow constrictions (<100 nm) separated by wider and deeper regions (a few microns). See Han & Craighead (2000) Science 288:1026-1029. Huang et al. disclose a hexagonal array of posts which act as a sieving matrix in pulsed-field electrophoresis. See Huang et al. (2002) Nat. Biotechnol. 20:1048. U.S. Patent Publication 20040144651 discloses an array of obstacles wherein molecules are separated according to size.
All separation techniques work via a competition between mobilization and retention or dissipation transport mechanisms. In many conventional methods, the retention and drag mechanisms are stochastic. If these mechanisms can be modeled as a sequence of N discrete stochastic interactions, then the peak resolving power of these separations, at best scales as N−1/2. At a constant average interaction rate therefore, the peak resolving power at best scales as t1/2, where t is the duration of the separation process (this t1/2 scaling is quite general and is not restricted to retention and drag mechanisms that rely on discrete events). Each interaction is separated by a diffusive transport step through a mobile phase.
Moreover, incoherent retention and drag interactions essentially depend on diffusion or Brownian motion. For example, in conventional chromatography, a particle undergoing separation must diffuse between the stationary and mobile phases. This essential diffusive transport sets a limit on the rate of interactions a particle experiences. Fast, high-resolution separations require short diffusion times which in turn require small diffusion distances, small molecules, or both. A conventional approach to improving the separation resolving power for a given separation time is to reduce the diffusion distance by packing or otherwise porously filling a separation column or channel. If the mobile phase is moved by an applied pressure gradient, the small molecular diffusion distance comes at the cost of a correspondingly small viscous diffusion distance. Consequently the absolute pressure applied must be large, typically tens to many hundreds of atmospheres, to achieve a flow rate that is high enough that diffusive peak broadening does not reduce the resolving power. Even with such packings and high mobilization fields, these conventional diffusion-rate-limited separations perform relatively poorly for slowly diffusing particles of practical industrial, medical, and scientific interest, e.g., proteins and other biological macromolecules, polymers, and nanoparticles of natural, biological, and synthetic origin. Consequently, these prior art methods separate particles using diffusion mediated transport which detrimentally limits the sorting rate for large molecules.
Other prior art methods employ techniques in which particles come into direct contact with surfaces such that the particles experience steric effects. Such contact is detrimental, particularly for small particles, because steric effects increase sensitivity to surface fouling and increase the likelihood of surface fouling and create additional issues including complicated or high-precision fabrication requirements.
There is therefore a need for devices and methods for rapidly separating, concentrating, and assaying particles which are not diffusion-rate-limited or result in steric effects.
The present invention provides devices and methods for rapidly separating, concentrating, and assaying particles which are not diffusion-rate-limited or result in steric effects. In particular, the present invention provides methods and devices for manipulating a particle in a fluid using coherent nonlinear chromatography (CNC).
In some embodiments, the present invention provides a method of manipulating an analyte in a fluid in a channel which comprises subjecting the analyte to a primary flow field and a secondary flow field produced by at least one field non-uniformity resulting from at least one perturber, with the proviso that where the perturber is a ridge obstacle or a valley obstacle, the primary flow field is not an electrokinetic field and the secondary flow field is not a dielectrophoretic field. In some embodiments, the primary flow is an electrokinetic flow or a hydrodynamic flow. The perturber is an obstacle, a patch, or a projection. In preferred embodiments, the perturber is elongated. In some embodiments, the secondary flow field is an electrophoretic field, a dielectrophoretic field, a magnetophoretic field, an electrostriction field, a photophoretic field, a thermophoretic field, an entropic field, an acoustical field, or a chemical field. In some embodiments, the secondary flow field is produced by a plurality of field non-uniformities in a coherent array. In some embodiments, the methods include placing the perturber at an angle that is substantially perpendicular to the primary flow field. In some embodiments, the methods include placing the perturber at an angle to the perpendicular of the primary flow field. In some embodiments, the methods include placing the field non-uniformity at an angle that is substantially perpendicular to the primary flow field. In some embodiments, the methods include placing the field non-uniformity at an angle to the perpendicular of the primary flow field.
In some embodiments, the present invention provides an assay for an analyte in a fluid which comprises manipulating the analyte using the methods or devices described herein and observing or detecting the secondary flow of the analyte. In some embodiments, the assay further comprises comparing the secondary flow of the analyte with a control. In some embodiments, the control is the primary flow, the movement of a given or known analyte, and the like.
In some embodiments, the present invention provides a microfluidic device comprising at least one perturber capable of producing at least one field non-uniformity in a primary flow field in a channel, with the proviso that where the perturber is a ridge obstacle or a valley obstacle, the primary flow field is not an electrokinetic field and the secondary flow field produced by the field non-uniformity is not a dielectrophoretic field. The perturber is an obstacle, a patch, or a projection. In preferred embodiments, the perturber is elongated. In some embodiments, the device comprises a plurality of perturbers, which may be the same or different. In some embodiments, the device comprises two or more domains of perturbers which may be in series or parallel. The domains may have structure which separates them such as a ridge, a channel, a binning channel, a valve, or the like. In some embodiments, the perturber is at an angle that is substantially perpendicular to the primary flow field. In some embodiments, the perturber is at an angle to the perpendicular of the primary flow field. In some embodiments, the field non-uniformity is at an angle that is substantially perpendicular to the primary flow field. In some embodiments, the field non-uniformity is at an angle to the perpendicular of the primary flow field.
Both the foregoing general description and the following detailed description are exemplary and explanatory only and are intended to provide further explanation of the invention as claimed. The accompanying drawings are included to provide a further understanding of the invention and are incorporated in and constitute part of this specification, illustrate several embodiments of the invention, and together with the description serve to explain the principles of the invention.
This invention is further understood by reference to the drawings wherein:
The right panel of each figure shows the cross-sections of the particle potential energy perturbations produced by non-uniform fields. The fringes are contours of constant potential energy.
The present invention provides methods and devices for employing coherent particle scattering (CPS) to separate particles based on their volume interactions with competing mobilization fields. The application of CPS to particle sorting and separation is referred to as “coherent nonlinear chromatography” (CNC).
Coherent particle scattering (CPS) is transport produced by deterministic particle interactions with field non-uniformities. These interactions include electrostatic, dielectrophoretic, magnetic, electromagnetic, optical, inertial, hydrodynamic, and mechanical interactions that occur through a significant fraction of the cross-section or “bulk” of the flow channel. These “volume” interactions contrast with “surface” interactions like the hydrophobic interactions used in chromatography, and direct physical entanglement and mechanical-contact-based sieving techniques. Because the scattering events are deterministic, the peak resolving power of separations based on CPS can in principle scale linearly with time when they are driven coherently, e.g., by spatially periodic repetition of the perturbation, requiring far fewer interactions than conventional techniques to produce a desired separation.
CPS does not require pore- or channel-scale diffusion for each interaction and is thus not inherently diffusion-rate limited. At most, molecular-scale diffusion time is needed for interactions that involve thermal motion to relax or equilibrate from a perturbation in the physical arrangement or excited energy state, e.g., thermal relaxation of particle conformation following a mechanical distortion. Electrostatic, magnetic, electromagnetic, dielectrophoretic, and hydrodynamic interactions do not explicitly employ thermal relaxation or equilibration or diffusion. These interactions are rate dependent because of other finite-rate relaxation mechanisms, e.g., polarization relaxation in dielectrophoresis. Because the magnitude of CPS depends on finite relaxation rates, CNC can actually be used to sort particles by their perturbation relaxation rates, i.e., time required for a particle to return to an equilibrium state following a perturbation. If relaxation rates are sufficiently high, CNC can be performed in an ultrafast manner, e.g., inertial large protein separations can theoretically be conducted in the ten-millisecond time scale instead of the kilosecond time scale typical for conventional chromatography. On the other hand, if the relevant relaxation mechanism, i.e., the physical process by which a perturbed particle re-equilibrates, is relatively slow, the linear scaling of resolving power with the number of interactions N, as opposed to N1/2 for conventional chromatography, in principle, allows the separation to proceed as fast as is physically possible for a given perturbation and relaxation mechanism.
In some cases, channel-scale diffusion, i.e., diffusion through the channel depth, span, or other characteristic geometrical length scale, can improve the performance of CNC separations by averaging out streamline-dependent phenomena that produce hydrodynamic dispersion. A preferable alternative to diffusion for reducing hydrodynamic dispersion is focusing or concentration of the target particles toward preferred streamlines of the primary flow. An effect of the secondary flow, this primary-flow-transverse focusing forces particles into narrow streams that substantially follow particular flow streamlines. Such transverse focusing can significantly reduce the amount of diffusion needed to average over streamline-to-streamline variations in flight-times in CNC devices.
As provided herein, the present invention provides methods and devices for separating or selectively concentrating particles in a fluid using coherent nonlinear chromatography (CNC) in a channel, preferably a microchannel. As used herein, “channel” refers to a structure wherein a fluid may flow. A channel may be a capillary, a conduit, a strip of hydrophilic pattern on an otherwise hydrophobic surface wherein aqueous fluids are confined, and the like. As used herein, “microfluidic” refers to a system or device having one or more fluidic channels, conduits or chambers that are generally fabricated at the millimeter to nanometer scale. Thus, the “microfluidic channels” or alternatively referred to herein as “microchannels” of the present invention generally have cross-sectional dimensions ranging from about 10 nm to about 1 mm.
As used herein, a “fluid” refers to a substance that tends to flow and to conform to the outline of a container such as a liquid or a gas. Fluids include saliva, mucus, blood, plasma, urine, bile, breast milk, semen, tears, water, liquid beverages, cooking oils, cleaning solvents, hydrocarbon oils, fluorocarbon oils, ionic fluids, air, and the like. Fluids can also exist in a thermodynamic state near the critical point, as in supercritical fluids. If one desires to test a solid sample for a given analyte according to the present invention, the solid sample may be made into a fluid sample using methods known in the art. For example, a solid sample may be dissolved in an aqueous solution, ground up or liquefied, dispersed in a liquid medium, melted, digested, and the like. Alternatively, the surface of the solid sample may be tested by washing the surface with a solution such as water or a buffer and then testing the solution for the presence of the given analyte. A fluid may be a polydisperse fluid, i.e. a fluid comprising a variety of particles having different properties, particles having multiple properties, or both.
As used herein, “analyte” is used interchangeably with “particle” to refer to a particle that may be natural or synthetic chemicals and biological entities. Chemicals and biological entities (biomolecules) include industrial polymers, powders, latexes, emulsions, colloids, environmental pollutants, pesticides, insecticides, drugs such as cocaine and antibiotics, magnetic particles, high-magnetic-permeability particles, metal ions, metal ion complexes, inorganic ions, inorganic ion complexes, organometallic compounds, metals including aluminum, arsenic, cadmium, chromium, selenium, cobalt, copper, lead, silver, nickel, and mercury, and the like, amino acids, peptides, proteins, glycoproteins, nucleotides, nucleic acid molecules, carbohydrates, lipids, lectins, cells, viruses, viral particles, bacteria, organelles, spores, protozoa, yeasts, molds, fungi, pollens, diatoms, toxins, biotoxins, hormones, steroids, immunoglobulins, antibodies, supermolecular assemblies, ligands, catalytic particles, zeolites, and the like, biological and chemical warfare agents, agents used in explosives, and the like.
As used herein, “separating” is used interchangeably with “sorting”, “collecting,” “concentrating,” “filtering,” “assaying,” “detecting” “measuring, ” “monitoring,” and “analyzing”. As provided herein, particles are separated by CNC, a process in which particles are made to depart from a primary flow via a secondary flow either longitudinally, resulting in a modified time-of-flight of the particles through a channel, or transversely, resulting in a modified spatial distribution of particles in a channel, or a combination of longitudinal and transverse processes.
Specifically, the present invention provides methods and devices which separate particles based on one or more characteristics by competing a primary flow field (primary mobilization field) with a secondary flow field in a channel. As used herein, “mobilization field” refers to any force field that influences a particle to pass through a channel or region of a channel. Mobilization fields include hydrodynamic flow fields produced by pressure differences, gravity, linear or centripetal acceleration, electrokinetic flow fields, electroosmotic flow fields, magnetophoretic and thermophoretic flow fields, electric fields, optical fields, centrifugal fields, gravitational fields, combinations thereof, and the like.
The primary flow of the particles is the motion of particles (flow) resulting from a primary flow force exerted by the primary flow field. Primary flow is generally in a direction that is substantially parallel to the boundaries of a microchannel. As used herein, a “primary flow force” is the force on a particle that makes it follow the primary flow. Two classes of primary flow are considered herein, “hydrodynamic flows” which, as used herein, include pressure-gradient-, capillarity-, inertia-, gravity, centripetal-acceleration-, chemical reaction-, and magnetically-driven flows and the like and “electrokinetic” flows which are the superposition of electrophoretic and electroosmotic flows. The electrokinetic flows considered herein can have substantial electrophoretic and electroosmotic components or have substantially dominant electrophoretic or electroosmotic components either by the choice of channel boundaries, fluid composition, surface treatments, surfactants, dynamic coatings, gels, and the like, including those known in the art.
The secondary flow field retains or redirects particles from the primary flow. The secondary flow field is produced by mechanical interactions, inertial interactions, entropic interactions, electrostatic interactions, magnetic interactions, electromagnetic interactions, optical interactions, chemical interactions, or a combination thereof, with at least one field non-uniformity projected or produced from patterns in the channel.
Secondary flow generally refers to the motion of a particle resulting from its interactions with forces produced by the secondary flow field and the “secondary flow force” refers to the force that produces the secondary flow. The secondary flow in the present invention is produced by interactions that occur substantially throughout the cross-section of the primary flow at a region or regions in the channel and are referred to as “volume interactions”. As used herein, “volume interaction” refers to any force on a particle that a particle can experience substantially throughout the cross-section of a flow channel. Thus, “secondary flow” is the particle motion produced by volume interactions resulting from at least one spatially non-uniform field within the flow channel
Volume interactions are different from “surface interactions”, which occur only when a particle is in immediate proximity to a channel boundary. As used herein, “surface interaction” refers to any force on a particle that a particle only experiences in immediate proximity to a boundary of the flow channel. Such surface interactions include Van Der Waals and other “adhesive” forces, electrostatic forces within a Debye layer that is thin compared other channel dimensions, steric effects and mechanical reaction forces produced when particles are forced onto or collide with a surface, and the like. These surface interactions are not employed to produce a secondary flow according to the present invention.
As used herein, a “field non-uniformity” refers to a spatial gradient in a field. As provided herein, a field non-uniformity is produced within the channel by a perturber. As used herein, a “perturber” distorts an applied flow, an electric field, or the action of an area or region in a channel which produces gradients in an intrinsic field, e.g., the electric field within the Debye layer. A perturber may be a projection. As provided herein, a “projection” is a disruption projected into a uniform field to produce a field non-uniformity. Examples of disruptions include optical interference patterns, temperature fields, magnetic fields, acoustic energy fields, and the like. These disruptions may modulate particle motion directly, e.g., by acoustic streaming or electrostriction, or modulate the behavior of the particle in the primary flow, e.g., by modifying surface charge density and thereby mobility in an electrokinetic primary flow. Moreover, all the force for the secondary flow can be generated from the action of a non-uniform primary flow, e.g., dielectrophoresis in a high-field electrokinetic flow or inertia in a high-speed hydrodynamic flow. The degree of coupling between the primary and secondary flows can be quantified by a simple exponent, n, which is an important consideration in the design of CNC devices.
A perturber may be an obstacle. As provided herein, an “obstacle” is a protrusion or a cavity in a surface of a channel. For example, a ridge is an elongated protrusion and a valley is an elongated cavity in a surface of a channel. As used herein, “elongated” refers to an object that has a length that is greater than its width, but is not necessarily straight. As used herein, a “post” refers to an arbitrarily shaped object that spans the channel either straight or at an incline with respect to the channel boundaries. As used herein, a “hole” refers to an opening in the channel through which particles, fluid or both may pass. In preferred embodiments, the perturbers are elongated.
Obstacles of the present invention may be made from the same material as the material defining the microfluidic channel in which the obstacle is located or the obstacles may be made of a different material deposited or adhered to walls of the microchannels using methods known in the art. Suitable materials for the pertubers include materials that are insulative, conductive, semi-conductive, or a combination thereof.
As used herein, the word “conductivity” is used to describe the ease of flow of both conduction and displacement current. It is often mathematically described as a complex number that varies with the frequency of the applied electric field. Similarly, “conduction” is used to describe both conventional conduction and conduction of displacement currents. As used herein, “insulative” and “conductive” refers to the relative conductivity of the described item with respect to the fluid. Insulative materials have relatively low conductivity and include plastics, epoxies, photoresists, polymers, silicon, silica, quartz, glass, controlled pore glass, carbon, and the like, and combinations thereof. Preferred insulative materials include thermoplastic polymers such as nylon, polypropylene, polyester, polycarbonate and the like. Conductive materials, in comparison, have relatively high conductivity. Conductive materials include bulk, sputtered, and plated metals and semiconductors, carbon nanotubes, and the like.
A perturber may be flush with the surface of the channel and is herein referred to as a “patch.” A patch is region having at least one property that is different from the adjacent regions of the surface of the channel. Such properties include surface charge, conductivity, transparency, absorptivity, and dopant concentration and type (which may be produced statically during fabrication or dynamically during device operation), and the like. Suitable materials for the patches include materials that are, relative to the adjacent surface, insulative, conductive, photo-conductive, photo-cleavable, semi-conductive, charged, neutral, high dielectric constant, low dielectric constant, positive Zeta potential, negative Zeta potential, or a combination thereof.
One skilled in the art may readily combine different perturbers, arrays of the same perturbers, or arrays of different perturbers in parallel, series, or both to achieve a specific result, for example, separation or concentration of particles into discrete streams or collection areas, sequential separation or concentration through multiple stages, and the like.
Thus, the methods and devices of the present invention employ at least one field non-uniformity within a channel resulting from at least one perturber, such as a projection, an obstacle, a patch, or a combination thereof. In some embodiments, the present employs at least one coherent array, which is a plurality of field non-uniformities that amplify the effect of a secondary flow field by judicious, substantially periodic repetition and may be used to prevent or decrease fouling, extend the operating envelope, and enhance of separations.
The present invention competes a primary flow field with a secondary flow field produced by the interaction of a particle with a field non-uniformity to separate particles. Unlike prior art methods which retain particles based on surface phenomena such as affinity, hydrophobic, affinity, and steric interactions, the methods and devices of the present invention separates (retains) particles as a result of interactions with field non-uniformities that occur throughout the three-dimensional space of the channel, not merely the regions in close proximity to surfaces of the channel. These field non-uniformities are the result of at least one perturber in a microchannel.
The dimensions of a field non-uniformity and therefore its associated perturber are based on the average size of the particle or particles of interest. To avoid surface interactions, the minimum channel dimensions, including regions surrounding obstacles, if present, is about several particle diameters, i.e., greater than about 3 diameters, preferably greater than about 10 diameters. Characteristics of a projection should be designed and the dimension of an obstacle or patch constrained to about equal to and preferably greater than about 3 times, the width of the flow area around the obstacle or patch so that the field extrema produced locally by the perturber vary by less than (preferably) 5% to 500% throughout the adjacent flow. A preferred size range of perturbers is about 10 to about 100 particle diameters. The obstacles or patches can be one-thousand or more times larger than the particles of interest, thereby facilitating the use of conventional photolithography to sort macromolecular particles. However, large ratios of the patch or obstacle sizes to particle sizes produce slower separations than those where the size ratios are closer to the more moderate preferred range, e.g., about 10 to about 100. For secondary flow mechanisms that derive their energy from the primary flow, e.g., dielectrophoresis vs. electrokinesis, large size ratios require relatively larger primary flow fields to be applied to drive the secondary flows than for more moderate size ratios. The width of the channel may be selected to achieve a desired throughput using methods known in the art. These ranges of size scales are offered only for practical guidelines and do not represent absolute physical limitations. The dimensions of the non-uniformities depend on the fabrication technique, particle size, and many other application-specific constraints which may be readily determined by one skilled in the art.
Depending on the type of field non-uniformity produced by the perturber, a particle can interact via a variety of mechanisms, including, for example:
The types and details of the field non-uniformity produced by a perturber depend on the type of perturber, the nature of the applied field, and whether the perturber directly produces a field or produces non-uniformities in an otherwise applied field.
A projection is a perturber that is a non-uniform field projected externally into a channel, for example a non-uniform illumination pattern produced by an external diffractive optic or optical interference within the channel, a non-uniform acoustic excitation produced by an external non-uniform source or by acoustic interference within the channel.
Obstacles are perturbers that are geometrical protrusions or cavities which generally produce field non-uniformities in externally applied fields, often fields that propagate through the fluid within the channels.
Patches are perturbers that regions that are substantially flush with channel surfaces which produce field non-uniformities in externally applied fields or directly apply a field non-uniformity, e.g., via direct application of electric, optical, acoustic, or thermal perturbations.
Table 1 lists examples of perturber mechanisms that can be used to producing various secondary flows according to the methods and devices described herein:
For illustration, the interactions of a particle with field non-uniformities in a channel can be expressed via a particle perturbation potential energy field which is the surplus or deficit potential energy that a particle possesses at as a result of the interactions. The gradient of these potentials is the secondary flow force and the resulting component of particle motion produced by these forces is the secondary flow.
For simplicity, the figures show obstacles or patches only at the bottom surface of a microchannel. Nevertheless, obstacles or patches on more than one microchannel wall, e.g., both the top and bottom surfaces with aligned and out-of-phase patterns, are contemplated herein. Similarly, alternative perturber geometries are contemplated herein, e.g., patterned channel-spanning posts, patterned valleys, and different obstacle shapes, are substantially periodic at least over domains within a device.
Highly elongated projections (fringes), obstacles (ridges and valleys), and patches (stripes) are preferred perturbers for many CNC designs because they facilitate the construction of channels having useful and relatively easily specified distributions of field non-uniformities. An elongated perturber can be characterized by a local axial angle that is locally aligned with the most narrowly spaced sides of the perturber and a local normal direction which is at right angles with the local axial direction. Such elongated perturbers typically have a length that is greater than three times the width and have a maximum radius of curvature greater than three widths throughout the majority of the perturber. The dimensions and shapes of the perturbers may be modified, particularly in regions where particles are to be collected or released and at the ends of the perturbers. There is no maximum aspect ratio except that needed to facilitate fabrication, mechanical strength, and dimensional accuracy. A practical upper bound of aspect ratio is limited by sag and deflection of unsupported boundaries of the channel containing the perturber. For unpressurized channels, the maximum ratio of channel width to channel depth with simple etching has been found to be about 103, while about 102 or lower are preferred. Highly pressurized channels require lower ratios of unsupported channel width to height. These ratios can be increased by the addition of internal supports, the use of thick substrates, or the use of external stiffeners.
To clarify the action of obstacle perturbers, which generally modulate an otherwise applied field,
Generally, obstacles with sharper edges, such as those shown in
In alternative embodiments, the coherent arrays may be placed so that the perturbers and consequently the secondary flows have a substantial component transverse to the primary flow, as shown in
Spectrometric separations may be performed using a coherent array which spans the width of the fluid of interest at an angle. In preferred spectrometric embodiments, the fluid flow is at an angle with respect to fringe-like projections, ridge-like obstacles, or stripe-like patches. In other preferred embodiments, the fluid flow is at a small (about <15 degree) angle with respect to a coherent array produced by a plurality of perturbers such as posts, holes, protrusions, cavities or patches such that the secondary flow of particles causes the particles to be deflected from the toward the plurality of perturbers.
A particle is impeded from crossing such a perturber when the largest local normal component of the secondary flow force successfully opposes the local normal component of the primary flow force. As used herein, this condition is called “inhibition”. As used herein, the “inhibition threshold” is the locus of conditions that separate the case where a given particle does and does not experience inhibition.
The local angle of the long axis of a perturber with the primary flow in general affects the particle transport past the perturber and can affect the magnitude of the secondary flow force produced by the perturber. The nature of these angle effects depends on the how the normal force produced by the perturber, δ, scales with the primary mobilization field magnitude, μ. The perturbation scaling can be expressed approximately as a power of μ, i.e., δ˜μn. The dependence of the ratio of the secondary flow force to primary flow force across a ridge, γ, with the local angle, θ, between the perturber axis and primary flow direction is generally γ˜sinn−1 θ.
In the simplest case, the perturbation forces normal to the perturber axis are substantially independent of the primary flow magnitude, so the exponent of the power law, n, is zero, e.g., optically induced electrostriction and photophoresis vs. hydrodynamic or electrokinetic primary flow, dielectrophoretic forcing vs. hydrodynamic primary flow, and the like. In this case, there is no angle dependence of the secondary flow normal force, but there is a sinusoidal dependence of the force applied by the primary flow across the perturber on the local axial angle, so the ratio of the secondary flow normal force to primary flow normal force scales like the cosecant of the local axial angle. Thus the inhibition effect of a ridge is reduced by angling the ridge axis toward a right angle to the primary flow.
In some situations, the primary flow couples weakly to the secondary flow force, e.g., via convective charge polarization effects within Debye layers, particle alignment or distortion effects, and the like. Provided the actual exponent n<1, the angle effects of the perturber will remain qualitatively as described for n=0, but the variation of the inhibition effect with angle reduces until as n→1, there is no angle dependence of inhibition.
The power n>1 implies that the primary flow contributes nonlinearly to the secondary flow, i.e., the secondary flow is partly or completely powered by the primary flow. In this range the angle dependence switches such that the competition between primary and secondary flow becomes more favorable for the secondary flow as the perturber axis becomes more misaligned with the primary flow, reaching a peak when oriented normal to the primary flow. This angular variation is qualitatively the opposite of that for n<1.
The angle dependence of the inhibition thresholds enables a different class of particle spectrometers.
The limit n=1 implies a first-order dependence of the secondary flow on the primary flow. Such dependence can be introduced if the perturbation interaction couples to the primary flow, for example if the secondary flow is produced by optically perturbing the surface charge density of a particle in an electrokinetic primary flow. Because the normal components of the secondary and primary flows have the same angle dependence, the inhibition threshold has no angle dependence. A spectrometer made from such a perturber, cannot exploit an angle dependence of the inhibition threshold. Instead, the perturber must either operate as a disperser below the inhibition threshold, as shown in
Theoretically, several important phenomena obey the scaling n=2, e.g., a dielectrophoretic secondary flow vs. an electrokinetic primary flow and an inertial secondary flow vs. a hydrodynamic primary flow, and the like. At this scaling, the primary force normal to the ridge scales sinusoidally with angle, but the secondary force scales as the sine squared, so the ratio of the secondary flow normal force to primary flow normal force scales like the sine of the local axial angle with respect to the primary flow. In this case, a canonical spectrometer can be constructed from a ridge that curves as shown in
Table 2 shows the range of n, a measure of the coupling between the primary and secondary flows for various parings of these flows. The parameter n quantifies coupling between the primary and secondary flows, with n=0 indicating no coupling and n=2 indicating strong coupling.
Because the region of particle interaction with a perturber depends on the properties of the particle, asymmetrical perturbers can have a variety of novel functions.
The devices of the present invention are readily fabricated using methods known in the art including techniques conventionally used for silicon-based integrated circuit fabrication, embossing, casting, injection molding, and the like. See e.g. Becker, et al. (1986) Microelectr. Engineer. 4:35-56, which is herein incorporated by reference. Other suitable fabrication techniques include photolithography, electron beam lithography, imprint lithography, reactive ion etching, wet etch, laser ablation, embossing, casting, injection molding, and the like. See e.g. Becker, et al. (1998) Microelectr. Engineer. 8:24-28, which is herein incorporated by reference.
The devices of the present invention may be fabricated from materials that are compatible with the conditions present in the particular application of interest. Such conditions and considerations include pH, temperature, application of organic solvents, ionic strength, pressure, application of electric fields, surface charge, sticking properties, surface treatment, surface functionalization, bio-compatibility, and the like. The materials of the devices may be chosen for their optical properties, mechanical properties, and for their inertness to compounds to be exposed thereto. Such materials include glass, fused silica, silicone rubber, silicon, ceramics, polymers, and the like.
In some embodiments, particles are unloaded from the array using methods known in the art, including microfluidic channels at the end of the array and are then be routed for further use. In particular, binning channels may be employed to divert a fluid stream of interest to a detection area for observation or visualization, to a reaction area or another device for further manipulations including chemical and physical reactions, and the like.
Embodiments diagrammed herein show only the active region of the CNC flow channel, not the means of introducing or collecting particles, primary flows, or means of providing for flushing, cleaning, elution, and the like. Thus, it should be noted that the devices of the present invention may further comprise multiple ports, offset-t structures, electrodes, and other microfluidic structures and means known in the art for implementing sample introduction, manipulation and analysis.
Moreover, embodiments diagrammed herein do not show the means of or external apparatus for applying fields and the primary flow. The design and possible integration of such external apparatus is obvious or known in the art and can be conveniently and reliably accommodated.
In preferred embodiments, portions of the devices of the present invention are optically transparent such that optical detection methods known in the art, including fluorescence detection and imaging using inverted-optic microscopes, may be used. In preferred embodiments, the fluid flows and separations are monitored in real-time. In some embodiments, the exterior of the devices are constructed such that interfaces, including capillary ports, and the like, known in the art may be conveniently and reliably accommodated.
In preferred embodiments, the channels of the devices are constructed with materials and dimensions that exhibit low intrinsic fluorescence. Thus, in some embodiments, the substrate of the devices comprises fused silica as fused silica exhibits low intrinsic fluorescence. In some embodiments, the devices comprise binning channels for post-separation analysis or further manipulations. In preferred embodiments, the devices are made by subtractive processing methods known in the art that limit exposure of the native fused silica surface to only O2 plasmas.
Devices can be constructed from a sandwich of two or more substrates so that channels are bounded conduits with ports. Bonding of the substrates may be done using methods known in the art including thermal bonding of nanofluidic channels in fused silica See e.g. Tamaki, et al. (2003) Proc. MicroTotal Analysis Systems 1:681, which is herein incorporated by reference.
CNC devices may be combined with other devices that employ separation methods known in the art including on-chip using chromatography, such as electrochromatography (Singh (2002) Anal. Chem. 74:784-789, which is herein incorporated by reference), micellar electrokinetic chromatography, or reverse-phase high pressure liquid chromatography, and the like, as well as sample preparation methods, chemical processing methods, and biological methods known in the art.
In addition to the specific embodiments shown, it is to be understood that a variety of configurations of perturbers may be used for a particular application-combining one or a plurality of perturbers and perturber types, described above, in any combination. Further, various geometries and device configurations may, according to the present invention, be readily designed by one skilled in the art for desired versatility and performance.
To the extent necessary to understand or complete the disclosure of the present invention, all publications, patents, and patent applications mentioned herein are expressly incorporated by reference therein to the same extent as though each were individually so incorporated.
Having thus described exemplary embodiments of the present invention, it should be noted by those skilled in the art that the within disclosures are exemplary only and that various other alternatives, adaptations, and modifications may be made within the scope of the present invention. Accordingly, the present invention is not limited to the specific embodiments as illustrated herein, but is only limited by the following claims.
The present invention was made by employees of Sandia National Laboratories. The Government has certain rights in the invention.