PROCESS FOR THE OBTAINMENT OF SUSPENDED DOUBLE-FLAT SU-8 JANUS CHIPS, SAID SUSPENDED DOUBLE-FLAT SU-8 JANUS CHIPS AND SUSPENDED ARRAY THEREOF

Abstract

The invention relates to a process for the obtainment of suspended double-flat SU-8 Janus chips by means of SU-8 photolithography to create an arrangement of ordered SU-8 chips on a substrate and soft lithography to create a planar printed arrangement or a planar printed array on each chip, said process comprising steps for forming a solidified membrane that is peeled off and dissolved in an aqueous medium. Furthermore, the invention relates to the suspended double-flat SU-8 Janus chips and to a suspended array comprises at least two different suspended double-flat SU-8 Janus chips. Lastly, the invention relates to barcoding chips and to sensing devices comprising said suspended double-flat SU-8 Janus chips or said suspended array.

Claims

1. A process for the obtainment of suspended double-flat SU-8 Janus chips comprising: a plurality of double-flat SU-8 chips, wherein each SU-8 chip has a first flat surface and a second flat surface, and molecules, biomolecules, nanoparticles or a combination thereof, wherein the molecules, biomolecules, nanoparticles or the combination thereof are grafted onto the first and the second flat surface of each SU-8 chip, and wherein said process characterised in that it comprises the following steps: a) defining the shape and the size of SU-8 chips by SU-8 photolithography; thereby forming an arrangement of ordered SU-8 chips onto a substrate, wherein each SU-8 chip has a first flat surface and a second flat surface and wherein the second flat surface is in direct contact with the substrate; b) functionalizing, by soft lithography, the first flat surface of each SU-8 chip obtained in step (a) using a silane crosslinker; thereby forming a first reactive flat surface in each SU-8 chip, wherein the silane crosslinker comprises two functional groups: a silane functional group and a functional group selected from the list consisting of primary or secondary amines, epoxide, thiol, carboxyl, azide, vinyl, isocyanate or methacryloxy groups; c) grafting molecules, biomolecules, nanoparticles or a combination thereof onto the first reactive flat surface of each SU-8 chip obtained in step (b) by soft lithography; d) casting a mounting medium on top of the SU-8 chips obtained in step (c) and leaving to solidifying, thereby embedding the SU-8 chips obtained in step (c) into the mounting medium and forming a solidified membrane onto the substrate; e) peeling off the solidified membrane obtained in step (d) from the substrate, thereby unlocking the second flat surface of each SU-8 chip; f) functionalizing, by soft lithography, the unlocked second flat surface of each SU-8 chip obtained in step (e) using a silane crosslinker, wherein the silane crosslinker comprises two functional groups: a silane functional group and a functional group selected from the list consisting of primary or secondary amines, epoxide, thiol, carboxyl, azide, vinyl, isocyanate or methacryloxy groups; thereby forming a second reactive surface in each SU-8 chip; g) grafting molecules, biomolecules, nanoparticles or a combination thereof onto the second reactive surface of each SU-8 chip obtained in step (f) by soft lithography; h) dissolving the solidified membrane of the SU-8 chips obtained in step (g) in an aqueous medium; and i) recollecting the suspended double-flat SU-8 Janus chips obtained in step (h) via centrifugation.

2. The process according to claim 1, wherein step (a) is repeated thereby obtaining a double-height arrangement of ordered SU-8 chips on the substrate.

3. The process according to claim 1, wherein steps (b) and (c) are repeated.

4. The process according to claim 1, wherein the molecules, biomolecules or nanoparticles grafted onto the first flat surface of each SU-8 chip obtained in step (c) comprises only one type of molecules, biomolecules or nanoparticles grafted onto the first flat surface of each SU-8 chip; thereby forming a first planar printed arrangement.

5. The process according to claim 1, wherein the molecules, biomolecules or nanoparticles grafted onto the first flat surface of each SU-8 chip obtained in step (c) comprises the combination of molecules, biomolecules or nanoparticles grafted onto the first flat surface of each SU-8 chip; thereby forming a first planar array.

6. The process according to claim 1, wherein soft lithography of steps (b) and (c) is performed in the form line patterns and/or spots.

7. The process according to claim 1, wherein steps (f) and (g) are repeated.

8. The process according to claim 1, wherein the molecules, biomolecules or nanoparticles grafted onto the second flat surface of each SU-8 chip obtained in step (g) comprises only one type of molecules, biomolecules or nanoparticles grafted onto the second flat surface of each SU-8 chip; thereby forming a second planar printed arrangement.

9. The process according to claim 1, wherein the molecules, biomolecules or nanoparticles grafted onto the second flat surface of each SU-8 chip obtained in step (g) comprises the combination of molecules, biomolecules or nanoparticles grafted onto the second flat surface of each SU-8 chip; thereby forming a second planar array.

10. The process according to claim 1, wherein soft lithography of steps (f) and (g) is performed in the form line patterns and/or spots.

11. A suspended double-flat Janus chips, comprising of: a plurality of double-flat SU-8 chips, wherein each SU-8 chip has a first flat surface and a second flat surface, and molecules, biomolecules, nanoparticles or a combination thereof, wherein the molecules, biomolecules, nanoparticles or the combination thereof are grafted onto the first and the second flat surface of each SU-8 chip.

12. The suspended double-flat Janus chips of claim 11, wherein the molecules are selected from the list consisting of modified chromophores comprising N-Hydroxysuccinimidyl ester or Succinimidyl ester groups and modified fluorophores comprising N-Hydroxysuccinimidyl ester or Succinimidyl ester groups.

13. The suspended double-flat Janus chips of claim 11, wherein the biomolecules are selected from the list consisting of carbohydrates, proteins, antibodies, enzymes and nucleic acids.

14. The suspended double-flat Janus chips of claim 11, wherein the nanoparticles are selected from carbon-based nanoparticles comprising an amine functional group, metal nanoparticles comprising an amine functional group, ceramic nanoparticles comprising an amine functional group, polymeric nanoparticles comprising an amine functional group and semiconductor nanoparticles comprising an amine functional group.

15. A suspended array comprising at least two different suspended double-flat Janus chips of claim 11 .

16. A process for the obtainment of the suspended array of claim 15 characterized in that it comprises a step of mixing at least two different suspended double-flat Janus chips.

17. A barcoding chip comprising the suspended double-flat Janus chips of claim 11 .

18. The barcoding chip of claim 17, wherein said barcoding chip is a color barcoding chip, and wherein at least a nanoparticle is grafted on the first or the second flat surface of each SU-8 chip in the form of line patterns and/or spots and said nanoparticle is an amine-modified Quantum Dot.

19. A sensing device comprising the suspended double-flat Janus chips of claim 11 .

20. The sensing device of claim 19, wherein the sensing device is a pH sensing device, and wherein at least a molecule is grafted on the first or the second flat surface of each SU-8 chip, and the molecule is a pH sensing fluorophore comprising N-Hydroxysuccinimidyl ester or Succinimidyl ester groups.

21. The sensing device of claim 19, wherein the sensing device is DNA sensing device, and wherein at least a biomolecule is grafted on the first or the second flat surface of each SU-8 chip, and the biomolecule is a DNA probe.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0097] FIG. 1 Scheme of the preparation of suspended double-flat SU-8 Janus chip with grafted fluorophore, DNA probe, protein and Quantum Dots.

[0098] FIG. 2. Scanning electron microscopy images of SU-8 chips on the substrate identified by their customized physical anisotropy: (a) fiducial marker, (b) aspect ratio width:length 1:2, 1:3, and 1:4, (c) branching, and (d) faceting.

[0099] FIG. 3. Scheme of the lateral view of suspended of double-height double-flat SU-8 chips with grafted fluorophore, DNA probe, protein and Quantum Dots.

[0100] FIG. 4. Scanning electron microscopy of double-height SU-8 chip consisting of an initial fiducial chip and a secondary branching chip.

[0101] FIG. 5. Optical microscopy image of liberated chips resuspended in water.

[0102] FIG. 6. Fluorescence microscopy images of an arrangement of fiducial SU-8 chips grafted with the red-emitting fluorophores to define a) spots or b) lines on top flat surface of the chips and backfilled with a green-emitting fluorophore for visualization purposes. c) The whole top flat surface of the arrangement of chips patterned to graft a red-emitting fluorophore. d) The top flat surface and the lateral sides of the arrangement of chips grafted with red-emitting fluorophore.

[0103] FIG. 7. a) Fluorescence microscopy images of an arrangement of branching SU-8 chips on the substrate and grafted with red-emitting fluorophore. b) The arrangement of grafted chips is liberated and resuspended in water.

[0104] FIG. 8. a) Fluorescence microscopy images of liberated branched SU-8 chips with an initial epoxy reactive surface and grafted with a Texas-red-labelled oligo. b) Fluorescence microscopy images of a liberated Aspect Ratio SU-8 chips with an initial epoxy reactive surface and grafted with GFP.

[0105] FIG. 9. a) Fluorescence microscopy image of an arrangement of aspect ratio SU-8 chips grafted with QD545. b) Fluorescence microscopy image of a population of liberated aspect ratio SU-8 chips grafted with QD545. c) Fluorescence microscopy image of an arrangement of fiducial SU-8 chips grafted with QD525. d) Fluorescence microscopy image of a population of liberated fiducial SU-8 chips grafted with QD525.

[0106] FIG. 10. a) Red fluorescent microscopy channel image of liberated Fiducial chips grafted with red-emitting fluorophore on the top flat surface and green-emitting fluorophore on the bottom flat surface. b) The same suspended chips observed with the green fluorescent channel. c) Composite image of the previous images. d) Red fluorescent microscopy channel image of liberated Faceting chips grafted with red-emitting QD655 on the top flat surface and green-emitting fluorophore on the bottom flat surface.

[0107] FIG. 11. a) Optical microscopy image of liberated and suspended double-height SU-8 chips. b) Fluorescence microscopy image of the same double-height SU-8 chips grafted with QD655 on the branching side and QD545 on the Fiducial side.

[0108] FIG. 12. Fluorescence microscopy images of suspended Branched SU-8 chips grafted with pH sensitive red fluorophore at different pH: a) pH 4, b) pH 7, and c) pH 9.

[0109] FIG. 13. a) Red fluorescent microscopy channel image of liberated Fiducial chips grafted with QD655 on the top flat surface and green-emitting oligo hybridized to the probe grafted onto the bottom flat surface. b) The same suspended chips observed with the green fluorescent channel. c) Composite image of the previous images.

[0110] FIG. 14. Composite image of the red and green fluorescent channels of suspended Aspect Ratio SU-8 chips with distinct red- and green-emitting fluorophore spots on the top surface and QD545 grafted onto the bottom surface.

EXAMPLES

[0111] FIG. 1 shows a general scheme of the preparation of a suspended double-flat Janus chip with grafted fluorophore, DNA probe and protein molecules, and nanoparticles as Quantum Dots. [0112] a) The SU-8 chip (2) is part of an arrangement of ordered chips fabricated directly over a substrate (1) by means of SU-8 lithography. The top flat surface of the chip (3) is functionalized to obtain the reactive surface with selected cross-linkers (4) via microcontact printing. [0113] b) The arrangement of ordered chips with the reactive surface with selected cross-linkers is patterned with soft lithography as microcontact printing for a complete coverage of the chip or with Polymer Pen lithography to graft a planar array of the same molecules or nanoparticles (5). Alternatively, different molecules and nanoparticles can be patterned independently with successive Polymer pen lithography processes to graft planar array with selected molecules or nanoparticles in discreet regions of the chip (5.1, 5.2, 5.3). [0114] c) Mounting medium (6) is cast over the arrangement of ordered SU-8 chips with the reactive surface with selected cross-linkers with either the complete coverage of the same molecules and nanoparticles, or the planar array of the same molecules and nanoparticles, or the planar array of different molecules and nanoparticles, and left to solidify, embedding the chips in its matrix. [0115] d) The solidified mounting medium is peeled from the substrate hauling the chips along its matrix, exposing the bottom flat surface of the chips (7). The substrate (1) can be discarded. [0116] e) The exposed bottom flat surface (7) of the chips is subsequently patterned with soft lithography as microcontact printing to obtain a reactive surface with selected cross-linkers (8). [0117] f) The reactive surface with selected cross-linkers (8) from the bottom flat surface (7) of the SU-8 chips can be patterned with soft lithography as microcontact printing to graft molecules or nanoparticles (9). [0118] g) The solidified mounting medium (6) is dissolved in an aqueous medium to obtain the double-flat chips as Janus chips.

[0119] We fabricated polymeric chips of various sizes (3-12 .Math.m), thickness (0.5-1.2 .Math.m), and topographies, coupled with faceting, fiducial, aspect ratio, and branching dimensions. Then, we selectively functionalized the top and bottom flat surfaces of the chips to generate 0D, 1D, 2D, and 3D patterns of molecules as fluorescent probes, biomolecules (proteins and DNA strands), and nanoparticles as quantum dots (QDs) with high spectral resolution. Importantly, the functionalization allows the use of multi-chemistry strategies to pattern probes with different or interfering immobilization chemistries without the need to consider orthogonal chemistry. Finally, we demonstrate the sensing and detecting capabilities of the suspended double-flat Janus chips to detect pH changes in the environment and the selective recognition of DNA.

Materials and Methods

[0120] All printing stamps, for microcontact printing or polymer pen lithography, were fabricated using Sylgard 184 PDMS elastomer (Dow Corning), and all chips with the SU-8 2000.5 resin (MicroChem). The HIPR 6512 positive photoresist (Fujifilm Electronic Materials, USA) and the Sioetch® remover (Selectipur) were used during microfabrication. The 3-glycidoxypropyltrimethoxysilane (epoxy-silane) and the (3-Aminopropyl)triethoxysilane (APTES) silanes (Sigma-Aldrich) were used independently as crosslinkers between the SU-8 and the subsequent surface modification. 1H,1H,2H,2H-Perfluorooctyltrichlorosilane (PFOTCS) was acquired from Fluka Other reagents include ethylenediamine (EDA), anhydrous dimethylsulfoxide (DMSO), acetonitrile, disodium hydrogen phosphate (Na.sub.2HPO.sub.4), Fluoromount® aqueous mounting media, Hybridization solution, saline-sodium citrate (SSC) buffer 20x (Sigma-Aldrich), and ethanol (Panreac). All of the fluorescent probes were either Qdot® ITK® Amino (PEG) Quantum Dots (QDs), DyLight NHS Ester fluorophores or pHrodo® Red, succinimidyl ester (ThermoFisher Scientific). The modified oligonucleotide strands had an anchoring moiety and/or fluorescent probe (biomers.net).

Fabrication of PPL Stamp Mold

[0121] A 525 .Math.m-thick P-type <100> silicon wafer was wet-oxidized at 1100 ºC to obtain a 1 .Math.m-thick SiO2 layer. Then, a 1.2 .Math.m-thick layer of the HIPR 6512 photoresist was spun over the oxidized wafer and exposed to UV light through a photomask using a MA56 mask aligner (Karl Süss, Germany). After developing and hard-baking the resist at 200 ºC for 30 min, the SiO.sub.2 layer was dry-etched using a C2F6/CHF3 mixture in a Drytek Quad 484 RIE (Drytek, USA). Later 40% KOH anisotropic etching at 75 ºC for 4 min attacked the exposed Si to create the inverted pyramids. The remaining SiO.sub.2 was removed with Sioetch®. Lastly the mold was plasma activated for 30 s at 100 W and exposed to a saturated PFOTCS atmosphere for 1 h. After baking at 75° C. for 1 h, the mold was rinsed with ethanol and dried under a N.sub.2 flow.

Fabrication of PDMS Stamps

[0122] A 10:1 w/w prepolymer-catalyst mixture was thoroughly stirred, degassed and poured over either a pristine silicon wafer for flat stamps, or onto the selected silicon molds with the desired features. To prevent the contraction of the PDMS stamps, a plasma-activated glass slide was placed over the uncured PDMS and left to cross-link at 75° C. for 1 h to a final thickness of ≈100 .Math.m.

Fabrication of SU-8 Chips

[0123] Standard SU-8 photolithography was used to define the shape and size of the SU-8 chips. A pristine 4-in silicon wafer was spin-coated with SU-8 2000.5 to obtain a homogenous 500-nm-thick layer, which was subsequently baked and exposed to UV-light trough a photomask with a dose of 445 mJ cm-2. A final baking step was done before developing the uncrosslinked resin. The wafer was divided into 1 × 1 cm2 portions.

Reactive Surfaces With Selected Cross-Linkers

[0124] A flat PDMS stamp was incubated in either a 2% v/v epoxy-silane or a 2% v/v APTES ethanolic solution for 15 min, and subsequently dried with N.sub.2. The arrangement of SU-8 chips on the substrate were activated under oxygen plasma at 500 W during 30 s and were immediately contact-printed with the incubated stamp during 10 s. The arrangement of SU-8 chips with the reactive surface were subsequently cured at 100°C during 20 min in a nitrogen atmosphere and brought to room temperature rapidly to induce thermal shock at the SU-8-substrate boundary, to aid with the subsequent liberation of the chips. The same protocol was followed to functionalize the bottom surface of the chips, which is performed after completing the modification of the first (top) surface of the SU-8 chip and the peel-off of the solidified mounting medium.

.Math.Contact Printing and PPL of Fluorophores

[0125] The amine-reactive NHS ester fluorophores were initially diluted in DMSO and subsequently in a 4:3 v/v acetonitrile:30 mM Na.sub.2HPO.sub.4 solution to a final concentration of 100 .Math.g mL-1. The PDMS stamp was plasma-activated and subsequently incubated with the solution. After 2 min incubating, the stamp was blown dry with N.sub.2 and was brought into contact with the APTES-modified arrangement of SU-8 chips during 10 s. After lift-off, the ink was left to react during 1 h in a humid and dark chamber and rinsed thoroughly with Deionized (DI) water for 30 s.

.Math.Contact Printing of QDs

[0126] QDs with different emission were diluted in a 30 mM Na.sub.2HPO.sub.4 aqueous solution to a final 0.8 .Math.M concentration. The inked stamp contacted the epoxy-modified SU-8 arrangement of SU-8 chips during 10 s to transfer the QDs to their activated surface. The arrangement of SU-8 chips was left to react for 1 h. Afterwards, the unreacted epoxy moieties were blocked with a 2% v/v EDA solution in 30 mM Na.sub.2HPO.sub.4 buffer during 1 h and finally rinsed thoroughly with DI water for 30 s.

.Math.Contact Printing of DNA Strands

[0127] The following modified oligonucleotide strands were suspended in DDI water to an initial concentration of 100 .Math.M and subsequently in the Na.sub.2HPO.sub.4 solution to a final concentration of 10 .Math.M:

[0128] TS314: 5′-[Aminolink C6]-CTT GGA GCG AAC GAC CTA C-3′ (SEQ ID NO: 1) RP-TS314: 5′-[DY-485-XL]-GTA GGT CGT TCG CTC CAA G-3′ (SEQ ID NO: 2) TS315: 5′-[Aminolink C6]-CAA CAC TCA ACC CTA TCT CG-[TxRd] (SEQ ID NO: 3) RP-TS315: 5′-[DY-490]-CGA GAT AGG GTT GAG TGT TG-3′ (SEQ ID NO: 4)

[0129] Subsequently, a PDMS stamp was incubated with the oligo solution for 15 min, rinsed with Distilled De-lonized (DDI) water and printed onto the epoxy-modified arrangement of SU-8 chips for 10 s. The arrangement of SU-8 chips was left to react in dark and humid atmosphere for 1 h before blocking with a 2% v/v EDA solution in 30 mM Na.sub.2HPO.sub.4 buffer during 1 h. To hybridize, the complementary strand was suspended to a final concentration of 10 .Math.M in the hybridization buffer and left to react at 36 ºC during 2 h. Afterwards, the chips were rinsed in SSC 2x for 5 min, then rinsed in SSC 1x for 5 min, followed by rinsing during 5 min in SSC 0.1x and finally rinsed in DDI water. Between each rinsing step, the chips were concentrated by centrifugation and the supernatant was recollected and eliminated.

Liberation of Printed Chips

[0130] A drop of the aqueous mounting media was placed on top of the arrangement of SU-8 chips on the substrate and left to solidify at room temperature. A manual lateral force was later used to separate the solidified medium from the substrate. The solidified mounting media with the embedded chips was dissolved in DI water and the suspended chips were collected by centrifugation.

Example 1 Characterization of SU-8 Chips After Step (a) of Defining the Shape and the Size of the SU-8 Chips

[0131] We began by establishing the required physical properties to obtain the desired SU-8 chip. The physical definition dictates the size and shape of each SU-8 chip, together with morphological dimensions such as topography. Next, we defined the physical descriptor on a photomask. Standard photolithography was later used to transcribe the design onto SU-8 with a defined thickness (0.5-1.2 .Math.m). The arrangement of ordered SU-8 chips on the substrate was obtained after the development of the SU-8. In FIG. 1a, a single chip (2) from the arrangement of ordered SU-8 chips is represented over the substrate (1), with its exposed top flat surface (3).

[0132] FIG. 2 shows the shape and size of arrangements of SU-8 chips over the substrate using scanning electron microscopy. Each arrangement of SU-8 chips contains a specific physical trait: a) fiducial mark, b) aspect ratio, c) branching, and d) faceting.

[0133] This approach allows the fabrication of SU-8 chips with customizable shapes and sizes in a field dominated by spherical polymer microparticles, where the only parameter that can be customized is the radius of the spheres. The photolithographic step allows transferring designs with features as small as 1 .Math.m.

Example 2 Characterization of Double-Height SU-8 Chips: After Step (a) of Defining the Shape and the Size of the SU-8 Chips

[0134] Double-height SU-8 chips are fabricated following two consecutive photolithography steps, a first to define an initial SU-8 chip directly over the substrate and a second photolithography step to create the second chip over the initial one, as represented in FIG. 3. A resulting double height chip can be seen in FIG. 4.

[0135] Initially, an arrangement of ordered SU-8 chips is fabricated via SU-8 photolithography and left over the substrate. A second SU-8 photolithography process is performed over the initial arrangement of ordered SU-8 chips obtaining SU-8 chips with features at a secondary height (10). Molecules and nanoparticles are grafted onto the top flat surface (3) of the double height SU-8 chips as described in FIGS. 1a-b. The double height SU-8 chips are liberated with casting medium (6) as described in FIGS. 1c-d. Molecules and nanoparticles are grafted onto the bottom flat surface (7) of the double height SU-8 chips.

[0136] This fabrication method ensures the obtention of SU-8 chips with two opposing top and bottom flat surfaces for subsequent chemical functionalization. Also, the double-height chips can incorporate physical traits of two distinct chips in a single device.

Example 3 Characterization of Liberated SU-8 Chips

[0137] The liberation step is crucial to obtain the suspended grafted SU-8 chips yet it must provide protection to the surface functionalization. Some liberation methods required the elimination of a sacrificial layer between substrate and chips using harsh chemical methods, damaging the sensitive surface functionalization. Conversely, immersed ultrasound helped release the chips from the fabrication substrate, yet this method may shatter the chips and also may interfere with the stability and functionality of the surface modification. Alternatively, shear force has also been used to scrape the SU-8 chips from the substrate, yet, this may unevenly break the chips and generate debris.

[0138] Therefore, to liberate the grafted SU-8 chips obtained following the process of the present invention following the steps in Example 1, mounting medium cast on top of the grafted chips, (6) in FIG. 1c, and is then left to solidify at room temperature (t = 21 ºC, RH 50%), embedding the grafted SU-8 chips into the solidified matrix. The resulting solidified membrane is later peeled from the substrate hauling the grafted SU-8 chips along. This membrane with the SU-8 chips can be dissolved in an aqueous medium to free the arrangement of chips and obtain suspended chips, preventing the risk of chemical damage. A collection of the suspended SU-8 chips can be observed in the optical microscopy image in FIG. 5.

[0139] The chips can be recollected via centrifugation for further characterization or usage. This liberation method protects the physical integrity of the SU-8 chips and prevents the creation of debris.

Example 4 Characterization of Grafted SU-8 Chips With Fluorophores Creating Defined Patterns on the Top Flat Surfaces of the Chips

[0140] Heterobifunctional crosslinkers were then used to generate the reactive surface on the top surface of each SU-8 chip fixed on the substrate number (4) in FIG. 1a. We developed soft lithography and wet chemistry protocols to pattern the reactive surface of the SU-8 chips with selected inks. Microcontact printing (.Math.CP) was used to pattern the whole chip or to create line patterns on top of the fixed chips with the same molecule or nanoparticle, as represented in (5) in FIG. 1b. Polymer pen lithography (PPL) grafted micrometric resolvable features (spots) in selected positions, coupled with multiple molecules or nanoparticles with different light emission, obtaining the grafted features (5.1, 5.2, and 5.3) represented in FIG. 1b. Having multiple spots identifiable by their position over each SU-8 chip inks provides the base to create multiplexed chips having the spots emit at the same color, eliminating the restrictions of color-based multiplexed chips limited by the number of spectrally-resolved dyes.

[0141] An amine-bearing silane (APTES, see Materials and Methods) is fixed onto the top flat surface of an arrangement of SU-8 chips fabricated in Example 1 to create a reactive surface with the selected cross-linker. Two NHS-ester-derivatized fluorophores with red and green emissions were grafted onto the reactive surface via soft lithography or wet chemistry. In FIG. 6a, the red-emitting fluorophore was grafted using polymer pen lithography to create spots over the arrangement of immobilized chips. Alternatively, fluorophore lines can be grafted onto the top surfaces of the arrangement of chips with microcontact printing, as demonstrated in FIG. 6b. To better visualize with fluorescence microscopy, the arrangement of chips and the grafted spots and lines, a green-emitting fluorophore was backfilled to cover the rest of the top surfaces of the arrangement of chips. Microcontact printing is used to graft a fluorophore over the entire top flat surface of the arrangement of chips, which can be observed in FIG. 6c. Alternatively, an arrangement of chips can be submerged in a solution of the fluorophore to graft the fluorophores via wet chemistry to the lateral sides and top flat surface of the chips, as shown in FIG. 6d.

[0142] This grafting method creates customized patterns on the top surface of the arrangement of chips. Additionally, the arrangement of chips can be rinsed and washed after each patterning process to eliminate excess molecule or nanoparticle without losing SU-8 chips.

Example 5 Characterization of Grafted SU-8 Chips With Fluorophores and Their Subsequent Liberation

[0143] Fluorescent chips have been used to create tagging, identification and barcoding devices in applications at the microscale. The top flat surface of the present invention can be grafted with selected fluorophores to achieve similar purposes. To accomplish this, the top flat surface of an arrangement of branching SU-8 chips is first modified to create a reactive surface with a selected amine-bearing cross-linker. Secondly, the top flat surface is grafted with a red-emitting NHS-ester-derivatized fluorophore via microcontact printing. The resulting emission of the grafted fluorophores over the arrangement of branching SU-8 chips can be seen in FIG. 7a. The grafted SU-8 chips are liberated using the mounting medium presented in Example 3 and resuspended in water. The fluorescent emission of the red-emitting fluorophore grafted on the chips is seen in FIG. 7b.

[0144] The fluorescence emission is detected through the chips as the material’s optical transmittance is <95% on the selected wavelengths, observing the emission whether the grafted face is facing up or down, with negligible autofluorescence. This approach allows the customization of the top flat surface of the arrangement of SU-8 chips with selected cross-linkers with specific moieties such as amine, epoxy or thiol to create the reactive surface where the fluorophore or nanoparticle can covalently bind.

Example 6 Characterization of Grafted SU-8 Chips With Nucleic Acids and Proteins and the Subsequent Liberation of the Grafted SU-8 Chips

[0145] Alternatively, the covalent immobilization of nucleic acids and proteins onto the arrangement of SU-8 chips provide favourable stability and biomolecule accessibility for biosensing, biocatalysis, and point-of-care monitoring. Current functionalization methods employ wet chemistry to coat randomly the chips. To direct the functionalization towards the chosen position of surface of the chips, the top flat surface of the arrangement of SU-8 chips are initially functionalized with an epoxy-containing crosslinker creating a reactive surface, which reacts spontaneously with secondary amines present in modified oligos and in proteins.

[0146] To accomplish this, an arrangement of branching SU-8 chips with a reactive epoxy-silane (Materials and Methods) top flat surface was patterned via microcontact printing to graft a Texas-red-labelled, amine-derivatized oligo. Similarly, an arrangement of Aspect Ratio SU-8 chips with a reactive epoxy-silane (Materials and Methods) top flat surface was patterned via microcontact printing with green fluorescent protein (GFP). After the oligos and proteins were grafted, the chips were liberated and recollected for characterization following the process in Example 3. The resulting liberated grafted SU-8 chips can be characterized with fluorescent microscopy as seen in FIG. 8. The fluorescence signature in FIG. 8a confirms the presence of the Texas-red-labelled oligo present on the top surface of the chips. Similarly, the green fluorescence emission in FIG. 8b confirms the grafted GFP over the top surface of the liberated chips.

[0147] The liberation method protects the integrity of the grafted biomolecules so they remain functional for further utilization of the chips.

Example 7 Characterization of Grafted SU-8 Chips With Quantum Dots and the Subsequent Liberation of the Grafted SU-8 Chips

[0148] The present invention permits grafting Quantum Dots (QDs) onto the top flat surface of arrangements of SU-8 chips of all shapes and sizes and the subsequent liberation of the grafted chips. The arrangements of SU-8 chips were fabricated as stated in Example 1 and were initially functionalized with a reactive surface with selected epoxy-silane cross-linker. Subsequently amino-functionalized QDs with a fluorescence emission at 545 nm (QD545) were grafted onto an arrangement of Aspect Ratio SU-8 chips (FIG. 9a) and amino-functionalized QDs with a fluorescence emission at 525 nm (QD525) were grafted onto an arrangement of Fiducial SU-8 chips (FIG. 9c). Both grafting processes were accomplished via microcontact printing. Afterwards, the grafted arrangements of chips were liberated from the substrate with the mounting media following the process established in Example 3.

[0149] The normalized fluorescence emission of the liberated chips suspended in an aqueous medium demonstrate a uniform QD surface coverage, with small fluorescence emission dispersion and condensed emission intensities, as demonstrated in FIG. 9b and FIG. 9d. The fluorescence emission provides an individual signature that can be used to differentiate between subpopulations of liberated suspended SU-8 chips, each subpopulation grafted with a different QD. The efficiency of the signature is linked to the ability to discriminate one grafted SU-8 chip from the other. Collectively, the potential of the technology allows to obtain precise and reproducible QD patterns throughout the top surfaces of the SU-8 chips and the mild liberation process demonstrate the conservation of the customized physical and chemical traits on the top surface of the liberated SU-8 chips.

EXAMPLE 8 Characterization of SU-8 Chips Grafted on Their Top Surface With Molecules or Nanoparticles, the Subsequent Liberation of the Grafted SU-8 Chips, and the Second Fluorophore Grafting of the SU-8 Chips Bottom Surface

[0150] The present invention establishes a pathway to endow selected surface pattern properties on the top surfaces of the SU-8 chips. This can be further expanded with the inclusion the coverage and selective printing of the bottom surface of the chips to obtain Janus chips. To fabricate these chips, we take advantage of their flush and ordered embedding into the solidified mounting medium after release established in Example 3 and their subsequent bottom patterning.

[0151] Instead of dissolving the membrane, the flat underside of the grafted SU-8 chips (7 in FIG. 1d) permits derivatizing the exposed bottom flat surfaces to create a reactive surface with selected cross-linkers (8 in FIG. 1e) and their subsequent microcontact printing whilst embedded on the solidified mounting medium to graft selected molecules and nanoparticles (9 in FIG. 1f), obtaining suspended Janus chips after dissolving the membrane (FIG. 1g).

[0152] Accordingly, we initially fabricated Janus chips with two fluorophores on their opposing surfaces (FIGS. 10a-c). The exposed top surface of an arrangement of Fiducial chips was functionalized with APTES (Material and Methods) to create the reactive surface and successively printed with the NHS-ester-derivatized red fluorophore with microcontact printing. After liberating the chips following the process in Example 3, the bottom surface was also amino-derivatized to create a reactive surface on the bottom surface of the chips and subsequently printed with the NHS-ester-derivatized green fluorophore with microcontact printing. The red and green fluorescence channels (FIGS. 10a,b, respectively) show the resulting chips with the individual contribution of each fluorophore after dissolving the membrane and resuspended the chips in an aqueous medium. The composite image formed by the combination of the previous two images in FIG. 10c clearly describes the position of the red and green fluorescent emissions localized on the top and bottom surfaces of the suspended chips.

[0153] Similarly, the strategy allows the usage of different covalent bonding mechanisms to add specific traits on the top and bottom surfaces of the chips. In the present invention, an arrangement of Faceting SU-8 chips was modified with an epoxy-silane (Materials and Methods) to create a reactive surface on the top surface of the chips. Then, an amino-modified QD with fluorescence emission at 655 nm (QD655) was grafted with microcontact printing. After the arrangement of chips was liberated following the steps shown in Example 3, the now exposed bottom flat surface of the chips can be modified with an amine-bearing crosslinker to create a reactive surface for a subsequent patterning of green NHS-ester-derivatized and amine-reactive fluorophore. The red fluorescent image in FIG. 10d shows the emission of the QD655 and the green fluorescent emission in FIG. 10e shows the emission of the green-emitting fluorophore. The composite image (FIG. 10f) shows the combination of the two previous fluorescence emissions and demonstrates the localization of the QD655 and green-emitting fluorophore on each chip.

[0154] This multi-chemistry protocol allows to guide the bonding pathways to obtain Janus chips with chemically-interfering entities.

Example 9 Characterization of Double-Height SU-8 Chips Grafted on Their Top Surface With Nanoparticles, the Subsequent Liberation of the Grafted SU-8 Chips, and the Second Grafting of Nanoparticles on the SU-8 Chips Bottom Surface

[0155] The physical traits present in the double-height SU-8 chips can be exploited to form physical constrains on the top and bottom surface areas for further chemical patterns. As shown previously in Example 2, these chips have a top surface with features at two distinctive heights, thus the patterning occurs only over the raised features. Molecules (Example 5), biomolecules (Example 6), and nanoparticles (Example 7) can be patterned via soft lithography like microcontact printing or polymer pen lithography can be patterned over those areas. Moreover, the present invention establishes the means to liberate the patterned double-height chips as described in Example 3, and add functional groups to the now exposed bottom flat surface, to form a reactive surface with selected cross-linkers as demonstrated in Example 8. This bottom flat reactive surface can be patterned with molecules (Example 5), biomolecules (Example 6), and nanoparticles (Example 7) with microcontact printing.

[0156] An optical microscopy image of the features of the double-height chips is shown in FIG. 11a, fabricated with an initial layer consisting of an arrangement of Fiducial SU-8 chips and the second layer of Branching SU-8 chips, following the procedure detailed in Example 2. Then, the top flat surface of the arrangement of double-height chips was functionalized to endow a reactive surface with an epoxy-silane (Materials and Methods). Microcontact printing was later used to graft amino-functionalized QD655 onto the reactive top flat surface of the double-height chips, as detailed in Example 7. The double-height chips were liberated with the mounting medium following the steps detailed in Example 3. Then, the bottom flat surface of the chips embedded in the mounting media matrix was modified with an epoxy-silane to form the reactive surface where amino-functionalized-QD545 were subsequently patterned with microcontact printing.

[0157] The fluorescence microscopy image in FIG. 11b produces a clear assessment of the suspended chips with QD655 initially printed onto the branching side of the chip and a successive epoxy derivatization and QD545 printing on the fiducial part after liberation. The fluorescence emission indicates the correct shape and size of the selective patterning of QDs initially over the top surface and subsequently over the exposed bottom surface of the chips after liberation.

[0158] Altogether, a vast array of potential Janus chips can be obtained with the present invention. Simultaneously, the chips could be patterned using selected (bio)chemical or nanoparticle-based inks to obtain surface chemical anisotropies dictated by the initial physical properties without the need of a customized stamp. Furthermore, excluding the necessity of orthogonal chemistry to create multiplexed surfaces, paves the way for multi-chemistry functionalization in a single chip.

Example 10 Application of Suspended SU-8 Chips Grafted With a pH-Sensing Fluorophore for the Determination of pH

[0159] We designed a miniaturized sensing device with a customized shape and size and coupled it with sensing capabilities at the microscale. The devices consisted in an arrangement of branching chips derivatized with APTES (Materials and Methods) to form the reactive top surface. Subsequently, pHrodo® Red, succinimidyl was grafted with microcontact printing onto the reactive surface. Then, the chips were liberated as stated in Example 3 and were later exposed to environments at different pH (FIG. 12). The pH-sensing fluorophore pHrodo red increases its emission at low pH values; consequently, it was observed a 4-fold increase in fluorescence at a low pH (FIG. 12a) compared to the neutral environment (FIG. 12b). The opposite occurred at a high pH were the fluorescence was negligible (FIG. 12c), consequently, the fluorescence of the chips is not visible.

[0160] The detailed physical anisotropy for ease of identification could be extrapolated towards multiplexed studies using the same fluorescence emission wavelength in suspended chips with their customized physical attributes, and, due to their size in extraordinarily small volumes.

Example 11 Application of Suspended SU-8 Chips Grafted With a Sensing Biomolecule on the Top Surface and a Fluorescent Label on the Bottom Surface

[0161] The present invention demonstrates the detection capability by performing a single step bioassay that consists in a Janus chip with a sensing face on the top surface of the chip and a complementary labelled face on the bottom surface of the chip. The chip consists of a DNA-sensing face and a QD signature on the other face (FIG. 13).

[0162] An arrangement of Fiducial chips was first modified with the epoxy-silane (Materials and Methods) to obtain a reactive top surface. Subsequently, amine-modified oligos (‘probe 1’) were derivatized onto the top surface with microcontact printing, following the steps detailed in Example 6. The grafted chips were later liberated with the mounting media as detailed in Example 3 and a reactive surface was endowed on the bottom face of the chips while embedded in the mounting media with APTES (Materials and Methods). Then, amino-derivatized QD655 was printed onto the reactive bottom surface with microcontact printing following the steps in Example 9. The mounting media was later dissolved and the suspended chips were then incubated with a probe (‘probe 2’) modified with a green-emitting fluorescent marker complementary to ‘probe1’ with a perfect base-pair match to promote hybridization. The suspended chips with the hybridized ‘probe2’ were washed, and lastly recollected via centrifugation.

[0163] The chips are visible with the QD655 grafted onto the bottom surface and is used as a label to identify the chips (FIG. 13a).

[0164] The analysis of the bioassay with fluorescent microscopy, shows the targeting of ‘probe2’ towards the printed ‘probe1’ resulting in a green emission signature (FIG. 13b).

[0165] This could offer a great advantage in DNA coded recognition with suspended devices in a multiplexed subpopulation. This approach can use different QDs to create independent fluorescent signatures for a population of chips derivatized with unique DNA sequences and cDNA strands all labelled with the same fluorophore, thus, eliminating the drawbacks present with the limited available fluorophores for DNA labelling.

Example 12 Application Towards the Creation of Barcoding Libraries With Suspended SU-8 Chips

[0166] The present invention demonstrates Janus multiplexed chips combining multi-chemistry and surface pattern designs, coupled with a fiducial mark for correct code reading, for barcoding at extremely small volumes. An arrangement of Aspect ratio SU-8 chips was derivatized with APTES (Materials and Methods) to endow a reactive moiety onto the top surface of the chips. Then, NHS-ester-derivatized and amine-reactive fluorophores were grafted with polymer pen lithography creating discreet fluorescence-emitting spots on the top surface of the arrangement of SU-8 chips. The color emission and the position of the spots create the coding elements of the barcode. The arrangement of chips is later liberated with the mounting medium as explained in Example 3 and the exposed bottom surface of the embedded chips was functionalized with an epoxy-silane (Materials and Methods) to create a reactive surface. Then, microcontact printing is used to graft amino-modified QD655 onto the reactive bottom surfaces of the chips. QDs were printed in this case for easy identification of the chips, yet can be substituted by any sensing molecule or nanoparticle. The solidified mounting medium is later dissolved in an aqueous medium to obtain the suspended chips (FIG. 14).

[0167] A numerical value can be assigned to the coding area: a red fluorophore spot with the value 2, the green fluorophore spot with the value 1 and an empty space represented a 0 of a ternary coding system.

[0168] Color-barcoded chips have demonstrated 6 coding features (m) in a total volume of ~0.63×106 .Math.m3 with up to 9 different colors (n), with a theoretical encoding density calculated by nm/V of ~0.8 codes .Math.m-3. This density can be expanded by augmenting the chip size to increase the number of coding features. Such approach is used in other reported chips containing 10 coding features in a volume of ~4.8×106 .Math.m3 coupled with 8 different colors, thus a calculated 223 codes .Math.m-3. The great barcoding potential of these chips is limited in applications that require further miniaturization, where the present invention could present a valid alternative. Interestingly, the parallel patterning coupled with just two different fluorophores in 9 possible spots, the 18 .Math.m3 Aspect Ratio chips could be coded to obtain a calculated coding density of 1,093 codes .Math.m-3 in a small volume. Consequently, these coded Janus chips expand their outreach by adding a bottom layer which does not interfere with the multiplexed planar array and can be subsequently used to expand the functionality or be used for increased barcoding.