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48 protocols using sylgard 184

1

Organic-Soluble Salmon DNA Fibers

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Enzyme‐isolation processed water‐soluble salmon DNA fibers were procured from GEnome Medical (GEM) corporation, Shiga, Japan. These DNA fibers were further modified with CTMA surfactant to synthesize an organically soluble substance. The detailed synthesis of the CDNA molecules is described in Section S1.1 in the Supporting Information. The MoS2 NPs (size: 90 nm) and CQDs with a quantum efficiency > = 5% were purchased from Sigma‐Aldrich. The PDMS prepolymer (SYLGARD 184) was mixed with a curing agent (SYLGARD 184) purchased from Sigma‐Aldrich. Single‐wall CNTs with an average diameter of 0.84 nm were purchased from Sigma‐Aldrich. A 0.6 mm thick Cu sheet was procured from Nilaco Corporation, Japan.
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2

Droplet Microfluidics Device Fabrication

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Droplet microfluidics devices were produced using soft lithography. Photomasks were ordered from CAD/Art Services, Inc. (Bandon, OR, USA). PDMS molds were produced by spin-coating wafers with SU-8 3000 photoresist (Microresist Technology, Berlin, Germany) according to manufacturer’s protocol to obtain 30 µm of channel height. PDMS devices were fabricated by mixing SYLGARD® 184 PDMS with SYLGARD® 184 curing agent (both from Merck) at 10:1 w/w before pouring the mixture onto the PDMS molds and curing for 2 h at 65 °C. Using a 1 mm biopsy puncher, holes for the inlets and outlet were punched. The obtained PDMS devices were bonded to glass slides using a plasma asher (Emitech, K1050X, Montigny-le-Bretonneux, France). After bonding, the channels were treated with 5% perfluorooctyltriethoxysilane in HFE-7500 fluorinated oil (both from Fluorochem, Hadfield, United Kingdom) in order to make channel walls hydrofobic, incubated for 1 h at 65 °C, flushed again with HFE-7500, and incubated overnight at 65 °C for thermal bonding.
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3

Fabrication of Soft PDMS Gels

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For the fabrication of 4 kPa and 1 MPa gels, two commercially available polymer reagents were mixed as follows: SYLGARD184 (Sigma-Aldrich, St. Louis, MO) was mixed in a 1:10 ratio (i.e., curing agent/monomer ratio) to prepare 1 MPa gels. NuSil Gel 8100 (Polymer Systems Technology, High Wycombe, UK) was prepared following the manufacturer’s instructions (1:1 A and B components). The gel mix was then supplemented with 1% of the prepared SYLGARD184 mix. After gentle stirring, the gels were spread on glass slides using razor blades, with 0.0625 mm Tape (3M 810 TAPE Scotch Magic Tape) as spacer, and subsequently cured at 65°C for 13 h, after which they were ready for experiments. The Young’s modulus of the soft PDMS gels was found to be 4.59 ± 0.35 kPa (n = 16), and creep response experiments showed a low viscous contribution, indicating that the gels were mostly elastic in their response (see Fig. S1).
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4

Fabrication of Striated Substrate Using Soft Lithography

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The preparation of the striated substrate is based on the soft lithography and micromoulding techniques as generally described in [35 (link)], and specifically applied to electrospun nanofiber mechanical measurements in [31 (link),32 (link),33 (link),34 (link)]. First, a PDMS (polydimethylsiloxane) stamp (negative (inverted) relief structure of the striated substrate) was created by pouring dimethyl siloxane mixed with a catalyst (Sylgard® 184, Sigma-Aldrich, St. Louis, MO, USA) onto an SU-8-silicon master grid in a large plastic Petri dish. A 1 cm × 1 cm stamp can then be excised with a scalpel. Excised stamps were stored in a 2% sodium dodecyl sulfate (SDS) solution to keep them clean; the stamps can be stored for at least several months and used repeatedly. To create the striated substrate, a drop of Norland Optical Adhesive-81 (NOA-81, Norland Products, Cranbury, NJ, USA) was placed on a 60 mm × 24 mm, #1.5 microscope cover slide (Thermo Fisher Scientific, Waltham, MA, USA). The PDMS stamp was pressed into the NOA-81 drop on the slide and cured with 365 nm UV light (Benchtop 3UV transilluminator, UVP, Upland, CA, USA) for several minutes. The substrate had ridges of width 7.3 μm and height 6 μm. The gaps between the ridges were 6 μm across.
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5

PDMS-PSPI Composite Fabrication

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All prepolymers were prepared in liquid state for uniform dispersion. PSPI (PIP 100, PNS technology, Anyang, Korea) was added to PDMS base and its cross-linking agent (Sylgard 184, Sigma-Aldrich, St. Louis, MO, USA) and then magnetically stirred for about 5 min. The mixtures were prepared by adjusting the weight ratio (PDMS:PSPI = 20:1, 10:1, 5:1, and 5:2). As-prepared mixtures was transferred onto silicon wafer (4SWP06, Prime grade, Silicon Technology Corp, Tokyo, Japan) and then spin-coated at 500 rpm for 1 min. Subsequently, the sample was cured for 1 h at 200 °C on a hot plate and then cooled to room temperature.
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6

Fabrication of Microstructured Surfaces

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To prepare the substrate with ridges and grooves, a drop of optical adhesive ((Norland Optical Adhesive NOA 81, Norland Products, Cranbury, NJ, USA) was placed in a petri dish (5 cm diameter). A 1 cm × 1 cm rectangular PDMS (Polydimethylsiloxane, Sylgard® 184, Sigma-Aldrich, St. Louis, MO, USA) stamp with imprinted ridges and grooves was pressed into the optical adhesive and exposed to UV light ((UPV, Upland, CA) and cured for 2 minutes before being peeled off. The PDMS stamp was prepared by pouring the PDMS onto a silicon master to a height of about 5 mm in a petri dish (10 cm diameter), letting it cure, and excising a 1 cm × 1 cm stamp with a scalpel. The grooves (spacing between ridges) and the lateral dimension of the ridges were both 12 μm.
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7

Paracetamol/HCl Sensing and Cleaning on MLagg Films

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The paracetamol/HCl sensing
and cleaning experiments are carried out on a MLagg film deposited
on a coverslip (Menzel #1.5). The MLagg films are prepared according
to the standard protocol but re-scaffolded with CB[7] molecules instead
of CB[5]. The films on the coverslip are then plasma bonded to a PDMS
chip (AuNP films face inside the channels of the chip) by a short
exposure (a few seconds) to oxygen plasma. Briefly, the PDMS chip
is manufactured by standard soft lithography from a template master
mold. For the process, the SU-8 2100 negative photoresist is spin-coated
evenly onto a silicon wafer to yield a layer height of ∼150
μm. After additional baking and exposure to UV light (through
photomask), the photoresist is developed by immersing the wafer into
PGMEA (1-methoxy-2propanol acetate) and then hard baked. A PDMS kit
(SYLGARD 184, Sigma-Aldrich) with a mixing ratio of 1:10 (curing agent
to PDMS monomer base) is used to manufacture the chips (baking for
30 min at 120 °C after degassing). For flow experiments, two
inlets and one outlet are punched (1 mm diameter) into the PDMS chip.
The inlets are connected to custom-made syringe pumps containing HCl
(1 M) and paracetamol (1.5 mM) solutions. Kinetic SERS measurements
are taken through a 63× (NA = 1.2) water-immersion objective
with 0.5 s integration time. The liquid flow is cycled between paracetamol
and HCl for 20 s each.48 (link)
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8

Pancreas Fixation and Stretching

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After fine dissection, pancreases were fixed in 4% paraformaldehyde for 3 hours either directly (endocrine pancreas anatomy and semi‐quantitative pancreas neurofilament density) or after stretching (PINS ganglia phenotype). Stretching consisted in pinning the pancreas flat in a dish lined with silicone (Sylgard®184; Sigma‐Aldrich, St Quentin Fallavier, France).7
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9

PDMS Fabrication and Material Procurement

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To eliminate the experimental error of mixing the base and curing agent, PDMS (SYLGARD® 184) with a fixed base and curing agent ratio of 10:1 is purchased from Sigma-Aldrich. For experiments to investigate the ratio influence and the pattern copy, PDMS (SYLGARD® 184) is purchased from Dow Corning, where the weight ratio of the base to curing agent can be varied. NOA 63 resist is purchased from Norland Products Inc. Perfluorodecyltrichlorosilane (FDTS) is bought from Alfa Aesar. Materials for OLED devices are purchased from Luminescence Technology Corp. and used after sublimation.
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10

Photopolymer Nanofabrication via Microfluidics

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Titanium(iv) isopropoxide, tantalum(v) ethoxide, allyl acetoacetate (AAAc), pentaerythritol tetrakis(3-mercaptopropionate) (PETMP), 2-(methacryloyloxy)ethyl acetoacetate (MAEAA), 2-hydroxy-2-methylpropiophenone (HMP), 1H,1H,2H,2H-perfluorodecyltrichlorosilane, and toluene were purchased from Sigma Aldrich and used as-received. Polydimethylsiloxane (PDMS) stamps were fabricated from Sylgard 184 purchased from Sigma Aldrich.
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