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1 PDMS devices are produced with uniform thicknesses rangi
2 PDMS microchannel network is reversibly bonded to a glas
3 PDMS solubility for the test compounds (log KOW 7.2-8.3)
4 PDMS was spin coated on micropatterned Parylene C obtain
5 PDMS-supported ionogels exhibited favorable ionic conduc
6 PDMS/glass hybrid chips were then produced using simple
7 capable of real-time pulse monitoring and a PDMS glove with multiple embedded sensors to provide com
11 integrated chip is only 1cm(2) (including a PDMS flow cell with a 50microm height microfluidic chann
13 ased FET-like structure is incorporated on a PDMS substrate with the IFN-gamma aptamer attached to gr
14 target preconcentration are implemented on a PDMS-based microfluidic chip (automaton), followed by si
15 consists of a TiO2-coated glass substrate, a PDMS micro-sized reaction chamber and two flow cells.
16 solid phase microextraction (HS-SPME) with a PDMS/Carboxen/DVB fibre, coupled with gas chromatography
18 iation of the cross-section of laser-ablated PDMS channel; (2) the volume of PeT chamber; and (3) the
20 rectional diffusion of ambient oxygen across PDMS preserving the gradient resolution and stability.
21 rroborate the hypothesis that the additional PDMS layer does not impair the extraction phase capacity
22 ilane, PtBA = poly(tert-butyl acrylate), and PDMS = polydimethylsiloxane) were created by the living
23 treatment of the wafer prior to casting and PDMS casting of the epoxy are discussed to preserve the
32 triblock comicelles M(PFS-b-PtBA)-b-M(PFS-b-PDMS)-b-M(PFS-b-PtBA) (M = micelle segment, PFS = polyfe
33 )-block-poly(2-methyl-2-oxa zoline) (PMOXA-b-PDMS-b-PMOXA), alpha,omega-acrylate-end-capped PMOXA-b-P
34 XA), alpha,omega-acrylate-end-capped PMOXA-b-PDMS-b-PMOXA, and poly(ethylene oxide)-block-poly(butadi
35 directed self-assembly of a cylindrical PS-b-PDMS block copolymer under solvent annealing guided by a
36 mary antibodies and a strong bonding between PDMS substrates and PC supports without increasing backg
38 he need for chemical cleanup, spiked blubber-PDMS extracts were dosed into the CAFLUX bioassay, which
40 ith long-term growth and imaging provided by PDMS microfluidic chambers, we demonstrate the capabilit
41 esenchymal stem cells was also unaffected by PDMS stiffness but regulated by the elastic modulus of P
42 Young's modulus of the composite Parylene C/PDMS was evaluated and it was found to be almost half wh
43 extraction, such as fiber coating (85mum CAR/PDMS), extraction time (2min for white and 3min for red
45 der optimal experimental conditions (DVB/CAR/PDMS fibre coating, 40 degrees C, 30min extraction time
46 nzene/carboxen/polydimethylsiloxane (DVB/Car/PDMS) and octadecyl/benzenesulfonic acid/polyacrylonitri
52 atic improvement when compared to commercial PDMS/DVB fiber coating applied in food analysis facilita
53 tigated the performance of matrix compatible PDMS-overcoated fibers (PDMS-DVB/PDMS) as compared to un
55 ming PAGE protein separations in a composite PDMS-glass microdevice, that toggles from an "enclosed"
56 using a capillary suspension ink containing PDMS in the form of both precured microbeads and uncured
57 ptofluidic platform, integrating liquid-core PDMS waveguides, that allows the accurate measurement of
58 d ionic liquids (ILs) was overcome to create PDMS-supported IL gels (ionogels) with IL loadings of up
61 The immiscibility of poly(dimethylsiloxane) (PDMS) and ionic liquids (ILs) was overcome to create PDM
62 nto the surface of a poly(dimethylsiloxane) (PDMS) elastomer and filled with EGaIn using a micro-tran
65 system consists of a poly(dimethylsiloxane) (PDMS) microchip sample injector featuring a pneumatic mi
66 ere synthesized in a poly(dimethylsiloxane) (PDMS) microfluidic chip by using an in-situ method, on t
68 and easily scalable poly(dimethylsiloxane) (PDMS) microfluidic device was fabricated using soft lith
69 per presents a novel poly(dimethylsiloxane) (PDMS) microfluidic immunosensor that integrates a comple
70 were patterned with poly(dimethylsiloxane) (PDMS) oligomers by thermally-assisted contact printing,
71 fluidic device where poly(dimethylsiloxane) (PDMS) or polystyrene (PS) were used to coat the sides of
77 , polyacrylamide and poly(dimethylsiloxane) (PDMS), is adapted for extrusion printing for integrated
82 OFS (using SU-8 and poly(dimethylsiloxane), PDMS) against the 36 most commonly used organic solvents
83 cing a 620 mum thick poly(dimethylsiloxane), PDMS, gasket with an opening of 3.2 cm x 1.5 cm on the c
84 separations, cyclic poly(dimethylsiloxanes) (PDMS) derived from the column's stationary phase have be
85 drawing micropillars from pipette-dispensed PDMS microdroplets using vacuum-chucked microspheres.
86 loxane (PDMS, 100 mum), PDMS/divinylbenzene (PDMS/DVB), Polyacrylate (PA) and PDMS 7 mum were evaluat
87 ed with polydimethylsiloxane-divinylbenzene (PDMS-DVB) and polyacrylate (PA) coated SPME fibers for t
88 MS) and polydimethylsiloxane/divinylbenzene (PDMS/DVB) TFME samplers were prepared using spin coating
90 comparison with a pure PDMS membrane and DVB/PDMS fiber for outdoor air sampling showed that the extr
93 compatible PDMS-overcoated fibers (PDMS-DVB/PDMS) as compared to unmodified PDMS/DVB coatings using
96 ed that the extraction efficiency of the DVB/PDMS membrane was significantly enhanced, especially for
98 polarity when compared to an unsupported DVB/PDMS membrane of similar shape and size which was prepar
99 Developmental Motor Scales (second edition; PDMS-2) score of greater than 10 points and an increase
100 ive sampling approach was tested by exposing PDMS to lipid-rich tissue (dugong blubber; 85% lipid) sp
101 es related to the capability of the external PDMS layer to protect the commercial coating, and showed
102 of matrix compatible PDMS-overcoated fibers (PDMS-DVB/PDMS) as compared to unmodified PDMS/DVB coatin
105 ure and detection chambers are produced from PDMS on machined molds and do not require lithography.
106 By stirring a mixture of a functionalized PDMS oligomer, formic acid, and an IL (or lithium-in-IL
109 e method has been used to create hydrophilic PDMS surfaces that allow for digital LAMP to be performe
110 00-300 nm, whereas BTZ and CFZ absorption in PDMS was approximately 5.0 and approximately 3.5 mum, re
114 e results highlight the biases that exist in PDMS devices and the importance of material selection in
116 ed the bias observed in IC50 values found in PDMS devices was directly related to the absorption of d
118 absorption of small hydrophobic molecules in PDMS specifically used to treat cancer and its subsequen
119 n IC50 of approximately 4.3x was observed in PDMS devices compared to both thermoplastic devices.
124 dified electrode arrays were integrated into PDMS microfluidic devices and incubated with U-937 cells
125 Lipid-PDMS partition coefficients (Klip-PDMS) ranged from 20 to 38, were independent of hydropho
126 efficients of determination (r(2)) for LDPE, PDMS, and POM were 0.68, 0.76, and 0.58, respectively.
127 es the focusing power of a weak sorbent like PDMS and allows narrow chromatographic peaks to be gener
128 oratory with synthesized highly cross-linked PDMS as a frit to immobilize carboxen (Car) particles fo
132 s properties of these two polymer materials: PDMS is permeable to O2 and the presence of O2 inhibits
133 d a simple, rapid method to directly measure PDMS solubilities of solid contaminants, SPDMS(S), which
134 enzymes to alumina (Al2O3) xerogel modified PDMS surface was demonstrated to be the best for prepari
136 The analytes were extracted with 100 mum PDMS fibres according to the factorial design matrix and
139 luding polydimethylsiloxane (PDMS, 100 mum), PDMS/divinylbenzene (PDMS/DVB), Polyacrylate (PA) and PD
143 abricated using a lead-free KNbO(3) nanowire-PDMS polymer composite are reported for the first time.
144 d, which has the structure of PVDF nanowires-PDMS composite film/indium tin oxide (ITO) electrode/pol
146 ctivated influenza viruses, replacing native PDMS microchips with hybrid microchips allowed the achie
150 this method, 96-well inserts constructed of PDMS act as an H(2)S-permeable membrane, eliminating non
151 on of a solid-phase microextraction fiber of PDMS/DVB into the oil matrix, followed by Gas Chromatogr
154 article, we utilized the wavy structures of PDMS microchannel sidewalls to initiate and cavitate bub
155 s of volatile extraction included the use of PDMS/DVB fibre, 2mL of wine, 30% of NaCl, 40 degrees C f
157 face coatings of collagen and fibronectin on PDMS maintained breast cancer cell phenotypes to be near
159 nm-scale roughness, the silver substrates on PDMS templates show larger roughness, on the order of 10
160 terminated polydimethylsiloxane (PDMS-DE or PDMS-DC) were encapsulated into the nanocapsules during
161 es similar to that exhibited by the original PDMS/DVB fiber toward triazole pesticides from water sam
162 on through the coating; therefore, the outer PDMS layer influences the uptake rate into the matrix co
163 onal boundary layer; as such, the overcoated PDMS does not affect uptake rate into the matrix-compati
165 muL chamber cast in polydimethoxylsiloxane (PDMS) atop a microfluidic chip consisting of a single cr
167 ive film composed of a polydimethylsiloxane (PDMS) layer incorporating molecules of cryptophane-A.
170 be transferred onto a polydimethylsiloxane (PDMS) microchannel through the soft lithography techniqu
172 In contrast, using a polydimethylsiloxane (PDMS) microfluidic deoxygenation device and ROXS, not on
173 ential applications, a polydimethylsiloxane (PDMS) wristband with an embedded microfluidic diaphragm
174 lture platform using a polydimethylsiloxane (PDMS)-based hanging drop array (PDMS-HDA) methodology.
175 abricated on glass and polydimethylsiloxane (PDMS) templates, on surface-enhanced Raman Spectroscopy
176 xymethylene (POM), and polydimethylsiloxane (PDMS), and organisms ranged from polychaetes and oligoch
179 ated by a carbon black/polydimethylsiloxane (PDMS)-photoacoustic lens, were introduced to trigger the
180 by fabricating bundled polydimethylsiloxane (PDMS) micro-pillars with graded heights and electrospinn
181 solid- and liquid-core polydimethylsiloxane (PDMS) waveguides that also provides fully functioning mi
182 nded in a high-density polydimethylsiloxane (PDMS) glue, which is spread onto a carbon fiber mesh.
183 ile and cost-effective polydimethylsiloxane (PDMS)/paper hybrid microfluidic device integrated with l
184 thography to fabricate polydimethylsiloxane (PDMS) devices consisting of linear channel segments with
185 coupled-optical-fiber-polydimethylsiloxane (PDMS) microdevice was developed, to quantify polyphenols
186 anotubes (CNTs) filled polydimethylsiloxane (PDMS) hybrid membrane was fabricated to evaluate its pot
189 those fabricated from polydimethylsiloxane (PDMS), collective understanding of the differences in ce
190 ass surface of a glass-polydimethylsiloxane (PDMS) microfluidic channel was modified to develop a sol
191 into a flexible hybrid polydimethylsiloxane (PDMS)-polycarbonate (PC) microfluidic chip with integrat
192 phenol using a hybrid polydimethylsiloxane (PDMS)/glass chronoimpedimetric microchip and its removal
193 annels were created in polydimethylsiloxane (PDMS) from a surface pattern of electrodeposited gold na
195 3 silicones, including polydimethylsiloxane (PDMS) and low-density polyethylene (LDPE) in methanol-wa
196 bre coatings including polydimethylsiloxane (PDMS, 100 mum), PDMS/divinylbenzene (PDMS/DVB), Polyacry
197 ched and embedded into polydimethylsiloxane (PDMS), thereby realizing a device with eight filter func
200 packed in a two-layer polydimethylsiloxane (PDMS) platform and were flowed through a narrow straight
202 n the wide adoption of polydimethylsiloxane (PDMS) for the rapid fabrication of microfluidic networks
203 icrowells comprised of polydimethylsiloxane (PDMS) surfaces coated with a hydrophilic film; no extern
204 d of a single piece of polydimethylsiloxane (PDMS) with three parallel channels interconnected to one
205 n, is made entirely of polydimethylsiloxane (PDMS), and does not require any additional coupling agen
206 The device is made of polydimethylsiloxane (PDMS), and ionic liquid is used to form the liquid elect
209 specific locations on polydimethylsiloxane (PDMS) posts printed in a square array (1 mm tall posts o
210 cer cell phenotypes on polydimethylsiloxane (PDMS) substrates and indicated that the cell phenotypic
212 polylactide (PLA), or polydimethylsiloxane (PDMS) macromonomer mediated by the third-generation meta
213 ess to surface pattern polydimethylsiloxane (PDMS) with ferromagnetic structures of varying sizes (mi
214 d a polycarbonate (PC)-polydimethylsiloxane (PDMS) hybrid microchip using a simple epoxy silica sol-g
216 tor comprises a single polydimethylsiloxane (PDMS) microchannel onto which an ion-selective layer of
217 oxylic acid terminated polydimethylsiloxane (PDMS-DE or PDMS-DC) were encapsulated into the nanocapsu
218 In this process, the polydimethylsiloxane (PDMS) membrane was prepared by employing water as solven
221 ted by partitioning to polydimethylsiloxane (PDMS) coated stir bars and analysis by ultrahigh resolut
223 minum tube template to polydimethylsiloxane (PDMS) via atomic layer deposition (ALD) assisted sacrifi
225 ilibrium sampling with polydimethylsiloxane (PDMS) has the potential for unbiased sampling of mixture
226 spectral encoding with polydimethylsiloxane (PDMS) microchambers for codetection of 42 immune effecto
227 living samples within polydimethylsiloxane (PDMS) microfluidic devices has facilitated the study of
229 ks to their chemical and physical properties PDMS and PAm hydrogel mimic the extracellular matrix (EC
231 hnique's utility and versatility, we realize PDMS micropillars on various unconventional substrate ar
235 d identical absorption capacities of several PDMS materials, whereas larger deviations from unity wer
236 photo-lithographically fabricated, silicone(PDMS)-based side-view flow chamber to dynamically visual
237 ), in comparison with polydimethyl siloxane (PDMS) coating, to assess volatiles in model wine solutio
238 ds the combination of polydimethyl-siloxane (PDMS) microfluidic technology with vibrational spectrosc
241 n external layer of poly(dimethyl siloxane) (PDMS) over the commercial PDMS/divinyl benzene (DVB) ext
243 e, multi-trap device, consisting of a single PDMS (polydimethylsiloxane) layer, which can immobilize
255 l for unbiased sampling of mixtures, and the PDMS extracts can be directly dosed into cell-based bioa
258 mall quantities of lipids coextracted by the PDMS were found to affect the kinetics in the regularly
259 me the inhibitory effects of O2, we coat the PDMS channel with a 10% benzophenone solution, which que
261 particles were uniformly distributed in the PDMS base, ensuring the repeatability of the membranes.
262 eous PDMS membrane, the CNTs filled into the PDMS membrane were beneficial for the improvement of but
263 ation, interfacing between both modules, the PDMS chip for electrokinetic concentration and the subst
264 the chips and the elastomeric nature of the PDMS allowed us to pull the microwires without the occur
267 h was taken to investigate the effect of the PDMS outer layer on the uptake rate of analytes during t
268 h or without oxygen-plasma treatments of the PDMS surfaces dramatically impacted the phenotypic equil
269 ancements in the matrix compatibility of the PDMS-modified fiber, and open new prospects for the deve
271 ids was allowed between the monolayer on the PDMS surface and the upper leaflet of the bilayer on the
275 .3 g/m(2).h and 32.9, respectively, when the PDMS membrane filled with 10 wt% CNTs was used to separa
277 cacy endpoint: 12 months after gene therapy, PDMS-2 scores were increased by a median of 62 points (I
279 nables the realization of microsphere-tipped PDMS micropillars on non-flat, highly space-constrained
281 in vitro culture from macroscopic culture to PDMS based devices can come with unforeseen challenges.
284 es in OSPW showed negligible partitioning to PDMS (i.e., DOW <1), however estimated DOW's for some sp
285 mina sol-gel encapsulation, physisorption to PDMS channels with, and without alumina xerogel modifica
286 PA coatings can be submitted to, respect to PDMS (220 degrees C the former two, 295 degrees C the la
290 ng ink is developed and printed onto treated PDMS with no visible signs of delamination and geometric
292 rs (PDMS-DVB/PDMS) as compared to unmodified PDMS/DVB coatings using aqueous samples and employing a
295 lls, separated by hydrophobic material (wax, PDMS) impermeable to aqueous solutions, and hydrophilic
296 l and optical stability of the SU-8, whereas PDMS suffered from unsealing or tearing in most cases.
298 new efficient technique for 3D printing with PDMS by using a capillary suspension ink containing PDMS
299 thermore, using a half-coated substrate with PDMS, nanoelectrodes could be retracted and positioned v
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