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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
8 ep casting with small applied pressure and a PDMS mould.
9 rane for free-flow zone electrophoresis in a PDMS microfluidic chip.
10 lyacrylamide gel electrophoresis (PAGE) in a PDMS/glass microfluidic chip.
11  integrated chip is only 1cm(2) (including a PDMS flow cell with a 50microm height microfluidic chann
12 mpletely sealed through the deformation of a PDMS membrane.
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
17                              In this work, a PDMS microchannel-based, colorimetric, autonomous capill
18 iation of the cross-section of laser-ablated PDMS channel; (2) the volume of PeT chamber; and (3) the
19 o wells in HF-etched glass and laser-ablated PDMS.
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
24 tyrene (PS), cyclo-olefin polymer (COP), and PDMS).
25 d fabricated structures made from copper and PDMS.
26 chip is made of two bare gold electrodes and PDMS microchamber of 36 nL volume.
27 nylbenzene (PDMS/DVB), Polyacrylate (PA) and PDMS 7 mum were evaluated.
28 bonding among starch granules, RB powder and PDMS polymer within the bio-elastomers.
29            For this purpose, EG-Silicone and PDMS polymeric phases were compared and, afterwards, the
30 hylsiloxane (PDMS)-based hanging drop array (PDMS-HDA) methodology.
31  particles either at the PDMS end-tips or at PDMS post bases.
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
37 nes with differently sized nanopores between PDMS slabs containing embedded microchannels.
38 he need for chemical cleanup, spiked blubber-PDMS extracts were dosed into the CAFLUX bioassay, which
39 al based on clay nanocomposites 3D molded by PDMS templates and capped with another LBL film.
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
44 ites, were obtained with a 50/30 mum DVB/CAR/PDMS coating fiber at 40 degrees C for 30 min.
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
47           Carboxen/polydimethylsiloxane (CAR/PDMS) and polydimethylsiloxane/divinylbenzene (PDMS/DVB)
48  solid-phase microextraction (SPME) Carboxen/PDMS SPME fiber.
49                            Overall, the CNTs/PDMS hybrid membrane with higher butanol flux and select
50 contact angle of the hydrophilic film-coated PDMS surface was only 14.3 degrees .
51 imethyl siloxane) (PDMS) over the commercial PDMS/divinyl benzene (DVB) extraction phase.
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
54               In addition, matrix-compatible PDMS-modified solid coatings, characterized by a new mor
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
59  dynamic-covalent boroxine bond to crosslink PDMS chain into 3D networks.
60 ll line patterns of poly (dimethylsiloxane) (PDMS).
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
63 m a commercial 7 mum poly(dimethylsiloxane) (PDMS) fiber.
64                      Poly(dimethylsiloxane) (PDMS) is a commonly used elastomer for fabricating micro
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
67 egrated emitter in a poly(dimethylsiloxane) (PDMS) microfluidic chip.
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
72 matching monomers in poly(dimethylsiloxane) (PDMS) porous membrane.
73 , wall-coated with a poly(dimethylsiloxane) (PDMS) stationary phase.
74 lected on a numbered poly(dimethylsiloxane) (PDMS) substrate with high viability.
75                      Poly(dimethylsiloxane) (PDMS) was determined to be an excellent material for mit
76  formed by bonding a poly(dimethylsiloxane) (PDMS) well to the glass substrate.
77 , polyacrylamide and poly(dimethylsiloxane) (PDMS), is adapted for extrusion printing for integrated
78 urtain" imaging with poly(dimethylsiloxane) (PDMS)-based microfluidics.
79 idic devices made of poly(dimethylsiloxane) (PDMS).
80 uidic system made of poly(dimethylsiloxane) (PDMS).
81 nked wall coating of poly(dimethylsiloxane) (PDMS).
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
89                             Avobenzone-doped PDMS (0.6% w/w) patterning confines UV exposure to the d
90 comparison with a pure PDMS membrane and DVB/PDMS fiber for outdoor air sampling showed that the extr
91 tional central composite design with CAR/DVB/PDMS fibre.
92 aqueous solution as compared to a 65 mum DVB/PDMS solid phase microextraction (SPME) fiber.
93  compatible PDMS-overcoated fibers (PDMS-DVB/PDMS) as compared to unmodified PDMS/DVB coatings using
94                                 The PDMS/DVB/PDMS coating exhibited superior features related to the
95        This work proposes the novel PDMS/DVB/PDMS fiber as a greener strategy for analysis by direct
96 ed that the extraction efficiency of the DVB/PDMS membrane was significantly enhanced, especially for
97 atrix-compatible coatings as compared to DVB/PDMS fibers.
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
103 erns was reduced by 14-fold compared to flat PDMS.
104 c olefin copolymer (COC) as alternatives for PDMS devices.
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
107 ss or plastic substrate to form hybrid glass-PDMS and plastic-PDMS microchannel structures.
108                Compared with the homogeneous PDMS membrane, the CNTs filled into the PDMS membrane we
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
111                Using nanofluidic channels in PDMS of cross section 500 nm x 2 mum, we demonstrate the
112 estimate KPDMSw and activity coefficients in PDMS.
113 s were packed with Car particles embedded in PDMS to simplify calculations in passive mode.
114 e results highlight the biases that exist in PDMS devices and the importance of material selection in
115 boosted by incorporating collagen fibrils in PDMS-HDA.
116 ed the bias observed in IC50 values found in PDMS devices was directly related to the absorption of d
117 abrication of PAGE molecular sieving gels in PDMS microchannel networks.
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.
120 ricated using replica moulding technology in PDMS patterned by high-aspect-ratio SU-8 moulds.
121 2 when exposed to UV, resulting in a PAGE-in-PDMS device.
122                          We see this PAGE-in-PDMS fabrication technique as expanding the application
123 s overcome through techniques to incorporate PDMS and PS.
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
129               New polymer-based (LDPE-lipid, PDMS-air) and multimedia partition coefficients (lipid-w
130                                        Lipid-PDMS partition coefficients (Klip-PDMS) ranged from 20 t
131                In contrast, subcooled liquid PDMS solubilities, SPDMS(L), were approximately constant
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
135 ext few years, 3D printing will replace most PDMS and plastic molding techniques in academia.
136     The analytes were extracted with 100 mum PDMS fibres according to the factorial design matrix and
137  The SPME fiber coating selected was 100 mum PDMS.
138 ur sputtered fibers and the commercial 7 mum PDMS fiber are essentially the same.
139 luding polydimethylsiloxane (PDMS, 100 mum), PDMS/divinylbenzene (PDMS/DVB), Polyacrylate (PA) and PD
140               Delamination from FN-muprinted PDMS precluded robust detection of myotubes.
141                           The nanostructured PDMS/titania tubes are superhydrophobic with water conta
142  cancer cells through plain and nanotextured PDMS microchannels showed clear differences.
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
145 ced when hybrid microchips instead of native PDMS microchips were used in the microENIA tests.
146 ctivated influenza viruses, replacing native PDMS microchips with hybrid microchips allowed the achie
147                 This work proposes the novel PDMS/DVB/PDMS fiber as a greener strategy for analysis b
148 ive properties of the cross-linking agent of PDMS.
149                Compared to a softer blend of PDMS muprinted with FN, myogenic index, myotube width, a
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
152                However, the vast majority of PDMS microfluidic devices are still made with extensive
153                 Experimental measurements of PDMS swelling were in accordance with previously reporte
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
156                  The combined utilization of PDMS microdroplets and microspheres not only enables the
157 face coatings of collagen and fibronectin on PDMS maintained breast cancer cell phenotypes to be near
158                    Assays are carried out on PDMS disposable microfluidic cartridges which require no
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
164 strate to form hybrid glass-PDMS and plastic-PDMS microchannel structures.
165  muL chamber cast in polydimethoxylsiloxane (PDMS) atop a microfluidic chip consisting of a single cr
166                        Polydimethylsiloxane (PDMS) and Polyacrylamide (PAm) hydrogel have been chosen
167 ive film composed of a polydimethylsiloxane (PDMS) layer incorporating molecules of cryptophane-A.
168 lls, encapsulated by a polydimethylsiloxane (PDMS) membrane.
169  in combination with a polydimethylsiloxane (PDMS) membrane.
170  be transferred onto a polydimethylsiloxane (PDMS) microchannel through the soft lithography techniqu
171                      A polydimethylsiloxane (PDMS) microfluidic channel is used to efficiently and re
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
177 2 nanotube arrays, and polydimethylsiloxane (PDMS).
178 rptive polymer such as polydimethylsiloxane (PDMS).
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
187              Thin-film polydimethylsiloxane (PDMS) passive samplers were exposed statically to intact
188  master structures for polydimethylsiloxane (PDMS)-based microfluidics.
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
194  to map liquid flow in polydimethylsiloxane (PDMS) microchannels.
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
198 oparticles (soot) into Polydimethylsiloxane (PDMS).
199 f specific interest is polydimethylsiloxane (PDMS).
200  packed in a two-layer polydimethylsiloxane (PDMS) platform and were flowed through a narrow straight
201       A replica molded polydimethylsiloxane (PDMS) microfluidic device with nanoliter sensing volumes
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
207  a 7 mum thick film of polydimethylsiloxane (PDMS).
208 le supporting layer of polydimethylsiloxane (PDMS).
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
211 ckled NRs supported on polydimethylsiloxane (PDMS).
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
215 ly(d,l-lactide) (PLA), polydimethylsiloxane (PDMS), or polystyrene (PS) macromonomer.
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
219 argon bubble or a thin polydimethylsiloxane (PDMS) layer.
220 cellular matrix, three polydimethylsiloxane (PDMS) layers were built into this array.
221 ted by partitioning to polydimethylsiloxane (PDMS) coated stir bars and analysis by ultrahigh resolut
222            Compared to polydimethylsiloxane (PDMS) microcontact printed (muprinted) with fibronectin
223 minum tube template to polydimethylsiloxane (PDMS) via atomic layer deposition (ALD) assisted sacrifi
224 atterns transferred to polydimethylsiloxane (PDMS).
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
228                     A polydimethyslsiloxane (PDMS) microchannel positioned over both the embedded tub
229 ks to their chemical and physical properties PDMS and PAm hydrogel mimic the extracellular matrix (EC
230                     A comparison with a pure PDMS membrane and DVB/PDMS fiber for outdoor air samplin
231 hnique's utility and versatility, we realize PDMS micropillars on various unconventional substrate ar
232 ma cells were integrated into reconfigurable PDMS microfluidic devices.
233                                The resulting PDMS structures are remarkably elastic, flexible, and ex
234 bly of the same polyelectrolytes on the same PDMS moulds.
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
239  than 2% due to the poly(dimethyl siloxane) (PDMS) body.
240 ated a microchip in poly(dimethyl siloxane) (PDMS) by soft lithography process.
241 n external layer of poly(dimethyl siloxane) (PDMS) over the commercial PDMS/divinyl benzene (DVB) ext
242                                     Silvered PDMS-supported pSi membranes, the most promising substra
243 e, multi-trap device, consisting of a single PDMS (polydimethylsiloxane) layer, which can immobilize
244                     The presence of a single PDMS-CaO(2) disk eliminated hypoxia-induced cell dysfunc
245 ets unlike planar control titania and smooth PDMS surfaces.
246 atin hydrogels compared to FN-muprinted soft PDMS constructs.
247           The obtained results indicate that PDMS-modified coatings reduce artifacts associated with
248                                          The PDMS CH3 groups are of "infinite" radiocarbon age due to
249                                          The PDMS chamber was bound to a polycarbonate membrane, whic
250                                          The PDMS coating showed higher relative areas for terpenes (
251                                          The PDMS fibre was chosen.
252                                          The PDMS microbeads are held together in thixotropic granula
253                                          The PDMS shell provides long-lasting mechanical support, ena
254                                          The PDMS/DVB/PDMS coating exhibited superior features relate
255 l for unbiased sampling of mixtures, and the PDMS extracts can be directly dosed into cell-based bioa
256 ces enriched with Pc particles either at the PDMS end-tips or at PDMS post bases.
257                                  Because the PDMS chambers are bonded to a coverslip, it is possible
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
260 sed here to detect H(2)S once it crossed the PDMS membrane.
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
265 ncer stem cells, while the variations of the PDMS elastic stiffness had much less such effects.
266                           Deflections of the PDMS membrane above the main microfluidic flow channels
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
270          Lipid monolayers were formed on the PDMS patterned surface while lipid bilayers were on the
271 ids was allowed between the monolayer on the PDMS surface and the upper leaflet of the bilayer on the
272                     This method requires the PDMS-water partition constants, KPDMSw, or activity coef
273                This study confirmed that the PDMS/DVB coating performs best for the quantification of
274  plug volumes could be achieved by using the PDMS microchip injector.
275 .3 g/m(2).h and 32.9, respectively, when the PDMS membrane filled with 10 wt% CNTs was used to separa
276 tu polymer inclusion membrane (PIM) with the PDMS.
277 cacy endpoint: 12 months after gene therapy, PDMS-2 scores were increased by a median of 62 points (I
278  contact printing, leaving behind 3 nm-thick PDMS patterns.
279 nables the realization of microsphere-tipped PDMS micropillars on non-flat, highly space-constrained
280 was found to be almost half when compared to PDMS.
281 in vitro culture from macroscopic culture to PDMS based devices can come with unforeseen challenges.
282              In contrast, approach curves to PDMS films allowed the rapid positioning of nanoelectrod
283 ds detected in ESI+ generally partitioned to PDMS to a greater extent than organic acids.
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
287 oplastics and ease of fabrication similar to PDMS.
288        The hydrophobicity of the transferred PDMS patterns was precisely tuned by the stamping temper
289  (Ab), a polyclonal anti-IgG, onto a treated PDMS surface.
290 ng ink is developed and printed onto treated PDMS with no visible signs of delamination and geometric
291  in the headspace and by immersion using two PDMS twisters.
292 rs (PDMS-DVB/PDMS) as compared to unmodified PDMS/DVB coatings using aqueous samples and employing a
293                                        Using PDMS chambers, we report that wild-type protonemal tissu
294                               This versatile PDMS/paper microfluidic platform has great potential for
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.
297  x 140 mum in cross section wall-coated with PDMS.
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
300  patens, can be continuously cultured within PDMS microfluidic chambers.

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