ライフサイエンスコーパス: PMMA

1 PMMA exists in three different isomeric forms, namely, i

2 PMMA fill patterns of clefted and unclefted VCFs were di

3 PMMA microcapillary electrophoresis (muCE) devices made

4 Nearly 100 PMMA chips were replicated using a single silicon master

5 hen coated with fibronectin: silicone (n=6), PMMA (n=6), and acrylic (n=6).

6 as been used to successfully pattern over 65 PMMA pieces using a single Si template.

7 A PMMA chip was employed as the microarray device, where z

8 A PMMA sheet with an imprinted microchannel was clamped to

9 A PMMA substrate is first imprinted with a Si template usi

10 epared for optical measurements by bonding a PMMA ring to the sclera in the region of the ciliary bod

11 dance one-bond (1)H-(13)C RDCs measured in a PMMA gel and a (3)J coupling constant analysis.

12 ge mapping of polyamine charge carriers in a PMMA matrix is reported.

13 electrophoretic separations of proteins in a PMMA-based microchip.

14 Additionally, the presence of a PMMA or PHEMA overlayer significantly decreased the sput

15 .5, 0.4, 0.6, and 0.1 ppm were obtained on a PMMA film containing 25% w/w di(2-ethylhexyl) phthalate

16 2+), and Pd(2+) were reduced and plated on a PMMA surface and Fe(CN)(6)(3-) was reduced to Fe(CN)(6)(

17 sed hairpin configuration when strapped to a PMMA surface as opposed to glass.

18 guiding layer and a sensing layer or with a PMMA waveguide and a chemically sensitive polymer.

19 s covalently attached onto this UV-activated PMMA surface were evaluated and compared with the same M

20 reaches Ca's bulk heat of sublimation on all PMMA surfaces, where pure, bulk-like Ca thin films form.

21 was determined that both silanized glass and PMMA gave working optodes, but the ones on PMMA did not

22 and 688 +/- 54 microm on silanized glass and PMMA, respectively, and the 0.50-mm tips produced diamet

23 microm were obtained on silanized glass and PMMA, respectively, using the polypropylene tips for spo

24 s, ceramics, and polymers, Ni, Si, HfO2, and PMMA, respectively.

25 rradiation, the junction between d(8)-PS and PMMA blocks is photocoupled through the anthracene photo

26 iency in the mixed 10/15 mum diameter PS and PMMA particle solutions tested.

27 Even when PS and PMMA particles have the same diameters, they exhibit str

28 rate these predictions by translating PS and PMMA particles simultaneously in a stationary flow.

29 Well defined PS and PMMA supramolecular polymers with molecular weights up t

30 homogeneity for the sputter yields of PS and PMMA.

31 S ((13)C-PS) and unlabeled PS ((12)C-PS) and PMMA were synthesized using atom-transfer radical polyme

32 ectra are presented for both bare silver and PMMA-coated silver gratings at a range of angles and pol

33 the PMMA resin at 0.1, 0.2, and 0.3 wt%, and PMMA resin without AgBr/NPVP served as the control.

34 Slow kinetics at PMMA-transferred graphene is attributed to the presence

35 2-3 orders of magnitude higher than those at PMMA-transferred graphene, which demonstrates an anomalo

36 bution of the isomeric content in an atactic PMMA sample is determined quantitatively by fractionatin

37 rrently, anthracene-functionalized d(8)-PS-b-PMMA BCP is one of the most promising candidates for the

38 -type phase behavior of its parent d(8)-PS-b-PMMA di-BCPs.

39 ual detection in SEC are evaluated with PS-b-PMMA diblock copolymers to determine the comonomer compo

40 The cation exchange capacity of bare PMMA capillaries was on the order of 1 pequiv/mm(2) with

41 Bonding of the embossed layer and a blank PMMA layer to generate the microchip was achieved by sol

42 mprinted microchannel was clamped to a blank PMMA sheet, and then 80 +/- 5 muL of acetone (bonding so

43 Surface binding by PMMA overlayers results in stable surface binding even a

44 e lower autofluorescence levels exhibited by PMMA at the detection wavelengths used and the improved

45 e, with PS chains forming a core shielded by PMMA chains.

46 ies confirmed a higher hydrocarbon uptake by PMMA in the presence of plasticizer.

47 5-keV Cs(+) bombardment, the characteristic PMMA secondary ion intensities decreased rapidly for pri

48 ed quasi-stabilization of the characteristic PMMA secondary ion intensities, and the decay of these i

49 Cylinders of coated PMMA were implanted in porcine corneas ex vivo for 2 wee

50 prepared on gold substrates by spin coating PMMA dissolved in toluene.

51 The sensor was fabricated by spin coating PMMA onto a quartz crystal, and the influence of plastic

52 nally, we examine the fabrication compatible PMMA coating as a viable passivation layer.

53 ponents of molecules dissolved in compressed PMMA gels, allowing a rapid and direct one-shot determin

54 In conclusion, PMMA-modified AFM probes have shown to be a reliable tec

55 We also show that contacting PMMA with Teflon depletes this electronic surface charge

56 e graphene films obtained using conventional PMMA-assisted transfer technique exhibits PMMA residues,

57 Fluorescent and positively charged core PMMA-NPs of nearly 60nm, obtained through an emulsion co

58 computations performed on analogue coronene/PMMA oligomers and a reasonable agreement was obtained.

59 th a deuterated poly(methyl methacrylate) (d-PMMA) film, and the interfacial silane structure has bee

60 ules traverse through the thickness of the d-PMMA film.

61 o 48.2 cP and suspensions of 10-mum-diameter PMMA particles with particle volume fractions phi = 0.16

62 ermore, it is found that blends of different PMMA isomers with similar molecular weights can be fract

63 ThFFF analysis of the different PMMA isomers in tetrahydrofuran, acetonitrile (ACN), and

64 the CRP assay, neutravidin-coated PQQ-doped PMMA nanospheres are used to bind with a biotinylated re

65 ole, and efficiencies comparable to embossed PMMA and laser ablated glass chips were obtained.

66 then used as a secondary mold for embossing PMMA, a polymeric substrate with a lower Tg ( approximat

67 al PMMA-assisted transfer technique exhibits PMMA residues, which degrade the sensing performance of

68 simplification of the process of fabricating PMMA devices and should lead to a widespread low-cost pr

69 For a series of mixed brushes with a fixed PMMA M(n) and systematically changed PS M(n), a transiti

70 ta(a)) from 74 degrees, the value for a flat PMMA surface, to 91 degrees, the value for a flat PS fil

71 Anti-TNF-alpha/FNAB/PMMA matrix was then integrated over comb structured gol

72 in undiluted serum using Anti-TNF-alpha/FNAB/PMMA/Au reveal that system can detect TNF-alpha in 100pg

73 For PMMA microchannels, the mobility was found to increase f

74 sion) and highly isospecific ([mm] > 95% for PMMA; [mm] > 99% for PBMA) via enantiomorphic-site contr

75 a from the same buffer are also obtained for PMMA (M = 49 kDa).

76 se, while measurable change was not seen for PMMA.

77 nt with acetic acid, a selective solvent for PMMA.

78 Four PMMA lenses received an excimer laser ablation of -6 D w

79 hydrocarbon sensitivity of plasticizer-free PMMA is negligible, while the sensitivity of plasticized

80 e polymers in the negative ion mode and from PMMA and PLA in the positive ion mode.

81 ) coupling to carboxylic acid functionalized PMMA micropillars.

82 th methyl methacrylate (MMA) yields PE-graft-PMMA with narrow polydispersities and increasing PMMA co

83 ides were demonstrated using the PEG-grafted PMMA muCE chips.

84 the general applicability of surface-grafted PMMA microdevices for a broad range of protein analyses.

85 ively a physical mixture of homo-PE and homo-PMMA is obtained.

86 Porphyrin-doped hybrid PMMA [poly(methyl methacrylate)] polymer films demonstra

87 ations in the K-ras gene was accomplished in PMMA microfluidic devices using sheath flows.

88 ip capillary electrophoresis (CE) devices in PMMA were created and tested.

89 strate that there are available electrons in PMMA that can participate in redox reactions at a rather

90 Laser engraving and holes in PMMA along with spacing from surface provide fluidic cha

91 The MSF architecture is manufactured in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)]

92 lated magnetic gamma-FeO(x) nanoparticles in PMMA matrix upon applying a magnetic field from 0 to 300

93 on and emission spectroscopy in solution, in PMMA and neat thin films.

94 for decreased IT band energies and widths in PMMA and provides important insight into electron transf

95 y to postprocedural pain response, including PMMA leakage.

96 with narrow polydispersities and increasing PMMA content at longer reaction times.

97 omparison study suggests that an inexpensive PMMA IOL design modification-a squared optic edge-could

98 n, along with the low cost of the integrated PMMA chip/detection system, should enhance the power and

99 microchip was prepared by hot embossing into PMMA from a brass mold master fabricated via high-precis

100 reduced beta (beta)-relaxation of isotactic PMMA most efficiently suppresses vibrational triplet dec

101 sion electron microscopy (TEM) measurements, PMMA oligomers conformally coat the metal-oxide nanopart

102 oven cytotoxicity, poly-methyl methacrylate (PMMA) resin is one of the most frequently and extensivel

103 Poly-methyl methacrylate (PMMA)-based dental resins with strong and long-lasting a

104 ulfate (CaSO4) and poly methyl methacrylate (PMMA).

105 wth substrate using polymethyl methacrylate (PMMA) and a wet etch to allow the user to transfer the f

106 (polystyrene (PS)-b-polymethyl methacrylate (PMMA) block copolymers (BCP)) using either ultralow ener

107 ridge integrating a polymethyl methacrylate (PMMA) micro-reactor with a polycarbonate (PC)-based pris

108 raphy at 100 kV and polymethyl methacrylate (PMMA) resist at different thicknesses.

109 laser engraving of polymethyl methacrylate (PMMA) sheet as off surface matrix was integrated in very

110 ointegration, using polymethyl methacrylate (PMMA)--the principal component of the Boston KPro--as a

111 Ultrathin poly(methyl methacrylate) PMMA films were prepared on gold substrates by spin coat

112 line coated with poly (methyl methacrylate) (PMMA) and a sensing line coated with a chemically sensit

113 lysorbate 80, and poly(methyl methacrylate) (PMMA) as analytes.

114 sensitivity of a poly(methyl methacrylate) (PMMA) based QCM sensor can be significantly enhanced for

115 and a hydrophobic poly(methyl methacrylate) (PMMA) block was developed to similarly reduce the minera

116 ene (d(8)-PS) and poly(methyl methacrylate) (PMMA) blocks, as well as a short middle block of poly(2-

117 n (LDR) and (2) a poly(methyl methacrylate) (PMMA) chip for the detection of the LDR products using a

118 ly used spherical poly(methyl methacrylate) (PMMA) colloids, suspended in an apolar organic medium.

119 c" hydroxyapatite/poly(methyl methacrylate) (PMMA) composites are developed by processing large-scale

120 We describe a poly(methyl methacrylate) (PMMA) dip-coating procedure, which results in surface st

121 iated with a thin poly(methyl methacrylate) (PMMA) film that is coupled to a silver-coated diffractio

122 mage of spin-cast poly(methyl methacrylate) (PMMA) films under 5-keV Cs(+) and 2.5-8.75-keV SF(5)(+)

123 the conventional poly(methyl methacrylate) (PMMA) for graphene transfer from a growth substrate.

124 Poly(methyl methacrylate) (PMMA) gels prepared by copolymerizing methyl methacrylat

125 micromachining on poly(methyl methacrylate) (PMMA) has the potential for flexible, low cost, rapid pr

126 470 nm) both in a poly(methyl methacrylate) (PMMA) matrix and in solution at 77 K.

127 The poly(methyl methacrylate) (PMMA) microchips feature integral in-plane contactless c

128 sis separation in poly(methyl methacrylate) (PMMA) microchips.

129 hemistries within poly(methyl methacrylate) (PMMA) microfluidic channels that enabled specific and se

130 respectively, on poly(methyl methacrylate) (PMMA) micropillar surfaces, as well as assessing ligand-

131 ive silver-coated Poly(methyl methacrylate) (PMMA) microspheres (50 mum diameter) into tailored patte

132 ystyrene (PS) and poly(methyl methacrylate) (PMMA) microspheres based entirely on their difference in

133 ), is loaded into poly(methyl methacrylate) (PMMA) nanospheres in the presence of methanol.

134 Poly(methyl methacrylate) (PMMA) optical fibers in a series of different diameters

135 system utilizes a poly(methyl methacrylate) (PMMA) or glass substrates sputtered by 40-nm-thick gold

136 ls in an embossed poly(methyl methacrylate) (PMMA) piece are filled with a heated liquid (paraffin wa

137 As poly (methyl methacrylate) (PMMA) remains the main material employed in the fabricat

138 by using a porous poly(methyl methacrylate) (PMMA) sacrificial layer, which creates a space between t

139 d for fabricating poly(methyl methacrylate) (PMMA) separation microchips is introduced.

140 netically coupled poly(methyl methacrylate) (PMMA) spheres with wavelength-scale diameters were recor

141 proximately 3 mm) poly(methyl methacrylate) (PMMA) spherical beads, threaded on a flexible string.

142 nnel assembled in poly(methyl methacrylate) (PMMA) substrate connected to an amperometric detector.

143 as immobilized on poly(methyl methacrylate) (PMMA) substrates activated using an oxygen plasma.

144 ss-transferred on poly(methyl methacrylate) (PMMA) substrates and are easily coupled to microfluidic

145 system exploited poly(methyl methacrylate) (PMMA) substrates of high optical quality to fabricate a

146 thermally bonding poly(methyl methacrylate) (PMMA) substrates to form microfluidic systems has been d

147 ite directly on a poly(methyl methacrylate) (PMMA) surface (also known as plexiglass or acrylic).

148 ectron-irradiated poly(methyl methacrylate) (PMMA) surfaces at 300 K has been studied by adsorption m

149 rts consisting of poly(methyl methacrylate) (PMMA) that provide enhanced performance levels for molec

150 s hot-embossed in poly(methyl methacrylate) (PMMA) to allow the detection of low-abundant mutations i

151 the separation of poly(methyl methacrylate) (PMMA) with regard to molecular microstructure.

152 st multilayers of poly(methyl methacrylate) (PMMA), poly(2-hydroxyethyl methacrylate) (PHEMA), and tr

153 fferent polymers, poly(methyl methacrylate) (PMMA), poly(ethylene terephthalate) (PET), poly(lactic a

154 Silanized glass, poly(methyl methacrylate) (PMMA), polycarbonate, and poly(dimethylsiloxane) were te

155 he thermoplastics poly(methyl methacrylate) (PMMA), polystyrene (PS), polycarbonate (PC), and cyclic

156 erimide (PEI) and poly(methyl methacrylate) (PMMA), were used to make the reusable secondary master a

157 es of interest on poly(methyl methacrylate) (PMMA)-covered monolayer MoS2 triangles.

158 al ligand loss in poly(methyl methacrylate) (PMMA).

159 styrene (PSR) and poly(methyl methacrylate) (PMMA).

160 lates composed of poly(methyl methacrylate) (PMMA).

161 ystyrene (PS) and poly(methyl methacrylate) (PMMA).

162 assembly of mixed poly(methyl methacrylate) (PMMA)/polystyrene (PS) brushes on silicon wafers was stu

163 yrene (PS) and poly(methylene methacrylate) (PMMA).

164 nnels poised on a poly(methyl methacrylate), PMMA, chip.

165 ere replicated in poly(methyl methacrylate), PMMA, from a metal mold master.

166 was fabricated in poly(methyl methacrylate), PMMA, using a single-step, double-sided hot-embossing ap

167 e, stereoregular poly(methyl methacrylates) (PMMAs) were separated according to tacticity on a carbon

168 a-exonuclease onto poly(methylmethacrylate) (PMMA) micropillars populated within a microfluidic devic

169 The poly(methylmethacrylate), PMMA, chip contained 8 devices, each equipped with 16 cu

170 polymer nano-composite (AgBr/NPVP)-modified PMMA-based dental resin.

171 owth was inhibited on the AgBr/NPVP-modified PMMA resin compared to the control (P < 0.05), and the a

172 ber of fungal cells attached to the modified PMMA resin was considerably lower than in the control.

173 -bound nanospheres (ca. 20,000 PQQ molecules/PMMA particle).

174 ity of polymethylmethacrylate nanoparticles (PMMA-NPs) to promote survivin MB uptake in human A549 ce

175 The carrier ability of PMMA-NPs in A549 was examined by confocal microscopy.

176 3)(2+) and S(2)O(8)(2-) with the addition of PMMA powder.

177 Small to moderate amounts of PMMA may escape from the vertebral body with no signific

178 ith two esters to form the Ca carboxylate of PMMA, because this reaction's heat would be close to tha

179 r dose for the breast simulated by 4.5 cm of PMMA was calculated with methods described in the "Europ

180 evaluated the use of a layered composite of PMMA (poly-methyl-methacrylate), PHEMA (poly-hydroxyl-et

181 By varying the concentration of PMMA, spin coating speed and curing condition, we obtain

182 nal to the PTFE surface area; the effects of PMMA and glass balls were negligible by comparison.

183 the vertebral body, followed by injection of PMMA cement.

184 o the proposal of an adsorption mechanism of PMMA on aluminum oxide, which shows the formation of met

185 25 to 0.94, and the molecular weight (Mn) of PMMA-b-PAA was controlled from 10 kDa to 90 kDa.

186 The damage profiles of PMMA under SF(5)(+) bombardment contained three distinct

187 This unprecedentedly high reactivity of PMMA-free CVD-grown graphene electrodes is fundamentally

188 This series of PMMA-b-PAA block copolymers was synthesized by reversibl

189 kyl catalysts: a constant syndiotacticity of PMMA produced over a wide polymerization temperature ran

190 slightly smaller than or similar to that of PMMA after treatment with acetic acid, a selective solve

191 with a PS M(n) slightly smaller than that of PMMA underwent self-reorganization, exhibiting a differe

192 faces, is believed to be superior to that of PMMA-mediated samples.

193 Four types of PMMA leakage and other potential predictors (patient age

194 I) can be controlled by changing the wt % of PMMA in the dipcoating solution.

195 HAp coatings were induced on PMMA discs after treatment with concentrated NaOH and co

196 on silanized glass and 839 +/- 28 microm on PMMA.

197 d PMMA gave working optodes, but the ones on PMMA did not fit the theoretical model.

198 h B) and fluorescein (FL), were performed on PMMA microchips to demonstrate the feasibility of the fa

199 the adhesion of Candida albicans cells onto PMMA surfaces by employing an atomic force microscopy (A

200 complement to the MBs when immobilized onto PMMA, and this was attributed to both the lower autofluo

201 ached to the acrylic than to the silicone or PMMA lenses (P<0.001).

202 individual sample targets within the overall PMMA-based MALDI sample plate.

203 rtebral levels injected, preprocedural pain, PMMA volume per vertebra) were related to postprocedural

204 n, we developed a simple, miniaturized paper/PMMA (poly(methyl methacrylate)) hybrid microfluidic mic

205 an age, 76 years) who underwent percutaneous PMMA vertebroplasty between 1996 and 1999, 245 were succ

206 ent of vertebral fractures with percutaneous PMMA vertebroplasty appears to be safe and results in su

207 riven by a microbial fuel cell (see picture; PMMA = poly(methyl methacrylate), E = electrode).

208 igible, while the sensitivity of plasticized PMMA was similar to or in some cases greater relative to

209 served trend in sensitivity for the polymers PMMA, poly(isobutylene), poly(epichlorohydrin), and poly

210 It was applied to a blend of two polymers, PMMA and PS.

211 to silicone (n=18), polymethylmethacrylate (PMMA; n=18), and acrylic (n=18) intraocular lenses in vi

212 to a 16-20 mum bore polymethylmethacrylate (PMMA) capillary.

213 used to apply dense polymethylmethacrylate (PMMA) microneedles to the skin models in a controlled an

214 luent reservoirs for polymethylmethacrylate (PMMA).

215 of a suspended Au NP/polymethylmethacrylate (PMMA) polymer close packed monolayer results in one-dime

216 uoroethylene (PTFE), polymethylmethacrylate (PMMA), and borosilicate glass with no headspace.

217 f a square-edge (SE) polymethylmethacrylate (PMMA) intraocular lens (IOL) modification in comparison

218 Suspended polymethylmethacrylate (PMMA) membranes were used as shadow masks for defining o

219 e different particle materials (polystyrene, PMMA, and silica) of the same size (2 mum) led to each b

220 Different combinations of polystyrene, PMMA, and silica particles with a commercially available

221 Cyphochilus, we fabricate ultra-thin, porous PMMA films by foaming with CO2 saturation.

222 On pristine PMMA, the initial sticking probability of Ca is 0.5, inc

223 We show that pristine PMMA can spontaneously transfer electrons to species in

224 n yield, the observed effects through the PS/PMMA interface can be greatly minimized, thereby signifi

225 nd (13)C secondary ion yields through the PS/PMMA interface; however, it is shown that this behavior

226 ncreased the force and work required to pull PMMA cylinders out of porcine corneas ex vivo.

227 ication in comparison with a round-edge (RE) PMMA IOL or an SE hydrophobic acrylic IOL (SE-Acrylic).

228 An RE-PMMA IOL was implanted in the fellow eye in 46 patients

229 IOL eyes compared with the contralateral RE-PMMA eyes at all follow-up visits (P < 0.05).

230 s were 2% for SE-PMMA IOLs versus 37% for RE-PMMA IOLs in group A (P < 0.001), and 4% for SE-PMMA IOL

231 The RE-PMMA PCO rate did not plateau and continued to increase

232 ne is attributed to the presence of residual PMMA.

233 The resulting PMMA substrate possessed the same features as those of t

234 diotactic, >70 000 g/mol molecular weight; s-PMMA) by a group transfer protocol-like (GTP-like) pathw

235 for bilateral phacoemulsification had an SE-PMMA IOL implanted in 1 eye.

236 A IOLs in group A (P < 0.001), and 4% for SE-PMMA IOLs versus 10% for SE-Acrylic IOLs in group B (P =

237 year Nd:YAG capsulotomy rates were 2% for SE-PMMA IOLs versus 37% for RE-PMMA IOLs in group A (P < 0.

238 PCO score was significantly lower in the SE-PMMA IOL eyes compared with the contralateral RE-PMMA ey

239 PCO score was statistically lower in the SE-PMMA IOL eyes compared with the contralateral SE-Acrylic

240 lon and Teflon beads, but leaves the smaller PMMA beads essentially uncharged; the resulting electros

241 bonding solvent (acetonitrile) and softened PMMA from filling the channels.

242 mined in toluene and acetonitrile solutions, PMMA layers, solid films, and crystal phase.

243 y indistinguishable densities-Nylon spheres, PMMA spheres, and drug spheres-demonstrate the applicabi

244 The aligning properties of the stretched PMMA gels were evaluated by monitoring the quadrupolar s

245 te complex 4, however, produces syndiotactic PMMA predominantly via chain-end control.

246 aration of highly isotactic and syndiotactic PMMAs of different molar masses.

247 to ester groups below the CH3/CH2-terminated PMMA surface.

248 We found that PMMA substrates welded together using this method could

249 Our measurements indicate that PMMA passivated black phosphorus thin film flakes can st

250 microscope (SEM) observations indicated that PMMA-b-PAA polymer treatment protected enamel from acid

251 The PMMA film sputtered in a controlled manner for SF(5)(+)

252 The PMMA films were transformed into highly reactive film co

253 The PMMA micro-chip was tested under an electric field stren

254 The PMMA microdevices were fabricated reproducibly and with

255 The PMMA sample plates were fabricated by a CNC milling tech

256 e waveguide surface by plasma activating the PMMA and the use of carbodiimide coupling chemistry.

257 surface was carried out by UV activating the PMMA to produce surface-confined carboxylate groups, whi

258 In solution and the PMMA matrix the S1 of BET-B relaxes to a correlated trip

259 reduced the inflammatory response around the PMMA implants in vivo.

260 Exposing the PMMA surface to electrons increases Ca's initial stickin

261 However, the PMMA used for a redox reaction or contacted with Teflon

262 asured by PALS was significantly less in the PMMA films compared to the PIB, and this result correlat

263 nted into fluidic channels embossed into the PMMA substrate.

264 mum ion dose limited by the thickness of the PMMA film.

265 The thickness of the PMMA overlayer on TiO2-Ru(II) can be controlled by chang

266 The erosion-preventing efficacy of the PMMA-b-PAA block copolymer in inhibiting HAP mineral los

267 As an example of the utility of the PMMA-based immobilization strategies developed for MBs,

268 These results demonstrate the ability of the PMMA-NPs to promote the survivin-MB internalization, sug

269 pulp cells were viable when cultured on the PMMA resin for 24 hours, while over 70% of the cells wer

270 (7 mm x 1 mm) positioned and centered on the PMMA substrate (33 mm x 9 mm).

271 nd where the SW bundles were embedded on the PMMA substrate, giving the electrode a high stability.

272 to graft poly(ethylene glycol) (PEG) on the PMMA surface.

273 lity were verified after adsorption onto the PMMA-NPs.

274 were evident by using the MB loaded onto the PMMA-NPs.

275 les of SWs that were highly ordered over the PMMA at the background where the SW bundles were embedde

276 y more negative reduction potential than the PMMA bonding electrons.

277 FTIR spectra confirmed that the PMMA-b-PAA block copolymer could bind to HAP via bridgin

278 (5)(+) impact energy while the damage to the PMMA film varied minimally with the SF(5)(+) impact ener

279 AgBr/NPVP was added to the PMMA resin at 0.1, 0.2, and 0.3 wt%, and PMMA resin with

280 ngal effects against Candida albicans to the PMMA resin, and it has low toxicity toward HDPCs, and it

281 ature transfer from the aluminum mold to the PMMA substrate was verified by profilometry.

282 hment of primary amine-containing MBs to the PMMA surface was carried out by UV activating the PMMA t

283 sticizer levels ( approximately 10% w/w) the PMMA film was more sensitive toward ethylbenzene and p-x

284 s showed that the adhesion of C. albicans to PMMA is morphology dependent, as hyphal tubes had increa

285 Compared to PMMA, CaSO4 had a more rapid short term rate of elution

286 The addition of NAC to PMMA resin significantly ameliorated its cytotoxicity to

287 amine-containing oligonucleotide tethered to PMMA surface) was optimized to maximize the loading leve

288 rated the application of the UV/O(3) treated PMMA films for the detection of microRNAs using a label-

289 ition, we obtained very smooth and ultrathin PMMA films.

290 Therefore, the interface of ultrathin PMMA films on native aluminum oxide, deposited by reacti

291 ocyte proliferation compared with unmodified PMMA surfaces.

292 etter with derivatized compared to untreated PMMA muCE chips.

293 F architecture is manufactured in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)], utilizes

294 Of note, when PMMA spheres occupy a volume greater than 18% of the foc

295 Moreover, protons were reduced when PMMA powder was dropped into a slightly acidic solution,

296 re is manufactured in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)], utilizes on-chip valv

297 approach is demonstrated in connection with PMMA microchips, it could be applied to other materials

298 ess AFM cantilevers were functionalized with PMMA microspheres and probed against C. albicans cells i

299 ich involved ball-milling of Cu powders with PMMA as solid carbon source, in-situ growth of graphene

300 AFM tips terminated with PMMA colloids are used to pattern molecules in both seri