ライフサイエンスコーパス: polycarbonate

1 branes constructed from nuclear track-etched polycarbonate.

2 excellent thermomechanical properties of the polycarbonate.

3 used in synthesis of an aromatic bisphenol A polycarbonate.

4 iently recover obliterated serial numbers in polycarbonate.

5 oss in the thermal stability compared to the polycarbonate.

6 ation of spiropyran in high T(g) bisphenol A polycarbonate.

7 he MPs were mainly composed of polyamide and polycarbonate.

8 through ortho ester linkages on an aliphatic polycarbonate.

9 oss in the thermal stability compared to the polycarbonate.

10 need for a readily degradable biocompatible polycarbonate.

11 ighboring dielectric material, either air or polycarbonate.

12 c series of leading aliphatic polyesters and polycarbonates.

13 t for 642 chemically distinct polyesters and polycarbonates.

14 egradable polymers, including polyesters and polycarbonates.

15 s on the thermal properties of the resulting polycarbonates.

16 , polyurethanes, polyureas, polyacetals, and polycarbonates.

17 and molecular weight distribution as virgin polycarbonates.

18 cracks propagating in opposite directions in polycarbonate, a material with high ductility and a larg

19 mpered glass, chemically tempered glass, and polycarbonate, all with 3.0-mm center thickness) were te

20 resistant to chemical degradation than their polycarbonate analogues and exhibit excellent mechanical

21 bilities compared to their oxygen-containing polycarbonate analogues and revealed variations in the e

22 ommon greenhouse materials such as glass and polycarbonate and are therefore depleted in many commerc

23 ) and storage container materials (including polycarbonate and polypropylene) for thiamine handling.

24 opolymer networks composed of lithium borate polycarbonates and poly(ethylene oxide) that improved th

25 gradable materials are aliphatic polyesters, polycarbonates and polyamides, which are often prepared

26 It is better known in the production of polycarbonates and polyesters, but is also a powerful ro

27 ries (polyvinyl chloride, polyurethanes, and polycarbonates) and in the activation of light hydrocarb

28 zed glass, poly(methyl methacrylate) (PMMA), polycarbonate, and poly(dimethylsiloxane) were tested as

29 polystyrene, acetonitrile-butadiene-styrene, polycarbonate, and poly(dimethylsiloxane), were used as

30 ined clusters of polyethylene terephthalate, polycarbonate, and polystyrene (max 50 ng MP m(-3)).

31 esters of cellulose, regenerated cellulose, polycarbonate, and polyvinylidene fluoride, were assayed

32 to convert these monomers to polyesters and polycarbonate, and the different end-of-use options for

33 mpered glass, chemically tempered glass, and polycarbonate, and with center thickness ranging from 1

34 polyacrylates, (bio)polyesters, polyamides, polycarbonates, and polyacrylonitriles.

35 educe emission by 1-6 tons of CO2 per ton of polycarbonates, and reduce polymer accumulation in landf

36 Aliphatic polycarbonates (aPCs) have become increasingly popular a

37 yl chloride), poly(methyl methacrylate), and polycarbonate are proposed for Py-GC/MS MPs mass determi

38 Aliphatic polyesters and polycarbonates are a class of biorenewable, biocompatibl

39 These polycarbonates are of interest as engineering materials

40 tential candidates, aliphatic polyesters and polycarbonates are promising materials due to their rene

41 ast, efficient catalysts for high molar mass polycarbonates are underinvestigated, and the resulting

42 cal polymerization of aniline on gold-coated polycarbonate asymmetric nanochannels.

43 A hydrolytically active polycarbonate backbone is used to construct the polymer

44 Herein, soft, elastomeric aliphatic polycarbonate-based materials were designed to undergo p

45 ps), polyurethanes (aliphatic, aromatic, and polycarbonate-based), and selected Fluka plasticizers (2

46 of selected dental ceramics bonded to clear polycarbonate bases (simulating crown/dentin structures)

47 CD polycarbonate bases were coated with these reflecting ma

48 e addition of carboxylic acid-functionalized polycarbonate block copolymers to commercially available

49 tral poly(ethylene oxide) block and terminal polycarbonate blocks with pendant 1,2-dithiolane functio

50 ufactured chemical, is found in canned food, polycarbonate-bottled liquids, and other consumer produc

51 uccessfully used to assess BPA leaching from polycarbonate bottles at 45 degrees C and 80 degrees C,

52 effectively depolymerized, while bisphenol A polycarbonate (BPA-PC) remained largely unaffected.

53 X = OAc, N(SiMe3)2, OMe, O(i)Pr all produced polycarbonate by the alternated insertion of CHO and CO2

54 ncing the optical properties of CO(2) -based polycarbonates by modifying the polymer's topological st

55 The resulting ABA triblock polycarbonate can be further functionalized with various

56 North Pacific and amended duplicate 20 liter polycarbonate carboys with nitrate or ammonium, tracking

57 single-molecule fluorescence measurements in polycarbonate chips using visible wavelengths for excita

58 carbon dioxide and epoxides into degradable polycarbonates (CO(2)-based copolymer) has been regarded

59 folding method to generate aligned graphene/polycarbonate composites with as many as 320 parallel la

60 The thus produced polycarbonate contained >99% carbonate linkages and had

61 Mn and Sr; BPA was detected in samples from polycarbonate containers.

62 ction of detailed solvent-resistance maps of polycarbonate copolymers and in determination of quantit

63 ion of the solvent resistance of a family of polycarbonate copolymers prepared from the reaction of b

64 This class of amphiphilic polycarbonates could embody a powerful platform for biom

65 ed 1L-WS(2) flakes transferred on a flexible polycarbonate cruciform substrate.

66 tly incorporated into a CO(2)-based triblock polycarbonate derived using a dicarboxylic acid chain-tr

67 odology was developed for the preparation of polycarbonates derived from glucose as a natural product

68 Polyesters and polycarbonates, derived from 6- and 7-membered heterocyc

69 uction by the i.p. implantation of 21 x 2 mm polycarbonate discs.

70 acid functionalities being installed in the polycarbonate domains for adhesive properties.

71 Here, we engineer a nanotube-polycarbonate film with a wide bandwidth (>300 nm) aroun

72 y on isolated single molecules of MEH-PPV in polycarbonate films that exclude O(2) reveals two distin

73 Aluminum coupon-based polycarbonate filter assemblies were deployed in the spa

74 mm diameter) of a 5-microm uniform pore size polycarbonate filter is continuously wetted by a 0.25 mL

75 Our results show that an 8 mum porosity polycarbonate filter placed on a Kevley slide enables pr

76 A thin (80 microm) colored polycarbonate filter was placed on the top of the embedd

77 , through a layer of Matrigel on a 5-um pore polycarbonate filter was stimulated up to 5-fold by 10(-

78 across platelets bound to fibronectin-coated polycarbonate filters by mAbs to Mac-1.

79 dent hippocampal neurons, we grew neurons on polycarbonate filters etched with 3 microm pores.

80 Intact retinas are placed on polycarbonate filters floating on explant culture medium

81 d at approximately the same rate on uncoated polycarbonate filters in the Boyden chambers.

82 icle SEM/EDX analysis of aerosols is done on polycarbonate filters or solid carbon substrates.

83 parations were evaluated over 6 hr utilizing polycarbonate filters ranging from 0.03 to 10 microns.

84 etermined on 24-mm Transwell (Cambridge, MA) polycarbonate filters with the End-Ohm device (World Pre

85 dothelial cells (BRECs) were grown on porous polycarbonate filters, and water flux across BREC monola

86 spheroplasts are lysed by extrusion through polycarbonate filters.

87 Stx was examined in four cell lines grown on polycarbonate filters.

88 rier for production of cyclic carbonates and polycarbonates for the two different classes of epoxides

89 levated temperatures, at ambient temperature polycarbonate formation is dominant.

90 )), reveals the transition state barrier for polycarbonate formation: DeltaG(*) = +92.6 +/- 2.5 kJ mo

91 By way of comparison, the similarly derived polycarbonate from the sterically less congested monomer

92 lvents cannot be used to selectively extract polycarbonates from mixtures of polymers with similar pr

93 ess than 30% of the cost of producing virgin polycarbonates from petroleum.

94 More than one million tons of polycarbonates from waste electrical and electronic equi

95 Aliphatic polycarbonates have gained increased attention as biomat

96 MPa, respectively) comparable to commercial polycarbonate, high optical clarity, and good barrier pr

97 rapidly generate libraries of polyester and polycarbonate homopolymers and block copolymers with exq

98 An amorphous polycarbonate host effectively disperses the chromophore

99 heir compatibility as guests in an amorphous polycarbonate host.

100 olyethylene, polypropylene, polystyrene, and polycarbonate, in seawater under laboratory-simulated ul

101 I)] catalyst is applied for CRM of aliphatic polycarbonates, including poly(cyclohexene carbonate) (P

102 fication of the topological structure of the polycarbonate is an efficient method of obtaining polyme

103 d Bacillus subtilis) on materials (Aluminum, Polycarbonate, Kevlar and Orthofabric) relevant to space

104 r membrane filters bonded between the mating polycarbonate layers.

105 lock polymers featuring controllable PEO and polycarbonate lengths are straightforwardly prepared usi

106 Under the test conditions of this study, polycarbonate lenses demonstrated greater impact resista

107 Polycarbonate lenses demonstrated resistance to impact f

108 The microdevice was attached to a polycarbonate manifold with external electrode reservoir

109 rom polydimethylsiloxane and gas impermeable polycarbonate materials that are integrated with multipl

110 These fundamental findings of glucose-based polycarbonates may facilitate the development of next-ge

111 A polycarbonate membrane (100-nm-diam pore size) hydrated

112 is sealed with either a viscous liquid or a polycarbonate membrane (no commercially available suppor

113 ents separated by either a porous alumina or polycarbonate membrane as a model system, diffusive flux

114 ists of a double-side gold-coated perforated polycarbonate membrane as part of a microfluidic system

115 ted with a one-pot hydrothermal method using polycarbonate membrane as the template.

116 images of relatively soft samples, such as a polycarbonate membrane filter and living diatoms in a co

117 mer on insulating substrates (glass slide or polycarbonate membrane filter).

118 ent the successful inclusion of track-etched polycarbonate membrane filters into the reservoirs of po

119 Polycarbonate membrane filters were used to assess prima

120 The polycarbonate membrane improved the quantification of Cd

121 an LEC migration assays were performed using polycarbonate membrane inserts and 20% fetal bovine seru

122 nducted in tissue culture plates fitted with polycarbonate membrane inserts exhibited mortality (100%

123 imary culture of human choroidal ECs through polycarbonate membrane inserts was quantified in the pre

124 f capturing proteins by interaction with the polycarbonate membrane of the NEE.

125 investigate whether an additional nuclepore polycarbonate membrane on the surface of DGT devices can

126 were grown to confluence on an 8-microM pore polycarbonate membrane precoated with an artificial base

127 by addressing microregions of a gold-filled polycarbonate membrane through the UMEs of an underlying

128 cells release NO, it flows through a porous polycarbonate membrane to the probe.

129 abeled GM1 RPE cells through a 2-microm-pore polycarbonate membrane using an extruder device.

130 he proteoliposomes after extrusion through a polycarbonate membrane was 94 +/- 4 nm.

131 ay (ANEMA) based on a Au-filled track-etched polycarbonate membrane was fabricated.

132 the seal between the gold nanowires and the polycarbonate membrane was not compromised as a result o

133 the number of ECs that migrated through the polycarbonate membrane was significantly higher than ECs

134 er chamber were allowed to migrate through a polycarbonate membrane with 8 microns pores toward VEGF

135 styrene spheres (43-150-nm diameter) using a polycarbonate membrane with conically shaped pores, the

136 ly differed from findings with an artificial polycarbonate membrane, which is a widely used model.

137 The PDMS chamber was bound to a polycarbonate membrane, which itself was bound to a mole

138 bias due to biofilms by using an additional polycarbonate membrane.

139 ipids and cholesterol by extrusion through a polycarbonate membrane.

140 ts whose bottoms are constructed of a porous polycarbonate membrane; this insert enables molecular tr

141 This principle is demonstrated by imaging polycarbonate membranes (6-12-microm thickness) containi

142 pH-induced hysteretic gating of track-etched polycarbonate membranes (TEPC) has been achieved by depo

143 ectrodes (RNEs) fabricated from track-etched polycarbonate membranes (TEPCMs) having cylindrical nano

144 Cells were plated on transwell polycarbonate membranes and stimulated by a stable vitam

145 st strategy to bond semiporous polyester and polycarbonate membranes between layers of PDMS microchan

146 Cellular invasion was investigated with polycarbonate membranes coated with collagen.

147 within the cylindrical pores of track-etched polycarbonate membranes compared to the multilayers on p

148 nterconnects, employing nuclear track-etched polycarbonate membranes containing nanometer-diameter ca

149 etching procedure based on the solubility of polycarbonate membranes in solvent mixtures is reported

150 rmability evaluated using filtration through polycarbonate membranes revealed that the cortical tensi

151 trolled etching of the surface layers of the polycarbonate membranes to expose up to 200-nm lengths o

152 The track-etched polycarbonate membranes were filled using a gold electro

153 ween single protein molecules and nanoporous polycarbonate membranes were investigated at the single

154 Polycarbonate membranes with 0.1-1-microm vertical pores

155 of magnitude higher than those of commercial polycarbonate membranes, despite having pore sizes an or

156 Cells were cultured on polycarbonate membranes, stimulated by stable Vitamin C,

157 nt lipids were prepared by extrusion through polycarbonate membranes.

158 Notably, the amphiphilic polycarbonate micelle rhenium catalyst suppresses H(2) g

159 Laminated polycarbonate microarray chips were developed for easy p

160 amide-modified DNA probes are immobilized in polycarbonate microfluidic channels via photopolymerizat

161 luorescent dyes at controlled locations in a polycarbonate microfluidic device.

162 Low-density polyethylene and polycarbonate microplastic particles were for the first

163 ayer of basement membrane-like Matrigel on a polycarbonate micropore filter was evoked by vasoactive

164 ally, the modification scheme was applied to polycarbonate microprojection arrays, and we show that t

165 Two similar polycarbonate models were used to simulate a single root

166 es into biomedical applications of aliphatic polycarbonates obtained by ring-opening polymerization o

167 erial comprised of polyethylene glycol and a polycarbonate of dihydroxyacetone (MPEG-pDHA).

168 icrofluidic channels ("biochannels") made of polycarbonate, optionally with an integrated pump.

169 elective preparation of either polyesters or polycarbonates or copoly(ester-carbonates).

170 Given the value of the polymer products-polycarbonates or polyether carbonates-it could provide

171 as 48.6, much higher than the corresponding polycarbonates or polythiocarbonates.

172 For polycarbonate, our results show that Ar4000+ bombardment

173 nitrate/cellulose acetate filter membranes, polycarbonate, paraffin, polyethylene terephthalate, pap

174 With the exception of polycarbonate (PC) baby bottles, little attention has be

175 fiably different for eDNA fragments with the polycarbonate (PC) binding the least and mixed cellulose

176 monella typhi (S. typhi) on modified isopore polycarbonate (PC) black membranes.

177 consisted of two different microchips: (1) a polycarbonate (PC) chip for performing an allele-specifi

178 nfiguration carried out in a microfabricated polycarbonate (PC) chip.

179 script, we discuss the use of photoactivated polycarbonate (PC) for purification of dye-labeled termi

180 This study is aimed to compare Tritan and polycarbonate (PC) from a point of view of migration of

181 ed bioreceptors modified 2D matrix of porous polycarbonate (PC) membrane with densely packed 20microm

182 into the pores of a templating track-etched polycarbonate (PC) membrane.

183 flexible hybrid polydimethylsiloxane (PDMS)-polycarbonate (PC) microfluidic chip with integrated scr

184 ure gradient gel electrophoresis (TGGE) in a polycarbonate (PC) microfluidic device, is reported.

185 the ammonia borane was encapsulated within a polycarbonate (PC) microtube array membrane, the tempera

186 ctrophoresis (CE) devices were fabricated in polycarbonate (PC) plastic material by compression moldi

187 ) is immobilized as a capturing agent on the polycarbonate (PC) surface of the track-etched templatin

188 piral microfluidic channel hot-embossed into polycarbonate (PC) that had three well-defined temperatu

189 aration channels that were hot-embossed into polycarbonate (PC) using a high-precision micromilled me

190 0 microm diameter posts, on a single 3" x 5" polycarbonate (PC) wafer fabricated by hot embossing.

191 thyl methacrylate) (PMMA), polystyrene (PS), polycarbonate (PC), and cyclic olefin copolymer (COC) as

192 deposition samples, with polyethylene (PE), polycarbonate (PC), and poly(ethylene terephthalate) (PE

193 erties are demonstrated in polystyrene (PS), polycarbonate (PC), and polyethylene (PE) by demonstrati

194 nds (compared to C-O bonds for PET) of waste polycarbonate (PC), largely forming xylenol (~38 %) and

195 Prior work demonstrated a core-shell polycarbonate (PC)-acrylonitrile butadiene styrene (ABS)

196 hyl methacrylate (PMMA) micro-reactor with a polycarbonate (PC)-based prism coated with a 50 nm Au fi

197 n resource-limited settings, we fabricated a polycarbonate (PC)-polydimethylsiloxane (PDMS) hybrid mi

198 th CO(2), via the epoxide manifold, to yield polycarbonate, PC(BiL(O)).

199 (Mem-dELISA) platform by using track-etched polycarbonate (PCTE) membranes to overcome these shortco

200 Amphiphilic polycarbonate/PEG copolymer with a star-like architectur

201 Bisphenol A (BPA) is found in polycarbonate plastic and epoxy resins and is used in a

202 ic chemical widely used in the production of polycarbonate plastic and epoxy resins found in numerous

203 umes and disposal of products made from BPA, polycarbonate plastic and epoxy resins, BPA has entered

204 l]propane, BPA), the monomer used to produce polycarbonate plastic and epoxy resins, is weakly estrog

205 BPA is used to manufacture polycarbonate plastic and epoxy resins; APs are used to

206 high production volume chemical used to make polycarbonate plastic and is found in many consumer prod

207 A (BPA) is widely used in the manufacture of polycarbonate plastic bottles, food and beverage can lin

208 These integrated devices were fabricated in polycarbonate plastic material by CO2 laser machining an

209 verages because of significant leaching from polycarbonate plastic products and the lining of cans.

210 ermination of bisphenol A migrated from some polycarbonate plastic products.

211 UV irradiation treatment of the hydrophobic polycarbonate plastic surfaces prior to thermal bonding.

212 n-volume chemical used in the manufacture of polycarbonate plastic, is associated with higher body we

213 The widespread use of bisphenol A (BPA) in polycarbonate plastics and epoxy resins has made it a pr

214 g compound, is a synthetic ingredient of the polycarbonate plastics and epoxy resins used in food con

215 a common chemical used in the manufacture of polycarbonate plastics and epoxy resins, and > 93% of U.

216 enol analogues are used in the production of polycarbonate plastics and epoxy resins.

217 ic compound widely used in the production of polycarbonate plastics and epoxy resins.

218 rial production and after degradation of the polycarbonate plastics and nonionic surfactants.

219 enoestrogen widely used in the production of polycarbonate plastics.

220 y, and the hard "A" block is a CO(2)-derived polycarbonate, poly(4-vinyl cyclohexene oxide carbonate)

221 rent types of plastic surfaces (polystyrene, polycarbonate, poly(methylmethacrylate), and polypropyle

222 ied as microplastics, composed of polyamide, polycarbonate, polyester, polyethylene terephthalate, po

223 nabling the synthesis of all-cis polyesters, polycarbonates, polyethers and polysulfites.

224 e butadiene styrene, polylactic acid, nylon, polycarbonate, polyethylene terephthalate, and chlorinat

225 Using this process to make low molar mass polycarbonate polyols is a commercially relevant route t

226 We discuss the use of a photoactivated polycarbonate (PPC) microfluidic chip for the solid-phas

227 Polycarbonate preforms containing microchannels with cro

228 , the initial intention was to expand beyond polycarbonates prepared by the copolymerization of oxeta

229 d as protecting side chains, while all other polycarbonates presented high thermal stabilities with a

230 134 degrees C, the highest yet reported for polycarbonates produced from CO(2)/epoxides coupling.

231 In contrast, high molar mass polycarbonates, produced from CO(2), generally under-del

232 These are shown to apply to polycarbonate production by the ring-opening copolymeriz

233 ken together, carboxylic acid-functionalized polycarbonates represent a promising class of bone cemen

234 an amniotic membrane corneal bandage with a polycarbonate ring, was placed in both eyes.

235 asurements on supported lipid bilayers and a polycarbonate sample using pipets with opening radii dow

236 ith a pressure of approximately 170 MPa in a polycarbonate sample, with a subsequent quantitative sta

237 (OR)(2)(OH)(2) (-) anions immobilized on the polycarbonate segments provide hydrogen-bonding chain cr

238 high selectivity (>99% CO(2) utilization and polycarbonate selectivity) for carbon dioxide and cycloh

239 reported TOF of 3200 h(-1) together with 99% polycarbonate selectivity.

240 larized monolayers on tissue culture-treated polycarbonate semipermeable supports were transduced wit

241 ust and the after-effects of mud formed on a polycarbonate sheet, which is commonly used as a protect

242 roximately 5-10 microm) nuclear track-etched polycarbonate sheets containing approximately 10(8) cm(-

243 er phantom was constructed with a 6-mm thick polycarbonate slab inserted at its center.

244 Results: The polycarbonate slab was resolvable in all reconstructed p

245 lysates or whole blood using a photactivated polycarbonate solid-phase reversible immobilization (PPC

246 We demonstrated that this polycarbonate structure coated with a critical thickness

247 The plates were then bonded to polycarbonate substrates and subjected to fatigue loadin

248 Monolithic glass plates were epoxy-bonded to polycarbonate substrates as a transparent model for an a

249 Monolithic glass plates were epoxy-joined to polycarbonate substrates as a transparent model for an a

250 c system features a compact design employing polycarbonate substrates that contain integrated microch

251 icroelectrospray emitters were fabricated on polycarbonate substrates using a laser etching technique

252 uch ability to modify characteristics of the polycarbonate surface could address the dust/mud-related

253 work required to remove the dry mud from the polycarbonate surface upon drying.

254 s then detected by an ELISA assay on the CNT-polycarbonate surface with an ECL assay.

255 hanical, and textural characteristics of the polycarbonate surface, and to increase the adhesion work

256 body-nanotube mixture was immobilized onto a polycarbonate surface.

257 phobicity via entrapment of nanoparticles in polycarbonate surfaces.

258 ne oil microdroplets in eyes using BD 1.0-mL polycarbonate syringes was significantly greater than BD

259 ith repackaged bevacizumab and the BD 1.0-mL polycarbonate syringes with aflibercept cause a higher l

260 % of eyes receiving aflibercept in 1.0-mL BD polycarbonate syringes, and 0% of eyes in controls.

261 BD 1.0-mL polypropylene syringes, BD 1.0-mL polycarbonate syringes, or controls (P < 0.001).

262 particles derived from a CO2 -based triblock polycarbonate system.

263 tubes within the conically shaped pores of a polycarbonate template membrane.

264 deposit Au nanotubules within the pores of a polycarbonate template membrane.

265 ctrodeposition within the conical pores of a polycarbonate template membrane.

266 ve been electrosynthesized using the conical polycarbonate template.

267 e first time the utility of tyrosine-derived polycarbonate terpolymer electrospun fiber mats as tunab

268 general for a wide variety of polyesters and polycarbonates, the catalyst system could selectively de

269 The construction of amphiphilic polycarbonates through epoxides/CO2 coupling is a challe

270 erization (ROCOP) allows for >30 wt % of the polycarbonate to derive from CO(2); so far, the field ha

271 protocol using poly(methyl methacrylate) and polycarbonate to produce functional scaffolds consisting

272 cylinder encased by sleeves of aluminum and polycarbonate to simulate trabecular bone, cortical bone

273 y replication of the pores of 70 nm diameter polycarbonate track etch membranes.

274 was fabricated by sandwiching two nanoporous polycarbonate track etched (PCTE) membranes with differe

275 wn on silicon carbide substrates to flexible polycarbonate track etched supports with well-defined cy

276 Among the four types of membrane sensors, polycarbonate track-etch (PCTE) membrane sensors exhibit

277 A thin layer of gold is plated onto polycarbonate track-etched nanoporous membranes via elec

278 scalable chemical vapor deposition (CVD) to polycarbonate track-etched supports.

279 AF, silicone rubber, track-etch hydrophilic polycarbonate, track-etch hydrophobic polycarbonate, tra

280 philic polycarbonate, track-etch hydrophobic polycarbonate, track-etch polyimide, nanoporous anodic a

281 riments and inhibited their invasion through polycarbonate Transwell filters.

282 ge evolution in a transparent glass/zirconia/polycarbonate trilayer, post mortem damage evaluation of

283 ical's well-established, radiopaque tyrosine-polycarbonate (Tyrocore) sirolimus-eluting DRS.

284 trospun medical-grade thermoplastic silicone-polycarbonate-urethane and is soft but tough (~15 megapa

285 ew bio-derived and degradable polyesters and polycarbonates via ring-opening polymerisation and ring-

286 First, we modified polycarbonate wafers using an electrophilic aromatic sub

287 The surface of polycarbonate was activated by UV radiation resulting in

288 weight (median; 10.4 mg/g dry weight), while polycarbonate was not detected in any sample.

289 A preformed T-microchannel imprinted in polycarbonate was postmodified with a pulsed UV excimer

290 This amphiphilic polycarbonate was shown to self-assemble in water to pro

291 e organobase catalyst employed, regioregular polycarbonates were obtained via ROP of monomers with et

292 Polycarbonates were successfully synthesized for the fir

293 rfaced with a photomultiplier tube through a polycarbonate window.

294 carbon dioxide to provide the corresponding polycarbonate with a minimal amount of ether linkages.

295 tively in a controlled fashion to afford the polycarbonate with a tunable degree of polymerization, n

296 The resulting polycarbonates with -OH end groups can thus be directly

297 e nonrandom chain packing for two commercial polycarbonates with decidedly different mechanical prope

298 The thermal behaviors of polycarbonates with ether and carbonate pendant groups w

299 and selectively depolymerize polyesters and polycarbonates with high ceiling temperatures (T(c) >200

300 g two mixed solvents is developed to recover polycarbonates with high yield (>95%) and a similar puri