ライフサイエンスコーパス: polymer

1 proach to fabricate Borromean linked organic polymer.

2 extent of zwitterionic functionality in the polymer.

3 first example of water-stable n-doping in a polymer.

4 and connectivity of pores within a model EPS polymer.

5 erties of the MOF and the flexibility of the polymer.

6 ning the head groups at the periphery of the polymer.

7 hole mobilities in this relatively amorphous polymer.

8 nefits from biodegradation of this synthetic polymer.

9 rated with a cyclobutane-fused lactone (CBL) polymer.

10 t control the growth and morphology of these polymers.

11 based only on transient binding to flexible polymers.

12 e that is distinct from that of cytoskeletal polymers.

13 of pai-stacking by formation of sigma-bonded polymers.

14 vations and broad applications of conducting polymers.

15 f the crowding agent BSA, but not by sucrose polymers.

16 ttention as organocatalysts and redox active polymers.

17 a host of new applications for CO(2)-derived polymers.

18 eutral, internally ion-paired supramolecular polymers.

19 rojunction devices based on narrow-gap donor polymers.

20 logical strategy toward high-mobility p-type polymers.

21 orks, amorphous analogues, and 1D conjugated polymers.

22 rs have not been described for branched PLGA polymers.

23 ulation of [Au(25)(Cys)(18)] and CV into the polymer activates potent photobactericidal activity.

24 These polymers afford the producing bacteria protection from a

25 ranules are composed of two distinct glucose polymers - amylose and amylopectin.

26 is the first example of ultrasound-assisted polymer analogues transformation of chitin unaccompanied

27 ransfer to organic solvents commonly used in polymer and peptide synthesis results in the alteration

28 consist of mixtures of up to nine different polymers and contain various elements of the periodic ta

29 ecretory trafficking of a protein that forms polymers and large intracellular inclusions.

30 grams of macromolecules, including synthetic polymers and proteins.

31 rength), different durable and biodegradable polymers - and in some cases no polymer (to improve vasc

32 of TLR2 agonists to antigens, carbohydrates, polymers, and fluorophores.

33 ble, due to the superior properties of novel polymers, and have the biocompatibility and hemodynamics

34 functions to replace nonrenewable plastics, polymers, and metals.

35 acteristic process of natural supramolecular polymers, and such recognition processes allow for dynam

36 GPC-4D) has been previously applied to other polymers, and the relevant mathematical parameters for t

37 Here we present a polymer- and transfer-free direct-etching method for bat

38 ciprofloxacin hydrochloride and FDA-approved polymers are fabricated.

39 en photochromic molecules and semiconducting polymers are far from being fully understood.

40 Different second-component polymers are introduced to change the properties of a po

41 Solution-processable highly conductive polymers are of great interest in emerging electronic ap

42 Carbon nanotubes (CNTs) embedded polymers are of increasing interest to scientific and in

43 Conducting polymers are promising material candidates in diverse ap

44 The polymers are synthesized using a new, highly active orga

45 Polymers are synthesized with rigid and contorted backbo

46 By comparing a conventional pai-conjugated polymer as the active material to a perdeuterated analog

47 fficiencies in TRLC despite the use of bulky polymers as stationary phases in HPLC.

48 ater through an approach that we refer to as polymer-attenuated Coulombic self-assembly.

49 rrent research, we reveal that a dendronized polymer augments the efficacy of an oncolytic peptide (O

50 otherapy by exploiting (i) "flexible" linear polymer backbone to facilitate interactions with biomemb

51 ng to the inherent stability provided by the polymer backbones and their ability to capture micropoll

52 nder various conditions and within different polymer backbones.

53 , we disclose a series of supramolecular (co)polymers based on water-soluble benzene-1,3,5-tricarboxa

54 are essential to realise the concept of all-polymer-based biosensors that do not depend on tradition

55 We have classified these compounds into polymer-based mass-tag reagents, nonpolymer-based mass-t

56 While great progress has been achieved, polymer-based mixed conductors frequently experience sig

57 The organic polymer-based monolithic columns have been evaluated as

58 umor uptake and biodistribution of SN22 as a polymer-based prodrug (PEG-[SN22](4)) compared with SN38

59 de electrochemical cells to form solid-state polymer batteries with good interfacial charge-transport

60 way of Cr (VI) to Cr (III) in graphene-based polymer beads.

61 tment, which digests anionic sulfated glycan polymers, before exposure rendered cells insensitive to

62 Through reference to theories of bottlebrush polymer behavior, we demonstrate that the experimental v

63 itic domains to intercalated assemblies with polymer bilayers between sheets.

64 r the development of a range of advanced all-polymer biosensors.

65 e wafers were composed of a series of binary polymer blends of carboxymethylcellulose (CMC) and algin

66 Polymer brush coatings are effective in preventing blood

67 Here we report a technique termed Polymer Brush Hypersurface Photolithography, which produ

68 Polymer brush patterns have a central role in establishe

69 The characterization of these polymers by mass spectrometry (MS) continues to be very

70 p pave the way for future developments of 2D polymers by those interested in joining the effort with

71 The 3D-printed conducting polymers can also be converted into highly conductive an

72 Furthermore, we demonstrate that these polymers can be imbued with advanced functionalities.

73 100 kPa, well below values typical of linear polymer CANs (1 MPa).

74 ect molecular-based design of functionalized polymer/carbon spheres.

75 al distribution of Ti species throughout the polymer-catalyst composite particle shows that the conti

76 essful preservation of the nickel complex at polymer chain ends is evidenced by nuclear magnetic reso

77 mbrane becomes crowded by ENTH proteins, the polymer chain extends, increasing the fluorescence lifet

78 realize protein-like behaviour at the single-polymer-chain level in a predictable manner.

79 the negative mode, sulfonic acid-terminated polymer chains can be more sensitively detected than thi

80 omplementary measurement of the length of PE polymer chains extending through the crystalline lamella

81 The hydration of polymer chains generates a large amount of weakly bounde

82 vage, and as this drug release proceeds, the polymer chains losing hydrophobicity are then disassocia

83 Unstructured protein or polymer chains pack loosely and readily rearrange, leadi

84 thod for validation of the segmental size of polymer chains with varying topology by using the revisi

85 mistry, a mechanical force, transduced along polymer chains, is used to activate covalent bonds in me

86 overlooked, namely, the isolation of living polymer chains.

87 hose aggregation is solely controlled by the polymer chains.

88 The reported polymer channel, having an average molecular weight of 1

89 curately discriminate between highly similar polymer chemistries or identify heterogeneities within i

90 merizations currently play a central role in polymer chemistry.

91 tical work addresses the characterization of polymer-coated nanoparticles via the analysis of Taylor

92 ting reaction discovery, and optimization of polymer coatings.

93 e both critical for the obtainment of stable polymer colloids as carbon precursors.

94 Here, we develop hydrogels with identical polymer components but different crosslinking capacities

95 study offers new insight into supramolecular polymers composed of custom-designed anion and receptor

96 Here, a novel magnetic shape memory polymer composite is reported to achieve this.

97 predictive models of mechanical behaviour in polymer-composite materials, particularly at the resin-f

98 tribution, concentration, particle size, and polymer compositions of microplastics in Lake Michigan a

99 lycine linker, making a monovalent quinidine-polymer conjugate, which was then evaluated for its inte

100 mprised of an ultra-pH sensitive amphiphilic polymer, conjugated with indocyanine green, which rapidl

101 unctional, proteolytically resistant peptide-polymer conjugates for intracellular delivery.

102 onomer units, the helical sense of a dynamic polymer constructed from achiral monomer units can be di

103 Here we report a photobactericidal polymer containing crystal violet (CV) and thiolated gol

104 llaboration as well as his following work in polymer-controlled drug releasing systems.

105 loading of 10 +/- 1.0% (w/w) while the same polymer could only load 1.6 +/- 0.4 (w/w) CH-3-8 using t

106 rent approaches to synthesize pai-conjugated polymers (CPs) are dominated by thermally driven, transi

107 Polymer crosslinking imbues chemical stability to thin f

108 Stage III is controlled by polymer degradation and involves release of the remainin

109 As particle size decreased, polymer degradation increased, indicating an increase in

110 Polymer density estimates indicated that 85 and 74% of o

111 ay are applied to cross-link hyaluronic acid polymers derivatised with a pendant bisphosphonate to ge

112 nts treated with polymer-free versus durable polymer DES.

113 ine (PTAA)) is employed to partially replace polymer donors in the active layer of PBDB-T/Y1.

114 Hydroxyl polymer doping thus offers a pathway for efficient H dop

115 dronized pyropheophorbide a (Ppa)-conjugated polymer (DPP) is reported, and a linear Ppa-conjugated p

116 o the thin-strut second-generation permanent polymer drug-eluting stent.

117 Polymer-drug conjugates are promising as strategies for

118 The nacre-like ceramic/polymer electrolyte (NCPE) simultaneously possesses a mu

119 ltimate flexural modulus (7.8 GPa) than pure polymer electrolytes (20 MPa).

120 ctive site also appeared to be important for polymer elongation.

121 The control of the tacticity of synthetic polymers enables the realization of emergent physical pr

122 To enhance the stability of chlorophyll, a polymer encapsulation method was proposed.

123 vances in creating assembled structures from polymers, engineering the assembly of polymeric material

124 In devices integrated on flexible polymers, enhanced room-temperature dielectric permittiv

125 The supramolecular polymer ensures the efficient intracellular delivery and

126 The polymers exhibited perfect regioregularity, and their mo

127 s a head-to-tail noncentrosymmetric columnar polymer, exhibiting a nucleation-elongation polymerizati

128 the membrane provides a real-time readout of polymer extension.

129 Polymer extraction from brain homogenates from Syrian ha

130 rovides access to the precise fabrication of polymers featuring diradical character which are potenti

131 x harboring a conoid, made of unique tubulin polymer fibers.

132 Here, several polymer films with similar main chains but different fun

133 lth of physico-chemical processes, including polymer folding and information storage.

134 The coating was comprised of an amphiphilic polymer followed by three crosslinked amphiphilic polyme

135 lecular weight, branched, and functionalized polymers for protein conjugation and drug delivery.

136 re we study the molecular mechanism of hGBP1 polymer formation as it is a crucial state of this enzym

137 Furthermore, engineering similar hetero-polymer formation into angiosperm crop plants may improv

138 es in outcomes between patients treated with polymer-free versus durable polymer DES.

139 Efforts to synthesize degradable polymers from renewable resources are deterred by techni

140 are similar to those previously reported on polymer-functionalized carbon-aerogels.

141 s these terms across all size categories and polymer groups to determine the fate and danger of plast

142 Within the second phase of polymer growth, opened hGBP1 molecules can be incorporat

143 The polymer has a donor fluorophore at its free end, such th

144 Coarse-grained modeling of conjugated polymers has become an increasingly popular route to inv

145 However, the fabrication of conducting polymers has mostly relied on conventional approaches su

146 performance of other temperature responsive polymers has rarely been compared under identical condit

147 Bacterial polymers have important roles in pathogenicity, and thei

148 ndependently control monomer composition and polymer height of each pixel.

149 Here, we report on the formation of polymer hexosomes whose inverted cylinders orient in an

150 However, the emergence of conducting polymer hydrogels with a desirable network structure can

151 pronounced spectral differences for the same polymer in the two polyMOF lattices.

152 metabolism dynamically assemble filamentous polymers in cells, often in response to changes in physi

153 The behavior of imprinted polymers in fluid solvents was also investigated by empl

154 ems can be exploited to generate "unnatural" polymers in the presence of "host" cells, thus setting u

155 ties of physisorbed zwitterionic bottlebrush polymers in the presence of multivalent ions using the s

156 tensity of all synthesized iodine-containing polymers, in comparison to non-iodinated poly(lactic aci

157 al design principle for synthesizing abiotic polymer inhibitors of enzymes.

158 at appeared after 200 degrees C due to small polymer interaction that shifted the OCT peak.

159 ding root mucilage and the proposed adhesive polymers involved in the formation of rhizosheaths at ro

160 plete 3D organization of the whole chromatin polymer is an inverse problem.

161 le ionic aggregates in single-ion conducting polymers is a crucial step toward exceptional transport

162 The reactivity of these end-capped polymers is illustrated here via functionalization with

163 demonstrate that the high stability of FimA polymers is primarily caused by the specific interaction

164 experiments on multiple push-pull conjugated polymers, it is argued that the size of the donor push u

165 nd hydrolysis to mechanical movement along a polymer lattice.

166 electrosynthesis of an amino moiety-bearing polymer layer on the graphene channel.

167 citation energy transfer from a photoexcited polymer layer to the underlying perovskite.

168 efficient and stable lanthanide coordination polymers (LCPs) with tunable luminescence as a new optio

169 nce from a three-dimensional hybrid microrod/polymer LED array and demonstrate its improved optical p

170 However, it is unclear if exceptional polymer length of vHMM-HA is important for longevity.

171 of the switching and obtain photocontrol of polymer length.

172 erms of how the concentration profile of the polymer-length distribution adjusts to changes in protom

173 PP) is reported, and a linear Ppa-conjugated polymer (LPP) is reported as a control.

174 of template induced 1-1 diad repeats in the polymer main chain shedding unique light on the relative

175 ally stable proteins, the synthesis of novel polymer materials that undergo ultrarapid, isochoric, an

176 ons, ranging from small molecules to dynamic polymer materials.

177 Nanocomposites consisting of a polymer matrix and metallic nanoparticles can merge the

178 In polymer mechanochemistry, a mechanical force, transduced

179 ange of Vps24 for Did2 induces a tilt in the polymer-membrane interface, which triggers transition fr

180 The tight polymer membranes and the inward oriented enzyme caused

181 designing solution-processable ion-selective polymer membranes with both intrinsic microporosity and

182 peptide nanopores, track-etched nanopores in polymer membranes, and hydroxylated and functionalized n

183 nosheets, amorphous MOF liquids and glasses, polymers, metal nanoparticles, metal carbide nanoparticl

184 vironmentally friendly molecularly imprinted polymer (MIP) coated on silica-carbon quantum dots (SiCQ

185 Numerous conducting molecularly imprinted polymer (MIP) films are deposited by electropolymerizati

186 The lab-made molecularly imprinted polymers (MIP), selective for simple coumarins, were use

187 fter modification with molecularly imprinted polymers (MIPs) for determination of thiabendazole (TBZ)

188 mical sensing based on molecularly imprinted polymers (MIPs) has become an interesting field for envi

189 of such a device using molecularly imprinted polymers (MIPs).

190 Our minimal polymer model reproduces the formation of lamin-associat

191 elease of individual vaccine components from polymer multilayers.

192 sed naphthalene diimide (NDI)-based acceptor polymer (N2200), by systematically replacing a certain a

193 al use of microalgal biomass encapsulated in polymer nanofibers to develop a colorimetric pH indicato

194 scribe a process for engineering a synthetic polymer nanoparticle (NP) that functions as an effective

195 based on electroactive molecularly imprinted polymer nanoparticles (nanoMIP) was developed.

196 eted drug tocilizumab (TCZ) is conjugated to polymer nanoparticles (PNPs) to develop the first NIR-II

197 e (thin or grafted layers, polymer ordering, polymer nanopores), architecture (branched vs linear), f

198 review we will discuss the influence of the polymer nanostructure (thin or grafted layers, polymer o

199 Macrocycle-containing covalent polymer networks have begun to attract attention in the

200 alyses demonstrates that the spectrum of the polymer non-backtracking operator resolves the true comp

201 Bacteria are protected by a polymer of peptidoglycan that serves as an exoskeleton(1

202 tabilization required binding of long GlcNAc polymers of greater than 20 units.

203 We focus on synthetic brush polymers of oligonucleotides, oligosaccharides, and olig

204 , dolichols and their derivatives are linear polymers of several isoprene units.

205 lymer nanostructure (thin or grafted layers, polymer ordering, polymer nanopores), architecture (bran

206 e distribution and clearance of the injected polymer over time.

207 We employ a dextran polymer particle to overcome the inherent lipophilicity

208 prepared by using a 2-pyridone-based diblock polymer (PEG-Py) to encapsulate a semiconducting, heavy-

209 nanotransformer-based vaccine, comprising a polymer-peptide conjugate-based nanotransformer and load

210 enzymes that modify the essential cell-wall polymer peptidoglycan by O-acetylation.

211 uch as lipidation of antigen, conjugation to polymers, phosphonic acids, and other linkers to achieve

212 and most structural materials (e.g., natural polymers, plastics, steels, and alloys).

213 of a nanofibrillar coating of the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT).

214 The conducting polymer poly(3,4-ethylenedioxythiophene) has shown great

215 uoride is simply admixed with the conjugated polymer poly(N,N'-bis(7-glycol)-naphthalene-1,4,5,8-bis(

216 A hole-transporting large-bandgap polymer (poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine

217 Porous organic polymers (POPs) have shown significant promise owing to

218 nique and complementary means to probe these polymers, precisely because they are sensitive to differ

219 s required by the Pel synthase machinery for polymer production.

220 examined unidentified chemical bonds in the polymer products, other than ester bonds, with NMR spect

221 Given the value of the polymer products-polycarbonates or polyether carbonates-

222 ion of [Au(25)(Cys)(18)] into the CV treated polymer promotes redox reactions through generation of a

223 -infrared (NIR) dye Cy5.5 was coupled to the polymer providing live-animal imaging capability to trac

224 ynthesis tool and an alternative for capsule polymer provision.

225 he synthesis of a new benzocyclobutene based polymer, PSBBB, designed as a dielectric material for us

226 ever, their application for the synthesis of polymers remains rare.

227 rials based on conducting and semiconducting polymers represent an exciting class of materials for bi

228 feasible or desirable, as it can damage the polymer's integrity, leading to loss of function and pro

229 the molecular orientation studies focused on polymer samples with a well-defined molecular axis.

230 bound lactose 3'-sulfate ligated to an inert polymer scaffold, and binding was inhibited by competing

231 Here we use biodegradable polymer scaffolds seeded with autologous cells to restor

232 the superiority of thin-strut biodegradable polymer second-generation drug-eluting stent to the firs

233 Gaining control over polymer self-assembly via molecular design to influence

234 ronic device consisting of patterned organic polymer semiconductors interfaced with an electrolyte so

235 In these "condensation reactions", the polymer serves as a steric guide to limit DNA hybridizat

236 Polymer simulations show that such C-walks are consisten

237 arge craniotomies for implanting transparent polymer skulls for cortex-wide imaging access and skull

238 ASDs were prepared from selected polymers, specifically a somewhat hydrophobic polymer th

239 r identify heterogeneities within individual polymer spots.

240 es thick-in which warp and weft single-chain polymer strands remain associated through periodic mecha

241 ability to polymerize GMT in a hydrolysable polymer structure, and engineer NPs of this polymeric ch

242 for these types of applications are based on polymer substrates that are not suitable for biostable,

243 trategy to obtain micropatterned graphene on polymer substrates using a direct curing process is demo

244 ):polystyrene sulfonate, and +10 to +15% for polymers such as poly(2-(3,3'-bis(2-(2-(2-methoxyethoxy)

245 he oxidation state of a film of a conducting polymer, such as poly(3-octylthiophene) [POT], that is i

246 ugh a sequential three segment ligation on a polymer support via a maleimide anchor.

247 ctivity is retained after conjugation to the polymer, supportive of retention of effective therapeuti

248 ching lipid bilayers to polydimethylsiloxane polymer supports, producing "soft bilayers" with physiol

249 ons for plasticizers in equilibrium with the polymer surface (y(0)).

250 l binding was significantly increased on all polymer surfaces after incubation with fibronectin and v

251 simulations demonstrate that the first-stage polymer/surfactant-surface sorption rate is at least 1 o

252 We introduce the bioconjugation of polymers synthesized by RAFT polymerization, bearing no

253 s during doping and dedoping of a conjugated polymer system via X-ray scattering.

254 or dynamic self-alteration, yielding complex polymer systems with extraordinarily high efficiency in

255 potential for the rapid development of novel polymer systems.

256 ontrast opals formed by the self-assembly of polymer-tethered particles.

257 beta-hydroxybutyrate (PHB) is an alternative polymer that can be considered environment friendly and

258 ces exploit a bioresorbable dynamic covalent polymer that facilitates tight bonding to itself and oth

259 olymers, specifically a somewhat hydrophobic polymer that was extremely effective at inhibiting drug

260 rmation of a highly constricted Did2-Ist1 co-polymer that we show is competent to promote fission whe

261 Conducting polymers that possess good electrochemical properties, n

262 uses only the structure of the chemical and polymer, the weight fraction, and physical-chemical prop

263 Complementing these experimental tools, co-polymers theoretical methods are necessary to determine

264 Drawing on polymer theory, we use this change in lifetime to calcul

265 centration of thermodesorbed pollutants on a polymer thin film and then, their quantification by ATR-

266 Polymer thin films that emit and absorb circularly polar

267 the thermoelectric performance of conjugated polymers, thus also providing new insights into the mole

268 ered yet extended two- and three-dimensional polymers to create topologically well-defined polygonal

269 nto the assembly of well-defined amphiphilic polymers to form functional structures remains elusive,

270 , which triggers transition from flat spiral polymers to helical filament to drive the formation of m

271 om a variety of materials, ranging from soft polymers to rigid ceramics.

272 iodegradable polymers - and in some cases no polymer (to improve vascular biocompatibility) - and new

273 Secretion steers the polymers toward a common exit point, which could facilit

274 mechanochemically generated thiol-terminated polymers undergo a Michael-type addition to Diels-Alder

275 Polydextrose (PDX) is a branched glucose polymer, utilized as a soluble dietary fiber.

276 esized using biodegradable and biocompatible polymers via self-assembly.

277 gs established that the CMC/ALG binary blend polymer wafers have the potential to improve the subling

278 The new polymer was utilized for modifying a GCE to generate a n

279 e aggregation of the resulting As(V)-Fe(III) polymers was enhanced by the presence of Mn.

280 imuli-responsive comonomer in a mostly inert polymer, we can cooperatively amplify the effect of the

281 oposed local conversion of actin monomers to polymers, we demonstrate a surprising role for shuttling

282 Using these polymers, we have developed a series of smart nanocarrie

283 Glycosyl-imprinted polymers were formed by electro-polymerization with poly

284 molecules can be incorporated in the growing polymer where the opened structure is stabilized, simila

285 ered the stage as a new generation of porous polymers which stand out by virtue of their crystallinit

286 The reaction affords aldehyde end-capped polymers whose molecular weight can be tuned by varying

287 Polyacrylates are important polymers widely used in pharmaceutical industry such as

288 chromatin behaves as an unconstrained Rouse polymer with excluded volume, while condensin constrains

289 ycarbonate backbone is used to construct the polymer with pH-dependent degradation kinetics.

290 ore than three metal atoms, and coordination polymers with a heterometallic metal-metal bonded backbo

291 -square error of 13 degrees C for conjugated polymers with alkyl side chains.

292 r level integration of inherently conductive polymers with bioactive hydrogels using bi-functional mo

293 ted following doping of conjugated push-pull polymers with both F(4) TCNQ (2,3,5,6-tetrafluoro-7,7,8,

294 Microtubules are tubular polymers with essential roles in numerous cellular activ

295 s (MOFs), which are crystalline coordination polymers with high porosity, have been proposed as key b

296 uaramide synthons resulted in supramolecular polymers with increased fiber flexibility and lower degr

297 Two conjugated polymers with rigid planar backbones, but with disordere

298 are an emerging class of crystalline porous polymers with tailor-made structures and functionalities

299 a range of organophosphate esters (OPEs) and polymers with varying physicochemical properties.

300 ne-diene rubber (23%) were the most abundant polymers within the water samples and polyethylene-chlor