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1 polypropylene, nylon-6, polyvinyl chloride, polystyrene).
2 the unfolding of the hydrophobic homopolymer polystyrene.
3 acid) (PLA) and a biodegradable analogue of polystyrene.
4 nt for safe MALDI mass analysis of ATRP-made polystyrene.
5 unds that inhibit adhesion of C. albicans to polystyrene.
6 poly(dimethyl siloxane), and tissue culture polystyrene.
7 cal fiber [a Pt(II) porphyrin immobilized in polystyrene].
8 bined use of two polymer-supported reagents (polystyrene-1,5,7-triazabicyclo[4,4,0]dec-5-ene/Cu and p
9 e-1,5,7-triazabicyclo[4,4,0]dec-5-ene/Cu and polystyrene-2-iodoxybenzamide) overcomes the thermodynam
12 We demonstrate here that antigen-conjugated polystyrene (Ag-PS) NPs, although effective for the prop
13 y the fluorescent labeling of functionalized polystyrene and by using Cu-C and Cu-Fe as catalysts.
15 izable norbornene-on the kinetics of ROMP of polystyrene and poly(lactic acid) MMs initiated by (H2IM
17 [polystyrene-block-poly(acrylic acid)-block-polystyrene and polystyrene-block-poly(acrylic acid)-blo
19 ofiles are also acquired from a multilayered polystyrene and polyvinylpyrrolidone film and from a pol
20 cation of small polyethylene, polypropylene, polystyrene, and nylon-6 particles, which frequently occ
21 contrast, plasticized poly(vinyl chloride), polystyrene, and poly(acrylate) ionophore-based membrane
22 ensor, coated with a single layer of atactic polystyrene (aPS) onto which a specific, high affinity a
23 toluene solution of amine end-functionalized polystyrene are completely suppressed, allowing the jett
24 um fabricated from electrospinning of liquid polystyrene are suitable scaffolds for concentric membra
25 , our results show that TMAO and urea act on polystyrene as a protectant and a denaturant, respective
27 mains of a phase-separated (polynorbornene-g-polystyrene)-b-(polynorbornene-g-poly(ethylene oxide)) c
29 to control the phase separation of symmetric polystyrene-b-poly(2-vinylpyridine) (PS-b-P2VP) in dispe
30 ethylene oxide), from the triblock copolymer polystyrene-b-poly(ethylene oxide)-b-polystyrene was inv
31 ive etch masks are formed by thin films of a polystyrene-b-poly(ferrocenylisopropylmethylsilane) dibl
32 S) were admixed and covalently attached to a polystyrene based-microtiter plate (MTP), pretreated wit
34 otein-specific primary antibody to MCMV, and polystyrene bead "anchors," which were functionalized wi
35 ld CD1 (43 eyes) and B6 mice (42 eyes) using polystyrene bead injection into the anterior chamber wit
36 as possible to achieve 2+-fold enrichment of polystyrene beads (5 mum in diameter) in the center daug
43 neutral, anionic and cationic nanoparticles (polystyrene beads and liposomes, 20-135nm diameter, -49
45 coding of soft hydrogels, rigid copper bars, polystyrene beads and silicon chiplets into three-dimens
48 ucleic acid (gamma-PNA) probes conjugated to polystyrene beads have been reported for the detection o
49 ers, and we show that the presence of 10 mum polystyrene beads is required to fully rupture cells and
50 In a second form, WGMs within phagocytized polystyrene beads of different sizes enable individual t
52 h 0.095 M NaCl electrolyte containing 10 mum polystyrene beads to visualize and quantify fluid flow u
53 ossible due to the use of 200 nm fluorescent polystyrene beads which firmly embed in the extracellula
54 essfully separated 2- and 10-microm-diameter polystyrene beads with a separation efficiency of approx
55 ately 99%, and separated 7.3- and 9.9-microm-polystyrene beads with an efficiency of approximately 97
56 From movies of neutrophil phagocytosis of polystyrene beads, we measure the fractional engulfment
57 taxa had the capacity to ingest 1.7-30.6 mum polystyrene beads, with uptake varying by taxa, life-sta
60 block copolymer (poly(2-vinlypyridine)-block-polystyrene-block-poly(2-vinylpyridine)] is doped with c
61 ock-poly(acrylic acid)-block-polystyrene and polystyrene-block-poly(acrylic acid)-block-poly(3,4-ethy
62 Amphiphilic star-like triblock copolymers [polystyrene-block-poly(acrylic acid)-block-polystyrene a
63 y of an ABC block terpolymer consisting of a polystyrene-block-poly(ethylene oxide) (PS-b-PEO) dibloc
64 preparation of nanoscopic line patterns from polystyrene-block-poly(ethylene oxide) featuring a photo
65 a sulfonated charge selective polymer film, polystyrene-block-poly(ethylene-ran-butylene)-block-poly
66 e triblock copolymer employed in the gel was polystyrene-block-poly(methyl methacrylate)-block-polyst
68 ous network structures of polyisoprene-block-polystyrene-block-poly(propylene carbonate) where the po
69 nge lateral ordering of low-molecular-weight polystyrene-block-polydimethylsiloxane with a lattice sp
72 BTBT) from a blended solution of C8-BTBT and polystyrene by using a novel off-centre spin-coating met
73 we use a microfluidic approach to fabricate polystyrene capsules triggered by a toluene stimulus.
75 CNT thread partially insulated with a thin polystyrene coating to define the microelectrode area wa
79 These devices incorporate a carbon nanotube-polystyrene composite, containing different inorganic el
83 wax and polystyrene-poly(ethylene-butylene)-polystyrene copolymer, was used as yarn guest to give an
84 oporphyrin (PtTPTBPF) was entrapped into the polystyrene core (oxygen nanosensors) and a pH sensitive
85 crylic acid) swellable tip and non-swellable polystyrene core, conical microneedles penetrate tissue
86 ymethyloxazoline shells and oxygen-permeable polystyrene cores crosslinked with metal-free purely org
88 ations and 8 neutral aromatic solutes on two polystyrene CXRs, MN500 and Amberlite 200, was examined.
89 alized hydroxyethyl cellulose and a cationic polystyrene derivative decorated with methylviologen moi
94 y was to calibrate and evaluate an existing, polystyrene-divinylbenzene copolymeric resin-based passi
96 utron scattering experiments with deuterated polystyrene (dPS) grafted silica and poly(vinyl methyl e
97 d on SPE of sulfonamides on hypercrosslinked polystyrene, elution with acetonitrile and off-line deri
98 te)-block-polystyrene, where the solvophobic polystyrene end blocks associate into micellar cross-lin
104 diameter of 50 nm, and 0.0005% yellow-green polystyrene fluorescent particles of 1 mum diameter.
106 colloidal self-assembly is used to organize polystyrene-grafted Au nanocrystals at a fluid interface
108 rile butadiene styrene (ABS) and high-impact polystyrene (HIPS) filaments (ranging from approximately
109 p of reference MS(2) spectra obtained from a polystyrene homopolymer and polystyrene end-capped with
111 , SarA-regulated biofilms formed on uncoated polystyrene in nutrient-rich bacteriological medium were
112 the production of MOF-5-polystyrene wherein polystyrene is grafted and uniformly distributed through
114 1 order of magnitude lower than those of the polystyrene latex nanoparticles, likely as a result of s
116 This is demonstrated for a mixture of three polystyrene latex particles with different sizes as well
119 results demonstrated that the use of treated polystyrene may be one factor that leads to falsely elev
120 ed to high emission fossil polymers, such as polystyrene (mean GHG savings up to 1.4 kg CO2e/kg corn
121 ity was then compared with that of a trapped polystyrene microbead as a function of the applied acous
123 this paper, we describe the use of colloidal polystyrene microbeads as a sacrificial template to crea
124 flow zone electrophoresis, we used silica or polystyrene microbeads between 3-6 mum in diameter and p
125 those obtained by replacing the bacteria by polystyrene microbeads to demonstrate the internalizatio
127 adhesion dynamics of Vibrio crassostreae on polystyrene microparticles (micro-PS) using electronic a
129 eractions to drive controlled aggregation of polystyrene microparticles, either through reversible co
133 a vector for transport of microplastics, (2) polystyrene microplastics can alter the properties and s
135 noporous support membrane, on top of which a polystyrene microspacer was thermally bonded to control
136 Here, we show that acute aqueous exposure to polystyrene microspheres (8 mum) with different surface
139 thelial growth factor receptor antagonist in polystyrene microspheres (PE) + tyrosine kinase inhibito
141 ng of two almost identically sized dye-doped polystyrene microspheres placed on adjacent holes at the
143 n between optical image and ADFF analysis of polystyrene microspheres with known dimensions and has a
145 in-2 (LCN2) by functionalizing a KOH-treated polystyrene microtiter plate with multiwalled carbon nan
146 Three lots of custom-made frozen 96-well polystyrene microtiter plates were used and prepared wit
148 ed the influence of treated versus untreated polystyrene microtiter trays on caspofungin MICs using 2
149 s of a nucleophilic substitution, leading to polystyrene molecules holding different terminations, de
154 180 mum sized polyethylene (micro-PE), 70 nm polystyrene (nano-PS), multiwalled carbon nanotubes (MWC
156 s to investigate disposition and toxicity of polystyrene nanoparticles (NPs) in early development of
157 s of varying length and amino-functionalized polystyrene nanoparticles (PS NP) without and with diffe
158 the immunological imprints of inert nontoxic polystyrene nanoparticles 50 nm in diameter (PS50G) and
159 transfer (TR-LRET) with donor europium(III) polystyrene nanoparticles and acceptor-labeled protein a
161 cross sections has been developed that uses polystyrene nanoparticles as the external reference.
162 abolism of the fish; hence, we conclude that polystyrene nanoparticles have severe effects on both be
165 n, we report on-chip detection of individual polystyrene nanoparticles, adenoviruses and influenza A
166 nds on different types of nanoparticles like polystyrene nanoparticles, semiconductor nanocrystals (S
167 d nanocapsules, polyvinyl acetate (PVAc) and polystyrene nanoparticles, were characterized for size,
170 of soft particles of various size and type: polystyrene nanosphere size standards, lipid droplets (L
173 gnetic tunnel junction nanopillars that uses polystyrene nanospheres as a lithographic template.
174 tion events of antibodies, enzymes, DNA, and polystyrene nanospheres can be differentiated from the b
175 , bacteriophages MS2, fr, GA, and Qbeta) and polystyrene nanospheres onto a positively charged model
176 motor by release of Ag(+) ions from a Janus polystyrene/Ni/Au/Ag activator motor to the activated Ja
177 of the HUVECs monolayer towards fluorescent polystyrene NPs (pNPs) of different sizes, which was det
178 s of conformation change when binding to the polystyrene NPs, which could potentially influence prote
180 ymer of the S(IS')3 type, where S and S' are polystyrenes of different lengths and I is poly(isoprene
181 dispersed nanospheres monolayers (Au-MNM) of polystyrene offers an unprecedented selectivity and the
183 operties that greatly exceed those of either polystyrene or the poly(thioether) network homopolymers
184 n over 24 h varied by larval age and size of polystyrene particle (ANOVA, P < 0.01), and surface prop
185 ructural characterization of the homogeneous polystyrene particle films during compression reveal an
187 ein to micrometer-sized carboxylate modified polystyrene particles and detection of two-photon excite
191 eposit morphology of drying drops containing polystyrene particles of different surface properties wi
192 (Crassostrea gigas) larvae (3-24 d.p.f.) to polystyrene particles spanning 70 nm-20 mum in size, inc
193 formation and shape recovery of micron-sized polystyrene particles via nanoimprint lithography is rep
195 s on cells was enhanced further by replacing polystyrene particles with pure chemotherapeutic drug na
200 s outperform traditional streptavidin-coated polystyrene plates under flow, validating their use in f
201 n fibrils over a few hours when incubated on polystyrene plates under physiological conditions throug
203 ility of three different particle materials (polystyrene, PMMA, and silica) of the same size (2 mum)
204 set of model surfaces, i.e., nitrocellulose, polystyrene, poly(methyl methacrylate), and poly(butyl m
206 thin identical regions of a cylinder-forming polystyrene-poly(ethylene oxide) diblock copolymer (PS-b
207 lastic material, comprising paraffin wax and polystyrene-poly(ethylene-butylene)-polystyrene copolyme
208 m in diameter) derived from cylinder-forming polystyrene-poly(methylmethacrylate) diblock copolymers.
209 nanosheets through in situ polymerization of polystyrene-polyacrylamide copolymers is established.
210 ene and polyvinylpyrrolidone film and from a polystyrene/polymethylmethacrylate bilayer, in the forme
213 orted as a major concern in mass analysis of polystyrene prepared by atom transfer radical polymeriza
215 In this study, we demonstrate separation of polystyrene (PS) and poly(methyl methacrylate) (PMMA) mi
216 have been demonstrated for materials such as polystyrene (PS) and poly(methyl methacrylate) (PMMA).
217 d the molecular-size of a mixture of various polystyrene (PS) and polyacrylate (PACR) nanoparticles h
218 yclic aromatic hydrocarbons (PAHs) on virgin polystyrene (PS) and PS marine debris led us to examine
220 ion mass spectrometry (TOF-SIMS) spectra of polystyrene (PS) films supported on silicon wafers were
222 ) encompassing the deposition of monolayered Polystyrene (PS) followed by a convective self-assembly
226 t was performed using commercially available polystyrene (PS) microparticles with a size comparable t
228 microbeads (Dynabeads((R)) anti-Salmonella), polystyrene (PS) microtitre plate and glutaraldehyde act
230 ate large area 2-D close-packed monodisperse polystyrene (PS) particle monolayers at air/water interf
231 sing droplets containing different number of polystyrene (PS) particles and by varying the applied vo
234 multaneously both as a solvent for recycling polystyrene (PS) waste and as a monomer that undergoes U
235 evice where poly(dimethylsiloxane) (PDMS) or polystyrene (PS) were used to coat the sides of a fluidi
236 ch as polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyethylene terephthalate (PET) a
237 ) and weakly on hydrophobic polymers such as polystyrene (PS), and the extent of adsorption decreased
238 fabricated using three different materials (polystyrene (PS), cyclo-olefin polymer (COP), and PDMS).
239 trixes of varying oxygen permeability, viz., polystyrene (PS), ethyl cellulose (EC) and an organicall
240 opolymerize with a norbornene-functionalized polystyrene (PS), polylactide (PLA), or polydimethylsilo
241 d for single-layer graphene transferred onto polystyrene (PS), semiconducting thienoazacoronene (EH-T
242 octyloxy)-1,4-phenylenevinylene] (MDMO-PPV), polystyrene (PS), thus breaking a new ground on the cont
243 ular depth profiling of structured polymers (polystyrene (PS)-b-polymethyl methacrylate (PMMA) block
244 m silicon oxide (Si) and 100 nm carboxylated polystyrene (PS-COOH) NPs cloaked by human plasma HC wer
246 structures were obtained with up to 97 wt % polystyrene, remarkably leaving the poly(isoprene) layer
247 The tested compounds were flowed through a polystyrene resin functionalized with an oligonucleotide
248 cordingly, the measured instantaneous CTE of polystyrene resin varied from 5.86 x 10(-5) degrees C(-1
254 created by chemically treating thermoplastic polystyrene sheets to form a thin skin layer and then he
261 ed the thermal fluctuations of a 1 mum-sized polystyrene sphere, which was placed in defined distance
263 phases nucleate exclusively on carboxylated polystyrene spheres along with calcite, whereas aragonit
264 stretching carboxylate-modified fluorescent polystyrene spheres into rod shapes with aspect ratios o
265 latinum solutions spiked with 6 mum diameter polystyrene spheres, filtered and unfiltered samples gav
267 ve polymer, poly(3,4-ethylenedioxythiophene)-polystyrene sulfonate ( PEDOT: PSS) as a cation-selectiv
268 ing polymer poly(3,4-ethylenedioxythiophene)/polystyrene sulfonate (PEDOT/PSS) which was synthesized
270 erein, we report a new approach to construct polystyrene sulfonate (PSS) threaded HKUST-1 metal-organ
271 e membrane by infiltrating sulfonated sodium polystyrene sulfonate and (2) micro-fabricated paper cha
272 e)-modified poly(3,4-ethylenedioxythiophene) polystyrene sulfonate as a transparent and stretchable a
275 m](+) (PDDA), [Polyethyleneimine](+) (PEI), [Polystyrene sulfonate](2-) (PSS) and neutral polymer Pol
277 ucleation and growth of CaCO3 in a matrix of polystyrene sulphonate (PSS), we show that the binding o
280 favorable interactions between OA-IONPs and polystyrene surfaces compared to silica, which is hypoth
281 are coupled separately onto Fe3 O4 @SiO2 and polystyrene surfaces of a unique polystyrene/Fe3 O4 @SiO
284 iocompatible protein nanorods from spherical polystyrene templates using the layer-by-layer (LBL) tec
285 affinity with the collapsed conformation of polystyrene than with the extended conformation, while t
286 n, carboxylated (PS-COOH) and amine (PS-NH2) polystyrene, the latter being a less common variant, kno
288 spofungin MICs were measured using untreated polystyrene trays and both the YeastOne and Etest assays
290 block copolymer poly(3-hexylthiophene)-block-polystyrene using a one-dimensional self-seeding techniq
291 ifferent substrate surfaces (from silicon to polystyrene), various silica precursors (TEOS, fumed sil
292 polymer polystyrene-b-poly(ethylene oxide)-b-polystyrene was investigated by means of liquid chromato
294 r and approaching surfaces of mica, gold, or polystyrene, we observed adhesion of the T4P to all of t
295 The capture anti-AFP (Ab1) was coated onto polystyrene well plates and bovine serum albumin (BSA) w
296 the jejunum or ileum, high concentrations of polystyrene were detected in the liver, kidneys, and lun
297 tyrene-block-poly(methyl methacrylate)-block-polystyrene, where the solvophobic polystyrene end block
298 is illustrated with the production of MOF-5-polystyrene wherein polystyrene is grafted and uniformly
299 bundance of polyethylene, polypropylene, and polystyrene, which covered more than 75% of all polymer
300 t plastic with low affinity for POPs such as polystyrene will have a marginal decreasing effect on bi
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