ライフサイエンスコーパス: micellar

1 due to the solubilisation of catechin in pre-micellar aggregates and then in micelles.

2 more hydrophilic molecules forming nanosized micellar aggregates including peptide nanofibres, molecu

3 ned in dimethylsulfoxide, while nanorods and micellar aggregates were observed in aqueous solutions.

4 to detect the first hybrid silica-surfactant micellar aggregates, prior to the precipitation of the m

5 fusion of polymeric ligands into cylindrical micellar aggregates.

6 e tumor model studies demonstrate that these micellar agonists have therapeutic efficacy in vivo.

7 emblies that are the building blocks of both micellar and chromonic lyotropic liquid crystals.

8 l interactions under a fairly broad range of micellar and environmental conditions.

9 sensitive to structural differences between micellar and lamellar aggregates.

10 ar phase promotes on-pathway fibrils, pseudo-micellar and micellar phases promote predominantly off-p

11 In vitro, physically loaded micellar and SCK nanotherapeutics demonstrated IC50 valu

12 In this work various micellar and thermodynamic parameters of SDS like critic

13 We show that these micellar aptamers retain their native secondary structur

14 DSCs, was encapsulated within the L2 inverse micellar aqueous domains of the lipid core of these nano

15 rotein code" that directs self-assembly into micellar architectures in aqueous conditions.

16 l be discussed in detail, including multiple micellar as well as high internal phase emulsion templat

17 sed copolymer junction and disruption of the micellar assembly.

18 evant changes in temperature could influence micellar behavior of bile salts, and in turn whether thi

19 rical micelles of PS(n)-AC(60), indicating a micellar behavior that changes from small molecular surf

20 ry to ensure stability in transit, but rapid micellar breakdown and concomitant drug release, when in

21 e, behaved similarly, with ~75% reduction in micellar breakdown at 25 degrees C compared to 37 degree

22 C showed STC to have a U shaped reduction in micellar breakdown between 37 degrees C and 15 degrees C

23 Thus micellar breakdown of bile salts is essential for their

24 We thus studied micellar breakdown of STC using isothermal titration cal

25 The micellar brushes can also be grown on ultrathin two-dime

26 ensity, length, and coronal chemistry of the micellar brushes can be precisely tuned, and post-growth

27 that involves the fabrication of cylindrical micellar brushes on a silicon wafer through seeded growt

28 with entangled, branched, and multiconnected micellar bundles, as evidenced by electron microscopy.

29 sclera was significantly prolonged with the micellar carrier systems as compared to the control afte

30 Micellar carrier systems can be a suitable transscleral

31 These micellar carrier systems can be efficiently delivered in

32 study was to investigate the feasibility of micellar carrier systems for sustained drug delivery in

33 sport experiments were conducted using these micellar carrier systems in side-by-side diffusion cells

34 ound that the solubilization capacity of the micellar carrier systems increased as the total lipid co

35 The micellar carrier systems were first characterized for th

36 after cathodal iontophoretic delivery of the micellar carrier systems, whereas more than ~50% of DEX

37 Saturated DEX solution without the micellar carriers was used as a control.

38 y protein isolate (WPI) solutions as well as micellar casein (MC) dispersions and mixtures were treat

39 olymer nanoblends were synthesized to detect micellar casein (MC), the main milk protein and an indic

40 peptides generated by triptic hydrolysis of micellar casein and beta-casein from bovine milk have be

41 sein matrices were prepared, by renneting of micellar casein concentrate (MCC), with modulation of sa

42 is work was to monitor the digestion of milk micellar casein in the porcine upper intestinal tract an

43 alcium phosphate and the ratio of soluble to micellar casein.

44 In this study, structural changes in micellar caseins and whey proteins due to high pressure-

45 Micellar catalysis enables copper-catalyzed silylcuprati

46 Application of micellar catalysis holds much promise for encoded chemis

47 catalysis under mild conditions, enabled by micellar catalysis in recyclable water as the reaction m

48 formed in situ and used in combination with micellar catalysis, catalyze Suzuki-Miyaura cross-coupli

49 The use of micellar catalysis, where water is the global reaction m

50 ouplings are run can be found in the form of micellar catalysis, wherein nanoparticles composed of ne

51 g delivery but also for applications such as micellar catalysis.

52 hermodynamic parameters of SDS like critical micellar concentration (CMC), standard Gibbs free energy

53 ociate to form micelles, termed the critical micellar concentration (CMC).

54 these exist as micelles above their critical micellar concentration (CMC).

55 lipophilic balance (HLB) value, and critical micellar concentration (CMC).

56 ged, and this lipid displays a high critical micellar concentration compared to housekeeping phosphol

57 taurine, which promotes a high intraluminal micellar concentration to facilitate lipid absorption.

58 cholate at concentrations below the critical micellar concentration, and even under hypertonic condit

59 dynamic light scattering, above the critical micellar concentration, the latter being determined by i

60 roach to the model-free analysis of critical micellar concentrations (CMCs) of surfactant mixtures th

61 otes RPT aggregation at both submicellar and micellar concentrations via non-specific binding with un

62 assemble into small micelles at low critical micellar concentrations, demonstrating that the short br

63 etal-catalyzed reactions have been run under micellar conditions to evaluate this surfactant relative

64 pled to an online radiometric detector under micellar conditions using 1-2% (v/v) 1-butanol mobile ph

65 oid content in certain samples; however, the micellar content was generally not lower for processed p

66 ribed by two drug partitioning coefficients (micellar core/shell K(p1) ~ 24, and shell/bulk solvent K

67 pening polymerizations of dithiolanes in the micellar cores to induce the cross-linking and gelation

68 Micellar coverage was approximately 50% of the MNP-oSUD

69 phobic polystyrene end blocks associate into micellar cross-links in the versatile ionic liquid 1-eth

70 selective detection of cyanide in an aqueous micellar CTABr solution.

71 STAT3 inhibition with micellar curcumin also suppressed postablation stimulati

72 ith or without a STAT3 inhibitor (S3I-201 or micellar curcumin, eight arms).

73 or an important comparison of AOT at smaller micellar (curved) and planar oil-water interfaces.

74 ate the great potential of enzyme-responsive micellar delivery platforms due to the ability to tune t

75 orce and diffusion constants appropriate for micellar diffusion and provide a measure of autochemotac

76 with acetonitrile and then diluted with the micellar diluent (demonstrating the reduction of tedious

77 d by injection of a long plug of sample in a micellar diluent after injection of a CD solution plug i

78 We show that LHC proteins form micellar, disc-shaped aggregates that are kinetically st

79 Aqueous micellar dispersions enabled compound synthesis under of

80 arative pharmacokinetic study of a nanoscale micellar docetaxel (DTX) prodrug, Procet 8, and commerci

81 In this manuscript, we present a novel micellar drug delivery system that is not only capable o

82 plied to introduce these interactions to the micellar drug delivery systems, as well as the effects o

83 ffects, we developed a unique tumor-targeted micellar drug-delivery platform.

84 An accurate, simple and rapid micellar electrokinetic capillary chromatographic method

85 of nitromidazole residues in egg by means of micellar electrokinetic capillary chromatography in comb

86 Micellar electrokinetic capillary chromatography with el

87 noparticles was developed through the use of micellar electrokinetic chromatography (MEKC) coupled to

88 A simple, inexpensive micellar electrokinetic chromatography (MEKC) method wit

89 of the SSC is demonstrated with LSERs for 74 micellar electrokinetic chromatography (MEKC) systems ta

90 y micelle to cyclodextrin stacking (MCDS) in micellar electrokinetic chromatography (MEKC) using sodi

91 ion of transient isotachophoresis (tITP) and micellar electrokinetic chromatography (MEKC) with subse

92 54 distinct systems and 16 decoy systems) in micellar electrokinetic chromatography (MEKC).

93 ds: capillary zone electrophoresis (CZE) and micellar electrokinetic chromatography (MEKC).

94 k samples previous to their determination by micellar electrokinetic chromatography (MEKC).

95 es the development of a methodology based on micellar electrokinetic chromatography for the separatio

96 ic separation of dopamine and catechol and a micellar electrokinetic chromatography separation of dop

97 mance liquid chromatography systems, and the micellar electrokinetic chromatography system of sodium

98 ictions and experimental tests show that the micellar electrokinetic chromatography system of sodium

99 st dimension analysis were then separated by micellar electrokinetic chromatography using sodium dode

100 the separation of dopamine and serotonin by micellar electrokinetic chromatography with amperometric

101 Micellar electrokinetic chromatography with electrochemi

102 a method for cotinine analysis by combining micellar electrokinetic chromatography with enrichment t

103 A new chiral micellar electrokinetic chromatography-laser induced flu

104 Furthermore, the micellar electrolyte promotes a transformation of one of

105 and mixed (anionic and nonionic surfactants) micellar eluent for determination of the total PET radio

106 line-geranate species in blood indicative of micellar/emulsion structures which eventually dissociate

107 Of the micellar ensemble of helical conformations only a limite

108 zinc powder, TMEDA, and an alkyl halide in a micellar environemnt containing catalytic amounts of Cu(

109 one should rationally choose the appropriate micellar environment to preserve native protein folding.

110 a(1-42) indeed oligomerizes over time in the micellar environment, forming hexamers with collision cr

111 beta-Sheet formation could be induced by a micellar environment, similarly to that of the parent pe

112 clohexadienone transients in homogeneous and micellar environment.

113 rane proteins are often studied in detergent micellar environments (proteomicelles), but how such pro

114 es its native three-dimensional structure in micellar environments but, remarkably, near-native helic

115 nnel function, and the measured stability in micellar environments with differing physicochemical pro

116 probe the micellar solubilisation and inter-micellar exchange of polyphenols using the 2,2-diphenyl-

117 ion (CPE) in which only a few microliters of micellar extracting phase is sufficient for determinatio

118 We used reverse micellar extraction to achieve this goal and carried out

119 the lipolysis induced by GTL, increased the micellar form of its fatty acid, lowered the increase in

120 Transformations among canonical micellar forms of polymer assemblies-spherical micelles,

121 d to DOX-loaded POEG-b-PCCDas micelles and a micellar formulation co-loaded with DOX and DAS.

122 in and beta-carotene bioaccessibility to the micellar fraction (and also carotenoid bioavailability)

123 educed carotenoid levels and transfer to the micellar fraction.

124 lipoteichoic acid (LTA) was identified in a micellar fraction.

125 is, particle size, and zeta potential of the micellar fractions were investigated.

126 tion between two molecular moieties, for the micellar hydrophobic core, tends to expose a reacting fr

127 The same micellar imprinting applied to simple as well as complex

128 The micellar incorporation of carotenoids (lycopene, alpha-

129 sitive linear relation was found between the micellar incorporation of carotenoids and lipid digestio

130 lglycerides, formation of FFAs and MAGs, and micellar incorporation of carotenoids, FFAs and MAGs.

131 Rate constants of carotenoid micellar incorporation were inversely proportional to th

132 O when it reacts with a radical probe in the micellar interface.

133 different strategies for the preparation of micellar IPECs, i.e., structures where such IPEC domains

134 Here, we developed docetaxel (DTX)-loaded micellar-like nanoparticles (MLNPs), designed to address

135 r these data demonstrate that the terpolymer micellar-like nanoparticles with reducible crosslinks ha

136 hase raises the fundamental question whether micellar-like spheres forming 3D phases generated from o

137 This demonstration of chirality in micellar-like spheres of a Frank-Kasper phase raises the

138 hirality of classic isotropic supramolecular micellar-like spheres, generated from conical dendrons,

139 o 480 conical dendrons self-assemble to form micellar-like spheres, with a molar mass of up to 1.1 x

140 A micellar liquid chromatographic method was developed for

141 mbrane liquid chromatography (IAM-LC) and by micellar liquid chromatography (MLC) employing sodium do

142 ofloxacin, ciprofloxacin and enrofloxacin by micellar liquid chromatography - fluorescence detection

143 bolite analysis of PET radioligands based on micellar liquid chromatography using an anionic surfacta

144 measurements of the elastic constants in the micellar lyotropic liquid crystals (LLCs) that are forme

145 1-butyl-3-methylimidazolium bromide (BMIMBr) micellar matrix with a conductivity 4 times greater than

146 lectrocatalytic activity in both aqueous and micellar media toward the oxidation of NIC at Britton-Ro

147 ji-Trost reaction, applied in a photochromic micellar media under conventional heating and microwave

148 tes under N(2) atmosphere in homogeneous and micellar media was investigated by means of steady-state

149 Inside the confined micellar media, with laser flash photolysis corroborated

150 Safranine O) are not oxidized in the reverse micellar media.

151 roxybenzophenone derivatives was observed in micellar media.

152 The use of SDBS as the micellar medium enhanced the fluorescence intensities of

153 sent in the hydrophobic core of the confined micellar medium in aqueous surfactant is described for t

154 as found that the PEDOT generated in aqueous micellar medium possesses relatively shorter polymeric c

155 An anionic micellar medium was added to the mobile phase for increa

156 nd autoxidation of linoleic acid in Tween 20 micellar medium) and compared with three widely used ant

157 The coupling only occurs in an aqueous micellar medium, where a radical process is likely, supp

158 lecules target Na(+) ions in nanospaces near micellar membranes with excellent selectivity against H(

159 recognized as a sequence of self-assembling micellar mesophases.

160 and even the experimental elucidation of the micellar mixing behavior of surfactant mixtures remain c

161 We present a micellar model of fl TIA1 wherein RRM2 and RRM3 are colo

162 able of successfully characterizing multiple micellar morphological evolutions (induced by the additi

163 ar concentration range [>0.25 (wt) %], their micellar morphological formation of spheres, cylinders,

164 phiphiles exhibited versatile self-assembled micellar morphologies which can be tuned by changing var

165 C) block can provide additional ways to vary micellar morphologies, but the formation of uniform mice

166 cidic pH values and also induces a spherical micellar morphology at high pH and concentration ranges.

167 ion range of equal or less than 0.25 (wt) %, micellar morphology of the series of PS(n)-AC(60) studie

168 In the second type of micellar nanocarrier the hydrophobic molecular cargo was

169 hese amphiphilic hybrids self-assembled into micellar nanocarriers with their cargo covalently encaps

170 g or probe molecules from stimuli-responsive micellar nanocarriers.

171 The Actinia-like micellar nanocoagulant has a core-shell structure and re

172 Here we show an innovative biomimetic micellar nanocoagulant that imitates the structure of Ac

173 hen injected into mice, the Herceptin-loaded micellar nanocomplex demonstrates better tumour selectiv

174 The micellar nanocomplex is obtained by complexation of olig

175 er proteins leads to the formation of stable micellar nanocomplexes, which have greater anticancer ef

176 hiphilic hybrids self-assemble in water into micellar nanocontainers that can disassemble and release

177 )-loaded PLGA MS, CM2 strongly prevented the micellar nanoenvironmental pH (pH 6.6 within 5days and t

178 We therefore developed a micellar nanoparticle (NP) to encapsulate and colloidall

179 esign and synthesis of multifunctional lipid-micellar nanoparticles (LMNs) containing Mn oxide (M-LMN

180 The one-pot synthetic approach yielded micellar nanoparticles at high concentrations and at sca

181 Micellar nanoparticles based on linear polyethylene glyc

182 We demonstrate that polymeric micellar nanoparticles can serve as a carrier and help t

183 ymer conjugate that assembles into spherical micellar nanoparticles displaying a dense shell of nucle

184 ar MRI of collagen, paramagnetic/fluorescent micellar nanoparticles functionalized with a collagen-bi

185 The micellar nanoparticles have been decorated with a high-a

186 on of individual amphiphilic block copolymer micellar nanoparticles in solution, in real time with na

187 DNA-paclitaxel conjugate, which forms stable micellar nanoparticles in solution.

188 lymeric amphiphiles assembled into spherical micellar nanoparticles that undergo a morphology transit

189 We describe the preparation of the synthetic micellar nanoparticles together with their characterizat

190 The size of the micellar nanoparticles was tuned by varying the lengths

191 Micellar nanoparticles were formed by a spatially segreg

192 DNA-containing micellar nanoparticles with distinctly different and hig

193 lymer amphiphiles are assembled as spherical micellar nanoparticles, and undergo a morphological tran

194 olymers self-assembled into 25-30nm diameter micellar nanoparticles.

195 We report a (1)O2-responsive micellar nanoplatform subject to considerable size-expan

196 lusion, we have developed a mPEG-b-PLA based micellar nanoplatform that could prevent drug resistance

197 The fabricated Targeted Micellar Nanoprobe (TMNP) had exceptionally high encapsu

198 lymer and permits it to self-assemble into a micellar nanostructure in water.

199 induce the cross-linking and gelation of the micellar network.

200 egree of atomic ordering is observed for the micellar NPs in H(2) atmosphere at all sizes studied, po

201 Simulations of a recent micellar nuclear magnetic resonance structure of the nat

202 vesicles under the same conditions, both the micellar nucleation event and the subsequent evolution i

203 tion regimes containing non-micellar, pseudo-micellar or micellar phases.

204 o of ten tumors treated with either PEG-PDLA micellar or nanoemulsion formulation recurred after the

205 ve not been observed in non-atomic (that is, micellar or nanoparticle) systems, where real-space info

206 It is based on the induction of micellar organised media by using Triton X-100 as an ext

207 ompared to that of the intravenous Cremophor micellar paclitaxel solution used off-label in previous

208 excels at removing redundant information for micellar phase characterization and retaining principal

209 ads to a comprehensive interpretation of the micellar phase classification.

210 While the non-micellar phase promotes on-pathway fibrils, pseudo-micel

211 Micellar phase separation at cloud point temperature of

212 roducts (i.e. contained within the bile salt micellar phase).

213 micellar phase and Peak B (340-440nm) on the micellar phase.

214 iminated the affinity of the analytes to the micellar phase.

215 otes on-pathway fibrils, pseudo-micellar and micellar phases promote predominantly off-pathway oligom

216 btle differences among those closely located micellar phases.

217 t is ineffective in defining the grouping of micellar phases.

218 containing non-micellar, pseudo-micellar or micellar phases.

219 gies (barge vs. tanker), in which liposomal, micellar, porous silica, polymeric, viral, noble metal,

220 ined FA concentration regimes containing non-micellar, pseudo-micellar or micellar phases.

221 lipoprotein A1 (apoA1) chains, (2) the lipid micellar-pseudolamellar organization, and (3) the solven

222 factor of the analytes in the presence of a micellar pseudostationary phase.

223 re and chemical composition of size-selected micellar Pt nanoparticles ( approximately 1 nm) supporte

224 ontaining aza-beta(3)-amino acids in aqueous micellar SDS were determined and demonstrate that the hy

225 cyclohexane, acetonitrile, and methanol) and micellar (SDS) solution was investigated by means of tim

226 ood agreement with the classification by the micellar selectivity triangle (MST).

227 e full range of exine types, was obtained by micellar self-assembly.

228 Computer simulations indicate that micellar shape changes are associated with different bin

229 d diagnostic assay that employs fluorescent, micellar silica nanosensors capable of specifically dete

230 when cast into thin films and their reduced micellar size in solution.

231 eic acid shell of the resulting cross-linked micellar SNA enhances their stability in physiological m

232 ere a spectrophotometric method to probe the micellar solubilisation and inter-micellar exchange of p

233 the role of cowpea peptide fractions in the micellar solubilisation of cholesterol, in the 3-hydroxy

234 l, as indicated by inhibition of cholesterol micellar solubility and pancreatic lipase activity, was

235 owpeas were more effective in inhibiting the micellar solubility of cholesterol than the raw ones but

236 this second part, the interplay between the micellar solubilization of (pro)vitamins (beta-carotene

237 The kinetics of micellar solubilization of lipophilic micronutrients (bi

238 en by interfacial Marangoni flows induced by micellar solubilization of the oil phase.

239 caprylin digestion (intestinal lipolysis and micellar solubilization).

240 nhance biodegradation of soil-sorbed PAHs by micellar solubilization, which increase the cell exposur

241 trated by the long injection of samples in a micellar solution followed by injection of a cyclodextri

242 on repeated dosing, the paclitaxel/Cremophor micellar solution showed cumulative toxicity whereas the

243 The samples were ultrasonicated in a micellar solution, free of organic solvent, to extract t

244 ometer-sized particles immersed in a nematic micellar solution.

245 ciency, relative to the paclitaxel/Cremophor micellar solution.

246 resent study reveals the effect of non-ionic micellar solutions of Brij30 and Brij35 on the extent of

247 adical probes 1 in buffered (pH 7), aqueous, micellar solutions of reduced Triton-X 100.

248 fferent surfaces upon water evaporation from micellar solutions of triblock copolymers containing a c

249 consider the flow of two semidilute wormlike micellar solutions through microposts, focusing on their

250 ol and oleuropein are investigated in pH 5-6 micellar solutions through the reduction of the DPPH rad

251 europium(III) at wavelengths up to 450 nm in micellar solutions, and its performance was compared to

252 A one-pot synthesis of micellar spherical nucleic acid (SNA) nanostructures usi

253 rtant interplay between molecular structure, micellar stability, and cell internalization pathways, p

254 usion dynamics and aggregation of PAs in the micellar stage.

255 We show that the micellar state of an inhibitory lipid can have a very si

256 d different bile salts in the submicellar or micellar state was investigated by intrinsic fluorescenc

257 propriate for micellization and, when in the micellar state, does not self-quench.

258 ended the study to the biologically relevant micellar state, using, to our knowledge, a novel reactio

259 es show depressed pyrogenicity in both free (micellar) state and in liposomal formulations when teste

260 Under certain flow conditions, micellar structural transitions follow different traject

261 This polymer assembles into a micellar structure in water.

262 troscopy (2D DOSY) NMR was used to probe the micellar structure of sodium dodecyl sulfate (SDS) and s

263 ase was doubled through cross-linking of the micellar structure to form SCKs.

264 smembrane association is entirely based on a micellar structure, we propose a revised model for the a

265 may have complex effects on the membrane or micellar structure.

266 Micellar structures and nanoporous patterns formed after

267 DLS and TEM rule out the formation of micellar structures and suggest that SP-B(1-25) promotes

268 to facilitate the formation of the branched micellar structures as a kinetically trapped morphology.

269 The self-assembly of micellar structures from diblock polymers that contain h

270 nd over the past half-century, these natural micellar structures have inspired a vast diversity of in

271 poly(2-vinylpyridine) arms) and unimolecular micellar structures serve as nanocarriers for hydrophobi

272 onsequently, the outer monolayer forms mixed micellar structures within the outer monolayer.

273 uestering their aggregation-prone regions in micellar structures, where the very soluble N-terminal d

274 as compared to the states observed in mixed micellar structures.

275 ion ranges based on the expected predominant micellar structures.

276 ough compartmentalization using a core-shell micellar support in an aqueous environment.

277 released peptide monomers were bound to the micellar surface.

278 We demonstrate that chemotaxis along micellar surfactant gradients can guide these swimmers t

279 ale oil droplets of different chemistries in micellar surfactant solutions can result in predator-pre

280 perties of sodium dodecylsulfate (SDS) based micellar system and thus making it appropriate for food

281 more effective additive in order to make SDS micellar system better for its potential applications as

282 rent polarity and with peroxyl radicals in a micellar system mimicking the amphiphilic environment of

283 This redox-responsive prodrug micellar system provides an attractive strategy for effe

284 ic-C60-monoadduct with sodium dodecylsulfate micellar system, in the presence of chlorambucil as a mo

285 rin (Gd-Tx) complex encapsulated in an IVECT micellar system, stabilized through Fe(III) cross-linkin

286 rature was found to be 307.5 K for the mixed micellar system.

287 cs depend intimately on the specific reverse micellar system.

288 a3 (hPLCbeta3) were evaluated in a cell-free micellar system.

289 acidity and basicity (a), and the cluster IV micellar systems are characterized by their strong hydro

290 explores the use of SDS-salicylic acid based micellar systems for their potential use in fruits posth

291 Micellar systems have excellent food applications due to

292 lysis, we found several key aspects of mixed micellar systems that preserve the activity of hA(2)aR,

293 nation of partition constants of radicals in micellar systems was thus validated as a reliable and se

294 by the formation of inclusion complexes and micellar systems with higher solubility values obtained

295 We established a composite micellar thermosensitive hydrogel made of clinically app

296 This micellar to monomer transition may involve complex therm

297 mic clusters of ordered lipids in comparable micellar topology and disagrees with some recent interpr

298 This species demonstrates various micellar transformations upon leaving equilibrium/nonequ

299 ults open perspectives to the use of aqueous micellar two-phase systems as an integrative methodology

300 d liquid-liquid extractions by using aqueous micellar two-phase systems was evaluated as potential to