ライフサイエンスコーパス: micelle

1 he concave interfaces of a reverse spherical micelle.

2 ibility with the clinically used PEG-b-PDLLA micelle.

3 ce quenching of pyrene by the radical in the micelle.

4 in the receptor and stiffening the detergent micelle.

5 egrates into the hydrophobic interior of the micelle.

6 es, and we docked the bound structure to the micelle.

7 e stability and enzymatic degradation of the micelles.

8 with rhodopsin reconstituted into detergent micelles.

9 to self-assembly and formation of spherical micelles.

10 structure of phycocyanin and the anionic SDS micelles.

11 rk with the presence of aggregates of casein micelles.

12 egral membrane protein, OmpF, solubilised in micelles.

13 ghly similar in lipid vesicles and detergent micelles.

14 bile phase consistent with small vesicles or micelles.

15 n, because the reaction proceeds only in the micelles.

16 compared to DOX and DOX-loaded POEG-b-PCCDas micelles.

17 oceeded faster than their incorporation into micelles.

18 oes not take place in liposomes but in mixed micelles.

19 are essential for accessing SM in bile salt micelles.

20 rbonate-graft-dodecanol; PEG-PCD) to prepare micelles.

21 y encapsulation in mixed phosphatidylcholine micelles.

22 he "self-seeding" process of crystalline BCP micelles.

23 t only non-ionised quercetin partitions into micelles.

24 in we studied its interaction with bile salt micelles.

25 lycero-3-phosphocholine (LLPC, zwitterionic) micelles.

26 s, upconversion nanoparticles, and polymeric micelles.

27 tion protein drk was encapsulated in reverse micelles.

28 by studying quercetin's interaction with SDS micelles.

29 tocycle intermediates as GtACR1 in detergent micelles.

30 o lyso-myristoyl phosphatidylglycerol (LMPG) micelles.

31 vironment than are the widely used detergent micelles.

32 ptake of [(3)H]cholesterol from taurocholate micelles.

33 on monodisperse cylindrical block copolymer micelles.

34 s between proteins and mixed lipid/detergent micelles.

35 ction amounts to 66% in nanodiscs and 82% in micelles.

36 that accelerate GlpG's folding in detergent micelles.

37 edium both, spherical and elongated branched micelles.

38 precludes high monomer concentration within micelles.

39 g gamma-cyclodextrin and sodium taurocholate micelles.

40 ase are additional advantages with polymeric micelles.

41 form a silicate trimer along the surface of micelles.

42 broad range of mutual miscibilities in mixed micelles.

43 ydrophobicity and stability of the assembled micelles.

44 spectively, leaving the remaining RL in free micelles.

45 ipid monolayers and Aerosol-OT (AOT) reverse micelles.

46 a higher concentration of FFAs in the mixed micelles.

47 New folic acid (FA) coupled three layered micelles (3LM) were designed to encapsulate DNA, and the

48 hanolamine-PEG (DSPE-PEG), which forms 12-nm micelles above the critical micelle concentration, accum

49 Herein, C60-monoadduct (the head group of micelle) actually served as a nanomediator for electroni

50 Upon drying, micelle aggregation and a kinetically controlled crystal

51 the procedure in the presence of small seed micelles allows the scalable formation of low dispersity

52 on of denatured whey protein with the casein micelle, an increase in casein micelle size, and reducti

53 tions between the head groups in the reverse micelle and the test protein.

54 nt, given that the water pool in the reverse micelle and the water pore in the gyroid phase have roug

55 (4T1.2) compared to DOX-loaded POEG-b-PCCDas micelles and a micellar formulation co-loaded with DOX a

56 NMR structure of its transmembrane domain in micelles and collect structural data on overlapping frag

57 ibe the formation of diamond-shaped platelet micelles and concentric "patchy" block co-micelles by us

58 different for vitamin D-re-assembled casein micelles and control fortified milks after 21days of ref

59 me active site binds carbon monoxide in both micelles and fibers, demonstrating that the heme active

60 oidal systems, including polymers, proteins, micelles and hard spheres, have been studied in thermal

61 oid proteases, can be used both in detergent micelles and in liposomes, and contain red-shifted fluor

62 molecules that self-assemble into spherical micelles and increase the local interfacial density of C

63 tive peptides and polymers, redox-responsive micelles and nanogels, thermo- or magnetic-responsive na

64 In summary, PEG-b-PLA micelles and PLGA-b-PEG-b-PLGA sol-gels may safely enabl

65 eclinical and clinical research on PEG-b-PLA micelles and PLGA-b-PEG-b-PLGA sol-gels that has focused

66 col)-block-poly(D,L-lactic acid) (PEG-b-PLA) micelles and poly(D,L-lactic-co-glycolic acid)-block-pol

67 residues 15-24 and 29-35 in the presence of micelles and structure-inducing solvents.

68 w light on host-guest interaction in polymer micelles and such pronounced host-guest specificities in

69 The high density of micelles and variety of interactions provided by this so

70 However, unlike spherical micelles and vesicles, control over their dimensions in

71 the template interacted with the surfactant micelles and, ultimately, with the MINP receptors.

72 on (via monomer solubilization in surfactant micelles) and adherence of graft-polymer to the membrane

73 , nanoemulsions, drug-loaded block-copolymer micelles, and nanocrystal-core reconstituted high-densit

74 droxypropyl)methacrylamide (HPMA), polymeric micelles, and nanoparticle carriers are explored with re

75 ed arrangements of spherical and cylindrical micelles, and stacks of bilayers, whose structures respo

76 luble vitamin loading in re-assembled casein micelles, and to evaluate vitamin D stability of dry for

77 he hydrophobic core of amphiphilic copolymer micelles, and was used to coordinate with biocompatible

78 esence and absence of sodium dodecyl sulfate micelles, and we docked the bound structure to the micel

79 rties of P-gp in native membranes, detergent micelles, and when reconstituted in artificial membranes

80 PEG-b-PLA micelles are a first-generation platform for the systemi

81 The micelles are highly sensitive to light irradiation: (1)O

82 col)-block-poly(d,l-lactic acid) (PEG-b-PLA) micelles are nanocarriers for poorly water-soluble antic

83 between readily degradable and undegradable micelles are rather minor, points to the critical roles

84 he dual interaction ability of mixed hemi/ad-micelle array of SDS molecules not only induce an effect

85 tion of both organclay and BDTA in excess or micelle as a one pot adsorption system appears to be the

86 nted inventions and recent advances of these micelles as effective carriers for ocular drug delivery

87 Nile Red demonstrates the potential of these micelles as redox-responsive nanocarriers.

88 de units, leading to full disassembly of the micelles, as confirmed by detection of pure unimers (DLS

89 We show that these micelles associate non-covalently with the bacterial out

90 te the formation of platelet and cylindrical micelles at concentrations up to 25% solids via a one-po

91 copolymers self-assemble into bridged flower micelles at high concentrations.

92 hiphilic block copolymers that form discrete micelles at low concentrations and enter a phase of stro

93 colloidally stable electroactive fibre-like micelles based on common pi-conjugated block copolymers

94 Using a micelle-based nanoparticle therapy that recognizes integ

95 to form robust, self-supporting macroscopic micelle-based thin films with useful mechanical properti

96 ntion, multi-responsive boronate crosslinked micelles (BCM) for ovarian cancer therapy.

97 such as membranes, lipid vesicles, detergent micelles, bicelles, oriented bilayers, or nanodiscs, in

98 self-assembly into size-specific cylindrical micelle building blocks for the hierarchical constructio

99 eaction stoichiometry or aspect ratio of the micelle building blocks.

100 separating and characterizing not only pure micelles but also mixed micelles prepared from polystyre

101 et micelles and concentric "patchy" block co-micelles by using seeds of the charge-terminated homopol

102 an intrascaffold "handshake" to generate DNA-micelle cages, which have increased structural stability

103 The SAXS data for pure RL micelles can be described by prolate core-shell structur

104 Systemic administration of micelles carrying paclitaxel and rubone inhibited orthot

105 ecognition for silicic acid, followed by the micelle coalescence.

106 fferent U-shaped conformation within reverse micelles compared to within solution, which is in sharp

107 inhibitor QZ59-SSS was observed in detergent micelles compared with native or artificial membranes.

108 nonionic), all diastereomers have a critical micelle concentration (CMC) in the micromolar range.

109 oncentrations much greater than the critical micelle concentration (CMC), the fluorescence anisotropy

110 rcetin and pyrene reported a higher critical micelle concentration for bile salts than for SDS.

111 hich forms 12-nm micelles above the critical micelle concentration, accumulates heavily inside choles

112 of the fibres can be varied by altering the micelle concentration, reaction stoichiometry or aspect

113 ate is not due to a decrease in the critical micelle concentration.

114 absolute surface tension curves and critical micelle concentrations (CMC) determined for these aeroso

115 The presence of detergents at increasing micelle concentrations, on the other hand, resulted in m

116 A BDTA hydrophobic core micelle coupled with a positive electric charge forms an

117 ncluding hydrogels, polymer-drug conjugates, micelles, dendrimers, and polymersomes.

118 e with endogenous lipids, detergents, and/or micelles during blue native gel electrophoresis (BN-PAGE

119 he analysis gives complexes of two connected micelles, each containing 10 RL and one protein in the s

120 psin can be released from the octylglucoside-micelle efficiently on all three instruments (MS-mode),

121 purified human or mouse P-gp in a detergent micelle environment.

122 detergent at the binding site in a detergent micelle environment.

123 In addition, DOX-loaded POEG-b-PSSDas micelles exhibited triggered DOX release under a redox e

124 tion of disulfide linkage into POEG-b-PSSDas micelles facilitated efficient cleavage of DAS from prod

125 easing the peptides that were bound to these micelles, facilitating peptide retention in the sample a

126 nto the hydrophobic regions of Pluronic F127 micelles, followed by chemical cross-linking and subsequ

127 tion of 20-30nm, SN-38-encapsulated photonic micelles for effectively trimodal cancer therapy.

128 decanol into cetyltrimethylammonium chloride micelles for the assembly of lyotropic liquid crystals g

129 ck copolymers into size-specific cylindrical micelles for the hierarchical construction of mechanical

130 ed hydrophobic tail were cross-linked in the micelle form on the surface and in the core in the prese

131 These micelles, whether in the pure or mixed micelle form, often exist as multiple morphologies (sphe

132 The kinetics of lipolysis, micelle formation and carotenoid bioaccessibility were m

133 , while Pluronic block copolymers capable of micelle formation showed slight effects at high concentr

134 riven self-assembly for precise control over micelle formation to prepare a new recyclable catalyst p

135 exes with bile salts/fatty acids, inhibiting micelle formation.

136 Micelles formed by the self-assembly of block copolymers

137 The introduction of a micelle-forming cationic surfactant allows for the templ

138 of the present study was to investigate the micelle-forming properties of saponins from Quillaja sap

139 A micelle formulation of the 7-methine facilitated SWIR im

140 cules were enriched using oppositely charged micelles from sodium dodecyl sulfate and cetyltrimethyla

141 Oligomeric micelles from sodium undecylenate (oSUD) were chemisorbe

142 being highly water soluble, these polymeric micelles generate clear aqueous solutions which allows e

143 logy and dimensions of block copolymer (BCP) micelles has attracted interest due to the potential of

144 sappears, and the stacking ends when all the micelles have electrophoretically migrated to the bounda

145 Over the past decades, polymeric micelles have emerged as one of the most promising drug

146 Cylindrical block copolymer micelles have shown considerable promise in various fiel

147 Our data suggest that Dox-HK-MPEG-PCL micelles have the potential to be applied clinically in

148 , of linoleic acid in sodium dodecyl sulfate micelles, have been determined in terms of oxygen consum

149 mic stacking boundary formed between charged micelles (i.e., from long chain ionic surfactants) and n

150 ical analysis indicated that DOX-HK-MPEG-PCL micelles improved Dox's anti-tumor effect by enhancing t

151 lipids are incorporated into the surrounding micelle in solution, and complex formation occurs indepe

152 for sorbent systems with free surfactant or micelle in solution.

153 ns and enter a phase of strongly interacting micelles in a gradual manner with increasing concentrati

154 multaneously, and could be released from the micelles in an extended period in vitro.

155 his molecule is solubilizing the cholesterol micelles in LBC agar.

156 PEG-dendron hybrids and their self-assembled micelles in order to determine their structure-stability

157 acts between the protein and detergent/lipid micelles in the electrospray droplet.

158 Similarly, a depletion of empty micelles in the wake of a droplet swimmer causes negativ

159 tated efficient cleavage of DAS from prodrug micelles in tumor cells/tissues, leading to a higher lev

160 olactone) 1D (cylindrical) and 2D (platelet) micelles in water and alcoholic solvents via crystalliza

161 These polymers self-assemble into 28+/-5 nm micelles in water.

162 s of inhibition of the lipid peroxidation in micelles, in view of bibliographic data, have been made.

163 he DNA acting as a pseudophase, analogous to micelles, in which all reaction components are concentra

164 Here, by investigating micelle incorporation in calcite with atomic force micro

165 While micelle incorporation is the limiting factor for caroten

166 Compared to POEG-b-PCCDas micelles, incorporation of disulfide linkage into POEG-b

167 the physicochemical modifications of casein micelles induced by Ser2 and to confirm its implication

168 LXR agonists reduced SR-B1-dependent lipidic-micelle-induced Erk phosphorylation.

169 Furthermore, Dox-HK-MPEG-PCL micelles inhibited glioma growth more significantly than

170 Key features of the polypeptide-micelle interaction include the anchoring of a hydrophob

171 lectrokinetic movement of DS(-) monomers and micelles into the capillary.

172 he formation of a dilute phase of individual micelles is prevented in polyelectrolyte complexation-dr

173 id beta peptide is encapsulated in a reverse micelle, it folds into a structure that may nucleate amy

174 ed transition from spheres to large compound micelles (LCM) in dilute solution, underwent phase separ

175 olecular assembly to evolve with time from a micelle-like assembly to a vesicular assembly.

176 ns with alpha-lac and promote formation of a micelle-like complex structure.

177 of morphology of lutein ester loaded saponin micelles (LMS), cryo-TEM micrographs showed depending on

178 onounced host-guest specificities in polymer micelles may not only be interesting in drug delivery bu

179 this TSIL a cloud point extraction (CPE) or micelle mediated extraction procedure was developed for

180 he results obtained by size-dependent UF and micelle-mediated CPE do not necessarily coincide, probab

181 MNPs) by the combination of nonionic reverse micelle method and Fe3O4 nanoparticles.

182 tip of the capillary served to collapse the micelles migrating into the capillary, thereby releasing

183 d substrates residing in or on membranes and micelles must also have important signaling roles, spurr

184 ently encapsulated into a targeted polymeric micelle nano-delivery system (SUNb-PM), working in a syn

185 ular drug delivery system using unimolecular micelle nanoparticles (unimNPs) to prevent RGC loss.

186 ibited higher stability than non-crosslinked micelles (NCM) in the presence of plasma or serum.

187 geometric constraints imposed by the reverse micelles need to be considered.

188 xorubicin, self-assembled into monodispersed micelles [NP(BTZ-DOX)] with small particle sizes (20-30

189 and a unique class of photonic nanoporphyrin micelles (NPM), the extremely hydrophobic SN-38 was succ

190 The incorporation of carotenoids into mixed micelles occurred faster and reached a higher final valu

191 ose of water confined in a reverse spherical micelle of a sulfonate surfactant, given that the water

192 ic nanostructures (FIOMNs) and mixed hemi/ad-micelle of sodium dodecyl sulfate (SDS) was designed for

193 quantitatively map the intracellular fate of micelles of a recombinant polypeptide conjugated with do

194 le, low-dispersity, electroactive fibre-like micelles of controlled length from pi-conjugated diblock

195 embly of diblock copolymers into cylindrical micelles of controlled length has emerged as a promising

196 ion of low dispersity samples of cylindrical micelles of controlled length up to three micrometres.

197 f uniform, monodisperse rectangular platelet micelles of controlled size by means of seeded-growth me

198 tritrpticin (TRP3), a cathelicidin AMP, and micelles of different chemical composition.

199 es of the GPCR rhodopsin are investigated in micelles of dodecyl maltoside (DDM) and in phospholipid

200 it cell, in which 30 sub-2-nm quasispherical micelles of five discrete sizes are arranged into a tetr

201 re, we report the preparation of cylindrical micelles of length in the wide range of 70 nm to 1.10 mu

202 netically pre-programming self-assembly into micelles of varied size and shape.

203 rophobes into the self-assembled aggregates (micelles) of surfactants.

204 Polymer micelles offer the possibility to create a nanoscopic en

205 sing effect of sodium dodecyl sulphate (SDS) micelles on pH-induced colour variations of phycocyanin

206 We find that similar to ionic micelles, on one hand, such aggregates can disrupt nativ

207 d HC surfactants form only one type of mixed micelle or rather demix into two micelle populations, na

208 bility, they are often superior to detergent micelles or liposomes for membrane protein solubilizatio

209 The stability of "detergentless" micelles or microemulsions in such mixtures was proposed

210 ation in the presence of either zwitterionic micelles or monodispersed PIs.

211 regeneration of structural biopolymers into micelles or nanoparticles suspended in water has enabled

212 chain lengths from 350 Da-30 kDa in DSPE-PEG micelles, or increasing DSPE-PEG content in an array of

213 demonstrate that vitamin E-derived designer micelles, originally developed for use in synthetic chem

214 Upon reconstitution in lipid micelles, p75-TM-WT forms the disulfide-linked dimers sp

215 ith an average size of 7.7 nm, bound by oSUD micelles (particle average diameter of ca. 200 nm).

216 d and entrapped in phosphatidylcholine mixed micelles (PCS) with 96.8% efficiency (particle size 3.0+

217 y was formed at the cyclodextrin zone as the micelles penetrated this zone.

218 oline headgroup gives rise to two coexisting micelle populations at high mole fractions of the FC mal

219 pe of mixed micelle or rather demix into two micelle populations, namely, FC-rich and HC-rich ones.

220 icrystalline nanoparticles, as a function of micelle pore expander concentration or stirring rate.

221 Micelles prepared from amphiphilic block copolymers (ABC

222 rizing not only pure micelles but also mixed micelles prepared from polystyrene-poly(ethylene oxide)

223 The solid and hollow 2D micelles provide a tunable platform for further function

224 (LA)n-PTX improves PTX delivery by PEG-b-PLA micelles, providing a strong justification for clinical

225 However, PEG-b-PLA micelles rapidly release PTX, resulting in widespread bi

226 form with the assumption of only one type of micelle regardless of the mixing ratio, whereas combinin

227 bly, o(LA)8-PTX and o(LA)16-PTX in PEG-b-PLA micelles resisted backbiting chain end scission, based o

228 The mucoadhesive nature of these polymeric micelles results in enhanced contact with the ocular sur

229 , reconstituted in liposomes or in detergent micelles, revealed in all cases the existence of a uniqu

230 -PMTEGE block copolymers formed well-defined micelles (Rh approximately 9-15 nm) in water, studied by

231 igh-density lipoprotein ([S]-HDL), polymeric micelles ([S]-PM), and liposomes ([S]-LIP), that are loa

232 nding crystalline homopolymer to cylindrical micelle seeds.

233 b-PtBA)-b-M(PFS-b-PDMS)-b-M(PFS-b-PtBA) (M = micelle segment, PFS = polyferrocenyldimethylsilane, PtB

234 dine), PtBA = poly(tert-butyl acrylate), M = micelle segment].

235 1 (SR-B1, encoded by SCARB1) mediates lipid-micelle sensing to promote assembly and secretion of chy

236 catanionic coacervates consist of elongated micelles, sequester a wide range of solutes including wa

237 these sub-100nm, SN-38-encapsulated photonic micelles show great promise for multimodal cancer therap

238 Simulation of the probes inside the micelle showed that this trend could be rationalized by

239 tein in the serum, and a reduction in casein micelle size (P<.05).

240 th the casein micelle, an increase in casein micelle size, and reductions in concentrations of serum

241 herapy with SN-38-encapsulated nanoporphyrin micelles (SN-NPM) enhanced the in vitro antitumor activi

242 ediate concentrations, and finally worm-like micelle structures at high concentrations.

243 onists through multivalent presentation on a micelle surface and that the activity of already active

244 r molecules that are not held tightly to the micelle surface only detected a Na(+) amplification fact

245 nd formation, and deformation of the reverse micelle surface to facilitate interactions with the surf

246 bic residue cluster into gaps in the reverse micelle surface, the formation of a beta turn at the anc

247 This pH/reduction dual-responsive micelle system provides a new platform for high fidelity

248 i-microsecond simulation of the same reverse micelle system that was studied experimentally.

249 tantly, we demonstrate that in the detergent micelle system, commonly used for the enzymatic analyses

250 ation initiated by soybean lipoxygenase in a micelle system.

251 as retained in vitamin D-re-assembled casein micelles than control powders during storage, while vita

252 (LA)n-PTX was more compatible with PEG-b-PLA micelles than PTX, increasing drug loading from 11 to 54

253 between BamA, B, D and E, and the detergent micelle that suggest communication between BAM and the l

254 Using micelles that change their fluorescent properties upon d

255 After self-assembly into polymeric micelles, they are capable of circulating in the physiol

256 y sequestered by, and incorporated into, the micelles, thus leading to efficient labelling of the mem

257 This is because of the micelle to solvent stacking mechanism (effective electro

258 e was formed by self-assembly of BSA-dextran micelles to envelope solid lipid via a pH- and heating-i

259 mote temperature triggered attachment of the micelles to membranes, thus rescuing by self-assembly th

260 ield-enhanced conditions and were focused by micelle-to-solvent stacking.

261 us changes in the stability of the assembled micelles toward enzymatic degradation.

262 The nanoscale micelles transform into submicrometer vesicles and grow

263 Molecular imprinting within cross-linked micelles using 4-vinylphenylboronate derivatives of carb

264 a of the peripheral block in the 2D block co-micelles using Pt nanoparticles followed by dissolution

265 loop 3 (ICL3) was crystallized in detergent micelles using vapor-phase diffusion.

266 n of coordination, sequence, and morphology (micelles versus fibers) in a series of simple peptide am

267 res, including complexes with nucleic acids, micelles, vesicles, hybrid nanoparticles, and hydrogels.

268 ses used for the creation of the 2D block co-micelles was confirmed by selected area electron diffrac

269 The Na(+) concentration near anionic micelles was found to be higher than that in bulk water

270 er-compatible C60-monoadduct based imprinted micelles was synthesized by the self-assembly of vinylic

271 ates in boroxole-functionalized cross-linked micelles, we prepared nanoparticle receptors for a wide

272 surface of surface-core doubly cross-linked micelles, we synthesized water-soluble nanoparticle rece

273 Accordingly, various types of detergent micelles were extensively screened to identify one that

274 retrieval with acetonitrile, these imprinted micelles were immobilized at the surface of ionic liquid

275 More importantly, DOX-loaded POEG-b-PSSDas micelles were more effective in inhibiting the tumor gro

276 These micelles, whether in the pure or mixed micelle form, oft

277 rm strong electrostatic complexes with mixed micelles, which could decrease the transport and absorpt

278 s water-induced self-assembly into spherical micelles, which pack into a previously unknown, low-symm

279 s solubilized and highly concentrated within micelles, which results in a significantly increased deg

280 of this region in the presence of detergent micelles, which was prevented by an AH-disrupting missen

281 Moreover, non-spherical micelles-which are promising for many applications-are g

282 spherical counterion atmosphere around each micelle, while maximizing counterion-mediated electrosta

283 The alphaLA-SDS complexes contain a prolate micelle with a core radius of 11-14 A and a shell of 8-1

284 alphaLA-RL complex agree with a 12-molecule micelle with a single protein molecule in the shell.

285 e SAXS data for SDS agree with oblate-shaped micelles with a core of 20 A, core eccentricity 0.7, and

286 Patchy block copolymer micelles with a corona consisting of two chemically diff

287 that self-assemble into nanoscale polymeric micelles with a densely functionalized aptamer-displayin

288 the preparation of monodisperse cylindrical micelles with a LC poly(2-(perfluorooctyl)ethyl methacry

289 r morphologies, but the formation of uniform micelles with controllable dimensions from LC BCPs has n

290 th crystalline cores yields uniform platelet micelles with controlled dimensions.

291 In selective solvents functional micelles with core-shell structures are formed.

292 nerated by the sonication of block copolymer micelles with crystalline cores yields uniform platelet

293 titumor activity of DAS and could form mixed micelles with DOX.

294 In conclusion, re-assembled casein micelles with high loading efficiency show promise for i

295 efficient and reproducible method of loading micelles with hydrophobic drugs.

296 structure of TriA1 in dodecylphosphocholine micelles with lipid II has been determined, and molecula

297 y rapidly solubilized in the bile salt mixed micelles with no fractionation according to the FA carbo

298 particles occurs via irreversible packing of micelles with non-uniform size distribution.

299 romising route to core-corona nanoparticles (micelles) with a wide range of potential uses.

300 ase activity was observed in heme-containing micelles yet was significantly reduced in heme-containin