ライフサイエンスコーパス: microcapsule

1 hilic and hydrophobic cargos within a single microcapsule.

2 from two different locations within the same microcapsule.

3 sequestered within a permeable, charged-film microcapsule.

4 es (CPN) were incorporated into PNA hydrogel microcapsule.

5 co-microcapsules than the oil released from microcapsules.

6 better thermal stability of resistant starch microcapsules.

7 s in yogurts protected using MTGase-mediated microcapsules.

8 oss-linking ability of laccase, or CaCl2, on microcapsules.

9 em as templates to fabricate polyelectrolyte microcapsules.

10 ructure than the lentil protein-maltodextrin microcapsules.

11 f small molecules and active biomolecules in microcapsules.

12 ignificantly higher MEEs than those of GE-AG microcapsules.

13 lyoxypropylenetriamine into hollow polymeric microcapsules.

14 ferric reducing power than did whey protein microcapsules.

15 f Saccharomyces boulardii within spray dried microcapsules.

16 and aid in the generation of multifunctional microcapsules.

17 its the survivability of S. boulardii within microcapsules.

18 e-glutamine degradable polylysine (A-GD-PLL) microcapsules.

19 oxidant molecules was observed in gum arabic microcapsules.

20 t for the elasticity and osmotic collapse of microcapsules.

21 mer shell in the form of aqueous dispersible microcapsules.

22 bserved in spray-dried double emulsion (SDE) microcapsules.

23 in we report a general route to programmable microcapsules.

24 cantly affect retention of bioactives in the microcapsules.

25 c and intestinal fluids predominated for FDE microcapsules.

26 ibution of CSO on the surface and within the microcapsules.

27 tween populations of non-lipid semipermeable microcapsules.

28 the surface and in the interior of the solid microcapsules.

29 ounds and to improve the thermal behavior of microcapsules.

30 emical images obtained from each type of the microcapsules.

31 resin modified with anisole and PMMA-filled microcapsules.

32 2AP-ZnCl(2) microcapsules (0.081% (w/w) 2AP loading) and unprotected

33 The microcapsules (13-42mum) promoted protection against oil

34 histological analysis reveals a safe dose of microcapsules (20 x 10(6)), which has not lead to irreve

35 sed to incorporate living cells into the PNA microcapsules (~500 um diameter).

36 For these dual-loaded microcapsules, a programmable and sequential release of

37 However, TEM inspection of these microcapsules after an alcohol challenge revealed no evi

38 of droplet size distribution around 9 mum), microcapsules after spray drying and double emulsions af

39 Uniform core-shell alginate microcapsules (AMCs), 60-300 mum in diameter, were fabri

40 ng ideas to provide new functionality to the microcapsule and nanocapsule is layer-by-layer depositio

41 Overall, this novel design of PNA microcapsule and the one-step method of cell encapsulati

42 The pattern of release of oil from the microcapsules and co-microcapsules was similar.

43 neered thermogenic response in biocompatible microcapsules and implanted them into the left and right

44 The in-vitro digestibility of the co-microcapsules and microcapsules was studied in terms of

45 Due to the cell-like attributes of polymeric microcapsules and polymersomes, material systems are ava

46 y of encapsulated oil, microstructure of the microcapsules and protection of fatty acids, especially

47 ution with the lowest particle size for both microcapsules and the corresponding emulsions after rehy

48 between the molecule localization inside the microcapsules and the reactivity against the specific re

49 oma cells, HepG2, were encapsulated into the microcapsules and their physio-chemical properties were

50 the microcapsules (W) were evaluated for the microcapsules and two non-encapsulated systems: ethanoli

51 Conventional poly-l-lysine-cross-linked microcapsules and unencapsulated islets were included as

52 ects (e.g., polystyrene beads, drug delivery microcapsules, and living cells) are patterned in respon

53 Intracranially implanted DOX and TMZ microcapsules are compared with systemic administration

54 The light-responsive microcapsules are composed of photocleavable o-nitrobenz

55 e-modified DNA shells, and the pH-responsive microcapsules are made of a cytosine-rich layer cross-li

56 the autonomous repair of damaged materials, microcapsules are needed that release their contents in

57 After 24 h microcapsules are not observed in the target kidney when

58 The size and wall thickness of the microcapsules are precisely controlled.

59 Hollow composite microcapsules are prepared by the assembly of pre-formed

60 Polyelectrolyte complex microcapsules are prepared using a novel template- and s

61 The microcapsules are produced spontaneously by ultrasonical

62 ure while the alginate and chitosan/alginate microcapsules are spherical with a smooth surface.

63 The microcapsules are stable under typical industrial operat

64 Although the microcapsules are too large to enter the cracks, their f

65 potential effectiveness of using 2AP-ZnCl(2) microcapsules as a flavoring agent.

66 ior to homogenization led to block copolymer microcapsules, as expected.

67 estimate the half-life of anthocyanin in the microcapsule at room temperature (37 degrees C) clearly

68 Agglomeration of BSO was observed in all microcapsules at pH 4.5 due to slow gelling process and

69 ol) barium sulfate to create barium-alginate microcapsules (BaCaps) that contained hMSCs.

70 n of mechanical damage is achieved through a microcapsule-based polymeric material system.

71 tivity in intact synthetic and biodegradable microcapsules before and after cell delivery as well as

72 We manufactured two new formulations of microcapsules (BioBullets).

73 that intravenous administration of alpha2MG-microcapsules (but not empty microcapsules) promoted neu

74 ts osmotic stress, hence we generated hybrid microcapsules by mixing PEG and ALG (MicroMix) or by coa

75 This study aimed to prepare anthocyanin-rich microcapsules by spray and freeze-drying complex coacerv

76 The interior of the microcapsule can be loaded with water-soluble hydrophili

77 Moreover, the size selectivity of the microcapsules can be adjusted by changing the type of de

78 These findings suggest that the microcapsules can be applied for loading anthocyanins as

79 The microcapsules can be rendered visible during the first s

80 The interfacially assembled supramolecular microcapsules can benefit from the diversity of polymeri

81 We show that these microcapsules can find the cracks on a surface and selec

82 Due to their geometry and elasticity, these microcapsules can uniquely serve as quantitative mechani

83 S), and the third group consisted of control microcapsules (CM), with no cross-linking.

84 The all-polysaccharide based polyelectrolyte microcapsules combining copigmentation for anthocyanin e

85 Polymer microcapsules composed of liquid carbonate cores and hig

86 nt capacities of gum arabic and maltodextrin microcapsules containing antioxidant molecules (trolox,

87 le more rationale layer-by-layer assembly of microcapsules containing biologically active molecules f

88 ication of "photonic pigments" consisting of microcapsules containing dense amorphous packings of cor

89 nsport and simultaneously rupturing adjacent microcapsules containing gallium-indium liquid metal (to

90 n efficiency was high (>=89%) and oil within microcapsules containing MC exhibited higher (p < 0.05)

91 , conjugated dienes increased more slowly in microcapsules containing MC.

92 brane emulsification (ME) enabled to produce microcapsules containing procyanidins.

93 Fish oil was loaded into the microcapsule core and protected with a shell composed of

94 olic activity, indicating that the 3D PNA-10 microcapsule could be suitable to maintain better vitali

95 GG microcapsules could be readily visualized with positive-

96 n of the membrane building blocks to produce microcapsules covered in a chemically distinct, dense ne

97 with laccase (MCL), the second group was the microcapsules cross-linked with divalent cationic CaCl2

98 The first group was the microcapsules cross-linked with laccase (MCL), the secon

99 The two microcapsule DEET formulations exhibited 36-40% higher c

100 rom the PLGA-GLN pellet resulted in A-GD-PLL microcapsule degradation and eventual PC12 cell death fo

101 Uneaten microcapsules degrade and become biologically inactive w

102 These microcapsule devices provide a safe, reliable vehicle fo

103 ore effective than soluble alpha2MG or empty microcapsules (devoid of active protein).

104 hydrogel-layer (~150 nm) provides the inner microcapsule (diameter ~2.5 mum).

105 Injection of non-safe microcapsule dose leads to carriers staying in glomeruli

106 encapsulation efficiency was higher for LBL microcapsules (e.g. 99.6 +/- 0.4% for 2.5% citral) than

107 ainst the test microorganisms compared to IN microcapsules, especially at concentrations of 100mg/mL.

108 The chitosan microcapsules exhibited the maximum release rate at pH 2

109 um release rate at pH 2.5 while the alginate microcapsules exhibited the maximum release rate at pH 6

110 We show that the design of the microcapsules facilitates the suppression of incoherent

111 In this approach, a flexible microcapsule filled with a solution of nanoparticles rol

112 tudy was to produce and characterise xylitol microcapsules for use in foods, in order to prolong the

113 into chitosan-calcium alginate double layer microcapsules, for the production of a Pale Ale beer.

114 g the chitosan-calcium alginate double layer microcapsules, for the production of Riesling sparkling

115 ops, which can then be used as templates for microcapsule formation.

116 Microcapsules, formed by employing these experimental co

117 ws from the surface toward the center of the microcapsule, forming an onion-like arrangement.

118 ulations were studied: a previously reported microcapsule formulation (Formulation A); a newly-develo

119 rmulation (Formulation A); a newly-developed microcapsule formulation (Formulation B); and a non-enca

120 Hence, colloidosome microcapsule formulations successfully provide good prot

121 Spray-dried microcapsules from double (DM) and multilayered (MM) fis

122 c resonance (TD-NMR) were applied to analyse microcapsules glass transition temperature (Tg).

123 to those observed for the other two types of microcapsules (>5%, w/w).

124 The chitosan microcapsules had a brain-like structure while the algin

125 The complex coacervation based microcapsules had a significantly lower oil content (~2%

126 Whey protein microcapsules had comparably lower release rates but hig

127 During in vitro digestion, gum arabic microcapsules had high release rates of phenolics with h

128 The results showed that the microcapsules had significantly greater 2AP stability co

129 mbly of metal-organic frameworks (MOFs) into microcapsules has attracted great interest because of th

130 The prepared MOF/CW microcapsules have excellent stability and enable the st

131 The resulting BCNU-loaded PLGA microcapsules have significantly higher drug encapsulati

132 Layer-by-layer assembled microcapsules have the potential to be versatile cell de

133 idics can be used to fabricate solid-shelled microcapsules having precisely controlled release behavi

134 s for the assembly of the shell of nano- and microcapsules holds great promise for the tailor-made de

135 partial pressure of oxygen (pO2) in alginate microcapsules implanted intraperitoneally in healthy non

136 for one-step fabrication of polyelectrolyte microcapsules in aqueous conditions.

137 phology, size, and chemical structure of PNA microcapsules in cell culture media.

138 ver, we demonstrate the application of these microcapsules in encapsulation and release of proteins w

139 ucibly mitigate the CO of implanted alginate microcapsules in mice, dogs and pigs.

140 It was possible to apply the microcapsules in yogurt, without compromising the rheolo

141 In addition, a pH-responsive microcapsule-in-microcapsule system is loaded with gluco

142 The acidification of the microcapsule-in-microcapsule system leads to the trigger

143 layer (thickness of ~150 nm) that yields the microcapsule-in-microcapsule system.

144 nsive nucleic acid-based hydrogel-stabilized microcapsule-in-microcapsule systems is introduced.

145 this work also demonstrates the inclusion of microcapsules into 3D printing resins to incorporate add

146 r/antioxidant), and incorporate the obtained microcapsules into yogurt.

147 a dual-function nanoparticle-loaded hydrogel microcapsule is developed that enables graft retrieval u

148 The inner microcapsule is separated from an outer aqueous compartm

149 The formulation of these probiotics into microcapsules is an emerging method to reduce cell death

150 ng how an advancing crack interacts with the microcapsules is critical to optimizing performance thro

151 Although many techniques exist for preparing microcapsules, it is still challenging to fabricate them

152 g the o-nitrobenzyl phosphate-functionalized microcapsules, lambda = 365 nm, or subjecting the pH-res

153 by sodium caseinate alone and layer-by-layer microcapsules (LBL) stabilized by sodium caseinate and p

154 lsions and the characteristics of CEO-loaded microcapsules like morphology, moisture, wettability, so

155 ending recent observations made with dextran-microcapsules loaded with alpha2MG in experimental sepsi

156 o assemble light-responsive or pH-responsive microcapsules loaded with different loads (tetramethylrh

157 is presented to optimize the formulation of microcapsules loaded with labile compounds.

158 ioluminescent enzyme luciferase in different microcapsule locations has on activity in intact synthet

159 t and bioaccessibility, the type of fish oil microcapsules may be selected as a function of the type

160 ffects of transplanting alginate (ALG)-based microcapsules (Micro) in the confined and well-vasculari

161 different emulsifier compositions: monolayer microcapsules (ML) stabilized by sodium caseinate alone

162 WPI-CMC stabilized microcapsules not only showed the highest procyanidin co

163 Particle size analysis indicated that the microcapsules obtained had a mean particle size of 60.97

164 The optimized co-encapsulated microcapsules obtained in this work showed an improved b

165 The microcapsules obtained under optimal conditions were sto

166 Microcapsules obtained using the optimized combination o

167 The microcapsules obtained were characterised in terms of pa

168 application of spray-chilled paraffin-coated microcapsules of 2AP zinc chloride complex (2AP-ZnCl(2))

169 Additionally, microcapsules of mucilage achieved the retention of beta

170 Solid co-microcapsules of omega-3 rich tuna oil and probiotic bac

171 on the physical and structural properties of microcapsules of pure carrot juice.

172 The microcapsules of xylitol showed desirable characteristic

173 Compared with nonfluorinated alginate microcapsules, PFOB fluorocapsules increased insulin sec

174 ulated using hyperbarically-loaded polymeric microcapsules (PMC).

175 We also examine the effect of microcapsule position on cell transfection with plasmid

176 Freeze-dried double emulsion (FDE) microcapsules possessed higher total anthocyanin and tot

177 io (HR=1.38-1.44) values showed that all the microcapsules prepared correspond to the "poor" flowabil

178 The yogurt containing microcapsules, presented a pH range from 3.89 to 4.17 an

179 The microcapsules produced are extremely monodisperse in siz

180 Among four PNA microcapsule products (PNA-0, PNA-10, PNA-30, and PNA-50

181 We present a new type of microcapsule programmed with a tunable active release me

182 ion of alpha2MG-microcapsules (but not empty microcapsules) promoted neutrophil migration into perito

183 Initially, emulsion and microcapsule properties as a function of oil (20%-30%),

184 umin (OVA) and sodium alginate (AL), and the microcapsule properties were characterized.

185 aterials, allowing for fine control over the microcapsule properties.

186 coacervate microdroplets and protein-polymer microcapsules (proteinosomes) that interact via electros

187 The A-GD-PLL microcapsules provided a 3-D microenvironment for good s

188 crofluidics to produce monodisperse polyurea microcapsules (PUMC) with a limonene core.

189 Upon mechanical damage, ruptured microcapsules release a liquid indicator molecule.

190 In the simulations, signaling microcapsules release agonist particles, whereas target

191 es release agonist particles, whereas target microcapsules release antagonist particles and the perme

192 We have demonstrated that microcapsules released Lf in small intestine allowing 6.

193 m 39% to 85% for gum arabic and maltodextrin microcapsules, respectively, suggesting that this carote

194 rst-order and Higuchi models for SDE and FDE microcapsules, respectively.

195 The inulin microcapsules retained 94.1% of its antioxidant capacity

196 Rehydrated gum arabic microcapsules retained more total ACNs but less ferric r

197 All wine microcapsules revealed significant activity against medi

198 ns (3D) the dynamic process of crack growth, microcapsule rupture and progressive release of solvent

199 tal oxidation (Totox): 26.5), followed by SD microcapsules (SD-M) (34.9) and RPO (56.7).

200 SEDS microcapsules (SEDS-M) were the most oxidatively stable

201 t, the anisotropic single-crystal-containing microcapsules selectively display-at certain orientation

202 anocarriers for hydrophobic molecules in the microcapsule shell.

203 to pH = 5.0, results in the cleavage of the microcapsule shells and the release of the loads.

204 These microcapsules show non-iridescent structural colors that

205 The SIO microcapsules showed a high encapsulation efficiency of

206 The lentil protein-maltodextrin-alginate microcapsules showed better oxidative stability and had

207 The empty microcapsules showed capacity to scavenge all the studie

208 The microcapsules showed high stability in gastric condition

209 r transform infrared (FT-IR) spectroscopy of microcapsules showed peaks in the region of 900-1300cm(-

210 CS-CMS microcapsules showed significantly higher MEEs than thos

211 t the antibacterial activity of the obtained microcapsules significantly depends on both citral conce

212 ater activity, moisture and oil content, and microcapsule size distribution was investigated.

213 to trap a small hydrophilic molecule in the microcapsule skin as cargo.

214 aim of this work was to produce solid lipid microcapsules (SLMs) loaded with AA using microfluidic t

215 ological characterization indicated that the microcapsules so obtained were oval to round in shape an

216 omitant increase in oil droplet diameter and microcapsule surface oil content, and a decrease in oil

217 In addition, a pH-responsive microcapsule-in-microcapsule system is loaded with glucose oxidase (GOx)

218 The acidification of the microcapsule-in-microcapsule system leads to the triggered unlocking of

219 Self-healing is achieved with a dual-microcapsule system utilizing epoxy-amine chemistry in a

220 of ~150 nm) that yields the microcapsule-in-microcapsule system.

221 id-based hydrogel-stabilized microcapsule-in-microcapsule systems is introduced.

222 anthocyanin retention during storage for all microcapsules tested.

223 acids was higher in the oil released from co-microcapsules than the oil released from microcapsules.

224 This protocol details methods to create microcapsules that are visible by X-ray, ultrasound (US)

225 ical processing ensures allergen-free pollen microcapsules that can be loaded with vaccine antigens.

226 we develop models for a colony of synthetic microcapsules that communicate by producing and releasin

227 l modeling, we design colonies of biomimetic microcapsules that exploit chemical mechanisms to commun

228 cles with EDTA yields the stimuli-responsive microcapsules that include the respective loads.

229 The use of this approach to fabricate microcapsules that only release their contents when expo

230 The type of fish oil microcapsules, the processing and/or culinary cooking an

231 Tocotrienol microcapsules (TM) were formed by firstly preparing Pick

232 e applied dextran-based layer-by-layer (LbL) microcapsules to deliver alpha-2-macroglobulin (alpha2MG

233 olayered (MO) and multilayered (MU) fish oil microcapsules to meat model systems and determines the e

234 by create adhesion gradients that propel the microcapsules to move.

235 da = 365 nm, or subjecting the pH-responsive microcapsules to pH = 5.0, results in the cleavage of th

236 Selective cytotoxicity of the DOX-D-loaded microcapsules toward cancer cells is demonstrated.

237 address the cytotoxicity of the DOX-D-loaded microcapsules toward MDA-MB-231 breast cancer cells and

238 unosuppression, but thus far islets in large microcapsules transplanted in the peritoneal cavity have

239 Nevertheless, samples containing microcapsules up to 5%wt were not distinguished from the

240 Methods to make microcapsules - used in a broad range of healthcare and

241 ing tocotrienols, which was then gelled into microcapsules using alginate and chitosan.

242 Thus, the formulation of these bacteria into microcapsules using appropriate biomaterials is a promis

243 Microencapsulation efficiency (MEE) of the microcapsules varied from 84.9% to 94.7%.

244 ferric reducing antioxidant activity of the microcapsules (W) were evaluated for the microcapsules a

245 f nanoparticles is made possible by the thin microcapsule wall (comparable to the diameter of the nan

246 M) revealed that the internal surface of the microcapsule was honeycomb-like networks containing nonh

247 t activity of the intestinal fluids when the microcapsule was spray-dried with pure W.

248 where the controlled release function of the microcapsules was clearly exhibited.

249 release of oil from the microcapsules and co-microcapsules was similar.

250 ro digestibility of the co-microcapsules and microcapsules was studied in terms of survival of L. cas

251 g time, TOTOX values of SDASO in MRP-derived microcapsules were 29-87% lower than that of the non-cro

252 rried out every 15 days, and the most stable microcapsules were achieved with maltodextrin DE(4-7) pr

253 The microcapsules were also additionally analyzed for the pa

254 ability, and chemical composition of the PNA microcapsules were analysed by light microscopy, fluores

255 Thirteen microcapsules were analysed by scanning electron microsc

256 and droplet size distribution of redispersed microcapsules were analyzed.

257 tal oil ratios in all the three types of the microcapsules were closely similar to the original non-p

258 ed on the surface and in the interior of the microcapsules were compared based on the average spectra

259 n were preloaded in CaCO3 scaffold, and then microcapsules were created by coating the sacrificial Ca

260 nanofibre-integrated alginate (PNA) hydrogel microcapsules were designed using NIM technology.

261 oxidant capacity and color difference of the microcapsules were determined.

262 The microcapsules were evaluated for particle size, accelera

263 The microcapsules were evaluated structurally with respect t

264 roperties and release characteristics of the microcapsules were evaluated.

265 The microcapsules were formed using two different microfluid

266 Multi-core microcapsules were formed when the mixed microencapsulat

267 The microcapsules were further classified into three sub-gro

268 ween aggregates of 0.5-mm or 1.5-mm alginate microcapsules were identified in vivo by looking at thei

269 The microcapsules were loaded with Cur up to about 55% w/w w

270 an macrophage phagocytosis: in both settings microcapsules were more effective than soluble alpha2MG

271 The effect of cross-linking agents on the microcapsules were more significant when the microcapsul

272 vels of anthocyanin losses in blueberry wine microcapsules were much greater: 19.9% (HP-beta-CD) and

273 The microcapsules were multinucleated, not very water-solubl

274 s showed that spherical nano-, submicro- and microcapsules were obtained through both techniques, alt

275 Blueberry ACN microcapsules were prepared from two wall materials (whe

276 The microcapsules were prepared with two different emulsifie

277 microcapsules were more significant when the microcapsules were produced by microfluidics.

278 In this study, chia seed oil (CSO) microcapsules were produced using three types of shell m

279 tivities of blackcurrant and chokeberry wine microcapsules were stable and remained unchanged during

280 The microcapsules were subsequently placed within a poly(eth

281 bited a SICA effect when the cPPA core-shell microcapsules were suspended in ion-containing acidic me

282 Significant amounts of Lf released from microcapsules were then absorbed into bloodstream and ac

283 al characteristics and microstructure of the microcapsules, were investigated.

284 an efficient encapsulation of alpha2MG into microcapsules, which enhanced i) human leukocyte recruit

285 he simulated gastric fluid was found for SDE microcapsules, while erosion-controlled release in simul

286 observations, we developed cPPA programmable microcapsules whose payload release rates depend on the

287 Specifically, the creation of a bimetallic microcapsule with controlled payload release and precise

288 Microcapsules with 20% oil, 2% protein and 18% maltodext

289 Polymeric microcapsules with a light-absorbing dye incorporated in

290 ds from bilberries was achieved by designing microcapsules with bilberry seed oil (BSO) distributed i

291 ses microfluidic droplets to generate porous microcapsules with easily customizable functionality.

292 tions and geometrical characteristics of the microcapsules with exceptional precision.

293 dy demonstrated the formulation of oxidative microcapsules with natural materials present in chitosan

294 e progress made so far of bringing nano- and microcapsules with shells of densely packed colloidal pa

295 owever, it remains a challenge to obtain MOF microcapsules with size selectivity at the molecular sca

296 ort materials to assemble MOF/cell wall (CW) microcapsules with size-selective permeability.

297 tions was suitable for spray drying, wherein microcapsules with smooth and spherical morphologies wer

298 ic (GA) coacervates was optimized to produce microcapsules with superior oxidative stability compared

299 epresented the best wall material to produce microcapsules with the highest entrapment efficiency ( a

300 icles (PHMs) are thin-walled, hollow polymer microcapsules with tunable nanoporous shells.

301 epoxy self-healing material, 150 um diameter microcapsules within 400 um of the crack plane are found