ライフサイエンスコーパス: particle size

1 etics, product distributions, and changes in particle size.

2 attern that was strongly depended on the MPs particle size.

3 n the out-of-plane displacement depending on particle size.

4 tion in plant and insects was independent of particle size.

5 that the electron transfer is dependent upon particle size.

6 le with vertical thickness comparable to the particle size.

7 rticles (NPs), are strongly dependent on the particle size.

8 nt on particle composition, and therefore on particle size.

9 n of smaller particles, reducing the average particle size.

10 tron transfer process that is independent of particle size.

11 particle size distribution, and reduced mean particle size.

12 matite with greater surface area and smaller particle size.

13 aircase that is correlated with the measured particle size.

14 ed to about a threefold increase of the mean particle size.

15 er-scale variations in both redox status and particle size.

16 ted by HXL-SOA, likely due to differences in particle size.

17 ion of particulate mass and determination of particle size.

18 , excellent structural robustness, and small particle size.

19 en the measured and modeled effectiveness by particle size.

20 timizing column length, eluent velocity, and particle size.

21 known skin irritants, and a modest change in particle size.

22 icroplastics (i.e., <1 mm) with a decreasing particle size.

23 s been predicted to increase with decreasing particle size.

24 eld and all the devices showed a micro-scale particle size.

25 tions, although the change is nonlinear with particle size.

26 small supported metal particles scales with particle size.

27 delivery systems are highly dependent on the particle size.

28 uilibrium structures correlate strongly with particle size.

29 f precipitates showing greater turbidity and particle sizes.

30 arrangements on the FeO6 octahedra for both particle sizes.

31 s reasonably limited due to relatively large particle sizes.

32 ite layer on the surfaces was independent of particle sizes.

33 ducting La and Pr complexes have the largest particle sizes.

34 me-of-flight mass spectrometry (ATOFMS), the particle size (0.3-1.5 mum), chemical composition and mi

35 lation of GEOs in water-based microemulsion (particle size 10.1nm) showed better antimicrobial activi

36 coration of nanostructured zirconia (average particle size 13 nm) on reduced graphene oxide (ZrO2-RGO

37 Freeze-drying increased particle size (199-283nm), and slightly decreased zeta p

38 Three different particle sizes (2<coarse<3.5, 1.6<medium<3.0, 0.5<fine<2

39 1%, 2%, and 4% of addition) at two different particle sizes (2.7mum and 5.7mum), added at the beginni

40 ter a seven-day treatment with nZnO (average particle size 20 nm, concentration 4 mg L(-1)).

41 odispersed micelles [NP(BTZ-DOX)] with small particle sizes (20-30 nm) for dual drug delivery.

42 mixed micelles (PCS) with 96.8% efficiency (particle size 3.0+/-0.06nm).

43 at), pore volume (0.51-0.66 cm(3)/gcat), and particle size (5.4-5.8 nm) were kept constant.

44 ical responses at these levels were 151.68nm particle size, 7.17% p-anisidine and 88.64% antioxidant

45 y produced stable nanodispersions with small particle sizes (72.88-142.85nm) and narrow PSDs (polydis

46 of starch damage (7.37%) and finest average particle size (8.52mum).

47 DLS and TEM revealed a particle size about 170nm for the double walled nanogels

48 The particle size (about 34 nm), morphology, X-ray Powder Di

49 The microcapsules were evaluated for particle size, accelerated oxidation by Rancimat, and si

50 from 300nm to 3.5mum and they retained their particle size after moulding of bilayer MN arrays.

51 Particle size/aggregation was a key parameter in modulat

52 validate the sub-micrometer precision of the particle size analysis based on a scattering model of sp

53 c multiple reaction monitoring and a 1.8-mum particle size analytical column, was developed to determ

54 and 5mL/min) were investigated at 0.5mm mean particle size and 20bar pressure.

55 ts of coadjuvant (2-4% when using the larger particle size and 4% when using the smaller one), with a

56 able, GC concentration-dependent increase in particle size and a reduction of the zeta-potential, and

57 local nanoparticle concentration with fixed particle size and channel size.

58 med by two different tissues in composition, particle size and colour terms, so two different flours

59 Apart from the importance of particle size and composition in droplet activation, we

60 Differences in Cu(2)(+)-tartrate complexes particle size and concentration were measured as a funct

61 orous rubber particles, through selection of particle size and concentration, and demonstrate tunabil

62 The formulations were characterized for particle size and encapsulation efficiency.

63 in consumer products, there is evidence that particle size and formulation influences skin permeabili

64 present study was to evaluate the effect of particle size and heat treatments on lutein and beta-car

65 The optimum formulations with minimum particle size and high zeta potential value were PW and

66 d uniformity and cloud stability by reducing particle size and increasing viscosity and yield stress

67 The particle size and lutein encapsulation efficiency of nan

68 growth and multiphase reactions to increase particle size and mass, which results in (3) further dim

69 n powder and aqueous suspension (absorbance, particle size and microstructure, free sulfhydryl conten

70 is likely to be strongly dependent upon the particle size and morphology.

71 pact Gag oligomerization as well as immature particle size and morphology.IMPORTANCE A key aspect in

72 Whereas, the experimental values for particle size and nanoemulsion stability were 156.13+/-2

73 The influence of particle size and optical properties on the stability of

74 grams of the SHG intensities as functions of particle size and orientation agreed nicely with predict

75 ic and combined electrostatic-steric) on the particle size and particle size distribution (PSD) of th

76 Our results reveal how particle size and phase morphology affects transformatio

77 Both VLDL particle size and plasma cholesterol levels were signifi

78 tuning various design factors, including the particle size and polymer length, we can use the supramo

79 time had significant effects (p<0.05) on the particle size and PSD.

80 ze and shape spectrum' (SSS) includes litter particle size and shape and their consequent effect on f

81 We describe the effect of varying particle size and shape on the SERS signal, focusing on

82 to extract spatiotemporal fields of internal particle size and shape orientation distributions during

83 as (i) an easy and precise control over the particle size and shape, (ii) a high encapsulation effic

84 he dependent variables were the temperature, particle size and solute:solvent ratio.

85 strumentation should be useful in studies of particle size and structure effects on given catalytic r

86 od should be particularly useful in studying particle size and structure effects.

87 The particle size and structure of masticated almonds have a

88 e characteristics of fullerene including its particle size and surface charge.

89 The collection efficiency increased with particle size and the cutoff diameter was between 0.5 an

90 By measuring the particle size and the particle number distribution, we w

91 aspects of our route, including the role of particle size and the voltages needed, are studied in de

92 ore proceeds by first selecting an available particle size and then optimizing eluent velocity and co

93 eractions caused marked increases in protein particle size and viscosity of the heated systems; conve

94 r(2)=-0.75) and positive correlation between particle size and water absorption index (r(2)=0.94) was

95 A negative correlation between particle size and wettability (r(2)=-0.75) and positive

96 ogel networks were characterized in terms of particle size and zeta (zeta) potential with average val

97 The high-resolution single particle size and zeta potential characterisation will p

98 enoid bioaccessibility (p<0.001), lipolysis, particle size and zeta potential.

99 urthermore, we report a shift towards larger particle sizes and a decrease in volume specific surface

100 ls (a class of BrC) appear brownish at small particle sizes and blackish at large sizes.

101 counted for, thereby posing a lower limit of particle sizes and limiting the accuracy of the size dis

102 t responses to CeO2 exposure varied with the particle sizes and the growth stages of plants.

103 ncentrations should be done across different particle sizes and types.

104 combined two-dimensional distribution of the particle-size and the molecular-size of a mixture of var

105 particle core (via the particle symmetry and particle size) and ligands (via the ligand length) on cr

106 d blueshift of the resonance with increasing particle sizes) and multiple electric resonances of the

107 LOD is subjected to particle stacking, small particle size, and compact cluster.

108 to spray-drying had lower moisture, aw, and particle size, and greater solubility, while the freeze-

109 copicity, glass transition temperature (Tg), particle size, and microstructure of the powders were ev

110 after a dry milling process) quantity, bran particle size, and milled bran thickness, and to investi

111 ng from organ-specific clearance mechanisms, particle size, and the molecular specificity of nanopart

112 isothermal storage conditions on turbidity, particle size, and thermal reversibility of vitamin E-en

113 Additionally, lipolysis, particle size, and zeta potential of the micellar fracti

114 es C), size reduced and separated into three particles sizes, and extracted with compressed propane a

115 n colour development, ionic calcium, protein particle size, apparent viscosity and pseudoplastic rheo

116 ound selenium were measured as a function of particle size at the inlet and outlet of the scrubber.

117 arameter optimization so long as one changes particle size at the prescribed crossover points.

118 All nanodispersions showed constant particle sizes at temperatures between 30 and 60 degrees

119 Emulsion particle sizes at the end of the gastric phase were dire

120 to produce nanodispersions successfully with particle sizes below 100nm.

121 kinetics depends on partition coefficients, particle size, boundary conditions, and time.

122 depends solely on the detector flow rate and particle size but not on the type of the soft particle.

123 bility of these droplets by decreasing their particle size by decreasing the number of surface pores;

124 ) the high RH induces an increase of aerosol particle size by enhanced hygroscopic growth and multiph

125 The direct online determination of particle size by ICPMS gave similar results than ELPI fo

126 lar, for less ripened olives, 1-2% of larger particle size calcium carbonate addiction determined a s

127 icles down to a final stage where the target particle size can be concentrated.

128 d several Lipoplex properties (i.e., reduced particle size, changed surface charge, modified composit

129 double walled nanogel was characterized for particle size, charge and thermal properties followed by

130 polylysine had pronounced influences on the particle size, charge, and aggregation state throughout

131 atic effects on important properties such as particle size, charge, and solubility.

132 ) concentration, relative humidity (RH), and particle size control reaction rates and mechanisms.

133 rogeneous catalysis because of their uniform particle sizes, controllable shapes, and tunable composi

134 The three clay types differ in particle size, crystal structure, and their accumulation

135 independent of RH, the reaction products and particle size depend upon H2O.

136 The role of particle size-dependent Mie scattering and absorption ef

137 However, such sites display strong particle-size-dependent reactivity because of very subtl

138 same NP suspension, was used to confirm the particle size determined with NTA and the equivalent par

139 Herein, the particle size distribution (PSD) of aluminium oxyhydroxi

140 ectrostatic-steric) on the particle size and particle size distribution (PSD) of the nanodispersions

141 ing protocol is developed to reveal the true particle size distribution from HAADF-STEM images, which

142 nship with pasting temperature while average particle size distribution had a significant, strong neg

143 We find that the particle size distribution is independent of the bean or

144 Herein we report on the influence of the particle size distribution of activated carbon material

145 milled rice grains on the damaged starch and particle size distribution of flour produced from a new

146 The relatively wide particle size distribution of PLGA NMP was shown to be i

147 (p<0.05) affected starch damage content and particle size distribution of rice flour.

148 We measured particle size distribution of wheat flour, photographed

149 e of this study was to examine the effect of particle size distribution on physical, chemical and fun

150 ions for at least 2 mo without any effect on particle size distribution or gas carrying capacity.

151 Analysis of particle size distribution showed a slight shift to smal

152 Soil pH and particle size distribution showed no significant correla

153 s coupled with the high efficiency of narrow particle size distribution silica.

154 significant changes in apparent stability or particle size distribution under the conditions examined

155 es of single origin coffee beans affects the particle size distribution upon grinding.

156 A bi-modal particle size distribution was found for all materials d

157 The particle size distribution was monomodal, shifting to sm

158 all fractions and only minor differences in particle size distribution were found between wines.

159 ing that grinding cold results in a narrower particle size distribution, and reduced mean particle si

160 rosols on climate is highly dependent on the particle size distribution, concentration, and compositi

161 ucidate the influence of bean temperature on particle size distribution, concluding that grinding col

162 n to systematically investigate (changes to) particle size distribution, dissolution, reprecipitation

163 PSF model, used the fractal dimension of the particle size distribution, exhibited an accepted perfor

164 hocolates were evaluated for their physical (particle size distribution, texture) and sensory propert

165 unction of their size and thus determine the particle size distribution.

166 eement with the value predicted based on the particle size distribution.

167 of the poly(nBA) microspheres with a narrow particles size distribution from 0.6 mum up to 1.8 mum.

168 owder inhaler while sampling for aerodynamic particle size distributions (APSD) by inertial impaction

169 We measured particle size distributions and spatial patterns of part

170 ter ruling out any support effects, the gold particle size distributions in different catalysts are q

171 The particle size distributions of the chocolates were mostl

172 and energy-dispersive X-ray analysis and the particle size distributions using optical methods.

173 itions applied during photodeposition on (i) particle size distributions, (ii) oxidation states of th

174 roven to be a powerful tool for the study of particle size distributions, particle shapes, and intera

175 effects of varying experimental conditions (particle size, dose, mixing time) on concentrations in p

176 nse of few-nm plasmonic particles depends on particle size due to effects such as nonlocality and ele

177 All the emulsions had no change in their particle size during storage (28days at 5, 20 and 40 deg

178 ppropriate acoustic frequency to the desired particle size, each particle population can be selective

179 A substantial AC particle size effect was observed.

180 n NPs, which is consistent with the observed particle size effect.

181 racer exchange data sets that explore pH and particle size effects, we developed a stochastic simulat

182 Emulsions were characterized by particle size, emulsifying activity index, surface prote

183 98, 99.184, 0.008, 0.008, 2.43 and 16.65 for particle size, emulsion stability, turbidity loss rate,

184 finite water-uptake ability at all sites and particle sizes examined.

185 radiation: (1)O2 triggering induced dramatic particle size expansion due to the conversion of imidazo

186 ncreasing catalytic activity with decreasing particle size for other transition metal catalysts also,

187 practitioner to rapidly identify the correct particle size for use in tackling a particular separatio

188 crease in hygroscopic growth with decreasing particle size (for particle diameters <150 nm) that is i

189 Larger particle size fractions showed slower starch digestion r

190 cine pancreatic alpha-amylase for a range of particle size fractions.

191 Soil particle-size fractions with higher bioavailability (i.e

192 After coating, changed particle size from 50.76 +/- 2.21 nm to 88.64 +/- 1.25 n

193 ndow it with unique advantages for measuring particle size from the nano- to the microscale.

194 l, and cobalt) were synthesized with average particle sizes from 0.9 to 1.4 nanometers, with tight si

195 The main particle size in exposure media was in the size range of

196 In addition, the particle size in nanoscale can provide short diffusion l

197 nd were evaluated to determine the effect of particle size in nutrient bioaccessibility.

198 At the inlet, the M-values for all particle sizes in blood were <0.2, suggesting that non-f

199 Particle sizes in plant-based milk substitutes, expresse

200 nstrates exceptional potential for resolving particle sizes in solution with sub-nm resolution.

201 ult of the limited availability of different particle sizes in using two-parameter optimization when

202 d no margination, which was observed for all particle sizes in water.

203 liter mass (HLM), hundred kernel mass (HKM), particle size index (PSI), percentage vitreous endosperm

204 ming possible disadvantages due to sample or particle size inhomogeneity.

205 Cure time, cure temperature, levonorgestrel particle size, initial levonorgestrel loading and silico

206 The average particle size is 7.6 +/- 1.2 nm.

207 Particle size is controlled by the self-assembly and uni

208 In such a distribution, the average particle size is correlated with the peak area ratio.

209 tructure, surface properties, impurities and particle size, is also discussed.

210 rsibly form and remove crystalline LiOH with particle sizes larger than 15 micrometers during dischar

211 The results revealed that a decrease in particle size led to an increased rate and extent of lip

212 ry of phenolics could be achieved with shell particle size less than 0.5mm when extracted with aceton

213 Drug-loaded ISNPs had particle size less than 158nm with mono-dispersed distri

214 0.5nm thin layer of SiO2 nanostructures with particle size lesser than 70nm.

215 0.4 [PM2.5], 0.35 [BC], approximately 0.25 [particle size]), low bias (<4%) and absolute bias (2-18%

216 Control of sub-nanometre particle size may be used for tuning catalysed hydrogena

217 The particle size (mean +/- SD) was 515 +/- 171 mum.

218 safe FDA approved drug for diuresis) through particle size measurement and forster resonance energy t

219 Turbidity and particle size measurements indicated that while spray-dr

220 use of resistive pulse sensors for submicron particle size measurements relies on a clear understandi

221 impact of two different iron-based magnetic particle sizes (micro- and nanosized particles) to deter

222 the final core-shell architecture, including particle size, monolayer coverage, and heterometallic co

223 in resistance and lipoprotein dysfunction by particle size, number, and functional assessment.

224 mass obtained from CeFFF retention data and particle size obtained from the TEM images were used to

225 Upon milling coarse bran with an average particle size of 1687 mum down to 77 mum, the specific s

226 ic and spherical-shaped vesicles with a mean particle size of 174.6+/-17.3nm and polydispersity index

227 The obtained AuNCs have a particle size of 2.7 +/- 0.1 nm and maximum fluorescence

228 g, which self-assembled into micelles with a particle size of 30-50 nm and high ICG loading.

229 h p.i.) was achieved using an optimized PPN particle size of approximately 10 nm, as measured by usi

230 The mean particle size of liposomal nanovesicles containing PF30

231 The particle size of liposomes was in the range of 82.4-107.

232 The particle size of Mg2Sn decreased from 100 nm to 50 nm wi

233 ups, a distribution that responds to average particle size of not only AgNPs, but also gold nanoparti

234 solute zeta-potential values and reduced the particle size of oat protein particles.

235 The particle size of PLGA NMP ranged from 300nm to 3.5mum an

236 g another satellite product sensitive to the particle size of silicate minerals.

237 tron microscopy images show that the average particle size of SiO2(LuPc2)PANI(PVIA)-CNB was between 1

238 ron microscopy reveals marked differences in particle size of the different members of the Ln series

239 The particle size of the fresh liposomes ranged from 75.7 to

240 ncapsulation with the ternary blends reduced particle size of the probiotic powders thereby offering

241 diverse grain size effects depending on the particle size of the starting powder and sintering tempe

242 The average particle size of the tannin fraction was 75-89 nm, and i

243 Approximately 80% of products have average particle sizes of 300 nm or lower.

244 The effect of reduced particle size on composition and several physicochemical

245 f the corresponding responses to extract the particle size on the surface.

246 In this study, we report the effects of particle sizes on the carbonation of wollastonite (CaSiO

247 suspensions of nC60 aggregates of different particle size or via organic solvents on soils with diff

248 Particle size, organic carbon content, and pore saturati

249 es and reactant gases depend strongly on the particle size, particularly in the subnanometer regime w

250 While particle size played some role, the NP capping agent/fab

251 We introduce a new estimator of particle size polydispersity for dynamic light scatterin

252 linked nanogels, crosslinking did not change particle size, polydispersity index (PDI) and morphology

253 3%w/w) and characterized by considering the particle size, polydispersity index (PDI), zeta potentia

254 cochemical properties (such as drug loading, particle size, porosity, and morphology) as well as the

255 ontrolled by external factors not limited to particle size, presence of intact cell wall and other no

256 i0.5O4 is capable of fast rate even at large particle size, presenting an enigma yet to be understood

257 e, and rituximab to determine the effects of particle size, protein size, and crosslinking density on

258 *) and b( *) values decreased by increasing particle size (r(2)=-0.94, r(2)=0.72, r(2)=0.73 respecti

259 of encapsulated protein over the micro-scale particle size range studied.

260 The developed nanocarriers presented particle sizes ranging from 71 to 366nm, leading to exce

261 Here we measure particle sizes ranging from around 50 to 200 nm.

262 am as a function of system composition f and particle size ratio r is outlined.

263 ic, converts to a single-phase reaction when particle size reaches approximately 25 nm.

264 Reduction of particle size resulted in a three- to fourfold increase

265 ng variables, namely pressure, temperatures, particle size, SC-CO2 flow rate and co-solvent, on SC-CO

266 However, the interplay between particle size, shape and surface chemistry has not been

267 pattern can be uniquely associated with the particle size, shape, and orientation producing it.

268 ometry was used to characterize in real-time particle size, shape, density, and quantitative composit

269 Particle size showed no significant effect on overall de

270 s transverse to the flow direction (vy), all particle sizes showed a larger standard deviation of vy

271 Particle size significantly effected color, water absorb

272 oxide value (PV), volatile compounds (VOCs), particle size, size distribution, zeta potential and mor

273 Various solvents, particle size, solid-solvent ratio and extraction time h

274 ces are attributed to complex effects of Eg, particle size, surface morphology, phase purity and the

275 targeting nanoplatforms, based on changeable particle sizes, switchable surface charges and activatab

276 Larger particle size tended to show higher TOF and smaller reac

277 bers and the detection of a broader range of particle sizes than the enzymatic digestion approach, hi

278 tally and theoretically examine the range of particle sizes that can be captured in fluid streamlines

279 In terms of flow rates, for a given particle size, the higher the flow rate, the higher the

280 larly bioavailability, rises with decreasing particle size, the knowledge of the MP proportion in hab

281 ly dependent on the solidus temperature, the particle sizes, the temperature-dependence of the viscos

282 ng electron microscopy, encapsulation yield, particle size, thermogravimetry, Fourier transform infra

283 Using a simple particle size threshold model to describe transfection a

284 um emulsion stability and viscosity, minimum particle size, turbidity loss rate, size index and perox

285 ese methods may include difficult control in particles size, use of surfactants & polymer, and low ra

286 The as-synthesized CDs exhibited small particle size variation (2.7 +/- 0.2 nm) and narrow emis

287 ining either XG or XG-LBG mixtures had large particle sizes, viscosity, droplet aggregation, and crea

288 (89.2 +/- 0.3%) was calculated when the mean particle size was 455 +/- 2 nm.

289 Particle size was controlled by the concentration of the

290 The particle size was larger (29.9mum) when cashew gum was u

291 Particle size was more variable in moss closer to indust

292 HDL functionality and particle size were determined.

293 Particle sizes were measured by atomic force microscopy

294 True density increased with decreased particle size whereas porosity and bulk density increase

295 ubstitute pastes of different HA content and particle size with autologous bone and empty defects, at

296 By labeling different particle sizes with dyes/QDs for LCN1 and TNF-alpha, we

297 es and FD encapsulated powder yielded larger particle sizes with flaky structure.

298 he lutein ester incorporation as revealed by particle size, zeta potential and colour measurements.

299 Particle size, zeta potential, span value, and pH of CSO

300 the resultant HPHs were evaluated for their particle sizes, zeta potential and surface hydrophobicit