ライフサイエンスコーパス: Tween

1 pids in a PLA-type manner and also hydrolyze Tween.

2 ular changes: a) increased vasoconstriction (Tween, 14.9 +/- 1.0%) in response to hypoxia compared wi

3 ly, when the assay buffer contains traces of Tween 20 (0.0001%), darbufelone appears inactive with PG

4 sence of low concentrations of the detergent Tween 20 (0.05-0.1%, v/v) in the wash buffer as well as

5 ey protein concentrate hydrolysate (WPCH) or Tween 20 (TW20) were used as the emulsifiers.

6 The Tween 20 allowed lower detection limits to be obtained f

7 formulations with aqueous solutions of 0.03% Tween 20 altered the time of dissolution for all cases.

8 m the Schirmer strip in 0.5 M NaCl with 0.5% Tween 20 and analyzed using multiplex assay kits to exam

9 pted by exposure to mild neutral detergents (Tween 20 and CHAPS) at concentrations from 0.25 to 2.0%.

10 mines the potential of two buffer additives (Tween 20 and DTT) to improve the solubility of proteins

11 elicited as 30 mg of cholesterol, 150 mg of Tween 20 and feeding time of 1 min at a stirring rate of

12 formation is inhibited by concentrations of Tween 20 and several other detergents well below their c

13 promising ratio between the two surfactants, Tween 20 and Span 60, in terms of entrapment efficiency

14 nanoemulsions emulsified by modified starch, Tween 20 and whey protein isolate, respectively, were pr

15 hed three times, then solubilized with 0.04% Tween 20 at a detergent/protein (w/w) ratio of 0.1.

16 A tween 20 coating method is developed to inhibit non-spec

17 gents such as Triton X-100, Nonidet P-40 and Tween 20 did not affect the activities, while anionic de

18 In contrast, formulations containing Tween 20 dissolved faster in the Tween 20 solution when

19 Salt and sucrose formulations without Tween 20 dissolved more slowly in a Tween 20 solution th

20 rol (0.5% carboxymethyl cellulose and 0.025% Tween 20 in distilled water) or 750 mg silibinin/kg body

21 affect darbufelone in this way, in place of Tween 20 in our PGHS buffers.

22 containing 0.5% methyl cellulose and 0.025% Tween 20 in two different protocols.

23 were prepared from mixtures of olive oil and Tween 20 in water.

24 ic acid and autoxidation of linoleic acid in Tween 20 micellar medium) and compared with three widely

25 However, Tween 20 micelles did appear to be able to solubilise le

26 E(8), followed by exchange of C(12)E(8) with Tween 20 on a Superose 6 column.

27 thesis could be abolished by the addition of Tween 20 or Triton X-100.

28 Moreover, the influence of Tween 20 over the analytical parameters was studied.

29 The emulsion produced with Tween 20 resisted coalescence in the gastric phase and s

30 riments with purified sGC in the presence of Tween 20 showed that cinaciguat activates the heme-free

31 y bound cardiolipin (CL) can be removed from Tween 20 solubilized bovine cytochrome bc(1) (EC 1.10.2.

32 Phospholipid removal from the Tween 20 solubilized enzyme, including the tightly bound

33 without Tween 20 dissolved more slowly in a Tween 20 solution than in water alone.

34 containing Tween 20 dissolved faster in the Tween 20 solution when compared to dissolution in water.

35 Tween 20 stabilized corn O/W emulsions at pH 7.0 were pr

36 Lastly, Tween 20 substantially and selectively increases NTPDase

37 a Tris-HCl buffer containing the surfactant Tween 20 to aid in the prevention of surface adhesion of

38 ngth of the desalted serum and also utilized Tween 20 to serve as the passivation agent by surface mo

39 PBS that contains 1 M NaCl and 2% Tween 20 was determined to be the optimal extraction buf

40 PBS that contains 1 M NaCl and 2% Tween 20 was determined to be the optimal extraction buf

41 ulsions consisting of water, tricaprylin and Tween 20 were prepared, thermally treated and the format

42 a, Polyethylene glycol sorbitan monolaurate (Tween 20) and Cetylpyridinium chloride (CPC) in Tris/HCl

43 e buffer (pH 8.8 containing 1% BSA and 0.05% Tween 20) and pipetted onto the sample-cum-conjugate pad

44 on of nonionic surfactants (Triton X-100 and Tween 20) arrays from the second series exhibit signific

45 m) were formed using a non-ionic surfactant (Tween 20) as emulsifier and long chain triglycerides (LC

46 sein, whey protein) and surfactants (Citrem, Tween 20) on the in vitro digestion and oxidation of lin

47 ions, from the nonionic class (Triton X-100, Tween 20) or from the zwitterionic class (3-[(3-cholamid

48 ution (1.5% carboxymethylcellulose with 0.2% Tween 20) via gastrointestinal gavage.

49 The detergent polysorbate 20 (Tween 20) was used successfully to facilitate the remova

50 ta-lactoglobulin) or a non-ionic surfactant (Tween 20).

51 glucoside, dodecyl maltoside, Triton X-100, Tween 20, 3-[(3-cholamidopropyl)dimethylammonio]-1-propa

52 For steric emulsifiers, Tween 20, 40, 60 and 80 were used to produce nanodispers

53 factant-to-oil ratio (SOR), surfactant type (Tween 20, 40, 60, 80 and 85), and stirring conditions on

54 d to study the influence of surfactant type (Tween 20, 60 and 80) and oil type (Vitamin E, vitamin D(

55 a major impact of non-ionic surfactant type (Tween 20, 60 or 80) on the formation and properties of t

56 in their ability to grow in the presence of Tween 20, a detergent that inhibits a kinase which can s

57 ied starch and whey protein isolate, but not Tween 20, affected the cell viability/proliferation more

58 was observed in W-1, Chaps, octyl glucoside, Tween 20, and Brij 35.

59 tion was inhibited by the nonionic detergent Tween 20, and several lipids did not enhance enzymatic a

60 ol, W-1, octyl glucoside, dodecyl maltoside, Tween 20, and sodium cholate allow varying degrees of Ba

61 e substrate in 50 mM NaOAc, 150 mM KF, 0.05% Tween 20, pH 5.5, with apparent first-order kinetics wit

62 which neutral additives (e.g., Triton X-100, Tween 20, poly(ethylene glycol)) are removed from protei

63 Other detergents, e.g., Tween 20, sodium cholate, sodium deoxycholate, CHAPS, or

64 fish oil-in-water emulsions stabilized with Tween 20, where emulsion physical stability was unaffect

65 Dilution experiments of cinaciguat/Tween 20-preincubated sGC revealed the irreversible char

66 ctoglobulin-stabilised nanoemulsions than in Tween 20-stabilised ones.

67 e and lauryl gallate in the aqueous phase of Tween 20-stabilized and CTAB-stabilized emulsions, respe

68 rson correlation coefficients showed that in Tween 20-stabilized emulsions, aqueous lauryl gallate, i

69 le to colour fading than those stabilized by Tween 20.

70 eased when the enzyme assays contained 0.02% Tween 20.

71 molecular-weight oligomers are stabilized by Tween 20.

72 formulations containing sucrose, salts, and Tween 20.

73 the growth of 8830R2::Cm in the presence of Tween 20.

74 n X-100 (RTX-100), octylglucopyranoside, and Tween 20.

75 led these strains to grow in the presence of Tween 20.

76 1 hour) and chemical inactivation with 0.5% Tween-20 against a high titer of Ebola virus (species Za

77 Three types of emulsifiers, lecithin, Tween-20 and sodium dodecyl sulphate (SDS) were tested.

78 mass spectrometric analyses, the presence of Tween-20 did not prevent detection of ricin peptides, an

79 method based on dichlorodimethylsilane (DDS)-Tween-20 for in vitro single-molecule studies, which, un

80 ed assays performed in buffers that included Tween-20 gave better results than assays performed using

81 Tween-20 ligand showed the best binding affinity by hydr

82 nd poorly to MTP, but its preincubation with Tween-20 resulted in significantly increased binding to

83 The DDS-Tween-20 surface was simple and inexpensive to prepare a

84 dentified an optimized formulation of 1% w/v Tween-20, 0.8 ug/uL bovine serum albumin, 1 M betaine in

85 ates, in emulsions prepared with lecithin or Tween-20, indicating the greater relevance of having thr

86 In contrast, for emulsions prepared with Tween-20, the antioxidants seem to follow the polar para

87 d autoxidation within single oil droplets in Tween-20-stabilized oil-in-water emulsion was achieved b

88 nt of black currants with 0.02mM MJ in 0.05% Tween-20.

89 wells; unbound AFP was then washed away with Tween-20.

90 r and StartingBlock phosphate buffer saline- Tween-20; (PBS-T20) blocking buffer was utilized to mini

91 E Delta%), was significantly increased after Tween (23.9 +/- 3.0, I-E Delta%) compared with baseline

92 activity was stimulated by Triton X-100 and Tween 40 at concentrations of up to 1%.

93 and methylene selectivity were observed when Tween 40 was included in the formulation, using decane/d

94 e combined with a small molecule surfactant (Tween 40).

95 ,9-tetramethyl-5-decyne-4,7-diol ethoxylate, Tween 40, Triton X-405, and Tetronic 701.

96 s extracted from these marginal edges with a Tween-40/deoxycholate buffer that solubilizes the actin

97 5); and b) increased mean vascular diameter (Tween, 41.2 +/- 1.5 microm) compared with the mean diame

98 surfactant concentration, using Tween 80 and Tween 60 (1-5 mg).

99 and 0.88 mg), acetone (6 and 10.25 ml), and Tween 60 (3.0 and 4.25 mg), with 90.9 and 71.9 nm for OF

100 to be able to solubilise less lemon oil than Tween 60 or 80 micelles, presumably due to their smaller

101 3:1 mole ratio of Span 60:Tween 60, 4mg/ml of alpha-TOC and 25:12.5:2.5 mole ratio

102 S-01A), emulsions with Span 80 (50% v/v) and Tween 80 (10% v/v), and a control without additives, ena

103 on of SRHA (20 mg C/L), SRFA (20 mg C/L), or Tween 80 (1000 mg/L) to the influent nC(60) suspensions

104 to the aqueous solution (130 mL) containing Tween 80 (195 mg).

105 Tween 80 (2%) was used as a control.

106 erent from that of emulsions stabilized with Tween 80 (43.56 +/- 3.71%), whereas vitamin E bioaccessi

107 a surfactant mixture of Span 80 (37.4%) and Tween 80 (62.6%) were emulsified in water by high intens

108 pH7.4 HEPES buffered-saline containing 0.02% Tween 80 (all media contained 0.02% sodium azide).

109 c), sodium caseinate (electrosteric) and SDS-Tween 80 (combined electrostatic-steric) emulsifiers.

110 Tween 80 (steric) was then chosen for further comparison

111 ifiers evaluated were soybean lecithin (SL), Tween 80 (T80) and a mixture of SL:T80 (50:50).

112 The self-assembly of Tween 80 (T80) micelles loaded with plant-based oregano

113 lease was tested over 9 weeks in PBS + 0.02% Tween 80 + 0.02% sodium azide pH 7.4 (PBST) at 37 degree

114 or NEOBEE(R)1053-MCT) and emulsifiers (WPI, Tween 80 - T80 or WPI/T80 mixture).

115 or NEOBEE(R)1053-MCT) and emulsifiers (WPI, Tween 80 - T80 or WPI/T80 mixture).

116 rotocol consisting of morphology on cornmeal Tween 80 agar and trehalose fermentation at 42 degrees C

117 fungal cell wall, (b) the membrane softener Tween 80 allows the passage of the Transfersomes into th

118 riments, mice administered farnesol alone or Tween 80 alone remained normal throughout a 14-day obser

119 nanoemulsion was fabricated using 0.5 wt% of tween 80 and 5 wt% oil phase comprising 30 % of Ostwald

120 ons composed of a 30% monoglyceride oil, 20% Tween 80 and 50% aqueous buffer were evaluated using an

121 whey proteins and two synthetic emulsifiers (Tween 80 and Croduret), and exposed to conditions simula

122 bility of FODE in buffer is enhanced with 1% Tween 80 and ethanol.

123 ability, a major improvement over the use of Tween 80 and hydrogenated Triton X-100.

124 -12 ml); and surfactant concentration, using Tween 80 and Tween 60 (1-5 mg).

125 ith prodigiosin in ethanol (1:1), and adding Tween 80 as an emulsifier.

126 s Labrasol, Cremophor EL, Gelucire 44/14 and Tween 80 as edge activators (EAs) in the lipid bilayer.

127 sulfate (SDS), sodium caseinate (SC) and SDS-Tween 80 as the emulsifiers.

128 Ps (d(43) ~ 570-780 nm) were stabilized with Tween 80 at a surfactant-to-oil ratio (SOR) of 0.1.

129 t diameters (d<200 nm) could be formed using Tween 80 at SOR1 at high stirring speeds (800 rpm).

130 utical industry to develop soya lecithin and Tween 80 based vitamin D delivery system for food additi

131 oil using the surfactants Pluronic F127 and Tween 80 by mechanical agitation (Emulsion_Tw and Emulsi

132 Besides, Tween 80 can be proposed as a good and greener alternati

133 Tween 80 dispersed the highest oleoresin mass (6.21 +/-

134 ulations composed of isopropyl myristate and Tween 80 encapsulating a fluorescent dye were applied to

135 ies of nitrate reduction, catalase activity, Tween 80 hydrolysis, tellurite reduction, or arylsulfata

136 ependent, and is affected by the presence of Tween 80 in the culture media; (ii) show that AM is prod

137 ds on a high concentration of the surfactant Tween 80 in their membrane.

138 tics in phosphate-buffered saline containing Tween 80 led us to suspect that a significant fraction o

139 The tween 80 micelle provides a mimic of natural lipoprotein

140 croscopy to visualize lycopene delivery from tween 80 micelles into PC-3 prostate cancer cells.

141 l components for nucleic acids detection and Tween 80 micelles to absorb the SDS and allow enzymatic

142 tion) followed by PAI-749 sequestration with Tween 80 micelles yielded active PAI-1; thus, PAI-749 di

143 Cur was first dissolved in a corn oil/Tween 80 mixture to prepare the oil phase.

144 ithin-PVA nanoparticles, MTX loaded Lecithin-Tween 80 nanoparticles) as well as their respective cont

145 The Tween 80 opacity test is simple and economical to prepar

146 examined for their respective responses to a Tween 80 opacity test.

147 , is stimulated as detergent concentrations (Tween 80 or Triton X-100) are increased up to their crit

148 ng agitated phosphate buffered saline +0.02% Tween 80 pH7.4, including rate of PLGA hydrolysis, mass

149 e from 1154 to 70-300 nm whereas addition of Tween 80 reduced it optimally to 5-25 nm.

150 The presence of adsorbed Tween 80 resulted in nC(60) BTCs characterized by a decl

151 A Pluronic F-68 + Tween 80 surfactant mixture with the lowest oleogel/aque

152 hort chain monoglycerides could be used with Tween 80 to prepare transparent beta-carotene-encapsulat

153 itions in the presence of propionic acid and TWEEN 80 to stimulate the production of odd-chain PUFAs.

154 combined with the addition of the surfactant Tween 80 to the buffer solution that is used in forming

155 pene Raman signal, Raman scattering from the tween 80 vehicle is also mapped in the cells.

156 s larger than for di- and triglycerides when Tween 80 was used as surfactant.

157 ised by a protein or by phosphatidyl-choline/Tween 80 were submitted to gastro-intestinal in vitro co

158 GK)3 NGs were obtained using polysorbate 80 (TWEEN 80) and sorbitane monooleate 80 (SPAN 80) as collo

159 ) and non-ionic surfactants (polysorbate 80, Tween 80) at varied concentrations on the generation and

160 and its formulation vehicle polysorbate 80 (Tween 80) in human plasma samples is described.

161 ial oil, ripening inhibitor, and surfactant (Tween 80) into 5mM sodium citrate buffer (pH 3.5).

162 eed oil plus orange oil) and 10% surfactant (Tween 80) were titrated into 80% aqueous phase.

163 some concentration of nonionic surfactants (Tween 80) with natural surfactant (soya lecithin) and to

164 300%), external surfactants (rhamnolipid and Tween 80), and salinity levels (0.5-2%).

165 stic reaction mix containing polysorbate 80 (Tween 80).

166 formulation START (0.9% sodium chloride, 1% Tween 80, 1% powdered ataluren, 1% carboxymethylcellulos

167 In the presence of Tween 80, 1-(3',4'-diethoxyphenyl)-1-hydroxy-2-(4'-metho

168 ives used to enhance nanoparticle stability (Tween 80, a nonionic surfactant), and residual contamina

169 sed in-channel through chemical agitation by Tween 80, also vacuum-dried within the microchannels.

170 , reconstituting fluid, 0.2% glycerol, 0.05% Tween 80, and 0.05% bovine serum albumin (BSA) were test

171 composed of ovalbumin, xanthan gum, MgCl(2), Tween 80, and canola oil, satisfying the dysphagia diet

172 excipients such as PEG400, propylene glycol, Tween 80, and hydroxypropyl-beta-cyclodextrin on the acc

173 ne lignin model compounds in the presence of Tween 80, and in three- to fourfold lower yield in its a

174 Notably, arbutin, L-arabinose, Tween 80, and succinamic acid demonstrated a strong posi

175 microscopic morphology on cornmeal agar with Tween 80, and when necessary, conventional biochemical t

176 ower oil emulsions stabilized with 0.5%(w/v) Tween 80, as affected by pectin molecular characteristic

177 The impact of emulsifier types (Tween 80, BSA and quillaja saponins) on the formation of

178 ity after extended culture in the absence of Tween 80, indicating that a stable amount of GC polysacc

179 Lutein nanodispersions were prepared using Tween 80, sodium dodecyl sulfate (SDS), sodium caseinate

180 le that contains membrane softeners, such as Tween 80, to make it ultra-deformable.

181 of PA emulsions generated using surfactants: Tween 80, Triton X100, Sodium Dodecyl Sulfate (SDS) and

182 B), and polyoxyethylene sorbitan monooleate (Tween 80, Tween), on the size and stability of the collo

183 tionic surfactant CTAB and the nonionic one, Tween 80, were taken into consideration.

184 impact of emulsifier type (quillaja saponin, Tween 80, whey protein and casein) and antioxidant type

185 sed >95% of curcumin at pH 1.2 HCl with 0.1% Tween 80, which was ascribed in part to curcumin amorphi

186 sequently oxidized by MnP in the presence of Tween 80, yields of 3,4-diethoxybenzaldehyde, 4-methoxya

187 berculous and nontuberculous isolates by the Tween 80-based method ranged from 22 to 92% and 27 to 93

188 hat combines NALC and NaOH (NALC-NaOH) and a Tween 80-based method.

189 Only Tween 80-stabilized nanodispersion was stable against th

190 Tween 80-stablized clove oil nanoemulsion displayed high

191 hate buffer (PB, pH 7.4) containing 0.1% v/v Tween 80.

192 rticles and particles coated with citrate or Tween 80.

193 sence and, in lower yield, in the absence of Tween 80.

194 the reaction was conducted in the absence of Tween 80.

195 gnificant interference effects of PEG400 and Tween 80.

196 s grown either with or without the detergent Tween 80.

197 owth in media with and without the detergent Tween 80.

198 oth strains was decreased in the presence of Tween 80.

199 mutants and is dependent upon the detergent Tween 80.

200 s were disappeared with the incorporation of Tween 80.

201 e or supplemented with propionic acid and/or TWEEN 80.

202 culation in nanodispersion stabilized by SDS-Tween 80.

203 gonorrhoeae were incubated for 5 min with 1% Tween 80.

204 AMG9810 (50 mg/kg) or vehicle (2% DMSO/5% Tween 80/10 ml/kg saline) was injected intraperitoneally

205 ons for mixed surfactants (Soya lecithin and Tween 80; 2:3) based nanoemulsions.

206 phate buffered-saline (PBS) containing 0.02% Tween 80; pH7.4 PBS containing 1.0% triethyl citrate (PB

207 e inhibitor stock solution or by addition of Tween-80 detergent.

208 ropanol (D-PDMP), solubilized in vehicle (5% Tween-80 in PBS); the placebo group received vehicle onl

209 unds were soluble in 0.5% methylcellulose/2% Tween-80 in water (MC/T) for oral administration.

210 and co-surfactant mixture using labrafil and tween-80 to obtain SED.

211 y human serum albumin, bovine serum albumin, Tween-80, Triton X-100, and Pluronic-F68.

212 sions by using food grade mixed surfactants (Tween:80 and lecithin; 3:1) to replace some concentratio

213 ris-HCl and 200 mM KCl, with or without 0.5% Tween added to the buffer, and the motion was recorded.

214 detergents Triton X-100, Nonidet P-40, Brij, Tween, and octylglucoside all inactivated the enzyme.

215 d discovered little-to-no difference between Tween- and SDS-containing reaction mixtures, compared to

216 or without membrane permeabilizers EDTA and Tween, as a donor plant on broccoli, cauliflower and kal

217 Tween caused a heterogenous lung injury with areas of no

218 Intratracheal instillation of Tween causes a heterogeneous surfactant deactivation in

219 f 40 mug/L was reached after just 6 h in the Tween-coated particle systems, accounting for ca. 3% of

220 Diminishing the link be-tween control of food intake and energy balance may cont

221 reover, substantial amounts of both CTAB and Tween distributed into the KTP-rich phase from the aqueo

222 Fatty acids delivered via Tween esters rapidly reduced the rate of fatty acid synt

223 was achieved upon feeding oleic acid (18:1) Tween esters that resulted in the intracellular accumula

224 ignal responsible for feedback, a variety of Tween esters were tested for their effects on the rate o

225 Tween feeding did not affect fatty acid elongation in th

226 4 hours: Control group (n = 3) surgery only; Tween group (n = 4) subjected to intratracheal Tween (su

227 Type I alveoli in either the control or Tween group demonstrated minimal change in alveolar area

228 In the Tween group, type II alveoli increased significantly in

229 ) larger in the control as compared with the Tween group.

230 er inflection point, whereas the curve after Tween has an inflection point at 8 mm Hg and a second at

231 on by Tween lavage (1.5 mL/kg 5% solution of Tween in saline).

232 o crystallization/orientation of interfacial Tween, increasing alignment and ultimately a greater dip

233 gas exchange in acid-induced ALI, yet not in Tween-induced surfactant depletion.

234 5% methanol or DMF, though surfactants like Tweens inhibit its function.

235 in which lung injury was induced by tracheal Tween instillation, causing surfactant deactivation (n =

236 models of ALI induced by hydrochloric acid, Tween instillation, or in antibody-mediated transfusion-

237 rfactant deactivation was induced in pigs by Tween instillation.

238 intervention plus surfactant deactivation by Tween lavage (1.5 mL/kg 5% solution of Tween in saline).

239 were subjected to surgical intervention, and Tween lavage pigs (n = 5) were subjected to surgical int

240 e alveoli caused by surfactant deactivation (Tween lavage).

241 wed for 4 hours: Control (n=3) surgery only; Tween (n=4) subjected to intratracheal Tween (surfactant

242 an 20% (LEC-PVA nanoparticles) and 2.3% (LEC-Tween nanoparticles), demonstrating that nanoparticles a

243 Results showed that the Tween-NPs had a much higher bioaccessibility (84.1 +/- 1

244 However, the Tween-NPs had a significantly higher cytotoxicity agains

245 ratrol, while a reduction in cytotoxicity of Tween-NPs was observed after the digestion.

246 aining a zein core surrounded by surfactant (Tween-NPs) or carboxymethyl chitosan (CMCS-NPs) shell we

247 lyoxyethylene sorbitan monooleate (Tween 80, Tween), on the size and stability of the colloidal ketop

248 echin-3-gallate (EGCG) oxidation (400muM) in Tween- or sodium dodecyl sulphate (SDS)-stabilised hexad

249 activator causing alveolar instability); and Tween + PEEP group (n = 4) subjected to Tween with incre

250 t deactivator causing alveolar instability); Tween+PEEP (n=4) subjected to Tween with increased PEEP

251 ormulated with peppermint oil and a blend of Tween(R) 20 and various amounts of sunflower lecithin wa

252 osed of 5 % w/w fish oil and stabilized with Tween(R) 20.

253 igating different surfactants, in particular Tween(R) 60.

254 .5% w/w dry matter) and totally substituting Tween(R)20 with MC.

255 The SLNs were prepared from Geleol(R) and Tween(R)80 as a lipid matrix and stabilizer, respectivel

256 The 5x HotSHOT+Tween reagent exhibited minimal inhibition and high extr

257 e sterically dispersed particles coated with Tween released silver quicker than did bare- and citrate

258 The combined use of HPMC with CTAB or Tween resulted in a further decrease in the thermodynami

259 ty of coffee oil as a natural substitute for Tween series of surfactants.

260 uld not be formed using vitamin D or E in 1% Tween solutions, due to the relatively large size of the

261 only; Tween (n=4) subjected to intratracheal Tween (surfactant deactivator causing alveolar instabili

262 een group (n = 4) subjected to intratracheal Tween (surfactant deactivator causing alveolar instabili

263 ifferential expression of virulence genes be-tween the two disease-causing biotypes of Vibrio cholera

264 uidic Taylor-Couette flow - flow confined be-tween two concentric independently rotating cylinders -

265 veolar type after surfactant deactivation by Tween was notably different.

266 and Tween + PEEP group (n = 4) subjected to Tween with increased PEEP (15 cm H2O) to stabilize alveo

267 instability); Tween+PEEP (n=4) subjected to Tween with increased PEEP (15cmH20) to stabilize alveoli