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 The Tween 20 allowed lower detection limits to be obtained f

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 Lastly, Tween 20 substantially and selectively increases NTPDase

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 molecular-weight oligomers are stabilized by Tween 20.

59 formulations containing sucrose, salts, and Tween 20.

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

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

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

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

64 1 hour) and chemical inactivation with 0.5% Tween-20 against a high titer of Ebola virus (species Za

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 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

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

81 3:1 mole ratio of Span 60:Tween 60, 4mg/ml of alpha-TOC and 25:12.5:2.5 mole ratio

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

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

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

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

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

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

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

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

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

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

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

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

94 -12 ml); and surfactant concentration, using Tween 80 and Tween 60 (1-5 mg).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

132 Only Tween 80-stabilized nanodispersion was stable against th

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

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

135 gnificant interference effects of PEG400 and Tween 80.

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

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

138 culation in nanodispersion stabilized by SDS-Tween 80.

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

140 mutants and is dependent upon the detergent Tween 80.

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

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

143 rticles and particles coated with citrate or Tween 80.

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

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

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

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

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

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

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

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

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

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

154 Tween caused a heterogenous lung injury with areas of no

155 Intratracheal instillation of Tween causes a heterogeneous surfactant deactivation in

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

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

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

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

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

161 Tween feeding did not affect fatty acid elongation in th

162 4 hours: Control group (n = 3) surgery only; Tween group (n = 4) subjected to intratracheal Tween (su

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

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

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

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

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

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

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

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

171 rfactant deactivation was induced in pigs by Tween instillation.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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