ライフサイエンスコーパス: clean up

1 ted sources, eliminating the need for sample clean up.

2 f lysine with minimal sample preparation and clean-up.

3 st and effective solutions for environmental clean-up.

4 sing a validated method that uses SAX column clean-up.

5 n followed by a solid-phase extraction (SPE) clean-up.

6 omising alternative technology for pollutant clean-up.

7 s employed for online analyte enrichment and clean-up.

8 cobalt recycling, recovery and environmental clean-up.

9 acetate-buffered QuEChERS extraction without clean-up.

10 sing hazardous solvents or requiring further clean-up.

11 (18) and Na(2)SO(4) aided by low-temperature clean-up.

12 often depend on costly immunoaffinity sample clean-up.

13 only used in this type of matrices as sample clean-up.

14 dividuals involved in oil spill response and clean-up.

15 olvent extraction followed by immunoaffinity clean-up.

16 hase extraction has been employed for sample clean-up.

17 een exposed to nerve agents and subsequently cleaned up.

18 erms of the sorbents used for extracting and cleaning-up.

19 ded full sets of BAHD superfamily genes, and cleaned up a few existing annotation errors, importantly

20 uch faster (<4min), however, a preceding SPE clean-up abolishes this benefit in time saving.

21 ltrimethoxysilane (TEOS-MTMOS) was used as a clean-up adsorbent in magnetic solid phase extraction (M

22 @G-TEOS-MTMOS is reusable up to 7 times as a clean-up adsorbent with good recovery (>85%).

23 workers and volunteers involved in oil spill clean-up after the Deepwater Horizon disaster.

24 RBS) that integrates read quality assessment/clean-up, alignment, methylation data extraction, annota

25 otential respiratory effects associated with cleaning up an oil spill.

26 ion absorbent, was applied for the selective clean up and quantification of benzoate in beverage samp

27 enge, here we present an enzymatic method to clean up and reconfigure DNA-origami structures.

28 method for the automatic pre-concentration, clean up and sensitive determination of OTA in wine.

29 od for the simultaneous extraction, separate clean-up and analysis of 21 free amino acids and 10 free

30 Triton X-114 was used for sample clean-up and as a fluorophore, whose fluorescence was qu

31 omizable wettability, solar-driven oil-water clean-up and demulsification technologies.

32 g PAHs using liquid-liquid extraction (LLE), clean-up and detection by liquid chromatography with flu

33 methods by optimizing lysis, elution, sample clean-up and detection of interacting proteins by multid

34 se microextraction's (SPME) efficient sample clean-up and enrichment and ambient MS's fast analysis a

35 LLE and SPE were employed for sample clean-up and enrichment of EGCG over caffeine.

36 manner, but often requires a range of sample clean-up and extraction steps.

37 d-liquid extraction with acetonitrile, d-SPE clean-up and final reconstitution of extract in ethyl ac

38 tonitrile extraction, dispersive solid phase clean-up and finally determination using liquid chromato

39 ocol was set up and coupled with extraction, clean-up and GC x GC-ToF/MS multianalyte method to monit

40 mbined with a freeze-based fat precipitation clean-up and HPLC-DAD-FLD-MS detection is described for

41 The method applied, based on rapid clean-up and LC-MS/MS determination, was previously deve

42 Sample preparation included SPE clean-up and liquid-liquid extraction for ice-cream and

43 Clean-up and off-line concentration were achieved by a n

44 uently used as SPE sorbent for the selective clean-up and pre-concentration of 3NT from standard solu

45 ds that coupled sample pre-treatment (sample clean-up and pre-concentration) with sensitive detection

46 The approach was applied to clean-up and preconcentrate bisphenols from milk samples

47 ompared to mini and micro-versions including clean-up and spiking procedures.

48 e (sample-to-sample) of 7 min, including the clean-up and the re-equilibration of the column.

49 mists need to be able to assess the costs of cleaning up and to develop incentive schemes to increase

50 mpleting training for oil spill response and clean-up) and 2225 non-workers (completed training but w

51 mple solid-liquid extraction without further clean-up, and analysis by ultra-high performance liquid

52 thod involving extraction, lipase treatment, clean-up, and detection and quantification by LC-ESI-MS/

53 Chromatographic conditions, extraction, clean-up, and matrix effect were studied.

54 n, 3D cell culture, micro reactor, oil spill clean-up, and oil/water separation.

55 he results obtained from solvent extraction, clean-up, and targeted GC-MS analysis.

56 ilica was used as solid phase for the sample clean-up, and the analyte determination was carried out

57 NaCl as extraction salts, MgSO(4)/PSA/C18 as clean-up, and the non-dilution of extracts.

58 re homogenized, extracted, pre-concentrated, cleaned up, and examined.

59 e physiologically relevant extracts are then cleaned up, and the analytes are preconcentrated onto a

60 the assay on-chip, the potential for sample clean-up; and the low volume of sample required.

61 ated areas, phytoremediation may be a viable clean-up approach.

62 imised and different extraction solvents and clean-up approaches were tested, obtaining the most effi

63 micals, novel methods of decontamination and clean-up are required.

64 We show that an image series can be cleaned up before arbitrary-region RICS (ARICS) analysis

65 tracted with methanol/water 80:20 (v/v), and cleaned up by a reversed phase/strong cation exchange so

66 tracted from food commodities with methanol, cleaned up by alumina-SPE column, and then determined by

67 dified ethyl acetate, MgSO4 and CH3COONa and cleaned up by dispersive SPE with PSA.

68 lohexane-ethyl acetate mixture (1:1 v/v) and cleaned up by florosil column.

69 racted by pressurized liquid extraction, and cleaned up by liquid-liquid partitioning.

70 The extract was cleaned-up by dispersive solid-phase extraction with MgS

71 ere extracted with methanol and the extracts cleaned-up by solid-phase extraction using Oasis HLB (60

72 nto dichloromethane on a ChemElut column and cleaned-up by solid-phase extraction.

73 xidative remediation tools and strategies to clean up chlordecone-polluted environments would benefit

74 dispersing agent and Envi-Carb-II/SAX/PSA as clean-up co-column.

75 .0g of octadecyl bonded silica (C18), as the clean-up co-sorbent.

76 2/H2) and natural gas upgrading (natural gas clean-up, CO2/CH4).

77 nts, sample throughput and effectiveness for cleaning-up complex samples.

78 Sample extraction and clean-up conditions were carefully studied and factors a

79 rtant factor in the selection of remedies to clean up contaminated sites.

80 mine whether phytoremediation can be used to clean up contaminated sites.

81 id extraction is a long-standing strategy to clean up contaminated water sources.

82 r valley there was widespread flooding, with clean-up costs of over pound1 billion.

83 cost, and indeed the wider implications, of cleaning up depends upon how it is done.

84 od is advantageous over classical methods as clean up/ derivatization of samples is not required for

85 The fabricated sponge can be used to clean up different types of oil, organic solvents, toxic

86 hese new explosives, feasible strategies for cleaning up DNAN from soil and water have not been devel

87 promising stepwise recoveries of extraction, clean-up, drying-reconstitution of most analytes ranging

88 be cheaper alternative receptors for sample clean-up due to their wide availability.

89 jected in the chromatographic system with no clean-up, during a total run time of 4 min.

90 timal Tc scavenger with the highest reported clean-up efficiency, while first-principle simulations r

91 ts, which is needed for supporting effective clean-up efforts and scientific evidence-based policy ma

92 itter on marine ecosystems, we conclude that clean-up efforts are a vital management action for islan

93 The use of plants and bacterial to clean up environmental pollutants has gained momentum in

94 Phytoremediation is the use of plants to clean up environmental pollution.

95 ified specific responsible attributes of the clean-up experience.

96 (FPSE) platform was developed for the matrix clean-up, extraction and preconcentration of five triazi

97 t professionals showed dead bed bugs are not cleaned up following treatment.

98 eatment, for the simultaneous extraction and clean-up for the determination of ionophore coccidiostat

99 production pipeline through effective sample clean up from more complex AAV matrices such as cell cul

100 ightforward sample treatment based on silica clean-up, GCxGC-ToFMS detection and automated data proce

101 al wines (Extremadura, Spain) without sample clean-up has been carried out by HPLC with spectrofluori

102 cing automobile exhaust and other emissions, cleaning up hazardous wastes (including the Three Mile I

103 e test tubes was discovered by chance during clean-up in preparation for a laboratory move.

104 eported procedure includes fractionation and clean-up in RPLC, selection of the fraction to be transf

105 sing a modified QuEChERS method, without any clean-up, including a dilution to obtain good peak shape

106 employed as an alternative solid support for clean-up is presented during the development and validat

107 ads (gamma-CD-EPI-MB) have been evaluated as clean-up materials for fish flesh extracts containing CT

108 p a simple but effective online column-based clean-up method (reversed-phase column in a size exclusi

109 SPE GCB/PSA proved to be the most effective clean-up method and enabled 225 pesticide residues to be

110 velopment of a QuEChERS-based extraction and clean-up method facilitated the quantification of 25 rel

111 To this end, an automated clean-up method for the pesticide extracts of bee pollen

112 The proposed preconcentration-clean-up method is environmentally friendly and convenie

113 novel lipid isolation, preconcentration, and clean-up method using pipettes containing immobilized me

114 A C18 solid-phase-extraction clean-up method was used to reduce matrix effects and in

115 Using this clean-up method, recoveries for samples spiked at 1 and

116 , 10, 20 min, extraction steps; 1-5) and two clean-up methods (n-hexane washing vs. low temperature f

117 Robusta) were analyzed through GC-MS and two clean-up methods were compared.

118 In this work, different extraction and clean-up methods were evaluated for the simultaneous ext

119 ized for direct PSD with on-the-probe sample clean-up methods.

120 nt before fertilization, and then shift into clean-up mode after the egg-to-embryo transition.

121 Clean up of labeled glycans via removal of excess of lab

122 that includes the extraction and dispersive clean up of the samples followed by the GC-MS determinat

123 valuated for the simultaneous extraction and clean-up of aflatoxins B1, B2, G1 and G2 from rice.

124 to perform efficient in situ separations and clean-up of biological samples.

125 The sample loading and electrophoretic clean-up of biosamples can be done in parallel within 20

126 This method enables clean-up of crude extracts within 18min and screening an

127 Rapid clean-up of drinking ponds immediately after a surge eve

128 Clean-up of extracts was performed by solid-phase extrac

129 (CSMISPE) was used for pre-concentration and clean-up of lincomycin in the milk matrix prior to analy

130 eparation science of Cs as it relates to the clean-up of nuclear waste.

131 ll have numerous applications, including the clean-up of oil spills, wastewater treatment, fuel purif

132 were observed when graphene was used during clean-up of onion extract and when chitosan was used for

133 th dispersive solid-phase extraction (d-SPE) clean-up of QuEChERS (quick, easy, cheap, effective, rug

134 was applied for the selective isolation and clean-up of tetracyclines (oxytetracycline, tetracycline

135 No clean-up of the digestion mixtures was needed prior to i

136 h, an ethyl acetate extraction followed by a clean-up of the extract by gel permeation chromatography

137 Clean-up of the sample and extraction of 11 analytes fro

138 investigated for simultaneous extraction and clean-up of thiamethoxam and thiacloprid from light and

139 Engineering bacteria to clean-up oil spills is rapidly advancing but faces regul

140 s by UPLC with fluorescence detection, after clean up on molecularly imprinted polymers, is herein de

141 esponse (18.0%), support operations (17.5%), clean-up on water (17.4%) or land (14.6%), decontaminati

142 p format, incorporating a solid-phase sample clean-up on-chip.

143 d the supernatant, after centrifugation, was cleaned up on a graphitized carbon solid-phase extractio

144 This allows the analyte to be cleaned up on the probe surface by simply washing the ta

145 uoroalkyl substances (PFAS) are expensive to clean up once emitted.

146 , which equates to around $10,000 per day of clean-up operations or $8,900 per tonne of litter.

147 collapsed, and those working in recovery and clean-up operations were exposed to severe psychological

148 samples for PAHs without the need for sample clean up or instrumental modifications for different mat

149 flows with arbitrary numbers of reaction and clean-up or capture steps.

150 als who worked on the oil spill response and clean-up or received safety training.

151 ht into specific activities on site, such as clean-up or structural change.

152 absence of unwanted matrix compounds in the cleaned-up PAH fraction down to the low picogram range u

153 t extraction to preconcentrate, extract, and clean up PAHs and PCDDs from human serum using the nonio

154 nt and environmental-friendly technology for cleaning up polluted soils.

155 Engineered plants can clean up pollution and recover technology-critical metal

156 f complex chromatographic separation, sample clean-up, preconcentration, and derivatization protocols

157 A clean up-preconcentration procedure was done prior to in

158 ible with column chromatography-based sample clean-up prior to analyte quantification.

159 soluble carbon was removed by the ENVI-Carb clean-up prior to the TOP assay.

160 A clean-up procedure based on PSA, GCB and MgSO4 was studi

161 ffective when added in the final step of the clean-up procedure instead of during extraction.

162 ) developed a gentler and simpler analytical clean-up procedure involving the use of a strong basic r

163 A QuEChERS method was used as extraction and clean-up procedure prior to separation and quantificatio

164 The clean-up procedure was performed by freezing samples ove

165 ported as well as the standards used for the clean-up procedure.

166 MSPD integrated the extraction and clean-up procedures into a single step, which provides t

167 Advanced sample clean-up procedures significantly impact total cell yiel

168 Solid-phase extraction clean-up procedures were performed as necessary followed

169 o improve the quality of PDB data, through a clean up programme that addresses inconsistencies and in

170 tly applied in serum; only requires a simple clean-up protocol.

171 he effects of three independent variables of clean-up replicate (A), extraction time (B), and solid-t

172 he optimal extraction conditions were 7 h, 3 clean-up replicates, and 1:4 solid to liquid ratio.

173 olution of DNA sequencing fragments when the cleaned up sample solution was used.

174 ng improvements aimed at preconcentrating or cleaning up samples.

175 Using M13mp18 as template, the resulting cleaned-up single DNA sequencing fragments could routine

176 amounts of sample (0.2 g), solvents (2 mL), clean-up sorbents (25 mg sorbent + 150 mg MgSO(4)) and p

177 Dispersive solid-phase clean-up sorbents (C18, GCB, Florisil, chitosan and grap

178 ied with amino groups (NH(2)), as dispersive clean-up sorbents for multi-component extraction of 21 p

179 Different clean-up sorbents were tested, and the best results were

180 cription-coupled nucleosome assembly, and to clean up spurious interactions.

181 -buffered version of QuEChERS, followed by a clean-up step and a concentration step to enhance sensit

182 extraction using acetonitrile, followed by a clean-up step based on dispersive solid-phase extraction

183 , followed by an immunoaffinity column (IAC) clean-up step before mass spectrometric detection (precu

184 solid-liquid extraction (SLE), followed by a clean-up step by solid phase extraction (SPE), were comp

185 is performed with acidified methanol, and a clean-up step by solid-phase extraction with polymeric c

186 hese results highlight the importance of the clean-up step for more reliable data in studies of healt

187 and simple extraction methods followed by a clean-up step is still lacking.

188 Furthermore, the method proposed requires no clean-up step of the acrylamide derivative to be perform

189 a dispersive solid-phase extraction (d-SPE) clean-up step to evaluate the phenolic composition, anti

190 e, sodium carbonate and sodium chloride, and clean-up step using dispersive solid-phase extraction by

191 acid (1%) was performed, while in nuts, the clean-up step was modified.

192 The clean-up step which employed chitosan proved to be effec

193 The proposed method uses a single clean-up step with acetic acid, resulting in a quick, lo

194 asonic solid-liquid extraction (FUSLE) and a clean-up step with Envi-Carb sorbent was validated and a

195 extraction with ethyl acetate, followed by a clean-up step with florisil.

196 icrowave extraction procedure consisted of a clean-up step with n-heptane and a subsequent dissolutio

197 ction is about 12min per sample and, for the clean-up step, a total solvent volume of 13ml is require

198 be used as sorbents, such as chitosan in the clean-up step, are cheap and green options.

199 he use of 1 g of sample, without preliminary clean-up step, sea sand as dispersant, temperature of 10

200 em after dilution and filtration without any clean-up step.

201 exane and isopropanol mixture, and a further clean-up step.

202 uces only one (17)O product, and requires no clean-up step.

203 subsequent reduction, alkylation and sample clean-up steps effectively reducing total analysis time

204 Neither dilution nor further clean-up steps of the extracts were needed.

205 EChERS extraction and dispersive solid-phase clean-up steps was applied.

206 trile (acetic acid 1% (v/v)), and additional clean-up steps were not necessary.

207 hod, which does not require extensive sample clean-up steps, was developed and validated.

208 ives quantitative results with no additional clean-up steps.

209 potential of trace plutonium assay to inform clean-up strategies of fast breeder legacies.

210 sociated with invasive physical and chemical clean-up strategies, there is an unparalleled interest i

211 This clean-up strategy provides at least 4.6 and 3.0-fold hig

212 ecause of the inherent danger and expense of cleaning up such wastes by physicochemical methods, othe

213 lentils and other pulses, using an effective clean-up system and UHPLC-MS/MS (triple quadrupole) meth

214 ctly into an automated turbulent flow sample clean-up system, coupled to a liquid-chromatography-high

215 ed to reduce the latter and so, for example, clean up tarnished steel.

216 Despite these concerns, plastic clean-up technologies can play an important role in redu

217 Although laudable, unregulated clean-up technologies may be inefficient and have uninte

218 ution by 2024, the implementation of plastic clean-up technologies should be regulated to secure thei

219 ommended as added value of implementation of clean-up technologies.

220 amental importance to the development of new clean-up technologies.

221 idely pursued in recent years as a favorable clean-up technology and is an area of intensive scientif

222 strategy rather than the converse, acting to clean up the motor noise resulting from low-fidelity exp

223 closely with the UniProt group at the EBI to clean up the taxonomy and sequence cross-reference infor

224 e extraction microcolumn, thus enriching and cleaning up the analytes.

225 Echo/anti-Echo signal detection cleans up the spectrum.

226 the early 1970s and directed individuals to clean up their local environment with the ultimate goal

227 rest of the sample as part of a solid-phase clean-up (thereby removing any contributions from the ba

228 roundwater sites around the world but can be cleaned up through bioremediation.

229 evelopment of phytoremediation strategies to clean up TNT from polluted military sites.

230 Diluted paint required clean up to remove 6:2 fluorotelomer phosphate diester (

231 indicated calibrants do not need to undergo clean-up to account for analyte loss.

232 may be needed during sample preparation and clean-up to address the issue of matrix effects.

233 framework for all protocol steps, from data clean-up to statistical analysis.

234 ave undergone minimal gas-phase collisional "clean-up" to retain native-like stoichiometries are disc

235 The planar clean-up took 7 min per sample, which is 5-fold faster t

236 e been proposed for environmental release to clean up toxic dump sites or as biopesticides.

237 generally based on liquid-liquid extraction, clean-up using an immunoaffinity column (IAC), and ident

238 Liquid-solid extraction, clean-up using immunoaffinity solid phase extraction chr

239 ollowed by dispersive solid phase extraction clean-up using primary secondary amine along with zircon

240 nd shoot process coupled with on-line sample clean-up using restricted access media with LC-MS/MS.

241 t samples were extracted by ultrasonication, cleaned up using a QuEChERS method, and PFASs were measu

242 a mixture of methanol/water (80:20; v/v) and cleaned up using immunoaffinity columns.

243 Samples were cleaned up using solid-phase extraction.

244 solvent extraction, then the extractant was cleaned-up using a coagulation process, and finally, the

245 extraction cartridges, and the extracts are cleaned-up using an anion-exchange cartridge (SAX) stack

246 L aliquot of the partitioned supernatant was cleaned-up using d-SPE and in-vial filtration with a com

247 s were washed with methanol and subjected to clean up via liquid/liquid and solid phase extraction pr

248 A final clean up via SPE on polyamide cartridges was also employ

249 Next on-line sample clean-up was achieved on the pretreatment precolumn Chro

250 Clean-up was achieved using solid phase extraction in ne

251 After the digestion of fat, the clean-up was carried out using solid phase extraction si

252 e extracted with acetonitrile and subsequent clean-up was done using dispersive solid phase extractio

253 llowed by primary secondary amines and C(18) clean-up was found suitable for the analysis of fifty fo

254 ed by rotary-evaporation and derivatized; no clean-up was necessary.

255 ollowed by solid phase extraction for sample clean-up was optimized.

256 Extraction of free phenolic acids and clean-up was performed by an optimised solid-phase extra

257 ssue by liquid-liquid extraction and further clean-up was performed by solid phase extraction using O

258 tion using dispersive solid-phase extraction clean-up was proposed for the trace level determination

259 h organic solvents and a final concentration/clean-up, we achieved recovery values from 90.7 to 108.6

260 Different polymeric and silica sorbents for clean up were tested and the combination of Florisil and

261 The extraction and clean-up were combined into a single step, thanks to the

262 Extraction and clean-up were performed according to QuEChERS principles

263 Different Solid Phase Extractions (SPE) and clean-up were selected to optimise the purification step

264 xtraction with Z-Sep+ and PSA dispersive-SPE clean-up were used for sample preparation.

265 n coffee was acetate buffer and chitosan for clean-up, while no-buffer extraction and the PSA + C18 m

266 oroacetic acid 5% and solid phase extraction clean up with STRATA X cartridge.

267 Direct injection and sample clean-up with a mixed-mode sorbent was compared.

268 ombination of site-selective conjugation and clean-up with ABC-tagged proteins also allows for facile

269 ers oligomers, following a modified QuEChERS clean-up with alumina/primary secondary amine, in pasta.

270 ollowed by dispersive solid-phase extraction clean-up with C(18) and Lipifiltr(R) and LC-HRMS for sim

271 sodium chloride, followed by dispersive SPE clean-up with diatomaceous earth.

272 ged, and safe) extraction and mixed-mode SPE clean-up with different sorbents in sample preparation.

273 It includes solid-liquid extraction and clean-up with dispersive solid phase extraction followed

274 QuEChERS-based extraction and clean-up with dispersive solid phase extraction were use

275 oyed acetonitrile for extraction followed by clean-up with EMR-Lipid(R) sorbent and trichloracetic ac

276 n solid-liquid extraction with acetonitrile, clean-up with Envicarb II/PSA cartridges and subsequent

277 d-SPE clean-up with PSA and C18 minimized the matrix effects b

278 urine samples prepared by direct dilution or clean-up with solid-phase extraction after acidic hydrol

279 ultrasonic extraction with ethylacetate and clean-up with SPE was also evaluated for these samples.

280 effect was observed due to efficient extract clean-up with ZrO2-based sorbents.

281 The sample was extracted with 5% TCA and cleaned up with Florisil providing 83.7% recoveries.

282 amples were extracted with ethyl acetate and cleaned up with primary secondary amine and graphitized

283 ction followed by immunoaffinity columns for clean-up, with recoveries of 86-92%, standard deviations

284 findings provide evidence that response and clean-up work is associated with adverse psychological e

285 Oil spill response and clean-up work was associated with increased prevalence o

286 INTERPRETATION: Oil spill clean-up workers with high amounts of total hydrocarbon

287 One full-scale version will be applied to clean up Z1 and Z2 harmonic errors in the MIT 1.3-GHz hi