ライフサイエンスコーパス: reversed-phase

1 graphy (HPLC) separation of proteins in both reversed phase and ion exchange modes.

2 ve validated the credentialing platform with reversed-phase and hydrophilic interaction liquid chroma

3 upon eluent composition explains the typical reversed-phase behavior (decreasing in retention followi

4 f peptides fractionated off-line by basic pH reversed-phase (bRP) chromatography.

5 First, Au-NPs are loaded onto a reversed phase C-18 (RP-C18) column, and then ligand-ass

6 romatographic separation is carried out on a reversed-phase C(18) column using 10% methanol/water.

7 romatographic separation was achieved with a reversed phase C18 column.

8 the sample and purification of oxysterols by reversed phase C18-SPE followed by HPLC-MS/MS analysis.

9 were eluted isocratically within 5 min on a reversed-phase C18 column without interference from endo

10 duced protein digests were separated using a reversed-phase C18 column, partially reduced by post-col

11 and 3D LC-MS/MS separation protocols (all of reversed-phase C18 functionality) to a tryptic digest of

12 of the samples with solid-phase extractions: reversed-phase (C18) and strong cation-exchange (SCX).

13 ne UHPLC separation into 8 fractions using a reversed-phase C4 column led to approximately twice as m

14 arried out by binary gradient technique on a reversed-phase C8 Zorbax column and the detection was ma

15 per demonstrates for the first time that C18 reversed-phase capillary liquid chromatography (Cap-LC)

16 en heated in boiling water and purified on a reversed-phase cartridge.

17 The method entails an aqueous extraction and reversed phase chromatographic separation using pentaflu

18 tribute to explain the retention behavior of reversed-phase chromatographic columns when used under h

19 gated the selectivity differences of various reversed-phase chromatographic sorbents.

20 After a short reversed-phase chromatographic step for desalting the sa

21 (ACE) in the first separation dimension and reversed phase chromatography (RP) in the second separat

22 y ionizable or retained analytes amenable to reversed phase chromatography and electrospray ionizatio

23 Ion exchange and high pH reversed phase chromatography are often used for this pu

24 g separation techniques for LC-IRMS, such as reversed phase chromatography at normal temperatures, io

25 HPLC-ICP-MS based on ion-paired reversed phase chromatography for the selenium speciatio

26 extracts of apple peels were fractionated by reversed phase chromatography using gradient elution of

27 Reversed phase chromatography, electrospray ionization-M

28 (salt-free) ion exchange chromatography and reversed phase chromatography-mass spectrometry allowed

29 Using complementary reversed-phase chromatography (RPC) and hydrophilic inte

30 graphy seleno-amino acids were determined by reversed-phase chromatography (RPC) coupled to ICP-MS.

31 Prymnesins were separated by reversed-phase chromatography and detected by positive-m

32 es were isolated using cationic exchange and reversed-phase chromatography and identified by (1)H NMR

33 Following trypsin cleavage, reversed-phase chromatography and mass spectrometry (MS)

34 ample preparation, off-line fractionation by reversed-phase chromatography at pH 10, immobilization o

35 Here, we show that nonaqueous reversed-phase chromatography can be coupled to mass-spe

36 collected, pooled together and subjected to reversed-phase chromatography for further purification.

37 tography (HILIC) for the aqueous extract and reversed-phase chromatography for the organic.

38 it is orthogonal to hydrophobicity on which reversed-phase chromatography is based.

39 ge of the analysis using subzero temperature reversed-phase chromatography is presented.

40 Reversed-phase chromatography revealed that most SAR11 b

41 techniques and peptide retention modeling in reversed-phase chromatography to generate a data set suf

42 14 to 36 carbon atoms are separated by C(8) reversed-phase chromatography using a water-methanol gra

43 Purification was based on miniature reversed-phase chromatography, a procedure suitable for

44 AH was separated using ultra-filtration and reversed-phase chromatography, and assessment of the fra

45 scent assay components are then separated by reversed-phase chromatography, and NBD-serine is quantif

46 e to separate the isomers, or who were using reversed-phase chromatography, gave rise to multi-modal

47 etylation resulted in increased retention in reversed-phase chromatography, whereas methylation, incl

48 actionated by off-gel isoelectrofocusing and reversed-phase chromatography.

49 tissue patches were directly collected on a reversed phase column and analyzed using an on-column ex

50 se, cellulase), the compounds separated on a reversed phase column by gradient elution and detected b

51 ographic separation was achieved using a C18 reversed phase column with gradient elution of basic mob

52 In contrast, on the reversed phase column, most metabolites eluted very rapi

53 A separation by LC was achieved using a reversed-phase column and a gradient of water/acetonitri

54 hat alanine and sarcosine coelute on an HPLC reversed-phase column and the mass spectrometer cannot d

55 EX elution steps are transferred onto the 2D reversed-phase column to further separate proteins.

56 step, van 't Hoff plots were measured with a reversed-phase column using the temperature control unit

57 A Kinetex C18 reversed-phase column was proposed under gradient elutio

58 d detection of tryptophan are performed on a reversed-phase column with fluorescence detection within

59 A C-18 reversed-phase column, acetonitrile-trifluoroacetic acid

60 ipped with a UV-detector, using a commercial reversed-phase column.

61 age of the gradient profile from a 150-mm C3 reversed-phase column.

62 sing high performance liquid chromatography (reversed phase columns, UV-Vis diode array detector) at

63 constructed with strong cation-exchange and reversed-phase columns, followed by MS/MS detection of t

64 Smaller (ca. 3 microm), normal and reversed-phase, core-shell diamond particles have been u

65 A high pH, low pH, reversed-phase data independent 2D-LC-MS(E) proteomic pl

66 ses strong cation-exchange (SCX) followed by reversed-phase desalting to remove Ficoll, a synthetic p

67 gradient mode were performed both in common reversed-phase eluents and environmental friendly ethano

68 2 under normal-phase and 3.74 and 4.34 under reversed-phase elution conditions.

69 e generation of droplets is also possible in reversed phase gradient elution mode as demonstrated by

70 , and 50 microm capillaries evaluated in the reversed phase gradient separation of three proteins sho

71 ing TFA as an acid modifier to a formic acid/reversed phase gradient, providing additional resolving

72 A targeted reversed-phase gradient UPLC-MS/MS assay has been develo

73 resent study was aimed to develop a low cost reversed phase high performance liquid chromatographic (

74 n phenols isolated from lake sediments using reversed phase high performance liquid chromatography (H

75 embranes, cation exchange chromatography and reversed phase high performance liquid chromatography wa

76 tion with solid phase extraction followed by reversed phase high performance liquid chromatography.

77 Reversed phase high pressure liquid chromatography (RP-H

78 gated for their phenolic profile by means of reversed phase high-performance liquid chromatography co

79 Analyzing the enriched samples by reversed phase high-performance liquid chromatography in

80 A robust analytical method, using reversed phase high-performance liquid chromatography wi

81 planar chromatography, using water-wettable reversed phase high-performance thin-layer chromatograph

82 A rapid reversed-phase high performance liquid chromatographic m

83 ere separated and quantified by an isocratic reversed-phase high performance liquid chromatography (H

84 the degrading microspheres was monitored by reversed-phase high performance liquid chromatography (H

85 cids in sour cassava starch wastewater using reversed-phase high performance liquid chromatography (H

86 Reversed-phase high performance liquid chromatography (R

87 ermination of vitamin E, being comparable to reversed-phase high performance liquid chromatography ch

88 Cleavage products were analyzed with reversed-phase high performance liquid chromatography, a

89 broadly be categorised into normal phase or reversed-phase high performance liquid chromatography.

90 d against immunoaffinity column (IAC) tandem reversed-phase high pressure liquid chromatography with

91 affinity column (IAC), and identification by reversed-phase high pressure liquid chromatography with

92 A method combining aqueous extraction, reversed-phase high-performance capillary liquid chromat

93 Both, reversed-phase high-performance liquid chromatography (H

94 tudy, we present the development of coupling reversed-phase high-performance liquid chromatography (H

95 A strategy using reversed-phase high-performance liquid chromatography (H

96 Here we describe a facile, reversed-phase high-performance liquid chromatography (H

97 These subunits were separated by ion-pair reversed-phase high-performance liquid chromatography (I

98 rometry (ICPMS), coupled to nano ion pairing reversed-phase high-performance liquid chromatography (n

99 iltration, gel filtration chromatography and reversed-phase high-performance liquid chromatography (R

100 The reversed-phase high-performance liquid chromatography (R

101 rapid determination of phenolic compounds by reversed-phase high-performance liquid chromatography (R

102 Reversed-phase high-performance liquid chromatography an

103 se peptide chemistry and characterized using reversed-phase high-performance liquid chromatography an

104 A reversed-phase high-performance liquid chromatography me

105 developed a stability-indicating, ion-pair, reversed-phase high-performance liquid chromatography me

106 Quantitation of protein concentrations by reversed-phase high-performance liquid chromatography pr

107 We used C18 reversed-phase high-performance liquid chromatography to

108 y solid-phase peptide synthesis, purified by reversed-phase high-performance liquid chromatography, a

109 sulfate polyacrylamide gel electrophoresis, reversed-phase high-performance liquid chromatography, a

110 tions of the Osborne fractions determined by reversed-phase high-performance liquid chromatography, s

111 culating phylloquinone was measured by using reversed-phase high-performance liquid chromatography.

112 ially available labeling kit and isolated by reversed-phase high-performance liquid chromatography.

113 The labeled product was purified by reversed-phase high-performance liquid chromatography.

114 (18)F-FB-IL2 was purified by reversed-phase high-performance liquid chromatography.

115 a commercially available kit and isolated by reversed-phase high-performance liquid chromatography.

116 mass spectrometry (MS), in combination with reversed-phase high-pressure liquid chromatography (HPLC

117 Reversed-phase, high-performance liquid chromatography (

118 pounds of non-V. vinifera grapes, using both reversed phase-high performance liquid chromatography (R

119 protein fractions generated were analyzed by reversed phase-high performance liquid chromatography an

120 ed to identify and quantify the saponins and reversed phase-high performance liquid chromatography co

121 ex, and its subsequent detection by Ion-Pair-Reversed Phase-High Performance Liquid Chromatography-Di

122 ased on enzymatic extraction with subsequent reversed-phase-high-pressure liquid chromatography (RP-H

123 monosulfate products that were identified by reversed phase HPLC and by LC-MS/MS.

124 AGE modification sites in plasma proteins by reversed phase HPLC mass spectrometry in tryptic plasma

125 Reversed phase HPLC provided multiple turnover rates and

126 s) in plant extracts was developed, based on reversed phase HPLC separation of extract components, fo

127 disk taken from the DPS sample, followed by reversed phase HPLC separation, combined with multiple r

128 punch taken from the DBS sample, followed by reversed phase HPLC separation, combined with selected r

129 ylcobalamin (OH-Cbl), were well separated by reversed phase HPLC with a C8-HPLC column as the station

130 Several conditions of ion-paired reversed phase HPLC-ICP-MS, such as pH of the mobile pha

131 med based on the retention times obtained by reversed phase HPLC.

132 nal NMR spectroscopy, mass spectrometry, and reversed-phase HPLC (log k(w)) and in one case by X-ray

133 s with mAb MF6 and subsequent analysis by C8 reversed-phase HPLC and MS/MS spectrometry and (ii) anal

134 The treated samples were characterized using reversed-phase HPLC and size-exclusion HPLC with absorpt

135 Here we used a reversed-phase HPLC coupled with tandem mass spectrometr

136 ze exclusion chromatography for homogeneity, reversed-phase HPLC for purity (99%), peptide digest LC-

137 ans- and cis-beta-Carotenes were analyzed by reversed-phase HPLC method using a mobile phase containi

138 We report here a 35-min reversed-phase HPLC method using a single C30 column kep

139 purification by HPLC, enzymatic hydrolysis, reversed-phase HPLC resolution of the ribonucleosides, a

140 (BioLCCC) describes polypeptide retention in reversed-phase HPLC using the basic principles of statis

141 The derivatives were separated via reversed-phase HPLC with gradient elution.

142 lmethoxycarbonyl chemistry, characterized by reversed-phase HPLC, and matrix-assisted laser desorptio

143 hioarsenolipids showed much sharper peaks on reversed-phase HPLC, which facilitated their resolution

144 he main aspects of polypeptide separation in reversed-phase HPLC.

145 and wax ester species were separated on the reversed-phase HPTLC plates.

146 igosaccharides, separated by size exclusion, reversed phase ion-pairing chromatography, and chip-base

147 We present a reversed phase ion-pairing HPLC-ICP-MS method for the se

148 Using a reversed-phase ion pair HPLC/MS method to evaluate inter

149 al key factors influencing the separation by reversed-phase ion pairing chromatography, specifically

150 Here we describe and apply a novel reversed-phase ion-pair liquid chromatography purificati

151 ort RNA strands have been developed based on reversed-phase ion-pair liquid chromatography.

152 We have analyzed GAGs in C. elegans using reversed-phase ion-pairing HPLC, mass spectrometry and i

153 from the analyses by enzymatic digestion and reversed-phase ion-pairing liquid chromatography mass sp

154 metabolites can be efficiently separated by reversed phase LC and ionized by electrospray ionization

155 ide molecular weight and retention time on a reversed phase LC column.

156 e the elution strength of aqueous eluents in reversed phase LC is the application of high temperature

157 The reversed phase LC method, with a cycle time 25 min, invo

158 0 to 100% MeOH and analyzed with untargeted reversed phase LC-MS showed that the highest number of m

159 by the combination of online two-dimensional reversed-phase LC (2D-LC) operated in high and low pH bu

160 omics analyses because it can interfere with reversed-phase LC separations and electrospray ionizatio

161 poor chromatographic retention properties in reversed-phase LC, the complex biological matrices, and

162 tes amino acid analysis by standard nanoflow reversed-phase LC-MS setups used for proteomics.

163 For a reversed-phase LC-MS/MS analysis of nine algal strains,

164 A reversed phase liquid chromatographic-tandem mass spectr

165 5 kDa proteolytic fragments were analyzed by reversed phase liquid chromatography (LC) coupled online

166 al phases for 2D gas chromatography (GC) and reversed phase liquid chromatography (RPLC) separations.

167 hic separation techniques, such as nanoscale reversed phase liquid chromatography and capillary elect

168 nitines was assessed by off-line coupling to reversed phase liquid chromatography coupled to time-of-

169 Reversed phase liquid chromatography coupled with MS-MS

170 are compared to those derived by denaturing reversed phase liquid chromatography using an oa-ToF MS

171 rvone, is performed by using on-line coupled reversed phase liquid chromatography with gas chromatogr

172 Reversed phase liquid chromatography with mass spectrome

173 up level of analysis, its complementarity to reversed phase liquid chromatography, and its hyphenatio

174 An online reversed phase liquid chromatography-gas chromatography

175 A novel approach involving the use of reversed phase liquid chromatography-mass spectrometry (

176 Wetting phenomena in reversed-phase liquid chromatographic (RPLC) stationary

177 nce of organic modifiers on the structure of reversed-phase liquid chromatographic (RPLC) stationary

178 The following isocratic high-performance reversed-phase liquid chromatographic conditions were so

179 The strategy capitalizes on high-resolution reversed-phase liquid chromatographic separations for an

180 separation of hydrophilic ionic analytes on reversed-phase liquid chromatographic stationary phases.

181 italizes on multidimensional high-resolution reversed-phase liquid chromatography (LC) separation for

182 s indicated that incorporation of m-NBA into reversed-phase liquid chromatography (LC) solvents impro

183 The platform combines reversed-phase liquid chromatography (LC) with online fl

184 ne method combining size-exclusion (SEC) and reversed-phase liquid chromatography (RP-HPLC) using a n

185 ophilic interaction chromatography (HILIC) x reversed-phase liquid chromatography (RP-LC) separation

186 hilic interaction chromatography (HILIC) and reversed-phase liquid chromatography (RP-LC) were employ

187 ated the utility of SERS in conjunction with reversed-phase liquid chromatography (RP-LC), for the de

188 Reversed-phase liquid chromatography (RPLC) and matrix a

189 adequate removal of the stationary phase of reversed-phase liquid chromatography (RPLC) columns.

190 ds mostly rely on gas chromatography (GC) or reversed-phase liquid chromatography (RPLC) coupled with

191 Reversed-phase liquid chromatography (RPLC) is a widely

192 ptake of eluent components by a C(18)-bonded reversed-phase liquid chromatography (RPLC) packing and

193 Most analytical methods rely on reversed-phase liquid chromatography (RPLC), which is qu

194 Reversed-phase liquid chromatography (RPLC), which uses

195 analysis has so far fallen far below that of reversed-phase liquid chromatography (RPLC)-MS/MS.

196 a combination of single-molecule imaging and reversed-phase liquid chromatography (RPLC).

197 tides were separated into 25 fractions using reversed-phase liquid chromatography (RPLC).

198 nteraction liquid chromatography (HILIC) and reversed-phase liquid chromatography (RPLC)] together wi

199 pipeline that combines superficially porous reversed-phase liquid chromatography (SPLC), Fourier tra

200 d/l-peptide epimers were separated by online reversed-phase liquid chromatography and fragmented by c

201 ties increased by up to 100-fold compared to reversed-phase liquid chromatography and hydrophilic int

202 The cells were labeled and analyzed by reversed-phase liquid chromatography and pulsed Q dissoc

203 The FAIMS approach is compared with reversed-phase liquid chromatography and strong cation e

204 r multilinear double pH/solvent-gradients in reversed-phase liquid chromatography are developed by di

205 rs Nochowski from 2012 and 2013 season using reversed-phase liquid chromatography combined with negat

206 een light/heavy pairs under various gradient reversed-phase liquid chromatography conditions, major c

207 Reversed-phase liquid chromatography coupled to electros

208 pe stripping of human skin, were analyzed by reversed-phase liquid chromatography coupled to high-res

209 s from different sources by high-temperature reversed-phase liquid chromatography coupled to isotope

210 Reversed-phase liquid chromatography coupled to negative

211 Reversed-phase liquid chromatography has become the pref

212 This platform combines reversed-phase liquid chromatography in parallel with bi

213 er, incorporation of the same modifiers into reversed-phase liquid chromatography solvents improves s

214 ple cleanup in a 96-well-plate format before reversed-phase liquid chromatography tandem mass spectro

215 analysis (CSIA) by coupling high-temperature reversed-phase liquid chromatography to isotope ratio ma

216 latform encompassing separation via ion-pair reversed-phase liquid chromatography using monolithic st

217 Peptide separation selectivity in reversed-phase liquid chromatography was investigated us

218 ituted in 25muL acetonitrile and analyzed by reversed-phase liquid chromatography with tandem mass sp

219 nd development of these materials for use in reversed-phase liquid chromatography, wide adoption cont

220 crofluidic device capable of two-dimensional reversed-phase liquid chromatography-capillary electroph

221 protein groups were identified in single-run reversed-phase liquid chromatography-electrospray ioniza

222 Here, we present a targeted reversed-phase liquid chromatography-high-resolution mas

223 vity in the separation of intact proteins by reversed-phase liquid chromatography-mass spectrometry (

224 olecule is not attainable using conventional reversed-phase liquid chromatography-mass spectrometry m

225 ILIC-MS/MS) for polar pesticides, and; (iii) reversed-phase liquid chromatography-tandem mass spectro

226 erum using liquid-liquid extraction prior to reversed-phase liquid chromatography-tandem mass spectro

227 ics and amine metabolomics analyses via nano reversed-phase liquid chromatography-tandem mass spectro

228 parison to over 600 other materials used for reversed-phase liquid chromatography.

229 actosamine), were shown to coelute following reversed-phase liquid chromatography.

230 a combination of hydrophilic interaction and reversed-phase liquid chromatography.

231 A reversed-phase liquid chromatography/mass spectrometry (

232 ion products were analyzed and quantified by reversed-phase liquid chromatography/tandem mass spectro

233 separation of longer peptides, combined with reversed phase-liquid chromatography (RP-LC) using colum

234 flight MS, and hydrophilic interaction- and reversed phase-liquid chromatography-quadrupole time-of-

235 pillary column packed with Waters YMC ODS-AQ reversed phase materials.

236 selectivity compared to conventional bonded reversed-phase materials, along with good peak shape and

237 any previous SPE of phenolic compounds using reversed-phase materials.

238 uch as they differ from the well-studied C18 reversed phase media.

239 We herein show how this previously described reversed phase method can baseline separate the cis-tran

240 Reversed-phase microfluidic liquid chromatography (LC) o

241 ethod for predicting UPLC retention times in reversed phase mode.

242 methanol-water (6:5:6:5 v/v) was used in the reversed phase mode.

243 Despite the use of reversed phase modes in both dimensions, a satisfactory

244 oint using a combination of ion-exchange and reversed phase modes.

245 thod for the profiling of polar lipids using reversed-phase nano high-performance liquid chromatograp

246 or sensitivity over a silica-based medium in reversed-phase nanocapillary LC, with detection of prote

247 -affinity flow configuration hyphenated with reversed phase nanoflow chromatography and coupled with

248 olumn in the first dimension for enrichment, reversed phase nanoLC column in the second dimension for

249 ndem C18/C30 column system under non-aqueous reversed phase (NARP) chromatography conditions.

250 iter scale, by using a single octanol-filled reversed-phase, octadecylsilane-modified (C18-silica) ch

251 00 cm columns fabricated with 5 mum diameter reversed phase particles and integrated electrospray emi

252 rapping region and an LC channel packed with reversed-phase particles.

253 d into their corresponding enantiomers under reversed-phase, polar organic and normal-phase condition

254 a 15 cm long separation column containing a reversed-phase polymethacrylate monolith as a stationary

255 ystals demonstrating negative refraction and reversed phase propagation.

256 mode column that has both anion-exchange and reversed-phase properties was used in the first dimensio

257 he trapping of proteolytic peptides onto the reversed phase resin.

258 ferent stationary phases are plotted against reversed phase retention data and examined as two-dimens

259 h is better in HILIC mode than in C5 and C18 reversed phase (RP) chromatography.

260 Nine state-of-the-art reversed phase (RP) columns for ultra-high performance l

261 Furthermore, polymeric reversed phase (RP) is created by octadecyl amine (ODA)

262 syl labeled metabolites can be captured on a reversed phase (RP) trap column for large volume injecti

263 tion step by strong cation exchange (SCX) or reversed phase (RP), and LC-MS analysis.

264 ssed three liquid chromatographic platforms: reversed phase (RP), aqueous normal phase (ANP), and hyd

265 ites, providing complementary information to reversed-phase (RP) chromatography.

266 ter-soluble metabolites depending on whether reversed-phase (RP) or hydrophilic interaction liquid ch

267 oaches that is facilitated by intact protein reversed-phase (RP)LC concurrently coupled with Fourier

268 hilic interaction chromatography (HILIC) and reversed-phase (RPLC) chromatography within one analytic

269 ethyl-functionalized silica gel, followed by reversed-phase semipreparative high-performance liquid c

270 hydrophobic chemistry was then used for the reversed phase separation in the orthogonal second dimen

271 ysteine-containing peptides in monolith with reversed phase separation of all other peptides, while t

272 Results are presented from reversed-phase separation of peptides on a 1 mm i.d. col

273 ration with 2 retention time segments, while reversed-phase separation was accomplished within 5.5 mi

274 Reversed-phase separations of nucleosides, nucleotides,

275 romatography (TLC) plates (alox, silica gel, reversed phase silica gel).

276 s, samples (20 mL) were concentrated using a reversed-phase solid-phase extraction (SPE) cartridge, f

277 cross-links as nucleosides, enrichment by a reversed-phase solid-phase extraction column, and nanoLC

278 ersus those measured for hydrophilic balance reversed-phase sorbents and the same mixed-mode polymer

279 imization of elution solvent composition for reversed phase SPE of a model system.

280 rophilic peptides than the traditional C(18) reversed-phase SPE, but it did so at the expense of an i

281 from analyzed samples by means of polymeric reversed phase Strata X solid phase extraction (SPE) car

282 extracted sample was chromatographed using a reversed phase system involving an Atlantis T3-C18 colum

283 lated peptides are more strongly retained by reversed phase than nonfarnesylated peptides.

284 icity of these new tracers was determined by reversed-phase thin-layer chromatography.

285 Antibodies were immobilized onto reversed-phase tips, which allows easy and flexible samp

286 and desalting the fractions onto a series of reversed phase trap cartridges with subsequent on-line a

287 g power (0.375nm) was further purified using reversed-phase UFLC and subjected to matrix assisted las

288 PE) step, and the analytes were separated by reversed-phase ultra high performance liquid chromatogra

289 analysis (EDA) was carried out by combining reversed-phase ultra performance liquid chromatography f

290 of biliverdin were subsequently annotated by reversed-phase ultra-high performance liquid chromatogra

291 Additionally, reversed-phase ultra-high performance liquid chromatogra

292 ethanesulfonate, (3) sequential ion-exchange/reversed-phase (ultra) high-performance liquid chromatog

293 these less commonly described conjugates by reversed-phase ultrahigh performance liquid chromatograp

294 re trapped online and then analyzed using an reversed-phase ultrahigh-performance liquid chromatograp

295 ligosaccharides was developed using ion-pair reversed-phase ultraperformance liquid chromatography co

296 An ion-pairing, reversed-phase, ultraperformance liquid chromatography (

297 A fast reversed-phase UPLC method was developed for squalene de

298 approach was based on scaling a conventional reversed-phase UPLC-MS method for urinary profiling from

299 r PA composition using normal-phase HPLC and reversed-phase UPLC-TQD-MS.

300 trimodal phase incorporating polar embedded reversed phase, weak anion exchange, and strong cation e