ライフサイエンスコーパス: reverse-phase

1 bed flow or oscillatory DF containing a flow-reversing phase.

2 lycoproteins with integrated, sequential C18 reverse phase and porous graphitized carbon-LC-ESI-QTOF-

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

4 We report here the important features of reverse phase-based nanoLC-MS/MS analysis of permethylat

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

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

7 eparation of vitamin D2 was carried out on a reverse phase C18 column with photo diode array detector

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

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

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

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

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

13 mine) guard columns connected in series to a reverse-phase (C18) analytical column.

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

15 determined by HPLC-PDA-MS (APCI(+)), using a reverse phase C30 column.

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

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

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

19 ow changes in sialic acid composition affect reverse phase chromatographic retention times: sialic ac

20 A rapid and economically affordable reverse-phase chromatographic approach based on a core-s

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

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

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

24 sSEC fractions could be further separated by reverse phase chromatography (RPC) coupled online with h

25 C with ion exchange chromatography (IEC) and reverse phase chromatography (RPC) for intact protein se

26 e HIC mobile phases is orthogonal to that of reverse phase chromatography (RPC).

27 ion as a hybrid form of conventional HIC and reverse phase chromatography.

28 protein extracts obtained were separated by reverse-phase chromatography (RP-HPLC-UV).

29 peptides, can be challenging to separate by reverse-phase chromatography with optimal efficiency.

30 ones in culture supernatants fractionated by reverse-phase chromatography, and mass spectrometry was

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

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

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

34 Reversed phase chromatography, electrospray ionization-M

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

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

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

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

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

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

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

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

43 Reversed-phase chromatography revealed that most SAR11 b

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

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

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

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

48 ns, iodate and nitrate, is demonstrated on a reverse phase column by a transient prior injection of h

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

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

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

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

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

54 ize exclusion, anion exchange, and capillary reverse phase columns coupled to IM-MS.

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

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

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

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

59 Thin-film hydration and reverse-phase evaporation techniques were evaluated in t

60 ance liquid chromatography method with a C18 reverse-phase fused-core column has been developed for t

61 e protein array (RPPA), termed polymer-based reverse phase glycoprotein array (polyGPA), to capture a

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

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

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

65 sed a central composite design to optimise a reverse phase high performance liquid chromatographic me

66 Catechin fractions were identified using reverse phase high performance liquid chromatography (HP

67 Some phenolic components were analyzed by reverse phase high performance liquid chromatography (RP

68 Reverse phase high performance liquid chromatography (RP

69 tate, alpha-tocopherol and gamma-tocopherol, reverse phase high performance liquid chromatography for

70 peptides was verified by LC-ESI-MS/MS and a reverse phase high performance liquid chromatography met

71 nt study, a new chromatographic method using reverse-phase high performance liquid chromatography cou

72 can be resolved and purified using ion-pair, reverse-phase high-performance liquid chromatography (HP

73 Ion-pair, reverse-phase high-performance liquid chromatography (HP

74 w concentrations of organic Fe ligands using reverse-phase high-performance liquid chromatography (HP

75 On the basis of reverse-phase high-performance liquid chromatography (RP

76 l filtration chromatography and two steps of reverse-phase high-performance liquid chromatography.

77 ic and dimeric flavan-3-ols were analyzed by reverse-phase high-pressure liquid chromatography, while

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

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

80 Reversed phase high pressure liquid chromatography (RP-H

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

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

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

84 A rapid reversed-phase high performance liquid chromatographic m

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

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

87 Reversed-phase high performance liquid chromatography (R

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

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

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

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

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

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

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

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

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

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

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

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

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

101 A reversed-phase high-performance liquid chromatography me

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

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

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

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

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

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

108 Reversed-phase, high-performance liquid chromatography (

109 Species separation was accomplished with reverse phase-high performance liquid chromatography (HP

110 DO cheeses were analysed using Urea-PAGE and reverse phase-high performance liquid chromatography (RP

111 ng a C18 matrix followed by semi-preparative reverse phase-high performance liquid chromatography (SP

112 The reverse phase-high pressure liquid chromatography chroma

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

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

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

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

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

118 ts of samples (10 mug), we developed high-pH reverse phase (Hp-RP) combined with stop-and-go extracti

119 Reverse phase HPLC show higher hydrophobicity of fluorin

120 and FMOC-derivatization preceded analysis by reverse phase HPLC with fluorescence.

121 sted backbiting chain end scission, based on reverse-phase HPLC analysis.

122 purified from salivary gland homogenates by reverse-phase HPLC and identified by mass spectrometry a

123 solubility, as measured by UV absorbance and reverse-phase HPLC experiments.

124 ing of a double filtration step coupled with reverse-phase HPLC fractionation of Chlamydia-infected H

125 dases upon cheese proteins were separated by reverse-phase HPLC to give 28 fractions.

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

127 Reversed phase HPLC provided multiple turnover rates and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

145 Reverse-phase LC-MS afforded fast separation according t

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

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

148 0 to 100% MeOH and analyzed with untargeted reversed phase LC-MS showed that the highest number of m

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

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

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

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

153 h-resolution accurate mass spectrometry with reverse phase liquid chromatography fractionation and ma

154 used method for peptide mapping is based on reverse phase liquid chromatography with mass spectromet

155 proteases, and was partially purified using reverse phase liquid chromatography.

156 However, their reverse-phase liquid chromatograph mass spectrometry pep

157 Reverse-phase liquid chromatographic methods using a hyd

158 up, cation exchange chromatography (CEX) and reverse-phase liquid chromatography (RPLC) were used as

159 th the collected fractions being analyzed by reverse-phase liquid chromatography coupled with tandem

160 abeling with amino acids in cell culture and reverse-phase liquid chromatography mass spectrometry, w

161 a liquid:liquid extraction and quantified by reverse-phase liquid chromatography tandem MS (LC-MS/MS)

162 ients were analyzed for 2HG concentration by reverse-phase liquid chromatography-mass spectrometry.

163 In this work, a reverse-phase liquid chromatography/tandem mass spectrom

164 5 kDa proteolytic fragments were analyzed by reversed phase liquid chromatography (LC) coupled online

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

166 Reversed phase liquid chromatography coupled with MS-MS

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

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

169 Reversed phase liquid chromatography with mass spectrome

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

193 Reversed-phase liquid chromatography has become the pref

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

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

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

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

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

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

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

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

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

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

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

205 A reversed-phase liquid chromatography/mass spectrometry (

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

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

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

209 oor retention of UDP-linked intermediates on reverse phase media, an ion-pairing (IP) approach using

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

211 By combining forward and reverse phase microarrays into an innovative three-dimen

212 A C18 reverse-phase mini-column was coupled to a continuous fl

213 -EtOAc-MeOH-H2O mixtures in normal-phase and reverse phase mode, respectively.

214 rmal-phase chromatography and carotenoids by reverse-phase mode.

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

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

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

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

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

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

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

222 iates some of the challenges associated with reverse-phase peptide separations.

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

224 ystals demonstrating negative refraction and reversed phase propagation.

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

226 High PLK1 expression was confirmed by reverse phase protein and tissue microarrays.

227 tream transcriptional response by exploiting reverse phase protein array (RPPA) and mRNA expression d

228 from 11 tumor types using the antibody based reverse phase protein array (RPPA) technology.

229 in expression after radiation, we utilized a reverse phase protein array (RPPA) to identify significa

230 Reverse phase protein array (RPPA) was performed on 205

231 ed a cohort of 129 ALL patient samples using reverse phase protein array (RPPA) with ErbB2 and phosph

232 Here, we report a novel functionalized reverse phase protein array (RPPA), termed polymer-based

233 Through reverse phase protein array analysis, we demonstrate tha

234 liquid chromatography-mass spectrometry and reverse phase protein array data from human MM cell line

235 -TRAP1 transgenic mice by RNA sequencing and reverse phase protein array reveals modulation of oncoge

236 We also used Reverse Phase Protein Array screening to identify differ

237 Unbiased reverse phase protein array studies and subsequent valid

238 Reverse phase protein array suggested that high expressi

239 Reverse phase protein array, tissue microarray, and quan

240 ons and did protein profiling analysis using reverse phase protein array; ii) computationally develop

241 Here, we describe the use of Reverse Phase Protein Arrays (RPPAs or RPLAs) to profile

242 Thus using a combination of RNAi screening, reverse phase protein arrays, and small molecules testin

243 proteomic platforms (planar and bead array, reverse phase protein microarray, phosphoflow, AQUA and

244 eptor (EGFR) phosphorylation, as assessed by reverse-phase protein analysis.

245 High-throughput reverse-phase protein array (RPPA) technology allows for

246 Reverse-phase protein array analysis of phospho-proteomi

247 Reverse-phase protein array analysis of PKCiota wild-typ

248 Phosphoproteomic profiles from reverse-phase protein array analysis supported by mRNA p

249 ignaling was studied by Western blotting and reverse-phase protein array analysis.

250 nalyzed whole exome sequencing (n = 374) and reverse-phase protein array data (n = 212) from head and

251 Analysis of reverse-phase protein array data indicated that increase

252 Reverse-phase protein array data show that PEA15 levels

253 alysis of human breast cancer microarray and reverse-phase protein array data was performed to identi

254 ant NRAS melanoma, we used a high-throughput reverse-phase protein array platform to identify signali

255 A reverse-phase protein array revealed that HuR-mediated r

256 Our screening, using a reverse-phase protein array, revealed distinct mechanism

257 Of the proteins screened in the reverse-phase protein array, we found that insulin recep

258 Reverse-phase protein arrays (RPPA) represent a powerful

259 Here we use reverse-phase protein arrays to analyse 3,467 patient sa

260 We first identified, by reverse-phase protein arrays, the lymphocyte cell-specif

261 Using reverse-phase protein arrays, we measured expression lev

262 Downstream events, measured by time-series reverse-phase protein microarrays, high-content imaging,

263 ry using the omics platforms: microarray and Reverse Phase Proteomic Array.

264 , miR-222-3p, miR-24-1-5p, and miR-31) using reverse-phase proteomic arrays.

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

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

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

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

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

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

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

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

273 Reversed-phase separations of nucleosides, nucleotides,

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

275 Reverse phase solid phase extraction was used to fractio

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

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

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

281 njection to assess each tracer metabolism by reverse-phase thin-layer chromatography.

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

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

284 eous HCl solution; unlike current processes, reverse phase transfer is achieved simply using water.

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

286 In the present study reverse-phase UHPLC-PDA technique was developed at 60 de

287 Reverse-phase ultra-high-pressure liquid chromatography

288 Then the samples were analyzed by reverse-phase ultra-performance liquid chromatography (U

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

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

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

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

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

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

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

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

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

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

299 Pressure Liquid Chromatography (MPLC) on the reverse phase using 5L of grape juice.

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