ライフサイエンスコーパス: HPLC

1 HPLC analysis revealed a decrease in carotenoid levels o

2 HPLC analysis revealed that PS flour added compounds whi

3 HPLC analysis showed that EPP was high in HG (homogalact

4 HPLC separation coupled with off-line determination by N

5 HPLC-DAD analysis showed a 25-78% increase in total phen

6 HPLC-DAD-ESI-MS/MS analysis identified cyanidine glycosi

7 HPLC-ESI-MS of procyanidins-rich fraction without any re

8 HPLC-ESI-UV/MS/MS-(IT) analysis recorded the presence of

9 trospray ionization mode (ESI(-)), an RP-18e-HPLC column and valve switch were exploited.

10 demonstrate that MS/MS data derived from 1D-HPLC strategies under different gradient schemes and sea

11 ed method was based on the heart-cutting 2D- HPLC technique in which only the specific portions of th

12 liquid chromatography/mass spectrometry (3D-HPLC/MS) approach for the monitoring of glycosylation pa

13 A HPLC-UV/FLD method was validated for the quantification

14 t was compared with the one obtained using a HPLC/DAD method.

15 diated peptide exchange binding assay and an HPLC-based competition binding assay.

16 In this paper, we developed an HPLC-MS/MS method for the simultaneous detection and qua

17 This study presents an HPLC-ESI-Q-TOF method for simultaneous quantification of

18 meat, by on-line coupling of LOC-FLEME to an HPLC system.

19 characterised using phytochemical analysis (HPLC fingerprint) to improve knowledge about this plant

20 potentials were determined by HPLC-MS(2) and HPLC equipped with an on-line ABTS(+) antioxidant detect

21 although traditional techniques (GC-ECD and HPLC-DAD) are still commonly used due to their accessibi

22 92), considering 4, 55 and 18 TLC, ELISA and HPLC-based studies (including 354, 9224 and 2606 samples

23 acids and soluble sugars through GC-FID and HPLC-RI, respectively, as well as the mineral profile, i

24 gastrocnemius by 1H-MRS and HPLC to compare signal quality and convergent validity.

25 UM-159PT TNBC cells, along with LC-MS/MS and HPLC metabolomics profiling, we found here that exposure

26 ls were measured using in vivo (31)P NMR and HPLC, respectively.

27 (1)H NMR, (13)C NMR and HPLC-DAD-MS were used to elucidate the acylation sites a

28 lts with discontinuous data of osmometry and HPLC showed an excellent agreement between the different

29 Using PAGE and HPLC analysis, we observed that the IP6K1/2-knockout cel

30 DPPH, FRAP, ABTS methods), total phenols and HPLC to detect individual phenolic and furanic compounds

31 ison between the two point-of-care tests and HPLC showed concordance between the three testing method

32 Testing of SPH membrane ultrafiltration and HPLC fractions indicated that smaller and non-polar pept

33 to the innovative integration of MA-XRF and HPLC-MS/MS to investigate these delicate artworks, the s

34 ance liquid chromatography with diode array (HPLC-DAD) and liquid chromatograph triple quadrupole mas

35 itional methods to codetect purines, such as HPLC with microdialysis, are robust but lack the tempora

36 ysis of such metal binding in a custom-built HPLC-ICP-MS system.

37 ation ranges: 5.10(-6)-1.10(-4) mol L(-1) by HPLC-UV and 1.10(-7)-5.10(-5) mol L(-1) by GC-MS techniq

38 emoTypeSC, 100% with SickleSCAN, and 100% by HPLC, and a sensitivity of 100% with HemoTypeSC, 100% wi

39 emoTypeSC, 100% with SickleSCAN, and 100% by HPLC.

40 e chlorinated and brominated acetic acids by HPLC-ICPMS/MS in Austrian surface, ground, and tap water

41 rs were fluorescently tagged and analysed by HPLC, combined with highly sensitive LC-MS/MS, MALDI-TOF

42 of reaction products, which were analysed by HPLC-ELSD.

43 performed a multi-step N-glycan analysis by HPLC and various exoglyosidase and chemical treatments i

44 will be made accessible prior to analysis by HPLC.

45 d polyphenol concentrations were analyzed by HPLC coupled to tandem MS after enzymatic hydrolysis.

46 nfrared spectrometers (NIRS) and analyzed by HPLC for total isoflavone and total saponin composition,

47 Consequently, we have analyzed by HPLC-ESI(+)/APCI(+)-hrTOF-MS(2) the accurate composition

48 sition in these milk samples was analyzed by HPLC.

49 was monitored spectrophotometrically, and by HPLC and LC-MS respectively, while antioxidant capacity

50 to those obtained by iodine titration and by HPLC-UV; all three methods were within 1.3% of the overa

51 of a highly efficient resolution approach by HPLC.

52 spectrophotometry, and major carotenoids by HPLC-DAD.

53 hy-bioautography method and characterised by HPLC-MS(n).

54 f polyphenols with MGO were characterized by HPLC-MS/MS.

55 ehensive analysis of phenolic composition by HPLC-DAD-Q-ToF-MS seed kernel from different cultivars (

56 terols, squalene, and phenolics compounds by HPLC-DAD, and the structures of the latter were confirme

57 rent methods, and (ii) identify compounds by HPLC-DAD-ESI-MS.

58 lfoselenide compounds which are confirmed by HPLC-QTof-MS.

59 aluated by SEM microscopy, sugars content by HPLC and sucrose melting temperature and enthalpy by DSC

60 fty-nine phenolic compounds were detected by HPLC-DAD-MS(n).

61 yptic digestion, and subsequent detection by HPLC-HRMS/MS.

62 and imazethapyr (IMT) with determination by HPLC-PAD (High performance liquid chromatography - photo

63 paper strip compared to those determined by HPLC was between 13.4 and 59.6% for tetracycline and 2.0

64 ation of AFB(1) and AFM(1) was determined by HPLC with fluorescence detection.

65 caffeoylquinic acids contents (determined by HPLC) as well as antioxidant activity (evaluated by Foli

66 d caffeine concentrations were determined by HPLC-DAD.

67 ttonseed ethanol extracts were determined by HPLC-MS analysis to be essentially free of toxic gossypo

68 nd antioxidant potentials were determined by HPLC-MS(2) and HPLC equipped with an on-line ABTS(+) ant

69 as in the chemical composition determined by HPLC-MS.

70 ion of NEPs molecular weight distribution by HPLC-SEC demonstrated that EAE extracted NEPs with high

71 rol and another that was analysed for DON by HPLC.

72 varying spectrum of polyphenols estimated by HPLC.

73 In this study, we have evaluated by HPLC-DAD, DLS and MALDI-TOF a synergic effect of the coe

74 of folic acid from flour samples followed by HPLC determination.

75 ng polymer nano- and microfibers followed by HPLC with spectrophotometric detection has been develope

76 rbent (in spinal syringe format) followed by HPLC-UV.

77 (SH4) and confirmed production of GM2/GD2 by HPLC.

78 Products were identified by HPLC, ESI-MS, FT-IR, and [Formula: see text] spectroscop

79 her compounds were tentatively identified by HPLC-DAD-ESI-MS(n).

80 43 metabolites were identified by HPLC-DAD-ESI-QTOF (8 betaxanthins, 8 betacyanins, 13 fla

81 of 46 phenolic compounds were identified by HPLC-DAD-ESI/MS(n) and quantified by HPLC-DAD, namely 19

82 amides and lignanamides, were identified by HPLC-ESI-QTOF-MS/MS.

83 ut also separately for each ET identified by HPLC-MS.

84 n aggregates composition was investigated by HPLC-tandem mass spectrometry.

85 d tocopherol isoform levels were measured by HPLC at the second trimester and 3 years of age, respect

86 ides for each grain species were measured by HPLC-MS/MS.

87 tB, venemycin production can be monitored by HPLC and NMR.

88 d cyanidin-3-O-glucoside levels monitored by HPLC-DAD-ESI/MS were used as response criteria.

89 susceptible moieties, is mainly monitored by HPLC-MS techniques.

90 ood donor-derived anti-D Ig were obtained by HPLC and mass spectrometry using 3 methods.

91 The speciation results obtained by HPLC-HG-AFS analysis indicated that the addition of As(I

92 the analyte determination was carried out by HPLC coupled to a fluorescence detector.

93 ea batatas native from Peru was performed by HPLC-QTOF-MSMS.

94 and metabolite levels in liver and plasma by HPLC.

95 and flavonoids content, phenolics profile by HPLC, and antioxidant activity of ten fruit beer produce

96 We characterized this complex protein by HPLC, light scattering, MS analysis, differential scanni

97 Purification by HPLC and analyses of the isolated peaks by NMR, MS, and

98 fied by HPLC-DAD-ESI/MS(n) and quantified by HPLC-DAD, namely 19 hydroxycinnamic acids, 2 hydroxybenz

99 ochemicals were identified and quantified by HPLC-ESI-TOF-MS.

100 on of QuEChERS and DLLME), and quantified by HPLC-FLD.

101 were separated, identified and quantified by HPLC-PDA-MS/MS.

102 vitro digestion and lutein was quantified by HPLC.

103 ied 44 polyphenols in the different seeds by HPLC-DAD-ESI-qTOF (MS/MS).

104 The polyphenol profile was studied by HPLC-ESI-MS/MS, while the antioxidant capacity was measu

105 These studies were further supported by HPLC analysis.

106 -pyridyl phosphorothioate) (CP) in tomato by HPLC-DAD.

107 tor was successfully used within a capillary HPLC system and could offer a miniaturized, rapidly stab

108 h-performance liquid chromatography (2D chip-HPLC) approach, which enables multiple transfers from th

109 high-performance liquid chromatography (chip-HPLC) with ion mobility spectrometry (IMS) via fully int

110 essants demonstrated the performance of chip-HPLC/IMS as a miniaturized two-dimensional separation te

111 ed, allowing for a robust coupling with chip-HPLC.

112 enantioselective synthesis as well as chiral HPLC methods were developed to give enantiopure R- and S

113 tic precursors were first screened by chiral HPLC for resolvability into enantiomers.

114 les of enantioenriched sulfoxides for chiral HPLC to enable reproducible results is clear.

115 MS), High-Performance Liquid Chromatography (HPLC) (for the quantification of eight organic acids), U

116 ) by high-performance liquid chromatography (HPLC) (this information was obtained from a guidebook "E

117 High performance liquid chromatography (HPLC) analysis of KG hydrolysate indicated its mannoolig

118 onal high-performance liquid chromatography (HPLC) and mass spectrometry (MS) is limited due to the s

119 sing high-performance liquid chromatography (HPLC) and minerals by inductively coupled plasma mass sp

120 IdeS-high-performance liquid chromatography (HPLC) column as a first dimension ((1)D) for on-line dig

121 and high-performance liquid chromatography (HPLC) data for these late-stage diversified cyclic RGD p

122 s by high-performance liquid chromatography (HPLC) in fecal samples from 301 one-year-old children fr

123 sing high-performance liquid chromatography (HPLC) in selected food products, in the aspect of consum

124 iral high-performance liquid chromatography (HPLC) into its enantiomers, and all four inherently chir

125 h as high-performance liquid chromatography (HPLC) or total organic carbon, often lead to extending t

126 rect high-performance liquid chromatography (HPLC) resolution or, when configurational lability was t

127 d by high-performance liquid chromatography (HPLC) to measure whole amino acid profiles for various f

128 NMR, high-performance liquid chromatography (HPLC), and mass spectrometry demonstrates that they work

129 anoflow high-pressure liquid chromatography (HPLC), current state-of-the-art systems still suffer fro

130 sing high-performance liquid chromatography (HPLC), fourier transform infrared spectroscopy (FTIR) an

131 SA), High-Performance Liquid Chromatography (HPLC), Mass Spectrum, and immunohistochemistry (IHC).

132 s by high-performance liquid chromatography (HPLC)-ICPMS/MS but none about utilizing this technique f

133 sing high-performance liquid chromatography (HPLC)-tandem mass spectrometry (LC-MS/MS), we found that

134 est, high-performance liquid chromatography (HPLC).

135 d by high performance liquid chromatography (HPLC).

136 sing high performance liquid chromatography (HPLC).

137 used high-performance liquid chromatography (HPLC).

138 sing high-performance liquid chromatography (HPLC).

139 and High Performance Liquid Chromatography (HPLC).

140 d by high performance liquid chromatography (HPLC).

141 d by high-performance liquid chromatography (HPLC).

142 d by high-performance liquid chromatography (HPLC).

143 s by high performance liquid chromatography (HPLC).

144 by a high-performance liquid chromatography (HPLC-FD) with a limit of detection (LOD) of 0.05 ng/mL f

145 d by High Performance Liquid Chromatography (HPLC-UV), BTEX (Benzene, Toluene, Ethylbenzene and Xylen

146 on (high-performance liquid chromatography - HPLC).

147 n ratios determined on a phospholipid coated HPLC column (IAM-HPLC) closely aligned with SSLM K(MW) v

148 Migration from conventional HPLC to UHPLC allowed a 60% reduction in analysis.

149 atography-tandem mass spectrometry coupling (HPLC-MS/MS) is classically used to characterize post-tra

150 Finally, calibrated CSMISPE-HPLC-UV method was used for lincomycin residue checking

151 d chromatography with ultraviolet detection (HPLC-UV).

152 id chromatography with diode array detector (HPLC-DAD).

153 id chromatography equipped with UV detector (HPLC-UV).

154 trometry (CRMS) coupled with two-dimensional HPLC (2D-LC).

155 in comparison with the corresponding direct HPLC standard method.

156 purified by reverse phase or anion exchange HPLC, yielding triethylammonium or ammonium salts in 32%

157 An ion-exchange-HPLC (with anion and cation exchange columns) and an ICP

158 id chromatography-ultra violet-fluorescence (HPLC-UV/FL) analysis.

159 were found to be between 89.2 and 98.3% for HPLC-UV system.

160 values of cobalt in cobalamin and cobalt for HPLC-ICP-OES system were calculated as 0.07 mg/kg (as Co

161 nzoyl chloride pre-column derivatisation for HPLC-UV determination of twelve biogenic amines (BAs) in

162 alteu, Total Polyphenols Index, DPPH, FRAP), HPLC (phloroglucinolysis), voltammetric analysis (Linear

163 cases and matched controls using label-free HPLC-tandem mass spectrometry.

164 the choice of components for the metal-free HPLC-DAD system and sector-field ICP-MS detection (ICF-s

165 Furthermore, HPLC-MS confirmed the methylation signals on mitochondri

166 Liquids and aerosols were analyzed by GCMS, HPLC, and fluorescence.

167 ed on a phospholipid coated HPLC column (IAM-HPLC) closely aligned with SSLM K(MW) values.

168 BZF was identified (HPLC-DAD-ESI-MS/MS) only in the dry outer scales of onio

169 versed-phase/cation-exchange columns (RP/IEX-HPLC), UV/vis detector, and a Rheodyne valve were instal

170 witch and NP-HPLC-UV/vis/FLD-bioassay-RP/IEX-HPLC-UV/vis-ESI(+/-)-MS with or without it.

171 in addition to determination of cobalamin in HPLC system.

172 se of bulky polymers as stationary phases in HPLC.

173 A stability-indicating HPLC-DAD method for simultaneous determination of all ni

174 n collection programs tailored to individual HPLC methods.

175 potential in microseparation techniques like HPLC and lab-on-a-chip devices.

176 rement results obtained using the macroscale HPLC method does not exceed 6.0%.

177 Anthocyanins were analyzed using micro-HPLC-MS/MS.

178 We analyzed this phenotype by microscopy, HPLC, gene functional characterization, genome structure

179 al data for a variable path length (0-60 mm) HPLC detection cell indicate that an exponential model f

180 -methodological approach, including NMR, MS, HPLC-PDA, GC-MS and spectrophotometric analyses, was pro

181 tudy describes the use of a multidimensional HPLC (2D and 4D) system for a faster and more effective

182 ifunctional tag that allows multidimensional HPLC purification and production of a tagged glycan libr

183 illar array column to a widely used nanoflow HPLC column for the proteomics analysis of 10 ng of tryp

184 To this purpose, a new HPLC-DAD method was developed and validated.

185 -UV/vis-ESI(-)-MS with a valve switch and NP-HPLC-UV/vis/FLD-bioassay-RP/IEX-HPLC-UV/vis-ESI(+/-)-MS

186 perhyphenations were successfully proven: NP-HPLC-UV/vis/FLD-bioassay-RP-HPLC-UV/vis-ESI(-)-MS with a

187 ug L(-1)) and demonstrates the advantages of HPLC-ICPMS/MS for the analysis of environmental water sa

188 lts of electrochemical approach with that of HPLC technique.

189 Use of HPLC and Florisil column enabled the separation of OxyTP

190 interactions on ESI response were studied on HPLC-QTOF.

191 ultra-performance -UPLC and high-performance-HPLC) coupled with mass spectrometry (MS) is conventiona

192 are identified/quantified by reversed phase HPLC coupled to tandem mass spectrometry by atmospheric

193 Also reversed phase HPLC-DAD method was developed and validated for estimati

194 Here, employing reversed-phase HPLC coupled with sensitive mass spectrometry, we demons

195 Reversed-phase HPLC enables the isolation of the all-trans isomer of th

196 d assisted extraction (UAE) and the platform HPLC-ESI-TOF-MS was employed to characterize these compo

197 The sum of 14 polyphenols (HPLC quantitation) was positively correlated with the me

198 Manual fraction collection from a prep-HPLC is a common method; however, it often lacks the rep

199 igh-performance liquid chromatographic (prep-HPLC) systems are used in many research schemes includin

200 ndous resource for any lab that employs prep-HPLC methods.

201 Automated fraction collectors for prep-HPLC systems can add thousands of dollars to the cost of

202 add thousands of dollars to the cost of prep-HPLC and are thus not always available to budgetary cons

203 rtition chromatography (CPC) and preparative HPLC.

204 ng TM complexes were isolated by preparative HPLC on a chiral stationary phase in good yields and exc

205 extraction technique followed by preparative HPLC.

206 thocyanins were isolated by semi-preparative HPLC, weighed, dried, and redissolved in acidic methanol

207 The polyphenol profile (HPLC-MS/MS) and antioxidant capacity (PCL(ACW), ABTS, FR

208 f the isolated (211)At was assessed by radio-HPLC.

209 min), AIF is routinely determined with radio-HPLC of blood sampled frequently during the PET experime

210 ich allow streamlining the extraction of raw HPLC data into TIBCO Spotfire for the graphical display

211 th those obtained with ELISA and a reference HPLC method (AOAC No.

212 Further enrichment by repetitive HPLC fractionation resulted in the quantitation of 6 add

213 The resulting HPLC-DAD-ICP-sfMS system has detection limits in the pic

214 The second one is RP- HPLC.

215 RP-HPLC was similarly able to quantify the main phenolics a

216 this study was to develop and validate an RP-HPLC-DAD method for the simultaneous quantification of t

217 fully proven: NP-HPLC-UV/vis/FLD-bioassay-RP-HPLC-UV/vis-ESI(-)-MS with a valve switch and NP-HPLC-UV

218 of activated platelets were separated by RP-HPLC demonstrating the coelution of 12(S)-HETE with frac

219 e high-performance liquid chromatography (RP-HPLC).

220 e liquid chromatography coupling with MS (RP-HPLC-MS).

221 d for nitrate and nitrite by an optimised RP-HPLC technique with isocratic elution using n-octylamine

222 e <=3 kDa were characterized by SDS-page, RP-HPLC and MALDI-TOF-MS.

223 The beta-carotene was quantified using RP-HPLC at bimonthly intervals for a period of six months.

224 n High Performance Liquid Chromatography (SE-HPLC) (Biosep-SEC-s2000, 5 um).

225 n-high performance liquid chromatography (SE-HPLC).

226 The SE-HPLC method was successfully compared to references: Kje

227 Lipids were separated using semipreparative HPLC, and specific lipid classes were identified using l

228 Rapid, precise, accurate, and sensitive HPLC-UV method for each drug was successfully developed,

229 regioisomers were quantified within a single HPLC run.

230 For speciation, HPLC coupled to ICP-MS was employed.

231 matography-high-resolution mass spectrometry HPLC-HRMS in the absence of chemical standards.

232 oupled plasma-optical emission spectrometry (HPLC-ICP-OES) in addition to determination of cobalamin

233 rospray-ionization tandem mass spectrometry (HPLC-ESI-MS/MS) to simultaneously quantify adenine nucle

234 nce liquid chromatography-mass spectrometry (HPLC-MS) analysis, without the need of preconcentrating

235 romatography coupled with mass spectrometry (HPLC-MS) and gas chromatography coupled with mass spectr

236 dney biopsy tissue, using mass spectrometry (HPLC-MS/MS) (n = 27) and immunohistochemistry (IHC) (n =

237 raphy - Mass Spectrometry/Mass Spectrometry (HPLC-MS/MS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) fre

238 uid chromatography tandem mass spectrometry (HPLC-MS/MS) was explored for the first time with applica

239 tograph triple quadrupole mass spectrometry (HPLC-MS/MS) were used to characterize raw and fermented

240 quadrupole time-of-flight mass spectrometry (HPLC-Q-TOF MS) with univariate and multivariate statisti

241 quadrupole time-of-flight mass spectrometry (HPLC-QTOF-MS) was developed to screen for the presence o

242 quadrupole time of flight mass spectrometry (HPLC-QTOF-MS) was used to analyze residues in fish.

243 me, liquid chromatography/mass spectrometry (HPLC/MS) was used to differentiate bovine bone gelatin f

244 niques including FTIR, UV spectrophotometry, HPLC and LC-MS analysis.

245 , most will rely on UV-Visible spectroscopy, HPLC and LC-MS methods.

246 valuable and enriching addition to standard HPLC and MS analysis of conformational isomers of disulf

247 In this study, HPLC/MS(2) experiments based on gas-phase ion-molecule r

248 The HPLC analysis of chitinase degraded shellfish waste reve

249 balt in cobalamin and cobalt detected by the HPLC-ICP-OES system were calculated in the range of 87.4

250 in good agreement with the results from the HPLC-UV reference method.

251 decreased, the signal-to-noise ratio of the HPLC peaks decreased more than the signal-to-noise ratio

252 Therefore, the HPLC part of this analysis was the primary limiting fact

253 The developed approach was applied to the HPLC-FLD determination of phenols (phenol, o-cresol, p-c

254 According to the HPLC-MS analysis of the caprylate esters, EGC-4'-O-capry

255 was only possible to determine DMA using the HPLC-ICP-MS mode.

256 ites) in rats' physiological fluids with the HPLC-MS/MS method proves betacyanin absorption from the

257 between concentration of triazoles and their HPLC peak areas in the range of 0.5-100 ug L(-1).

258 Thioglycolysis-HPLC-ESI-MS identified five oxidation markers of PCs wit

259 te reaction quenching was determined through HPLC and mass spectrometry.

260 The quantification was carried out through HPLC.

261 to fractionate minor metabolites compared to HPLC.

262 ofile of the polymers and then coupled it to HPLC to obtain discernible mass spectra of key impuritie

263 tion, with similar separation performance to HPLC, but with improved speed and lower sample volumes.

264 eloped for extraction of aflatoxins prior to HPLC-FD.

265 nt compound racemic mixture was subjected to HPLC enantioseparation, and the identification of the eu

266 subjected to metabolomics analysis by ultra-HPLC (uHPLC), coupled to a photodiode array (PDA) and ta

267 Using targeted ultra-HPLC-tandem MS (UPLC-MS/MS), we measured sphingolipids (

268 rformance liquid chromatography-ultraviolet (HPLC-UV).

269 We then used HPLC-MS/MS to assess the beta-glucosidase activity of pu

270 Using HPLC-DAD we analyzed saffron plants grown at various con

271 quantification method for gallic acid using HPLC-UV was developed and validated.

272 s of Highbush and Rabbiteye blueberry, using HPLC-DAD-ESI-MS(n).

273 All the analyses were performed by using HPLC-MS/MS followed by pooling the variables with princi

274 and lariciresinol) in green coffee by using HPLC-MS/MS.

275 eous evaluation of these MLs in cheese using HPLC and fluorescence detection.

276 statherins/P-B peptide, and cystatins) using HPLC-UV and fluorescence.

277 different stages of tuber development, using HPLC-DAD and UHPLC-MS.

278 , have been separated into enantiomers using HPLC with a chiral stationary phase.

279 bfractions (thylakoids and envelopes), using HPLC high-resolution tandem mass spectrometry, thin-laye

280 tion of ALA in food items was examined using HPLC-UV and GC-MS systems.

281 and folates in fresh and frozen fruits using HPLC-UV analyses.

282 nding increases in MAAs under FR light using HPLC analysis.

283 ryptic-digested gelatins were measured using HPLC/MS and, subsequently, two powerful chemometrics app

284 ow-cost multipurpose analytical method using HPLC-UV-DAD was developed and validated, following inter

285 pal phenolic compounds was carried out using HPLC method.

286 PAHs analysis was performed using HPLC-FLD/DAD and confirmed by GC-MS.

287 r prospective thiols was then proposed using HPLC with high resolution MS, and verified with authenti

288 phenolics in lentil hulls were studied using HPLC-DAD-ESI-MS(n) and their antioxidant potential deter

289 impact on the metabolome were studied using HPLC-ESI-QTOF-MS analysis of polar and apolar compounds.

290 and dihydrocapsiate for the first time using HPLC-ESI/MS(QTOF).

291 Here we describe a novel method utilizing HPLC-ESI-MS/MS to identify and quantify multiple full-le

292 Finally, a validated HPLC method offering good precision (0.12-0.94%) and acc

293 ined were compared to those of the validated HPLC-MS method.

294 gurational lability was too high, through VT-HPLC analysis on the chiral stationary phase (DeltaG(*)

295 ing four vegetal examples and beginning with HPLC-MS/MS in precursor ion scan mode, after extraction

296 nd in SMCs, ICC and PDGFRalpha(+) cells with HPLC-FLD, we report that (1) in tissues, eNAD is degrade

297 LOQs for MISPE offline coupled with HPLC were less than 1.5 ug mL(-1) and 12 ng mL(-1) for U

298 rtho-phenylenediamine, we analyzed 3-DG with HPLC-UV.

299 ical determination method was evaluated with HPLC as a standard determination method.

300 ioning evaluated using UV detection, or with HPLC coupled to either charged aerosol detection or ESI-