ライフサイエンスコーパス: liquid chromatography

1 2 hours over a 7-day period by high-pressure liquid chromatography.

2 ) levels were quantified by high-performance liquid chromatography.

3 ing SERS and confirmed with high-performance liquid chromatography.

4 usion experiments, and experiments employing liquid chromatography.

5 n-PyC3A metabolism by using high-performance liquid chromatography.

6 amino acid (AA) contents were determined by liquid chromatography.

7 n apple juices and ciders were studied using liquid chromatography.

8 tion, and analyzed by ultra-high performance liquid chromatography.

9 tched healthy volunteers by high-performance liquid chromatography.

10 18)F-FCP was verified using high-performance liquid chromatography.

11 retinol and alpha-, and gamma-tocopherol by liquid chromatography.

12 ma of a rhesus monkey using high-performance liquid chromatography.

13 h 80% (v/v) aqueous methanol and purified by liquid chromatography.

14 in-layer chromatography and high-performance liquid chromatography.

15 ch were separated by chiral high-performance liquid chromatography.

16 ations that involve the use of both gas- and liquid-chromatography.

17 ss the motivations for doing two-dimensional liquid chromatography (2D-LC) and describe the commonly

18 the development of an online two-dimensional liquid chromatography (2D-LC) method where the first dim

19 Ultra-Performance Liquid Chromatography analyses indicate that MLG in brow

20 High-performance liquid chromatography analyses of hamster ear extracts s

21 use blood was determined by high-performance liquid chromatography analysis of blood samples.

22 tment strategy coming from metabolomics with liquid chromatography analysis using a silica bonded C18

23 Fluorescence microscopy and high performance liquid chromatography analysis were performed to determi

24 As shown by high-performance liquid chromatography analysis, levels of 11-cis-RAL in

25 RYM1 was evaluated by radio-high-performance liquid chromatography analysis.

26 raterellus tubaeformis) using high precision liquid chromatography analysis.

27 ns was determined by an on-line method using liquid chromatography and an electrochemical detector fo

28 Tandem mass spectrometry, when combined with liquid chromatography and applied to complex mixtures, p

29 mobility spectrometry (FAIMS) combined with liquid chromatography and mass spectrometry (LC-FAIMS-MS

30 re liquid chromatography, ultrahigh pressure liquid chromatography and SDS-PAGE gels.

31 eeks 4 and 12 using a commercially available liquid chromatography and tandem mass spectrometry assay

32 e acids were profiled using high-performance liquid chromatography and the composition of the microbi

33 omparable to reversed-phase high performance liquid chromatography chosen as reference method.

34 separated and identified by high-performance liquid chromatography coupled to a mass spectrometer.

35 ed to determine flubendiamide in honey using liquid chromatography coupled to a selective mass spectr

36 ve quantification and ultra-high-performance liquid chromatography coupled to accurate-mass, high-res

37 Liquid chromatography coupled to high resolution mass sp

38 Using liquid chromatography coupled to high-resolution accurat

39 Nontarget screening by liquid chromatography coupled to high-resolution mass sp

40 ctrospray ionization (ESI) is widely used in liquid chromatography coupled to mass spectrometry (LC-M

41 g BRCA1 pathogenic mutations by non-targeted liquid chromatography coupled to mass spectrometry techn

42 nalysis was performed using high-performance liquid chromatography coupled to photodiode-array detect

43 Here we optimized conditions for liquid chromatography coupled to tandem mass spectrometr

44 biodistribution of EDHB were analyzed using liquid chromatography coupled to tandem mass spectrometr

45 A normal-phase ultraperformance liquid chromatography coupled to tandem mass spectrometr

46 specific method using ultra-high performance liquid chromatography coupled to tandem mass spectrometr

47 Liquid chromatography coupled to ultra-high-definition a

48 (NIT) in livestock feeds by high performance liquid chromatography coupled to ultraviolet oxidation h

49 Liquid chromatography coupled with electrospray ionizati

50 n-up, and analysis by ultra-high performance liquid chromatography coupled with fluorescence detectio

51 Sample analyses were performed using liquid chromatography coupled with mass spectrometry, SD

52 ocalibrated by their (14)C-isotopologues via liquid chromatography coupled with radioactivity detecti

53 ugar profile was determined by high-pressure liquid chromatography coupled with refractive index dete

54 an optimisation and validation process using liquid chromatography coupled with tandem mass spectrome

55 eved, using optimized solvent extraction and liquid chromatography coupled with tandem mass spectrome

56 Liquid chromatography, coupled to a diode array detector

57 employed a combination of ultra-performance liquid chromatography-coupled electrospray ionization ta

58 The peroxy acids were separated using liquid chromatography, detected via negative mode electr

59 High performance liquid chromatography-diode array detection- tandem mass

60 A commercial liquid chromatography/drift tube ion mobility-mass spect

61 raphy/mass spectrometry and high-performance liquid chromatography electrospray ionization tandem mas

62 With this in mind, we developed a liquid chromatography-electrospray ionization tandem mas

63 ctrometric screens based on high-performance liquid chromatography-electrospray ionization-tandem mas

64 uronidase (E. coli K12) and then analyzed by liquid chromatography-electrospray ionization-triple qua

65 screening methods with ultrahigh-performance liquid chromatography-electrospray ionization/quadrupole

66 , mass spectrometry-based approaches such as liquid chromatography/electrospray ionization multiple r

67 ic acid were identified by ultra-performance liquid chromatography/electrospray ionization-quadruple

68 , ciprofloxacin and enrofloxacin by micellar liquid chromatography - fluorescence detection in commer

69 ldehyde (OPA) reagent using high-performance liquid chromatography-fluorescence detection.

70 ion of gas chromatography-mass spectrometry, liquid chromatography-fluorescence, and mass spectrometr

71 ccurate mass spectrometry with reverse phase liquid chromatography fractionation and mass spectrometr

72 A real time monitoring of fouling in liquid chromatography has been presented.

73 nic compounds from marine biota samples by a liquid chromatography-heated electrospray ionization/tan

74 s were extracted three times and analyzed by liquid chromatography high resolution mass or time-of-fl

75 necarboxylic acid (3-QCA), was identified by liquid chromatography high resolution tandem mass spectr

76 s work, a sensitive method based on nanoflow liquid chromatography high-resolution mass spectrometry

77 graphy mass-spectrometry (GC x GC/MS) and/or liquid-chromatography high-resolution accurate-mass mass

78 Here liquid-chromatography high-resolution mass spectrometry

79 Using a suspect screening workflow based on liquid chromatography-high resolution (Orbitrap) mass sp

80 This study therefore applies liquid chromatography-high resolution mass spectrometry

81 he potential to enhance different aspects of liquid chromatography-high-resolution mass spectrometry

82 tabolomic profiling by ultrahigh-performance liquid chromatography-high-resolution mass spectrometry

83 hybridizing ligand binding assay (LBA) with liquid chromatography-high-resolution mass spectrometry

84 Here, we present a targeted reversed-phase liquid chromatography-high-resolution mass spectrometry-

85 The hydrophilic interaction liquid chromatography (HILIC) coupled to a negative-ion

86 acid derivatives and hydrophilic interaction liquid chromatography (HILIC) in combination with mass s

87 ish tissue, based on hydrophilic interaction liquid chromatography (HILIC).

88 determined by using on-line high-performance liquid chromatography (HPLC) analysis combined with 2,2'

89 Results from high performance liquid chromatography (HPLC) analysis indicated high con

90 A normal phase high performance liquid chromatography (HPLC) method was developed to sim

91 s were investigated using a high performance liquid chromatography (HPLC) platform coupled to photo d

92 ation (VG) device to couple high-performance liquid chromatography (HPLC) separation and inductively

93 Measurements using high-performance liquid chromatography (HPLC) showed that the activity of

94 High performance liquid chromatography (HPLC) was employed for the measur

95 quantitative capability of high-performance liquid chromatography (HPLC) with charged aerosol detect

96 avanones were determined by high-performance liquid chromatography (HPLC) with diode array detection,

97 phase extraction (SPE) and high performance liquid chromatography (HPLC) with fluorescence detection

98 , radiolabeling followed by high-performance liquid chromatography (HPLC) with radiodetection, the de

99 d infant formula samples by high performance liquid chromatography (HPLC) with visible detection.

100 says (ELISA), Western blot, high performance liquid chromatography (HPLC), spectrophotometry and flow

101 nts, and indirectly through high-performance liquid chromatography (HPLC)-fluorescence detection of B

102 s measured as plasma PLP by high-performance liquid chromatography (HPLC).

103 llic acid, as quantified by high performance liquid chromatography (HPLC).

104 ovide a set of quantitative high-performance liquid-chromatography (HPLC) approaches to determine CSF

105 measured by immobilized artificial membrane liquid chromatography (IAM-LC) and by micellar liquid ch

106 mic analysis of plasma samples using gas and liquid chromatography in combination with mass spectrome

107 High-performance liquid chromatography inductively coupled plasma mass-sp

108 ic species were measured by high performance liquid chromatography-inductively coupled plasma mass sp

109 We analyzed samples by ultraperformance liquid chromatography ion mobility-mass spectrometry.

110 extraction tool to export defined slices of liquid chromatography/ion mobility/mass spectrometry (LC

111 by ion-pair reversed-phase high-performance liquid chromatography (IP-RP-HPLC) and detected by UV sp

112 ive parameter for optimization in chip-based liquid chromatography is an important step toward high-s

113 tion with contemporary ultrahigh performance liquid chromatography is demonstrated with the resulting

114 modulation for comprehensive two-dimensional liquid chromatography is introduced.

115 ments, where an orthogonal separation (e.g., liquid chromatography) is missing.

116 on of each vegetable oil, using normal-phase liquid chromatography, is described and the chemometric

117 Online two-dimensional (2D) comprehensive liquid chromatography (LC x LC) has become increasingly

118 msPurity, a vendor-independent R package for liquid chromatography (LC) and direct infusion (DI) MS(2

119 ents a microwave flow detector technique for liquid chromatography (LC) application.

120 However, commonly used nanoflow liquid chromatography (LC) approaches hamper sample thro

121 Liquid chromatography (LC) coupled to the negative elect

122 ctroscopy as a detection method coupled with liquid chromatography (LC) has recently attracted consid

123 surface analysis (HR-LESA) followed by micro-liquid chromatography (LC) separation and a data-indepen

124 tidimensional high-resolution reversed-phase liquid chromatography (LC) separation for target peptide

125 port on the online coupling of FcRn affinity liquid chromatography (LC) with electrospray ionization

126 creased demand for universal methods such as liquid chromatography (LC)-mass spectrometry (MS) for th

127 ed the data obtained by LESA-MS to that from liquid chromatography (LC)-MS and matrix-assisted laser

128 t affect the overall run time of traditional liquid chromatography (LC)-MS-based metabolomics and lip

129 onium ions and glycan fragments from tandem (liquid chromatography (LC)-MS/MS) mass spectra for glyca

130 ility of DRILL has also been demonstrated by liquid chromatography (LC)-MS: a stable isotope labeled

131 ample preparation and compound separation by liquid chromatography (LC).

132 (3% w/v) and measured migration using tandem liquid chromatography (LC)/mass spectrometry (MS) and LC

133 nce chemical isotope labeling (CIL) nanoflow liquid chromatography mass spectrometry (nanoLC-MS) for

134 of plasma metabolites using ultraperformance liquid chromatography mass spectrometry to identify pati

135 enin, an enamel-forming protein, by nanoflow liquid chromatography mass spectrometry.

136 Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry.

137 tula macrosclereid cells, a high performance liquid chromatography-mass spectrometry (HPLC-MS) assay

138 tric waveform ion mobility spectrometry with liquid chromatography-mass spectrometry (LC-FAIMS-MS) ha

139 bsequent analysis of the residual protein by liquid chromatography-mass spectrometry (LC-MS) after gl

140 o extract and analyze isotopic patterns from liquid chromatography-mass spectrometry (LC-MS) and gas

141 We applied high-resolution liquid chromatography-mass spectrometry (LC-MS) and tand

142 Analysis of liquid chromatography-mass spectrometry (LC-MS) data req

143 package that takes high resolution wide-scan liquid chromatography-mass spectrometry (LC-MS) data set

144 he follow up time period clustered, based on liquid chromatography-mass spectrometry (LC-MS) data, wi

145 d solid-phase extraction (MISPE) followed by liquid chromatography-mass spectrometry (LC-MS) for biom

146 A novel liquid chromatography-mass spectrometry (LC-MS) interfac

147 Contrary to the main steps of a typical liquid chromatography-mass spectrometry (LC-MS) metabolo

148 enriched PAHSAs enabled the development of a liquid chromatography-mass spectrometry (LC-MS) method t

149 Liquid chromatography-mass spectrometry (LC-MS) methods

150 e times in the millisecond range for typical liquid chromatography-mass spectrometry (LC-MS) peaks, e

151 diabetic (n = 6) and healthy (n = 6) dogs by liquid chromatography-mass spectrometry (LC-MS) profilin

152 We employed shotgun liquid chromatography-mass spectrometry (LC-MS) proteomi

153 actices for each common analytical platform: liquid chromatography-mass spectrometry (LC-MS), gas chr

154 In spite of the liquid chromatography-mass spectrometry (LC-MS)-based de

155 edures for sample collection and processing, liquid chromatography-mass spectrometry (LC-MS)-based me

156 sitive strains of P. falciparum by combining liquid chromatography-mass spectrometry (LC-MS)-based pr

157 ntifying the oxidation level by both NMR and liquid chromatography-mass spectrometry (LC-MS).

158 this study, we used low- and high-resolution liquid chromatography-mass spectrometry (LC/MS) techniqu

159 D2, D3, D5, E1 and 17-HDHA, were measured by liquid chromatography-mass spectrometry and tested for a

160 first time a metabolomics approach based on liquid chromatography-mass spectrometry for revealing su

161 riety of techniques and finally evaluated by liquid chromatography-mass spectrometry in the capillary

162 istry and electron microscopy, and performed liquid chromatography-mass spectrometry on optic gliomas

163 files were analyzed by ultrahigh-performance liquid chromatography-mass spectrometry over a period of

164 tablish that BONCAT can be coupled to tandem liquid chromatography-mass spectrometry to identify and

165 D [25(OH)D] with the use of high-performance liquid chromatography-mass spectrometry, assessed dietar

166 antification of 15 mycotoxins in cow milk by liquid chromatography-mass spectrometry, is presented.

167 Using liquid chromatography-mass spectrometry, we measured 25(

168 Samples were analyzed using liquid chromatography-mass spectrometry-based metabolomi

169 Endocannabinoid levels were measured using liquid chromatography-mass spectrometry.

170 rrots on the basis of features determined by liquid chromatography-mass spectrometry.

171 by partial resistance to restriction and by liquid chromatography-mass spectrometry.

172 identification of the unmodified analyte by Liquid Chromatography-Mass Spectrometry.

173 each period and analyzed by high-resolution liquid chromatography-mass spectrometry.

174 ts with and 9 without T1R were conducted via liquid chromatography-mass spectrometry.

175 ity and compare well to results from NMR and liquid chromatography-mass spectrometry.

176 tensin analysis was performed using a unique liquid chromatography-mass spectrometry/mass spectroscop

177 Untargeted liquid-chromatography-mass spectrometry (LC-MS)-based me

178 When using liquid chromatography/mass spectrometry (LC/MS) to perfo

179 By using targeted liquid chromatography/mass spectrometry metabolomics, we

180 lldown assays combined with high sensitivity liquid chromatography/mass spectrometry to identify nove

181 rometry, and nonvolatile organic analysis by liquid chromatography/mass spectrometry.

182 y available fluorometric-enzymatic assay and liquid chromatography/mass spectrometry.

183 A rapid high-performance liquid chromatography method with a C18 reverse-phase fu

184 A high performance liquid chromatography method, coupled to diode-array and

185 ation and comparison with the results of the liquid chromatography method, where a linear correlation

186 However, other compounds interfere in the liquid chromatography methods used for this analysis.

187 quid chromatography (IAM-LC) and by micellar liquid chromatography (MLC) employing sodium dodecyl sul

188 ble for their activity using medium pressure liquid chromatography (MPLC).

189 ichment, enzymatic digestion, and nano-scale liquid chromatography MS/MS analysis.

190 tion was analyzed via ultra-high performance liquid chromatography-MS.

191 lactolipid measurements were performed using liquid chromatography-multiple reaction monitoring/mass

192 Liquid chromatography-multistage mass spectrometry (LC-M

193 itive method, relying on the use of nanoflow liquid chromatography-nanoelectrospray ionization-tandem

194 ed on stable isotope dilution (SID) nanoflow liquid chromatography nanospray ionization tandem mass s

195 n nESI direct infusion, but also in nanoflow liquid chromatography (nLC)/MS experiments.

196 This work demonstrates on-line liquid chromatography (on-line LC) as a PAT tool for mon

197 examined samples using the ultra-performance liquid chromatography photodiode detector-quadrupole/tim

198 children with the use of an ultraperformance liquid chromatography-photodiode array.

199 High-performance liquid chromatography-photodyode array detector-mass spe

200 yproline, using preparative high-performance liquid chromatography (Prep-HPLC).

201 n spiked urine using hydrophilic interaction liquid chromatography prior to FAIMS-MS separation, with

202 ate with 4-HBZA followed by high-performance liquid chromatography purification.

203 ixture and beta-TBECH using ultraperformance liquid chromatography-Q-Exactive Orbitrap mass spectrome

204 Liquid chromatography quadrupole time-of-flight mass spe

205 re evaluated by untargeted ultra-performance liquid chromatography-quadrupole time-of-flight mass spe

206 Samples were analyzed by means of liquid chromatography-quadrupole time-of-flight mass spe

207 rate mass measurement using ultraperformance liquid chromatography-quadrupole-time-of-flight-mass spe

208 A liquid chromatography-(quadrupole-time of flight)-mass s

209 Reverse-phase ultra-high-pressure liquid chromatography (RP-UHPLC) analysis of acid-releas

210 st analytical methods rely on reversed-phase liquid chromatography (RPLC), which is quite limited for

211 egies, a serial RPLC-hydrophilic interaction liquid chromatography (RPLC-HILIC) coupling and an analy

212 ques such as size exclusion ultraperformance liquid chromatography (SE-UPLC).

213 Gas liquid chromatography shows that the fatty acid composit

214 combines superficially porous reversed-phase liquid chromatography (SPLC), Fourier transform mass spe

215 hatidylcholine were measured with the use of liquid-chromatography-stable-isotope dilution-multiple-r

216 Several liquid chromatography stationary and mobile phases were

217 bridged hybrid phenyl ultra-high-performance liquid chromatography stationary phase allowed fast sepa

218 pad, and solid organ tissue samples typed by liquid chromatography tandem mass spectrometry (LC-MS).

219 xchange chromatography (SCX) and analysis by liquid chromatography tandem mass spectrometry (LC-MS/MS

220 Liquid chromatography tandem mass spectrometry (LC-MS/MS

221 hieved using a sequential approach combining liquid chromatography tandem mass spectrometry (LC-MS/MS

222 lm solid phase microextraction (TF-SPME) and liquid chromatography tandem mass spectrometry (LC-MS/MS

223 Liquid chromatography tandem mass spectrometry (LC-MS/MS

224 oth compounds can be detected sensitively by liquid chromatography tandem mass spectrometry (LC-MS/MS

225 extraction coupled to ultra-high-performance liquid chromatography tandem mass spectrometry (MAE-SPE-

226 (SALLE) combined with ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS

227 C-OH) in milk, liver and hemp seeds based on liquid chromatography tandem mass spectrometry has been

228 Analysis by liquid chromatography tandem mass spectrometry identifie

229 d and PAH target antigens were identified by liquid chromatography tandem mass spectrometry, confirme

230 ombining blue-native gel electrophoresis and liquid chromatography tandem mass spectrometry, showed t

231 Using liquid chromatography tandem mass spectrometry, we confi

232 nalysis of NL, using micro laser capture and liquid chromatography tandem mass spectrometry.

233 metabolomic profiling using high performance liquid chromatography tandem mass spectroscopy (LC/MS-MS

234 gh validation of structural assignment using liquid chromatography tandem mass-spectrometry (LC-MS/MS

235 Analyses of DC were assayed by liquid chromatography - tandem mass spectrometry method.

236 methods were developed and validated, using liquid chromatography-tandem mass spectrometric detectio

237 ble pesticides; (ii) hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS

238 entic water, we developed a high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/

239 Methods based on liquid chromatography-tandem mass spectrometry (LC-MS/MS

240 eatures or known activity were identified by liquid chromatography-tandem mass spectrometry (LC-MS/MS

241 cts (TP) (mainly phase-I) were quantified by liquid chromatography-tandem mass spectrometry (LC-MS/MS

242 e identification of peptides and proteins is liquid chromatography-tandem mass spectrometry (LC-MS/MS

243 an leukocyte antigen (HLA)-bound peptides by liquid chromatography-tandem mass spectrometry (LC-MS/MS

244 chromatography-mass spectrometry (GC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS

245 e-linked) phenolic acids were examined using liquid chromatography-tandem mass spectrometry (LC-MS/MS

246 An effective and simultaneous liquid chromatography-tandem mass spectrometry (LC-MS/MS

247 were digested with trypsin and analyzed with liquid chromatography-tandem mass spectrometry (LC-MS/MS

248 Liquid chromatography-tandem mass spectrometry (LC-MS/MS

249 tect histamine release from LAD2 cells using liquid chromatography-tandem mass spectrometry (LC-MS/MS

250 ts, and DHE plasma levels were determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS

251 The obtained derivatives were determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS

252 lly used to calibrate (13)C6-metabolites via liquid chromatography-tandem mass spectrometry (LC-MS/MS

253 Sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS

254 polar pesticides, and; (iii) reversed-phase liquid chromatography-tandem mass spectrometry (UHPLC-MS

255 Here we report the generation and multimodal liquid chromatography-tandem mass spectrometry analysis

256 Liquid chromatography-tandem mass spectrometry analysis

257 The 25(OH)D was measured by liquid chromatography-tandem mass spectrometry and categ

258 Liquid chromatography-tandem mass spectrometry confirmed

259 y based on fat and protein precipitation and liquid chromatography-tandem mass spectrometry for the d

260 ting.We measured 677 serum metabolites using liquid chromatography-tandem mass spectrometry in a cros

261 To this end, a solid-phase extraction-liquid chromatography-tandem mass spectrometry method wa

262 ophoresis of microalgal membranes coupled to liquid chromatography-tandem mass spectrometry proved to

263 The quantification was carried out by liquid chromatography-tandem mass spectrometry with elec

264 -dimensional gel electrophoresis followed by liquid chromatography-tandem mass spectrometry, in order

265 ver 12 h postprandially via high-performance liquid chromatography-tandem mass spectrometry.

266 oviral concentrations using high-performance liquid chromatography-tandem mass spectrometry.

267 analytes were measured in serum or urine by liquid chromatography-tandem mass spectrometry.

268 d electron microscopy; and their proteome by liquid chromatography-tandem mass spectrometry.

269 OEA and PEA were measured by liquid chromatography-tandem mass spectrometry.

270 on procedure and instrumental analysis using liquid chromatography-tandem mass spectrometry.

271 XAs) were measured in plasma with the use of liquid chromatography-tandem mass spectrometry.

272 in D Standardization Program with the use of liquid chromatography-tandem mass spectrometry.

273 ed by analysis of the target compounds using liquid chromatography-tandem mass spectrometry.

274 ing state for metabolomics analysis by using liquid chromatography-tandem mass spectrometry.

275 tabolomics study using ultrahigh performance liquid chromatography-tandem mass spectroscopy and gas c

276 The quality of top-down liquid chromatography-tandem MS (LC-MS/MS) data sets is

277 combines theoretical peptidome analysis and liquid chromatography-tandem MS (LC-MS/MS), we selected

278 ve liquid-liquid microextraction (DLLME) and liquid chromatography/tandem mass spectrometry (LC-MS(2)

279 tures of these glycans were revealed through liquid chromatography/tandem mass spectrometry (LC/MS-MS

280 Traditional data-dependent liquid chromatography/tandem mass spectrometry (LC/MS/MS

281 ion and comparison with the ultraperformance liquid chromatography technique, and a correlation of 10

282 analyzed for HMOs by using high-performance liquid chromatography.There was an effect of the cohort

283 n incorporated into an ultrahigh performance liquid chromatography (UHPLC) and time-of-flight mass sp

284 were identified using ultrahigh-performance liquid chromatography (UHPLC) coupled to LTQ OrbiTrap ma

285 vegetable oils using ultra high performance liquid chromatography (UHPLC) with photodiode array dete

286 me consuming processes such as high pressure liquid chromatography, ultrahigh pressure liquid chromat

287 icroanalysis was performed using a capillary liquid chromatography-ultraviolet detection system.

288 (Durham, NC), using ultrahigh-performance liquid chromatography (UPLC) and high-resolution MS.

289 raphy (GC), and phenols by ultra-performance liquid chromatography (UPLC), both with mass spectrometr

290 an analytical method using ultra performance liquid chromatography (UPLC)/negative electrospray ioniz

291 o those derived by denaturing reversed phase liquid chromatography using an oa-ToF MS system (1.56 +/

292 Extracted components were separated by liquid chromatography, whereby the selected ethylene-bri

293 tes of oligonucleotides using capillary flow liquid chromatography with column switching coupled to a

294 esticides was conducted via high performance liquid chromatography with diode-array detection (HPLC-D

295 odextrin in raw milk, using high-performance liquid chromatography with evaporative light scattering

296 or peptide mapping is based on reverse phase liquid chromatography with mass spectrometry.

297 nally, reversed-phase ultra-high performance liquid chromatography with photodiode array detection (R

298 extract analyzed with ultra high performance liquid chromatography with photodiode array detection.

299 traction (DLLME) coupled to high performance liquid chromatography with ultraviolet detector (HPLC-UV

300 ne MISPE method followed by high-performance liquid chromatography with UV diode-array detection was