2019
DOI: 10.1016/j.jpba.2018.10.030
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Chemical profiles and quality evaluation of Buddleja officinalis flowers by HPLC-DAD and HPLC-Q-TOF-MS/MS

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Cited by 40 publications
(15 citation statements)
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“…Identification of 5‐caffeoylquinic acid (peak 3) was confirmed by comparison with retention time of a commercial standard; however, the identity of caffeoylquinic acid isomer (peak 2) was not confirmed as a result of a lack of coincidence of the retention time of the peak with the available standards 3‐caffeoylquinic and 4‐caffeoylquinic acid. Identification of the quercetin‐hexoside (peak 5) isomer was also not confirmed as a result of a lack of coincidence with the retention time of the commercial standard quercetin‐3‐glucoside; for this reason, this compound may possibly correspond to quercetin‐5‐glucoside or quercetin‐7‐glucoside, all with similar fragmentation patterns characterized by a pseudomolecular ion with m / z 463 and a product ion of m / z 301 in the negative ion mode . It is important to consider that glucoside and galactoside derivatives present similar fragmentation patterns by MS, characterized by a neutral loss to m / z 162; however, 3‐galactoside was discarded as a result of the elution order, ecause galactoside derivatives must eluted at lower retention times than glucoside derivatives .…”
Section: Resultsmentioning
confidence: 99%
“…Identification of 5‐caffeoylquinic acid (peak 3) was confirmed by comparison with retention time of a commercial standard; however, the identity of caffeoylquinic acid isomer (peak 2) was not confirmed as a result of a lack of coincidence of the retention time of the peak with the available standards 3‐caffeoylquinic and 4‐caffeoylquinic acid. Identification of the quercetin‐hexoside (peak 5) isomer was also not confirmed as a result of a lack of coincidence with the retention time of the commercial standard quercetin‐3‐glucoside; for this reason, this compound may possibly correspond to quercetin‐5‐glucoside or quercetin‐7‐glucoside, all with similar fragmentation patterns characterized by a pseudomolecular ion with m / z 463 and a product ion of m / z 301 in the negative ion mode . It is important to consider that glucoside and galactoside derivatives present similar fragmentation patterns by MS, characterized by a neutral loss to m / z 162; however, 3‐galactoside was discarded as a result of the elution order, ecause galactoside derivatives must eluted at lower retention times than glucoside derivatives .…”
Section: Resultsmentioning
confidence: 99%
“…Compound 122, as shown in Figure S10 (supporting information), exhibited quasi-molecular ion at 2390, 420.2283, 292.2012, 204.1013, and 147.0440 could be observed. It was tentatively identified as safflospermidine B, referring to the literature (Xie et al, 2019). In addition, three isomers of safflospermidine B were detected and identified as N 1 (Z),N 5 (Z),N 10 (E)-tri-p-coumaroyl spermidine, N 1 (E),N 5 (Z),N 10 (E)-trip-coumaroylspermidine, and N 1 ,N 5 ,N 10 (E)-tri-p-coumaroylspermidine from CF (Xie et al, 2019).…”
Section: Identification Of Spermidine Alkaloidsmentioning
confidence: 99%
“…Fortunately, multi-component quantitative analysis has been developed as a reliable method to control the quality of TCM [15,16,17]. In addition, HPLC-ESI-Q-TOF-MS/MS and HPLC fingerprint combined with chemometrics as an effective, reliable and comprehensive method were also successfully applied for quality consistency assessment of TCM [18,19,20]. Therefore, the simultaneous qualitative and quantitative of TCM can be achieved by the combination of HPLC-ESI-Q-TOF-MS/MS, HPLC fingerprint and multicomponent quantitative analysis.…”
Section: Introductionmentioning
confidence: 99%