Quantitative Analysis of Eight Triterpenoids and Two Sesquiterpenoids in Rhizoma Alismatis by Using UPLC-ESI/APCI-MS/MS and Its Application to Optimisation of Best Harvest Time and Crude Processing Temperature
Autor: | Qiurong Zhang, Ruihua Xie, Fuxian Zou, Kedan Chu, Xiaoyan Li, Jia Wang, Wen Xu, Shuisheng Wu, Tai Yanni, Mingqing Huang, Ronghui Rao |
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Rok vydání: | 2019 |
Předmět: |
Detection limit
Electrospray lcsh:QD71-142 Chromatography Article Subject 010405 organic chemistry Chemistry ved/biology General Chemical Engineering 010401 analytical chemistry ved/biology.organism_classification_rank.species lcsh:Analytical chemistry Atmospheric-pressure chemical ionization Repeatability Tandem mass spectrometry 01 natural sciences High-performance liquid chromatography 0104 chemical sciences Computer Science Applications Analytical Chemistry Alisma orientale Instrumentation Quantitative analysis (chemistry) Research Article |
Zdroj: | Journal of Analytical Methods in Chemistry, Vol 2019 (2019) Journal of Analytical Methods in Chemistry |
ISSN: | 2090-8873 2090-8865 |
Popis: | Rhizoma Alismatis (RA), widely known as “Ze-Xie” in China, is the tuber of Alisma orientale (Sam.) Juzep (Alismaceae), a Chinese herbal medicine that has been used to treat hyperlipidemia, diabetes, hypertension, dysuria, and inflammation. In this study, a sensitive and reliable method based on an ultra-performance liquid chromatography (UPLC) couple with two ionisation modes, including electrospray ionisation (ESI) and atmospheric pressure chemical ionisation (APCI) tandem mass spectrometry (MS), namely, UPLC-ESI/APCI-MS/MS was developed and validated to simultaneously determine 8 triterpenoids (ESI mode) and 2 sesquiterpenoids (APCI mode) in RA. Ten marker compounds were analysed with a Waters’ CORTECS UPLC C18 column (200 mm × 2.1 m, 1.6 μm) and gradient elution with water (contained 0.1% formic) and acetonitrile within 7 min. The established method was validated for linearity, intra- and interday precisions, accuracy, recovery, and stability. The calibration curve for 10 marker compounds showed good linear regression (r > 0.9971). The limits of detection and quantification for analytes were 0.14–1.67 ng/mL and 0.44–5.65 ng/mL, respectively. The relative standard deviations (RSD, %) and accuracy (RE, %) of intra- and interday precisions were less than 3.83% and 1.21% and 3.22% and 1.46%, repeatability and stability for real samples were less than 2.78% and 3.19%, respectively. All recoveries of the 10 marker compounds ranged from 97.24% to 102.49% with RSDs less than 4.05%. The developed method efficiently determined the 10 marker compounds in RA and was subsequently applied to optimise harvest time and crude processing temperature. The result indicated the 90% wilted phase and 70°C (or lower) may be the best harvest time and the processing temperature of RA. |
Databáze: | OpenAIRE |
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