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Rapid Quantitative Analysis of 19 Bioactive Components in Fangji Huangqi Decoction Based on UHPLC–MS/MS

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Abstract Fangji Huangqi Decoction (FHD) is a classic prescription of traditional Chinese medicine which is recorded in “Jin Gui Yao Lue”. The purpose of this study is to develop a method for simultaneous determination multicomponent in FHD. The separation of the 19 compounds that included calycosin, calycosin-7-O-β-D-glucoside, formononetin, ononin, methylnissolin, methylnissolin-3-O-glucoside, isomucronulatol, tetrandrine, fangchinoline, atractylenolide-I, atractylenolide-III, liquiritigenin, liquiritin, isomucronulatol-7-O-β-D-glucoside, astragaloside-I, astragaloside-II, astragaloside-III, astragaloside-IV and glycyrrhetinic acid were achieved by linear gradient elution. The 19 components were identified by comparing the chromatographic peaks with the reference compounds and were quantitatively analyzed by multiple reaction monitoring. This method was strict validated with recovery (96.10–101.70%), precision [relative standard deviation (RSD), 1.34–3.34%], stability (RSD, 1.49–3.80%) and repeatability (RSD, 1.60–3.49%), respectively. All the compounds showed good linearities (R2 > 0.999). The limit of detection (LOD) and limit of quantitation (LOQ) for the 19 compounds were in the range of 0.03–0.27 μg/mL (LODs) and 0.05–1.23 μg/mL (LOQs). The correlation analysis indicated that astragalus flavonoids were negatively correlated with astragalosides, tetrandrine and their corresponding flavonoid glycosides, and atractylenolides were positively correlated with astragalosides and fangchinoline. This method proved to be reliable and effective, which would give a helpful basis for the quality control, pharmacological and pharmacokinetic of FHD.
Title: Rapid Quantitative Analysis of 19 Bioactive Components in Fangji Huangqi Decoction Based on UHPLC–MS/MS
Description:
Abstract Fangji Huangqi Decoction (FHD) is a classic prescription of traditional Chinese medicine which is recorded in “Jin Gui Yao Lue”.
The purpose of this study is to develop a method for simultaneous determination multicomponent in FHD.
The separation of the 19 compounds that included calycosin, calycosin-7-O-β-D-glucoside, formononetin, ononin, methylnissolin, methylnissolin-3-O-glucoside, isomucronulatol, tetrandrine, fangchinoline, atractylenolide-I, atractylenolide-III, liquiritigenin, liquiritin, isomucronulatol-7-O-β-D-glucoside, astragaloside-I, astragaloside-II, astragaloside-III, astragaloside-IV and glycyrrhetinic acid were achieved by linear gradient elution.
The 19 components were identified by comparing the chromatographic peaks with the reference compounds and were quantitatively analyzed by multiple reaction monitoring.
This method was strict validated with recovery (96.
10–101.
70%), precision [relative standard deviation (RSD), 1.
34–3.
34%], stability (RSD, 1.
49–3.
80%) and repeatability (RSD, 1.
60–3.
49%), respectively.
All the compounds showed good linearities (R2 > 0.
999).
The limit of detection (LOD) and limit of quantitation (LOQ) for the 19 compounds were in the range of 0.
03–0.
27 μg/mL (LODs) and 0.
05–1.
23 μg/mL (LOQs).
The correlation analysis indicated that astragalus flavonoids were negatively correlated with astragalosides, tetrandrine and their corresponding flavonoid glycosides, and atractylenolides were positively correlated with astragalosides and fangchinoline.
This method proved to be reliable and effective, which would give a helpful basis for the quality control, pharmacological and pharmacokinetic of FHD.

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