穿心莲内酯
色谱法
化学
药代动力学
选择性反应监测
电喷雾电离
高效液相色谱法
生物利用度
质谱法
校准曲线
萃取(化学)
液相色谱-质谱法
代谢物
检出限
串联质谱法
药理学
医学
生物化学
作者
Ruopeng Yang,Wanyu Hu,Cong Xie,Dafu Tang,Zhao Xiaojie,Bingxuan Fu,Jianming Wu,Ling Ye,Rongxin Liao
出处
期刊:Current Drug Metabolism
[Bentham Science]
日期:2022-09-01
卷期号:23 (11): 905-911
标识
DOI:10.2174/1386207326666221020110217
摘要
Andrographolide is a promising natural substance with numerous pharmacotherapy uses. 14-deoxy-12(R)-sulfo andrographolide (SAP) is the main metabolite of andrographolide in the intestine.To investigate the pharmacokinetic properties of SAP, a precise and sensitive ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of SAP concentration in rat plasma was developed and validated in this study.Chromatographic separation was achieved on an Acpuity UPLC BEH C18 column with gradient elution that consisted of methanol and water at a flow rate of 0.3 mL/min. MS/MS detection was carried out by the multiple reaction monitoring (MRM) mode with negative electrospray ionization (ESI-) source, with the transitions of m/z 413.2→m/z 287.2 for SAP and m/z 269→m/z 133 for genistein [which was used as an internal standard (IS)].The calibration curve of SAP was linear over the concentration range of 5-120 ng/mL. The selectivity, precision, accuracy, extraction recovery, matrix effect, and stability of the method were within acceptable ranges. This SAP quantification method was then successfully applied to a pharmacokinetic study of SAP. The area under the curve (AUC) of SAP in rats treated with SAP at 60 mg/kg by intravenous administration was 7498.53 ± 2405.02 mg/L·min. The AUC of SAP in rats treated with SAP at 60 mg/kg by oral administration was 97.74 ± 39.56 mg/L·min. Thus, the absolute oral bioavailability of SAP was determined to be 1.40%.
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