School of Pharmacy, Jilin medical University, 5 Jilin Street, Fengman District, Jilin 132013, China.
J Chromatogr Sci. 2022 Jun 6;60(5):458-464. doi: 10.1093/chromsci/bmab116.
Fangji Huangqi Decoction is composed of Stephaniae Tetrandrae Radix, Astragli Radix, Atractylodis Macrocephalae Rhizoma and Glycyrrhizae Radix Et Rhizoma. It is a classic traditional Chinese medicine formula for the treatment of chronic glomerulonephritis in China. However, its pharmacokinetic characteristics in vivo are still unclear. In this study, a method for quantifying fangchinoline, tetrandrine and calycosin-7-O-β-D-glucoside, the main active constituents of Fangji Huangqi Decoction, in rat plasma by using ultrahigh-performance liquid chromatography-tandem mass spectrometry technique was developed. Plasma samples were processed with a deproteinization procedure using acetonitrile, followed by chromatographic separation on a Shim-pack XR-ODS C18 column using gradient elution of 0.1% aqueous formic acid and acetonitrile at 0.4 mL/min. The analytes and internal standard, diphenhydramine hydrochloride, were detected using positive electrospray ionization in multiple reactions monitoring mode. The optimized mass transition ion-pairs (m/z) were 609.3/367.3 for fangchinoline, 623.3/174.3 for tetrandrine, 447.2/285.1 for calycosin-7-O-β-D-glucoside and 256.2/167.1 for diphenhydramine hydrochloride, respectively. The developed method was validated for intraday and interday precision and accuracy whose values fell in the acceptable limits. Recovery efficiency of all the analytes was found to be >90.5%. Matrix effect was found to be negligible. Stability results showed that the analytes were stable under all conditions. The validated method was successfully used for studying the pharmacokinetics of the three compounds in rat plasma after oral administration of Fangji Huangqi Decoction.
防己黄芪汤由粉防己、黄芪、白术和甘草组成,是中国治疗慢性肾小球肾炎的经典中药方剂。然而,其体内药代动力学特征尚不清楚。本研究建立了一种超高效液相色谱-串联质谱法同时测定大鼠血浆中防己碱、粉防己碱和汉黄芩素-7-O-β-D-葡萄糖苷等主要活性成分的方法。采用乙腈沉淀蛋白法处理血浆样品,然后在 Shim-pack XR-ODS C18 柱上以 0.1%甲酸水溶液和乙腈为流动相进行梯度洗脱,流速为 0.4 mL/min。采用正离子电喷雾电离多反应监测模式检测分析物和内标(盐酸苯海拉明)。优化后的质量转换离子对(m/z)分别为 609.3/367.3 用于防己碱,623.3/174.3 用于粉防己碱,447.2/285.1 用于汉黄芩素-7-O-β-D-葡萄糖苷,256.2/167.1 用于盐酸苯海拉明。该方法日内和日间精密度和准确度的验证结果均在可接受范围内。所有分析物的回收率均>90.5%。发现基质效应可以忽略不计。稳定性结果表明,在所有条件下分析物均稳定。该验证方法成功用于研究防己黄芪汤灌胃后大鼠血浆中三种化合物的药代动力学。