Zhang Kaihui, Lu Zenghui, Wang Qian, Liu Fangle, Wang Meiqi, Lin Chaozhan, Zhu Chenchen
School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China.
School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China.
Front Pharmacol. 2022 Jul 4;13:936846. doi: 10.3389/fphar.2022.936846. eCollection 2022.
Liandan Xiaoyan Formula (LXF), a classic Traditional Chinese medicine (TCM) formula, is composed of two Chinese herbal medicines for treating bowel disease under the TCM theory. This study aimed to develop a rapid, stable, sensitive, and reliable method based on ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) to simultaneously determine four major bioactive components of LXF (andrographolide, dehydroandrographolide, 1-methoxicabony-β-carboline, 4-methoxy-5-hydroxy-canthin-6-one) in rat serum and evaluate the pharmacokinetic characteristics of LXF in ulcerative colitis (UC) and control rats. After pretreating by protein precipitation with methanol, separation was performed on a UPLC C18 column using gradient elution with a mobile phase consisting of acetonitrile and 0.1% formic acid at a flowing rate of 0.4 ml/min. Detection was performed on Triple-TOF™ 5600 mass spectrometry set at the positive ionization and multiple reaction monitoring (MRM) mode. The validated method showed good linearity ( ≥ 0.9970), the intra- and inter-day accuracy were within ±11.58%, whereas the intra- and inter-day precision were less than 13.79%. This method was validated and applied to compare the pharmacokinetic profiles of the analytes in serum of UC induced by dextran sulphate sodium (DSS) and control rats after oral administration of LXF. The results showed that four major bioactive components of LXF were quickly absorbed after oral administration in both groups, with higher exposure levels in the UC group. This relationship between the active ingredients' pharmacokinetic properties provided essential scientific information for applying LXF in clinical.
连丹消炎方(LXF)是一种经典的中药方剂,由两味中药组成,依据中医理论用于治疗肠道疾病。本研究旨在建立一种基于超高效液相色谱 - 串联质谱法(UPLC - MS/MS)的快速、稳定、灵敏且可靠的方法,以同时测定大鼠血清中连丹消炎方的四种主要生物活性成分(穿心莲内酯、脱水穿心莲内酯、1 - 甲氧基羰基 - β - 咔啉、4 - 甲氧基 - 5 - 羟基 - 咔啉 - 6 - 酮),并评估连丹消炎方在溃疡性结肠炎(UC)大鼠和对照大鼠中的药代动力学特征。采用甲醇蛋白沉淀法进行预处理后,在UPLC C18柱上进行分离,流动相为乙腈和0.1%甲酸,采用梯度洗脱,流速为0.4 ml/min。在设置为正离子模式和多反应监测(MRM)模式的Triple - TOF™ 5600质谱仪上进行检测。验证后的方法显示出良好的线性关系(r≥0.9970),日内和日间准确度在±11.58%以内,而日内和日间精密度均小于13.79%。该方法经过验证并应用于比较硫酸葡聚糖钠(DSS)诱导的UC大鼠和对照大鼠口服连丹消炎方后血清中分析物的药代动力学特征。结果表明,连丹消炎方的四种主要生物活性成分在两组大鼠口服给药后均迅速吸收,UC组的暴露水平更高。活性成分的药代动力学性质之间的这种关系为连丹消炎方在临床上的应用提供了重要的科学依据。