Department of Traditional Chinese Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province 450052, People's Republic of China.
Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province 450052, People's Republic of China.
Drug Des Devel Ther. 2020 May 13;14:1837-1850. doi: 10.2147/DDDT.S235646. eCollection 2020.
Shenkang injection, a traditional Chinese herbal prescription, had been widely used in renal disease due to its perfect curative effect. In this research, a novel, sensitive, accurate and rapid liquid chromatography-tandem mass spectrometric method was developed to simultaneously detect the seven active ingredients in rat plasma of Shenkang injection and investigate its pharmacokinetic behaviors with metabolism profiling meanwhile.
For accurate pharmacokinetic quantitation, a WATERS ACQUITY UPLC BEH C18 column was used to perform a separation and acetonitrile-water (0.1% formic acid) was selected as mobile phase for gradient elution with a flow rate of 0.20 mL/min. A heated electrospray ionization with selective reaction monitoring mode was used to monitor the precursor-product ion transitions for all the analytes and IS.
They all showed good linearity over a wide concentration range (>0.996 3) and the lower limit of quantification (LLOQ) was 0.1-1.0 ng/mL for analytes. The validation parameters were all within the acceptable limits. Furthermore, for metabolism profiling study, metabolites of the seven ingredients were identified from the rat plasma based on the accurate mass and fragment ions. The metabolic pathways mainly focus on reduction, dehydration and conjugation.
This study provided an overview of disposition of Shenkang injection, which is highly instructive for better understanding the effectiveness and toxicity of this drug.
肾康注射液是一种中药复方制剂,由于其疗效确切,已广泛应用于肾脏疾病。本研究建立了一种灵敏、准确、快速的液相色谱-串联质谱法,同时检测肾康注射液在大鼠血浆中的 7 种活性成分,并进行代谢物谱分析,以研究其药代动力学行为。
为了进行准确的药代动力学定量分析,采用沃特世 ACQUITY UPLC BEH C18 柱进行分离,以乙腈-水(0.1%甲酸)为流动相进行梯度洗脱,流速为 0.20 mL/min。采用加热电喷雾电离,选择反应监测模式,监测所有分析物和内标的前体-产物离子跃迁。
它们在较宽的浓度范围内(>0.996 3)均表现出良好的线性关系,分析物的定量下限(LLOQ)为 0.1-1.0 ng/mL。验证参数均在可接受范围内。此外,为了进行代谢物谱研究,根据精确质量和碎片离子,从大鼠血浆中鉴定出 7 种成分的代谢物。代谢途径主要集中在还原、脱水和结合。
本研究概述了肾康注射液的处置情况,这对更好地理解该药物的疗效和毒性具有重要意义。