Dai Guo-Liang, Ma Shi-Tang, Liu Shi-Jia, Cheng Xiao-Gui, Zang Yu-Xin, Ju Wen-Zheng, Tan Heng-Shan
College of Pharmacy of Nanjing University of Traditional Chinese Medicine, Nanjing 210029, China.
Department of Clinical Pharmacology, Affiliated Hospital of Nanjing University of Traditional Chinese Medicine, Nanjing 210029, China.
Zhongguo Zhong Yao Za Zhi. 2013 Nov;38(21):3753-7.
To establish a LC-MS/MS method to determine caffeic acid, chlorogenic acid in rat plasma and study their pharmacokinetics in rats. Six Sprague-Dawley rats were intravenously injected with 4 mL x kg(-1) of Dengzhanxixin injection, respectively. Their drug plasma concentration was determined by LC-MS/MS, with tinidazole as an internal standard. The pharmacokinetic parameters were calculated by DAS 1.0. The linear concentration ranges of caffeic acid, and chlorogenic acid were 2-128 microg x L(-1) (r = 0.998 1) and 3-384 microg x L(-1) (r = 0.998 7), respectively. The methodological test showed conformance to the requirements. The intraday and inter-day variable coefficients were both less than 10.0%, indicating that both of legitimate precise and accuracy were in conformity with the requirements of biological sample analysis. For caffeic acid, the pharmacokinetic parameter t1/2beta AUC0-t, and CL were (130.91 +/- 38.77) min, (4.89 +/- 0.96) mg x min x L(-1) and (0.12 +/- 0.02) L x min(-1) x kg(-1), respectively. For chlorogenic acid, the pharmacokinetic parameter t1/2beta , AUC0-t, and CL were (49.38 +/- 8.85) min, (9.54 +/- 0.95) mg x min x L(-1) and (0.09 +/- 0.003) L x min(-1) x kg(-1), respectively. The LC-MS/MS analysis method established in this study was proved to be so accurate and sensitive that it can be applied to the pharmacokinetic study of caffeic acid and chlorogenic acid.
建立一种液相色谱-串联质谱法测定大鼠血浆中咖啡酸、绿原酸,并研究它们在大鼠体内的药代动力学。6只Sprague-Dawley大鼠分别静脉注射4 mL·kg⁻¹的灯盏细辛注射液。以替硝唑为内标,采用液相色谱-串联质谱法测定其血药浓度。用DAS 1.0计算药代动力学参数。咖啡酸和绿原酸的线性浓度范围分别为2~128 μg·L⁻¹(r = 0.998 1)和3~384 μg·L⁻¹(r = 0.998 7)。方法学考察结果符合要求。日内和日间变异系数均小于10.0%,表明精密度和准确度均符合生物样品分析要求。咖啡酸的药代动力学参数t1/2β、AUC0-t和CL分别为(130.91±38.77) min、(4.89±0.96) mg·min·L⁻¹和(0.12±0.02) L·min⁻¹·kg⁻¹。绿原酸的药代动力学参数t1/2β、AUC0-t和CL分别为(49.38±8.85) min、(9.54±0.95) mg·min·L⁻¹和(0.09±0.003) L·min⁻¹·kg⁻¹。本研究建立的液相色谱-串联质谱分析方法准确、灵敏,可用于咖啡酸和绿原酸的药代动力学研究。