Chen Chen, Sheng Yunhua, Hu Yue, Sun Jie, Li Wei, Feng Hongmin, Tang Liming
School of Pharmacy, Fudan University, Shanghai, China.
Shanghai Institute for Food and Drug Control, Shanghai, China.
Biomed Chromatogr. 2019 Jul;33(7):e4530. doi: 10.1002/bmc.4530. Epub 2019 Apr 25.
The aim of the present study was to develop a method based on gas chromatography-tandem mass spectrometry (GC-MS/MS) to determine and quantify the d-limonene in mouse plasma and tissue samples. This new method was validated for the quantification of d-limonene with the linearity ranges 1.0-1000.0 ng/mL (r > 0.9952) for plasma samples and 5.0-5000.0 ng/g (r > 0.9940) for tissue samples. The intra- and inter-day assay of precisions in plasma and tissues were <13.4% and the accuracies were within 91.1-105.8%. In the oral/inhalation administration pharmacokinetics and tissue distribution studies, the main pharmacokinetic parameters were the peak concentration = (97.150 ± 34.450)/(4336.415 ± 1142.418) ng/mL, the area under the curve = (162.828± 27.447)/(2085.721 ± 547.787) h ng/mL and the half-life = (3.196 ± 0.825)/(0.989 ± 0.095) h. The tissue distribution of d-limonene in mice after oral/inhalation administration demonstrated a decreasing tendency in different tissues (liver > kidney > heart > lung > spleen).
本研究的目的是开发一种基于气相色谱 - 串联质谱法(GC-MS/MS)的方法,用于测定和定量小鼠血浆和组织样本中的d-柠檬烯。该新方法针对d-柠檬烯的定量进行了验证,血浆样本的线性范围为1.0 - 1000.0 ng/mL(r>0.9952),组织样本的线性范围为5.0 - 5000.0 ng/g(r>0.9940)。血浆和组织中日内和日间精密度测定结果均<13.4%,准确度在91.1 - 105.8%范围内。在口服/吸入给药的药代动力学和组织分布研究中,主要药代动力学参数为峰浓度 =(97.150 ± 34.450)/(4336.415 ± 1142.418)ng/mL,曲线下面积 =(162.828 ± 27.447)/(2085.721 ± 547.787)h ng/mL,半衰期 =(3.196 ± 0.825)/(0.989 ± 0.095)h。口服/吸入给药后小鼠体内d-柠檬烯的组织分布在不同组织中呈现出下降趋势(肝脏>肾脏>心脏>肺>脾脏)。