Liu Bin, Gou Xiaoli, Bai Xupeng, Hou Xiangyu, Li Dongshun, Zhong Guoping, Jin Jing, Huang Min
School of Pharmaceutical Science, Sun Yat-sen University, Guangzhou, China.
School of Pharmaceutical Science, Sun Yat-sen University, Guangzhou, China.
J Pharm Biomed Anal. 2015 Mar 25;107:346-54. doi: 10.1016/j.jpba.2015.01.001. Epub 2015 Jan 10.
A rapid, sensitive and reliable method has been developed and validated for the simultaneous determination of seven taxoids including 10-deacetylbaccatin III (10-DAB III), baccatin III, 5-epi-canadensene, taxinine M, 10-deacetyltaxol (10-DAT), cephalomannine and paclitaxel in rat plasma using docetaxel as the internal standard (IS). The plasma samples were pretreated by liquid-liquid extraction with methyl tert-butyl ether. The chromatographic separation was achieved on a C18 column (50 mm × 2.1 mm, 1.8 μm, Waters, USA) with a gradient elution program consisting of methanol and water (containing 0.1% formic acid) at a flow rate of 0.2 mL/min. Detection was performed under the selected reaction monitoring (SRM) scan using an electrospray ionization (ESI) in the positive ion mode. The mass transitions were as follows: m/z 567.4→444.9 for 10-DAB III, m/z 609.0→549.3 for baccatin III, m/z 617.4→496.9 for 5-epi-canadensene, m/z 709.6→649.3 for taxinine M, m/z 834.8→307.9 for 10-DAT, m/z 854.5→285.4 for cephalomannine, m/z 876.8→307.3 for paclitaxel and m/z 830.8→549.6 for IS, respectively. All calibration curves exhibited good linearity (r(2)>0.99) over a wide concentration range for all components. The intra-day and inter-day precisions at three different levels were both less than 14.3% in terms of relative standard deviation (RSD) and the accuracies ranged from -8.3% to 14.8% in terms of relative error (RE). The extraction recoveries of the seven compounds ranged from 62.5% to 100.5%. The developed method was successfully applied to the pharmacokinetic study of the seven taxoids in rat plasma after oral administration of the crude extract of the twigs and leaves of Taxus yunnanensis.
已开发并验证了一种快速、灵敏且可靠的方法,以多西他赛为内标(IS),同时测定大鼠血浆中的七种紫杉烷类化合物,包括10-去乙酰巴卡亭III(10-DAB III)、巴卡亭III、5-表加拿大紫杉烯、紫杉宁M、10-去乙酰紫杉醇(10-DAT)、三尖杉宁碱和紫杉醇。血浆样品通过用甲基叔丁基醚进行液-液萃取进行预处理。色谱分离在C18柱(50 mm×2.1 mm,1.8μm,美国沃特世公司)上进行,采用由甲醇和水(含0.1%甲酸)组成的梯度洗脱程序,流速为0.2 mL/min。在选定反应监测(SRM)扫描下,使用正离子模式的电喷雾电离(ESI)进行检测。质量跃迁如下:10-DAB III为m/z 567.4→444.9,巴卡亭III为m/z 609.0→549.3,5-表加拿大紫杉烯为m/z 617.4→496.9,紫杉宁M为m/z 709.6→649.3,10-DAT为m/z 834.8→307.9,三尖杉宁碱为m/z 854.5→285.4,紫杉醇为m/z 876.8→307.3,内标为m/z 830.8→549.6。所有校准曲线在所有组分的宽浓度范围内均表现出良好的线性(r(2)>0.99)。在三个不同水平下,日内和日间精密度的相对标准偏差(RSD)均小于14.3%,准确度的相对误差(RE)范围为-8.3%至14.8%。七种化合物的萃取回收率范围为62.5%至100.5%。所开发的方法成功应用于云南红豆杉枝叶粗提物口服给药后大鼠血浆中七种紫杉烷类化合物的药代动力学研究。