Liang Xiaoming, Liu Zhenzhen, Shi Huiyan, Zhang Yuanyuan, Wang Shixiao, Bi Kaishun, Chen Xiaohui
Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.
Department of Functional Science, School of Medicine, Yangtze University, No.1 Nanhuan Road, Jingzhou City 434100, China.
J Pharm Anal. 2017 Apr;7(2):118-122. doi: 10.1016/j.jpha.2016.11.002. Epub 2016 Nov 19.
Larotaxel, a new taxane compound prepared by partial synthesis from 10-deacetyl baccatin III, is active against tumors. In this research, a selective LC-MS method was developed and validated for the study of degradation kinetics of larotaxel, which was carried out in aqueous solutions with different pH (1.5, 3.0, 5.0, 6.5, 7.4, 9.0, 10 and 11.0) and temperature (0, 25, 37 and 45 °C). The linear range was 0.5-25 μg/mL, the intra- and inter-day precisions were less than 7.0%, and accuracy ranged from 97.4-104.5% for each analyte. The observed rate obtained by measuring the remaining intact larotaxel was shown to follow first-order kinetics. The activation energies for degradation were 126.7 and 87.01 kJ/mol at pH 1.5 and 11, respectively. Although larotaxel was stable in pH 5, 6.5 and 7.4 buffers at 37 °C for 24 h during our study, increasing or decreasing the pH of the solutions would decrease its stabilities. Moreover, three main degradation products in alkaline condition were separated by HPLC and identified by Q-TOF-MS. The three degradation products were confirmed as 10-deacetyl larotaxel, 7, 8-cyclopropyl baccatin Ⅲ and 10-deacetyl-7, 8-cyclopropyl baccatin Ⅲ.
拉罗他赛是一种通过对10-去乙酰浆果赤霉素III进行部分合成制备的新型紫杉烷化合物,具有抗肿瘤活性。在本研究中,开发并验证了一种选择性液相色谱-质谱法,用于研究拉罗他赛在不同pH值(1.5、3.0、5.0、6.5、7.4、9.0、10和11.0)和温度(0、25、37和45℃)的水溶液中的降解动力学。线性范围为0.5 - 25μg/mL,日内和日间精密度均小于7.0%,各分析物的准确度范围为97.4 - 104.5%。通过测量剩余完整拉罗他赛获得的观测速率显示遵循一级动力学。在pH 1.5和11时,降解的活化能分别为126.7和87.01kJ/mol。尽管在我们的研究中,拉罗他赛在37℃的pH 5、6.5和7.4缓冲液中24小时内稳定,但溶液pH值的升高或降低都会降低其稳定性。此外,通过高效液相色谱分离并通过Q-TOF-MS鉴定了碱性条件下的三种主要降解产物。这三种降解产物被确认为10-去乙酰拉罗他赛、7,8-环丙基浆果赤霉素Ⅲ和10-去乙酰-7,8-环丙基浆果赤霉素Ⅲ。