Zheng Nan, Lian Bin, Du Wenwen, Xu Guobing, Ji Jiafu
Key laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), National Drug Clinical Trial Center, Peking University Cancer Hospital & Institute, Beijing 100142, China.
Key laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Renal Cancer and Melanoma, Peking University Cancer Hospital & Institute, Beijing 100142, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Jan 1;1072:347-354. doi: 10.1016/j.jchromb.2017.12.002. Epub 2017 Dec 6.
Paclitaxel-loaded polymeric micelles (PTX-PM) are commonly used as tumor-targeted nanocarriers and display outstanding antitumor features in clinic, but its accumulation and distribution in vitro are lack of investigation. It is probably due to the complex micellar system and its low concentration at the cellular or subcellular levels. In this study, we developed an improved extraction method, which was a combination of mechanical disruption and liquid-liquid extraction (LLE), to extract the total PTX from micelles in the cell lysate and subcellular compartments. An ultra-performance liquid chromatography tandem mass spectroscopy (UPLC-MS/MS) method was optimized to detect the low concentration of PTX at cellular and subcellular levels simultaneously, using docetaxel as internal standard (IS). The method was proved to release PTX totally from micelles (≥95.93%) with a consistent and reproducible extraction recovery (≥75.04%). Good linearity was obtained at concentrations ranging from 0.2 to 20ng/mL. The relative error (RE%) for accuracy varied from 0.68 to 7.56%, and the intra- and inter-precision (relative standard deviation, RSD%) was less than 8.64% and 13.14%, respectively. This method was fully validated and successfully applied to the cellular uptake and distribution study of PTX-loaded PLGA-PEG micelles in human breast cancer cells (MCF-7).
载紫杉醇聚合物胶束(PTX-PM)通常用作肿瘤靶向纳米载体,在临床上显示出出色的抗肿瘤特性,但其体外的积累和分布缺乏研究。这可能是由于胶束系统复杂以及其在细胞或亚细胞水平的浓度较低。在本研究中,我们开发了一种改进的提取方法,该方法是机械破碎和液液萃取(LLE)的组合,用于从细胞裂解物和亚细胞区室中的胶束中提取总PTX。优化了超高效液相色谱串联质谱(UPLC-MS/MS)方法,以多西他赛作为内标(IS),同时检测细胞和亚细胞水平的低浓度PTX。该方法被证明能从胶束中完全释放PTX(≥95.93%),具有一致且可重复的提取回收率(≥75.04%)。在0.2至20ng/mL的浓度范围内获得了良好的线性。准确度的相对误差(RE%)在0.68至7.56%之间变化,批内和批间精密度(相对标准偏差,RSD%)分别小于8.64%和13.14%。该方法经过充分验证,并成功应用于载PTX的PLGA-PEG胶束在人乳腺癌细胞(MCF-7)中的细胞摄取和分布研究。