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采用液相色谱-串联质谱法检测 A549 细胞细胞内区室中甲紫杉醇的超敏分析方法。

Ultra-sensitive assay for paclitaxel in intracellular compartments of A549 cells using liquid chromatography-tandem mass spectrometry.

机构信息

Clinical Pharmacology Center, Research Institute of Translational Medicine, The First Bethune Hospital of Jilin University, Dongminzhu Street, Changchun 130061, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Jan 1;912:93-7. doi: 10.1016/j.jchromb.2012.10.033. Epub 2012 Nov 2.

Abstract

A high-performance liquid chromatography-tandem mass spectrometric (LC-MS/MS) method for the determination of paclitaxel in intracellular compartments using docetaxel as internal standard (IS) has been developed and validated. A549 cancer cells (10(6)) were incubated with paclitaxel (2ng/mL) for up to 4h and then subjected to sequential extraction of cytosolic, membrane/organelle, nuclear and cytoskeleton soluble protein. Fractions were ultrasonicated to release protein bound paclitaxel after which drug was extracted using liquid-liquid extraction with diethyl ether:dichloromethane (2:1, v/v). Chromatographic separation was then carried out on an Ascentis Express C18 column (50mm×4.6mm, 2.7μm) with a mobile phase of acetonitrile:0.1% formic acid in water (50:50, v/v). Detection involved electrospray positive ionization followed by multiple reactions monitoring of the precursor-to-product ion transitions of paclitaxel at m/z 854.4→286.3 and docetaxel at m/z 808.6→226.1. Assay validation based on samples of total cell extract in the same buffer as protein fractions showed the assay was linear over the range 2-600pg/mL with intra- and inter-day precision (as relative standard deviation) and accuracy (as relative error) of <7% and <±12%, respectively. Recovery was approximately 70% and matrix effects were minimal. The distribution of paclitaxel in subcellular components of A549 cancer cells was mainly into the cytoskeletal compartment.

摘要

建立并验证了一种使用多西他赛(docetaxel)作为内标(IS)的高效液相色谱-串联质谱(LC-MS/MS)法,用于测定细胞内区室中的紫杉醇。将 A549 癌细胞(10(6))孵育 2ng/mL 的紫杉醇长达 4 小时,然后对细胞质、膜/细胞器、核和细胞骨架可溶性蛋白进行顺序提取。各馏分经超声处理以释放蛋白结合的紫杉醇,然后用二乙醚:二氯甲烷(2:1,v/v)进行液液萃取提取药物。然后在 Ascentis Express C18 柱(50mm×4.6mm,2.7μm)上进行色谱分离,流动相为乙腈:水(50:50,v/v)中的 0.1%甲酸。检测采用电喷雾正离子化,随后对紫杉醇的前体到产物离子跃迁进行多重反应监测,m/z 854.4→286.3,多西他赛 m/z 808.6→226.1。基于与蛋白馏分相同缓冲液中的总细胞提取物样品进行的分析验证表明,该测定法在 2-600pg/mL 范围内呈线性,日内和日间精密度(相对标准偏差)和准确度(相对误差)均<7%和<±12%。回收率约为 70%,基质效应最小。紫杉醇在 A549 癌细胞的亚细胞成分中的分布主要进入细胞骨架区室。

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