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Quantitative subcellular study of doxorubicin in MCF-7/Adr cells using liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法定量研究MCF-7 / Adr细胞中阿霉素的亚细胞

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摘要

A rapid, sensitive and selective high-performance liquid chromatography-tandem mass spectrometric (LC-MS/MS) method has been developed and validated for the determination of doxorubicin in intracellular compartments using glibenclamide as internal standard (IS). MCF-7/Adr cancer cells (1 x 10(6)) were incubated with doxorubicin (8 mu g/mL) for 0.5, 1,2 and 4 h and then subjected to sequential extraction of cytosolic, membrane/organelle, nuclear and cytoskeleton soluble protein. Samples were extracted using protein precipitation with methanol. Chromatographic separation was carried out on a C-18 column with acetonitrile and 0.1% formic acid water as mobile phase and with gradient elution at a flow rate of 0.2 mL/min. The method was linear over the range of 1-300 ng/mL with a lower limit of quantification (LLOQ) of 1 ng/mL. The distribution of doxorubicin in subcellular components of MCF-7/Adr cancer cells was mainly in nucleic protein fraction. (C) 2015 Elsevier B.V. All rights reserved.
机译:已经开发了一种快速,灵敏且选择性的高效液相色谱-串联质谱(LC-MS / MS)方法,并已验证了使用格列本脲作为内标(IS)测定细胞内隔室中阿霉素的含量。将MCF-7 / Adr癌细胞(1 x 10(6))与阿霉素(8μg / mL)孵育0.5、1,2和4 h,然后依次提取胞质,膜/细胞器,核和细胞骨架可溶性蛋白。使用蛋白质沉淀和甲醇提取样品。在C-18色谱柱上进行色谱分离,以乙腈和0.1%的甲酸水为流动相,并以0.2 mL / min的流速进行梯度洗脱。该方法在1-300 ng / mL范围内是线性的,定量下限(LLOQ)为1 ng / mL。阿霉素在MCF-7 / Adr癌细胞的亚细胞成分中的分布主要在核酸蛋白组分中。 (C)2015 Elsevier B.V.保留所有权利。

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