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一种灵敏且快速的液相色谱串联质谱法,用于定量测定含基于脂质体的7-乙基-10-羟基喜树碱(SN-38,即LE-SN38)的人血浆中的7-乙基-10-羟基喜树碱(SN-38)。

A sensitive and rapid liquid chromatography tandem mass spectrometry method for quantitative determination of 7-ethyl-10-hydroxycamptothecin (SN-38) in human plasma containing liposome-based SN-38 (LE-SN38).

作者信息

Khan Sumsullah, Ahmad Ateeq, Ahmad Imran

机构信息

Pharmacokinetics, Metabolism and Bioanalytical, Research and Development, NeoPharm Inc., Waukegan, IL 60085, USA.

出版信息

Biomed Chromatogr. 2003 Dec;17(8):493-9. doi: 10.1002/bmc.257.

Abstract

7-Ethyl-10-hydroxycamptothecin (SN-38) is an active metabolite of Irinotecan (CPT-11), an anticancer pro-drug. To support clinical pharmacokinetic studies for liposome based formulation of SN-38 (LE-SN38) in cancer patients, a rapid, simple and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method has been developed and validated for the quantification of total SN-38 in human plasma. Sample preparation was carried out by one-step protein precipitation using cold acetonitrile with 0.5% acetic acid (v/v). Camptothecin was used as an internal standard (IS). Chromatographic separation of SN-38 and IS was achieved using a Synergi Hydro-RP column (C(18), 50 x 2 mm, 4 micro m), with a gradient elution of acetonitrile and 0.1% acetic acid. After ionization in electrospray source (positive ions), the acquisition was performed in the multiple reactions monitoring mode. Quantitation was accomplished using the precursor-->product ion combinations of m/z 393.1-->349.2 for SN-38 and 349.1-->305.1 for IS. The quantification limit of 0.05 ng/mL was achieved by using much lower volume (0.2 mL) of plasma and in the presence of LE-SN38. The method was validated over the concentration range of 0.05-400 ng/mL. Accuracy was within +/-12% of nominal at all concentration levels. Inter-day and intra-day precisions expressed as percentage coefficient of variation (%CVs) for quality control (QC) samples were less than 14 and 5%, respectively.

摘要

7-乙基-10-羟基喜树碱(SN-38)是抗癌前体药物伊立替康(CPT-11)的活性代谢产物。为支持在癌症患者中开展基于脂质体的SN-38制剂(LE-SN38)的临床药代动力学研究,已开发并验证了一种快速、简便且灵敏的液相色谱串联质谱(LC-MS/MS)方法,用于定量测定人血浆中的总SN-38。样品制备采用一步法,使用含0.5%乙酸(v/v)的冷乙腈进行蛋白沉淀。喜树碱用作内标(IS)。使用Synergi Hydro-RP柱(C(18),50×2 mm,4μm)对SN-38和内标进行色谱分离,采用乙腈和0.1%乙酸梯度洗脱。在电喷雾源(正离子)中离子化后,以多反应监测模式进行采集。使用m/z 393.1→349.2(用于SN-38)和349.1→305.1(用于内标)的前体→产物离子组合进行定量。通过使用低得多的血浆体积(0.2 mL)并在存在LE-SN38的情况下,实现了0.05 ng/mL的定量限。该方法在0.05 - 400 ng/mL的浓度范围内进行了验证。在所有浓度水平下,准确度在标称值的±12%以内。质量控制(QC)样品的日间和日内精密度以变异系数百分比(%CVs)表示,分别小于14%和5%。

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