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采用液相色谱-电喷雾串联质谱法验证测定含铂抗癌药物小瓶外表面污染的方法。

Validated method using liquid chromatography-electrospray ionization tandem mass spectrometry for the determination of contamination of the exterior surface of vials containing platinum anticancer drugs.

机构信息

Department of Hospital Pharmacy, Hamamatsu University School of Medicine, Higashi-ku, Hamamatsu, Japan.

出版信息

Talanta. 2011 Sep 15;85(3):1614-20. doi: 10.1016/j.talanta.2011.06.059. Epub 2011 Jun 29.

DOI:10.1016/j.talanta.2011.06.059
PMID:21807230
Abstract

Contamination of the exterior surface of vials of cytostatic drugs by the drugs themselves is a potential hazard to human health. This study developed a validated method using liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) for the determination of contamination of the exteriors of vials of cisplatin and carboplatin. Large Alpha® sampling swabs were employed to wipe the vial exterior. Cisplatin or carboplatin and gold(III) as an internal standard were derivatized by N,N-diethyldithiocarbamate (DDTC). Pt(DDTC)(3)(+) and Au(DDTC)(2)(+) were monitored by the respective transitions of m/z 639.3-490.9 and 493.0-345.0, respectively. Each separation was completed within 9 min using a 3 μm particle ODS-column. Calibration curves for cisplatin and carboplatin were linear over concentration ranges of 30-10,000 and 30-30,000pgvial(-1), respectively. The accuracies and precisions were 96.1-102.5% and within 8.2% for intra-assay and 99.6-103.3% and within 7.6% for inter-assay, respectively. Their lower limit of quantification was 30 pg vial(-1). Amounts of 0.17-17.0 ng vial(-1) as cisplatin and 0.48-794 ng vial(-1) as carboplatin were detected from the exterior surface of the vials. This validated method using LC-ESI-MS/MS for the determination of platinum anticancer drugs is helpful for monitoring contamination of the exterior surface of drug vials.

摘要

铂类抗癌药物外表面污染检测的 LC-ESI-MS/MS 方法研究

药物外瓶表面受自身药物污染是对人类健康的潜在危害。本研究采用液相色谱-电喷雾串联质谱法(LC-ESI-MS/MS)建立了一种经确证的方法,用于测定顺铂和卡铂外瓶表面的污染情况。采用 Alpha®大采样拭子擦拭外瓶表面。顺铂或卡铂和金(III)作为内标,用 N,N-二乙基二硫代氨基甲酸盐(DDTC)衍生化。Pt(DDTC)(3)(+)和 Au(DDTC)(2)(+)分别通过 m/z 639.3-490.9 和 493.0-345.0 的相应跃迁进行监测。使用 3μm 粒径 ODS 柱,每种分离物在 9 分钟内完成。顺铂和卡铂的校准曲线在浓度范围 30-10000 和 30-30000pg 瓶-1 内呈线性。内测定的准确度和精密度分别为 96.1-102.5%和 8.2%, 间测定的准确度和精密度分别为 99.6-103.3%和 7.6%。定量下限为 30pg 瓶-1。从瓶外表面检测到顺铂为 0.17-17.0ng 瓶-1,卡铂为 0.48-794ng 瓶-1。本研究建立的 LC-ESI-MS/MS 法可用于测定铂类抗癌药物,有助于监测药物外瓶表面的污染情况。

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