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采用自建聚合物添加剂库的 UPLC-QTOF MS 检测和识别塑料包装材料中疫苗的浸出物。

Detection and Identification of Leachables in Vaccine from Plastic Packaging Materials Using UPLC-QTOF MS with Self-Built Polymer Additives Library.

机构信息

College of Science, Beijing Key Laboratory of Environmentally Harmful Chemical Analysis, Beijing University of Chemical Technology , Beijing, China 100029.

Beijing Key Laboratory of Diagnostic and Traceability Technologies for Food Poisoning, Beijing Center for Disease Control and Prevention , Beijing, China 100013.

出版信息

Anal Chem. 2016 Jul 5;88(13):6749-57. doi: 10.1021/acs.analchem.6b01027. Epub 2016 Jun 15.

Abstract

The direct contact of plastic parts with the medical products raises the possibility that plastic-related contaminants (leachables) may be present in the finished medical product. The leachable components from plastic materials may impact the safety and efficacy of the final medical product, so identification and determination of the leachables are essential for the safety assessment of medical products. A method to identify main leachables-polymer additives in medical products was developed by ultraperformance liquid chromatography-quadrupole time-of-flight-mass spectrometry (UPLC-QTOF MS) and a self-built library. The library contains 174 additives and the information on their names, formulas, structures, retention times, fragments, classifications, origin, and corresponding MS(E) and MSMS spectra. The reliability of the construction process of the library was guaranteed by the system stability and suitability test. Identification parameters of library application, such as mass error, retention times, fragments, and isotope pattern, were evaluated. Leachables in real vaccine and the intermediates were identified using automatic library searching. In vaccine, the peak m/z 239.0887 that could not be assigned by the library was identified as dimethyl 2-hydroxy-1,3-cyclohexanedicarboxylate using a series of elucidation tools. As a result, the concentrations of leachables in vaccine and the intermediates ranged from 0.85 to 21.91 μg/L.

摘要

塑料部件与医疗产品的直接接触增加了塑料相关污染物(可浸出物)可能存在于最终医疗产品中的可能性。塑料材料中的可浸出成分可能会影响最终医疗产品的安全性和有效性,因此确定和确定可浸出物对于医疗产品的安全性评估至关重要。本研究通过超高效液相色谱-四极杆飞行时间质谱(UPLC-QTOF MS)和自建库建立了一种识别医疗产品中主要可浸出物-聚合物添加剂的方法。该库包含 174 种添加剂及其名称、公式、结构、保留时间、碎片、分类、来源以及相应的 MS(E)和 MSMS 图谱的信息。该库构建过程的可靠性通过系统稳定性和适用性测试得到保证。评估了库应用的鉴定参数,如质量误差、保留时间、碎片和同位素模式。使用自动库搜索鉴定了真实疫苗和中间体中的可浸出物。在疫苗中,使用一系列解析工具将无法通过库分配的峰 m/z 239.0887 鉴定为二甲基 2-羟基-1,3-环己烷二甲酸酯。结果,疫苗和中间体中可浸出物的浓度范围为 0.85 至 21.91 μg/L。

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