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Development and Validation of Gas Chromatography-Triple Quadrupole Mass Spectrometric Method for Quantitative Determination of Regulated Plasticizers in Medical Infusion Sets

机译:气相色谱-三重四极杆质谱联用技术定量测定医用输液器中增塑剂的开发与验证

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摘要

A method for the quantitative determination of dibutyl phthalate (DBP), benzyl butyl phthalate (BBP), bis(2-ethylhexyl) adipate (DEHA), bis(2-ethylhexyl) phthalate (DEHP), di-n-octyl phthalate (DNOP), dioctyl terephthalate (DOTP), diisononyl phthalate (DINP), and diisodecyl phthalate (DIDP) in medical infusion sets was developed and validated using gas chromatography coupled with triple quadrupole mass spectrometry (GC-MS/MS) in the multiple reaction monitoring (MRM) mode. Solvent extraction with polymer dissolution for sample preparation was employed prior to GC-MS/MS analysis. Average recoveries of the eight target analytes are typically in the range of 91.8–122% with the relative standard deviations of 1.8–17.8%. The limits of quantification (LOQs) of the analytical method were in the ranges of 54.1 to 76.3 ng/g. Analysis using GC-MS/MS provided reliable performance, as well as higher sensitivity and selectivity than GC-MS analysis, especially for the presence of minority plasticizers at different concentrations.
机译:一种定量测定邻苯二甲酸二丁酯(DBP),邻苯二甲酸苄基丁酯(BBP),己二酸双(2-乙基己基)酯(DEHA),邻苯二甲酸二(2-乙基己基)酯(DEHP),邻苯二甲酸二正辛酯(DNOP)的定量方法),开发了医用输液器中的对苯二甲酸二辛酯(DOTP),邻苯二甲酸二异壬酯(DINP)和邻苯二甲酸二异癸酯(DIDP),并在多反应监测中使用气相色谱和三重四极杆质谱(GC-MS / MS)进行了验证( MRM)模式。在进行GC-MS / MS分析之前,先采用溶剂溶解法和聚合物溶解法进行样品制备。八个目标分析物的平均回收率通常在91.8–122%的范围内,相对标准偏差为1.8–17.8%。该分析方法的定量限(LOQ)在54.1至76.3ng / g的范围内。与GC-MS分析相比,使用GC-MS / MS进行分析可提供可靠的性能以及更高的灵敏度和选择性,特别是对于存在不同浓度的少数增塑剂而言。

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