测定灭活 Covid-19 疫苗中 β-丙内酯残留量的气相色谱-质谱方法

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of chromatographic science Pub Date : 2024-09-17 DOI:10.1093/chromsci/bmae049
Seyedeh Zohreh Mirjalili, Zahra Tamiji, Mehrnoosh Shirangi, Mohsen Amini
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引用次数: 0

摘要

β-丙内酯是疫苗中常用的灭活剂。由于 β-丙炔内酯具有致癌性,因此必须将其完全水解,以防止在哺乳动物细胞中产生细胞毒性。因此,临床上应更多地关注β-丙炔内酯,并对其痕量进行测量。由于其不稳定性,β-丙内酯的分析具有挑战性。为定量检测 2019 年冠状病毒病灭活疫苗(Covid-19)中残留的 β-丙内酯,我们开发了一种简单快速的气相色谱-质谱法。在样品溶液中使用己内酯作为内标;用乙酸乙酯从疫苗培养基中提取分析物后进行分析。该方法的线性范围为0.2-20 μg/mL,检出限为0.07 μg/mL,定量限为0.20 μg/mL,r2为0.99。样品中未检测到目标分析物β-丙炔内酯,表明检测样品合格。所建立的方法可用于 Covid-19 灭活疫苗的质量控制。
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A GC–MS Method for Determination of β-Propiolactone Residues in Inactivated Covid-19 Vaccines
β-propiolactone is a common inactivator agent used in vaccines. Due to β-propiolactone carcinogenicity, complete hydrolysis of it is necessary to prevent cytotoxicity in mammalian cells. As a result, more attention should be paid to it at the clinic, and it is important to measure its trace amounts. β-propiolactone analysis is challenging due to its instability. A simple and fast gas chromatography–mass spectrometry method was developed for quantitation of residual β-propiolactone in inactivated coronavirus disease 2019 (Covid-19) vaccines. Caprolactone was used as an internal standard in sample solutions; the analysis was performed after extraction of analyte from vaccine media by ethyl acetate. The validity of the method was studied with a linearity of r2 > 0.99 over the concentration range of 0.2–20 μg/mL with the limit of detection and the limit of quantification of 0.07 and 0.20 μg/mL, respectively. The target analyte β-propiolactone was not detected in the samples, demonstrating the test samples were qualified. The established method can be used for quality control of inactivated Covid-19 vaccines.
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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