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采用罗丹明 B 酰肼作为衍生化试剂的高效液相色谱法测定新型冠状病毒灭活疫苗中β-丙内酯残留量的研究。

Development of a high-performance liquid chromatography using rhodamine B hydrazide as the derivatization reagent for determination of β propiolactone residues in inactivated COVID-19 vaccines.

机构信息

Department of Drug and Food Control, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2024 Aug 15;1244:124241. doi: 10.1016/j.jchromb.2024.124241. Epub 2024 Jul 15.

Abstract

β-propiolactone (BPL) is an alkylating agent used for inactivation of biological samples such as vaccines. Due to its known carcinogenic properties, complete hydrolysis of BPL is essential, and the detection of trace amounts is crucial. In this study a novel High-Performance Liquid Chromatography-Ultraviolet (HPLC-UV) method was developed. Rhodamine B hydrazide (RBH) was synthesized and utilized as a derivatizing reagent to react with BPL. The reaction was optimized in a weak acidic solution, resulting in a high yield. The separation of the RBH-derivatized BPL was achieved on a C8 column and detected by a UV detector at a wavelength of 560 nm. The method's validation demonstrated a high linearity (r2 > 0.99) over a concentration range of 0.5-50 µg/mL, with detection and quantification limits of 0.17 µg/mL and 0.5 µg/mL, respectively. The average recovery of samples was 85.20 % with a relative standard deviation (RSD) of 1.75 %. This method was successfully applied for BPL residue analysis in inactivated COVID-19 vaccines. This novel derivatization method offers a promising solution for monitoring BPL residues in the vaccine production process for quality control purposes and compliance with regulatory standards.

摘要

β-丙内酯(BPL)是一种烷化剂,用于灭活疫苗等生物样本。由于其已知的致癌特性,必须完全水解 BPL,并且检测痕量 BPL 至关重要。在这项研究中,开发了一种新的高效液相色谱-紫外(HPLC-UV)方法。合成了罗丹明 B 腙(RBH)并用作衍生化试剂与 BPL 反应。在弱酸性溶液中优化了反应,得到了高产率。RBH 衍生化 BPL 的分离在 C8 柱上实现,并在 560nm 处的 UV 检测器检测。方法验证表明,在 0.5-50μg/mL 的浓度范围内具有高线性度(r2>0.99),检测限和定量限分别为 0.17μg/mL 和 0.5μg/mL。样品的平均回收率为 85.20%,相对标准偏差(RSD)为 1.75%。该方法成功应用于灭活 COVID-19 疫苗中 BPL 残留分析。这种新的衍生化方法为监测疫苗生产过程中 BPL 残留提供了一种有前途的解决方案,有助于质量控制和符合监管标准。

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