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[使用尺寸排阻色谱法测定灭活口蹄疫疫苗中的146S抗原]

[Using size-exclusion chromatography to quantify the 146S antigen in inactivated foot-and-mouth disease vaccine].

作者信息

Xu Yuan, Zou Xingqi, Li Cui, Zhu Yuanyuan, He Tianci, Yang Yanli, Lin Xuan, Song Yanmin, Zheng Jinlai, Zhang Songping, Zhao Qizu

机构信息

China Institute of Veterinary Drug Control, Beijing 100081, China.

National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2018 May 25;34(5):676-684. doi: 10.13345/j.cjb.170392.

Abstract

The aim of this study is to quantify the 146S antigen in foot-and-mouth disease virus (FMDV) inactivated vaccine by size-exclusion chromatography (SEC). The analysis was performed on a TSKgel G4000SWXL column (7.8 mm×30 cm), with a pH 7.2 buffer salt system as the mobile phase. The flow rate was 0.6 mL/min, the injection volume was 100 μL and the detection wavelength was 259 nm. The calibration curve was established by using purified inactivated FMDV (serotype O) 146S antigen; 3 batches of vaccine formulated by inactivated antigen solution were tested to verify the accuracy, reproducibility, specificity and tolerability of the method. At last 16 batches of vaccine were determined by the SEC method. Results showed a good linearity between peak area and concentration of 146S antigen in the range between 0.56 and 67.42 μg/mL (R2=0.996, n=10), and the average recovery rate of 146S antigen in the 3 batches of vaccine formulated in lab were 93.6% (RSD=2.7%, n=3), 102.3% (RSD=2.6%, n=3), and 95.5% (RSD=5.1%, n=3). The method was proved accurate and reliable with good reproducibility (RSD=0.5%, n=6), and applied to determine 16 batches of the commercial FMDV vaccine. According to the above results, the SEC method is high effective for 146S antigen quantify in the inactivated FMDV vaccine and would provide strong support for the vaccine quality control.

摘要

本研究旨在通过尺寸排阻色谱法(SEC)对口蹄疫病毒(FMDV)灭活疫苗中的146S抗原进行定量分析。分析在TSKgel G4000SWXL柱(7.8 mm×30 cm)上进行,以pH 7.2缓冲盐系统作为流动相。流速为0.6 mL/min,进样量为100 μL,检测波长为259 nm。通过使用纯化的灭活FMDV(O型)146S抗原建立校准曲线;对3批由灭活抗原溶液配制的疫苗进行检测,以验证该方法的准确性、重现性、特异性和耐受性。最后用SEC法对16批疫苗进行测定。结果表明,在0.56至67.42 μg/mL范围内,146S抗原的峰面积与浓度之间具有良好的线性关系(R2 = 0.996,n = 10),实验室配制的3批疫苗中146S抗原的平均回收率分别为93.6%(RSD = 2.7%,n = 3)、102.3%(RSD = 2.6%,n = 3)和95.5%(RSD = 5.1%,n = 3)。该方法经证明准确可靠,重现性良好(RSD = 0.5%,n = 6),并应用于测定16批市售FMDV疫苗。根据上述结果,SEC法在灭活FMDV疫苗中146S抗原定量方面高效,可为疫苗质量控制提供有力支持。

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