The conjugation of serotype 31 pneumococcal polysaccharide and CRM197 in N,N-dimethylformamide

Q3 Medicine
Chengli Zong, Hongzhao Mao, Huiting Li, Shiyan Mai
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引用次数: 0

Abstract

Traditionally, PCV (pneumococcal conjugate vaccine) was prepared by the coupling of aldehyde-activated polysaccharide, with a carrier protein via NaCNBH3 (sodium cyanoborohydride) mediated reductive amination in water. However, the reaction is very slow and may take up to several days, which is a significant burden for pharmaceutical companies. Here we report the detailed reaction process of the reductive amination of structurally reassigned serotype 31 polysaccharide and cross reacting material (CRM197) in an organic solvent (N,N-dimethylformamide, DMF) by using STAB (sodium triacetoxyborohydride). The product has been characterized by size exclusion chromatography, nuclear magnetic resonance and transmission electron microscopy. Compared with the traditional method, the reaction can finish within hours and elicited a comparable immune response. The new strategy has the potential of being applied in the preparation of next-generation polysaccharide conjugate vaccines.

血清31型肺炎球菌多糖与CRM197在N,N-二甲基甲酰胺中的结合
传统上,PCV(肺炎球菌结合疫苗)是通过醛活化多糖与载体蛋白在水中通过NaCNBH3(氰硼氢化钠)介导的还原胺化反应偶联制备的。然而,反应非常缓慢,可能需要几天的时间,这对制药公司来说是一个很大的负担。本文报道了三乙酰氧基硼氢化钠(STAB)在有机溶剂(N,N-二甲基甲酰胺,DMF)中对31型血清多糖和交叉反应物质(CRM197)进行胺化还原的详细反应过程。产品经粒度排斥层析、核磁共振、透射电镜等表征。与传统方法相比,该反应可在数小时内完成,并引起类似的免疫反应。该方法具有应用于制备下一代多糖结合疫苗的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Vacunas
Vacunas Medicine-Infectious Diseases
CiteScore
3.90
自引率
0.00%
发文量
138
审稿时长
62 days
期刊介绍: Sin duda una de las mejores publicaciones para conocer los avances en el campo de las vacunaciones preventivas, tanto en el ámbito de la investigación básica como aplicada y en la evaluación de programas de vacunaciones. Su alta calidad y utilidad la ha llevado a estar indexada en los prestigiosos índices IME y SCOPUS.
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