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应用 PNMR 定量评估肺炎链球菌荚膜多糖中的 C-多糖。

Quantitative assessment of C-polysaccharide in capsular polysaccharides of Streptococcus pneumoniae by PNMR.

机构信息

Finlay Institute of Vaccines, Havana, Cuba.

Finlay Institute of Vaccines, Havana, Cuba.

出版信息

J Pharm Biomed Anal. 2021 Jan 5;192:113670. doi: 10.1016/j.jpba.2020.113670. Epub 2020 Oct 8.

Abstract

Capsular polysaccharides of Streptococcus pneumoniae are key components of commercially available anti-pneumococcal vaccines; meanwhile C-polysaccharide is considered an impurity. World Health Organization recommends a strict control over the presence of this biomolecule due to the possibility of introducing an undesired response. An alternative way for assessing this impurity is focused on detect the phosphocholine residues by means of quantitative H-NMR. This could be tricky due to the amounts of this substituent may vary generating two C-polysaccharides forms. In this work we propose an improved quantitative NMR methodology based on P-NMR for the quantification of C-polysaccharide on capsular polysaccharide preparations. The technique also focuses on phosphocholine but, conversely to above-mentioned methods, allows to discriminate between phosphocholine linked in different positions. The methodology was run on samples of eleven vaccine serotypes, including seven with phosphate groups. From a rational acceptance criterion of 10 wt%, the method allows to quantified from 30 μg of the impurity in 3 mg of total polysaccharide (1 wt%) with a signal/noise ratio of 16:1. Repeatability and intermediate precision evaluation showed a relative standard deviation of 3.33 % and 8.34 % respectively. Additionally, the method provides information about structural identity of phosphate contained in capsular polysaccharides and C-polysaccharide species. This constitutes a new contribution from the NMR that highlights the power of these techniques for assessing imperative parameters in carbohydrate-based vaccines.

摘要

肺炎链球菌荚膜多糖是市售肺炎球菌疫苗的关键成分;而 C 多糖则被认为是一种杂质。世界卫生组织建议严格控制这种生物分子的存在,因为它有可能引发不良反应。评估这种杂质的替代方法侧重于通过定量 H-NMR 检测磷酸胆碱残基。由于取代基的数量可能会有所不同,从而产生两种 C 多糖形式,因此这可能具有挑战性。在这项工作中,我们提出了一种基于 P-NMR 的改进的定量 NMR 方法,用于定量荚膜多糖制剂中的 C 多糖。该技术还专注于磷酸胆碱,但与上述方法相反,它允许区分不同位置连接的磷酸胆碱。该方法在 11 种疫苗血清型的样品上进行了测试,其中包括 7 种带有磷酸基团的样品。从 10wt%的合理接受标准来看,该方法可以在 3mg 总多糖(1wt%)中定量检测 30μg 的杂质,信噪比为 16:1。重复性和中间精密度评估分别显示相对标准偏差为 3.33%和 8.34%。此外,该方法还提供了有关荚膜多糖和 C 多糖中所含磷酸的结构同一性的信息。这是 NMR 的一个新贡献,突出了这些技术在评估基于碳水化合物的疫苗中重要参数方面的强大功能。

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