肺炎球菌荚膜多糖中C多糖的定量1H-NMR和31P-NMR法测定

    Determination of Pneumococcal C-polysaccharide in Capsular Polysaccharides from Streptococcus Pneumoniae by the Quantitative 1H-NMR and 31P-NMR Method

    • 摘要:
      目的  利用1H-NMR和31P-NMR核磁定量法测定肺炎球菌荚膜多糖中C多糖残留量。
      方法 采用Bruker AVANCE NEO 600 MHz核磁共振波谱仪,以六甲基磷酰胺(hexamethylphosphoramide,HMPA)作为内标物,对不同血清型及不同浓度荚膜多糖溶液中C多糖进行定量1H-NMR和31P-NMR分析。
      结果 在定量1H-NMR中二甲基亚砜的回收率为96.52%~103.31%,RSD值均<2.00%,表明定量1H-NMR具有较好的准确度和精密度。在定量1H-NMR中,当荚膜多糖样品浓度>9 mg·mL−1时满足信噪比要求,而定量31P-NMR中测定浓度需>15 mg·mL−1。对于7F型荚膜多糖在浓度15~25 mg·mL−1时2种方法测定结果差异无统计学意义。而对于4型荚膜多糖在浓度为3~15 mg·mL−1时定量1H-NMR测定结果差异无统计学意义。通过定量1H-NMR和31P-NMR法测定多种不同血清型荚膜多糖中C多糖含量,结果显示,19种血清型荚膜多糖中C多糖含量为0.57%~5.07%。
      结论 以HMPA为内标建立的C多糖定量1H-NMR和31P-NMR测定法,其操作简单,准确性高,重复性好,可作为肺炎球菌C多糖残留量检测的一种有效手段。

       

      Abstract:
      OBJECTIVE  To establish a method for detection of the content of residual C-polysaccharide(C-Ps) in the capsular polysaccharide from Streptococcus pneumoniae by the quantitative 1H-NMR and 31P-NMR method.
      METHODS  All NMR experiments were carried out on Bruker AVANCE NEO 600 MHz spectrometer using hexamethylphosphoramide(HMPA) as internal standard. Quantitative 1H-NMR and 31P-NMR analysis of C-Ps in different concentrations solution of multiple serotypes capsular polysaccharide were performed.
      RESULTS  The recovery of DMSO in quantitative 1H-NMR were 96.52%−103.31%, and the RSD values were all <2.00%, indicating that the quantitative 1H-NMR possessed good accuracy and precision. The signal-to-noise ratio met requirement when the concentration was >9 mg·mL−1 in quantitative 1H-NMR, while 15 mg·mL−1 for quantitative 31P-NMR. For serotype 7F capsular polysaccharides, there was no significant difference between the two methods under concentrations of 15−25 mg·mL−1. And for serotype 4 capsular polysaccharides, there was no significant difference under concentrations of 3−15 mg·mL−1 in quantitative 1H-NMR. The content of C-Ps in multiple serotypes were determined by quantitative 1H-NMR and 31P-NMR, and the results showed that the content of C-Ps in 19 serotypes capsular polysaccharides was 0.57%−5.07%.
      CONCLUSION  The quantitative1H-NMR and 31P-NMR methods established with HMPA as the internal standard for the determination of pneumococcal C-Ps are simple, accurate and reproducible, and can be used as an efficient method for the detection of pneumococcal C-Ps.

       

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