丁黎, 陈建华, 安登魁. 衍生化GC法测定生物转化产品L-山梨糖及其中残余D-山梨醇的含量J. 药学学报, 1998, 33(3): 217-221.
引用本文: 丁黎, 陈建华, 安登魁. 衍生化GC法测定生物转化产品L-山梨糖及其中残余D-山梨醇的含量J. 药学学报, 1998, 33(3): 217-221.
Ding Li, Chen Jianhua , An Dengkui, . DETERMINATION OF L-SORBOSE PREPARED BY BIOCONVERSIONAND RESIDUAL D-SORBITOL IN IT BY DERIVATIVE GC METHODJ. Acta Pharmaceutica Sinica, 1998, 33(3): 217-221.
Citation: Ding Li, Chen Jianhua , An Dengkui, . DETERMINATION OF L-SORBOSE PREPARED BY BIOCONVERSIONAND RESIDUAL D-SORBITOL IN IT BY DERIVATIVE GC METHODJ. Acta Pharmaceutica Sinica, 1998, 33(3): 217-221.

衍生化GC法测定生物转化产品L-山梨糖及其中残余D-山梨醇的含量

DETERMINATION OF L-SORBOSE PREPARED BY BIOCONVERSIONAND RESIDUAL D-SORBITOL IN IT BY DERIVATIVE GC METHOD

  • 摘要: 设计了生物转化产品L-山梨糖及其中残余D-山梨醇的衍生化GC测定方法。以乙酸酐—吡啶(1∶1)为衍生化试剂对样品中残余D-山梨醇进行乙酰化GC测定,再以四氢硼钠为还原剂、乙酸酐为乙酰化试剂对样品中L-山梨糖进行还原乙酰化GC测定。结果表明,D-山梨醇及L-山梨糖分别在0.01999~2.999μg及4.00~24.00μg范围内呈线性。本法精密度及回收率均较好,可用于监测L-山梨糖生物转化终点及其成品中L-山梨糖及残余D-山梨醇的含量。

     

    Abstract: A derivative GC method with n-tetracosane as the internal standard was developed for the determination of L-sorbose prepared by bioconversion and residual D-sorbitol in it. The method includes two procedures. The first procedure involves acetylation of bioconversion samples with a solution of acetic anhydride: pyridine(1∶1) at 90℃ for 20 min. The resulting products were assayed by GC to determine residual D-sorbitol. The second procedure involves reduction of the bioconversion samples with NaBH4 in aqueous solution at 40℃ for 1 hour followed by reaction with the mixture of acetic anhydride: pyridine(1∶1) at 90℃ for 20 min. The resulting products were assayed by GC to determine L-sorbose. Chromatography was performed on a 5% OV-17 stainless steel column(2 m×3 mm ID) with nitrogen as carrier gas. The detector was FID. The standard curves of D-sorbitol and L-sorbose were linear in the ranges of 0.01999~2.999 μg and 4.000~24.000 μg respectively. The method has been applied to assay L-sorbose and residual D-sorbitol in bioconversion products and to monitor bioconversion termination point of L-sorbose.

     

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