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酶解液相色谱法测定硫酸软骨素钠含量 被引量:9

Enzymolysis-HPLC determination of the content of chondroitin sulfate sodium
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摘要 目的:建立酶解液相色谱法测定硫酸软骨素钠的含量。方法:使用硫酸软骨素ABC酶酶解硫酸软骨素钠,使用强阴离子交换高效液相色谱测定酶解产生的二糖,通过计算二糖峰面积总和确定硫酸软骨素钠的含量。色谱柱为Zorbax SAX(250 mm×4.6 mm,5μm);流动相为pH 3.5的水和pH 3.5的2 mol.L-1的氯化钠溶液,流速为1.0 mL.min-1,检测波长为232 nm,柱温为40℃。结果:硫酸软骨素钠的线性范围为0.25~1.50 mg.mL-1,r=0.9999;精密度RSD为0.3%;回收率为101.2%,RSD为1.6%(n=5);最低检测限为4.0μg.mL-1,定量限为11.9μg.mL-1。结论:该方法具有专属性好,灵敏度高,重现性好的优点。 Objective :To estabhsh enzymolysis -HPLC method for determining of the content of chondroitin sul- fate sodium. Methods: Chondroitin sulfate sodium was first digested by chondroitinase ABC. The CS disaccha- rides produced were analyzed by SAX - HPLC and CS content was quantified by calculating the total peak areas of the disaccharides. Zorbax SAX column(250 mm ×4.6 mm,5 μm)was adopted the mobile phase of water (pH 3.5 ) and 2 mol . L^-1NaCl( pH 3.5 ) at 40 ~C with flow rate of 1.0 mL .min^-1, detecting wavelength being 232 nm. Results: The calibration curve was linear in the range of 0. 25 - 1.50 mg . mL^-1 with correlation coefficient of 0. 9999. The method precision RSD was 0. 3%. The average recovery was 101.2% and its RSD was 1.6% (n =5). The low detection limit was 4.0 μg . mL^-1 and the quantitative limit was 11.9 μg .mL^-1. Conclusion: This method is reproducible, sensitive and suitable for the determination of the content of chon- droitin sulfate sodium.
出处 《药物分析杂志》 CAS CSCD 北大核心 2012年第7期1246-1248,1258,共4页 Chinese Journal of Pharmaceutical Analysis
关键词 硫酸软骨素钠 酸性黏多糖 酶解液相色谱法 含量测定 标准提高 chondroitin sulfate sodium acidic mucopolysaccharide enzymolysis - HPLC assay standard improve-merit
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