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引用本文:杨庆,马鲁南,刘忠,张贵民.分子排阻色谱法测定德谷胰岛素高分子蛋白含量[J].中国现代应用药学,2020,37(23):2879-2882.
YANG Qing,MA Lunan,LIU Zhong,ZHANG Guimin.Quantitation of High Molecular Weight Proteins in Insulin Degludec by Size Exclusion Chromatography[J].Chin J Mod Appl Pharm(中国现代应用药学),2020,37(23):2879-2882.
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分子排阻色谱法测定德谷胰岛素高分子蛋白含量
杨庆1, 马鲁南1, 刘忠1, 张贵民2
1.山东新时代药业有限公司, 山东省蛋白类药物工程实验室, 山东 临沂 273400;2.鲁南制药集团股份有限公司, 哺乳动物细胞高效表达国家工程实验室, 山东 临沂 276006
摘要:
目的 建立德谷胰岛素高分子蛋白质的定量分析测定方法。方法 采用Insulin HMWP色谱柱(7.8 mm×300 mm,10 μm),以冰醋酸-异丙醇-水(4:3:10)为流动相,流速为0.5 mL·min-1,检测波长为280 nm,利用分子排阻色谱法分离德谷胰岛素单体以及高分子蛋白质,并对高分子蛋白质进行定量分析。结果 该方法的检测限和定量限分别为0.18和0.47 μg;仪器精密度RSD为0.51%,德谷胰岛素在0.125~4.0 mg·mL-1内与峰面积呈良好的线性关系,回归方程为Y=20.864 1X-0.125 9,R2=1.000 0;德谷胰岛素主峰与高分子蛋白质峰的分离度>2.0。结论 建立的方法操作简便,灵敏度高,可有效地对德谷胰岛素高分子蛋白质进行定量分析。
关键词:  德谷胰岛素  高分子蛋白质  分子排阻色谱法
DOI:10.13748/j.cnki.issn1007-7693.2020.23.011
分类号:R927.2
基金项目:
Quantitation of High Molecular Weight Proteins in Insulin Degludec by Size Exclusion Chromatography
YANG Qing1, MA Lunan1, LIU Zhong1, ZHANG Guimin2
1.Shandong New Time Pharmaceutical Co., Ltd., Shandong Provincial Engineering Laboratory of Protein Pharmaceutical, Linyi 273400, China;2.Lunan Pharmaceutical Group Co., Ltd., State Engineering Laboratory of High Expression of Mammalian Cells, Linyi 276006, China
Abstract:
OBJECTIVE To establish a quantitative analysis method of the high molecular weight proteins in insulin degludec. METHODS The column was Insulin HMWP column(7.8 mm×300 mm, 10 μm). The mobile phase was acetic acid-isopropanol- water (4:3:10). The flow rate was 0.5 mL·min-1. The detection wavelength was set at 280 nm. The high molecular weight proteins were separated and accurately determined by size exclusion chromatography. RESULTS The detection limit and quantitative detection limit were 0.18, 0.47 μg, respectively. The RSD of instrument precision test was 0.51%. The concentration of insulin degludec at the range of 0.125-4.0 mg·mL-1 showed good linear relationship to the peak area, of which the regression equation was Y=20.864 1X-0.125 9, with R2=1.000 0. The resolution of main peak and molecular protein peak was >2.0. CONCLUSION The established method is simple, sensitive and can effectively quantitatively analyze the high molecular protein of insulin degludec.
Key words:  insulin degludec  high molecular weight proteins  size exclusion chromatography
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