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作 者:韩秋俊[1] 毕葳[2] 王伟[1] 李取胜[1] 王鹏龙[1] 徐士勋[1] 王艳慧[1] 绪扩[1] 汪林[1] 程亚涛[1] 李强[1] 雷海民[1]
机构地区:[1]北京中医药大学中药学院,北京100102 [2]中国中医科学院中药研究所,北京100700
出 处:《中国实验方剂学杂志》2012年第24期86-88,共3页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(81073017)
摘 要:目的:建立双缩脲反应-酶联免疫检测仪对肽类的快速定量方法,测定鳖甲炮制前后肽类含量差异,探讨鳖甲炮制科学性。方法:应用0.02 g.mL-1酒石酸钠钾50μL,5%氢氧化钠20μL,0.5%硫酸铜50μL的双缩脲显色剂测定鳖甲炮制前后肽类含量,检测波长580 nm。结果:鳖甲七肽在0.10~5.00 g.L-1与吸光度呈良好的线性关系,醋鳖甲平均总肽含量为6.99%,生鳖甲平均总肽含量为1.04%。结论:醋鳖甲总肽含量明显高于生鳖甲总肽含量,醋制法可提高鳖甲有效成分溶出度。Objective: A rapid method was established for quantitative determination of peptide based on biuret reaction-enzyme-linked immunosorbent detector, and peptide content in the same geographical origin of pre- and-post-processed Trionycis Carapax was analyzed. Method: The developer was 0.02 g·mL^-1 sodium potassium tartrate solution (50 μL), 5% NaOH (20 μL), 1% CuSO4 ·5H2O (50 μL). The wavelength of detection was at 580 nm. Result: The calibration curves were linear in the ranges of 0.00-5.00 g ·L^-1 for septa-peptide from Trionycis Carapax. Peptide content in vinegar-processed samples was 6.99% , while the same content in crud samples was 1.04%. Conclusion: Peptide content in vinegar-processed samples was significantly higher than the one in crud samples. The content of Trionycis Carapax is increased greatly after vinegar by decoction.
关 键 词:鳖甲 寡肽 双缩脲反应-酶联免疫检测仪 含量测定
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