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机构地区:[1]沈阳药科大学,沈阳110044 [2]大连市药品检验所,大连116021 [3]大连医科大学,大连116044
出 处:《中国新药杂志》2011年第4期372-375,共4页Chinese Journal of New Drugs
基 金:大连市科技计划项目(大连市科委2007E11SF059)
摘 要:目的:建立用生色底物法(chromogenic substrate assay,CSA)测定大鼠血浆中重组水蛭素(re-combinant hirudin,rH)含量的方法,并用该法研究rH在大鼠血浆中的药动学。方法:以TGPApNA(tosyl-gly-cyl-polyl-arginine-para-nitraniline)为底物,凝血酶(thrombin,Th)能水解TGPApNA释放出对-硝基苯胺(para-nitraniline,pNA),pNA在405nm处有特异性吸收,通过测定反应体系中未被rH中和的Th量,间接测定rH的活性。结果:CSA法能有效地测定大鼠血浆中rH的含量;rH的浓度在3.125~40 ng.mL-1范围内呈线性关系;日间和日内精密度相对标准偏差均符合要求。应用上述方法测定大鼠iv 2.0 mg.kg-1的rH后不同时间的血药浓度,结果表明该药符合二室模型一级动力学过程。结论:用生色底物法测定大鼠血浆中rH具有准确、可靠、重现性好的特点,可用于rH药动学的研究。Objective: To develop a chromogenic substrate assay for determining the concentrations of the recombinant hirudin(rH) in plasma of rats.Methods: Because thrombin can specifically bind to rH and can hydrolyze chromogenic substrate(tosyl-glycyl-polyl-arginine-para-nitraniline) to release para-nitraniline with specific absorption at 405nm.Thus,it was used to detect the concentration of rH in plasma of rats.Results: The method could effectively and accurately detect the concentration of rH in plasma of rats.The linear range of rH was 3.125~40 ng·mL-1.The RSD of intra-day and inter-day was satisfactory.Applying the method,the concentration of the rH in plasma of rats was detected at different time points after iv 2.0 mg·kg-1.The results showed that the change in drug concentration met two-compartment model.Conclusion: Chromogenic substrate assay is an accurate and reproducible method and can be used in pharmacokinetic study to detect rH concentration in plasma of rats.
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