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作 者:许健[1] 彭婷婷 Xu Jian;Peng Tingting(Department of Pharmacy,the First Affiliated Hospital of Bengbu Medical College Bengbu 233000;Department of Spine Surgery,the First Affiliated Hospital of Bengbu Medical College,Bengbu 233000,China)
机构地区:[1]蚌埠医学院第一附属医院药剂科,安徽蚌埠233000 [2]蚌埠医学院第一附属医院脊柱外科,安徽蚌埠233000
出 处:《广东化工》2020年第21期148-149,共2页Guangdong Chemical Industry
基 金:蚌埠医学院校级课题重点项目[BYKY1829ZD]。
摘 要:目的:比较内标法和外标法用于测定人血中多西他赛药物浓度的差异。方法:分别以内标法和外标法建立人血中多西他赛药物浓度测定的超高效液相测定方法,并进行方法学验证,最后测定不同的血液样本,比较两种方法的测定结果。结果:以内标法和外标法为基础的多西他赛超高效液相测定方法均通过方法学验证,对于人血中多西他赛的含量测定,内标法和外标法无显著性差异。结论:外标法操作简便,结果准确,适用于人血中多西他赛的含量测定。Objective: To compare the internal standard method and the external standard method used to determine the difference in the concentration of docetaxel in human blood. Methods: The internal standard method and the external standard method were used to establish the ultra-high performance liquid method for the determination of the concentration of docetaxel in human blood, and the method was verified. Finally, different blood samples were measured and the results of the two methods were compared. Results: Both the internal standard method and the external standard method based on the ultra-high performance liquid method for the determination of docetaxel passed the methodological verification. For the determination of the content of docetaxel in human blood, the internal standard method and the external standard method are not significant difference. Conclusion: The external standard method is simple and accurate, and it is suitable for the determination of docetaxel in human blood.
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