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作 者:李芹[1] 梁永广[1] 赵秀杰[1] 赵焰[2] 郭瑞臣[3]
机构地区:[1]山东省聊城市人民医院药学部,聊城252000 [2]山东大学药学院药剂实验室,济南250012 [3]山东大学齐鲁医院临床药理研究所,济南250012
出 处:《中国临床药理学杂志》2002年第5期371-373,共3页The Chinese Journal of Clinical Pharmacology
摘 要:目的:研究羟甲烟胺对环孢菌素A药物动力学参数的影响。方法:采用荧光偏振免疫分析法(FPIA)测定18名健康志愿者单服环孢菌素及同服羟甲烟胺后环孢菌素的血药浓度,用3P97程序分析处理数据,比较两组药动学参数的变化。结果:单服环孢菌素及同服羟甲烟胺后环孢菌素的Cmax和AUC(0-∞)有极显著性差异(P<0.001),而t1/2(β)、tmax无显著性差异(P>0.05)。结论:羟甲烟胺可促进环孢菌素的吸收,提高环孢菌素的峰浓度及药时曲线下面积,但不影响环孢菌素的代谢。OBJECTIVE: To study the influence of Nicotinylmethylamide (BILOCID) on the pharmacokinetics parameters of Cyclosporin A (CsA). METHODS: Whole blood CsA concentrations were measured by a fluorescence polarization immunoassay (FPIA) in 18 healthy volunteers administrated single CsA or co-administrated bil ocid. The data of time-blood concentrations of CsA were analyzed by 3P97 Practical Pharmacokinetics Program and the analysis of variance and two one-sided t-test were used to compare the main pharmacokinetics parameters of CsA in the two administrations. RESULTS: The results implied that Cmax and AUC(0-∞) ofCsA had statistically significant difference between the single CsA group and co-administration of bil ocid group (P<0.001), while t1/2(β) and tmax of CsA had no statistically significant difference between the two groups (P>0.05). CONCLUSION: bil ocid could improve the absorption of CsA and increase the Cmax and AUC of CsA, but had no influence on the metabolism of CsA.
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