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国产新药和福喷丁在人体内药代动力学研究
引用本文:方治平,王浴生,杨芳炬,孔古娅,徐金枝.国产新药和福喷丁在人体内药代动力学研究[J].中国药理学通报,1989(1).
作者姓名:方治平  王浴生  杨芳炬  孔古娅  徐金枝
作者单位:华西医科大学药理教研室,华西医科大学药理教研室,华西医科大学药理教研室,华西医科大学药理教研室,四川抗菌素研究所 成都,成都,成都,成都
摘    要:9名志愿受试者口服利福喷丁(Rifapentine)连续给药10d,随后改为每周两次的间隙给药连续3周的药代动力学研究结果,与利福定作比较。发现利福喷丁吸收、排泄均较利福定慢,在体内维持时间长,T1/2为15h。连服药10d,血中药浓先是逐渐上升,4、5d达到最高,随后下降,这可能与利福霉素激活肝药酶有关。

关 键 词:利福喷丁  利福定  半衰期  肝药酶  药代动力学

STUDY ON THE PHARMACOKINETIC OF RIFAPENTINE IN VOLUNTEERS
Fang Zhiping,Wang Yusheng Yang Fangju et.STUDY ON THE PHARMACOKINETIC OF RIFAPENTINE IN VOLUNTEERS[J].Chinese Pharmacological Bulletin,1989(1).
Authors:Fang Zhiping  Wang Yusheng Yang Fangju et
Abstract:The pharmacokinetic study of Rifapentine by daily oral administration for 10d and followed by twice weekly for another 3 weeks in 9 volunteers and in comparism with Rifandin were reported. The results showed that the absorption and excretion of Rifapentine were markedly slower than that of Rifandin, its T1/2 was 15h. The Peak plasma level and T1/2 decreased after repeated administration of the drug. This suggested that Rifapentine and Rifandin in similar to Ri-fampin were hepatic microsomal enzyme inducers.
Keywords:Rifapentine  Rifandin  Plasma half life  Pharmacokinetic  Hepatic microsomal enzyme  
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