替硝唑在汉族健康人体的药动学  被引量:3

Pharmacokinetics of Tinidazole in Chinese Healthy Volunteers

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作  者:郭涛[1] 常馨予[1] 夏东亚[1] 

机构地区:[1]沈阳军区总医院药剂科,沈阳110016

出  处:《中国药学杂志》2008年第17期1336-1338,共3页Chinese Pharmaceutical Journal

基  金:全军医学科学技术研究“十一五”计划科技攻关课题基金资助项目(06G023)

摘  要:目的研究汉族健康志愿者单剂量po替硝唑片的药动学。方法健康志愿者10名(其中男性5名,女性5名),单剂量po替硝唑片剂1 g,采用高效液相色谱法测定血浆中替硝唑的含量。用DAS软件程序进行数据处理,用SPSS软件对不同性别药动学参数进行统计分析。结果受试者单剂量po1 g替硝唑的主要药动学参数:ρmax为(19.04±2.42)mg·L-1,tmax为(2.15±0.47)h,t1/2为(16.94±2.40)h,AUC0-72 h为(454.37±59.74)mg·h·L-1,AUC0-∞为(486.14±65.63)mg·h·L-1。结论汉族健康志愿者单剂量po替硝唑片的体内药动学过程符合一室模型。经统计学分析,汉族健康志愿者药动学过程存在性别差异。OBJECTIVE To study the pharmacokinetics of tinidazole tablets after a single oral dose in Han healthy volunteers.METHODS Five healthy male volunteers and five healthy female volunteers were involved in the study.Each subject received a single dose of 1 g tinidazole tablets.The plasma concentration was determined by HPLC.The pharmacokinetic parameters were calculated by DAS software and were statistical analyzed by SPSS software.RESULTS The main pharmacokinetic parameters were as follows: ρmax was(19.04±2.42) mg·L-1,tmax was(2.15±0.47) h,t1/2 was(16.94±2.40) h,AUC0-72 h was(454.37±59.74) mg·h·L-1,AUC0-∞ was(486.14±65.63) mg·h·L^-1.CONCLUSION The results showed that the plasma concentration-time curve of tinidazole were fitted to an one-compartment model and the main pharmacokinetic parameters of tinidazole have significant differences between male and female volunteers.

关 键 词:替硝唑 高效液相色谱法 药动学 

分 类 号:R969.1[医药卫生—药理学]

 

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