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甲磺酸帕珠沙星氯化钠注射液健康志愿者单剂给药药动学
http://www.100md.com 《中国抗生素杂志》 2007年第1期
甲磺酸帕珠沙星氯化钠注射液;,药动学;,健康志愿者,,甲磺酸帕珠沙星氯化钠注射液;,药动学;,健康志愿者,1材料与方法,2结果,3讨论,参考文献
     摘要: 目的 研究健康志愿者静脉滴注单剂甲磺酸帕珠沙星氯化钠注射液后药动学特征,为该药Ⅱ期临床试验提供依据。方法 采用2剂量2周期交叉试验设计。10名健康受试者单剂静脉滴注甲磺酸帕珠沙星氯化钠注射液300、500mg,HPLC法测其血清、尿药物浓度。结果 受试者静脉滴注甲磺酸帕珠沙星氯化钠注射液后,人体耐受良好,体内过程符合二室开放模型。主要药动学参数与给药剂量呈线性关系,cmax分别为83和1107μg/ml,AUC0-∞分别为1366和2404μg·h/ml,V值分别为289和40L,t1/2β分别为177和227h,36h尿药累积回收率约为79%。结论 甲磺酸帕珠沙星氯化钠注射液静脉滴注血峰浓度高,组织分布较广,消除半衰期短,300mg每日2次可用于治疗敏感菌感染。

    关键词: 甲磺酸帕珠沙星氯化钠注射液; 药动学; 健康志愿者

    Pharmacokinetics of pazufloxacin mesylate sodium chloride injection in healthy volunteers after a singledose administration

    Cai Sufang and Huang Wenxiang

    (The First Affiliated Hospital, Chongqing University of Medical Sciences, Chongqing 400016)

    ABSTRACT Objective To study the pharmacokinetics of pazufloxacin mesylate sodium chloride injection in healthy volunteers after singledose administration. Method A singledose of 300 or 500mg pazufloxacin mesylate sodium chloride injection were administered venoclysisly to ten healthy volunteers in autocross test; the concentrations of pazufloxacin in serum and urine were detected by HPLC. Results Pazufloxacin was well tolerated. The concentrationtime data after single dose of 300 or 500mg pazufloxacin conformed to a twocompartment open model and there were linear relationship between dosages and major parameters, cmax were 83, 1107μg/ml respectively; AUC0-∞ were 1366, 2404 μg·h/ml respectively; V were 289, 40L respectively; t1/2β were 177, 227h respectively. 79% of the administered doses were recovered in the urine within 36h. Conclusion These results indicate that pazufloxacin has a favorable pharmacokinetic properties with high blood concentration and good tissue distribution. 300mg twice daily dose may be used for the treatment of bacterial infections caused by susceptible organisms. ......

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