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首页> 外文期刊>European journal of drug metabolism and pharmacokinetics >Pharmacokinetic evaluation of guar gum-based colon-targeted oral drug delivery systems of metronidazole in healthy volunteers.
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Pharmacokinetic evaluation of guar gum-based colon-targeted oral drug delivery systems of metronidazole in healthy volunteers.

机译:基于瓜尔胶的甲硝唑在结肠中靶向结肠的口服药物递送系统的药代动力学评估。

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The present study was carried out to find the in vivo performance of guar gum-based colon-targeted tablets of metronidazole as compared to an immediate release tablets in human volunteers. Six healthy volunteers participated in the study and a crossover design was used. Blood samples were obtained at different time intervals and the plasma concentration of metronidazole was estimated by reverse phase HPLC. The immediate release tablets of metronidazole produced peak plasma concentration (Cmax of 2990 +/- 574.6 ng/mL) within 2.8 +/- 0.6 h. On oral administration of colon-targeted tablets, metronidazole started appearing in the plasma between 5 h and 8 h, and reached the peak concentration (Cmax of 1940.0 +/- 528.4 ng/mL) at 11.1 +/- 2.1 h (Tmax). The AUC(0-infinity) and t(1/2) of metronidazole were unaltered on administering the drug as a colon-targeted tablet indicating that the extent of absorption and elimination were not affected by targeting the drug to the colon. However, colon-targeted tablets showed delayed tmax and absorption time (ta), decreased Cmax and decreased absorption rate constant as compared to immediate release tablets. This in turn indicated that metronidazole was delivered to the colon resulting in a slow absorption of the drug and making it available for local action in the colon.
机译:进行本研究以发现与瓜耳胶基结肠靶向甲硝唑的片剂相比,在人类志愿者中的速释片剂的体内性能。六名健康志愿者参加了研究,并使用了交叉设计。在不同的时间间隔获得血样,并通过反相HPLC估算甲硝唑的血浆浓度。甲硝唑的速释片在2.8 +/- 0.6小时内产生了峰值血浆浓度(Cmax为2990 +/- 574.6 ng / mL)。口服结肠靶向片剂后,甲硝唑开始在5小时至8小时之间出现在血浆中,并在11.1±2.1小时(Tmax)时达到峰值浓度(Cmax为1940.0 +/- 528.4 ng / mL)。甲硝唑以结肠靶向片剂给药时,AUC(0-无穷大)和t(1/2)未改变,表明吸收和消除程度不受靶向药物对结肠的影响。但是,与速释片剂相比,结肠靶向片剂显示出tmax和吸收时间(ta)延迟,Cmax降低和吸收速率常数降低。这又表明甲硝唑被递送至结肠,导致药物吸收缓慢,使其可用于结肠局部作用。

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