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Oral pharmacokinetics of the acidic drugs diclofenac and sulfamonomethoxinein male Shiba goats

机译:酸性药物双氯芬酸和磺胺单甲辛的口服药代动力学在雄性柴犬山羊中

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摘要

In the present study, we examined the oral pharmacokinetics of the acidic drugs, diclofenac (DF) and sulfamonomethoxine (SMM), which have different physicochemical properties, in Shiba goats. DF and SMM were intravenously and orally administered to 5 male goats using a crossover design. The Tmax of DF and SMM were reached 1.5 and 5.6 hr after they have been orally administered, respectively, and this was followed by their slow elimination. The elimination of both drugs was markedly faster after being intravenously rather than orally administered, which indicated flip-flop phenomena after the oral administration. The mean absorption times (MATs) of DF and SMM were 6 and 15 hr, respectively. This slow absorption may have been due to slow gastric emptying in goats. The large difference observed in MATs between DF and SMM may have been because DF, which is more lipophilic than SMM, was partly absorbed from the forestomach. Therefore, these results suggest that the absorption of highly lipophilic drugs from the forestomach may be markedly high in Shiba goats. In case of drugs whose elimination is quite fast, their efficacies may appear from the early stage after oral administration even in ruminants, because elimination rate is the determinant factor of Tmax in flip-flop phenomena. Such drugs may be used orally even in ruminants.
机译:在本研究中,我们检查了芝巴山羊中具有不同理化特性的酸性药物双氯芬酸(DF)和磺胺单甲辛(SMM)的口服药代动力学。使用交叉设计对5只雄性山羊静脉和口服给予DF和SMM。 DF和SMM的Tmax在口服后分别达到1.5和5.6小时,然后缓慢消除。静脉内给药而非口服给药后,两种药物的清除速度明显加快,这表明口服给药后会出现翻转现象。 DF和SMM的平均吸收时间(MATs)分别为6和15 hr。这种缓慢的吸收可能是由于山羊胃排空缓慢造成的。 DF和SMM之间在MATs中观察到的巨大差异可能是因为比SMM更具亲脂性的DF被部分从前胃中吸收。因此,这些结果表明,在什巴山羊中,从前胃中吸收的高度亲脂性药物可能明显较高。对于消除速度非常快的药物,即使在反刍动物中,它们的功效也可能从口服后的早期开始出现,因为消除率是触发现象中Tmax的决定因素。这样的药物甚至可以在反刍动物中口服使用。

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