Weitschies W, Friedrich C, Wedemeyer R S, Schmidtmann M, Kosch O, Kinzig M, Trahms L, Sörgel F, Siegmund W, Horkovics-Kovats S, Schwarz F, Raneburger J, Mönnikes H
Department of Biopharmaceutics, University of Greifswald, Greifswald, Germany.
Eur J Pharm Biopharm. 2008 Oct;70(2):641-8. doi: 10.1016/j.ejpb.2008.05.011. Epub 2008 Jun 5.
The rate and extent of amoxicillin and clavulanic acid absorption from pharmacokinetically enhanced extended release (ER) tablets is strongly influenced by the intake conditions. In order to investigate the cause of the food effects, a pharmacokinetic study with simultaneous imaging of the in vivo behaviour of the ER tablets by magnetic marker monitoring (MMM) was performed. Under fasting conditions the amoxicillin AUC (1854+/-280microg min ml(-1)) was significantly lower than after intake at the beginning of the breakfast (2452+/-354microg min ml(-1)) or after the breakfast (2605+/-446microg min ml(-1)). In contrast, clavulanic acid AUC was well comparable after tablet intake under fasting conditions and intake at the beginning of a breakfast (191+/-46 and 189+/-44microg min ml(-1), respectively) but significantly lower following a breakfast (126+/-71microg min ml(-1)). The localization data showed that the reduced bioavailability of amoxicillin under fasting conditions is due to early gastric emptying in combination with poor absorption from deeper parts of the small intestine. Prolonged gastric residence of clavulanic acid caused by intragastric tablet deposition in the proximal stomach was identified as the reason for the decreased bioavailability of clavulanic acid after tablet intake following the meal.
阿莫西林和克拉维酸从药代动力学增强型缓释(ER)片剂中的吸收速率和程度受摄入条件的强烈影响。为了研究食物影响的原因,进行了一项药代动力学研究,通过磁性标记监测(MMM)对ER片剂的体内行为进行同步成像。在禁食条件下,阿莫西林的AUC(1854±280μg·min·ml⁻¹)显著低于早餐开始时摄入后(2452±354μg·min·ml⁻¹)或早餐后(2605±446μg·min·ml⁻¹)。相比之下,克拉维酸的AUC在禁食条件下片剂摄入后与早餐开始时摄入后具有良好的可比性(分别为191±46和189±44μg·min·ml⁻¹),但在早餐后显著降低(126±71μg·min·ml⁻¹)。定位数据表明,禁食条件下阿莫西林生物利用度降低是由于胃排空过早以及小肠深部吸收不良。胃内片剂在胃近端沉积导致克拉维酸在胃内停留时间延长,这被确定为餐后片剂摄入后克拉维酸生物利用度降低的原因。