Ogata H, Aoyagi N, Kaniwa N, Ejima A
Int J Clin Pharmacol Ther Toxicol. 1986 Jun;24(6):279-82.
The effect of food on the bioavailability of metronidazole from three commercial sugar-coated tablets varying markedly in drug dissolution behavior relative to pH was determined after oral administration in healthy male subjects with low gastric acidity. Four subjects, whose gastric acidities were evaluated as low (hypo- or anacidity) by using a non-intubation method (Gastrotest tablets administration method), received, in a cross-over fashion, a single 250 mg dose in sugar-coated tablet during periods of fasting and non-fasting. The tablet having the fastest and most pH-independent dissolution rate gave significantly higher Cmax and AUC0-32 than the other tablets having extremely slow dissolution at pH 5 or 7.2, when the drug was administered in the fasting state. However, there were no statistically significant differences in the above parameters among the tablets tested when they were administered postprandially. The improvement of the bioavailability of the tablets exhibiting poorer dissolution in the pH range of 5 to 7.2 is ascribed to suggestible vigorous agitation in the digestive tract stimulated by food intake.
在胃酸分泌较低的健康男性受试者口服给药后,测定了食物对三种市售糖衣片甲硝唑生物利用度的影响,这三种糖衣片的药物溶解行为相对于pH值有显著差异。通过非插管法(胃功能测试片给药法)评估为胃酸分泌较低(胃酸过少或无酸)的四名受试者,采用交叉方式,在禁食和非禁食期间分别单次服用250mg糖衣片剂量。当在禁食状态下给药时,具有最快和最不依赖pH值溶解速率的片剂,其Cmax和AUC0-32显著高于在pH值为5或7.2时溶解极慢的其他片剂。然而,餐后给药时,受试片剂在上述参数上没有统计学上的显著差异。在pH值为5至7.2范围内溶解较差的片剂生物利用度的提高,归因于食物摄入刺激消化道中可能出现的剧烈搅动。