EVALUATION OF THE INTESTINAL-ABSORPTION OF ERYTHROMYCIN IN MAN - ABSOLUTE BIOAVAILABILITY AND COMPARISON WITH ENTERIC-COATED ERYTHROMYCIN

被引:23
作者
SOMOGYI, AA
BOCHNER, F
HETZEL, D
WILLIAMS, DB
机构
[1] ROYAL ADELAIDE HOSP,DEPT CLIN PHARMACOL,ADELAIDE,SA 5000,AUSTRALIA
[2] ROYAL ADELAIDE HOSP,DEPT GASTROENTEROL,ADELAIDE,SA 5000,AUSTRALIA
关键词
ERYTHROMYCIN; INTESTINAL ABSORPTION; PHARMACOKINETICS; BIOAVAILABILITY;
D O I
10.1023/A:1016215510223
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To determine the role of acid hydrolysis on the gastrointestinal absorption of erythromycin, six healthy subjects received erythromycin as a 240 mg Intravenous dose, a 250 mg oral solution administered via endoscope directly into the duodenum and bypassing the stomach, and an enteric-coated 250 mg capsule. Blood samples were collected for 6 hours and serum erythromycin quantified by a microbiological method. The time to achieve maximum serum concentrations for the solution was 0.25 +/- 0.08 (mean +/- SD) hours and for the capsule was 2.92 +/- 0.55 hours. The absolute bioavailability of erythromycin from the capsule was 32 +/- 7% and for the duodenal solution 43 +/- 14%. The ratio of the areas under the serum erythromycin concentration-time curve of capsule to solution was 80 +/- 28% (range 38 to 110%). There is substantial loss of erythromycin apart from gastric acid hydrolysis, which cannot be accounted for by hepatic first-pass metabolism. Attempts to further improve the oral bioavaitability of erythromycin beyond 50% by manipulation of formulation are likely to be futile.
引用
收藏
页码:149 / 154
页数:6
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