Sjövall J, Westerlund D, Alván G, Magni L, Nord C E, Sörstad J
Chemotherapy. 1984;30(3):137-47. doi: 10.1159/000238260.
The relative bioavailability of bacampicillin hydrochloride, a pro-drug of ampicillin, was compared after rectal and oral administration. Bacampicillin was administered rectally as a microenema . The oral formulation was an aqueous microcapsule suspension. They were given as single doses of 400 mg to 12 healthy volunteers after overnight fasting using a randomized cross-over design. Ampicillin and bacampicillin were determined in plasma and blood, respectively, using HPLC. Bacampicillin was rapidly absorbed from the rectum but to a much smaller degree compared to the oral dose. The median t-max was 0.5 and 0.75 h after the rectal and oral doses, respectively. The mean (SD) Cp-max was 1.2 (0.33) mg/l after rectal and 4.8 (0.98) mg/l after oral administration, respectively. Blood concentrations of bacampicillin were extremely low or undetectable with no indication of differences between the two modes of administration. The 95% confidence limits for the relative bioavailability of the microenema were 22.4-39.2 and 22.5-40.4% based on area under the plasma concentration time curve and urinary recovery, respectively. The rectal dose was followed by distress, diarrhea or pain, in 7 subjects. There were no adverse reactions after the oral dose. Bacampicillin was unaffected by beta-lactamases produced by intestinal bacteria.
比较了氨苄西林前体药物盐酸巴氨西林经直肠和口服给药后的相对生物利用度。巴氨西林以微灌肠剂形式经直肠给药。口服制剂为水性微胶囊混悬液。采用随机交叉设计,在隔夜禁食后,给12名健康志愿者单次服用400mg剂量。分别采用高效液相色谱法测定血浆和血液中的氨苄西林和巴氨西林。巴氨西林从直肠迅速吸收,但与口服剂量相比程度要小得多。直肠给药和口服给药后,中位达峰时间分别为0.5小时和0.75小时。直肠给药后平均(标准差)峰浓度为1.2(0.33)mg/l,口服给药后为4.8(0.98)mg/l。巴氨西林的血药浓度极低或无法检测到,两种给药方式之间无差异迹象。基于血浆浓度-时间曲线下面积和尿回收率,微灌肠剂相对生物利用度的95%置信区间分别为22.4 - 39.2%和22.5 - 40.4%。7名受试者直肠给药后出现不适、腹泻或疼痛。口服给药后无不良反应。巴氨西林不受肠道细菌产生的β-内酰胺酶影响。