Pedersen-Bjergaard L, Petersen K E
Clin Pharmacokinet. 1977 Nov-Dec;2(6):451-6. doi: 10.2165/00003088-197702060-00005.
In a cross-over study, the oral absorption following equimolar doses of ampicillin corresponding to 16.7 mg/kg administrered as pivampicillin ('Pondocillin') suspension and ampicillin ('Doktacillin') suspension respectively, was investigated in 11 children aged from 8 months to 4.5 years. Pivampicillin produced a mean peak serum concentration of 10.7 microgram ampicillin/ml compared with 5.8 microgram/ml after ampicillin. The mean area under the serum concentration-time curves was 29.2 microgram/ml-h after pivampicillin and 16.7 microgram/ml-h after ampicillin, reflecting the superior bioavailability of the ester form. In 4 of the children aged between 8 and 12 months, the serum levels after pivampicillin were consistenly lower than those recorded in the remaining 7 children beyound the age of 1 year. The mechanism and therapeutic implications of this finding require further study.
在一项交叉研究中,对11名年龄在8个月至4.5岁的儿童,分别给予等摩尔剂量相当于16.7mg/kg的匹氨西林(“邦多西林”)混悬液和氨苄西林(“多可西林”)混悬液,研究其口服吸收情况。匹氨西林产生的氨苄西林平均血清峰值浓度为10.7微克/毫升,而氨苄西林给药后为5.8微克/毫升。匹氨西林给药后的血清浓度-时间曲线下平均面积为29.2微克/毫升·小时,氨苄西林给药后为16.7微克/毫升·小时,这反映出酯型药物具有更高的生物利用度。在4名年龄在8至12个月的儿童中,匹氨西林给药后的血清水平始终低于其余7名1岁以上儿童记录的水平。这一发现的机制及其治疗意义需要进一步研究。