Kees F, Lukassek U, Naber K G, Grobecker H
Lehrstuhl für Pharmakologie, Universität Regensburg, Straubing, Fed. Rep. of Germany.
Arzneimittelforschung. 1991 Aug;41(8):843-6.
In a three-way cross-over study the bioavailability of cefuroxime was determined in 12 healthy volunteers after oral administration of 250 mg as cefuroxime axetil (Elobact; CAS 64544-07-6) in a plain aqueous suspension and as tablets from different batches. The tablet formulations showed nearly identical pharmacokinetic parameters and were bioequivalent. The mean maximum serum concentration was 4.7 micrograms/ml, achieved after 2.1 h. The serum half-live was 1.2-1.4 h, the area under the serum concentration-time curve was 14.3-14.4 micrograms/ml.h and the urinary recovery of unchanged cefuroxime was 54%. The bioavailability of cefuroxime after administration of cefuroxime axetil in aqueous suspension was lower, but bio-inequivalence was not demonstrated.
在一项三交叉研究中,对12名健康志愿者口服250毫克头孢呋辛酯(Elobact;化学物质登记号64544 - 07 - 6)后的生物利用度进行了测定,药物以普通水悬浮液及不同批次的片剂形式给药。片剂制剂显示出几乎相同的药代动力学参数,并且具有生物等效性。平均最大血清浓度为4.7微克/毫升,在2.1小时后达到。血清半衰期为1.2 - 1.4小时,血清浓度 - 时间曲线下面积为14.3 - 14.4微克/毫升·小时,未变化的头孢呋辛经尿液回收量为54%。头孢呋辛酯以水悬浮液形式给药后,头孢呋辛的生物利用度较低,但未显示出生物不等效性。