Lode H, Stahlmann R, Koeppe P
Antimicrob Agents Chemother. 1979 Jul;16(1):1-6. doi: 10.1128/AAC.16.1.1.
In a randomized crossover study, the pharmacokinetics of three new cephalosporin antibiotics, cefaclor, cefadroxil, and CGP 9000, in comparison to cephalexin, were determined after oral administration, by capsules, of 1,000 mg on an empty stomach in 12 normal subjects. Serum concentrations were measured during a period of 8 h, and urine recovery was measured during 24 h. The significant parameters of bioavailability of an orally administered substance were determined. The maximal serum concentrations (y(max)) for cephalexin, cefaclor, cefadroxil, and CGP 9000 (in milligrams per liter) were: 38.8 +/- 8.1; 34.6 +/- 7.8; 33.0 +/- 5.4; and 23.3 +/- 7.3, respectively. The areas under the curve (in hours x milligrams per liter) were: 93.0 +/- 14.8; 74.5 +/- 9.9; 70.1 +/- 9.0; and 108.5 +/- 18.4, respectively. In a further crossover study with six subjects, 1,000 mg of cephalexin and of cefadroxil were given during a standard breakfast. The y(max) of cephalexin decreased to 23.1 +/- 6.6 mg/liter, in contrast to cefadroxil, with an unchanged y(max) of 32.7 +/- 3.4 mg/liter.
在一项随机交叉研究中,12名正常受试者空腹口服1000毫克胶囊装的三种新型头孢菌素抗生素(头孢克洛、头孢羟氨苄和CGP 9000),并与头孢氨苄进行比较,测定其药代动力学。在8小时内测定血清浓度,在24小时内测定尿回收率。确定了口服给药物质生物利用度的重要参数。头孢氨苄、头孢克洛、头孢羟氨苄和CGP 9000的最大血清浓度(以毫克/升计)分别为:38.8±8.1;34.6±7.8;33.0±5.4;和23.3±7.3。曲线下面积(以小时×毫克/升计)分别为:93.0±14.8;74.5±9.9;70.1±9.0;和108.5±18.4。在另一项有6名受试者参与的交叉研究中,在标准早餐期间给予1000毫克头孢氨苄和头孢羟氨苄。与头孢羟氨苄不同,头孢氨苄的最大血清浓度降至23.1±6.6毫克/升,而头孢羟氨苄的最大血清浓度不变,为32.7±3.4毫克/升。