Guibert J, Kitzis M D, Yvelin C, Acar J F
J Antimicrob Chemother. 1983 Jan;11 Suppl:201-6. doi: 10.1093/jac/11.suppl_a.201.
The pharmacokinetic parameters of cefotetan were determined in six healthy adults after intramuscular (im) and intravenous (iv) administration of a single dose. After an iv bolus injection of 1 g cefotetan the mean peak serum level was 179.6 mg/l (S.E.M. +/- 14.2 mg/l) at 2 min. The apparent volume of distribution was 10.29 l (S.E.M. +/- 0.66 l). After im injections of 500 mg and 1 g of cefotetan the mean peak levels were 35 mg/l (S.E.M. +/- 1.6 mg/l) and 74 mg/l (S.E.M. +/- 3.6 mg/l) at 82 and 97 min respectively; the level at 12 h was 4.5 mg/l after 500 mg and 10.4 mg/l after 1 g. Cefotetan was slowly eliminated. The serum half-life was about 3.1 h after 1 g iv injection and varied from 3.4 to 3.7 h after the 500 mg and 1 g im injections. About 75% of the dose was excreted in the urine during the first 24 h after 1 g iv bolus injection; after 500 mg and 1 g im injection 60 to 65% of the dose was recovered in the urine during the same time period.
在6名健康成年人单次肌内注射(im)和静脉注射(iv)头孢替坦后,测定了其药代动力学参数。静脉推注1g头孢替坦后,2分钟时血清平均峰值水平为179.6mg/L(标准误±14.2mg/L)。表观分布容积为10.29L(标准误±0.66L)。肌内注射500mg和1g头孢替坦后,平均峰值水平分别在82分钟和97分钟时为35mg/L(标准误±1.6mg/L)和74mg/L(标准误±3.6mg/L);500mg注射后12小时的水平为4.5mg/L,1g注射后为10.4mg/L。头孢替坦消除缓慢。静脉注射1g后血清半衰期约为3.1小时,肌内注射500mg和1g后半衰期在3.4至3.7小时之间。静脉推注1g后,约75%的剂量在24小时内从尿液中排出;肌内注射500mg和1g后,在同一时间段内60%至65%的剂量可在尿液中回收。