Cho N, Fukunaga K, Kunii K
Jpn J Antibiot. 1982 Jul;35(7):1855-76.
Pharmacokinetic studies of cefotaxime (CTX) were carried out in perinatal mothers and infants. CTX was promptly absorbed after intravenous injection, intravenous drip infusion and intramuscular injection in pregnant women, producing dose-related peak blood levels. Placental passage to the fetus was favorable. After intravenous injection, intravenous drip infusion and intramuscular injection of 500--1,000 mg of CTX, drug concentrations of the cord blood, amniotic fluid and fetal blood exceeded MICs of the main pathogenic organisms. By administration of this dose 1 to 2 times daily it is possible to successfully prevent or treat uterine infections. Passage of CTX into the milk of lactating mothers was minimal, suggesting that only minute quantities can possibly be transferred from the milk to newborn infants. Absorption of CTX in neonatal infants was prompt. The peak blood levels of 47.9 micrograms/ml were attained 15--30 minutes after intravenous injection of 20 mg/kg. The half-life ranged from 2.4--5.56 hours, depending on the number of days postpartus. CTX was effective in the prophylaxis and therapy of perinatal uterine infections.
对围产期母婴进行了头孢噻肟(CTX)的药代动力学研究。在孕妇中,静脉注射、静脉滴注和肌内注射后,CTX能迅速被吸收,产生与剂量相关的血药峰浓度。药物通过胎盘进入胎儿的情况良好。静脉注射、静脉滴注和肌内注射500 - 1000mg CTX后,脐血、羊水和胎儿血中的药物浓度超过了主要致病微生物的最低抑菌浓度(MIC)。通过每日给药1 - 2次该剂量,有可能成功预防或治疗子宫感染。CTX进入哺乳期母亲乳汁的量极少,这表明从乳汁转移到新生儿体内的量可能微乎其微。新生儿对CTX的吸收迅速。静脉注射20mg/kg后15 - 30分钟达到血药峰浓度47.9μg/ml。半衰期为2.4 - 5.56小时,取决于产后天数。CTX在围产期子宫感染的预防和治疗中有效。