Wise R, Andrews J M
Eur J Clin Microbiol. 1983 Oct;2(5):505-8. doi: 10.1007/BF02013917.
One gram each of moxalactam and cefotaxime and 0.5 g of ceftriaxone was administered intravenously to six volunteers. The pharmacokinetics and tissue penetration (as measured by a blister fluid model) were studied. The initial (i.e. 15 min) concentrations of the agents were 89.7 mg/l, 101 mg/l and 55 mg/l for ceftriaxone, moxalactam and cefotaxime respectively. The serum half-lives differed considerably, being 8.8, 2.8 and 1.2 h respectively. All agents penetrated the blister fluid rapidly the maximum penetration being found with ceftriaxone, namely 32.7 mg/l.
给6名志愿者静脉注射1克羟羧氧酰胺菌素、1克头孢噻肟和0.5克头孢曲松。研究了它们的药代动力学和组织穿透性(通过水疱液模型测量)。头孢曲松、羟羧氧酰胺菌素和头孢噻肟的初始(即15分钟时)浓度分别为89.7毫克/升、101毫克/升和55毫克/升。血清半衰期差异很大,分别为8.8小时、2.8小时和1.2小时。所有药物均能迅速穿透水疱液,头孢曲松的穿透性最强,即32.7毫克/升。