Nicolau D P, Freeman C D, Nightingale C H, Coe C J, Quintiliani R
Department of Pharmacy, Hartford Hospital, Connecticut 06115.
Antimicrob Agents Chemother. 1994 Jul;38(7):1515-8. doi: 10.1128/AAC.38.7.1515.
The purpose of this study was to determine the penetration of minocycline and vancomycin into cardiac vegetations and to determine their efficacy in a rabbit model of endocarditis caused by oxacillin-resistant Staphylococcus aureus. Animals were randomized into three groups: control (no antibiotic), minocycline (6 mg/kg given intravenously every 8 h), and vancomycin (50 mg/kg given intravenously every 8 h). Penetration of the antibiotics into aortic valve vegetations was determined by using the tissue/serum area under the concentration-time curve ratio. The reductions in the bacterial density of the vegetations caused by both vancomycin (4.8 +/- 1.2 CFU/g) and minocycline (5.3 +/- 1.6 CFU/g) were significantly different from that of controls (8.7 +/- 1.8 CFU/g). Although the penetration of minocycline was twice that of vancomycin, they were equally effective in reducing the bacterial density of the vegetations, since the concentrations of both agents in tissue remained above their MICs for oxacillin-resistant S. aureus. For organisms for which the MICs are higher, however, these penetration differences may result in treatment differences.
本研究的目的是确定米诺环素和万古霉素在心脏赘生物中的渗透情况,并确定它们在由耐苯唑西林金黄色葡萄球菌引起的心内膜炎兔模型中的疗效。将动物随机分为三组:对照组(不使用抗生素)、米诺环素组(每8小时静脉注射6 mg/kg)和万古霉素组(每8小时静脉注射50 mg/kg)。通过使用浓度-时间曲线下面积的组织/血清比值来确定抗生素在主动脉瓣赘生物中的渗透情况。万古霉素(4.8±1.2 CFU/g)和米诺环素(5.3±1.6 CFU/g)引起的赘生物细菌密度降低与对照组(8.7±1.8 CFU/g)相比有显著差异。尽管米诺环素的渗透是万古霉素的两倍,但它们在降低赘生物细菌密度方面同样有效,因为两种药物在组织中的浓度均保持在高于耐苯唑西林金黄色葡萄球菌的最低抑菌浓度之上。然而,对于最低抑菌浓度较高的微生物,这些渗透差异可能导致治疗差异。