McColm A A, Ryan D M
Antimicrob Agents Chemother. 1985 Jun;27(6):925-7. doi: 10.1128/AAC.27.6.925.
The penetration of ceftazidime, administered in a dose of 100 mg/kg intramuscularly, into cardiac vegetations and subcutaneously implanted fibrin clots was compared in rabbits with experimental Staphylococcus aureus endocarditis. Significant pharmacokinetic differences between the time-concentration curves for the two compartments were observed. Concentrations of ceftazidime in vegetations peaked at 30 min after dosing at a level slightly lower than that in plasma and thereafter declined in parallel with concentrations in plasma throughout the 8-h sampling period. Concentrations in fibrin clots increased more slowly than those in plasma and vegetations, reaching a maximum at 120 min. This was followed by a slow elimination phase yielding concentrations in excess of concurrent plasma and vegetation levels and a greater area under the curve. These features were observed for both large (2-ml volume) and small (0.1-ml volume) clots. Contrary to previous reports, these observations suggest that fibrin clots do not provide an accurate model for predicting antibiotic concentrations in cardiac vegetations produced in endocarditis and that concentrations of antimicrobial agents in vegetations can be predicted more accurately from concomitant plasma levels.
在患有实验性金黄色葡萄球菌性心内膜炎的兔子中,比较了以100mg/kg剂量肌内注射头孢他啶后,其在心脏赘生物和皮下植入的纤维蛋白凝块中的渗透情况。观察到两个隔室的时间-浓度曲线之间存在显著的药代动力学差异。给药后30分钟,赘生物中头孢他啶浓度达到峰值,略低于血浆浓度,此后在整个8小时采样期内与血浆浓度平行下降。纤维蛋白凝块中的浓度比血浆和赘生物中的浓度升高得更慢,在120分钟时达到最大值。随后是一个缓慢消除阶段,其浓度超过同期血浆和赘生物水平,曲线下面积更大。对于大(2ml体积)小(0.1ml体积)凝块均观察到这些特征。与先前的报道相反,这些观察结果表明,纤维蛋白凝块不能为预测心内膜炎中产生的心脏赘生物中的抗生素浓度提供准确模型,并且从同期血浆水平可以更准确地预测赘生物中抗菌药物的浓度。