Craig W A
William S Middleton Memorial VA Hospital, Madison, Wisconsin 53705, USA.
J Chemother. 1995 Jun;7 Suppl 2:47-52.
The pharmacodynamic characteristics of isepamicin and other aminoglycosides, both in terms of efficacy and toxicity, explain why once-daily administration of these agents should be the optimal dosing regimen. Isepamicin, as with other aminoglycosides, exhibits concentration-dependent bactericidal activity and produces prolonged post-antibiotic effects against susceptible organisms. High concentrations of these drugs would be expected to produce more rapid and extensive bacterial killing than lower levels. Furthermore, the post-antibiotic effect would protect against bacterial regrowth when serum and tissue concentrations fall below inhibitory levels. In animal models, the magnitude of the peak serum concentration or the area under the concentration-time curve, are the important determinants of efficacy for isepamicin and the other aminoglycosides. Isepamicin also exhibits the "first-exposure effect", i.e. initial exposure of bacteria to isepamicin down-regulates subsequent uptake of the drug. During this period of down-regulation, bacteria exhibit decreased killing and shorter post-antibiotic effects. Since the first-exposure effect lasts for several hours, once-daily administration of the aminoglycosides allows for this effect to dissipate completely between doses. High peak concentrations, greater than 8-10 times the minimum inhibitory concentration (MIC), will also decrease the emergence of resistant strains. With regard to toxicity, one of the first steps in the uptake of aminoglycosides into sites of toxicity is their binding to the brush borders of renal cells and to the cochlea and vestibular membranes. Binding to these membranes demonstrates saturable kinetics. As a result, uptake of the aminoglycosides is more efficient with low sustained concentrations than with high intermittent levels. Once-daily dosing of aminoglycosides has consistently been less toxic than more frequent dosing in animals. In clinical studies, once-daily dosing of aminoglycosides compared to two-or three-times daily administration has generally exhibited similar efficacy and toxicity. However, a few studies has shown greater efficacy or lower toxicity with once-daily dosing of aminoglycosides. Once-daily dosing of the aminoglycosides has the potential to enhance efficacy, reduce toxicity, and lower administration costs for this drug class.
异帕米星和其他氨基糖苷类药物的药效学特征,无论是在疗效还是毒性方面,都解释了为何这些药物每日一次给药应是最佳给药方案。与其他氨基糖苷类药物一样,异帕米星表现出浓度依赖性杀菌活性,并对敏感菌产生延长的抗生素后效应。预期这些药物的高浓度比低浓度能更快速、更广泛地杀灭细菌。此外,抗生素后效应可在血清和组织浓度降至抑制水平以下时防止细菌再生长。在动物模型中,血清峰浓度或浓度-时间曲线下面积的大小是异帕米星和其他氨基糖苷类药物疗效的重要决定因素。异帕米星还表现出“首次暴露效应”,即细菌首次接触异帕米星会下调其随后对该药物的摄取。在下调期,细菌的杀灭作用减弱且抗生素后效应缩短。由于首次暴露效应持续数小时,氨基糖苷类药物每日一次给药可使该效应在两次给药之间完全消散。高于最低抑菌浓度(MIC)8至10倍的高浓度峰也会减少耐药菌株的出现。关于毒性,氨基糖苷类药物摄取到毒性部位的第一步是它们与肾细胞的刷状缘以及耳蜗和前庭膜结合。与这些膜的结合表现出饱和动力学。因此,低持续浓度时氨基糖苷类药物的摄取比高间歇浓度时更有效。在动物中,氨基糖苷类药物每日一次给药的毒性始终低于更频繁给药。在临床研究中,与每日两次或三次给药相比,氨基糖苷类药物每日一次给药通常表现出相似的疗效和毒性。然而,一些研究表明氨基糖苷类药物每日一次给药具有更高的疗效或更低的毒性。氨基糖苷类药物每日一次给药有可能提高疗效、降低毒性并降低该类药物的给药成本。