Mousa S A, Ritger R C, Smith R D
Pharmaceuticals and Biotechnology Research Division, Du Pont Merck Pharmaceutical Company, Wilmington, Delaware 19880-0400.
J Cardiovasc Pharmacol. 1992 Mar;19(3):425-9. doi: 10.1097/00005344-199203000-00019.
The efficacy and safety of deferoxamine conjugated to hydroxyethyl starch (HES-DFO) was evaluated in an in vitro rat cardiac membrane lipid peroxidation (CMLP) assay and in a swine model of regional myocardial ischemia/reperfusion injury in comparison to DFO. The rat CMLP results demonstrate that HES-DFO is at least as potent as DFO (IC50 = 10 and 13 microM, respectively). HES-DFO given intravenously (i.v.) at the equivalence of 25 mg/kg and 100 mg/kg DFO in a swine model of regional myocardial ischemia [20-min left anterior descending coronary artery (LAD) occlusion followed by 60-min reperfusion] showed no significant changes in hemodynamics as compared with DFO at 25 mg/kg i.v. In addition, HES-DFO was at least as potent as DFO with regard to recovery of regional segment shortening function (%SS). Furthermore, both HES-DFO and DFO significantly reduced tissue water content (edema) in the area at risk (AAR). We conclude that conjugation of DFO to HES improves the safety without any interference in the efficacy of DFO.
在体外大鼠心脏膜脂质过氧化(CMLP)试验以及猪局部心肌缺血/再灌注损伤模型中,与去铁胺(DFO)相比,评估了与羟乙基淀粉结合的去铁胺(HES-DFO)的疗效和安全性。大鼠CMLP结果表明,HES-DFO的效力至少与DFO相同(IC50分别为10和13微摩尔)。在猪局部心肌缺血模型[左冠状动脉前降支(LAD)闭塞20分钟,随后再灌注60分钟]中,以相当于25毫克/千克和100毫克/千克DFO的剂量静脉注射(i.v.)HES-DFO,与静脉注射25毫克/千克DFO相比,血流动力学无显著变化。此外,在恢复局部节段缩短功能(%SS)方面,HES-DFO的效力至少与DFO相同。此外,HES-DFO和DFO均显著降低了危险区域(AAR)的组织含水量(水肿)。我们得出结论,DFO与HES结合可提高安全性,且不会干扰DFO的疗效。