Gordon Center for Medical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.
Department of Pharmaceutical Sciences, Northeastern University, Boston, MA, 02115, USA.
Nat Commun. 2019 Nov 13;10(1):5134. doi: 10.1038/s41467-019-13143-z.
Iron chelators have been widely used to remove excess toxic iron from patients with secondary iron overload. However, small molecule-based iron chelators can cause adverse side effects such as infection, gastrointestinal bleeding, kidney failure, and liver fibrosis. Here we report renal clearable nanochelators for iron overload disorders. First, after a singledose intravenous injection, the nanochelator shows favorable pharmacokinetic properties, such as kidney-specific biodistribution and rapid renal excretion (>80% injected dose in 4 h), compared to native deferoxamine (DFO). Second, subcutaneous (SC) administration of nanochelators improves pharmacodynamics, as evidenced by a 7-fold increase in efficiency of urinary iron excretion compared to intravenous injection. Third, daily SC injections of the nanochelator for 5 days to iron overload mice and rats decrease iron levels in serum and liver. Furthermore, the nanochelator significantly reduces kidney damage caused by iron overload without demonstrating DFO's own nephrotoxicity. This renal clearable nanochelator provides enhanced efficacy and safety.
铁螯合剂已被广泛用于从患有继发性铁过载的患者体内去除多余的毒性铁。然而,基于小分子的铁螯合剂会引起不良反应,如感染、胃肠道出血、肾衰竭和肝纤维化。在这里,我们报告了用于铁过载疾病的可经肾脏清除的纳米螯合剂。首先,与天然去铁胺(DFO)相比,单次静脉注射后,纳米螯合剂表现出良好的药代动力学特性,如肾脏特异性生物分布和快速肾脏排泄(4 小时内超过 80%注射剂量)。其次,纳米螯合剂的皮下(SC)给药改善了药效学,这表现为与静脉注射相比,尿液中铁排泄效率提高了 7 倍。第三,对铁过载的小鼠和大鼠进行 5 天的每日 SC 注射纳米螯合剂,可降低血清和肝脏中的铁含量。此外,纳米螯合剂可显著降低铁过载引起的肾脏损伤,而不会表现出 DFO 自身的肾毒性。这种可经肾脏清除的纳米螯合剂提供了增强的疗效和安全性。