Department of Pharmaceutical & Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602-2352, USA.
Department of Pathology, College of Veterinary Medicine, University of Georgia, Athens, GA 30602-7388, USA.
J Control Release. 2018 Aug 10;283:84-93. doi: 10.1016/j.jconrel.2018.05.025. Epub 2018 May 22.
Iron-mediated generation of highly toxic Reactive Oxygen Species (ROS) plays a major role in the process leading to iron overload-related diseases. The long-term subcutaneous administration of Deferoxamine (DFO) is currently clinically-approved to improve patient symptoms and survival. However, non-specific toxicity and short circulation times of the drug in humans often leads to poor patient compliance. Herein, thioketal-based ROS-responsive polymeric nanogels containing DFO moieties (rNG-DFO) were designed to chelate iron and to degrade under oxidative stimuli into fragments <10 nm to enhance excretion of iron-bound chelates. Serum ferritin levels and iron concentrations in major organs of IO mice decreased following treatment with rNG-DFO, and fecal elimination of iron-bound chelates increased compared to free DFO. Furthermore, rNG-DFO decreased iron mediated oxidative stress levels in vitro and reduced iron-mediated inflammation in the liver of IO mice. The study confirms that ROS-responsive nanogels may serve as a promising alternative to DFO for safer and more efficient iron chelation therapy.
铁介导的高毒性活性氧(ROS)的产生在导致铁过载相关疾病的过程中起主要作用。目前,长期皮下给予去铁胺(DFO)被临床批准用于改善患者症状和生存。然而,药物在人体内的非特异性毒性和短循环时间常常导致患者顺应性差。在此,设计了包含 DFO 部分的基于硫缩酮的 ROS 响应性聚合物纳米凝胶(rNG-DFO),以螯合铁,并在氧化刺激下降解成 <10nm 的片段,以增强铁结合螯合物的排泄。IO 小鼠用 rNG-DFO 治疗后,血清铁蛋白水平和主要器官中的铁浓度降低,与游离 DFO 相比,铁结合螯合物的粪便消除增加。此外,rNG-DFO 降低了体外铁介导的氧化应激水平,并减少了 IO 小鼠肝脏中铁介导的炎症。该研究证实,ROS 响应性纳米凝胶可能是 DFO 的一种有前途的替代品,用于更安全、更有效的铁螯合治疗。