Yu Bohong, Yang Yinxian, Liu Qi, Zhan Aiyan, Yang Yang, Liu Hongzhuo
Wuya college of innovation, Shenyang Pharmaceutical University, No.103, Wenhua Road, Shenyang 110016, China.
Collage of Pharmacy, Shenyang Pharmaceutical University, No.103, Wenhua Road, Shenyang 110016, China.
Pharmaceutics. 2020 Apr 7;12(4):329. doi: 10.3390/pharmaceutics12040329.
The traditional iron chelator deferoxamine (DFO) has been widely used in the treatment of iron overload disease. However, DFO has congenital disadvantages, including a very short circular time and non-negligible toxicity. Herein, we designed a novel multi-arm conjugate for prolonging DFO duration in vivo and reducing cytotoxicity. The star-like 8-arm-polyethylene glycol (8-arm-PEG) was used as the macromolecular scaffold, and DFO molecules were bound to the terminals of the PEG branches via amide bonds. The conjugates displayed comparable iron binding ability to the free DFO. Furthermore, these macromolecule conjugates could significantly reduce the cytotoxicity of the free DFO, and showed satisfactory iron clearance capability in the iron overloaded macrophage RAW 246.7. The plasma half-life of the 8-arm-PEG-DFO conjugate was about 190 times than that of DFO when applied to an intravenously administered rat model. In conclusion, research indicated that these star-like PEG-based conjugates could be promising candidates as long circulating, less toxic iron chelators.
传统的铁螯合剂去铁胺(DFO)已被广泛用于治疗铁过载疾病。然而,DFO存在先天性缺陷,包括循环时间非常短以及毒性不可忽视。在此,我们设计了一种新型多臂缀合物,以延长DFO在体内的持续时间并降低细胞毒性。星状八臂聚乙二醇(8臂-PEG)用作大分子支架,DFO分子通过酰胺键与PEG支链的末端相连。这些缀合物表现出与游离DFO相当的铁结合能力。此外,这些大分子缀合物可显著降低游离DFO的细胞毒性,并在铁过载的巨噬细胞RAW 246.7中显示出令人满意的铁清除能力。当应用于静脉给药的大鼠模型时,8臂-PEG-DFO缀合物的血浆半衰期约为DFO的190倍。总之,研究表明这些基于星状PEG的缀合物有望成为长效循环、低毒的铁螯合剂。