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细胞通透型咪唑-去铁胺缀合物的合成及体外评价。

Cell Permeable Imidazole-Desferrioxamine Conjugates: Synthesis and In Vitro Evaluation.

机构信息

Centre for Excellence in Basic Sciences , Mumbai 400098 , India.

Bio-Organic Division , Bhabha Atomic Research Centre , Trombay, Mumbai 400085 , India.

出版信息

Bioconjug Chem. 2019 Mar 20;30(3):841-852. doi: 10.1021/acs.bioconjchem.8b00924. Epub 2019 Feb 22.

Abstract

Desferrioxamine (DFO), a clinically approved iron chelator used for iron overload, is unable to chelate labile plasma iron (LPI) because of its limited cell permeability. Herein, alkyl chain modified imidazolium cations with varied hydrophobicities have been conjugated with DFO. The iron binding abilities and the antioxidant properties of the conjugates were found to be similar to DFO. The degree of cellular internalization was much higher in the octyl-imidazolium-DFO conjugate (IV) compared with DFO, and IV was able to chelate LPI in vitro. This opens up a new avenue in using N-alkyl imidazolium salts as a delivery vector for hydrophilic cell-impermeable drugs.

摘要

去铁胺(DFO)是一种临床批准的铁螯合剂,用于治疗铁过载,但由于其细胞通透性有限,无法螯合不稳定的血浆铁(LPI)。在此,我们将具有不同疏水性的烷基链修饰的咪唑阳离子与 DFO 连接起来。研究发现,这些配合物的铁结合能力和抗氧化性能与 DFO 相似。与 DFO 相比,辛基-咪唑-DFO 配合物(IV)的细胞内化程度要高得多,并且能够在体外螯合 LPI。这为将 N- 烷基咪唑盐用作亲水性细胞不可渗透药物的递送载体开辟了新途径。

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