高分子纳米载体处理全身铁超载。

Molecular and cellular therapies Pub Date : 2015-03-24 eCollection Date: 2015-01-01
Jasmine L Hamilton, Jayachandran N Kizhakkedathu
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引用次数: 0

摘要

去铁胺(DFO)、去铁素(L1)和去铁asirox (ICL-670)是临床批准的铁螯合剂,用于治疗继发性铁超载。尽管自20世纪60年代以来,铁螯合剂已被广泛使用,现有的治疗方法也有了很大的改进,但由于长期疗效和药物毒性有限,仍然需要新的候选药物。此外,目前所有获批准的铁螯合剂均为低分子量(MW) (
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polymeric nanocarriers for the treatment of systemic iron overload.

Polymeric nanocarriers for the treatment of systemic iron overload.

Polymeric nanocarriers for the treatment of systemic iron overload.

Polymeric nanocarriers for the treatment of systemic iron overload.

Desferrioxamine (DFO), deferiprone (L1) and desferasirox (ICL-670) are clinically approved iron chelators used to treat secondary iron overload. Although iron chelators have been utilized since the 1960s and there has been much improvement in available therapy, there is still the need for new drug candidates due to limited long-term efficacy and drug toxicity. Moreover, all currently approved iron chelators are of low molecular weight (MW) (<600 Da) and the objectives reported for the "ideal" chelator of low MW, including possessing the ability to promote iron excretion without causing toxic side effects, has proven difficult to realize in practice. With prolonged iron chelator use, patients may develop toxicities or become insensitive. In contrast, the limited research that has been geared towards developing higher MW, polymeric, long circulating iron chelators has shown promise. The inherent potential of polymeric iron chelators toward longer plasma half-lives and reduction in toxicity provides optimism and may be a significant addition to the currently available low MW iron chelators. This article reviews knowledge pertaining to this theme, highlights some unique advantages that these nanomedicines have in treating systemic iron overload as well as their potential utility in the treatment of other disease states.

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