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阿霉素铁的时间依赖性修饰

Time-dependent modifications of ferric-adriamycin.

作者信息

Gelvan D, Berg E, Saltman P, Samuni A

机构信息

Department of Molecular Biology, Hebrew University Hadassah Medical School, Jerusalem, Israel.

出版信息

Biochem Pharmacol. 1990 Apr 15;39(8):1289-95. doi: 10.1016/0006-2952(90)90005-6.

Abstract

The biological and chemical properties of the ferric-Adriamycin complex changed with time after its preparation. Our experiments demonstrated that the toxicity of the iron-chelate in mice decreased as a function of its age. The reduced toxicity can be correlated with changes in the difference spectrum of ferric-Adriamycin vs Adriamycin (ADR), where a peak around 610 nm shifted to the 570 nm region. When ferric-Adriamycin "aged", the affinity of the drug for iron increased. Concurrently, the redox properties of the chelate changed, such that the bound iron was no longer reduced by glutathione or cysteine. The time-dependent changes observed did not involve the formation of polynuclear iron, as shown by electron spin resonance. Thin-layer chromatography showed that ADR undergoes accelerated degradation in the presence of iron. The iron-catalyzed degradation was oxygen independent. The changes evolving in the spectral and chemical properties of the chelate were shown to stem from transfer of the iron from ADR to one of the degradation products.

摘要

阿霉素铁复合物的生物学和化学性质在制备后随时间发生变化。我们的实验表明,铁螯合物在小鼠体内的毒性随其存放时间的延长而降低。毒性降低与阿霉素铁和阿霉素(ADR)差示光谱的变化相关,其中610nm左右的峰移至570nm区域。当阿霉素铁“老化”时,药物对铁的亲和力增加。同时,螯合物的氧化还原性质发生变化,使得结合的铁不再被谷胱甘肽或半胱氨酸还原。电子自旋共振显示,观察到的随时间变化不涉及多核铁的形成。薄层色谱表明,在铁存在下ADR会加速降解。铁催化的降解与氧无关。螯合物光谱和化学性质的变化表明是由于铁从ADR转移到一种降解产物所致。

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