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阿霉素-铁络合物被磷脂双层的物理和化学修饰

Physical and chemical modifications of adriamycin:iron complex by phospholipid bilayers.

作者信息

Samuni A, Chong P L, Barenholz Y, Thompson T E

出版信息

Cancer Res. 1986 Feb;46(2):594-9.

PMID:3940630
Abstract

Adriamycin (ADM) and the ADM:Fe(III) complex both interact with phosphatidylcholine bilayers in aqueous vesicle dispersions. The immediate interaction of either ADM or ADM:Fe(III) with phospholipid causes little change in their absorption or emission spectra, but considerably increases the steady-state fluorescence anisotropy of both species. This is followed by a conversion of the ADM:Fe(III) complex (but not of metal-free ADM) into a new compound in periods ranging from minutes to hours depending upon the Fe(III) concentration. This reaction does not require the presence of unsaturated acyl chains, net negatively charged phospholipid head groups, or the participation of molecular oxygen. This new compound has a characteristic absorption and fluorescence emission spectra which differ from those of the ADM:Fe(III) or of metal-free ADM. It can be isolated from the aqueous lipid dispersion by Folch extraction under acidic conditions. It is very lipophilic in comparison to ADM or the ADM:Fe(III) complex. It may be similar to the compound reported to form between cardiolipin and Adriamycin. Preliminary results indicate that it also forms spontaneously in intact biological membranes. Its highly lipophilic character may confine it to bilayers and membranes.

摘要

阿霉素(ADM)以及阿霉素:铁(III)络合物都能与水相囊泡分散体系中的磷脂酰胆碱双层膜相互作用。阿霉素或阿霉素:铁(III)与磷脂的直接相互作用对它们的吸收光谱或发射光谱影响不大,但会显著增加这两种物质的稳态荧光各向异性。随后,阿霉素:铁(III)络合物(而非无金属的阿霉素)会在几分钟到几小时不等的时间内(取决于铁(III)的浓度)转化为一种新化合物。该反应不需要不饱和酰基链、带净负电荷的磷脂头部基团的存在,也不需要分子氧的参与。这种新化合物具有独特的吸收光谱和荧光发射光谱,与阿霉素:铁(III)或无金属的阿霉素不同。在酸性条件下通过福氏提取法可将其从水相脂质分散体系中分离出来。与阿霉素或阿霉素:铁(III)络合物相比,它具有很强的亲脂性。它可能类似于报道的在心肌磷脂和阿霉素之间形成的化合物。初步结果表明,它在完整的生物膜中也能自发形成。其高度亲脂的特性可能使其局限于双层膜和膜中。

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