Saha A, De A U, Sengupta C
Department of Chemical Technology, University Calcutta, 92, A P C Road, Calcutta 700 009, India.
Indian J Exp Biol. 2000 Sep;38(9):912-5.
Considering the lipophilicity of aspirin (log P = -1.15), a significant contributor to its action mechanism, interaction of the drug with the whole lipids of goat blood have been investigated using phospholipid binding and lipid peroxidation phenomena as the parameters under investigation. The lipid content change along with the peroxidation induced by aspirin and its suppression with ascorbic acid had been quantitatively measured. Significant loss in phospholipid was observed after incubation of whole blood with aspirin in varying periods of time. This may be ascribed to binding affinity of aspirin with lipid constituents in blood, which may have potential role in its therapeutic effect. Lipid peroxidation induction potential of aspirin caused significant extent of peroxidation. Ascorbic acid, an antioxidant could significantly reduce aspirin induced lipid peroxidation.
考虑到阿司匹林的亲脂性(log P = -1.15),这是其作用机制的一个重要因素,已使用磷脂结合和脂质过氧化现象作为研究参数,研究了该药物与山羊血液中全部脂质的相互作用。已定量测定了阿司匹林诱导的脂质含量变化以及过氧化作用,并测定了抗坏血酸对其的抑制作用。在全血与阿司匹林在不同时间段孵育后,观察到磷脂有显著损失。这可能归因于阿司匹林与血液中脂质成分的结合亲和力,这可能在其治疗效果中发挥潜在作用。阿司匹林诱导脂质过氧化的潜力导致了显著程度的过氧化。抗氧化剂抗坏血酸可以显著降低阿司匹林诱导的脂质过氧化。