Schreier S, Malheiros S V, de Paula E
Departmento de Bioquimica, Instituto de Quimica, Universidade de Saõ Paulo, Brazil.
Biochim Biophys Acta. 2000 Nov 23;1508(1-2):210-34. doi: 10.1016/s0304-4157(00)00012-5.
Many pharmacologically active compounds are of amphiphilic (or hydrophobic) nature. As a result, they tend to self-associate and to interact with biological membranes. This review focuses on the self-aggregation properties of drugs, as well as on their interaction with membranes. It is seen that drug-membrane interactions are analogous to the interactions between membranes and classical detergents. Phenomena such as shape changes, vesiculation, membrane disruption, and solubilization have been observed. At the molecular level, these events seem to be modulated by lipid flip-flop and formation of non-bilayer phases. The modulation of physicochemical properties of drugs by self-association and membrane binding is discussed. Pathological consequences of drug-membrane interaction are described. The mechanisms of drug solubilization by surfactants are reviewed from the physicochemical point of view and in relation to drug carrying and absorption by the organism.
许多药理活性化合物具有两亲性(或疏水性)。因此,它们倾向于自我缔合并与生物膜相互作用。本综述聚焦于药物的自聚集特性以及它们与膜的相互作用。可以看出,药物与膜的相互作用类似于膜与传统洗涤剂之间的相互作用。已经观察到诸如形状变化、囊泡形成、膜破坏和增溶等现象。在分子水平上,这些事件似乎受脂质翻转和非双层相形成的调节。讨论了药物通过自缔合和膜结合对其物理化学性质的调节。描述了药物与膜相互作用的病理后果。从物理化学角度并结合药物在生物体中的携带和吸收情况,综述了表面活性剂增溶药物的机制。