Anteneodo C, Bisch P M, Marques J F
Centro Brasileiro de Pesquisas Físicas/CNPq, RJ, Rio de Janeiro, Brazil.
Eur Biophys J. 1995;23(6):447-52. doi: 10.1007/BF00196833.
The interaction of chlorpromazine (CPZ) with artificial membranes (egg-yolk phosphatidylcholine liposomes) has been studied. Measurements of the surface electric potential, which is modified in the presence of the ionized form of the drug, were obtained by electron paramagnetic resonance spectroscopy (EPR) using a positively charged amphiphilic spin-probe. This probe partitions between the aqueous and lipidic phases depending on the surface potential and on the structural state of the membrane. The surface potential was measured as a function of drug concentration in the range where the spectral line-shapes are not affected by the incorporation of the drug. From these experimental results and through an appropriate formalism we obtain information on the binding of the drug to the lipid bilayer and on the ionization of the drug in the lipidic phase.
已对氯丙嗪(CPZ)与人工膜(蛋黄磷脂酰胆碱脂质体)之间的相互作用进行了研究。使用带正电荷的两亲性自旋探针,通过电子顺磁共振光谱(EPR)测量了表面电势,该电势在药物离子化形式存在时会发生改变。这种探针根据表面电势和膜的结构状态在水相和脂质相之间分配。在光谱线形不受药物掺入影响的浓度范围内,测量了表面电势随药物浓度的变化。从这些实验结果出发,通过适当的形式体系,我们获得了关于药物与脂质双层结合以及药物在脂质相中的离子化信息。