Ferreira J, Chatelain P, Caspers J, Ruysschaert J M
Laboratoire de Chimie-Physique des Macromolécules aux Interfaces, Université Libre de Bruxelles, Belgium.
Biochem Pharmacol. 1987 Dec 15;36(24):4245-50. doi: 10.1016/0006-2952(87)90665-4.
Amiodarone is a potent antianginal and antiarrhythmic drug which affects the lipid dynamics. The influence of amiodarone ionization on the lipid transition temperature and enthalpy associated to the liquid crystalline to gel state transition was studied in multilamellar vesicles (MLV) of dipalmitoylphosphatidylcholine (DPPC) by differential scanning measurements (DSC) at different pH. These data were correlated with the calculated number of charged amiodarone molecules inserted into the lipid vesicles. The procedure of calculation requires the knowledge of the intrinsic ionization constant of amiodarone and the area occupied per amiodarone molecule in the close packed state; it can be applied successfully to water insoluble amphiphilic molecules. Only the ionized form of amiodarone molecule destabilizes the lipid matrix organisation whereas no effect was observed with the uncharged form. This destabilizing effect could be explained in terms of a modification of the drug structure induced by its ionization state or in terms of its distribution in the lipid matrix, as an isolated molecule or assembled in clusters depending on its ionization state.
胺碘酮是一种强效抗心绞痛和抗心律失常药物,会影响脂质动力学。通过在不同pH值下进行差示扫描量热法(DSC)测量,研究了胺碘酮电离对二棕榈酰磷脂酰胆碱(DPPC)多层囊泡(MLV)中与液晶态到凝胶态转变相关的脂质转变温度和焓的影响。这些数据与计算得出的插入脂质囊泡中的带电胺碘酮分子数量相关。计算过程需要了解胺碘酮的固有电离常数以及在紧密堆积状态下每个胺碘酮分子所占的面积;它可以成功应用于水不溶性两亲分子。只有胺碘酮分子的离子化形式会破坏脂质基质的组织,而未带电形式则未观察到影响。这种破坏作用可以从其电离状态引起的药物结构改变方面来解释,或者从其在脂质基质中的分布方面来解释,即根据其电离状态以孤立分子或聚集簇的形式存在。