Albertini G, Donati C, Phadke R S, Ponzi Bossi M G, Rustichelli F
Dipartimento di Scienze dei Materiali e della Terra, Ancona, Italy.
Chem Phys Lipids. 1990 Sep;55(3):331-7. doi: 10.1016/0009-3084(90)90171-m.
Some thermodynamic and structural aspects of propranolol-DPPC liposomes interaction were investigated by DSC and X-ray diffraction: the lamellar arrangement of the lipid matrix remains intact even at high concentrations of the drug (until 1:1 drug/lipid molar ratio). However, the bilayer thickness increases significantly and the chains become perpendicular to the lamellar planes, for increasing drug content. At still higher propranolol concentrations a hexagonal phase occurs followed by a lamellar phase, in which the liposomes are destroyed. Moreover, the presence of propranolol has been found to impart fluidity to the lipid matrix.
通过差示扫描量热法(DSC)和X射线衍射研究了普萘洛尔与二棕榈酰磷脂酰胆碱(DPPC)脂质体相互作用的一些热力学和结构方面:即使在高药物浓度下(直至药物/脂质摩尔比为1:1),脂质基质的层状排列仍保持完整。然而,随着药物含量的增加,双层厚度显著增加,且链变得垂直于层状平面。在更高的普萘洛尔浓度下,会出现六方相,随后是层状相,其中脂质体被破坏。此外,已发现普萘洛尔的存在会赋予脂质基质流动性。