Sospedra P, Alsina MA, Espina M, Reig F, Haro I, Mestres C
Physicochemistry Department, Facultat de Farmàcia, Av.Joan XXIII s.n., Barcelona, 08028, Spain
J Colloid Interface Sci. 2000 Jan 15;221(2):230-235. doi: 10.1006/jcis.1999.6585.
To prepare liposomes containing a synthetic hepatitis A virus antigen (HAV) [VP3(110-121)] as a vaccine, the miscibility of this peptide (with negative net charge) with a neutral lipid [dipalmitoylphosphatidylcholine (DPPC)], a negatively charged lipid [dipalmitoylphosphatidylglycerol (DPPG)], and a positively charged lipid [Stearylamine (SA)] was studied through compression isotherms of monolayers. Mixtures with DPPC and SA showed a low degree of interaction with the peptide, the composition of the monolayer being stable through compression. For DPPG-containing monolayers larger positive deviations from ideality were found, and the peptide was squeezed out from the monolayer at a DPPG/VP3(110-121) mole fraction of 0.8/0.2. All this suggests that besides hydrophobic interactions between the peptide and the lipid, electrostatic forces also play a role; thus it seems that neutral and positively charged lipids would be more suitable for preparing stable liposomes with VP3(110-121). Copyright 2000 Academic Press.
为了制备含有合成甲型肝炎病毒抗原(HAV)[VP3(110 - 121)]作为疫苗的脂质体,通过单分子层的压缩等温线研究了这种带负净电荷的肽与中性脂质[二棕榈酰磷脂酰胆碱(DPPC)]、带负电荷的脂质[二棕榈酰磷脂酰甘油(DPPG)]和带正电荷的脂质[硬脂胺(SA)]的混溶性。与DPPC和SA的混合物与该肽的相互作用程度较低,单分子层的组成在压缩过程中保持稳定。对于含DPPG的单分子层,发现与理想情况有较大的正偏差,并且在DPPG/VP3(110 - 121)摩尔分数为0.8/0.2时,该肽从单分子层中被挤出。所有这些表明,除了肽与脂质之间的疏水相互作用外,静电力也起作用;因此,中性和带正电荷的脂质似乎更适合用于制备含有VP3(110 - 121)的稳定脂质体。版权所有2000年,学术出版社。