Studies on molecular interactions between nalidixic acid and liposomes

被引:25
作者
Budai, M
Szabó, Z
Zimmer, A
Szögyi, M
Gróf, P
机构
[1] Semmelweis Univ, Fac Med, Inst Biophys & Radiat Biol, H-1444 Budapest, Hungary
[2] Karl Franz Univ, Fac Nat Sci, Inst Pharmaceut Chem & Pharmaceut Technol, A-8010 Graz, Austria
基金
新加坡国家研究基金会;
关键词
liposomes; nalidixic acid; DSC; DLS; zeta-potential; EPR;
D O I
10.1016/j.ijpharm.2004.04.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The interaction between nalidixic acid sodium salt (NANa) and liposomes prepared from alpha-L-dipalmitoyl-phosphatidylcholine (DPPC) or from its binary mixture with dioleoyl-phosphatidylcholine (DOPC) was studied with differential scanning calorimetry (DSC) and electron paramagnetic resonance (EPR) spectroscopy. We evaluated the role of broadband ultraviolet-B (UV-B) irradiation on the molecular interactions between the lipids and the NANa, and determined the decay-kinetics of the incorporated spin labeled fatty-acid free radicals. Multilamellar and unilamellar vesicles were prepared by sonication and extrusion. The entrapment efficiencies were determined spectrophotometrically. The size-distribution of the liposomes and its change in time was checked by dynamic light scattering (DLS). Our results indicate that NANa mainly interacts with lipid head groups. However, its effect and presumably the formation of the free radicals, induced by broadband ultraviolet-B, is not localized only to the head group region of the lipid molecules. Depending on DOPC content, interaction between the NANa and the lipids modifies the phase-transition parameters of the liposome dispersions. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 79
页数:13
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