Department of Pharmaceutics, Semmelweis University, Budapest, Hungary.
J Liposome Res. 2009;19(2):163-8. doi: 10.1080/17482940902724044.
The present studies were focused on the preparation and characterization of stericaly stabilized liposomes (SLs) encapsulating a recombinant organophosphorus hydrolyzing phosphotriesterase (OPH) enzyme for the antagonism of organophosphorus intoxication. Earlier results indicate that the liposomal carrier system provides an enhanced protective effect against the organophosphorus molecule paraoxon, presenting a more effective therapy with less toxicity than the most commonly used antidotes. Physicochemical characterization of the liposomal OPH delivery system is essential in order to get information on its in vitro stability and in vivo fate. Osmolarity, pH, viscosity, and encapsulation efficiency of the SL preparation and the surface potential of the vesicles were determined. The membrane rigidity and the impact of OPH enzyme on it was studied by electron-paramagnetic resonance spectroscopy, using spin probes. The in vitro stability of the liposomal preparations, the vesicle size distribution, and its alteration during a 3-week storage were followed by dynamic light-scattering measurements. Further, the stability of encapsulated and nonencapsulated OPH was compared in puffer and plasma.
本研究集中于制备和表征立体稳定脂质体(SL),用于包裹重组有机磷水解酶(OPH)以对抗有机磷中毒。早期结果表明,脂质体载体系统对有机磷分子对氧磷提供了增强的保护作用,与最常用的解毒剂相比,具有更低的毒性和更有效的治疗效果。为了了解其体外稳定性和体内命运,有必要对脂质体 OPH 递药系统进行理化特性表征。测定了 SL 制剂的渗透压、pH 值、粘度、包封效率和囊泡表面电位。通过电子顺磁共振波谱法,使用自旋探针研究了膜刚性以及 OPH 酶对其的影响。通过动态光散射测量,研究了脂质体制剂的体外稳定性、囊泡粒径分布及其在 3 周储存期间的变化。此外,还比较了在河豚鱼和血浆中包裹和未包裹的 OPH 的稳定性。