Perugini P, Pavanetto F
Department of Pharmaceutical Chemistry, University of Pavia, Italy.
J Microencapsul. 1998 Jul-Aug;15(4):473-83. doi: 10.3109/02652049809006874.
In the present work, liposomes loaded with Boronophenylalanine (BPA), with or without stabilization, were formulated for the application in boron neutron capture therapy. BPA was encapsulated into liposomes as a complex with fructose, but also as a free drug in two different pH buffers. The influence of critical variables (cholesterol content, drug:lipid molar ratio, osmotic stress of liposomes containing hyperosmotic drug solution) on liposome morphology and drug content was evaluated. The drug content and dissolution profile of different BPA loaded liposomes were also studied. The physical stability of liposomes in terms of changes in the size distribution in different osmotic pressure buffers and the chemical oxidation of phospholipids during storing conditions were investigated. The encapsulation efficiencies of all formulations were always satisfactory, being between 20-48%; even when the liposomes were exposed to high osmotic stress, the particle size was below 200 nm. The BPA-fructose complex loaded liposomes showed a slower drug release profile.
在本研究中,制备了负载有硼苯丙氨酸(BPA)的脂质体,有或没有进行稳定化处理,用于硼中子俘获疗法。BPA以与果糖形成的复合物形式被包封到脂质体中,同时也以游离药物形式存在于两种不同的pH缓冲液中。评估了关键变量(胆固醇含量、药物与脂质的摩尔比、含有高渗药物溶液的脂质体的渗透压)对脂质体形态和药物含量的影响。还研究了不同负载BPA的脂质体的药物含量和溶出曲线。研究了脂质体在不同渗透压缓冲液中尺寸分布变化方面的物理稳定性以及储存条件下磷脂的化学氧化情况。所有制剂的包封效率始终令人满意,在20%至48%之间;即使脂质体暴露于高渗透压下,粒径仍低于200nm。负载BPA-果糖复合物的脂质体显示出较慢的药物释放曲线。