摘要
目的:研究肺靶向穿心莲内酯脂质体的制备方法并考察其体外释药性质。方法:采用薄膜一冻融法制备穿心莲内酯脂质体;高效液相色谱法测定包封率;用透析法考察药物体外释放性质。结果:制得的脂质体平均粒径为6.325μm,包封率大于75%,稳定性好。药物体外释放符合Higuchi方程。结论:采用薄膜.冻融法可制得具有较高包封率及稳定性的穿心莲内酯脂质体,有助于提高穿心莲内酯的肺靶向性。
Objective: To study preparation and in vitro releasing characteristics of Andrographis liposomes. Method: To take the method of film-freeze-thaw for the preparation of Liposomal andrographolide; determine entrapment efficiency by HPLC; inspect in vitro releasing characteristics by dialysis. Results: The obtained liposomes average size was 6.325μm, entrapment efficiency was greater than 75%, stable. Released drugs in vitro were consistent with higuchi equation. Conclusion: To take the method of film-freeze-thaw could obtain better entrapment efficiency and stable Andrographis liposomes, help to improve lung targeting of andrographolide.
出处
《中医临床研究》
2010年第12期29-31,共3页
Clinical Journal Of Chinese Medicine
关键词
穿心莲内酯
脂质体
肺靶向
Andrographis
liposomes
Targeting at lung