摘要: |
为了减少痢菌净的毒副作用及临床用药次数,本实验特制备痢菌净缓释纳米乳。方法:用水包油法制备痢菌净纳米乳,并对其形态、粒径、稳定性及体外释放等性能进行了一定的研究。结果:纳米乳的稳定性较好,平均粒径在50nm左右,80小时体外释放率达到70%,具备明显的缓释功能。结论:本研究获得了制备痢菌净纳米乳较为满意的工艺。 |
关键词: 痢菌净;纳米乳 缓释. |
DOI: |
投稿时间:2010-11-12修订日期:2011-01-18 |
基金项目: |
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Mequindox nanoemulsion preparation and determination of in vitro release |
Feng xiao-hua |
(Hunan Institute of Animal and Veterinary Science) |
Abstract: |
To reduce mequindox clinical medication side effects and the number of special preparation of the experiment mequindox release nanoemulsion. Methods: Preparation of oil-water mequindox nanoemulsion and its morphology, particle size, stability and in vitro release properties were so certain of. Results: The stability of nanoemulsion good average diameter of about 50nm, 80-hour in vitro release rate of 70%, with significant release function. Conclusion: The obtained nanoemulsion preparation mequindox the more satisfactory process. |
Key words: Mequindox nanoemulsion release. |