首页|3,4,3″-三羟基对三联苯纳米混悬液制备工艺的筛选

3,4,3″-三羟基对三联苯纳米混悬液制备工艺的筛选

扫码查看
目的 筛选3,4,3″-三羟基对三联苯纳米混悬液的制备工艺.方法 采用纳米沉淀-微射流结合法制备纳米混悬液,以粒径为考察指标,通过单因素试验考察纳米沉淀过程搅拌速度及沉淀温度,微射流均质压力及循环次数对纳米混悬液粒径的影响,通过析因设计考察稳定剂的种类和用量对粒径的影响,从而筛选最佳制备工艺.结果 纳米混悬液的最佳制备工艺为沉淀温度0℃,搅拌速度900 rpm,微射流均质压力1600 bar,循环次数12次,处方组成比例为药物:泊洛沙姆188:卵磷脂为1:0.8:0.8.结论 通过优化制备工艺,成功制得粒径较低的纳米混悬液,为进一步研究奠定了基础.
Screening the Preparation Process of 3,4,3″-trihydroxy p-terphenyl Nanosuspension
Objective To screen the preparation process of 3,4,3″-trihydroxy p-terphenyl nanosuspension. Methods The nanosuspension was prepared in combination with the nanoprecipitation and microfluidization method. Taken the particle size for indicator, we investigated the stirring speed and precipitation temperature in the nanoprecipitation process, the homogeneous stress and cycles in the microfluidic process through single factor experiment. In addition, by factorial design, the variety and dosage of stabilizers are investigated. Results The excellent preparation condition of the nanosuspension are as follows: 0 ℃ for the precipitation temperature, 900 rpm for the stirring speed, 1600 bar for the microfluidization pressure and 12 times for cycles. The ingredient ratio for drug: poloxamer 188: lecithin is 1: 0.8: 0.8. Conclusion Through optimizing the preparation technology, we have successfully prepared nanosuspension with lower size , which will lay a foundation for further study.

nanosuspensionparticle sizesingle factor experimentfactorial design

田晓娜、王荣梅

展开 >

山东大学第二医院 药学部,山东 济南 250000

纳米混悬液 粒径 单因素考察 析因设计

2017

中国生化药物杂志
南京生物化学制药研究所,全国生化制药情报中心站,中国生化制药工业协会,中国药品生物制品检定所

中国生化药物杂志

ISSN:1005-1678
年,卷(期):2017.37(9)
  • 8