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丙基硫氧嘧啶固体脂质纳米粒的制备与质量评价

徐雄波 崔叶妹 宋红娟 卜振军 张青松 唐靖 马宁

中国药房2016,Vol.27Issue(7):946-948,949,4.
中国药房2016,Vol.27Issue(7):946-948,949,4.DOI:10.6039/j.issn.1001-0408.2016.07.25

丙基硫氧嘧啶固体脂质纳米粒的制备与质量评价

Preparation and Quality Evaluation of Propylthiouracil Solid Lipid Nanoparticles

徐雄波 1崔叶妹 1宋红娟 2卜振军 3张青松 1唐靖 1马宁1

作者信息

  • 1. 长沙医学院药学院,长沙 410219
  • 2. 徐州市妇幼保健院,江苏徐州 221003
  • 3. 湖南九典制药有限公司,长沙 410331
  • 折叠

摘要

Abstract

OBJECTIVE:To optimize the formulation and preparation technology of Propylthiouracil(PTU)solid lipid nanopar-ticles(PTU-SLN)and to evaluate the quality of PLN-SLN. METHODS:PTU-SLN was prepared by emulsion ultrasound dispersing method. The formulation of PTU-SLN was optimized by orthogonal design with the entrapment efficacy and particle size as index, using the amount of lipid material,soybean lecithin and poloxamer 188 and ultrasonic time as factors. The quality of prepared nanoparticles was evaluated with particle size,Zeta potential,entrapment efficiency,stability and in vitro drug release rate as in-dex. RESULTS:The optimal formulation and technology was as follows as lipid material 0.6 g,soybean lecithin 1.0 g,poloxamer 188 0.8 g,ultrasonic time 10 min. The obtained PTU-SLN was round and smooth in appearance and distributed evenly in particle size with average particle size of 93.5 nm,Zeta potential of -30.8 mV and average entrapment efficiency of 74.9%. Prepared nanoparticles had no significant change after placing for 15 d at 4 ℃. Accumulative release rate of PTU-SLN was 56.1% at 4 hour in vitro and reached 98.4% at 24 hour. CONCLUSIONS:PTU-SLN is prepared successfully and reasonable in technology,and can reach sustained-release effects.

关键词

丙基硫氧嘧啶/固体脂质纳米粒/包封率/体外释放/正交试验

Key words

Propylthiouracil/Solid lipid nanoparticicles/Encapsulation efficiency/in vitro release/Orthogonal test

分类

医药卫生

引用本文复制引用

徐雄波,崔叶妹,宋红娟,卜振军,张青松,唐靖,马宁..丙基硫氧嘧啶固体脂质纳米粒的制备与质量评价[J].中国药房,2016,27(7):946-948,949,4.

基金项目

湖南省医药卫生科研计划课题项目 ()

中国药房

OA北大核心CSTPCD

1001-0408

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