眼用氟尿嘧啶的制备及体外评价
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上海市科委纳米专项基金(0452nm015);全军“十一五”医药卫生科研基金(06MA177).


Preparation and in vitro evaluation of fluorouracil nanoparticles for ophthalmologic usage
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Supported by Fund for Nano-research of Shanghai Science and Technology Committee(0452nm015) and the “10th Five-Year Plan” for Medical Science Research Foundation of PLA(06MA177).

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    摘要:

    目的:应用滴入分散法制备眼用氟尿嘧啶-壳聚糖纳米粒(5-Fu-CS-NP),并对其体外释放进行考察。方法:将壳聚糖、聚丙烯酸与氟尿嘧啶通过滴入分散法形成聚电解质络合物制备5-Fu-CS-NP。考察纳米粒粒径、包封率、载药量以及体外释药特性。 结果和结论:5-Fu-CS-NP平均粒径为(144.6±3.1) nm,包封率为84.5%,载药量为3.91%。5-Fu-CS-NP有较好的缓释作用,能在3~7 d内持续释放药物。在pH值7.2~7.4的生理范围内,释放速率变化不大。

    Abstract:

    Objective:To prepare fluorouracil-loaded chitosan nanoparticle (5-Fu-CS-NP) for ophthalmologic usage and evaluate its releasing characteristics in vitro. Methods: 5-Fu-CS-NP was prepared with 5-Fu, polyacrylic acid and chitosan using dispersion method. The mean size, entrapment efficiency (EE%), drug loading (DL%) and the in vitro releasing characteristics of 5-Fu-CS-NP were investigated.Results and conclusion: The mean size of 5-Fu-CS-NP was (144.6±3.1) nm, the EE% was 84.5% and the DL% was 3.91%. 5-Fu-CS-NP had a satisfactory sustained-releasing effect and the releasing could last for 3-7 days, and the release behavior was not greatly changed within a pH value of 7.2-7.4.

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  • 收稿日期:2008-02-01
  • 最后修改日期:2008-05-19
  • 录用日期:2008-07-15
  • 在线发布日期: 2008-10-08
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