首页> 外文期刊>Reactive & Functional Polymers >Fabrication of core-shell microspheres using alginate and chitosan-polycaprolactone for controlled release of vascular endothelial growth factor
【24h】

Fabrication of core-shell microspheres using alginate and chitosan-polycaprolactone for controlled release of vascular endothelial growth factor

机译:用藻酸盐和壳聚糖-聚己内酯制备核-壳微球以控制释放血管内皮生长因子

获取原文
获取原文并翻译 | 示例

摘要

Alginate microspheres loaded with vascular endothelial growth factor (VEGF) were prepared via an emul-sification method using calcium chloride as a crosslinker. The microspheres with encapsulation efficiency of about 80% were coated by chitosan-polycaprolactone (CH-PCL) with various PCL percentages changing from around 15 to 42 wt.% to fabricate core-shell alginate/CH-PCL microspheres with an average size of around 40 μm. It was found that the CH-PCL coating layer on the core-shell microspheres could have a sandwich-like structure. The PCL content in the CH-PCLs and the concentration of CH-PCL solutions in preparing the microsphere functioned as two key factors to regulate the release profiles of the micro-spheres. Some selected alginate/CH-PCL microspheres were further crosslinked using genipin as a cross-linker, and the amount of genipin was found to be another impactful factor to mediate the release patterns of the microspheres. In vitro release measurements revealed that VEGF-release from these core-shell microspheres was controlled either by Fickian diffusion or non-Fickian transport that involves both diffusion and swelling. Some optimized core-shell microspheres were capable of maintaining sustained VEGF-release in an approximately linear manner over a period of time longer than 4 weeks and did not involve a significant initial burst.
机译:通过使用氯化钙作为交联剂的乳化法制备负载有血管内皮生长因子(VEGF)的藻酸盐微球。用壳聚糖-聚己内酯(CH-PCL)包覆包封效率约为80%的微球,使PCL的百分比从约15%变为42%(重量),以制造平均尺寸约为10%的核壳藻酸盐/ CH-PCL微球。 40微米发现核-壳微球上的CH-PCL涂层可以具有夹心状结构。 CH-PCL中PCL的含量和制备微球时CH-PCL溶液的浓度是调节微球释放曲线的两个关键因素。某些选定的藻酸盐/ CH-PCL微球使用Genipin作为交联剂进一步交联,发现Genipin的量是介导微球释放模式的另一个影响因素。体外释放测量表明,从这些核-壳微球中释放的VEGF受Fickian扩散或涉及扩散和溶胀的非Fickian转运的控制。一些优化的核-壳微球能够在超过4周的时间内以近似线性的方式维持VEGF的持续释放,并且不涉及明显的初始爆发。

著录项

  • 来源
    《Reactive & Functional Polymers》 |2012年第7期|p.427-437|共11页
  • 作者单位

    Department of Nuclear Medicine and Minnan PET Center, The First Affiliated Hospital of Xiamen University, Xiamen 316003, PR China;

    College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, PR China;

    Department of Stomatology, Hospital of Hubei Province - Direct Organizations, Wuhan 430071, PR China;

    School of Pharmaceutical Science & Technology, Tianjin University, Tianjin 300072, PR China;

    College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, PR China;

    College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, PR China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    alginate; chitosan-polycaprolactone; core-shell microsphere; vascular endothelial growth factor; controlled release;

    机译:海藻酸盐壳聚糖聚己内酯核壳微球血管内皮生长因子;控释;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号