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首页> 外文期刊>Acta biomaterialia >Fluorination of electrospun hydrogel fibers for a controlled release drug delivery system.
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Fluorination of electrospun hydrogel fibers for a controlled release drug delivery system.

机译:电纺水凝胶纤维的氟化用于控释药物递送系统。

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摘要

Electrospinning and fluorination were carried out in order to obtain a controlled release drug delivery system to solve the problem of both an initial burst of the drug and a limited release time. Poly(vinyl alcohol) was electrospun with Procion Blue as a model drug and heat treated in order to obtain cross-linked hydrogel fibers. Two different kinds of electrospun fibers of thin and thick diameters were obtained by controlling the electrospinning conditions. Thin fibers offer more available sites than thick fibers for surface modification during fluorination. Fluorination was conducted to control the release period by introducing hydrophobic functional groups on the surface of fibers. With an increase in the reaction pressure of the fluorine gas hydrophobic C-F and C-F(2) bonds were more effectively introduced. Over-fluorination of the fibers at higher reaction pressures of fluorine gas led to the introduction of C-F(2) bonds, which made the surface of the fibers hydrophobic and resulted in a decrease in their swelling potential. When C-F bonds were generated the initial drug burst decreased dramatically and total release time increased significantly, by a factor of approximately 6.7 times.
机译:进行静电纺丝和氟化,以获得控制的释放药物递送系统,以解决药物的初始爆发和有限释放时间的问题。将聚(乙烯醇)电纺器纺器具有涂层蓝作为模型药物和热处理以获得交联的水凝胶纤维。通过控制静电纺丝条件,获得两种不同类型的薄和厚直径的纤维。薄纤维提供比氟化在厚纤维的更多可用场地,用于氟化过程中的表面改性。通过在纤维表面上引入疏水官能团来进行氟化以控制释放期。随着氟气疏水的反应压力的增加,更有效地引入C-F(2)键。在氟气的较高反应压力下荧光的过氟化纤维导致引入C-F(2)键,这使得纤维表面疏水,导致它们的溶胀潜力降低。当产生C-F键时,初始药物爆发显着降低,总释放时间显着增加,倍率约为6.7倍。

著录项

  • 来源
    《Acta biomaterialia》 |2010年第1期|共8页
  • 作者

    Im JS; Yun J; Lim Y;

  • 作者单位

    Department of Fine Chemical Engineering and Applied Chemistry Chungnam National University Daejeon 305-764 Republic of Korea.;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物医学工程;
  • 关键词

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