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Functionalization of poly(ethylene oxide)-based diblock copolymer vesicles.

机译:聚(环氧乙烷)基二嵌段共聚物囊泡的功能化。

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摘要

The principal goal of this research is to achieve the chemical labeling and surface modification of block copolymer vesicles (polymersomes) made from amphiphilic diblock copolymer Poly(butadiene-b-ethylene oxide) (PBd120 -PEO89, MW 10400 g/mol) with the aim of developing possible drug carrier vehicles for controlled release of molecules triggered by stimuli-responsive environments.;The terminal hydroxyl group of poly(ethylene oxide) (PEO), or poly(ethylene glycol) is converted into its corresponding carboxylic acid by a novel one-pot two-phase oxidation reaction. This regioselective and catalytic reaction assures the preservation of important structural characteristic of the block copolymers. Vesicles formed by a mixture of the carboxylate and unmodified block copolymer exhibit an increment in the critical aggregation concentration (CAC) value while the averaged vesicle size decreases demonstrating that the negative charges in the modified diblock copolymer disrupt the vesicle formation process.;The carboxylated reactive intermediates are subsequently subjected to a covalent coupling reaction in organic solvent to replace the terminal hydroxyl of the PEO block. The obtained functionalized diblock copolymers are effectively incorporated into the vesicle bilayer. Also, surface density control in polymersomes of fluorescently modified diblock copolymers, synthesized by the amination reaction, is achieved.;To demonstrate the ability of this polymersomes as carrier vehicles, a Noradrenaline functionalized vesicle is placed in closed contact with rat aortic smooth muscle cells (RASMC) using the micropipette aspiration technique. A distinctive increase in fluorescent intensity of cells is observed. It indicates that the drug molecule has been transported by the polymersome and internalized by the cell. In addition, diblock copolymers containing a disulfide moiety and a fluorophore are synthesized and studied through fluorescent microscopy. Vesicles are formed with this polymer and a decrease in fluorescent intensity is observed in the vesicle's bilayer after its exposure to a reductive environment. These results indicate that fluorophore molecules are successfully released into solution.
机译:这项研究的主要目的是实现由两亲性二嵌段共聚物聚(丁二烯-b-环氧乙烷)(PBd120 -PEO89,MW 10400 g / mol)制成的嵌段共聚物囊泡(聚合物囊泡)的化学标记和表面改性研发可能的药物载体,以控制由刺激反应环境触发的分子的释放。聚环氧乙烷(PEO)或聚乙二醇的末端羟基被一种新颖的羧酸转化为其相应的羧酸锅两相氧化反应。这种区域选择性和催化反应确保了嵌段共聚物重要结构特征的保留。由羧酸盐和未改性的嵌段共聚物的混合物形成的囊泡显示出临界聚集浓度(CAC)值的增加,而平均囊泡大小减小,表明改性的二嵌段共聚物中的负电荷破坏了囊泡的形成过程。中间体随后在有机溶剂中进行共价偶联反应,以取代PEO嵌段的末端羟基。将获得的官能化的二嵌段共聚物有效地结合到囊泡双层中。同样,通过胺化反应合成的荧光改性二嵌段共聚物的聚合物囊泡中的表面密度控制得以实现。为了证明该聚合物囊泡作为载体的能力,将去甲肾上腺素官能化的囊泡与大鼠主动脉平滑肌细胞紧密接触( RASMC)使用微量移液器抽吸技术。观察到细胞的荧光强度显着增加。这表明药物分子已被多聚体转运并被细胞内化。另外,合成并包含二硫键部分和荧光团的二嵌段共聚物并通过荧光显微镜研究。用这种聚合物形成囊泡,暴露于还原性环境后,在囊泡的双层中观察到荧光强度降低。这些结果表明荧光团分子成功释放到溶液中。

著录项

  • 作者单位

    Texas A&M University.;

  • 授予单位 Texas A&M University.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 118 p.
  • 总页数 118
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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