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Poly(amino acids) for drug and gene delivery.

机译:用于药物和基因递送的聚氨基酸。

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摘要

Three classes of biodegradable poly(amino acids) have been developed for the potential application to drug and gene delivery. Hyperbranched polylysine has been synthesized by four methods to obtain molecular weights up to 16,000 g/mol and degrees of branching approaching 0.64. The initial investigation into the DNA complexation capability of hyperbranched polylysine led to their use as “macro-cores” in the design of a second class of materials. These polymers were used to graft short linear polylysine chains to provide a macromolecule effective in DNA condensation, but ineffective in the release of the genetic material. To improve the delivery ability, histidine units were introduced into the polymer to provide imidazole units to promote DNA release. As expected, the histidine-containing materials formed weaker complexes with DNA compared to the all lysine polymer.; One class of molecules investigated for drug delivery are amphiphilic polymers that are degradeable and biocompatible such as the previously synthesized hydraamphiphiles consisting of a Boc-terminated lysine dendrimer grown from a monofunctional PEG chain. The asymmetric nature of the lysine repeat unit may prevent the hydrophobic end groups from perfectly aligning at the periphery since the termini are non-equivalent. To investigate the effect this has on the surfactant properties, a hydraamphiphile isomeric to the PEG supported lysine dendrimer has been synthesized using isolysine, the symmetric isomer of lysine, as the dendritic building block. The dendrimer was grown onto a PEG chain using a Boc-protected isolysine monomer, which was prepared in 5 steps from 2-pyrollidinone and 2-bromoethylamine hydrobromide. The surfactant properties of generations 1–4 of these Boc-terminated dendrimers were examined and compared to those previously obtained for the lysine dendrons. Micelle size was somewhat dependent on generation and dendrimer symmetry as were the critical micelle concentrations (cmcs) and micelle aggregation numbers. The stability of oil in water emulsions using the PEG supported Boc-terminated isolysine dendrimers as the surfactant was also explored.
机译:已经开发出三类可生物降解的聚氨基酸,以潜在地应用于药物和基因递送。通过四种方法合成了超支化聚赖氨酸,获得的分子量高达16,000 g / mol,支化度接近0.64。对高支化聚赖氨酸的DNA络合能力的初步研究导致其在第二类材料的设计中用作“大核心”。这些聚合物用于接枝短的线性聚赖氨酸链,以提供对DNA缩合有效的大分子,但对遗传物质的释放无效。为了提高递送能力,将组氨酸单元引入聚合物中以提供咪唑单元以促进DNA释放。如所期望的,与所有赖氨酸聚合物相比,含组氨酸的材料与DNA形成较弱的复合物。被研究用于药物递送的一类分子是可降解的且具有生物相容性的两亲聚合物,例如先前合成的亲水两亲物,该亲水两亲物由从单官能PEG链生长的Boc端赖氨酸树状大分子组成。由于末端不等价,赖氨酸重复单元的不对称性质可能会阻止疏水端基在周边完全对齐。为了研究其对表面活性剂性能的影响,已使用异赖氨酸(赖氨酸的对称异构体)作为树状结构单元,合成了与PEG负载的赖氨酸树状聚合物的异构体的亲水两亲物。使用Boc保护的异赖氨酸单体将树枝状大分子生长到PEG链上,该单体由5个步骤由2-吡咯烷酮和2-溴乙胺氢溴酸盐制备。检查了这些Boc封端的树枝状大分子的第1-4代的表面活性剂性质,并将其与以前从赖氨酸树突中获得的性质进行了比较。胶束的大小在一定程度上取决于生成和树状聚合物的对称性,如临界胶束浓度(cmcs)和胶束聚集数。还探讨了使用PEG负载的Boc末端的赖氨酸树状大分子作为表面活性剂的水包油乳液的稳定性。

著录项

  • 作者

    Menz, Terri Lynn.;

  • 作者单位

    University of Pittsburgh.;

  • 授予单位 University of Pittsburgh.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 p.6109
  • 总页数 233
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

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