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From Drug-Eluting Stents to Biopharmaceuticals: Poly(ester amide) a Versatile New Bioabsorbable Biopolymer

机译:从药物洗脱支架到生物制药:聚酯酰胺是一种多功能的新型生物可吸收生物聚合物

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摘要

New biodegradable and tissue-resorbable co-poly(ester amides) (PEAs) useful for biomedical applications were prepared using a versatile Active PolyCondensation (APC) method, which involves di-p-toluenesulfonic acid salts of bis-(L-α-amino acid)-α,ω-alkylene diesters and active diesters of dicarboxylic acids as monomers. APC reactions were carried out at mild temperatures (40-60℃) and allowed the synthesis of regular, linear, polyfunctional PEAs with high molecular weights. The physical properties of PEAs are critically dependent upon the structure of the polymer backbone. A wide range of mechanical properties and biodegradation rates can be achieved by varying the three components in the backbone: a-amino acids, diols and dicarboxylic acids. Indeed, there is a growing need for wider variations of biocompatible PEA compositions and methods for the delivery of different therapeutic molecules at controlled rates, while affording enhanced mechanical and physical properties. Therefore, various types of new non-toxic building blocks based upon bulky diols (isosorbide, 17β-estradiol), unsaturated (fumaric) and aromatic diacids (hydroxycinnamic acid, 1,3-bis(4-carboxyphenoxy)-propane) were developed and successfullyrnincorporated into the main backbone of PEA. In vitro biodegradation tests with enzymes have shown that changes in the polymer backbone and functional groups resulted in a wide range of degradation rates that further exemplify the usefulness of these compositions in biomedical applications.
机译:使用通用的主动缩聚(APC)方法制备了可用于生物医学的新的可生物降解和组织可吸收的共聚(酯酰胺)(PEA),该方法涉及双-(L-α-氨基)的二对甲苯磺酸盐酸)-α,ω-亚烷基二酯和二羧酸作为单体的活性二酯。 APC反应在温和的温度(40-60℃)下进行,可以合成规则的,线性的,高分子量的多官能PEA。 PEA的物理性质关键取决于聚合物主链的结构。通过改变主链中的三个组分:α-氨基酸,二醇和二羧酸,可以实现广泛的机械性能和生物降解速率。确实,越来越需要生物相容性PEA组合物和方法的更广泛的变化,以便以受控的速率递送不同的治疗分子,同时提供增强的机械和物理性能。因此,开发了各种基于大分子二醇(异山梨醇,17β-雌二醇),不饱和(富马酸)和芳族二酸(羟基肉桂酸,1,3-双(4-羧基苯氧基)丙烷)的新型无毒建筑材料,成功纳入PEA的主要骨干。用酶进行的体外生物降解测试表明,聚合物主链和官能团的变化导致了广泛的降解速率,这进一步证明了这些组合物在生物医学应用中的实用性。

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  • 会议地点 San Francisco CA(US);San Francisco CA(US)
  • 作者单位

    MediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnMediVas LLC, 6275 Nancy Ridge Drive, San Diego, CA 92121;

    rnCenter for Medical Polymers and Biomaterials, Georgian Technical University, 69, Kostava Strasse, 0175 Tbilisi, Georgia;

    rnMediVas LLC, 6275 Nancy Ridge;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 TB347;
  • 关键词

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