首页> 外文期刊>Journal of the American Chemical Society >Biocompatible Polymeric Nanoparticles Degrade and Release Cargo in Response to Biologically Relevant Levels of Hydrogen Peroxide
【24h】

Biocompatible Polymeric Nanoparticles Degrade and Release Cargo in Response to Biologically Relevant Levels of Hydrogen Peroxide

机译:生物相容性聚合物纳米粒子降解和释放货物对生物相关水平的过氧化氢的响应

获取原文
获取原文并翻译 | 示例
           

摘要

Oxidative stress is caused predominantly by accumulation of hydrogen peroxide and distinguishes inflamed tissue from healthy tissue. Hydrogen peroxide could potentially be useful as a stimulus for targeted drug delivery to diseased tissue. However, current polymeric systems are not sensitive to biologically relevant concentrations of H_2O_2 (50-100 μM). Here we report a new biocompatible polymeric capsule capable of undergoing backbone degradation and thus release upon exposure to such concentrations of hydrogen peroxide. Two polymeric structures were developed differing with respect to the linkage between the boronic ester group and the polymeric backbone: either direct (1) or via an ether linkage (2). Both polymers are stable in aqueous solution at normal pH, and exposure to peroxide induces the removal of the boronic ester protecting groups at physiological pH and temperature, revealing phenols along the backbone, which undergo quinone methide rearrangement to lead to polymer degradation. Considerably faster backbone degradation was observed for polymer 2 over polymer 1 by NMR and GPC. Nanoparticles were formulated from these novel materials to analyze their oxidation triggered release properties. While nanoparticles formulated from polymer 1 only released 50% of the reporter dye after exposure to 1 mM H_2O_2 for 26 h, nanoparticles formulated from polymer 2 did so within 10 h and were able to release their cargo selectively in biologically relevant concentrations of H_2O_2. Nanoparticles formulated from polymer 2 showed a 2-fold enhancement of release upon incubation with activated neutrophils, while controls showed a nonspecific response to ROS producing cells. These polymers represent a novel, biologically relevant, and biocompatible approach to biodegradable H_2O_2-triggered release systems that can degrade into small molecules, release their cargo, and should be easily cleared by the body.
机译:氧化应激主要由过氧化氢的积累引起,并将发炎的组织与健康的组织区分开。过氧化氢可能潜在地用作将药物靶向递送至患病组织的刺激物。但是,当前的聚合物系统对生物学上相关的H_2O_2(50-100μM)浓度不敏感。在这里,我们报告了一种新型的生物相容性聚合物胶囊,该胶囊能够经受主链降解并因此在暴露于这种浓度的过氧化氢时释放。在硼酸酯基团和聚合物骨架之间的连接方面,开发了两种不同的聚合物结构:直接(1)或通过醚键(2)。两种聚合物在正常pH下在水溶液中均稳定,暴露于过氧化物会导致在生理pH和温度下除去硼酸酯保护基,从而沿主链显示出酚类,酚类经过醌甲基化物重排导致聚合物降解。通过NMR和GPC观察到聚合物2比聚合物1快得多的主链降解。由这些新型材料制成纳米颗粒,以分析其氧化触发的释放特性。由聚合物1配制的纳米颗粒在暴露于1 mM H_2O_2 26小时后仅释放了50%的报告染料,而由聚合物2配制的纳米颗粒在10 h内释放了该染料,并能够以生物学相关浓度的H_2O_2选择性地释放其货物。由聚合物2配制的纳米颗粒在与活化的嗜中性粒细胞孵育后显示出2倍的释放增强,而对照显示出对产生ROS的细胞的非特异性反应。这些聚合物代表了可生物降解的H_2O_2触发的释放系统的一种新颖的,具有生物学意义的生物相容性方法,该系统可降解成小分子,释放其货物,并应易于人体清除。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第38期|p.15758-15764|共7页
  • 作者单位

    Skaggs School of Pharmacy and Pharmaceutical Sciences, Departments of NanoEngineering and of Materials Science and Engineering, University of California at San Diego, La Jolla, California 92093, United States;

    Skaggs School of Pharmacy and Pharmaceutical Sciences, Departments of NanoEngineering and of Materials Science and Engineering, University of California at San Diego, La Jolla, California 92093, United States;

    Skaggs School of Pharmacy and Pharmaceutical Sciences, Departments of NanoEngineering and of Materials Science and Engineering, University of California at San Diego, La Jolla, California 92093, United States;

    Skaggs School of Pharmacy and Pharmaceutical Sciences, Departments of NanoEngineering and of Materials Science and Engineering, University of California at San Diego, La Jolla, California 92093, United States;

    Skaggs School of Pharmacy and Pharmaceutical Sciences, Departments of NanoEngineering and of Materials Science and Engineering, University of California at San Diego, La Jolla, California 92093, United States;

    Skaggs School of Pharmacy and Pharmaceutical Sciences, Departments of NanoEngineering and of Materials Science and Engineering, University of California at San Diego, La Jolla, California 92093, United States;

    Skaggs School of Pharmacy and Pharmaceutical Sciences, Departments of NanoEngineering and of Materials Science and Engineering, University of California at San Diego, La Jolla, California 92093, United States;

  • 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);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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