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Facile fabrication of pH-responsive nanoparticles from cellulose derivatives via Schiff base formation for controlled release

机译:通过Schiff碱基形成对纤维素衍生物的pH-响应纳米粒子的体积制备进行控制释放

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摘要

A controllable drug delivery system demonstrates a promising tool for diverse biomedical applications. In this work, a group of amphiphilic macromolecules was designed and prepared via Schiff base reactions between 2,3-dialdehyde cellulose (DAC) with oleylamine and amino-containing compounds. Benefiting from the self-assemble process of these amphiphilic macromolecules in the poor solvent, a group of novel pH-responsive nanoparticles (NPs) were facilely fabricated by using nanoprecipitation dropping technique. The high amount of aldehyde groups on DAC chains enabled immobilization of tunable amounts of amine compounds (up to 1.67 mmol/g) in the NPs. Furthermore, the Schiff base bonds in NPs allowed the efficient release of the drug in acidic tumor microenvironment by cleaving the Schiff base linkages. This study demonstrates the formation of a group of novel pH-sensitive and drug-loadable NPs, which provide a simple and efficient drug delivery system for the potential application for cancer treatment.
机译:可控药物递送系统演示了一种有前途的生物医学应用的工具。在这项工作中,通过2,3-二醛纤维素(DAC)与油胺和氨基化合物之间的Schiff基础反应设计和制备了一组两亲型大分子。受益于在不良溶剂中的这些两亲型大分子的自组装过程中,通过使用纳米沉淀滴技术,尤其化为一种新型pH-响应纳米颗粒(NPS)。 DAC链上的大量醛基使得能够在NPS中固定可调谐量的胺化合物(高达1.67mmol / g)。此外,NPS中的Schiff基础键允许通过切割席夫碱基联系,在酸性肿瘤微环境中有效释放药物。本研究表明,形成一组新型pH敏感和可负载的NPS,其为癌症治疗潜在施用提供了一种简单富有效的药物递送系统。

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