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一种具有可调节表面用于pH和谷胱甘肽双响应药物递送的聚乙烯醇包被的核壳纳米颗粒。

A poly (vinyl alcohol) coated core-shell nanoparticle with a tunable surface for pH and glutathione dual-responsive drug delivery.

作者信息

Li Jiagen, Hou Yuhang, Wu Hao, Chen Chunxia, Fu Xiaohong, Liu Jun, Li Lu, Shang Shuyong, Deng Guowei

机构信息

College of Chemistry and Life Science, Sichuan Provincial Key Laboratory for Structural Optimization and Application of Functional Molecules, Chengdu Normal University, Chengdu 611130, China.

College of Chemistry and Life Science, Sichuan Provincial Key Laboratory for Structural Optimization and Application of Functional Molecules, Chengdu Normal University, Chengdu 611130, China.

出版信息

Colloids Surf B Biointerfaces. 2025 Mar;247:114421. doi: 10.1016/j.colsurfb.2024.114421. Epub 2024 Dec 2.

Abstract

The surface characteristics of nanoparticles play a pivotal role in modulating the efficiency and functionality of drug delivery systems, particularly when addressing the complex challenges of targeted therapeutics. This study presents the development of a core-shell nanoparticle system (PMAA@DOX-PVA), incorporating poly(vinyl alcohol) (PVA) as a dynamic shell component to establish dual responsiveness to pH and glutathione levels. The hydrophilic PVA shell is covalently conjugated to the poly (methylacrylic acid) (PMAA) core via a boronic ester bond, establishing a robust platform for controlled release with tunable surface properties. Notably, our findings demonstrate a remarkable enhancement in drug loading efficiency from a modest 8 % (PMAA@DOX) to an impressive 18 % (PMAA@DOX-PVA-0.2). Furthermore, under physiological conditions (pH 7.4), the drug leakage after 62 hours is significantly reduced, dropping from 37 % (PMAA@DOX) to 21 % (PMAA@DOX-PVA-0.2). This suggests a potential improvement in stability during blood circulation. Intriguingly, the PVA ratio was found to influence drug release profiles under different environments distinctly. The possible mechanism was proposed offering insight into this tunable behavior. In vitro cytotoxicity assays on A549 cancer cells reveal that the blank carriers exhibit excellent biocompatibility, while the PVA-coated nanoparticles significantly boost anti-tumor efficacy. Collectively, these results present a promising strategy for designing core-shell nanoparticles with customizable surface properties, paving the way for next-generation, multifunctional drug delivery systems in diverse biomedical applications.

摘要

纳米颗粒的表面特性在调节药物递送系统的效率和功能方面起着关键作用,尤其是在应对靶向治疗的复杂挑战时。本研究展示了一种核壳纳米颗粒系统(PMAA@DOX-PVA)的开发,该系统将聚乙烯醇(PVA)作为动态壳层成分,以建立对pH值和谷胱甘肽水平的双重响应。亲水性PVA壳层通过硼酸酯键与聚甲基丙烯酸(PMAA)核共价共轭,建立了一个具有可调表面性质的控释强大平台。值得注意的是,我们的研究结果表明,药物负载效率从适度的8%(PMAA@DOX)显著提高到了令人印象深刻的18%(PMAA@DOX-PVA-0.2)。此外,在生理条件(pH 7.4)下,62小时后的药物泄漏显著减少,从37%(PMAA@DOX)降至21%(PMAA@DOX-PVA-0.2)。这表明在血液循环过程中的稳定性可能得到改善。有趣的是,发现PVA比例在不同环境下对药物释放曲线有明显影响。提出了可能的机制,以深入了解这种可调行为。对A549癌细胞的体外细胞毒性试验表明,空白载体具有优异的生物相容性,而涂有PVA的纳米颗粒显著提高了抗肿瘤功效。总的来说,这些结果为设计具有可定制表面性质的核壳纳米颗粒提供了一种有前景的策略,为各种生物医学应用中的下一代多功能药物递送系统铺平了道路。

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