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用于增强生物分子静电吸附的纳米颗粒表面功能化

Surface Functionalization of Nanoparticles for Enhanced Electrostatic Adsorption of Biomolecules.

作者信息

Gorohovs Marks, Dekhtyar Yuri

机构信息

Mechanical and Biomedical Engineering Institute, Riga Technical University, Kipsalas Street 6B, LV-1048 Riga, Latvia.

出版信息

Molecules. 2025 Jul 30;30(15):3206. doi: 10.3390/molecules30153206.

Abstract

Electrostatic adsorption plays a crucial role in nanoparticle-based drug delivery, enabling the targeted and reversible loading of biomolecules onto nanoparticles. This review explores the fundamental mechanisms governing nanoparticle-biomolecule interactions, with a focus on electrostatics, van der Waals forces, hydrogen bonding, and protein corona formation. Various functionalization strategies-including covalent modification, polymer coatings, and layer-by-layer assembly-have been employed to enhance electrostatic binding; however, each presents trade-offs in terms of stability, complexity, and specificity. Emerging irradiation-based techniques offer potential for direct modulation of surface charge without the addition of chemical groups, yet they remain underexplored. Accurate characterization of biomolecule adsorption is equally critical; however, the limitations of individual techniques also pose challenges to this endeavor. Spectroscopic, microscopic, and electrokinetic methods each contribute unique insights but require integration for a comprehensive understanding. Overall, a multimodal approach to both functionalization and characterization is essential for advancing nanoparticle systems toward clinical drug delivery applications.

摘要

静电吸附在基于纳米颗粒的药物递送中起着至关重要的作用,能够使生物分子靶向且可逆地负载到纳米颗粒上。本综述探讨了纳米颗粒与生物分子相互作用的基本机制,重点关注静电作用、范德华力、氢键以及蛋白质冠层的形成。已采用各种功能化策略,包括共价修饰、聚合物涂层和层层组装,以增强静电结合;然而,每种策略在稳定性、复杂性和特异性方面都存在权衡。新兴的基于辐照的技术为在不添加化学基团的情况下直接调节表面电荷提供了潜力,但仍未得到充分探索。生物分子吸附的准确表征同样至关重要;然而,个别技术的局限性也给这一努力带来了挑战。光谱、显微镜和电动方法各自提供了独特的见解,但需要整合才能全面理解。总体而言,功能化和表征的多模态方法对于推动纳米颗粒系统走向临床药物递送应用至关重要。

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Protein Corona of Nanoparticles: Isolation and Analysis.纳米颗粒的蛋白质冠层:分离与分析
Chem Bio Eng. 2024 Oct 3;1(9):757-772. doi: 10.1021/cbe.4c00105. eCollection 2024 Oct 24.

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