Cixi Institute of Biomedical Engineering, CAS Key Laboratory of Magnetic Materials and Devices & Key Laboratory of Additive Manufacturing Materials of Zhejiang Province, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, P. R. China.
Center for Microscopy-Microanalysis and Information Processing, University Politehnica of Bucharest, Bucharest 060042, Romania.
J Mater Chem B. 2020 Mar 25;8(12):2381-2392. doi: 10.1039/c9tb02902h.
A broad range of investigation methods and frameworks are currently used to throughly study the elasticity of various types of micro/nanoparticles (MNPs) with different properties and to explore the effect of such properties on their interactions with biological species. Specifically, the elasticity of MNPs serves as a key influencing factor with respect to important aspects of phagocytosis, such as the clathrin-mediated phagocytosis, caveolae-mediated phagocytosis, macropinocytosis, and cell membrane fusion. Achieving a clear understanding of the relationships that exist between the elasticity of MNPs and their phagocytic processes is essential to improve their performance in drug delivery, which is related to aspects such as circulation lifetime in blood, accumulation time in tissues, and resistance to metabolism. Resolving such aspects is very challenging, and related efforts require using the right tools/methods, which are not always easy to identify. This review aims to facilitate this by summarizing and comparing different cell phagocytosis pathways, while considering various MNPs exhibiting different elastic properties, shape change capabilities, and their effect on cellular uptake. We conduct an overview of the advantages exhibited by different MNPs with respect to both in vitro and in vivo delivery, taking computational simulation analysis and experimental results into account. This study will provide a guide for how to investigate various types of MNPs in terms of their elastic properties, together with their biomedical effects that rely on phagocytosis.
目前,广泛使用各种研究方法和框架来深入研究具有不同特性的各种微/纳米颗粒(MNPs)的弹性,并探索这些特性对其与生物物种相互作用的影响。具体而言,MNPs 的弹性是吞噬作用的重要影响因素,如网格蛋白介导的吞噬作用、小窝蛋白介导的吞噬作用、巨胞饮作用和细胞膜融合。清楚地了解 MNPs 的弹性与其吞噬过程之间的关系对于改善其在药物输送中的性能至关重要,这与药物在血液中的循环寿命、在组织中的积累时间以及对代谢的抵抗力等方面有关。解决这些方面具有挑战性,并且相关的努力需要使用正确的工具/方法,而这些方法并不总是容易识别的。本综述旨在通过总结和比较不同的细胞吞噬途径,同时考虑具有不同弹性特性、形状变化能力以及对细胞摄取影响的各种 MNPs,来促进这方面的研究。我们综述了不同 MNPs 在体内和体外输送方面的优势,同时考虑了计算模拟分析和实验结果。本研究将为如何研究各种类型的 MNPs 的弹性特性以及依赖于吞噬作用的生物医学效应提供指导。
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