Baudis Stefan, Roch Toralf, Balk Maria, Wischke Christian, Lendlein Andreas, Behl Marc
Institute of Active Polymers, Helmholtz-Zentrum Hereon, Kantstraße 55, 14513 Teltow, Germany.
Institute of Biochemistry and Biology, University of Potsdam, Karl-Liebknecht-Str. 24-25, 14476 Potsdam-Golm, Germany.
ACS Biomater Sci Eng. 2024 Mar 11;10(3):1481-1493. doi: 10.1021/acsbiomaterials.3c01803. Epub 2024 Feb 19.
Controlling cellular responses to nanoparticles so far is predominantly empirical, typically requiring multiple rounds of optimization of particulate carriers. In this study, a systematic model-assisted approach should lead to the identification of key parameters that account for particle properties and their cellular recognition. A copolymer particle library was synthesized by a combinatorial approach in soap free emulsion copolymerization of styrene and methyl methacrylate, leading to a broad compositional as well as constitutional spectrum. The proposed structure-property relationships could be elucidated by multivariate analysis of the obtained experimental data, including physicochemical characteristics such as molar composition, molecular weight, particle diameter, and particle charge as well as the cellular uptake pattern of nanoparticles. It was found that the main contributors for particle size were the polymers' molecular weight and the zeta potential, while particle uptake is mainly directed by the particles' composition. This knowledge and the reported model-assisted procedure to identify relevant parameters affecting particle engulfment of particulate carriers by nonphagocytic and phagocytic cells can be of high relevance for the rational design of pharmaceutical nanocarriers and assessment of biodistribution and nanotoxicity, respectively.
到目前为止,控制细胞对纳米颗粒的反应主要是凭经验,通常需要对颗粒载体进行多轮优化。在本研究中,一种系统的模型辅助方法应能识别出解释颗粒性质及其细胞识别的关键参数。通过苯乙烯和甲基丙烯酸甲酯的无皂乳液共聚的组合方法合成了共聚物颗粒库,从而得到了广泛的组成和结构范围。通过对获得的实验数据进行多变量分析,可以阐明所提出的结构-性质关系,这些数据包括物理化学特征,如摩尔组成、分子量、粒径和颗粒电荷,以及纳米颗粒的细胞摄取模式。研究发现,影响粒径的主要因素是聚合物的分子量和zeta电位,而颗粒摄取主要由颗粒的组成决定。这一知识以及所报道的用于识别影响非吞噬细胞和吞噬细胞对颗粒载体颗粒吞噬的相关参数的模型辅助程序,分别对于药物纳米载体的合理设计以及生物分布和纳米毒性评估具有高度相关性。