含亚砜侧链聚乙二醇在纳米医学中的亲水性和防污性能。

Polymer science & technology (Washington, D.C.) Pub Date : 2025-08-15 eCollection Date: 2025-09-23 DOI:10.1021/polymscitech.5c00084
Yuhao Zhang, Mingdi Hu, Ruijing Xin, Xin Xu, Ze Zhang, Hui Peng, Rong Cai, Chunying Chen, Andrew K Whittaker, Changkui Fu
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引用次数: 0

摘要

聚乙二醇(PEG)作为纳米药物的防污涂层材料被广泛应用,以提高纳米药物的稳定性和安全性。然而,越来越多的研究表明,聚乙二醇具有免疫原性,可能引起不必要的免疫反应,因此需要开发用于纳米医学的替代防污聚合物。在这项研究中,我们报道了一种创新的聚合物,聚-(2-(甲基亚砜基)-乙基缩水甘油醚)(PMSOEGE),由聚乙二醇骨架结构与含亚砜侧链组成。我们证明,由于存在高极性和亲水的亚砜结构,PMSOEGE比传统PEG具有高度的生物相容性和亲水性。此外,经体外竞争性酶联免疫吸附试验(ELISA)证实,PMSOEGE与抗peg抗体的相关性要低得多。我们将PMSOEGE作为氧化铁纳米颗粒(IONPs)的涂层材料,并证明与聚乙二醇化的IONPs相比,PMSOEGE涂层的IONPs被巨噬细胞摄取的细胞量明显降低。蛋白冠分析表明,与IONP@PMSOEGE相关的蛋白较少。结果突出了PMSOEGE优越的防污性能,并突出了其作为PEG替代品在各种生物应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced Hydrophilicity and Antifouling Performance of PEG with Sulfoxide-Containing Side Chains for Nanomedicine Applications.

Enhanced Hydrophilicity and Antifouling Performance of PEG with Sulfoxide-Containing Side Chains for Nanomedicine Applications.

Enhanced Hydrophilicity and Antifouling Performance of PEG with Sulfoxide-Containing Side Chains for Nanomedicine Applications.

Enhanced Hydrophilicity and Antifouling Performance of PEG with Sulfoxide-Containing Side Chains for Nanomedicine Applications.

Poly-(ethylene) glycol (PEG) has been widely used as an antifouling coating material for nanomedicines to improve their stability and safety. However, a growing number of studies have indicated that PEG is immunogenic and can cause unwanted immune responses, highlighting the need to develop alternative antifouling polymers for applications in nanomedicine. In this study, we report an innovative polymer, poly-(2-(methylsulfinyl)-ethyl glycidyl ether) (PMSOEGE), composed of a PEG backbone structure with sulfoxide-containing side chains. We demonstrated that PMSOEGE is highly biocompatible and more hydrophilic than conventional PEG due to the presence of highly polar and hydrophilic sulfoxide structures. Furthermore, PMSOEGE exhibits a much lower association with anti-PEG antibodies, as confirmed by an in vitro competitive enzyme-linked immunosorbent assay (ELISA). We applied PMSOEGE as a coating material for iron oxide nanoparticles (IONPs) and demonstrated that the PMSOEGE-coated IONPs showed significantly lower cellular uptake by macrophages compared with PEGylated IONPs. Protein corona analysis indicated that fewer proteins were associated with IONP@PMSOEGE. The results highlight the superior antifouling properties of PMSOEGE and highlight its potential to serve as a PEG alternative for various biological applications.

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