Masclef Jean-Baptiste, Acs Emmanuelle M N, Koehnke Jesko, Prunet Joëlle, Schmidt Bernhard V K J
School of Chemistry, University of Glasgow, Joseph Black Building, G12 8QQ Glasgow, U.K.
Institute of Food Chemistry, Leibniz University Hannover, 30167 Hannover, Germany.
Macromolecules. 2024 Jun 14;57(13):6013-6023. doi: 10.1021/acs.macromol.4c00528. eCollection 2024 Jul 9.
Hydrophilic polymers have found ubiquitous use in drug delivery and novel polymer materials to advance drug delivery systems are highly sought after. Herein, an amylose mimic (PEGose) was combined with poly(lactic acid) (PLA) in an amphiphilic block copolymer to form PEG-free nanoparticles as an alternative to PEG-based nanomedicines. The block copolymer self-assembled into 150-200 nm particles with a narrow dispersity in aqueous environment. The formed nanoparticles were capable of encapsulation, the sustained release of both hydrophilic and hydrophobic dyes. Moreover, the nanoparticles were found to be remarkably stable and had a very low cytotoxicity and a high propensity to penetrate cells. These results highlight the potential of PEGose--PLA to be used in drug delivery with a new hydrophilic building block.
亲水性聚合物在药物递送中有着广泛应用,人们对用于推进药物递送系统的新型聚合物材料有着很高的需求。在此,一种直链淀粉模拟物(聚乙二醇糖)与聚乳酸(PLA)在两亲性嵌段共聚物中结合,形成无聚乙二醇纳米颗粒,作为基于聚乙二醇的纳米药物的替代品。该嵌段共聚物在水性环境中自组装成粒径为150 - 200 nm且分散度窄的颗粒。所形成的纳米颗粒能够包封并持续释放亲水性和疏水性染料。此外,发现这些纳米颗粒非常稳定,细胞毒性极低且具有很高的细胞穿透倾向。这些结果突出了聚乙二醇糖 - PLA在使用新型亲水性结构单元进行药物递送方面的潜力。