| Literature DB >> 35651170 |
Zhiliang Gao1, Haiyan Zhu, Xiaoyu Li1, Peiyu Zhang1, Muthupandian Ashokkumar, Francesca Cavalieri, Jingcheng Hao1, Jiwei Cui1,2.
Abstract
Engineering functional nanoparticles (NPs) with low nonspecific interactions and a high specific targeting property is highly desired for improved drug delivery. Herein, we report a targeted poly(ethylene glycol) (PEG)-based chemotherapy system synthesized via a catalyst-free sono-polymerization process for drug delivery. The polymerization process was fast (20 min), and different monomers were able to be polymerized to form NPs in a one-pot process. Glutathione (GSH)-responsive platinum prodrugs and fluorescent dyes could be encapsulated in NPs by amidation formation. Cyclic peptides containing Arg-Gly-Asp (RGD)-modified PEG-based NPs possessed a much higher cell targeting (∼90%) than the unmodified PEG-based NPs (∼10%) after a 12 h incubation with U87 MG cells, which could improve drug delivery efficacy. The IC50 (50% inhibitory concentration) could also be reduced more than 50% compared to the nontargeted PEG-based NPs. Importantly, these PEG-based NPs can be freeze-dried into a powder form and redispersed in an aqueous solution without aggregation, which may facilitate the storage and transportation of nanomedicine. This study establishes a green and efficient method to engineer targeted drug carriers for drug delivery.Entities:
Year: 2019 PMID: 35651170 DOI: 10.1021/acsmacrolett.9b00576
Source DB: PubMed Journal: ACS Macro Lett ISSN: 2161-1653 Impact factor: 6.903