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ABSTRACT: Background
Surface engineering has emerged as a promising strategy to enhance the performance of nanomedicines. In particular, the PEGylation levels for chemotherapy drug 7-Ethyl-10-hydroxycamptothecin (SN38) prodrug nanoparticles (NPs) play a crucial role in determining their stability, drug release kinetics, cytotoxicity, cellular uptake, in vivo pharmacokinetics, biodistribution, and antitumor efficacy. The study aims to investigate the surface engineering for chemotherapy drugs, providing new solutions for improving their in vivo delivery.Methods
We systematically evaluated the effects of different PEGylation levels on NPs (WDSPE-mPEG2k/Wprodrug; 0%, 5%, 20%, 40%, 60%, 80%, 100%, 150%, and 200% NPs) incorporated on SN38 prodrug NPs via surface engi
SUBMITTER: Li YQ
PROVIDER: S-EPMC12452009 | biostudies-literature | 2025 Sep
REPOSITORIES: biostudies-literature