作者: Qinmei Li , Lijun Zhu , Ruigang Liu , Da Huang , Xin Jin
DOI: 10.1039/C2JM34136K
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摘要: A novel drug carrier with dual triggerable release properties based on keratin graft poly(ethylene glycol) (keratin-g-PEG) copolymers is reported. Keratin-g-PEG different densities are synthesized through thiol–ene click chemistry. Taking advantage of the amphiphilicity and thiol groups copolymer, nanoparticles stabilized PEG chains as core, bearing glutathione (GSH) cleavable cross-links, fabricated in aqueous solutions. The keratin-g-PEG copolymer can serve excellent carriers for doxorubicin hydrochloride salt (DOX·HCl) a highest loading capacity 18.1% (w/w). loaded DOX sensitive to concentration GSH, especially at GSH cellular level. Trypsin further trigger nanoparticles. In vitro uptake experiments indicate that released from DOX-loaded be internalized into cells efficiently, shows faster nuclei under higher concentrations. have promising applications intracellular delivery cancer therapy.