文摘
Controlled delivery of drugs in response to environments has the potential of targeting therapies and personalizedtreatments. Here, we described self-assembled peptide sequences that release therapeutic payloads upon specificinteraction with disease-associated proteases. The core peptide sequence consists of a protease cleavable regionflanked by two self-assembly motifs. In aqueous solution, the peptides self-assemble as a gel scaffold. Withtreatment of the model preparations with the appropriate protease, the matrix can be degraded in a controlledfashion, where the degradation rate is fine-tuned by varying the peptide compositions. Protease-mediated drugrelease was demonstrated by enzymatic treatment of a model therapeutic peptide incorporated into the optimizedmatrix. Our results suggest that this type of material may have far-reaching applications for functionally targeteddrug delivery.