| Literature DB >> 16602747 |
Benedict Law1, Ralph Weissleder, Ching-Hsuan Tung.
Abstract
Controlled delivery of drugs in response to environments has the potential of targeting therapies and personalized treatments. Here, we described self-assembled peptide sequences that release therapeutic payloads upon specific interaction with disease-associated proteases. The core peptide sequence consists of a protease cleavable region flanked by two self-assembly motifs. In aqueous solution, the peptides self-assemble as a gel scaffold. With treatment of the model preparations with the appropriate protease, the matrix can be degraded in a controlled fashion, where the degradation rate is fine-tuned by varying the peptide compositions. Protease-mediated drug release was demonstrated by enzymatic treatment of a model therapeutic peptide incorporated into the optimized matrix. Our results suggest that this type of material may have far-reaching applications for functionally targeted drug delivery.Mesh:
Substances:
Year: 2006 PMID: 16602747 DOI: 10.1021/bm050920f
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988