Ligation of anti-cancer drugs to self-assembling ultrashort peptides by click chemistry for localized therapy

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Abstract

Self-assembling ultrashort peptides from aliphatic amino acids were functionalized with platinum anti-cancer drugs by click chemistry. Oxaliplatin-derived hybrid peptide hydrogels with up to 40% drug loading were tested for localized breast cancer therapy. Stably injected gels showed significant tumor growth inhibition in mice and a better tolerance compared to the free platinum drug. © 2014 The Royal Society of Chemistry.

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Reithofer, M. R., Chan, K. H., Lakshmanan, A., Lam, D. H., Mishra, A., Gopalan, B., … Hauser, C. A. E. (2014). Ligation of anti-cancer drugs to self-assembling ultrashort peptides by click chemistry for localized therapy. Chemical Science, 5(2), 625–630. https://doi.org/10.1039/c3sc51930a

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