Abstract
The success of nanoparticle-based cancer therapies ultimately depends on their ability to selectively and efficiently accumulate in regions of disease. Outfitting nanoparticles to actively target tumor-specific markers has improved specificity, yet it remains a challenge to amass adequate therapy in a selective manner. To help address this challenge, we have developed a mechanism of nanoparticle amplification based on stigmergic (environment-modifying) signalling, in which a "Signalling" population of gold nanorods induces localized unveiling of cryptic collagen epitopes, which are in turn targeted by "Responding" nanoparticles bearing gelatin-binding fibronectin fragments. We demonstrate that this two-particle system results in significantly increased, selective recruitment of responding particles. Such amplification strategies have the potential to overcome limitations associated with single-particle targeting by leveraging the capacity of nanoparticles to interact with their environment to create abundant new binding motifs. © The Royal Society of Chemistry 2013.
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CITATION STYLE
Lo, J. H., Von Maltzahn, G., Douglass, J., Park, J. H., Sailor, M. J., Ruoslahti, E., & Bhatia, S. N. (2013). Nanoparticle amplification via photothermal unveiling of cryptic collagen binding sites. Journal of Materials Chemistry B, 1(39), 5235–5240. https://doi.org/10.1039/c3tb20619j
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