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https://doi.org/10.1038/ncomms10432
Title: | In vivo covalent cross-linking of photon-converted rare-earth nanostructures for tumour localization and theranostics | Authors: | Ai X. Ho C.J.H. Aw J. Attia A.B.E. Mu J. Wang Y. Wang X. Wang Y. Liu X. Chen H. Gao M. Chen X. Yeow E.K.L. Liu G. Olivo M. Xing B. |
Keywords: | 2 cyanobenzothiazole benzothiazole derivative cathepsin cysteine nanomaterial peptide photosensitizing agent singlet oxygen unclassified drug upconversion nanoparticle lanthanide nanomaterial benzene chemical reaction electron enzyme activity medicine nanoparticle oxygen peptide precision rare earth element tumor animal cell animal experiment animal model animal tissue Article chemical reaction controlled study covalent bond cross linking female human human cell irradiation mouse nonhuman photon protein cleavage theranostic nanomedicine tumor localization tumor microenvironment animal Bagg albino mouse chemistry HT-29 cell line NIH 3T3 cell line nude mouse procedures theranostic nanomedicine Animals Female HT29 Cells Humans Metals, Rare Earth Mice Mice, Inbred BALB C Mice, Nude Nanostructures NIH 3T3 Cells Photons Singlet Oxygen Theranostic Nanomedicine |
Issue Date: | 2016 | Publisher: | Nature Publishing Group | Citation: | Ai X., Ho C.J.H., Aw J., Attia A.B.E., Mu J., Wang Y., Wang X., Wang Y., Liu X., Chen H., Gao M., Chen X., Yeow E.K.L., Liu G., Olivo M., Xing B. (2016). In vivo covalent cross-linking of photon-converted rare-earth nanostructures for tumour localization and theranostics. Nature Communications 7 : 10432. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms10432 | Abstract: | The development of precision nanomedicines to direct nanostructure-based reagents into tumour-targeted areas remains a critical challenge in clinics. Chemical reaction-mediated localization in response to tumour environmental perturbations offers promising opportunities for rational design of effective nano-theranostics. Here, we present a unique microenvironment-sensitive strategy for localization of peptide-premodified upconversion nanocrystals (UCNs) within tumour areas. Upon tumour-specific cathepsin protease reactions, the cleavage of peptides induces covalent cross-linking between the exposed cysteine and 2-cyanobenzothiazole on neighbouring particles, thus triggering the accumulation of UCNs into tumour site. Such enzyme-triggered cross-linking of UCNs leads to enhanced upconversion emission upon 808 nm laser irradiation, and in turn amplifies the singlet oxygen generation from the photosensitizers attached on UCNs. Importantly, this design enables remarkable tumour inhibition through either intratumoral UCNs injection or intravenous injection of nanoparticles modified with the targeting ligand. Our strategy may provide a multimodality solution for effective molecular sensing and site-specific tumour treatment. | Source Title: | Nature Communications | URI: | https://scholarbank.nus.edu.sg/handle/10635/175441 | ISSN: | 20411723 | DOI: | 10.1038/ncomms10432 |
Appears in Collections: | Staff Publications Elements |
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