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Bioorthogonal Uncaging of Cytotoxic Paclitaxel through Pd Nanosheet–Hydrogel Frameworks
[Image: see text] The promising potential of bioorthogonal catalysis in biomedicine is inspiring incremental efforts to design strategies that regulate drug activity in living systems. To achieve this, it is not only essential to develop customized inactive prodrugs and biocompatible metal catalysts...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497487/ https://www.ncbi.nlm.nih.gov/pubmed/32787091 http://dx.doi.org/10.1021/acs.jmedchem.0c00781 |
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author | Pérez-López, Ana M. Rubio-Ruiz, Belén Valero, Teresa Contreras-Montoya, Rafael Álvarez de Cienfuegos, Luis Sebastián, Víctor Santamaría, Jesús Unciti-Broceta, Asier |
author_facet | Pérez-López, Ana M. Rubio-Ruiz, Belén Valero, Teresa Contreras-Montoya, Rafael Álvarez de Cienfuegos, Luis Sebastián, Víctor Santamaría, Jesús Unciti-Broceta, Asier |
author_sort | Pérez-López, Ana M. |
collection | PubMed |
description | [Image: see text] The promising potential of bioorthogonal catalysis in biomedicine is inspiring incremental efforts to design strategies that regulate drug activity in living systems. To achieve this, it is not only essential to develop customized inactive prodrugs and biocompatible metal catalysts but also the right physical environment for them to interact and enable drug production under spatial and/or temporal control. Toward this goal, here, we report the first inactive precursor of the potent broad-spectrum anticancer drug paclitaxel (a.k.a. Taxol) that is stable in cell culture and labile to Pd catalysts. This new prodrug is effectively uncaged in cancer cell culture by Pd nanosheets captured within agarose and alginate hydrogels, providing a biodegradable catalytic framework to achieve controlled release of one of the most important chemotherapy drugs in medical practice. The compatibility of bioorthogonal catalysis and physical hydrogels opens up new opportunities to administer and modulate the mobility of transition metal catalysts in living environs. |
format | Online Article Text |
id | pubmed-7497487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74974872020-09-18 Bioorthogonal Uncaging of Cytotoxic Paclitaxel through Pd Nanosheet–Hydrogel Frameworks Pérez-López, Ana M. Rubio-Ruiz, Belén Valero, Teresa Contreras-Montoya, Rafael Álvarez de Cienfuegos, Luis Sebastián, Víctor Santamaría, Jesús Unciti-Broceta, Asier J Med Chem [Image: see text] The promising potential of bioorthogonal catalysis in biomedicine is inspiring incremental efforts to design strategies that regulate drug activity in living systems. To achieve this, it is not only essential to develop customized inactive prodrugs and biocompatible metal catalysts but also the right physical environment for them to interact and enable drug production under spatial and/or temporal control. Toward this goal, here, we report the first inactive precursor of the potent broad-spectrum anticancer drug paclitaxel (a.k.a. Taxol) that is stable in cell culture and labile to Pd catalysts. This new prodrug is effectively uncaged in cancer cell culture by Pd nanosheets captured within agarose and alginate hydrogels, providing a biodegradable catalytic framework to achieve controlled release of one of the most important chemotherapy drugs in medical practice. The compatibility of bioorthogonal catalysis and physical hydrogels opens up new opportunities to administer and modulate the mobility of transition metal catalysts in living environs. American Chemical Society 2020-08-05 2020-09-10 /pmc/articles/PMC7497487/ /pubmed/32787091 http://dx.doi.org/10.1021/acs.jmedchem.0c00781 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Pérez-López, Ana M. Rubio-Ruiz, Belén Valero, Teresa Contreras-Montoya, Rafael Álvarez de Cienfuegos, Luis Sebastián, Víctor Santamaría, Jesús Unciti-Broceta, Asier Bioorthogonal Uncaging of Cytotoxic Paclitaxel through Pd Nanosheet–Hydrogel Frameworks |
title | Bioorthogonal Uncaging
of Cytotoxic Paclitaxel through
Pd Nanosheet–Hydrogel Frameworks |
title_full | Bioorthogonal Uncaging
of Cytotoxic Paclitaxel through
Pd Nanosheet–Hydrogel Frameworks |
title_fullStr | Bioorthogonal Uncaging
of Cytotoxic Paclitaxel through
Pd Nanosheet–Hydrogel Frameworks |
title_full_unstemmed | Bioorthogonal Uncaging
of Cytotoxic Paclitaxel through
Pd Nanosheet–Hydrogel Frameworks |
title_short | Bioorthogonal Uncaging
of Cytotoxic Paclitaxel through
Pd Nanosheet–Hydrogel Frameworks |
title_sort | bioorthogonal uncaging
of cytotoxic paclitaxel through
pd nanosheet–hydrogel frameworks |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497487/ https://www.ncbi.nlm.nih.gov/pubmed/32787091 http://dx.doi.org/10.1021/acs.jmedchem.0c00781 |
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