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In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma

[Image: see text] The ability to activate drugs only at desired locations avoiding systemic immunosuppression and other dose limiting toxicities is highly desirable. Here we present a new approach, named local drug activation, that uses bioorthogonal chemistry to concentrate and activate systemic sm...

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Autores principales: Mejia Oneto, Jose M., Khan, Irfan, Seebald, Leah, Royzen, Maksim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965853/
https://www.ncbi.nlm.nih.gov/pubmed/27504494
http://dx.doi.org/10.1021/acscentsci.6b00150
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author Mejia Oneto, Jose M.
Khan, Irfan
Seebald, Leah
Royzen, Maksim
author_facet Mejia Oneto, Jose M.
Khan, Irfan
Seebald, Leah
Royzen, Maksim
author_sort Mejia Oneto, Jose M.
collection PubMed
description [Image: see text] The ability to activate drugs only at desired locations avoiding systemic immunosuppression and other dose limiting toxicities is highly desirable. Here we present a new approach, named local drug activation, that uses bioorthogonal chemistry to concentrate and activate systemic small molecules at a location of choice. This method is independent of endogenous cellular or environmental markers and only depends on the presence of a preimplanted biomaterial near a desired site (e.g., tumor). We demonstrate the clear therapeutic benefit with minimal side effects of this approach in mice over systemic therapy using a doxorubicin pro-drug against xenograft tumors of a type of soft tissue sarcoma (HT1080).
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spelling pubmed-49658532016-08-08 In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma Mejia Oneto, Jose M. Khan, Irfan Seebald, Leah Royzen, Maksim ACS Cent Sci [Image: see text] The ability to activate drugs only at desired locations avoiding systemic immunosuppression and other dose limiting toxicities is highly desirable. Here we present a new approach, named local drug activation, that uses bioorthogonal chemistry to concentrate and activate systemic small molecules at a location of choice. This method is independent of endogenous cellular or environmental markers and only depends on the presence of a preimplanted biomaterial near a desired site (e.g., tumor). We demonstrate the clear therapeutic benefit with minimal side effects of this approach in mice over systemic therapy using a doxorubicin pro-drug against xenograft tumors of a type of soft tissue sarcoma (HT1080). American Chemical Society 2016-07-13 2016-07-27 /pmc/articles/PMC4965853/ /pubmed/27504494 http://dx.doi.org/10.1021/acscentsci.6b00150 Text en Copyright © 2016 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 Mejia Oneto, Jose M.
Khan, Irfan
Seebald, Leah
Royzen, Maksim
In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
title In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
title_full In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
title_fullStr In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
title_full_unstemmed In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
title_short In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
title_sort in vivo bioorthogonal chemistry enables local hydrogel and systemic pro-drug to treat soft tissue sarcoma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965853/
https://www.ncbi.nlm.nih.gov/pubmed/27504494
http://dx.doi.org/10.1021/acscentsci.6b00150
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