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Protease-Sensitive Nanomaterials for Cancer Therapeutics and Imaging
[Image: see text] Many diseases can be characterized by the abnormal activity exhibited by various biomolecules, the targeting of which can provide therapeutic and diagnostic utility. Recent trends in medicine and nanotechnology have prompted the development of protease-sensitive nanomaterials syste...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445504/ https://www.ncbi.nlm.nih.gov/pubmed/28572701 http://dx.doi.org/10.1021/acs.iecr.7b00990 |
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author | Anderson, Caleb F. Cui, Honggang |
author_facet | Anderson, Caleb F. Cui, Honggang |
author_sort | Anderson, Caleb F. |
collection | PubMed |
description | [Image: see text] Many diseases can be characterized by the abnormal activity exhibited by various biomolecules, the targeting of which can provide therapeutic and diagnostic utility. Recent trends in medicine and nanotechnology have prompted the development of protease-sensitive nanomaterials systems for therapeutic, diagnostic, and theranostic applications. These systems can act specifically in response to the target enzyme and its associated disease conditions, thus enabling personalized treatment and improved prognosis. In this Review, we discuss recent advancements in the development of protease-responsive materials for imaging and drug delivery and analyze several representative systems to illustrate their key design principles. |
format | Online Article Text |
id | pubmed-5445504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-54455042017-05-30 Protease-Sensitive Nanomaterials for Cancer Therapeutics and Imaging Anderson, Caleb F. Cui, Honggang Ind Eng Chem Res [Image: see text] Many diseases can be characterized by the abnormal activity exhibited by various biomolecules, the targeting of which can provide therapeutic and diagnostic utility. Recent trends in medicine and nanotechnology have prompted the development of protease-sensitive nanomaterials systems for therapeutic, diagnostic, and theranostic applications. These systems can act specifically in response to the target enzyme and its associated disease conditions, thus enabling personalized treatment and improved prognosis. In this Review, we discuss recent advancements in the development of protease-responsive materials for imaging and drug delivery and analyze several representative systems to illustrate their key design principles. American Chemical Society 2017-04-24 2017-05-24 /pmc/articles/PMC5445504/ /pubmed/28572701 http://dx.doi.org/10.1021/acs.iecr.7b00990 Text en Copyright © 2017 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 | Anderson, Caleb F. Cui, Honggang Protease-Sensitive Nanomaterials for Cancer Therapeutics and Imaging |
title | Protease-Sensitive Nanomaterials for Cancer Therapeutics
and Imaging |
title_full | Protease-Sensitive Nanomaterials for Cancer Therapeutics
and Imaging |
title_fullStr | Protease-Sensitive Nanomaterials for Cancer Therapeutics
and Imaging |
title_full_unstemmed | Protease-Sensitive Nanomaterials for Cancer Therapeutics
and Imaging |
title_short | Protease-Sensitive Nanomaterials for Cancer Therapeutics
and Imaging |
title_sort | protease-sensitive nanomaterials for cancer therapeutics
and imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445504/ https://www.ncbi.nlm.nih.gov/pubmed/28572701 http://dx.doi.org/10.1021/acs.iecr.7b00990 |
work_keys_str_mv | AT andersoncalebf proteasesensitivenanomaterialsforcancertherapeuticsandimaging AT cuihonggang proteasesensitivenanomaterialsforcancertherapeuticsandimaging |