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Bioresponsive matrices in drug delivery

For years, the field of drug delivery has focused on (1) controlling the release of a therapeutic and (2) targeting the therapeutic to a specific cell type. These research endeavors have concentrated mainly on the development of new degradable polymers and molecule-labeled drug delivery vehicles. Re...

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Detalles Bibliográficos
Autores principales: You, Jin-Oh, Almeda, Dariela, Ye, George JC, Auguste, Debra T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002303/
https://www.ncbi.nlm.nih.gov/pubmed/21114841
http://dx.doi.org/10.1186/1754-1611-4-15
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author You, Jin-Oh
Almeda, Dariela
Ye, George JC
Auguste, Debra T
author_facet You, Jin-Oh
Almeda, Dariela
Ye, George JC
Auguste, Debra T
author_sort You, Jin-Oh
collection PubMed
description For years, the field of drug delivery has focused on (1) controlling the release of a therapeutic and (2) targeting the therapeutic to a specific cell type. These research endeavors have concentrated mainly on the development of new degradable polymers and molecule-labeled drug delivery vehicles. Recent interest in biomaterials that respond to their environment have opened new methods to trigger the release of drugs and localize the therapeutic within a particular site. These novel biomaterials, usually termed "smart" or "intelligent", are able to deliver a therapeutic agent based on either environmental cues or a remote stimulus. Stimuli-responsive materials could potentially elicit a therapeutically effective dose without adverse side effects. Polymers responding to different stimuli, such as pH, light, temperature, ultrasound, magnetism, or biomolecules have been investigated as potential drug delivery vehicles. This review describes the most recent advances in "smart" drug delivery systems that respond to one or multiple stimuli.
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spelling pubmed-30023032010-12-16 Bioresponsive matrices in drug delivery You, Jin-Oh Almeda, Dariela Ye, George JC Auguste, Debra T J Biol Eng Review For years, the field of drug delivery has focused on (1) controlling the release of a therapeutic and (2) targeting the therapeutic to a specific cell type. These research endeavors have concentrated mainly on the development of new degradable polymers and molecule-labeled drug delivery vehicles. Recent interest in biomaterials that respond to their environment have opened new methods to trigger the release of drugs and localize the therapeutic within a particular site. These novel biomaterials, usually termed "smart" or "intelligent", are able to deliver a therapeutic agent based on either environmental cues or a remote stimulus. Stimuli-responsive materials could potentially elicit a therapeutically effective dose without adverse side effects. Polymers responding to different stimuli, such as pH, light, temperature, ultrasound, magnetism, or biomolecules have been investigated as potential drug delivery vehicles. This review describes the most recent advances in "smart" drug delivery systems that respond to one or multiple stimuli. BioMed Central 2010-11-29 /pmc/articles/PMC3002303/ /pubmed/21114841 http://dx.doi.org/10.1186/1754-1611-4-15 Text en Copyright ©2010 You et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
You, Jin-Oh
Almeda, Dariela
Ye, George JC
Auguste, Debra T
Bioresponsive matrices in drug delivery
title Bioresponsive matrices in drug delivery
title_full Bioresponsive matrices in drug delivery
title_fullStr Bioresponsive matrices in drug delivery
title_full_unstemmed Bioresponsive matrices in drug delivery
title_short Bioresponsive matrices in drug delivery
title_sort bioresponsive matrices in drug delivery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002303/
https://www.ncbi.nlm.nih.gov/pubmed/21114841
http://dx.doi.org/10.1186/1754-1611-4-15
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