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Photo cleavable thioacetal block copolymers for controlled release
We present a new light cleavable polymer containing o-nitrobenzene thioacetal groups in the main chain. By conjugation to a PEG block, we synthesized block copolymers capable of forming nanoparticles in aqueous solution. We studied drug encapsulation and release using the model drug Nile Red. Irradi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240465/ https://www.ncbi.nlm.nih.gov/pubmed/34262625 http://dx.doi.org/10.1039/d1py00514f |
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author | Men, Yongjun Brevé, Tobias G. Liu, Huanhuan Denkova, Antonia G. Eelkema, Rienk |
author_facet | Men, Yongjun Brevé, Tobias G. Liu, Huanhuan Denkova, Antonia G. Eelkema, Rienk |
author_sort | Men, Yongjun |
collection | PubMed |
description | We present a new light cleavable polymer containing o-nitrobenzene thioacetal groups in the main chain. By conjugation to a PEG block, we synthesized block copolymers capable of forming nanoparticles in aqueous solution. We studied drug encapsulation and release using the model drug Nile Red. Irradiation with UV-A light (365 nm) leads to efficient degradation of the polymers and associated burst release of the payload. Unlike other thioacetal and thioketal polymers, these polymers are stable to reactive oxygen species (ROS), preventing non-triggered release. Moreover, the nanocarriers showed low cytotoxicity in cell viability experiments. |
format | Online Article Text |
id | pubmed-8240465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-82404652021-07-12 Photo cleavable thioacetal block copolymers for controlled release Men, Yongjun Brevé, Tobias G. Liu, Huanhuan Denkova, Antonia G. Eelkema, Rienk Polym Chem Chemistry We present a new light cleavable polymer containing o-nitrobenzene thioacetal groups in the main chain. By conjugation to a PEG block, we synthesized block copolymers capable of forming nanoparticles in aqueous solution. We studied drug encapsulation and release using the model drug Nile Red. Irradiation with UV-A light (365 nm) leads to efficient degradation of the polymers and associated burst release of the payload. Unlike other thioacetal and thioketal polymers, these polymers are stable to reactive oxygen species (ROS), preventing non-triggered release. Moreover, the nanocarriers showed low cytotoxicity in cell viability experiments. The Royal Society of Chemistry 2021-06-08 /pmc/articles/PMC8240465/ /pubmed/34262625 http://dx.doi.org/10.1039/d1py00514f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Men, Yongjun Brevé, Tobias G. Liu, Huanhuan Denkova, Antonia G. Eelkema, Rienk Photo cleavable thioacetal block copolymers for controlled release |
title | Photo cleavable thioacetal block copolymers for controlled release |
title_full | Photo cleavable thioacetal block copolymers for controlled release |
title_fullStr | Photo cleavable thioacetal block copolymers for controlled release |
title_full_unstemmed | Photo cleavable thioacetal block copolymers for controlled release |
title_short | Photo cleavable thioacetal block copolymers for controlled release |
title_sort | photo cleavable thioacetal block copolymers for controlled release |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240465/ https://www.ncbi.nlm.nih.gov/pubmed/34262625 http://dx.doi.org/10.1039/d1py00514f |
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