Cargando…
Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment
The chemotherapy combined with photothermal therapy has been a favorable approach for the treatment of breast cancer. In present study, nanoparticles with the characteristics of photothermal/matrix metalloproteinase-2 (MMP-2) dual-responsive, tumor targeting, and size-variability were designed for e...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838055/ https://www.ncbi.nlm.nih.gov/pubmed/33532192 http://dx.doi.org/10.1016/j.apsb.2020.08.009 |
_version_ | 1783643086176387072 |
---|---|
author | Chen, Xiaojie Zou, Jiafeng Zhang, Ke Zhu, Jingjing Zhang, Yue Zhu, Zhihong Zheng, Hongyue Li, Fanzhu Piao, Ji-Gang |
author_facet | Chen, Xiaojie Zou, Jiafeng Zhang, Ke Zhu, Jingjing Zhang, Yue Zhu, Zhihong Zheng, Hongyue Li, Fanzhu Piao, Ji-Gang |
author_sort | Chen, Xiaojie |
collection | PubMed |
description | The chemotherapy combined with photothermal therapy has been a favorable approach for the treatment of breast cancer. In present study, nanoparticles with the characteristics of photothermal/matrix metalloproteinase-2 (MMP-2) dual-responsive, tumor targeting, and size-variability were designed for enhancing the antitumor efficacy and achieving “on-demand” drug release markedly. Based on the thermal sensitivity of gelatin, we designed a size-variable gelatin nanoparticle (GNP) to encapsulate indocyanine green (ICG) and doxorubicin (DOX). Under an 808 nm laser irradiation, GNP-DOX/ICG responded photothermally and swelled in size from 71.58 ± 4.28 to 160.80 ± 9.51 nm, which was beneficial for particle retention in the tumor sites and release of the loaded therapeutics. Additionally, GNP-DOX/ICG showed a size reduction of the particles to 33.24 ± 4.11 nm and further improved drug release with the degradation of overexpressed MMP-2 in tumor. In the subsequently performed in vitro experiments, it was confirmed that GNP-DOX/ICG could provide a therapeutic effect that was enhanced and synergistic. Consequently, GNP-DOX/ICG could efficiently suppress the growth of 4T1 tumor in vivo. In conclusion, this study may provide a promising strategy in the rational design of drug delivery nanosystems based on gelatin for chemo-photothermal therapy to achieve synergistically enhanced therapeutic efficacy against breast cancer. |
format | Online Article Text |
id | pubmed-7838055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78380552021-02-01 Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment Chen, Xiaojie Zou, Jiafeng Zhang, Ke Zhu, Jingjing Zhang, Yue Zhu, Zhihong Zheng, Hongyue Li, Fanzhu Piao, Ji-Gang Acta Pharm Sin B Original Article The chemotherapy combined with photothermal therapy has been a favorable approach for the treatment of breast cancer. In present study, nanoparticles with the characteristics of photothermal/matrix metalloproteinase-2 (MMP-2) dual-responsive, tumor targeting, and size-variability were designed for enhancing the antitumor efficacy and achieving “on-demand” drug release markedly. Based on the thermal sensitivity of gelatin, we designed a size-variable gelatin nanoparticle (GNP) to encapsulate indocyanine green (ICG) and doxorubicin (DOX). Under an 808 nm laser irradiation, GNP-DOX/ICG responded photothermally and swelled in size from 71.58 ± 4.28 to 160.80 ± 9.51 nm, which was beneficial for particle retention in the tumor sites and release of the loaded therapeutics. Additionally, GNP-DOX/ICG showed a size reduction of the particles to 33.24 ± 4.11 nm and further improved drug release with the degradation of overexpressed MMP-2 in tumor. In the subsequently performed in vitro experiments, it was confirmed that GNP-DOX/ICG could provide a therapeutic effect that was enhanced and synergistic. Consequently, GNP-DOX/ICG could efficiently suppress the growth of 4T1 tumor in vivo. In conclusion, this study may provide a promising strategy in the rational design of drug delivery nanosystems based on gelatin for chemo-photothermal therapy to achieve synergistically enhanced therapeutic efficacy against breast cancer. Elsevier 2021-01 2020-08-26 /pmc/articles/PMC7838055/ /pubmed/33532192 http://dx.doi.org/10.1016/j.apsb.2020.08.009 Text en © 2021 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Chen, Xiaojie Zou, Jiafeng Zhang, Ke Zhu, Jingjing Zhang, Yue Zhu, Zhihong Zheng, Hongyue Li, Fanzhu Piao, Ji-Gang Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment |
title | Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment |
title_full | Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment |
title_fullStr | Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment |
title_full_unstemmed | Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment |
title_short | Photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment |
title_sort | photothermal/matrix metalloproteinase-2 dual-responsive gelatin nanoparticles for breast cancer treatment |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838055/ https://www.ncbi.nlm.nih.gov/pubmed/33532192 http://dx.doi.org/10.1016/j.apsb.2020.08.009 |
work_keys_str_mv | AT chenxiaojie photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT zoujiafeng photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT zhangke photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT zhujingjing photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT zhangyue photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT zhuzhihong photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT zhenghongyue photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT lifanzhu photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment AT piaojigang photothermalmatrixmetalloproteinase2dualresponsivegelatinnanoparticlesforbreastcancertreatment |