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Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors
The integration of photothermal therapy and chemotherapy has been recognized to be an efficient strategy through the instant thermally ablation and long-term chemical inhibition, thus achieving high therapeutical effect. In the present work, we designed and prepared Cu(7)S(4)@SiO(2)/DOX nanocomposit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522791/ https://www.ncbi.nlm.nih.gov/pubmed/33042978 http://dx.doi.org/10.3389/fbioe.2020.579439 |
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author | Zhang, Leilei Pan, Hui Li, Yongyun Li, Fang Huang, Xiaolin |
author_facet | Zhang, Leilei Pan, Hui Li, Yongyun Li, Fang Huang, Xiaolin |
author_sort | Zhang, Leilei |
collection | PubMed |
description | The integration of photothermal therapy and chemotherapy has been recognized to be an efficient strategy through the instant thermally ablation and long-term chemical inhibition, thus achieving high therapeutical effect. In the present work, we designed and prepared Cu(7)S(4)@SiO(2)/DOX nanocomposites and used them as efficient nanoplatforms for synergistic photothermal-chemo therapy on melanoma tumors. The Cu(7)S(4)@SiO(2)/DOX was constructed by firstly synthesizing Cu(7)S(4) nanocrystals, then in situ growing SiO(2) shell on the surface of Cu(7)S(4) nanocrystals, and finally loading DOX within SiO(2) shell. The Cu(7)S(4)@SiO(2)/DOX was composed of Cu(7)S(4) core as the photothermal transducer, SiO(2) shell as DOX carrier and DOX as the model of anticancer drug. Once exposed to a 1064 nm laser, the Cu(7)S(4)@SiO(2)/DOX could simultaneous generate heat for photothermal therapy and accelerate the DOX release. When the Cu(7)S(4)@SiO(2)/DOX was injected into the center of tumor, the tumor exhibit rapid temperature elevation once exposed to the NIR laser and the tumor growth is significantly inhibited through the synergistic photothermal-chemo therapy, in comparison to the limited therapeutical effect of photothermal therapy or chemotherapy alone. Therefore, the Cu(7)S(4)@SiO(2)/DOX with photothermal-chemo function can be used as excellent nanoplatforms for treating solid tumor with high theoretical effect. |
format | Online Article Text |
id | pubmed-7522791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75227912020-10-09 Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors Zhang, Leilei Pan, Hui Li, Yongyun Li, Fang Huang, Xiaolin Front Bioeng Biotechnol Bioengineering and Biotechnology The integration of photothermal therapy and chemotherapy has been recognized to be an efficient strategy through the instant thermally ablation and long-term chemical inhibition, thus achieving high therapeutical effect. In the present work, we designed and prepared Cu(7)S(4)@SiO(2)/DOX nanocomposites and used them as efficient nanoplatforms for synergistic photothermal-chemo therapy on melanoma tumors. The Cu(7)S(4)@SiO(2)/DOX was constructed by firstly synthesizing Cu(7)S(4) nanocrystals, then in situ growing SiO(2) shell on the surface of Cu(7)S(4) nanocrystals, and finally loading DOX within SiO(2) shell. The Cu(7)S(4)@SiO(2)/DOX was composed of Cu(7)S(4) core as the photothermal transducer, SiO(2) shell as DOX carrier and DOX as the model of anticancer drug. Once exposed to a 1064 nm laser, the Cu(7)S(4)@SiO(2)/DOX could simultaneous generate heat for photothermal therapy and accelerate the DOX release. When the Cu(7)S(4)@SiO(2)/DOX was injected into the center of tumor, the tumor exhibit rapid temperature elevation once exposed to the NIR laser and the tumor growth is significantly inhibited through the synergistic photothermal-chemo therapy, in comparison to the limited therapeutical effect of photothermal therapy or chemotherapy alone. Therefore, the Cu(7)S(4)@SiO(2)/DOX with photothermal-chemo function can be used as excellent nanoplatforms for treating solid tumor with high theoretical effect. Frontiers Media S.A. 2020-09-15 /pmc/articles/PMC7522791/ /pubmed/33042978 http://dx.doi.org/10.3389/fbioe.2020.579439 Text en Copyright © 2020 Zhang, Pan, Li, Li and Huang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Zhang, Leilei Pan, Hui Li, Yongyun Li, Fang Huang, Xiaolin Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors |
title | Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors |
title_full | Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors |
title_fullStr | Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors |
title_full_unstemmed | Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors |
title_short | Constructing Cu(7)S(4)@SiO(2)/DOX Multifunctional Nanoplatforms for Synergistic Photothermal–Chemotherapy on Melanoma Tumors |
title_sort | constructing cu(7)s(4)@sio(2)/dox multifunctional nanoplatforms for synergistic photothermal–chemotherapy on melanoma tumors |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522791/ https://www.ncbi.nlm.nih.gov/pubmed/33042978 http://dx.doi.org/10.3389/fbioe.2020.579439 |
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