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Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications
Recently, photothermal therapy has become a promising strategy in tumor treatment. However, the therapeutic effect was seriously hampered by the low tissue penetration of laser. Therefore, in this study, radiofrequency (RF) with better tissue penetration was used for tumor hyperthermia. First, one t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399988/ https://www.ncbi.nlm.nih.gov/pubmed/28450782 http://dx.doi.org/10.2147/IJN.S128844 |
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author | Wang, Lei Li, Dong Hao, Yongwei Niu, Mengya Hu, Yujie Zhao, Hongjuan Chang, Junbiao Zhang, Zhenzhong Zhang, Yun |
author_facet | Wang, Lei Li, Dong Hao, Yongwei Niu, Mengya Hu, Yujie Zhao, Hongjuan Chang, Junbiao Zhang, Zhenzhong Zhang, Yun |
author_sort | Wang, Lei |
collection | PubMed |
description | Recently, photothermal therapy has become a promising strategy in tumor treatment. However, the therapeutic effect was seriously hampered by the low tissue penetration of laser. Therefore, in this study, radiofrequency (RF) with better tissue penetration was used for tumor hyperthermia. First, one type of gold nanorods (AuNRs) suitable for RF hyperthermia was selected. Then, poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) loaded with AuNRs and docetaxel (DTX) (PLGA/AuNR/DTX) NPs were constructed. Finally, manganese dioxide (MnO(2)) ultrathin nanofilms were coated on the surfaces of PLGA/AuNR/DTX NPs by the reduction of KMnO(4) to construct the PLGA/AuNR/DTX@MnO(2) drug delivery system. This drug delivery system can not only be used for the combined therapy of chemotherapy and RF hyperthermia but can also produce Mn(2+) to enable magnetic resonance imaging. Furthermore, the RF hyperthermia and the degradation of MnO(2) can significantly promote the controlled drug release in a tumor region. The in vitro and in vivo results suggested that the PLGA/AuNR/DTX@MnO(2) multifunctional drug delivery system is a promising nanoplatform for effective cancer theranostic applications. |
format | Online Article Text |
id | pubmed-5399988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53999882017-04-27 Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications Wang, Lei Li, Dong Hao, Yongwei Niu, Mengya Hu, Yujie Zhao, Hongjuan Chang, Junbiao Zhang, Zhenzhong Zhang, Yun Int J Nanomedicine Original Research Recently, photothermal therapy has become a promising strategy in tumor treatment. However, the therapeutic effect was seriously hampered by the low tissue penetration of laser. Therefore, in this study, radiofrequency (RF) with better tissue penetration was used for tumor hyperthermia. First, one type of gold nanorods (AuNRs) suitable for RF hyperthermia was selected. Then, poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) loaded with AuNRs and docetaxel (DTX) (PLGA/AuNR/DTX) NPs were constructed. Finally, manganese dioxide (MnO(2)) ultrathin nanofilms were coated on the surfaces of PLGA/AuNR/DTX NPs by the reduction of KMnO(4) to construct the PLGA/AuNR/DTX@MnO(2) drug delivery system. This drug delivery system can not only be used for the combined therapy of chemotherapy and RF hyperthermia but can also produce Mn(2+) to enable magnetic resonance imaging. Furthermore, the RF hyperthermia and the degradation of MnO(2) can significantly promote the controlled drug release in a tumor region. The in vitro and in vivo results suggested that the PLGA/AuNR/DTX@MnO(2) multifunctional drug delivery system is a promising nanoplatform for effective cancer theranostic applications. Dove Medical Press 2017-04-13 /pmc/articles/PMC5399988/ /pubmed/28450782 http://dx.doi.org/10.2147/IJN.S128844 Text en © 2017 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wang, Lei Li, Dong Hao, Yongwei Niu, Mengya Hu, Yujie Zhao, Hongjuan Chang, Junbiao Zhang, Zhenzhong Zhang, Yun Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications |
title | Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications |
title_full | Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications |
title_fullStr | Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications |
title_full_unstemmed | Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications |
title_short | Gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications |
title_sort | gold nanorod–based poly(lactic-co-glycolic acid) with manganese dioxide core–shell structured multifunctional nanoplatform for cancer theranostic applications |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399988/ https://www.ncbi.nlm.nih.gov/pubmed/28450782 http://dx.doi.org/10.2147/IJN.S128844 |
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