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Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics

Background: Multifunctional nanoplatforms with diagnostic-imaging and targeted therapeutic functionality (theranostics) are of great interest in the field of precision nanomedicine. The emerging sonodynamic therapy (SDT) combined with sonosensitizers under the guidance of photoacoustic (PA) imaging...

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Autores principales: Huang, Ju, Liu, Fengqiu, Han, Xiaoxia, Zhang, Liang, Hu, Zhongqian, Jiang, Qinqin, Wang, Zhigang, Ran, Haitao, Wang, Dong, Li, Pan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299698/
https://www.ncbi.nlm.nih.gov/pubmed/30613291
http://dx.doi.org/10.7150/thno.29569
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author Huang, Ju
Liu, Fengqiu
Han, Xiaoxia
Zhang, Liang
Hu, Zhongqian
Jiang, Qinqin
Wang, Zhigang
Ran, Haitao
Wang, Dong
Li, Pan
author_facet Huang, Ju
Liu, Fengqiu
Han, Xiaoxia
Zhang, Liang
Hu, Zhongqian
Jiang, Qinqin
Wang, Zhigang
Ran, Haitao
Wang, Dong
Li, Pan
author_sort Huang, Ju
collection PubMed
description Background: Multifunctional nanoplatforms with diagnostic-imaging and targeted therapeutic functionality (theranostics) are of great interest in the field of precision nanomedicine. The emerging sonodynamic therapy (SDT) combined with sonosensitizers under the guidance of photoacoustic (PA) imaging is highly expected to accurately eliminate cancer cells/tissue. Methods: Unique core/shell-structured theranostic FA-HMME-MNPs-PLGA nanoparticles (FHMP NPs, FA: folate, HMME: hematoporphyrin monomethyl ether, MNPs: melanin nanoparticles, PLGA: poly (lactic-co-glycolic) acid) were constructed by the integration of MNPs (for PA imaging) in the core and HMME in the shell for enhanced PA imaging-guided SDT, which were further functionalized with a tumor-targeting ligand, FA. The PA imaging-guided SDT was systematically and successfully demonstrated both in vitro and in vivo. The high biosafety of FHMP NPs was also systematically evaluated. Results: The synthesized FHMP NPs with a broad optical absorption not only possess high PA-imaging contrast enhancement capability but also exhibit significant SDT efficiency. Importantly, such a PLGA based nanoplatform improved light stability of HMME, enhancing sonodynamic performance and facilitated delivery of MNPs to the tumor region. Meanwhile, a combined effect between HMME and MNPs was discovered and verified. Furthermore, a sonosensitizer assisted by ultrasound irradiation engenders reactive oxygen species (ROS)-mediated cytotoxicity toward tumor cells/tissue. Both in vitro cell-level and systematic in vivo xenograft evaluations on tumor-bearing mice demonstrated that the selective killing effect of ROS on tumor cells was assisted by FHMP NPs, which played an active role in the suppression of tumor growth with high biosafety. Conclusion: A theranostic nanoplatform was successfully constructed, achieving PA imaging-guided SDT against breast cancer cells/tissue. More importantly, MNPs and HMME in one platform with combined effect for enhancing PA imaging was demonstrated. This unique theranostic nanoplatform with multiple capabilities paves a new way toward personalized medicine by rational utilization.
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spelling pubmed-62996982019-01-04 Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics Huang, Ju Liu, Fengqiu Han, Xiaoxia Zhang, Liang Hu, Zhongqian Jiang, Qinqin Wang, Zhigang Ran, Haitao Wang, Dong Li, Pan Theranostics Research Paper Background: Multifunctional nanoplatforms with diagnostic-imaging and targeted therapeutic functionality (theranostics) are of great interest in the field of precision nanomedicine. The emerging sonodynamic therapy (SDT) combined with sonosensitizers under the guidance of photoacoustic (PA) imaging is highly expected to accurately eliminate cancer cells/tissue. Methods: Unique core/shell-structured theranostic FA-HMME-MNPs-PLGA nanoparticles (FHMP NPs, FA: folate, HMME: hematoporphyrin monomethyl ether, MNPs: melanin nanoparticles, PLGA: poly (lactic-co-glycolic) acid) were constructed by the integration of MNPs (for PA imaging) in the core and HMME in the shell for enhanced PA imaging-guided SDT, which were further functionalized with a tumor-targeting ligand, FA. The PA imaging-guided SDT was systematically and successfully demonstrated both in vitro and in vivo. The high biosafety of FHMP NPs was also systematically evaluated. Results: The synthesized FHMP NPs with a broad optical absorption not only possess high PA-imaging contrast enhancement capability but also exhibit significant SDT efficiency. Importantly, such a PLGA based nanoplatform improved light stability of HMME, enhancing sonodynamic performance and facilitated delivery of MNPs to the tumor region. Meanwhile, a combined effect between HMME and MNPs was discovered and verified. Furthermore, a sonosensitizer assisted by ultrasound irradiation engenders reactive oxygen species (ROS)-mediated cytotoxicity toward tumor cells/tissue. Both in vitro cell-level and systematic in vivo xenograft evaluations on tumor-bearing mice demonstrated that the selective killing effect of ROS on tumor cells was assisted by FHMP NPs, which played an active role in the suppression of tumor growth with high biosafety. Conclusion: A theranostic nanoplatform was successfully constructed, achieving PA imaging-guided SDT against breast cancer cells/tissue. More importantly, MNPs and HMME in one platform with combined effect for enhancing PA imaging was demonstrated. This unique theranostic nanoplatform with multiple capabilities paves a new way toward personalized medicine by rational utilization. Ivyspring International Publisher 2018-11-29 /pmc/articles/PMC6299698/ /pubmed/30613291 http://dx.doi.org/10.7150/thno.29569 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Huang, Ju
Liu, Fengqiu
Han, Xiaoxia
Zhang, Liang
Hu, Zhongqian
Jiang, Qinqin
Wang, Zhigang
Ran, Haitao
Wang, Dong
Li, Pan
Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics
title Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics
title_full Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics
title_fullStr Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics
title_full_unstemmed Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics
title_short Nanosonosensitizers for Highly Efficient Sonodynamic Cancer Theranostics
title_sort nanosonosensitizers for highly efficient sonodynamic cancer theranostics
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299698/
https://www.ncbi.nlm.nih.gov/pubmed/30613291
http://dx.doi.org/10.7150/thno.29569
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