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The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer

Compared to conventional cancer treatment, combination therapy based on well-designed nanoscale platforms may offer an opportunity to eliminate tumors and reduce recurrence and metastasis. In this study, we prepared multifunctional microspheres loading (131)I-labeled hollow copper sulfide nanopartic...

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Autores principales: Liu, Qiufang, Qian, Yuyi, Li, Panli, Zhang, Sihang, Wang, Zerong, Liu, Jianjun, Sun, Xiaoguang, Fulham, Michael, Feng, Dagan, Chen, Zhigang, Song, Shaoli, Lu, Wei, Huang, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990345/
https://www.ncbi.nlm.nih.gov/pubmed/29881676
http://dx.doi.org/10.1016/j.apsb.2018.04.001
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author Liu, Qiufang
Qian, Yuyi
Li, Panli
Zhang, Sihang
Wang, Zerong
Liu, Jianjun
Sun, Xiaoguang
Fulham, Michael
Feng, Dagan
Chen, Zhigang
Song, Shaoli
Lu, Wei
Huang, Gang
author_facet Liu, Qiufang
Qian, Yuyi
Li, Panli
Zhang, Sihang
Wang, Zerong
Liu, Jianjun
Sun, Xiaoguang
Fulham, Michael
Feng, Dagan
Chen, Zhigang
Song, Shaoli
Lu, Wei
Huang, Gang
author_sort Liu, Qiufang
collection PubMed
description Compared to conventional cancer treatment, combination therapy based on well-designed nanoscale platforms may offer an opportunity to eliminate tumors and reduce recurrence and metastasis. In this study, we prepared multifunctional microspheres loading (131)I-labeled hollow copper sulfide nanoparticles and paclitaxel ((131)I-HCuSNPs-MS-PTX) for imaging and therapeutics of W256/B breast tumors in rats. (18)F-fluordeoxyglucose ((18)F-FDG) positron emission tomography/computed tomography (PET/CT) imaging detected that the expansion of the tumor volume was delayed (P<0.05) following intra-tumoral (i.t.) injection with (131)I-HCuSNPs-MS-PTX plus near-infrared (NIR) irradiation. The immunohistochemical analysis further confirmed the anti-tumor effect. The single photon emission computed tomography (SPECT)/photoacoustic imaging mediated by (131)I-HCuSNPs-MS-PTX demonstrated that microspheres were mainly distributed in the tumors with a relatively low distribution in other organs. Our results revealed that (131)I-HCuSNPs-MS-PTX offered combined photothermal, chemo- and radio-therapies, eliminating tumors at a relatively low dose, as well as allowing SPECT/CT and photoacoustic imaging monitoring of distribution of the injected agents non-invasively. The copper sulfide-loaded microspheres, (131)I-HCuSNPs-MS-PTX, can serve as a versatile theranostic agent in an orthotopic breast cancer model.
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spelling pubmed-59903452018-06-07 The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer Liu, Qiufang Qian, Yuyi Li, Panli Zhang, Sihang Wang, Zerong Liu, Jianjun Sun, Xiaoguang Fulham, Michael Feng, Dagan Chen, Zhigang Song, Shaoli Lu, Wei Huang, Gang Acta Pharm Sin B Original Article Compared to conventional cancer treatment, combination therapy based on well-designed nanoscale platforms may offer an opportunity to eliminate tumors and reduce recurrence and metastasis. In this study, we prepared multifunctional microspheres loading (131)I-labeled hollow copper sulfide nanoparticles and paclitaxel ((131)I-HCuSNPs-MS-PTX) for imaging and therapeutics of W256/B breast tumors in rats. (18)F-fluordeoxyglucose ((18)F-FDG) positron emission tomography/computed tomography (PET/CT) imaging detected that the expansion of the tumor volume was delayed (P<0.05) following intra-tumoral (i.t.) injection with (131)I-HCuSNPs-MS-PTX plus near-infrared (NIR) irradiation. The immunohistochemical analysis further confirmed the anti-tumor effect. The single photon emission computed tomography (SPECT)/photoacoustic imaging mediated by (131)I-HCuSNPs-MS-PTX demonstrated that microspheres were mainly distributed in the tumors with a relatively low distribution in other organs. Our results revealed that (131)I-HCuSNPs-MS-PTX offered combined photothermal, chemo- and radio-therapies, eliminating tumors at a relatively low dose, as well as allowing SPECT/CT and photoacoustic imaging monitoring of distribution of the injected agents non-invasively. The copper sulfide-loaded microspheres, (131)I-HCuSNPs-MS-PTX, can serve as a versatile theranostic agent in an orthotopic breast cancer model. Elsevier 2018-05 2018-04-07 /pmc/articles/PMC5990345/ /pubmed/29881676 http://dx.doi.org/10.1016/j.apsb.2018.04.001 Text en © 2018 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
Liu, Qiufang
Qian, Yuyi
Li, Panli
Zhang, Sihang
Wang, Zerong
Liu, Jianjun
Sun, Xiaoguang
Fulham, Michael
Feng, Dagan
Chen, Zhigang
Song, Shaoli
Lu, Wei
Huang, Gang
The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer
title The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer
title_full The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer
title_fullStr The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer
title_full_unstemmed The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer
title_short The combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer
title_sort combined therapeutic effects of (131)iodine-labeled multifunctional copper sulfide-loaded microspheres in treating breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990345/
https://www.ncbi.nlm.nih.gov/pubmed/29881676
http://dx.doi.org/10.1016/j.apsb.2018.04.001
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