The polyvinylpyrrolidone functionalized rGO/Bi sub(2)S sub(3) nanocomposite as a near-infrared light-responsive nanovehicle for chemo-photothermal therapy of cancer
Recently, a combination of chemotherapy with photothermal therapy (PTT) has received great attention for the construction of a near infrared (NIR)-controlled drug-delivery system for synergistic treatment of cancer, ultimately resulting in the enhancement of the therapeutic efficacy of anticancer dr...
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Veröffentlicht in: | Nanoscale 2016-06, Vol.8 (22), p.11531-11542 |
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creator | Dou, Ruixia Du, Zhen Bao, Tao Dong, Xinghua Zheng, Xiaopeng Yu, Miao Yin, Wenyan Dong, Binbin Yan, Liang Gu, Zhanjun |
description | Recently, a combination of chemotherapy with photothermal therapy (PTT) has received great attention for the construction of a near infrared (NIR)-controlled drug-delivery system for synergistic treatment of cancer, ultimately resulting in the enhancement of the therapeutic efficacy of anticancer drugs. Here, we developed a novel system for synergistic cancer therapy based on bismuth sulfide (Bi sub(2)S sub(3)) nanoparticle-decorated graphene functionalized with polyvinylpyrrolidone (PVP) (named PVP-rGO/Bi sub(2)S sub(3)). The as-prepared PVP-rGO/Bi sub(2)S sub(3) nanocomposite has a high storage capacity for anticancer drugs ( similar to 500% for doxorubicin (DOX)) and simultaneously has perfect photothermal conversion efficiency in the NIR region. The results of the in vitro accumulative drug release test manifests that the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be applied as a dual pH- and NIR-responsive nanotherapeutic carrier for the controlled release of DOX from DOX-loaded PVP-rGO/Bi sub(2)S sub(3) (PVP-rGO/Bi sub(2)S sub(3)-DOX). Moreover, the treatment of both cancer cells (including Hela, MCF-7, HepG2 and BEL-7402 cells) and BEL-7402 tumor-bearing mice with the PVP-rGO/Bi sub(2)S sub(3)-DOX complex followed by NIR laser irradiation produces significantly greater inhibition of cancer cell growth than the treatment with NIR irradiation alone or DOX alone, exhibiting a synergistic antitumor effect. Furthermore, due to the obvious NIR and X-ray absorption ability, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be employed as a dual-modal contrast agent for both photoacoustic tomography and X-ray computed tomography imaging. In addition to the good biocompatibility, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite paves a potential way for the fabrication of theranostic agents for dual-modal imaging-guided chemo-photothermal combined cancer therapy. |
doi_str_mv | 10.1039/c6nr01543c |
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Here, we developed a novel system for synergistic cancer therapy based on bismuth sulfide (Bi sub(2)S sub(3)) nanoparticle-decorated graphene functionalized with polyvinylpyrrolidone (PVP) (named PVP-rGO/Bi sub(2)S sub(3)). The as-prepared PVP-rGO/Bi sub(2)S sub(3) nanocomposite has a high storage capacity for anticancer drugs ( similar to 500% for doxorubicin (DOX)) and simultaneously has perfect photothermal conversion efficiency in the NIR region. The results of the in vitro accumulative drug release test manifests that the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be applied as a dual pH- and NIR-responsive nanotherapeutic carrier for the controlled release of DOX from DOX-loaded PVP-rGO/Bi sub(2)S sub(3) (PVP-rGO/Bi sub(2)S sub(3)-DOX). Moreover, the treatment of both cancer cells (including Hela, MCF-7, HepG2 and BEL-7402 cells) and BEL-7402 tumor-bearing mice with the PVP-rGO/Bi sub(2)S sub(3)-DOX complex followed by NIR laser irradiation produces significantly greater inhibition of cancer cell growth than the treatment with NIR irradiation alone or DOX alone, exhibiting a synergistic antitumor effect. Furthermore, due to the obvious NIR and X-ray absorption ability, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be employed as a dual-modal contrast agent for both photoacoustic tomography and X-ray computed tomography imaging. In addition to the good biocompatibility, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite paves a potential way for the fabrication of theranostic agents for dual-modal imaging-guided chemo-photothermal combined cancer therapy.</description><identifier>ISSN: 2040-3364</identifier><identifier>EISSN: 2040-3372</identifier><identifier>DOI: 10.1039/c6nr01543c</identifier><language>eng</language><subject>Cancer ; Drugs ; Graphene ; Nanocomposites ; Nanostructure ; Polyvinylpyrrolidone ; Therapy ; Tomography</subject><ispartof>Nanoscale, 2016-06, Vol.8 (22), p.11531-11542</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Dou, Ruixia</creatorcontrib><creatorcontrib>Du, Zhen</creatorcontrib><creatorcontrib>Bao, Tao</creatorcontrib><creatorcontrib>Dong, Xinghua</creatorcontrib><creatorcontrib>Zheng, Xiaopeng</creatorcontrib><creatorcontrib>Yu, Miao</creatorcontrib><creatorcontrib>Yin, Wenyan</creatorcontrib><creatorcontrib>Dong, Binbin</creatorcontrib><creatorcontrib>Yan, Liang</creatorcontrib><creatorcontrib>Gu, Zhanjun</creatorcontrib><title>The polyvinylpyrrolidone functionalized rGO/Bi sub(2)S sub(3) nanocomposite as a near-infrared light-responsive nanovehicle for chemo-photothermal therapy of cancer</title><title>Nanoscale</title><description>Recently, a combination of chemotherapy with photothermal therapy (PTT) has received great attention for the construction of a near infrared (NIR)-controlled drug-delivery system for synergistic treatment of cancer, ultimately resulting in the enhancement of the therapeutic efficacy of anticancer drugs. Here, we developed a novel system for synergistic cancer therapy based on bismuth sulfide (Bi sub(2)S sub(3)) nanoparticle-decorated graphene functionalized with polyvinylpyrrolidone (PVP) (named PVP-rGO/Bi sub(2)S sub(3)). The as-prepared PVP-rGO/Bi sub(2)S sub(3) nanocomposite has a high storage capacity for anticancer drugs ( similar to 500% for doxorubicin (DOX)) and simultaneously has perfect photothermal conversion efficiency in the NIR region. The results of the in vitro accumulative drug release test manifests that the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be applied as a dual pH- and NIR-responsive nanotherapeutic carrier for the controlled release of DOX from DOX-loaded PVP-rGO/Bi sub(2)S sub(3) (PVP-rGO/Bi sub(2)S sub(3)-DOX). Moreover, the treatment of both cancer cells (including Hela, MCF-7, HepG2 and BEL-7402 cells) and BEL-7402 tumor-bearing mice with the PVP-rGO/Bi sub(2)S sub(3)-DOX complex followed by NIR laser irradiation produces significantly greater inhibition of cancer cell growth than the treatment with NIR irradiation alone or DOX alone, exhibiting a synergistic antitumor effect. Furthermore, due to the obvious NIR and X-ray absorption ability, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be employed as a dual-modal contrast agent for both photoacoustic tomography and X-ray computed tomography imaging. In addition to the good biocompatibility, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite paves a potential way for the fabrication of theranostic agents for dual-modal imaging-guided chemo-photothermal combined cancer therapy.</description><subject>Cancer</subject><subject>Drugs</subject><subject>Graphene</subject><subject>Nanocomposites</subject><subject>Nanostructure</subject><subject>Polyvinylpyrrolidone</subject><subject>Therapy</subject><subject>Tomography</subject><issn>2040-3364</issn><issn>2040-3372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqVjbtOAzEQRS0EEuHR8AVTJsUSr73ZkBbEo6MgfWScWWzknTG2N9LyPXwoIUL0VOcU9-gKcVXL61rq1dy2lGS9aLQ9EhMlG1lpvVTHf942p-Is53cp25Vu9UR8rR1C5DDuPI0hjilx8FsmhG4gWzyTCf4Tt5Aen-e3HvLwOlWzlwP1DMgQW-4jZ18QTAYDhCZVnrpk0j4L_s2VKmGOTNnv8FDs0Hkb9hecwDrsuYqOCxeHqTcBfmjiCNyBNWQxXYiTzoSMl788F9OH-_XdUxUTfwyYy6b32WIIhpCHvKlv1KJZqlbV-h_Tb7I4aHo</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Dou, Ruixia</creator><creator>Du, Zhen</creator><creator>Bao, Tao</creator><creator>Dong, Xinghua</creator><creator>Zheng, Xiaopeng</creator><creator>Yu, Miao</creator><creator>Yin, Wenyan</creator><creator>Dong, Binbin</creator><creator>Yan, Liang</creator><creator>Gu, Zhanjun</creator><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20160601</creationdate><title>The polyvinylpyrrolidone functionalized rGO/Bi sub(2)S sub(3) nanocomposite as a near-infrared light-responsive nanovehicle for chemo-photothermal therapy of cancer</title><author>Dou, Ruixia ; Du, Zhen ; Bao, Tao ; Dong, Xinghua ; Zheng, Xiaopeng ; Yu, Miao ; Yin, Wenyan ; Dong, Binbin ; Yan, Liang ; Gu, Zhanjun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_18254726213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cancer</topic><topic>Drugs</topic><topic>Graphene</topic><topic>Nanocomposites</topic><topic>Nanostructure</topic><topic>Polyvinylpyrrolidone</topic><topic>Therapy</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dou, Ruixia</creatorcontrib><creatorcontrib>Du, Zhen</creatorcontrib><creatorcontrib>Bao, Tao</creatorcontrib><creatorcontrib>Dong, Xinghua</creatorcontrib><creatorcontrib>Zheng, Xiaopeng</creatorcontrib><creatorcontrib>Yu, Miao</creatorcontrib><creatorcontrib>Yin, Wenyan</creatorcontrib><creatorcontrib>Dong, Binbin</creatorcontrib><creatorcontrib>Yan, Liang</creatorcontrib><creatorcontrib>Gu, Zhanjun</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Nanoscale</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dou, Ruixia</au><au>Du, Zhen</au><au>Bao, Tao</au><au>Dong, Xinghua</au><au>Zheng, Xiaopeng</au><au>Yu, Miao</au><au>Yin, Wenyan</au><au>Dong, Binbin</au><au>Yan, Liang</au><au>Gu, Zhanjun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The polyvinylpyrrolidone functionalized rGO/Bi sub(2)S sub(3) nanocomposite as a near-infrared light-responsive nanovehicle for chemo-photothermal therapy of cancer</atitle><jtitle>Nanoscale</jtitle><date>2016-06-01</date><risdate>2016</risdate><volume>8</volume><issue>22</issue><spage>11531</spage><epage>11542</epage><pages>11531-11542</pages><issn>2040-3364</issn><eissn>2040-3372</eissn><abstract>Recently, a combination of chemotherapy with photothermal therapy (PTT) has received great attention for the construction of a near infrared (NIR)-controlled drug-delivery system for synergistic treatment of cancer, ultimately resulting in the enhancement of the therapeutic efficacy of anticancer drugs. Here, we developed a novel system for synergistic cancer therapy based on bismuth sulfide (Bi sub(2)S sub(3)) nanoparticle-decorated graphene functionalized with polyvinylpyrrolidone (PVP) (named PVP-rGO/Bi sub(2)S sub(3)). The as-prepared PVP-rGO/Bi sub(2)S sub(3) nanocomposite has a high storage capacity for anticancer drugs ( similar to 500% for doxorubicin (DOX)) and simultaneously has perfect photothermal conversion efficiency in the NIR region. The results of the in vitro accumulative drug release test manifests that the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be applied as a dual pH- and NIR-responsive nanotherapeutic carrier for the controlled release of DOX from DOX-loaded PVP-rGO/Bi sub(2)S sub(3) (PVP-rGO/Bi sub(2)S sub(3)-DOX). Moreover, the treatment of both cancer cells (including Hela, MCF-7, HepG2 and BEL-7402 cells) and BEL-7402 tumor-bearing mice with the PVP-rGO/Bi sub(2)S sub(3)-DOX complex followed by NIR laser irradiation produces significantly greater inhibition of cancer cell growth than the treatment with NIR irradiation alone or DOX alone, exhibiting a synergistic antitumor effect. Furthermore, due to the obvious NIR and X-ray absorption ability, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite could be employed as a dual-modal contrast agent for both photoacoustic tomography and X-ray computed tomography imaging. In addition to the good biocompatibility, the PVP-rGO/Bi sub(2)S sub(3) nanocomposite paves a potential way for the fabrication of theranostic agents for dual-modal imaging-guided chemo-photothermal combined cancer therapy.</abstract><doi>10.1039/c6nr01543c</doi></addata></record> |
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subjects | Cancer Drugs Graphene Nanocomposites Nanostructure Polyvinylpyrrolidone Therapy Tomography |
title | The polyvinylpyrrolidone functionalized rGO/Bi sub(2)S sub(3) nanocomposite as a near-infrared light-responsive nanovehicle for chemo-photothermal therapy of cancer |
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