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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nanoscale 2016-06, Vol.8 (22), p.11531-11542
Hauptverfasser: Dou, Ruixia, Du, Zhen, Bao, Tao, Dong, Xinghua, Zheng, Xiaopeng, Yu, Miao, Yin, Wenyan, Dong, Binbin, Yan, Liang, Gu, Zhanjun
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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.
ISSN:2040-3364
2040-3372
DOI:10.1039/c6nr01543c