Laser-triggered collaborative chemophotothermal effect of gold nanoparticles for targeted colon cancer therapy

[Display omitted] •Multi-functional gold NPs were prepared for colon cancer therapy.•The active and remarkable targeted ability of NPs owing to the AS1411 aptamer.•The improved cytotoxicity of NPs by the collaborative chemophotothermal effect.•Our NPs could be an advantageous nanoplatform for colon...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2020-10, Vol.130, p.110492, Article 110492
Hauptverfasser: Zhang, Yajie, Zhou, Lu, Tan, Jingwei, Liu, Jianling, Shan, Xiaoqing, Ma, Yong
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Sprache:eng
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Zusammenfassung:[Display omitted] •Multi-functional gold NPs were prepared for colon cancer therapy.•The active and remarkable targeted ability of NPs owing to the AS1411 aptamer.•The improved cytotoxicity of NPs by the collaborative chemophotothermal effect.•Our NPs could be an advantageous nanoplatform for colon cancer therapy. Nanotechnology has shown advantages for cancer treatment. Multimodal nanoparticles (NPs) combining chemotherapy and photothermal therapy are promising and elicit synergetic benefit. However, there were still less multifunctional nanomaterials with good targeting and anti-tumor property applied as the colon cancer therapeutic strategy. In this study, we designed the gold NPs modified with AS1411 and DNA riched of GC intercalation (hairpin DNA) with doxorubicin (DOX) for targeted chemotherapy and NIR laser-triggered chemo-photothermal effect (PTT). We took advantage of PTT effect to realize DOX release from hairpin DNA. We also demonstrated AS1411 based NPs exhibited remarkable targeted binding towards SW480 colon cancer cells in vitro and enhanced uptake inside the cells. Strikingly, AS1411 based NPs exhibited the most efficient cytotoxicity and markedly enhanced inhibition effect on cells proliferation to SW480 cells under laser exposure when compared to the NPs merely with PTT or chemotherapy. Our study appears to provide an alternative nanoplatform with good targeted and chemo-photothermal therapy against colon cancer.
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2020.110492