4.8 Article

Dendrimer-Modified MoS2 Nanoflakes as a Platform for Combinational Gene Silencing and Photothermal Therapy of Tumors

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 19, 页码 15995-16005

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b03371

关键词

MoS2 nanoflakes; dendrimers; photothermal therapy; gene silencing; tumors

资金

  1. National Natural Science Foundation of China [21273032, 81571679, 81271596]
  2. Fundamental Research Funds for the Central Universities
  3. Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning
  4. FCT-Foundation for Science and Technology [PEst-OE/QUI/U10674/2013]
  5. Madeira Chemistry Center - CQM + (Madeira) [M1420-01-0145-FEDER-000005]

向作者/读者索取更多资源

Exploitation of novel hybrid nanomaterials for combinational tumor therapy is challenging. In this work, we synthesized dendrimer-modified MoS2 nanoflakes for combinational gene silencing and photothermal therapy (PTT) of cancer cells. Hydro thermally synthesized MoS2 nanoflakes were modified with generation 5 (G5) poly(amidoamine) dendrimers partially functionalized with lipoic acid via disulfide bond. The formed G5-MoS2 nanoflakes display good colloidal stability and superior photothermal conversion efficiency and photothermal stability. With the dendrimer surface amines on their surface, the GS-MoS2 nanoflakes are capable of delivering Bcl-2 (B-cell lymphoma-2) siRNA to cancer cells (4T1 cells, a mouse breast cancer cells) with excellent transfection efficiency, inducing 47.3% of Bcl-2 protein expression inhibition. In vitro cell viability assay data show that cells treated with the G5-MoS2/Bcl-2 siRNA polyplexes under laser irradiation have a viability of 21.0%, which is much lower than other groups of single mode PTT treatment (45.8%) or single mode of gene therapy (68.7%). Moreover, the super efficacy of combinational therapy was further demonstrated by treating a xenografted 4T1 tumor model in vivo. These results suggest that the synthesized G5-MoS2 nanoflakes may be employed as a potential nanoplatform for combinational gene silencing and PTT of tumors.

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