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Combined Chemo-photothermal Antitumor Therapy Using Molybdenum Disulfide Modified with Hyperbranched Polyglycidyl
Kewei Wang1, Qianqian Chen1, Wei Xue1
1Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Department of Biomedical Engineering, Jinan University, No. 601 West Huangpu Road, Guangzhou 510632, China.
Hyperbranched polyglycidyl-modified molybdenum disulfide (MoS2-HPG) enhances cancer treatment by improving MoS2 stability and enabling combined chemo-photothermal therapy.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Cancer Therapy
Background:
- Molybdenum disulfide (MoS2) shows promise in cancer therapy as a photothermal agent and drug carrier.
- Poor aqueous dispersibility and stability of MoS2 hinder its clinical application.
- Linear polymers improve MoS2 properties but may have limitations in circulation.
Purpose of the Study:
- To develop a stable, hyperbranched polyglycidyl (HPG)-modified MoS2 (MoS2-HPG) for enhanced cancer treatment.
- To evaluate MoS2-HPG as a drug delivery system for doxorubicin hydrochloride (DOX).
- To investigate the efficacy of combined chemo-photothermal therapy using MoS2-HPG-DOX.
Main Methods:
- Synthesis of MoS2-HPG via surface adsorption of HPG onto MoS2.
- Characterization of physicochemical, photothermal, and biocompatibility properties of MoS2-HPG.
- In vitro evaluation of combined chemo-photothermal therapy efficacy using MoS2-HPG-DOX.
Main Results:
- MoS2-HPG exhibited excellent dispersion and stability in aqueous solutions.
- High photothermal conversion efficiency and good in vitro biocompatibility were observed for MoS2-HPG.
- MoS2-HPG-DOX demonstrated superior anticancer effects compared to individual therapies.
Conclusions:
- MoS2-HPG offers improved properties for cancer therapy applications.
- Combined chemo-photothermal therapy using MoS2-HPG-DOX is a potent strategy against cancer.
- MoS2-HPG holds potential as a therapeutic formulation for clinical cancer treatment.
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