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Design of injectable agar-based composite hydrogel for multi-mode tumor therapy
Chenyao Wu1, Jiulong Zhao2, Fei Hu1
1College of Science, University of Shanghai for Science and Technology, No. 334 Jungong Road, Shanghai 200093, People's Republic of China.
Carbohydrate Polymers
|November 7, 2017
Summary
This study introduces an injectable hydrogel for combined tumor photothermal therapy and chemotherapy. The novel Agar/MBP/DOX hydrogel enables controlled drug release and imaging, offering a promising cancer treatment strategy.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Oncology
Background:
- Current cancer therapies often lack specificity and can cause systemic side effects.
- Developing localized drug delivery systems is crucial for improving treatment efficacy and reducing toxicity.
Purpose of the Study:
- To design an injectable hydrogel for concurrent photothermal therapy and chemotherapy.
- To evaluate the hydrogel's drug retention, imaging capabilities, and therapeutic efficiency.
- To investigate the potential for on-demand drug release and antibiotic co-delivery.
Main Methods:
- Dissolving Molybdenum disulfide/Bismuth(III) sulfide-Polyethylene glycol (MoS2/Bi2S3-PEG) nanosheets, doxorubicin, and agar in water.
- Intra-tumoral injection of the solution, forming a hydrogel upon cooling to body temperature.
- Encapsulation of therapeutic agents and assessment of hydrogel properties and in-vivo performance.
Main Results:
- The Agar/MBP/DOX (AMD) hydrogel effectively retained nanosheets and doxorubicin, preventing systemic leakage.
- The hydrogel maintained photoacoustic and computed tomography imaging capabilities.
- Photothermal heating by MBP nanosheets promoted on-demand doxorubicin release, enhancing therapeutic outcomes.
- Co-encapsulation of antibiotics was feasible for preventing post-surgical wound infections.
Conclusions:
- The developed injectable AMD hydrogel is a promising platform for localized and concurrent tumor photothermal therapy and chemotherapy.
- The hydrogel facilitates controlled drug release, imaging, and potential infection prevention, improving cancer treatment strategies.

