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Development of a Chitosan-Based Smart Hydrogel Composite as a Controlled Release Drug Delivery Agent
Misba Jan1, Aabid H Shalla2, Kowsar Majid1
1Department of Chemistry, National Institute of Technology, Srinagar, Jammu and Kashmir 190006, India.
A novel chitosan-based hydrogel composite (CsP@Ag) was developed for sustained diclofenac sodium (Ds) delivery. This biocompatible material shows promising potential for advanced therapeutic applications due to its controlled release and environmental responsiveness.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Polymer Chemistry
Background:
- Diclofenac sodium (Ds) is a widely used anti-inflammatory drug.
- Developing effective and sustained drug delivery systems is crucial for improving therapeutic outcomes and patient compliance.
- Hydrogel composites offer potential for controlled drug release due to their tunable properties.
Purpose of the Study:
- To develop a multifunctional hydrogel composite (CsP@Ag) for sustained release of diclofenac sodium (Ds).
- To investigate the structural, physicochemical, and stimuli-responsive properties of the CsP@Ag hydrogel.
- To evaluate the in vitro drug release kinetics and biocompatibility of the developed system.
Main Methods:
- A chitosan (Cs)-based hydrogel composite (CsP@Ag) was synthesized using 2,6-pyridinedicarboxaldehyde and silver nitrate (AgNO3) via Schiff base condensation.
- Characterization included morphology (SEM), physicochemical properties, thermomechanical analysis, and swelling behavior under varying pH and temperature.
- Diclofenac sodium (Ds) loading and in vitro release studies were conducted at different pH conditions, followed by kinetic analysis (Korsmeyer-Peppas model).
- Cytotoxicity and biocompatibility tests were performed.
Main Results:
- The CsP@Ag hydrogel composite exhibited a honeycomb-like porous morphology with mesoporous structure (average pore diameter 38.8 nm).
- Incorporation of AgNO3 enhanced thermomechanical properties.
- The hydrogel demonstrated significant temperature-dependent swelling and pH responsiveness, with maximum swelling (4268%) at neutral pH.
- Sustained and controlled in vitro release of Ds was achieved, fitting the Korsmeyer-Peppas model.
- The system showed good biocompatibility and low cytotoxicity.
Conclusions:
- The developed CsP@Ag hydrogel composite is a promising biocompatible material for sustained drug delivery.
- Its stimuli-responsive properties (pH and temperature) enable tailored drug loading and release.
- The system holds potential for advanced therapeutic applications requiring prolonged drug release.
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