Novel biocompatible poly(acrylamide)-grafted-dextran hydrogels: Synthesis, characterization and biomedical
Sudha B Patil1, Syed Z Inamdar1, Kakarla Raghava Reddy2
1Department of Pharmaceutics, BLDEA's SSM College of Pharmacy and Research Centre, Vijayapur 586 103, Karnataka, India.
This study developed an electro-responsive transdermal drug delivery system (ETDS) using a novel copolymer for on-demand rivastigmine tartrate release. Electrical stimulation significantly enhanced drug permeability through the skin.
Area of Science:
- Materials Science
- Biomedical Engineering
- Pharmacology
Background:
- Transdermal drug delivery offers advantages over oral administration but faces challenges in controlling drug release rates.
- Electro-responsive materials present a novel approach to modulate drug permeation through biological barriers like the skin.
- Rivastigmine tartrate is a key therapeutic agent for managing cognitive decline in neurological disorders.
Purpose of the Study:
- To synthesize and characterize an electro-responsive polyacrylamide-grafted-dextran (PAAm-g-Dxt) copolymer.
- To develop an electro-responsive transdermal drug delivery system (ETDS) for rivastigmine tartrate using the synthesized copolymer.
- To evaluate the effect of electrical stimuli on the transdermal delivery of rivastigmine tartrate.
Main Methods:
- Synthesis and characterization of PAAm-g-Dxt copolymer using spectroscopic and analytical techniques.
- Fabrication of ETDS comprising a drug-loaded hydrogel reservoir and a cross-linked dextran-poly(vinyl alcohol) blend rate-controlling membrane.
- In vitro permeation studies with and without electrical stimuli, including varying current strengths and 'on-off' cycling.
- Histopathological examination of skin tissue post-application of electrical stimuli.
Main Results:
- The synthesized PAAm-g-Dxt copolymer demonstrated successful grafting and electro-responsive properties.
- ETDS exhibited significantly enhanced rivastigmine tartrate permeability (1.6-fold increase) under electrical stimulation.
- Drug permeability correlated positively with electrical current strength and showed dynamic 'on-off' release behavior.
- Histopathology confirmed skin structural integrity was maintained, with alterations only under electrical stimulation.
Conclusions:
- The developed PAAm-g-Dxt based ETDS provides a viable platform for electrically triggered, on-demand transdermal drug delivery.
- This system offers precise control over drug release kinetics, potentially improving therapeutic efficacy and patient compliance.
- The electro-responsive nature of the copolymer enables tunable drug release for systemic circulation.
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