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Diffusion and binding of 5-fluorouracil in non-ionic hydrogels with interpolymer complexation
1School of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing 312000, China.
International Journal of Pharmaceutics
|April 26, 2012
Summary
Novel hydrogels made from N-vinyl pyrrolidone and acrylamide (PVP-co-PAM) and poly(vinyl alcohol) (PVA) show enhanced swelling and drug binding. These hydrogen-bonded interpolymer complexes offer tunable properties for advanced drug delivery systems.
Area of Science:
- Polymer Science
- Materials Science
- Drug Delivery
Background:
- Hydrogen-bonded interpolymer complexes offer unique properties for novel dosage forms.
- Crosslinked hydrogels, including copolymer networks and interpenetrating polymer networks (IPN), can be designed using polymers like N-vinyl pyrrolidone and acrylamide (PVP-co-PAM) and poly(vinyl alcohol) (PVA).
- Non-ionic complexes formed through H-bonding act as additional crosslinks, influencing hydrogel properties.
Purpose of the Study:
- To synthesize and characterize two types of crosslinked hydrogels: PVP-co-PAM and IPNs of PVP-co-PAM/PVA.
- To investigate the effect of varying crosslinking degrees on hydrogel swelling, permeability, and drug binding.
- To explore the drug release kinetics and transport mechanisms of 5-fluorouracil (5-FU) from these hydrogel systems.
Main Methods:
- Synthesis of crosslinked PVP-co-PAM copolymer networks and PVP-co-PAM/PVA interpenetrating polymer networks (IPNs) at three different crosslinking densities.
- Swelling studies to determine hydrogel sensitivity.
- Permeability measurements to assess pore structure.
- Fourier transform infrared (FTIR) difference spectroscopy to probe drug-polymer interactions.
- Drug release studies analyzed using the Peppas model.
Main Results:
- Both hydrogel types exhibited significantly higher swelling sensitivity compared to ionizable hydrogels.
- IPNs showed increased permeability with PVA incorporation, indicating more open pores, which decreased with higher crosslinking density.
- FTIR analysis confirmed substantial hydrogen bonding between 5-FU and polymer side chains.
- Drug binding interactions were stronger in PVP-co-PAM copolymers than in IPNs.
- Both hydrogel systems demonstrated non-Fickian drug release kinetics, with slower release observed in copolymer hydrogels due to stronger drug-polymer interactions.
Conclusions:
- Synthesized hydrogels possess tunable swelling and permeability properties influenced by crosslinking degree and composition.
- Significant hydrogen bonding interactions between 5-FU and polymers contribute to controlled drug release.
- These hydrogen-bonded interpolymer complexes represent promising materials for developing advanced drug delivery systems with tailored release profiles.

