Effect of Poly (2-hydroxyethyl methacrylate) on the Release of Phenylacetaldehyde from Chitosan Matrix

Abstract To investigate the effect of Poly (2-hydroxyethyl methacrylate) on the extended release of Phenylacetalde-hyde, considered as a prototype of drug with aldehyde function, tow series of chitosan (CS) based systems were prepared; graft compolymers Chitosan-Phenylacetaldehyde– graft -poly(2-hydroxyethylmethacrylate) [CSPhAcAl- graft -PHEMA] with various PhAcAL ratios, and blends consisting of Chitosan-phenylacetaldehyde/Poly(2-hydroxyethylmethacrylate) [CSPhAcAl/PHEMA] with different PHEMA. PhAcAl was covalently attached to chitosan CS via Schiff base reaction assisted by pervaporation. FTIR and 1HNMR analyses confirmed chitosan Schiff base formation and its graft copolymerization with PHEMA, while distribution of PhAcAl within the copolymer matrix was examined using XRD and DSC analysis. Both systems exhibited pH-responsive swelling, however, significant differences were observed in their release behavior. CSPhAcAl/PHEMA systems with 3.74 and 8.98 wt% of PhAcAl content demonstrated the highest performance at pH 7. The release kinetics of the grafted systems followed the Korsmeyer-Peppas and Higuchi models, suggesting a Fickian diffusion-controlled mechanism. In contrast, blended systems demonstrated mixed behavior.

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Published
2025-12-01
DOI
https://doi.org/10.2478/pjct-2025-0019
Primary Topic
Hydrogels: synthesis, properties, applications
Type
article
Field-Weighted Citation Impact
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article

Effect of Poly (2-hydroxyethyl methacrylate) on the Release of Phenylacetaldehyde from Chitosan Matrix

Hassiba Benguergoura, Taı̈eb Aouak, Soufiane Rahal, Fethia Benmerad
Hydrogels: synthesis, properties, applications
article

Effect of Poly (2-hydroxyethyl methacrylate) on the Release of Phenylacetaldehyde from Chitosan Matrix

Hassiba Benguergoura, Taı̈eb Aouak, Soufiane Rahal, Fethia Benmerad
article en

Abstract

Abstract To investigate the effect of Poly (2-hydroxyethyl methacrylate) on the extended release of Phenylacetalde-hyde, considered as a prototype of drug with aldehyde function, tow series of chitosan (CS) based systems were prepared; graft compolymers Chitosan-Phenylacetaldehyde– graft -poly(2-hydroxyethylmethacrylate) [CSPhAcAl- graft -PHEMA] with various PhAcAL ratios, and blends consisting of Chitosan-phenylacetaldehyde/Poly(2-hydroxyethylmethacrylate) [CSPhAcAl/PHEMA] with different PHEMA. PhAcAl was covalently attached to chitosan CS via Schiff base reaction assisted by pervaporation. FTIR and 1HNMR analyses confirmed chitosan Schiff base formation and its graft copolymerization with PHEMA, while distribution of PhAcAl within the copolymer matrix was examined using XRD and DSC analysis. Both systems exhibited pH-responsive swelling, however, significant differences were observed in their release behavior. CSPhAcAl/PHEMA systems with 3.74 and 8.98 wt% of PhAcAl content demonstrated the highest performance at pH 7. The release kinetics of the grafted systems followed the Korsmeyer-Peppas and Higuchi models, suggesting a Fickian diffusion-controlled mechanism. In contrast, blended systems demonstrated mixed behavior.

Vol. 27(4)
King Saud University (SA), University Yahia Fares of Medea (DZ), University of Blida (DZ)
King Saud University
Clean water and sanitation
Openalex Percentile: Top 44%
Hydrogels: synthesis, properties, applications
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