Microwaved schiff base dialdehyde cellulose-chitosan hydrogels for sustained drug release with DFT calculations

Dialdehyde cellulose (DAC) prepared from sugarcane bagasse (SC) by an eco-friendly, fast and low-cost microwave method was used for loading and sustained release of 4-aminoacetophenone (4-AAP). DAC was reacted with chitosan (Ch) and 4-AAP via a Schiff base reaction. FTIR analysis confirmed successful Schiff base formation between DAC and Ch, evidenced by the disappearance of the DAC aldehyde peak at 1716 cm⁻<sup>1</sup> and the appearance of the imine peak at 1631 cm⁻<sup>1</sup>, as well as strong hydrogen bonding with incorporated 4-AAP, indicated by a shift in the O-H stretch from 3336 cm⁻<sup>1</sup> to 3330 cm⁻<sup>1</sup>.Swelling studies showed increased water absorption with higher 4-AAP content, with 4-AAP@DAC/Ch2 demonstrating pseudo-second-order kinetics and non-Fickian diffusion. The DFT calculations revealed that the 4-AAP@DAC/Ch hydrogel exhibited enhanced stability and reactivity. A significantly reduced HOMO-LUMO energy gap, coupled with negative Pi values, indicated strong interactions between DAC, chitosan, and 4-AAP. The high adsorption energy further supported the observed slow drug release, validating the experimental findings.

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Publication Details

Journal
BMC Chemistry
Published
2025-05-02
DOI
https://doi.org/10.1186/s13065-025-01469-3
Citations
15
Primary Topic
Hydrogels: synthesis, properties, applications
Type
article
Field-Weighted Citation Impact
8.87

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article

Microwaved schiff base dialdehyde cellulose-chitosan hydrogels for sustained drug release with DFT calculations

Hebat‐Allah S. Tohamy
15 citations
BMC Chemistry
Hydrogels: synthesis, properties, applications
8.87
article

Microwaved schiff base dialdehyde cellulose-chitosan hydrogels for sustained drug release with DFT calculations

Hebat‐Allah S. Tohamy
article en
15 citations

Abstract

Dialdehyde cellulose (DAC) prepared from sugarcane bagasse (SC) by an eco-friendly, fast and low-cost microwave method was used for loading and sustained release of 4-aminoacetophenone (4-AAP). DAC was reacted with chitosan (Ch) and 4-AAP via a Schiff base reaction. FTIR analysis confirmed successful Schiff base formation between DAC and Ch, evidenced by the disappearance of the DAC aldehyde peak at 1716 cm⁻<sup>1</sup> and the appearance of the imine peak at 1631 cm⁻<sup>1</sup>, as well as strong hydrogen bonding with incorporated 4-AAP, indicated by a shift in the O-H stretch from 3336 cm⁻<sup>1</sup> to 3330 cm⁻<sup>1</sup>.Swelling studies showed increased water absorption with higher 4-AAP content, with 4-AAP@DAC/Ch2 demonstrating pseudo-second-order kinetics and non-Fickian diffusion. The DFT calculations revealed that the 4-AAP@DAC/Ch hydrogel exhibited enhanced stability and reactivity. A significantly reduced HOMO-LUMO energy gap, coupled with negative Pi values, indicated strong interactions between DAC, chitosan, and 4-AAP. The high adsorption energy further supported the observed slow drug release, validating the experimental findings.

BMC ChemistryVol. 19(1)
National Research Centre (EG)
National Research Centre
Clean water and sanitation
Openalex Percentile: Top 2%
Hydrogels: synthesis, properties, applications
8.87
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Microwaved schiff base dialdehyde cellulose-chitosan hydrogels for sustained drug release with DFT calculations — Hebat‐Allah S. Tohamy · BMC Chemistry (2025) | TGRS Research Map | TGRS