Related Experiment Video
Updated: May 13, 2026

Gene-therapy Inspired Polycation Coating for Protection of DNA Origami Nanostructures
Published on: January 19, 2019
Chitosan-based Schiff base polymer derived from acetyl triazolyl uracil: Synthesis, characterization, evaluation of
Taghreed Hassan Abdalla1, Ahmed G Ibrahim2, Samia Elabbady1
1Chemistry Department, Faculty of Women of Arts, Science and Education, Ain Shams University, Heliopolis 11757, Egypt.
Abstract:
This work aimed to synthesize a new acetyl triazolyl uracil (UT) compound and subsequently utilize it to obtain a new chitosan-based Schiff base polymer (CH-UT). The new derivative was characterized using elemental analysis, FTIR, 1H NMR, XRD, TGA, DSC, and SEM analyses. Both UT and CH-UT were evaluated for their antibacterial activities against various Gram-positive and Gram-negative bacteria. The results demonstrated that the CH-UT displayed significant antibacterial activity against E. coli and L. monocytogenes, with inhibition ability of 44 % and 53 %, respectively, and low minimum inhibitory concentration (MIC) values of 31 μg/mL for E. coli and 15 μg/mL for L. monocytogenes. Additionally, the biofilm inhibitory activity showed that chitosan alone reduced E. coli biofilms by 10.25 %, whereas the combination of chitosan with UT in CH-UT increased inhibition to 43.00 %. The maximum biofilm inhibition for S. aureus was 42.02 % with UT alone, surpassing both chitosan and CH-UT. Furthermore, the CH-UT derivative showed notable antioxidant activity, with a value of 72.76 %. Results from frontier molecular orbitals (FMOs) analysis indicated that CH-UT exhibits higher reactivity due to its lower HOMO-LUMO energy gap and modified structure. The triazole group in CH-UT contributes to its potential antibacterial activity through hydrogen bonding and electronic properties.
More Related Videos
Related Concept Videos
Acid/Base Strengths and Dissociation Constants
Relative Strengths of Conjugate Acid-Base Pairs
Weak Base Solutions
Acid and Bases: Ka, pKa, and Relative Strengths
Solvating Effects
Extraction: Effects of pH

