Synthesis and Antibacterial Activity of Some New Drug Loaded Polymaleimide Derivatives

In this work new polymers have been synthesized via free radical polymerization method of 3 different drug substituted maleimides in THF using Azobisisobutyronitrile (AIBN) as initiator in nitrogen atmosphere at 65oC. for 18 hrs. The maleimides monomers were synthesized by conjugation of 4-maleimidobenzoic acid with amino group of three drugs (mesalzine, theophylline, and 4-aminoantipyrine). These monomers were polymerized to give three polymers (e-f). The synthesized polymers were characterized by using H-NMR, and FT-IR spectroscopic analytical techniques. Drug release and swelling percentage were examined at acidic and basic different pH. The intrinsic viscosities of these polymers were evaluated at 25 ºC using an Ostwald viscometer and based on their solubility. All produced monomers' physicochemical characteristics and the antibacterial activity of the derivatives was evaluated against Escherichia coli (E. coli), and Staphylococcus aureus (S. aureus).

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Publication Details

Journal
Cognizance Journal of Multidisciplinary Studies
Published
2024-12-30
DOI
https://doi.org/10.47760/cognizance.2024.v04i12.053
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
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article

Synthesis and Antibacterial Activity of Some New Drug Loaded Polymaleimide Derivatives

Hussein Ali Al‐Bahrani, Zahraa Ch. Hameed, Ammar Abdul-Hussein Awad, Mohammed Nawfal Abdul Maged
Cognizance Journal of Multidisciplinary Studies
Multicomponent Synthesis of Heterocycles
article

Synthesis and Antibacterial Activity of Some New Drug Loaded Polymaleimide Derivatives

Hussein Ali Al‐Bahrani, Zahraa Ch. Hameed, Ammar Abdul-Hussein Awad, Mohammed Nawfal Abdul Maged
article en

Abstract

In this work new polymers have been synthesized via free radical polymerization method of 3 different drug substituted maleimides in THF using Azobisisobutyronitrile (AIBN) as initiator in nitrogen atmosphere at 65oC. for 18 hrs. The maleimides monomers were synthesized by conjugation of 4-maleimidobenzoic acid with amino group of three drugs (mesalzine, theophylline, and 4-aminoantipyrine). These monomers were polymerized to give three polymers (e-f). The synthesized polymers were characterized by using H-NMR, and FT-IR spectroscopic analytical techniques. Drug release and swelling percentage were examined at acidic and basic different pH. The intrinsic viscosities of these polymers were evaluated at 25 ºC using an Ostwald viscometer and based on their solubility. All produced monomers' physicochemical characteristics and the antibacterial activity of the derivatives was evaluated against Escherichia coli (E. coli), and Staphylococcus aureus (S. aureus).

Cognizance Journal of Multidisciplinary StudiesVol. 4(12)
Clean water and sanitation
Openalex Percentile: Top 82%
Multicomponent Synthesis of Heterocycles
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