Novel kojic acid-polymer-based magnetic nanocomposites for medical applications

Samer Hasan Hussein-Al-Ali,1 Mohamed Ezzat El Zowalaty,2,5 Mohd Zobir Hussein,3 Maznah Ismail,1,4 Dena Dorniani,3 Thomas J Webster6,7 1Laboratory of Molecular Biomedicine, 2Laboratory of Vaccines and Immunotherapeutics, Institute of Bioscience, 3Materials Synthesis and Characterization Laboratory,...

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Autores principales: Hussein-Al-Ali SH, El Zowalaty ME, Hussein MZ, Ismail M, Dorniani D, Webster TJ
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Publicado: Dove Medical Press 2014
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spelling oai:doaj.org-article:8a8cb810b23743a0b84610247ab37f0f2021-12-02T04:52:23ZNovel kojic acid-polymer-based magnetic nanocomposites for medical applications1178-2013https://doaj.org/article/8a8cb810b23743a0b84610247ab37f0f2014-01-01T00:00:00Zhttp://www.dovepress.com/novel-kojic-acid-polymer-based-magnetic-nanocomposites-for-medical-app-a15438https://doaj.org/toc/1178-2013 Samer Hasan Hussein-Al-Ali,1 Mohamed Ezzat El Zowalaty,2,5 Mohd Zobir Hussein,3 Maznah Ismail,1,4 Dena Dorniani,3 Thomas J Webster6,7 1Laboratory of Molecular Biomedicine, 2Laboratory of Vaccines and Immunotherapeutics, Institute of Bioscience, 3Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, 4Department of Nutrition and Dietetics, Faculty of Medicine and Health Science, Universiti Putra Malaysia, Serdang, Selangor, Malaysia; 5Faculty of Public Health and Tropical Medicine, Jazan University, Jazan, Saudi Arabia; 6Department of Chemical Engineering and Program in Bioengineering, Northeastern University, Boston, MA, USA; 7Center of Excellence for Advanced Materials Research, King Abdulaziz University, Jeddah, Saudi Arabia Abstract: Iron oxide magnetic nanoparticles (MNPs) were synthesized by the coprecipitation of iron salts in sodium hydroxide followed by coating separately with chitosan (CS) and polyethylene glycol (PEG) to form CS-MNPs and PEG-MNPs nanoparticles, respectively. They were then loaded with kojic acid (KA), a pharmacologically bioactive natural compound, to form KA-CS-MNPs and KA-PEG-MNPs nanocomposites, respectively. The MNPs and their nanocomposites were characterized using powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, vibrating sample magnetometry, and scanning electron microscopy. The powder X-ray diffraction data suggest that all formulations consisted of highly crystalline, pure magnetite Fe3O4. The Fourier transform infrared spectroscopy and thermogravimetric analysis confirmed the presence of both polymers and KA in the nanocomposites. Magnetization curves showed that both nanocomposites (KA-CS-MNPs and KA-PEG-MNPs) were superparamagnetic with saturation magnetizations of 8.1 emu/g and 26.4 emu/g, respectively. The KA drug loading was estimated using ultraviolet–visible spectroscopy, which gave a loading of 12.2% and 8.3% for the KA-CS-MNPs and KA-PEG-MNPs nanocomposites, respectively. The release profile of the KA from the nanocomposites followed a pseudo second-order kinetic model. The agar diffusion test was performed to evaluate the antimicrobial activity for both KA-CS-MNPs and KA-PEG-MNPs nanocomposites against a number of microorganisms using two Gram-positive (methicillin-resistant Staphylococcus aureus and Bacillus subtilis) and one Gram-negative (Salmonella enterica) species, and showed some antibacterial activity, which could be enhanced in future studies by optimizing drug loading. This study provided evidence for the promise for the further investigation of the possible beneficial biological activities of KA and both KA-CS-MNPs and KA-PEG-MNPs nanocomposites in nanopharmaceutical applications. Keywords: chitosan, polyethylene glycol, magnetic nanoparticle, kojic acid, controlled release, biological activityHussein-Al-Ali SHEl Zowalaty MEHussein MZIsmail MDorniani DWebster TJDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2014, Iss Issue 1, Pp 351-362 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Hussein-Al-Ali SH
El Zowalaty ME
Hussein MZ
Ismail M
Dorniani D
Webster TJ
Novel kojic acid-polymer-based magnetic nanocomposites for medical applications
description Samer Hasan Hussein-Al-Ali,1 Mohamed Ezzat El Zowalaty,2,5 Mohd Zobir Hussein,3 Maznah Ismail,1,4 Dena Dorniani,3 Thomas J Webster6,7 1Laboratory of Molecular Biomedicine, 2Laboratory of Vaccines and Immunotherapeutics, Institute of Bioscience, 3Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, 4Department of Nutrition and Dietetics, Faculty of Medicine and Health Science, Universiti Putra Malaysia, Serdang, Selangor, Malaysia; 5Faculty of Public Health and Tropical Medicine, Jazan University, Jazan, Saudi Arabia; 6Department of Chemical Engineering and Program in Bioengineering, Northeastern University, Boston, MA, USA; 7Center of Excellence for Advanced Materials Research, King Abdulaziz University, Jeddah, Saudi Arabia Abstract: Iron oxide magnetic nanoparticles (MNPs) were synthesized by the coprecipitation of iron salts in sodium hydroxide followed by coating separately with chitosan (CS) and polyethylene glycol (PEG) to form CS-MNPs and PEG-MNPs nanoparticles, respectively. They were then loaded with kojic acid (KA), a pharmacologically bioactive natural compound, to form KA-CS-MNPs and KA-PEG-MNPs nanocomposites, respectively. The MNPs and their nanocomposites were characterized using powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, vibrating sample magnetometry, and scanning electron microscopy. The powder X-ray diffraction data suggest that all formulations consisted of highly crystalline, pure magnetite Fe3O4. The Fourier transform infrared spectroscopy and thermogravimetric analysis confirmed the presence of both polymers and KA in the nanocomposites. Magnetization curves showed that both nanocomposites (KA-CS-MNPs and KA-PEG-MNPs) were superparamagnetic with saturation magnetizations of 8.1 emu/g and 26.4 emu/g, respectively. The KA drug loading was estimated using ultraviolet–visible spectroscopy, which gave a loading of 12.2% and 8.3% for the KA-CS-MNPs and KA-PEG-MNPs nanocomposites, respectively. The release profile of the KA from the nanocomposites followed a pseudo second-order kinetic model. The agar diffusion test was performed to evaluate the antimicrobial activity for both KA-CS-MNPs and KA-PEG-MNPs nanocomposites against a number of microorganisms using two Gram-positive (methicillin-resistant Staphylococcus aureus and Bacillus subtilis) and one Gram-negative (Salmonella enterica) species, and showed some antibacterial activity, which could be enhanced in future studies by optimizing drug loading. This study provided evidence for the promise for the further investigation of the possible beneficial biological activities of KA and both KA-CS-MNPs and KA-PEG-MNPs nanocomposites in nanopharmaceutical applications. Keywords: chitosan, polyethylene glycol, magnetic nanoparticle, kojic acid, controlled release, biological activity
format article
author Hussein-Al-Ali SH
El Zowalaty ME
Hussein MZ
Ismail M
Dorniani D
Webster TJ
author_facet Hussein-Al-Ali SH
El Zowalaty ME
Hussein MZ
Ismail M
Dorniani D
Webster TJ
author_sort Hussein-Al-Ali SH
title Novel kojic acid-polymer-based magnetic nanocomposites for medical applications
title_short Novel kojic acid-polymer-based magnetic nanocomposites for medical applications
title_full Novel kojic acid-polymer-based magnetic nanocomposites for medical applications
title_fullStr Novel kojic acid-polymer-based magnetic nanocomposites for medical applications
title_full_unstemmed Novel kojic acid-polymer-based magnetic nanocomposites for medical applications
title_sort novel kojic acid-polymer-based magnetic nanocomposites for medical applications
publisher Dove Medical Press
publishDate 2014
url https://doaj.org/article/8a8cb810b23743a0b84610247ab37f0f
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