Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system

Abstract Zinc sulphide (ZnS) nanoparticles were synthesized by the coprecipitation method. The ZnS nanoparticle surface was polymerized with allyl glycidyl ether (AGE), and 3‐aminophenol was then deposited as a ligand on nanosorbent. The modified nanosorbent was investigated with Fourier transform i...

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Main Authors: Milad Abniki, Zahra Azizi, Homayon Ahmad Panahi
Format: Article
Language:English
Published: Wiley 2021-10-01
Series:IET Nanobiotechnology
Online Access:https://doi.org/10.1049/nbt2.12063
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spelling doaj-af1eb403a7ef458e84b5ba5dc942db982021-09-14T08:09:21ZengWileyIET Nanobiotechnology1751-87411751-875X2021-10-0115866467310.1049/nbt2.12063Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery systemMilad Abniki0Zahra Azizi1Homayon Ahmad Panahi2Department of Chemistry, Karaj Branch Islamic Azad University Karaj IranDepartment of Chemistry, Karaj Branch Islamic Azad University Karaj IranDepartment of Chemistry, Central Tehran Branch Islamic Azad University Tehran IranAbstract Zinc sulphide (ZnS) nanoparticles were synthesized by the coprecipitation method. The ZnS nanoparticle surface was polymerized with allyl glycidyl ether (AGE), and 3‐aminophenol was then deposited as a ligand on nanosorbent. The modified nanosorbent was investigated with Fourier transform infrared spectroscopy and thermogravimetric analysis. The particle size of the modified nanosorbent was studied with scanning electron microscopy. Some characteristic factors of the adsorption process such as pH and time were investigated for famotidine using the modified nanosorbent. The equilibrium adsorption study of famotidine by 3‐aminophenol‐grafted AGE/ZnS was analysed by adsorption isotherms of the Langmuir, Freundlich, and Temkin models. The famotidine‐releasing process was investigated in simulated biological fluids (intestinal fluid at pH of 7.4 and gastric fluid at pH of 1.2) and demonstrated 65% and 73% famotidine release during periods of 30 h (pH = 7.4) and 60 min (pH = 1.2), respectively. These results reveal the optimal performance of 3‐aminophenol‐grafted AGE/ZnS for sustained drug delivery.https://doi.org/10.1049/nbt2.12063
collection DOAJ
language English
format Article
sources DOAJ
author Milad Abniki
Zahra Azizi
Homayon Ahmad Panahi
spellingShingle Milad Abniki
Zahra Azizi
Homayon Ahmad Panahi
Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system
IET Nanobiotechnology
author_facet Milad Abniki
Zahra Azizi
Homayon Ahmad Panahi
author_sort Milad Abniki
title Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system
title_short Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system
title_full Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system
title_fullStr Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system
title_full_unstemmed Design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system
title_sort design of 3‐aminophenol‐grafted polymer‐modified zinc sulphide nanoparticles as drug delivery system
publisher Wiley
series IET Nanobiotechnology
issn 1751-8741
1751-875X
publishDate 2021-10-01
description Abstract Zinc sulphide (ZnS) nanoparticles were synthesized by the coprecipitation method. The ZnS nanoparticle surface was polymerized with allyl glycidyl ether (AGE), and 3‐aminophenol was then deposited as a ligand on nanosorbent. The modified nanosorbent was investigated with Fourier transform infrared spectroscopy and thermogravimetric analysis. The particle size of the modified nanosorbent was studied with scanning electron microscopy. Some characteristic factors of the adsorption process such as pH and time were investigated for famotidine using the modified nanosorbent. The equilibrium adsorption study of famotidine by 3‐aminophenol‐grafted AGE/ZnS was analysed by adsorption isotherms of the Langmuir, Freundlich, and Temkin models. The famotidine‐releasing process was investigated in simulated biological fluids (intestinal fluid at pH of 7.4 and gastric fluid at pH of 1.2) and demonstrated 65% and 73% famotidine release during periods of 30 h (pH = 7.4) and 60 min (pH = 1.2), respectively. These results reveal the optimal performance of 3‐aminophenol‐grafted AGE/ZnS for sustained drug delivery.
url https://doi.org/10.1049/nbt2.12063
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