Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption

Paracetamol, a popular analgesic, has been linked to harmful health effects, such as kidney and liver damage. The detection of paracetamol in the environment and its overdose use in humans and animals has raised global concerns, highlighting the need for its efficient removal or detection in real sa...

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Published in:JOURNAL OF MOLECULAR LIQUIDS
Main Authors: Asman, Saliza; Idris, Alya Athirah Mohd; Sambasevam, Kavirajaa Pandian
Format: Article
Language:English
Published: ELSEVIER 2024
Subjects:
Online Access:https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001265207500001
author Asman
Saliza; Idris
Alya Athirah Mohd; Sambasevam
Kavirajaa Pandian
spellingShingle Asman
Saliza; Idris
Alya Athirah Mohd; Sambasevam
Kavirajaa Pandian
Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
Chemistry; Physics
author_facet Asman
Saliza; Idris
Alya Athirah Mohd; Sambasevam
Kavirajaa Pandian
author_sort Asman
spelling Asman, Saliza; Idris, Alya Athirah Mohd; Sambasevam, Kavirajaa Pandian
Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
JOURNAL OF MOLECULAR LIQUIDS
English
Article
Paracetamol, a popular analgesic, has been linked to harmful health effects, such as kidney and liver damage. The detection of paracetamol in the environment and its overdose use in humans and animals has raised global concerns, highlighting the need for its efficient removal or detection in real samples. In this study, a deep eutectic solvent-molecularly imprinted polymer (DES-MIP) was synthesized and applied as an adsorbent to recognize the removal of paracetamol selectively. DES-MIP was synthesized using a deep eutectic solvent (DES) as a functional monomer, ethylene glycol dimethacrylate as a crosslinker, and paracetamol as a template. DES was initially prepared by combining choline chloride (ChCl) with methacrylic acid at a molar ratio of 1:2. A deep eutectic solvent-non-imprinted polymer (DES-NIP) was synthesized as a control. The characterization analysis, including Fourier transform infrared spectroscopy (FTIR), Scanning emission microscopy (SEM), and Brunauer-EmmettTeller (BET) was conducted for both polymers to confirm the synthesis occurred. The selectivity study inferred that DES-MIP (15.95 mg/g) was more selective towards paracetamol than DES-NIP (7.00 mg/g). Response surface methodology (RSM) coupled with central composite design (CCD) was employed to examine the effect of pH, contact time, and dosage on paracetamol adsorption. The analysis of variance (ANOVA) demonstrated the relative significance of process parameters in the adsorption process. The contact time and dosage were found to be more significant than the pH. The result indicated that the optimal conditions for paracetamol adsorption were pH 7, 35 min, and 5.5 mg. The behavior of paracetamol adsorption on DES-MIP was well-fitted using the second-order kinetic and Langmuir isothermal models, respectively. Then, the DES-MIP with optimized parameter studies was applied to herbs, medicine, and dietary supplements, achieving good recoveries of 94.46 %, 86.79 %, and 85.13 % and relative standard deviations (RSD) of 1.15 %, 2.39 %, and 2.52 %, respectively.
ELSEVIER
0167-7322
1873-3166
2024
408

10.1016/j.molliq.2024.125365
Chemistry; Physics

WOS:001265207500001
https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001265207500001
title Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
title_short Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
title_full Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
title_fullStr Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
title_full_unstemmed Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
title_sort Molecularly imprinted polymer based on deep eutectic solvent as functional monomer for paracetamol adsorption
container_title JOURNAL OF MOLECULAR LIQUIDS
language English
format Article
description Paracetamol, a popular analgesic, has been linked to harmful health effects, such as kidney and liver damage. The detection of paracetamol in the environment and its overdose use in humans and animals has raised global concerns, highlighting the need for its efficient removal or detection in real samples. In this study, a deep eutectic solvent-molecularly imprinted polymer (DES-MIP) was synthesized and applied as an adsorbent to recognize the removal of paracetamol selectively. DES-MIP was synthesized using a deep eutectic solvent (DES) as a functional monomer, ethylene glycol dimethacrylate as a crosslinker, and paracetamol as a template. DES was initially prepared by combining choline chloride (ChCl) with methacrylic acid at a molar ratio of 1:2. A deep eutectic solvent-non-imprinted polymer (DES-NIP) was synthesized as a control. The characterization analysis, including Fourier transform infrared spectroscopy (FTIR), Scanning emission microscopy (SEM), and Brunauer-EmmettTeller (BET) was conducted for both polymers to confirm the synthesis occurred. The selectivity study inferred that DES-MIP (15.95 mg/g) was more selective towards paracetamol than DES-NIP (7.00 mg/g). Response surface methodology (RSM) coupled with central composite design (CCD) was employed to examine the effect of pH, contact time, and dosage on paracetamol adsorption. The analysis of variance (ANOVA) demonstrated the relative significance of process parameters in the adsorption process. The contact time and dosage were found to be more significant than the pH. The result indicated that the optimal conditions for paracetamol adsorption were pH 7, 35 min, and 5.5 mg. The behavior of paracetamol adsorption on DES-MIP was well-fitted using the second-order kinetic and Langmuir isothermal models, respectively. Then, the DES-MIP with optimized parameter studies was applied to herbs, medicine, and dietary supplements, achieving good recoveries of 94.46 %, 86.79 %, and 85.13 % and relative standard deviations (RSD) of 1.15 %, 2.39 %, and 2.52 %, respectively.
publisher ELSEVIER
issn 0167-7322
1873-3166
publishDate 2024
container_volume 408
container_issue
doi_str_mv 10.1016/j.molliq.2024.125365
topic Chemistry; Physics
topic_facet Chemistry; Physics
accesstype
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url https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001265207500001
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