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Jahan Bakhsh Raoof

Jahan Bakhsh Raoof

Academic rank: Professor
ORCID:
Education: PhD.
ScopusId:
Faculty: Faculty of Chemistry
Address: Electroanalytical Chemistry Research Laboratory, Department of Analytical Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, 47416-95447, Iran
Phone: 01135302392

Research

Title
In-situ synthesis of flower like Co3O4 nanorod arrays on anodized aluminum substrate templated from layered double hydroxide as a nanosorbent for thin film microextraction of acidic drugs followed by HPLC-UV quantitation
Type
JournalPaper
Keywords
In-situ conversion; Box-Behnken design; Biological fluids; Thin film microextraction; Electrochemical Anodizing; Acidic drugs
Year
2020
Journal Journal of Chromatography B: Biomedical Sciences and Applications
DOI
Researchers Faezeh Alipour ، Jahan Bakhsh Raoof ، Milad Ghani

Abstract

The present study is the first report of in-situ growth and application of nanorods-flower like Co3O4 nanosorbent coated on the anodized aluminum substrate for thin film microextraction (TFME) approach. The flower like Co3O4 was successfully fabricated by conversion of Co-Al layered double hydroxide (LDH) precursor to Co3O4 using the simple calcinations process. The cheap and available aluminum foil was electrochemically anodized and used as a porous substrate. Response surface methodology (RSM) was explored for optimization step. Different acidic drugs, including: paracetamol, ibuprofen, aspirin and diclofenac were extracted from biological fluids in order to investigate the capability of the prepared sorbent. The extracted analytes were then analyzed using high performance liquid chromatography-ultraviolet detection (HPLC-UV). Under the optimized conditions, the limits of detection were between 0.2 - 1.7 µg L−1 in different selected matrices. The obtained limits of quantification were also calculated to be between 0.8-5.1 µg L−1 in the selected matrices. In addition the enrichment factors were also in the range of 105 to 195. Batch-to-batch reproducibility at 100 µg L−1 concentration level was also evaluated to be lower than 5.2% (n=3). Finally, the method was successfully used for analysis of these compounds in the biological fluids.