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Cadmium Separation in Human Biological Samples Based on Captopril-Ionic Liquid Paste on Graphite Rod Before Determination by Electrothermal Atomic Absorption Spectrometry Publisher



Azami K1 ; Aliomrani M2 ; Mobarake MD3, 4
Authors
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Authors Affiliations
  1. 1. Faculty of Pharmacy, Department of Toxicology Pharmacology, Tehran University of Medical Science, Tehran, Iran
  2. 2. Department of Toxicology and Pharmacology, School of pharmacy, Isfahan University of Medical Sciences (IUMS), Isfahan, Iran
  3. 3. Energy Technology Research Division, Research Institute of Petroleum Industry (RIPI), Tehran, Iran
  4. 4. Department of Chemistry, University of Siegen, North Rhine Westphalia, Adolf-Reichwein-Straße 2, Siegen, 57076, Germany

Source: Analytical Methods in Environmental Chemistry Journal Published:2019


Abstract

A mixture of captopril nanoparticles (CAP-NPs) and ionic liquid (IL, [HMIM] [PF6]) paste on micro graphite rod (CAP-IL-MGR) and was used for separation cadmium in human serum and urine samples by micro solid phase extraction (μ-SPE). 0.01 g of CAP-NPs and 0.1 g of [HMIM] [PF6] mixed with 1 mL of acetone and mixture passed physically on micro graphite rod (MGR) at 55oC. Then, the graphite probe placed on 10 mL of human biological samples with 5 min of sonication, then cadmium ions complexed by thiol group of captopril (CAP-SH) at pH=5.5. The cadmium ions on micro probe were back extracted with 0.25 mL of nitric acid (0.5 M) which was diluted with DW up to 0.5 mL and finally, the cadmium concentration determined by ET-AAS. By optimizing of amount of captopril, the absorption capacity and recovery were obtained 132.4 mg g-1 and more than 96%, respectively. The limit of detection (LOD), linear range (LR) and enrichment factor (EF) were achieved 2 ngL-1, 0.01-0.35 μg L-1 and 19.7, respectively (RSD %<5%). The validation was done by certified reference material (CRM, NIST) and ICP-MS analysis. © 2019, AMEC Publisher. All rights reserved.