Deep eutectic solvent based method for analysis of Niclosamide in pharmaceutical and wastewater samples - A green analytical chemistry approach

被引:40
作者
Faraz, Noor [1 ]
Ul Haq, Hameed [1 ,2 ]
Arain, Muhammad Balal [3 ]
Castro-Munoz, Roberto [2 ,4 ]
Boczkaj, Grzegorz [2 ,5 ]
Khan, Asif [1 ]
机构
[1] Abdul Wali Khan Univ Mardan, Dept Chem, Kpk 23200, Pakistan
[2] Gdansk Univ Technol, Fac Chem, Dept Proc Engn & Chem Technol, 11-12 Narutowicza Str, PL-80233 Gdansk, Poland
[3] Univ Karachi, Dept Chem, Sindh, Pakistan
[4] Tecnol Monterrey, Campus Toluca, Toluca De Lerdo 50110, Mexico
[5] Gdansk Univ Technol, EkoTech Ctr, G Narutowicza St 11-12, PL-80233 Gdansk, Poland
关键词
Extraction; Deep eutectic solvents; Drugs; Sample preparation; Spectroscopy; SPECTROPHOTOMETRIC METHODS; VOLTAMMETRIC DETERMINATION;
D O I
10.1016/j.molliq.2021.116142
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The paper presents a simple, but very effective and sensitive spectrophotometric method for trace analysis of Niclosamide based on liquid-liquid microextraction using deep eutectic solvents (DESs) prior to its quantification. Here, different DES systems, such as Choline chloride (ChCl) + Urea, ChCl + Citric acid, ChCl + Ethylene glycol and ChCl + Phenol, were synthesized and evaluated at different molar ratios, selecting ChCl + Phenol 1:2 as an extractive DES system. Optimization studies revealed that best performance were obtained at pH 8 with optimum volume of THF and DES as 0.3 mL and 0.4 mL, respectively. The developed method is characterized by good analytical performance, e.g., a recovery of 99.26% and precision described by RSD value as <2%. The inter-assay precision was 0.51% while intermediate precision was 0.0323%. The method was found linear from 4.8 to 48 mu g/L. LOD and LOQ were found as 0.112 and 0.374 mu g/L, respectively. The paper presents also examples of the application of the proposed method for the determination of Niclosamide in different pharmaceutical and wastewater samples. This alternative method reveals a better performance in respect to the British pharmacopoeia procedure, providing concurrently ease of operation and simplicity. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页数:6
相关论文
共 34 条
  • [1] Detection of the damage caused to DNA by niclosamide using an electrochemical DNA-biosensor
    Abreu, FC
    Goulart, MOF
    Brett, AMO
    [J]. BIOSENSORS & BIOELECTRONICS, 2002, 17 (11-12) : 913 - 919
  • [2] Al-Hadiya Badraddin M H, 2005, Profiles Drug Subst Excip Relat Methodol, V32, P67, DOI 10.1016/S0099-5428(05)32002-8
  • [3] Alemu H, 2003, B CHEM SOC ETHIOPIA, V17, P95
  • [4] Niclosamide quantification in methyl-β-cyclodextrin after derivatization to aminoniclosamide
    Algarra, Manuel
    Campos, Bruno B.
    Rodriguez-Borges, Jose E.
    Sanchez, Francisco G.
    Lopez-Romero, Juan M.
    da Silva, Joaquim C. G. Esteves
    [J]. JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 2012, 72 (1-2) : 89 - 94
  • [5] THE BIOLOGY AND TOXICOLOGY OF MOLLUSCICIDES, BAYLUSCIDE
    ANDREWS, P
    THYSSEN, J
    LORKE, D
    [J]. PHARMACOLOGY & THERAPEUTICS, 1982, 19 (02) : 245 - 295
  • [6] [Anonymous], 2014, SITTIGS HDB PESTICID
  • [7] [Anonymous], 2005, Current Step, V4, P1
  • [8] Niclosamide: Beyond an antihelminthic drug
    Chen, Wei
    Mook, Robert A., Jr.
    Premont, Richard T.
    Wang, Jiangbo
    [J]. CELLULAR SIGNALLING, 2017, 41 : 89 - 96
  • [9] Selective differential spectrophotometric methods for determination of niclosamide and drotaverine hydrochloride
    Daabees, HG
    [J]. ANALYTICAL LETTERS, 2000, 33 (04) : 639 - 656
  • [10] Sensitive Voltammetric Determination of Niclosamide at a disposable pencil graphite electrode
    Dede, Eda
    Saglam, Ozlem
    Dilgin, Yusuf
    [J]. ELECTROCHIMICA ACTA, 2014, 127 : 20 - 26