Designing a molecularly imprinted polymer-based electrochemical sensor for the sensitive and selective detection of the antimalarial chloroquine phosphate


Piskin E., Cetinkaya A., ÜNAL M. A., Pérez-López B., Gunatilake U. B., Sene S., ...Daha Fazla

Microchimica Acta, cilt.191, sa.12, 2024 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 191 Sayı: 12
  • Basım Tarihi: 2024
  • Doi Numarası: 10.1007/s00604-024-06820-4
  • Dergi Adı: Microchimica Acta
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Analytical Abstracts, Aqualine, Aquatic Science & Fisheries Abstracts (ASFA), Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, Chimica, Communication Abstracts, Food Science & Technology Abstracts, Metadex, Pollution Abstracts, Civil Engineering Abstracts
  • Anahtar Kelimeler: Chloroquine phosphate, Differential pulse voltammetry, Electrochemical sensor, Malaria, Modified glassy carbon electrode, Molecularly imprinted polymer, Prussian blue nanoparticles (PBNP)
  • Ankara Üniversitesi Adresli: Evet

Özet

For the first time an electrochemical sensor based on nanomaterial-supported molecularly imprinted polymers (MIPs) is applied to the sensitive and specific determination of chloroquine phosphate (CHL). The sensor was produced using an electropolymerization (EP) approach, and it was formed on a glassy carbon electrode (GCE) using CHL as a template and 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS) and aniline (ANI) as functional monomers. Incorporating Prussian blue polyethyleneglycol-amine nanoparticles (PB@PEG-NH2) in the MIP-based electrochemical sensor increased the active surface area and porosity. The developed CHL/AMPS-PANI/PB@PEG-NH2/MIP-GCE sensor was characterized morphologically and electrochemically using electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and scanning electron microscopy (SEM). The indirect measurement of CHL was accomplished in 5.0 mmol L−1 [Fe(CN)6]−3/−4 solution using differential pulse voltammetry, displaying linear response between 1.75 × 10−12 and 2.50 × 10−13 M, and limits of detection (LOD) and quantitation (LOQ) of 6.68 × 10−14 M and 2.23 × 10−13 M, respectively, in standard solutions. CHL recoveries in spiked serum and tablet form ranged from 99.13 to 101.51%, while the relative standard deviations (RSD%) were below 2.41% in both types of samples. In addition, the sensor’s excellent selectivity was successfully demonstrated in the presence of components with a chemical structure similar to CHL. Graphical Abstract: (Figure presented.)