Yayınlanmış 1 Ocak 2025 | Sürüm v1
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Highly sensitive electrochemical determination of cariprazine using a novel Ti<sub>3</sub>C<sub>2</sub>@CoAl<sub>2</sub>O<sub>4</sub> nanocomposite: application to pharmaceutical and biological sample analysis

  • 1. Ankara Univ, Fac Pharm, Dept Analyt Chem, TR-06560 Ankara, Turkiye
  • 2. Erciyes Univ, Fac Sci, Dept Chem, TR-38039 Kayseri, Turkiye

Açıklama

Cariprazine (CAR) is an atypical antipsychotic drug used for the treatment of schizophrenia and bipolar disorder. This study presents the development of a novel, highly sensitive electrochemical sensor based on a Ti3C2@CoAl2O2 nanocomposite-modified glassy carbon electrode (GCE) for the detection of CAR in pharmaceutical and biological samples. The innovative Ti3C2@CoAl2O2 composite, synthesized and characterized through Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy coupled with energy-dispersive spectroscopy, and thermogravimetric analysis, revealed exceptional structural integrity, morphology, composition, and thermal stability. The electrochemical properties of the modified electrode were evaluated using cyclic voltammetry and electrochemical impedance spectroscopy, demonstrating enhanced conductivity, an increased electroactive surface area, and reduced charge transfer resistance compared to the bare GCE. Differential pulse voltammetry was employed for CAR detection under optimized conditions, yielding a linear range of 0.2-5.6 mu M with a regression equation Ipa (mu A) = 0.133 CCAR (mu M) + 0.09 (R2 = 0.993). The limit of detection and limit of quantification were determined as 0.02 mu M and 0.07 mu M, respectively, highlighting the sensor's high sensitivity. The modified electrode exhibited excellent repeatability with a relative standard deviation (RSD) of = 2.9% and reproducibility (RSD = 2.8%), along with strong selectivity against common interfering substances. The sensor was successfully applied to human blood serum, urine, and CAR tablets, achieving high recovery values (98.52-103.94%), confirming its reliability for real-sample analysis. These findings underline the novelty and potential of the Ti3C2@CoAl2O2-modified GCE as a powerful tool for the accurate, selective, and sensitive determination of CAR in clinical and pharmaceutical applications.

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