Suchanek Małgorzata, Krakowska Agata, Szmuc Kamil, Łukowiec Dariusz, Zambrzycki Marcel, Piech Robert
Department of Analytical Chemistry and Biochemistry, Faculty of Materials Science and Ceramics, AGH University of Krakow, A. Mickiewicza 30 Av., 30-059 Krakow, Poland.
Department of Inorganic Chemistry and Pharmaceutical Analytics, Faculty of Pharmacy, Jagiellonian University Medical College, 9 Medyczna Street, 30-688 Krakow, Poland.
Int J Mol Sci. 2025 Sep 11;26(18):8861. doi: 10.3390/ijms26188861.
A novel voltammetric sensor was constructed by modifying a glassy carbon electrode with a composite material consisting of platinum-nickel-doped tin oxide and carbon black (PtNiSnO-CB/GCE), enabling highly sensitive differential pulse voltammetry (DPV) determination of trazodone HCl (TRZ). The DPV experimental parameters, including the composition of the supporting electrolyte and instrumental settings, were carefully optimized to achieve maximum analytical efficiency. Within the linear range of 1-10 µM, quantification of TRZ molecules could be performed without the preconcentration step. When applying a 60 s accumulation time (in the range 0.02-0.2 µM of TRZ), the detection limit reached 4.1 nM (1.67 mg L), indicating superior sensitivity compared to previously reported voltammetric techniques. The method demonstrated good reproducibility, with a relative standard deviation of 4.3% for 10 repeated measurements at 0.06 µM TRZ. The developed sensor exhibits excellent stability, simplicity of fabrication, and operational convenience. Its practical applicability was confirmed by the successful analysis of molecules of TRZ in diverse sample types, including pharmaceutical products, urine, plasma, river water, and artificial gastric and intestinal fluids, with recovery rates between 97.7% and 104.2%. Flow injection analysis (FIA) with amperometric detection was also performed for TRZ molecule determination.
通过用由铂 - 镍掺杂的氧化锡和炭黑组成的复合材料(PtNiSnO - CB/GCE)修饰玻碳电极,构建了一种新型伏安传感器,可实现对盐酸曲唑酮(TRZ)的高灵敏度差分脉冲伏安法(DPV)测定。仔细优化了DPV实验参数,包括支持电解质的组成和仪器设置,以实现最大分析效率。在1 - 10 μM的线性范围内,无需预富集步骤即可对TRZ分子进行定量。当施加60 s的积累时间(在0.02 - 0.2 μM的TRZ范围内)时,检测限达到4.1 nM(1.67 mg L),表明与先前报道的伏安技术相比具有更高的灵敏度。该方法具有良好的重现性,在0.06 μM的TRZ下进行10次重复测量的相对标准偏差为4.3%。所开发的传感器具有出色的稳定性、制备简单和操作方便的特点。通过成功分析包括药品、尿液、血浆、河水以及人工胃液和肠液在内的多种样品类型中的TRZ分子,回收率在97.7%至104.2%之间,证实了其实际适用性。还进行了带安培检测的流动注射分析(FIA)以测定TRZ分子。