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    A simple and efficient supramolecular solvent based liquid phase microextraction method for the preconcentration of nickel from dandelion tea samples before FAAS quantification, and the practicality and greenness assessment of developed method
    (Elsevier Inc., 2024) Kartoğlu, Bedrihan; Bodur, Süleyman; Gülhan Bakırdere, Emine; Bakırdere, Sezgin
    A sensitive, accurate and practical analytical method (supramolecular solvent based liquid phase microextraction – flame atomic absorption spectrometry (SUPRAS-LPME-FAAS) was developed for the determination of nickel in dandelion tea samples. All influential parameters of SUPRAS-LPME were optimized to attain low detection/quantification limits using a univariate optimization approach. Under the optimum SUPRAS-LPME-FAAS conditions, dynamic range, limit of detection (LOD) and limit of quantification (LOQ) were found to be 25.86–497.64 µg/kg, 8.20 µg/kg and 27.35 µg/kg, respectively. The detection power of FAAS system was augmented as 28-fold with the help of SUPRAS-LPME method. Recovery experiments were performed for the evaluation of the accuracy and the applicability of the SUPRAS-LPME-FAAS method and percent recovery results for the spiked dandelion tea samples were calculated between 86.0 and 131.8 % via matrix matching calibration strategy. Additionally, the practicality and greenness evaluations for the SUPRAS-LPME-FAAS method were carried out using BAGI and AGREEprep software, respectively. © 2024 Elsevier B.V.
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    Dispersive solid phase extraction and quadruple isotope dilution–mass spectrometry combination for the accurate and sensitive quantification of capsaicin in pepper, domestic wastewater and human saliva samples by GC–MS system
    (Elsevier Inc., 2025) Bodur, Süleyman; Bodur, Sezin Erarpat; Gürsoy, Selim; Ayyıldız, Merve Fırat; Kartoğlu, Bedrihan; Akbıyık, Hilal; Günkara, Ömer Tahir; Bakırdere, Sezgin
    In the presented study, reduced graphene oxide/Fe3O4 (rGO/Fe3O4) nanocomposites based dispersive solid phase extraction (DSPE) – gas chromatography–mass spectrometry (GC–MS) method was developed for the determination of capsaicin in domestic wastewater (DW), pepper (PP) and human saliva (HS) samples. All important parameters of the DSPE method affected the preconcentration factor were carefully optimized to achieve high signal to noise ratio for the analyte. After the optimization studies, the system analytical performance of DSPE-GC–MS system was evaluated using the aqueous standard solution of capsaicin. Limit of detection (LOD), limit of quantitation (LOQ) and dynamic range were figured out to be 0.54 µg/kg, 1.80 µg/kg and 2.66 – 487.35 µg/kg, respectively. Under the optimum experimental conditions, recovery studies were conducted with the spiked DW, PP and HS samples, and percent recovery results were recorded between 52.6 % and 183.6 % via matrix matching calibration strategy. After the implementation of ID4 strategy, percent recovery results for the spiked DW, PP and HS samples were calculated as 98.2 %–99.3 %, 99.7 %–100.7 % and 99.4 %–99.8 %, respectively. In addition, capsaicin content in Sivri (S)-PP, Kıl (K)-PP and Samandağ (SA)-PP samples were found to be 309.5 ± 11.8 mg/kg, 873.7 ± 26.7 mg/kg and 165.3 ± 5.1 mg/kg via DSPE-GC-ID4-MS method, respectively. As a result, the combination of quadruple isotope dilution (ID4) strategy and the DSPE-GC–MS method were successfully performed to boost the accuracy and precision of developed DSPE-GC–MS method. © 2024 Elsevier B.V.