PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection

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Author: search.filters.author.Boyaci, EzelPublication Index: search.filters.publicationIndex.Scopus

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  • Article
    Citation - WoS: 2
    Citation - Scopus: 2
    Speciation of Inorganic and Organometallic Arsenic in Various Matrices With a Novel Spme Fiber Functionalized With Iron Nanoparticles Prior To Lc-Icp Determination
    (Elsevier, 2025) Boyaci, Ezel; Cagir, Ali; Shahwan, Talal; Eroglu, Ahmet E.
    A novel SPME-LC-ICP-MS methodology is described for the simultaneous microextraction/speciation/determination of the metabolically critical inorganic and organoarsenic species, namely, As(III), As(V), dimethylarsinic acid (DMA), and monomethylarsonic acid (MMA) in natural waters such as drinking and geothermal waters, and biological fluids such as urine. The novelty of the study stems also from the use of home-made SPME fibers for the extraction process, and from the proposed methodology needing no derivatization step. SPME fibers were prepared with in-tube capillary template approach through the immobilization of iron nanoparticles into agarose matrix. The fibers demonstrated reproducible extraction (<10 % RSD), good mechanical strength and good solvent resistivity. The separation of the analytes was realized by HPLC with a strong anion exchange column via gradient elution using different concentrations of (NH4)(2)CO3 (pH 8.50), and the on-line detection of eluted analytes was achieved by ICP-MS. The validity of the proposed methodology was verified via the analysis of certified reference materials (SRM 1643e, Natural Water-Trace Elements, and SRM 2669, Arsenic Species in Frozen Human Urine) and through spike recovery tests. The values of percentage recovery for SRM 2669 were 90.7 % for As(III), 99.8 % for As(V), 93.6 % for DMA, and 85.9 % for MMA. A good correlation was also found between the certified (60.45 mu gL(-1)) and determined (59.00 mu gL(-1)) values for SRM 1643e. Moreover, the speciation capability of the method was demonstrated on various natural waters and biological fluids.
  • Article
    Citation - WoS: 1
    Citation - Scopus: 1
    Assessment of Thermal and Solvent Stable Spme Fibers for Metabolomics Studies Performed in Living Systems
    (Elsevier, 2025) Kahremanoglu, Kuebra; Jaroch, Karol; Szeliska, Paulina; Filipiak, Wojciech; Charemski, Bartlomiej; Zuchowska, Karolina; Boyaci, Ezel
    Solid phase microextraction (SPME), as a sampling/sample preparation technique, offers unique solutions for the most challenging applications, including metabolomics studies of living systems. However, for global metabolomics it is critical to use an SPME sampler facilitating the extraction of both volatiles and nonvolatiles, which at the same time is compatible with thermal and solvent-assisted desorption. As a promising universal coating, recently hydrophilic-lipophilic balanced (HLB) particles immobilized in PTFE have been introduced as a new SPME sampler to provide a wide-range of analyte coverage and compatibility with solvent and thermal desorption. Thus, making it suitable for both gas and liquid chromatography (GC/LC) based applications. However, its potential in metabolomics has not been investigated to date. In this study, HLB/PTFE SPME fibers were prepared, evaluated with selected polar and non-polar metabolites relevant to biological systems, and validated for cell-line studies. The validation proved that these fibers can extract a wide-range of molecules (LogP: 4.2 to 15.6) with acceptable accuracy (<= 19% RE%) and repeatability (intra-day <= 17% and inter-day 12% RSD%). The LOQ was determined to vary between 150.0 and 500.0 ng/mL. Upon validation, the fibers were used in a proof-of-concept study for extraction of endometabolome and exometabolome of melanoma B16F10 and lung cancer LL2 cell lines. The metabolome studies showed that HLB/ PTFE fibers provide lower coverage, but for some compounds higher extraction efficiency compared to HLB/PAN fibers used in LC-based metabolomics. Fibers also proved suitable for GC-MS analysis, allowing for the detection of 36 volatile organic compounds in the headspace of the cell lines and RPMI medium.