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Yayın A green electrochemical sensor based on molecular imprinting for etoposide detection in environmental matrices(Elsevier, 2026) Al Faysal, Abdullah; Kaya, Beril Sena; Dorreh, Setareh; Erdoğan, Taner; Gölcü, AyşegülA semisynthetic form of podophyllotoxin, etoposide (ETO), is frequently used to manage multiple types of cancer, including lung, testicular, bladder, prostate, and gastric malignancies. Having been utilized in clinical settings for over twenty years, it is one of the most frequently prescribed anticancer agents globally. The primary cytotoxic mechanism of ETO involves the inhibition of topoisomerase II. In the present work, an innovative electrochemical detection platform utilizing MIP was successfully established to enable both highly selective and exceptionally sensitive determination of ETO in pharmaceutical injection forms and environmental specimens. An ETO-specific MIP sensor was fabricated through a photopolymerization process and immobilized onto a GCE, where AMPS served as the active monomer, and EGDMA functioned as the cross-linking agent. This study marks the first instance of a MIP-based electrochemical sensor designed explicitly for ETO identification. The AMPS ETO@MIP/GCE sensor was subjected to electrochemical and morphological assessments through FTIR, SEM, CV, and EIS. An indirect measurement approach was employed using a 5.0 mM potassium ferricyanide/ferro cyanide system to ascertain the analytical detection range from 1.0 to 10.0 pM. The sensor demonstrated excellent sensitivity, reproducibility, and selectivity, enabling effective discrimination of ETO from structurally similar compounds while retaining reliable performance in complex matrices such as soil and tap water. Results from validation experiments in pharmaceutical matrices indicated superior recovery, supporting the sensor's practical effectiveness and stability. To further investigate the experimental results and better understand the nature of template–monomer interactions, a series of DFT calculations was performed. Binding energies were evaluated for ETO–AMPS complexes across varying template-to-monomer ratios.Yayın Electrophoretic approaches for investigating plant-derived compound interactions with dna and proteins(Wiley, 2026) Aydemir, Zeynep; Kaya, Beril Sena; Bakırcı, Meysera; Al Faysal, Abdullah; Kalaycıoğlu, Zeynep; Gölcü, AyşegülPlant-derived compounds are increasingly recognized as promising therapeutic agents due to their broad biological activities and structural diversity, making their interactions with DNA and proteins central to understanding mechanisms of action and guiding drug discovery. Electrophoretic techniques probe these interactions by tracking changes in electrophoretic mobility, conformation, complex formation, and biopolymer integrity. This review surveys electrophoretic strategies for characterizing plant-derived compound-DNA and -protein interactions, covering fundamental DNA-binding modes (intercalation, groove binding, electrostatic association, cleavage), representative phytochemicals and extracts, and analytical challenges of complex plant matrices, including chemical heterogeneity, synergistic and antagonistic effects, and active-constituent identification. Particular attention is given to capillary electrophoresis-based approaches (affinity CE, CE, and pressure-assisted frontal analysis) and gel-based methods (agarose gel electrophoresis, native PAGE, SDS-PAGE). The literature shows capillary electrophoresis excels at quantifying binding affinity, stoichiometry, and specificity, whereas gel electrophoresis better visualizes ligand-induced changes in DNA topology and protein behavior. HSA and BSA dominate as model proteins, while advanced methods remain underapplied to chemically complex extracts, gaps pointing toward broader protein targets and natural-product systems. Integrating mass spectrometry, advanced detection, and data-driven approaches could further strengthen the mechanistic and quantitative reach of electrophoretic analysis in this field.Yayın Green MIP-based electrochemical sensing platform for environmental ivermectin analysis(American Chemical Society, 2026) Aydemir, Zeynep; Kaya, Beril Sena; Dorreh, Setareh; Al Faysal, Abdullah; Erdoğan, Taner; Gölcü, AyşegülIvermectin (IVM), a macrocyclic lactone derived from Streptomyces avermitilis, is widely recognized as a “wonder drug” for its broad-spectrum efficacy against internal and external parasites in human and veterinary medicine. Owing to its potent pharmacological activity, precise quantification of IVM is essential for therapeutic monitoring and dose optimization. In this study, we report the design of a novel electrochemical sensor based on molecularly imprinted polymer (MIP) technology, specifically tailored for the selective detection of IVM. The sensor was fabricated via an electropolymerization strategy employing methacrylic acid (MAA) as the functional monomer and aniline as the comonomer in phosphate-buffered saline (PBS, pH 7.0). To the best of our knowledge, this represents the first electropolymerization-based MIP sensor developed for IVM determination. The resulting MAA-IVM@MIP/GCE sensor was thoroughly characterized using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). Electrochemical detection was achieved through an indirect redox probe approach with 5.0 mM [Fe(CN)6] 3−/4−, providing a wide linear range (1 × 10−12 −1 × 10−11 M) and remarkably low limits of detection (LOD: 2.91 × 10−13 M) and quantification (LOQ: 9.71 × 10−13 M). The sensor demonstrated high sensitivity, reproducibility, and selectivity, clearly distinguishing IVM from structurally related compounds. It maintained strong analytical performance in pharmaceutical formulations, biological matrices, and environmental samples such as tap water and soil, showing minimal matrix interference. These results confirm the platform’s robustness and applicability. Density functional theory (DFT) calculations were performed to evaluate template−monomer interactions and determine the optimal template:monomer ratio for the MIP-based sensor. The results revealed that the 1:1 complex exhibited the most favorable binding characteristics, consistent with the experimental findings. In addition, the sensor fabrication strategy was designed in accordance with green analytical chemistry principles. The electropolymerization process was performed in aqueous phosphate-buffered saline under mild conditions without the use of excessive cross-linkers or hazardous reagents. The approach minimizes organic solvent consumption, reduces energy requirements, and enables sensor reusability, thereby contributing to a sustainable and environmentally responsible analytical platform. Overall, this cost-effective, scalable, and environmentally conscious electrochemical sensor provides a practical tool for reliable IVM monitoring and has strong potential for clinical diagnostics, pharmacokinetics, and pharmaceutical quality control.Yayın Integrating green chemistry principles into the fabrication of MIP electrochemical sensors for heavy metal monitoring(Taylor & Francis, 2026) Dorreh, Setareh; Kaya, Beril Sena; Aydemir, Zeynep; Al Faysal, Abdullah; Gölcü, AyşegülHeavy metal contamination remains a critical global environmental issue due to the persistence, bioaccumulation, and toxicity of metal ions such as Pb2+, Cd2+, Hg2+, and As³+. Although conventional analytical techniques provide high sensitivity and accuracy, they often rely on energy-intensive instrumentation, hazardous reagents, and generate considerable chemical waste, raising concerns regarding their environmental sustainability. In this context, molecularly imprinted polymer (MIP)-based electrochemical sensors have emerged as promising alternatives, offering high selectivity, operational simplicity, and compatibility with miniaturized and in situ analysis. This review critically examines the integration of Green Analytical Chemistry (GAC) principles into the design and fabrication of MIP-based electrochemical sensors for heavy metal monitoring. Particular attention is given to material selection, polymerization strategies, template removal approaches, and electrode modification techniques, with emphasis on their environmental implications. The applicability of quantitative greenness assessment tools, including the Analytical Eco-Scale, GAPI, AGREE, and AGREEMIP, is discussed in the context of sensor development workflows, highlighting both their strengths and current limitations in addressing fabrication stages, nanomaterial synthesis, and end-of-life considerations. By identifying methodological bottlenecks, particularly solvent-intensive template removal and limited reusability, this review outlines practical directions for advancing more sustainable sensor platforms. Overall, the work provides a critical framework for aligning analytical performance with environmental responsibility in next-generation MIP-based electrochemical sensing systems.Yayın Utilization of terephthalic acid obtained from textile waste for environmental detection of mitoxantrone using molecularly imprinted electrochemical sensor technology(Wiley, 2026) Bakırcı, Meysera; Kaya, Beril Sena; Al Faysal, Abdullah; Erdoğan, Taner; Gölcü, AyşegülThe global textile industry generates substantial amounts of waste, much of which originates from polyethylene terephthalate (PET). Due to its resistance to natural degradation, PET accumulates in the environment and contributes to pollution and landfill growth. Chemical depolymerization offers a sustainable strategy for mitigating these impacts while recovering valuable monomers such as terephthalic acid (TPA) for high-value applications. In this study, five textile waste materials with varying PET content were subjected to alkaline hydrolysis using sodium hydroxide in a methanol–water medium. Pre-treated fabrics were cut into 2 mm pieces and reacted at 80◦C for 10–65 min. The recovered products were isolated by acidification and subsequently characterized by Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopy, with the obtained spectra confirming the successful recovery of TPA and its expected molecular structure. The efficiency of TPA recovery was strongly influenced by fabric composition and reaction time. Fabric 5, containing 50% PET, produced the highest yield (27.91%) at 50 min, followed by Fabric 4 (24.77%). Fabrics 1–3 yielded between 20.61% and 23.77%, with optimum recovery occurring between 20 and 60 min. Prolonged reaction times led to reduced yields, suggesting partial degradation or re-dissolution of the product. To demonstrate value-added utilization, the recovered TPA was employed as a functional monomer in the synthesis of a molecularly imprinted polymer (MIP) for the selective electrochemical detection of the anticancer drug mitoxantrone (MTX) in tap water. Density functional theory (DFT) calculations were performed to investigate MTX–TPA interactions at template-to-monomer ratios from 1:1 to 1:5. Both computational and experimental results identified the 1:1 ratio as optimal. The developed MIP-based sensor achieved a detection limit of 2.13 × 10− 13 M. These findings demonstrate the potential of converting textile waste into high-value functional materials for advanced environmental monitoring and analytical applications.
