Institute of Chemistry

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    Pharmacokinetics of different selenium supplements in healthy individuals and patients with autoimmune thyroiditis after oral administration
    (Society of Chemists and Technologists of Macedonia, 2025-06-24)
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    Stafilov, Trajče
    Selenium is essential for the function of key selenoproteins such as glutathione peroxidase, thiore-doxin reductase, and iodothyronine deiodinase, which have antioxidant properties and support thyroid hormone metabolism. Due to the low selenium content in European soils – particularly in the Southeast-ern regions, supplementation is often recommended, especially for conditions like Hashimoto's thyroidi-tis. However, careful consideration of selenium dosage and pharmacokinetics is crucial, as the margin be-tween essential and toxic levels is very narrow. The aim of this study was to investigate the pharmacoki-netics of selenium absorption and plasma concentration following oral administration of various selenium doses and chemical forms, both in the short and long term, in healthy individuals and patients with auto-immune thyroiditis. Selenium concentrations in blood plasma were measured using electrothermal atomic absorption spectrometry (ETAAS). The study found that L-selenomethionine is absorbed more efficiently than inorganic sodium selenite, with peak plasma concentrations reached and sustained within 6 – 8 hours. Selenium levels remained elevated 48 hours after ingestion compared to baseline. At a daily dose of 200 μg of selenium as L-selenomethionine, plasma selenium concentrations increased by approximate-ly 30 %, and by about 25 % at 100 μg/day, relative to the initial value. Long-term studies showed that plasma selenium concentrations rose significantly after the first month of supplementation, with a slower increase in subsequent months. After supplementation ended, selenium levels declined rapidly. Interest-ingly, no significant differences in selenium absorption or excretion were observed between patients with Hashimoto's thyroiditis and healthy controls.
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    Unmasking the Aliphatic Repertoire: New Polyunsaturated Metabolites in Bupleurum falcatum sensu lato Provide Chemotaxonomic Insights
    (MDPI AG, 2025-05-10)
    Nešić, Milica D.
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    Nešić, Milan S.
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    Raca, Irena Lj.
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    Radulović, Niko S.
    Bupleurum falcatum (Apiaceae) sensu lato includes multiple infraspecific taxa with longstanding taxonomic ambiguities, often resulting from incomplete morphological and chemical characterizations. Herein, diethyl ether extracts were analyzed from four Balkan populations that were tentatively identified as B. falcatum subsp. falcatum (syn. B. falcatum) and B. falcatum subsp. cernuum (syn. B. sibthorpianum). Comprehensive chro-matography and spectroscopic techniques (GC-MS and 1D/2D NMR) enabled the iso-lation of several newly identified aliphatic polyunsaturated esters, including com-pounds bearing uncommon conjugated tetraene and triyne backbones. These novel structures differ from canonical falcarinol derivatives by lacking the usual 3-hydroxylation, suggesting a divergent branch in the crepenynate pathway. The chemical profiles of each sample correlated closely with leaf morphology and infra-specific designations: for example, the Galičica Mt. population of B. falcatum featured a unique newly detected heptadecadientriyne, while the populations from Šar Planina and Suva Planina displayed distinct polyunsaturated repertoires. Extracts from B. sibthorpianum likewise contained stereoisomeric compounds that highlight metabolic divergence. Collectively, these findings demonstrate significant chemotypic variation within the Bupleurum falcatum complex and provide the first account of less-polar sec-ondary metabolites, including newly discovered polyunsaturated metabolites. Future research integrating molecular markers and bioactivity assays may elucidate how these specialized metabolites contribute to both the taxonomy and pharmacological potential of these understudied taxa.
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    Upcycling of plastic waste into multi-walled carbon nanotubes as efficient organic dye adsorbent
    (Slovenian Chemical Society, 2025-03-03)
    Bogoeva-Gaceva, Gordana
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    Sokolovska, Meri
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    Kovačič, Sebastijan
    Multi-walled CNTs with an average diameter of about 80 nm, a length of several micrometers and surface area (SBET) of 100 m2 g-1 were obtained by pyrolysis of low-density polyethylene waste. The potential of the resulting MWCNTs material to purify water containing organic dyes was tested with Bezaktiv Blau HE-RM (BB) and Bezaktiv Rot S-3B (BR) reactive dyes. 200 mg L-1 MWCNT material was used to follow the adsorption of 30 mg L-1, 40 mg L-1, 50 mg L-1 and 60 mg L-1 BB and BR at pH 3 and a temperature of ~25 oC. The results have shown that this material has a high potential as a sorbent, and its adsorption capacity of 257 mg g-1 (for Bezaktiv Blau HE-RM) and 213 mg g-1 (for Bezaktiv Rot) is close to some commercial MWCNTs and functionalized MWCNT-based adsorbents. The adsorption process was very fast, reaching 80-90 % of the dye removal in 10-15 minutes, and the equilibrium time was reached in 40-60 minutes. The adsorption isotherm showed that the Langmuir model was more suitable than the Freundlich model for describing the adsorption properties of the pollutants.
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    Infrared and Raman spectra of racemic ibuprofen sodium dihydrate – Spectra-structure correlations
    (Elsevier BV, 2025-10)
    Cvetkovska Bogatinovska, E.
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    Najkov, K.
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    Petrushevski, Gj.
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    Geskovski, N.
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    Koleva, V.
    Ibuprofen sodium dihydrate, a salt form of ibuprofen, is a widely used non-steroidal anti-inflammatory drug (NSAID) valued for its high solubility, which enhances absorption into blood plasma compared to standard ibuprofen. This study presents, for the first time, the infrared spectra of this compound and its deuterated analogues, recorded at room temperature (RT) and liquid nitrogen temperature (LNT). Additionally, room-temperature attenuated total reflectance (ATR) and Raman spectra were recorded. For the first time, spectral analyses and spectra-structure correlations for this compound were also conducted. Vibrational spectra were analyzed using factor group analysis. Comparison of RT and LNT infrared spectra of the protiated compound, as well as partially deuterated analogues, reveals that bands at 3340 cm-1, 3280 cm-1, and 3030 cm-1 correspond to HOH stretching vibrations, while a shoulder near 1580 cm-1 is attributed to HOH deformation modes. Bands at 901 cm-1, 827 cm-1, 749 cm-1, 607 cm-1, and 554 cm-1 in the LNT spectrum are linked to water librational modes. In the infrared spectrum of the slightly deuterated analogue (∼5% D) at RT, two new bands appear at 2477 cm-1 and ∼ 2325 cm-1. At LNT, three distinct bands are observed at 2479 cm-1, 2454 cm-1, and 2300 cm-1, suggesting the presence of a highly asymmetric water molecule in the structure. Unexpectedly, the spectra of the deuterated analogues lack bands associated with DOD deformation vibrations. Intense bands at 1547 cm-1 and 1415 cm-1 in the LNT spectrum are assigned to COO antisymmetric and symmetric stretching vibrations, respectively, while the band around 850 cm-1 is confidently attributed to γ(CH) vibrations.
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    Assessment of volatile organic compounds in indoor environments across North Macedonia and Kosovo using passive sampling
    (Society of Chemists and Technologists of Macedonia, 2024-12-28)
    Mula, Vllaznim
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    Petreska Stanoeva, Jasmina
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    Zeneli, Lulzim
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    Berisha, Avni
    <jats:p>Humans are exposed to various volatile organic compounds (VOCs) through ingestion, inhalation, or skin contact, potentially leading to adverse health consequences. In this study, the distribution of vari-ous VOCs in indoor air in North Macedonia and Kosovo was investigated for the first time. From March to December 2023, the monthly relative abundance of VOCs was monitored using Radiello® pas-sive/diffusive samplers, followed by gas chromatography mass spectrometry (GC MS) analysis.A total of 60 samples were collected from 17 sites, where over 70 individual VOCs belonging to several classes were identified. Benzene, toluene, ethylbenzene, and xylenes (BTEX) compounds were the most abundant in the chemical stockroom, contributing up to 77.84 % of the total VOC relative abun-dance. In the printing store/workplace, alkylbenzenes were predominant, comprising 69.72 %. Alcohols and ethers were primarily detected in the coffee shop, whereas organosiloxanes were dominant in the hair salon, accounting for 33.87 % and 54.46 % of the total VOCs, respectively. Terpenes were a significant component in the meat factory, representing 65.78 % of the total VOCs, while hydrocarbons were most prevalent in the oil & lubricants store, accounting for 58.23%. Halogenated compounds were primarily found in the superstore, constituting 20.42 % of total VOCs. The VOC composition results indicate that their presence in indoor environments may pose both acute and chronic health risks.</jats:p>
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    Vasorelaxant Effects of Ethanolic Extract from <i>Cydonia oblonga</i> Mill<i>.</i> Leaves on Isolated Rat Thoracic Aorta and Potential Mechanism of Action
    (SAGE Publications, 2024-09)
    Krasniqi, Donjeta
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    Uka, Albina
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    Rexhbeqaj, Era
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    Beretta, Giangiacomo
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    Petreska Stanoeva, Jasmina
    <jats:p> Objective: Cydonia oblonga Mill . leaves ethanolic extract (CydOL-EE) has shown different cardioprotective effects. However, no previous studies investigated its direct effect on the vascular smooth muscle tone. Therefore, the study aimed to test the potential vasodilator activity of CydOL-EE in ex-vivo rat thoracic aorta preparations with an additional investigation of its mechanistic effects. Methods: CydOL-EE phytochemical profile was first investigated by HPLC-DAD-ESI-MS/MS and then tested for the vasorelaxation/vasoreactivity effects in rat aortic rings. The NO synthase inhibitor N(ω)-nitro-L-arginine methyl ester (L-NAME) and cyclic guanosine monophosphate inhibitor 1H-[1,2,4]Oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) were used to explore of the involvement of NO-dependent pathways. Results: Chromatographic analysis of CydOL-EE revealed the presence of six flavonols and seven hydroxycinnamic acids. Moreover, CydOL-EE showed a decrease in vasoreactivity caused by dose-dependent phenylephrine (PE) (Control, Emax = 104.29 ± 3.67 vs CydOL-EE, Emax = 70.73 ± 3.67, P < .0001) and a direct relaxing activity to precontraction with PE (Emax = 79.63 ± 3.67%). These responses were abolished during e-NOS inhibition, demonstrating that the mechanism of action was predominately controlled by the participation of an endothelium-dependent system. Conclusion: The results of our study show that CydO-EE demonstrates vasorelaxation and reduction of vasoreactivity through a NO-dependent pathway. These findings provide scientific evidence for further understanding of CydOL-EE use in the treatment of cardiovascular disease. </jats:p>
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    Crossroads of vibrational (infrared and Raman) spectroscopy and X-ray powder diffraction in identification and characterization of some minerals – advantages and limitations. A review
    (Society of Chemists and Technologists of Macedonia, 2024-05-19)
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    Pejov, Ljupco
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    Jovanovski, Gligor
    <jats:p>Many analytical methods have been successfully employed for the study of minerals, in particular, vibrational infrared (FTIR) and Raman spectroscopies and X-ray powder diffraction (XRPD). The advantages of the vibrational spectroscopic techniques for identifying and characterizing minerals include: rapid and versatile use; qualitative and quantitative chemical signatures; distinctive chemical fingerprint of a material; indirect determination of the crystal features (polymorphism, isomorphism, coordination, degree of deformation of structural polyhedra); small sample quantity (area less than 1 μm2 for Raman); wide coverage of 4,000 – 50 cm−1 region in a single scan; in situ and direct measurements without sample preparation; nondestructive use; etc. On the other hand, XRPD is a destructive technique that, depending on the method used and the density of the material, requires from a few micrograms up to around 5 grams of sample quantity for analysis. In spite of that, it is a rapid and powerful technique used in mineral studies with relatively straightforward interpretation of the results. During the last decade, portable X-ray powder diffractometers for the nondestructive analysis of art and archeological materials have been developed along with the portable and hand-held vibrational spectroscopy instrument. Here, some advantages and limitations in the process of the complementary use of FTIR and Raman vibrational spectroscopy and XRPD for identification and characterization of minerals are outlined.</jats:p>
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    Coal: exploration, reserves, and utilization
    (Springer Science and Business Media LLC, 2024-02-12)
    Životić, Dragana
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    Jovanovski, Gligor
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    Simić, Vladimir
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    Boev, Ivan
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    Cvetkov, Vesna
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    Raman spectroscopy as a tool for predicting the dimensionality and octahedra connectivity in lead iodide perovskites
    (2023-12-05)
    Gjorgjevikj, K., Bukleski, M., Dimitrovska-Lazova, S., Aleksovska, S.
    The interesting properties of the perovskite materials, especially the organic-inorganic ones are a consequence of their structural characteristics. In order to define the origin of these properties, a detailed structural characterization involving analysis with vibrational spectroscopy techniques has been undertaken. In this work, several inorganic and organic-inorganic lead iodide perovskites (RbPbI3, CsPbI3, CH3NH3PbI3, CH(NH2)2PbI3, C(NH2)3PbI3, (CH3)2NH2PbI3, (CH2)4NH2PbI3) were investigated by means of vibrational spectroscopy at room and low temperature and X-ray powder diffraction. Focusing on the Raman spectra, we followed the differences appearing in perovskites with different dimensionality. The bands that occur below 200 cm–1, their shape, relative position, intensity and shift can be related to the octahedral connectivity of the PbI6 anions, which, on the other hand, influence the dimensionality of the perovskites. Therefore, Raman spectroscopy can be used as a supporting technique for fast and reliable identification of octahedral connectivity.
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    Rapid and in-situ determination of epoxy equivalent weight of bisphenol-based epoxides by micro-Raman spectroscopy
    (Springer Science and Business Media LLC, 2023-02)
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    Ivanoska-Dacikj, Aleksandra
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    Geskovski, Nikola
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    Gigopulu, Olga
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    Bogoeva-Gaceva, Gordana