1. A review of analytical techniques for the determination of e-liquid and electronic cigarette aerosol compositionMatjaž Rantaša, David Majer, Matjaž Finšgar, 2025, pregledni znanstveni članek Opis: Since the introduction of electronic cigarettes (ECs) to the global market, the composition of e-liquids has been a controversial topic. While some consider ECs to be an effective tool for quitting smoking, their primary criticism lies in the uncertain and varied composition of e-liquids. Manufacturers create the desired formulations by mixing different ratios of humectants, flavorings, nicotine, cannabinoids, and cooling agents. However, the health effects of inhaling these compounds are still not well understood. Regular analytical control of e-liquids and aerosols is crucial to gain valuable insights into e-liquid composition, generating new compounds during aerosolization, and the potential impact on human health. This work presents an overview of the analytical techniques used for the qualitative and quantitative determination of e-liquid and aerosol compounds, including a description of the methods used for aerosol collection. Gas and liquid chromatography are the most used analytical techniques for compound determination, followed by nuclear magnetic resonance spectroscopy. Additionally, inductively coupled plasma-mass spectrometry and inductively coupled plasma-optical emission spectroscopy are the most frequently used analytical techniques for elemental determination in e-liquids and their aerosols.
Ključne besede: electronic cigarettes, e-liquids, aerosol, gas chromatography, high-performance liquid chromatography, inductively coupled plasma mass spectrometry
Objavljeno v DKUM: 21.03.2025; Ogledov: 0; Prenosov: 2
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5. Reinforcing ethyl cellulose aerogels with poly(lactic acid) for enhanced bone regenerationGabrijela Horvat, Jan Rožanc, Uroš Maver, Matjaž Finšgar, Željko Knez, Zoran Novak, 2024, izvirni znanstveni članek Opis: Developing double porous biodegradable and biocompatible scafolds that can incorporate and release drugs in a controlled manner holds immense potential in regenerative medicine. This study presents a synthesis method for preparing a macro-mesoporous scafold, where poly(lactic acid) adds to the macroporous region and mechanical properties, and ethyl cellulose adds to the surface area (182 m2 /g). High surface area enables the incorporation of model drug indomethacin with an entrapment efciency of 17.0% and its later controlled release profle. The resulting scafold has desirable mechanical properties in the range of a natural trabecular bone with a compressive modulus of 22.4 MPa. The material is stable in the simulated body fuids for 120 days before the slow degradation starts. In vitro studies demonstrate the material’s ability to support bone cell adhesion, proliferation, and diferentiation, promoting osteogenic activity. Overall, the unique combination of poly(lactic acid) and ethyl cellulose produces advanced materials with tailored macro and mesopore properties, remarkable mechanical properties, optimal degradation rate, and drug delivery potential, making it a promising candidate for bone scafolds in regenerative medicine and tissue engineering
Ključne besede: bio composite, polymer-matrix composites (PMCs), polymers, porosity/voids, secondary ion mass spectrometry
Objavljeno v DKUM: 23.08.2024; Ogledov: 130; Prenosov: 7
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6. Simultaneous GC-MS determination of free and bound phenolic acids in Slovenian red wines and chemometric characterizationMilena Ivanović, Maša Islamčević Razboršek, Mitja Kolar, 2016, izvirni znanstveni članek Opis: Several phenolic acids (PAs), caffeic, vanillic, syringic, p-coumaric and ferulic acid, found in Slovenian red wines were studied using gas chromatography and mass spectrometry (GC-MS). For isolation of the PAs from wine samples, solid phase extraction (SPE) using hydrophilic modified styrene - HLB cartridges was used. The bound PAs were extracted after basic hydrolysis and o-coumaric acid was used as the internal standard (ISTD). The method developed was validated and the linear concentration range for all analytes was from 1 to 100 mg L$^{-1}$ with correlation coefficients above 0.999. We show that the method is repeatable (RSD<2%), recoveries were above 96%, and LOD and LOQ values were acceptable.
In all of the wine samples tested, caffeic and p-coumaric acid were determined to be the predominant PAs (17-72 mg L$^{-1}$), while other compounds were found in lower concentrations. Principal Component Analysis (PCA) and Cluster Analysis (CLU) were used to study differences between wines related towards varieties and Slovenian wine regions. The results demonstrate that variety has more influence on PAs content than wine regions in Slovenian red wines.
Ključne besede: phenolic acids, Slovenian red wines, gas chromatography, mass spectrometry, PCA, CLU
Objavljeno v DKUM: 25.08.2017; Ogledov: 2231; Prenosov: 388
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7. Determination of candesartan in human plasma with liquid chromatography - tandem mass spectrometryVanja Forjan, Lea Cvitkovič-Maričič, Helena Prosen, Darinka Brodnjak-Vončina, 2016, izvirni znanstveni članek Opis: A sensitive, specific and rapid liquid chromatography - tandem mass spectrometry method was developed and validated for the determination of candesartan in human plasma. Analyte was separated from endogenous components present in plasma by solid phase extraction. Chromatographic separation was performed on Gemini C18 analytical column using mobile phase acetonitrile – 5 mM ammonium formate pH 2 (90:10, v/v) at flow rate of 0.3 mL/min. For detection, tandem mass spectrometry in SRM mode with positive electrospray ionization was used. The mass transitions m/z 441.1 > 263.1 and 445.1 > 267.1 were used to determine candesartan by using candesartan-d4 as an internal standard. After development, the method was validated according to the requirements of EMA regulatory guidelines in the concentration range 1 - 400 ng/ml in human plasma. Limit of quantification (LLOQ) was 1 ng/ml. The developed and validated method proved to be very fast and reproducible and was therefore successfully implemented in pharmacokinetic and bioequivalence studies with large number of study samples.
Ključne besede: candesartan, liquid chromatography, tandem mass spectrometry, human plasma
Objavljeno v DKUM: 17.08.2017; Ogledov: 1548; Prenosov: 391
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8. Determination of major phenolic acids, phenolic diterpenes and triterpenes in Rosemary (Rosmarinus Officinalis L.) by gas chromatography and mass spectrometryMaša Islamčević Razboršek, Darinka Brodnjak-Vončina, Valter Doleček, Ernest Vončina, 2007, izvirni znanstveni članek Opis: A gas chromatographic-mass spectrometric (GC-MS) method for the simultaneous identification and quantification of seven major phenolic and terpenic compounds in Rosmarinus officinalis L. was developed. The compounds were identified as trimethylsilyl (TMS) derivatives of phenolic acids (caffeic and rosmarinic acid), phenolic diterpene (carnosic acid), and pentacyclic triterpenes (ursolic, oleanolic, betulinic acid and betulin). These compounds have been identified by retention time and comparison of mass spectra. The procedure involves ultrasonic extraction using solvent mixture of tetrahydrofuran and ethanol. Extracts were fractionated by size exclusion chromatography (SEC) after purifying on graphitised carbon. The fraction with phenolic and terpenic compounds was derivatised prior to GC-MS analysis using N-methyl-N-trimethylsilyl trifluoroacetamide (MSTFA) as a derivatisation reagent. The derivatisation process was optimized regarding temperature and reaction time. The linearity of the method was tested in concentration range 4-25 mg L$^{–1}$. The correlation coefficients ($r^2$) were in the range of 0.997 to 0.999. The average recoveries for all compounds ranged from 80 to 82%. The GC-MS technique is specific and sensitive, and can be used for simultaneous identification and determination of a wide range of phenolic and terpenic compounds in different plants even at trace levels.
Ključne besede: Rosmarinus officinalis, diterpenes, triterpenes, size exclusion chromatography, gas chromatography, mass spectrometry
Objavljeno v DKUM: 21.12.2015; Ogledov: 1915; Prenosov: 217
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