The initial research of this thesis involves the evaluation of different strategies for developing diverse chemistries of highly stable coatings for the automated 96-blade (thin-film) solid phase microextraction (SPME) system. Thin-film geometry increases the volume of extractive phase, and consequently improves the sensitivity of the analysis. Sol-gel technology was used for the preparation of octadecyl (C18)-silica gel thin-film coating. The evaluation of the C18-silica gel SPME extractive phase resulted in stable physical and chemical characteristics and long-term reusability with a high degree of reproducibility. Biocompatible polyacrylonitrile (PAN) polymer was used for the preparation of particle-based extractive phases in order to improve the biocompatible characteristics of SPME coatings for the extraction from biological samples. Three different immobilization strategies were evaluated for developing highly stable coatings for the automated 96-blade SPME system. The spraying was found to be the optimal method in terms of stability and reusability for long-term use. The optimized C18-PAN coating demonstrated improved biocompatibility, stability, and reusability for the extraction of benzodiazepines from human plasma in comparison with those of C18-silica gel coating. To improve the biocompatible properties of the C18-PAN SPME coating for long-term direct analysis from whole blood, different modification strategies were studied and evaluated. The modification of the coating with an extra layer of biocompatible polyacrylonitrile resulted in significant improvement in the blood compatibility in long-term use. ‘Extracted blood spot’ (EBS) sampling was introduced as a novel approach to overcome the limitations of dried blood spot sampling. EBS includes the application of a biocompatible SPME coating for spot sampling of blood or other biofluids. The compatibility of EBS sampling with different analytical methods was demonstrated. The utilization of EBS as a fast sampling and sample preparation method resulted in a significant reduction of matrix effects through efficient sample clean-up. Modified polystyrene-divinylbenzene (PS-DVB)-PAN and phenylboronic acid (PBA)-PAN 96-blade SPME coatings were developed and evaluated for the extraction of analytes in a wide range of polarity. These coatings demonstrated efficient extraction recovery for both polar and non-polar groups of compounds, and presented chemical and mechanical stabilities and reproducible extraction efficiencies for more than 100 usages in biological sample.

Aldehydes in lung cancer cell culture have been investigated using gas chromatography/mass spectrometry and solid-phase microextraction with on-fiber derivatization. In this study, the poly(dimethylsiloxane/divinylbenzene (PDMS/DVB) fiber was used and o-2,3,4,5,6-(pentafluorobenzyl) hydroxylamine hydrochloride (PFBHA) was first loaded on the fiber. Aldehydes in the headspace of lung cancer cell culture were extracted by solid-phase microextraction (SPME) fiber and subsequently derivatized by PFBHA on the fiber. Finally, the aldehyde oximes formed on the fiber were analyzed by gas chromatography/mass spectrometry (GC/MS). Using this method, acetaldehyde decrease was found in both non-small lung cancer cell cultures studied compared to the medium control study. The results of spiking the cell culture with acetaldehyde solution showed that 5 million SK-MES-1 cell lines could consume up to 4.5 uM acetaldehyde in 15-ml medium, and 5 million NCI-H522 cell lines could consume 5.9 uM acetaldehyde in 15-ml medium. The decrease of acetaldehyde may contribute to the metabolism of lung cancer cells. It was proved that GC/MS and SPME with on-fiber derivatization is a simple, rapid, sensitive and solvent-free method for the detection of aldehydes in lung cancer cell culture.

Source: Masters Abstracts International, Volume: 47-06, page: 3475. Advisers: Elaine Symanski; Thomas H. Stock. Includes bibliographical references

The feasibility of using solid phase micro-extraction (SPME) as an in vivo sampling tool for analysis of trace environmental contaminants in fish exposed to municipal wastewater effluents (MWWEs) was validated using controlled laboratory and field experiments. SPME was compared with traditional extraction techniques， including solid phase extraction (SPE) in water and solid-liquid extraction (SLE) in fish tissues to assess relative efficiencies. All three techniques were used to quantify the presence of eight compounds of interest in fish exposed to MWWEs in the laboratory, as well as in wild and field caged fish upstream and downstream of three wastewater treatment plants in the Grand River watershed. Atrazine, carbamazepine, naproxen, diclofenac, gemfibrozil, bisphenol A, fluoxetine and ibuprofen were selected as target compounds due to their diverse chemical characteristics and frequent detection in surface waters and sediments around the world. The distribution coefficients between various sample matrices (water, fish) and extraction phases (SPME fibers) were compared, as were extraction profiles and bioconcentration factors of target analytes in muscle of fish exposed to MWWEs under laboratory conditions, during field caging studies, or collected (wild) from the Grand River. Poly(dimethylsiloxane) (PDMS) medical grade tubing was utilized as the SPME extraction phase, which when kinetically calibrated, were effective at extracting and quantifying the target analytes from both water and fish tissue relative to traditional techniques. Caged and in wild fish exposed to MWWEs from all three municipal treatment plants bio-accumulated detectable levels of several of the target chemicals. All target analytes (except for fluoxetine) were identified in the MWWEs and exposed fish by SPME at low concentrations (ng/L). The presence and concentration of the targeted analytes in both water and wild fish living in the Grand River watershed varied with season and proximity to the wastewater outfalls. Results demonstrate that properly applied SPME can detect and quantify selected contaminants in fish tissues, surface water, and wastewater effluents. In vivo SPME allows for non-lethal sampling of fish, which creates the opportunity for monitoring contaminant exposure in receiving environments influenced by MWWEs or non-point-source runoff while minimizing the impact on the organisms.

The objective of the present work was systematic investigation of water-based headspace single-drop microextraction (SDME) technique, its conjunction with capillary electrophoresis, and application for the analysis of volatile inorganic compounds (cyanide and ammonium) in biomedical and environmental samples. Theoretically evaluated and experimentally confirmed that the manipulation in the volatility of the analyte by its chemical modification in the sample and/or in the acceptor phase is the most effective way to enhance the extraction performance in headspace SDME. Maximum extraction efficiency for cyanide was observed in the pH range 4.5–7.5, where cyanide anion is completely transferred into volatile HCN. Complete cyanide recoveries (≥96%) from metal-cyanide complexes were obtained by using two ligand-exchange reagents (ethylenediamine and dithizone). Maximum extraction efficiency was observed by the extraction of ammonia from alkaline samples (pH≥11) with neutral or slightly acidic acceptor phase (pH 3-7). Compared to existing methods water-based headspace SDME is significantly faster and simpler. In addition, proposed technique does not require any sample pre-treatment (deproteinization, acidic/alkaline distillation, etc.) and thus is much less susceptible to interferences. Finally, it offers possibility to choice of a wider variety of solvents and, consequently, enhances the range of extractable analytes as well as the range of analytical methods that can be coupled... [to full text] / Daktaro disertacijoje nuodugniai ištirtas mikroekstrakcijos iš viršerdvės vandens lašu metodas, apjungtas su kapiliarine elektroforeze bei pritaikytas lakių neorganinių junginių (cianido ir amonio) koncentravimui ir nustatymui biomedicininiuose ir aplinkos objektuose. Teoriniais skaičiavimais parodyta ir eksperimentiškai patvirtinta, kad efektyviausias būdas mikroekstrakcijos iš viršerdvės efektyvumui pagerinti – analitės lakumo didinimas chemiškai modifikuojant ją prieš ekstrakciją ir/arba jos lakumo mažinimas modifikuojant ją akceptorinėje fazėje. Maksimalus cianido mikroekstrakcijos efektyvumas pasiekiamas pH srityje 4,5- 7,5, kur cianidas kiekybiškai pervedamas į lakų HCN. Ištyrus cianido mikroekstrakciją tirpiklio lašu iš metalų cianidinių kompleksų tirpalų nustatyta, kad kiekybiškas silpnai surišto cianido suardymas (cianido išgavos siekia ≥96%) pasiekiamas panaudojus ligandų mainus etilendiamino ir ditizono mišiniu. Maksimalus amonio mikroekstrakcijos efektyvumas pasiekiamas ekstrahuojant jį iš pašarmintų mėginių (pH≥11) akceptorine faze, kurios pH 3-7. Lyginant su standartiniais metodais, siūlomas metodas yra greitesnis ir paprastesnis, visiškai eliminuojama mėginio matricos įtaka, nereikalingos jokios drastiškos (deproteinizacija, veikimas rūgštimis/šarmais, distiliacija ir pan.) manipuliacijos su mėginiu, todėl išvengiama mėginio matricos įtakos. Mikroekstrakcija iš viršerdvės vandens lašu praplečia mikroekstrakcijos metodų taikymo sritis: atveriama galimybė labai... [toliau žr. visą tekstą]

The aim of this work was to investigate and apply new DLLME systems coupled with LA-ICP-MS and ultra-performance liquid chromatography (UPLC) techniques for the preconcentration and determination of Cr(VI), Co(II), Cu(II) ir Ni(II) ions. / Šioje daktaro disertacijoje apibendrintų mokslinių tyrimų tikslas – ištirti ir pritaikyti naujus Cr(VI), Co(II), Cu(II) ir Ni(II) koncentravimo ir nustatymo metodus apjungiant dispersinę skystafazę mikroekstrakciją (DSME) su lazerinio išgarinimo induktyviai sužadintos plazmos masių spektrometrijos (LA-ICP-MS) bei ultraefektyviosios skysčių chromatografijos (UESCh) metodais.

Šioje daktaro disertacijoje apibendrintų mokslinių tyrimų tikslas – ištirti ir pritaikyti naujus Cr(VI), Co(II), Cu(II) ir Ni(II) koncentravimo ir nustatymo metodus apjungiant dispersinę skystafazę mikroekstrakciją (DSME) su lazerinio išgarinimo induktyviai sužadintos plazmos masių spektrometrijos (LA-ICP-MS) bei ultraefektyviosios skysčių chromatografijos (UESCh) metodais. / The aim of this work was to investigate and apply new DLLME systems coupled with LA-ICP-MS and ultra-performance liquid chromatography (UPLC) techniques for the preconcentration and determination of Cr(VI), Co(II), Cu(II) ir Ni(II) ions.

This dissertation will focus on the extraction of volatile organic compounds associated with gunshot residue from articles of clothing, followed by analysis with mass spectrometry. During the discharge of a weapon, a cloud of volatile organic gunshot residue (OGSR) is dispersed around a firearm. This will create a high probability of transfer between the OGSR and the clothing of individuals who are near a discharged weapon. The first part of this dissertation will be the development of a method for removal of volatile OGSR from articles of clothing. Extraction of OGSR will be completed by solid phase microextraction (SPME), followed by separation and analysis by gas chromatography-mass spectrometry (GC/MS). Many parameters will require optimization for proper extraction of OGSR from articles of clothing. Following development of a SPME procedure, figures of merit were determined such as linearity and limits of detection/quantification, obtaining levels of detection of 0.206 ng/cm2 on a 100 cm2 cotton cloth. Applications of this extraction method were investigated including the determination of the distance OGSR travels from a discharged weapon and the extraction of OGSR with different clothing materials by SPME. The second part of this dissertation will focus on the development of an on-line solvent extraction method for removal of OGSR from articles of clothing, followed by analysis with paper spray mass spectrometry. Issues using SPME of certain types of clothing materials required the development of an alternative method for removal of OGSR from articles of clothing. Use of an on-line solvent extraction technique of OGSR from articles of clothing followed by analysis with paper spray mass spectrometry allowed for detection of OGSR at comparable levels to a headspace SPME procedure. Use of paper spray with an ion trap mass spectrometer permitted the soft ionization of OGSR compounds followed by tandem mass spectrometry to obtain structural information. Extraction of OGSR from articles of clothing has potential to determine if an individual was present during the discharge of a firearm. Extraction of OGSR from articles of clothing will provide an alternative to traditional methods of gunshot residue analysis currently in use.

Sample preparation has a critical role as a first step in analytical processes, especially in bioanalysis and environmental analysis. A good sample preparation technique should be robust and stable, regardless of the sample matrix. The aim of this thesis is to design and synthesize molecularly imprinted polymers that can be used in various sample preparation techniques, such as on-line MEPS, on-line SPE and on-line monolithic pre-columns used for the extraction of drugs, hormones, and cancer biomarkers from human plasma and urine samples. Additional aim was to provide full automation, on-line coupling, short sample preparation time and high-throughput. In this thesis MIP in MEPS was used on-line with liquid chromatography-tandem mass spectrometry (LC/MS/MS) for the determination of sarcosine in human urine and plasma samples. The method was fully automated and the packed sorbent could be used for about hundred extractions. In additional work a coated needle with MIP-Sol-Gel as thin layer was prepared and used for the microextraction of bilirubin from human plasma and urine. Small sample volumes could be handled and the validation of the method showed that the method was robust and selective. In a further work MIP-SPE on-line with HPLC was used for the extraction and determination of dextromethorphan in human plasma samples. MIP-SPE showed a good selectivity and high recovery (87% - 92%). On-line MIP monolithic pre-column was prepared and used in a coupled system for the extraction of tramadol in human plasma and urine samples. The MIP monolithic pre-column showed good selectivity and high extraction recovery was obtained (91-96%). The extraction and analysis of human insulin in plasma and pharmaceutical formulation solutions were carried out using MIP-SPE on-line with HPLC. The validation of the method showed that the method was accurate and robust. / <p>At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 5: Submitted.</p>

Various needle trap devices (NTDs) with different designs for different applications have been developed during the past decade. A theoretical model on the fundamentals of the NTD was recently proposed, which employed the theory of frontal (gas-solid) chromatography to describe the sampling process, where a gaseous sample was continuously introduced into the sorbent bed. In this investigation, different types of sorbent particles with different dimensions were packed into the needle as adsorbents. The effect of particle dimension, which would affect the packing density and consequently the capacity, the extraction efficiency, and desorption efficiency of the NTD were experimentally investigated and the proposed theory was validated. The results demonstrated that NTDs packed with small particles possess higher extraction capacity and efficiency but much higher resistance to flow as well. The higher resistance did not necessarily result in poor desorption efficiency, because desorption efficiency was affected by both the sorbent bed structure and the desorption gas flow. The relationships observed among those physical parameters provide valuable guidance on how to design an NTD with high performance potential for future applications. For particulate sampling, it was found that NTDs packed with different particles presented high collection efficiency of the particulates being investigated, and the collection efficiency was dominated by the pore size and distribution of the sorbent bed packed inside the needle. Collection efficiency also increased with increase in solidity of the sorbent bed; the increase in humidity of the aerosol sample; and the decrease of sampling rate. The results also provide valuable guidance on the optimisation of needle trap for particulate collection.