Orientador: Susanne Rath / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Química / Made available in DSpace on 2018-08-16T00:51:54Z (GMT). No. of bitstreams: 1 Barros_LeonardoAugustode_M.pdf: 2516979 bytes, checksum: 9e6340ca4d81c25d9929cae4417e6fbf (MD5) Previous issue date: 2010 / Resumo: Esse trabalho teve como objetivo principal sintetizar um polímero de impressão molecular (MIP) para ser empregado em processo de extração em fase sólida (SPE), visando a determinação de resíduos de fenitrotiona (FNT) em tomates. Os reagentes da síntese foram selecionados a partir de estudos de modelagem molecular, usando para tanto o programa computacional Gaussian 03. As energias eletrônicas de ligação para a interação entre o monômero funcional e a FNT, no vácuo e no solvente, foram calculadas através do método DFT, no nível B3LYP e conjunto de base 6-31G(d). Os reagentes de síntese foram: FNT (molde), ácido metacrílico (monômero funcional), etilenoglicol dimetacrilato (reagente de ligação cruzada), AIBN (iniciador radicalar) e tolueno (solvente porogênico). Também foi sintetizado um polímero não-impresso (NIP). Por meio de estudos de adsorção foi avaliado o meio de melhor reconhecimento molecular. Foram construídas as isotermas de adsorção para cada um dos polímeros impresso e não impresso e foi avaliada a seletividade do MIP frente a análogos da FNT. Os polímeros foram caracterizados por infravermelho com transformada de Fourier, ressonância magnética nuclear de C, microscopia de varredura eletrônica e porosimetria de sorção de nitrogênio (BET). O MIP foi empregado como fase estacionária em SPE. Foi desenvolvido e validado um método para a determinação de FNT em tomates, usando a cromatografia líquida de alta eficiência. A eficiência de extração foi de 96%. A faixa linear foi de 130 a 2000 ng g, com uma linearidade superior a 0,99. A precisão intra-ensaio e inter-ensaio foram inferiores a 7,0% e 8,1%, respectivamente (níveis de fortificação 250, 500 e 1000 ng g). A exatidão foi superior a 89% no nível de fortificação em torno do limite máximo de resíduo de 500 ng g / Abstract: This work aimed the synthesis of a molecularly imprinted polymer (MIP) to be employed in process of solid phase extraction (SPE), for the determination of residues of fenitrothion (FNT) in tomatoes. The synthesis reagents were selected from molecular modeling, using the Gaussian 03 software. The electronic binding energies for the interaction between the functional monomer and the FNT, in vacuum and in solvent, were calculated by the DFT method in B3LYP level and 6-31G(d) basis set. The reagents of the synthesis were: FNT (template), methacrylic acid (functional monomer), ethyleneglycol dimethacrylate (cross-linker), AIBN (initiator) and toluene (porogenic solvent). Also, was synthesized a non-imprinted polymer. Through batch rebinding studies were evaluated the medium of the best molecular recognition. The adsorption isotherms for each imprinted and non-imprinted polymer were constructed and the selectivity of the MIP in relation to FNT analogues evaluated. The polymers were characterized by Fourier transform infrared, C nuclear magnetic resonance, scanning electron microscopy and nitrogen sorption porosimetry (BET). The MIP was employed as stationary phase in SPE. A method for the determination of FNT in tomatoes was developed and validated, using high performance liquid chromatography. The extraction efficiency was 96%. The linear range was 130 to 2000 ng g, with a linearity greater than 0.99. The intra-day and inter-day precision were lower than 7.0% and 8.1%, respectively (fortification levels 250, 500 e 1000 ng g). The accuracy was higher than 89% for a concentration level around the maximum residue limit of 500 ng g / Mestrado / Quimica Analitica / Mestre em Química

Les travaux de thèse ont porté sur la synthèse d’un MIP (polymère à empreintes moléculaires) spécifique d’un fongicide se trouvant dans la majorité des vins français : l’iprodione. Pour extraire l’iprodione à partir du vin, un challenge important se présentait : le milieu hydroalcoolique est un solvant dipolaire alors que l’interaction du MIP avec l’iprodione se base sur des interactions dipôle-dipôle. Les premières études d’extraction de l’iprodione ont été faites sur un MIP obtenu par polymérisation en masse à partir du méthacrylamide et de l'éthylène glycol diméthacrylate (EGDMA). Le MIP était plus efficace que le NIP (polymère non imprimé) dans des solutions hydroalcooliques ce qui vérifie que l’impression moléculaire était réussie. Un plan d’expériences 23 a été appliqué pour étudier l’influence de 3 facteurs de synthèse de MIP (la méthode de polymérisation, la nature de l'agent réticulant et le type de monomère fonctionnel) sur les propriétés de reconnaissance des polymères vis-à-vis de l’iprodione. 8 MIP et 8 NIP ont été ainsi synthétisés. Les isothermes d'adsorption de l'eau et de l’iprodione par les MIPs et les NIPs ont été déterminées. Des différences significatives entre les polymères ont été mises en évidences impliquant une relation entre l’adsorption de l’eau et l’adsorption de l’iprodione. La formation des empreintes moléculaires au sein des MIP a été démontrée par plusieurs techniques comme la calorimétrie différentielle à balayage et la résonance magnétique nucléaire. Les meilleures propriétés de reconnaissance de l’iprodione sont obtenues avec le MIP synthétisé par précipitation à partir du méthacrylamide comme monomère fonctionnel et de l’EGDMA comme réticulant. Ce MIP a été utilisé en extraction en phase solide (SPE) pour la pré-concentration de l’iprodione dans un vin blanc avec un facteur de pré-concentration égal à 6 et sa sélectivité par rapport à deux fongicides : le pyriméthanil et le procymidone a été démontrée. / The aim of this study was the synthesis of a MIP (molecularly imprinted polymer) specific for a fungicide that is found in the majority of the french wine: iprodione. The challenge for extracting iprodione from wine medium was that the hydoralcoholic solution is a dipolar solvent, whereas the interaction between the MIP and iprodione is based on dipolar interactions. The first extraction study of iprodione was made on a MIP synthesized by bulk polymerization using methacrylamide and ethylene glycol dimethacrylate (EGDMA). The MIP was found to be more efficient than the NIP (non-imprinted polymer) in hydroalcoholic solutions which demonstrates that the molecular imprinting was successful. Then we synthesized 8 MIPs and 8 NIPs following an 23 experimental design in order to study the influence of three synthesis factors (the polymerization method, the nature of the crosslinker and the type of the functional monomer) on the iprodione recognition properties of the polymers. The water and the iprodione adsorption isotherms for MIPs and NIPs were determined. The result showed significant differences between the polymers involving a relationship between the water adsorption and the adsorption of iprodione. The molecular imprinting has been demonstrated by several techniques such as the differential scanning calorimetry and the nuclear magnetic resonance. The best recognition properties of iprodione are obtained with the MIP which was synthesized by precipitation polymerization using methacrylamide as functional momonomer and EGDMA as crosslinker. This MIP was used in solid phase extraction (SPE) for pre-concentration of iprodione in a white wine with a pre-concentration factor of 6. Its selectivity versus two fungicides: procymidone and pyrimethanil has been demonstrated.

Orientadores: Susanne Rath, Rogério Custódio / Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química / Made available in DSpace on 2018-08-27T17:08:24Z (GMT). No. of bitstreams: 1 Barros_LeonardoAugustode_D.pdf: 4314419 bytes, checksum: 93a1b964e0a2949ef6a2379990e2f089 (MD5) Previous issue date: 2014 / Resumo: Esse trabalho teve como objetivo principal otimizar e sintetizar polímeros de impressão molecular (MIP) para serem empregados em processos de extração em fase sólida (SPE), visando a determinação de diuréticos tiazídicos em urina. Cálculos teóricos de modelagem molecular, usando o programa computacional Gaussian 09 e os métodos DFT e PCM, no nível B3LYP e conjunto de base 6-31G(d), foram realizados para selecionar o monômero funcional (MF) e o solvente porogênico mais adequados para serem utilizados na síntese dos MIP. Para o desenvolvimento dos MIP compatíveis com água, foi utilizado hidroclorotiazida, clorotiazida ou hidroflumetiazida como molde, acrilamida como MF, etilenoglicol dimetacrilato como reagente de ligação cruzada (RLC) e tetraidrofurano como solvente porogênico. Foram avaliados alguns parâmetros que afetam a eficiência do polímero de impressão, tais como a quantidade de MF e a natureza do RLC. Foram construídas as isotermas de adsorção para cada um dos polímeros sintetizados e foi avaliada a seletividade dos MIP frente a análogos estruturais dos moldes. Os polímeros foram caracterizados por infravermelho com transformada de Fourier, 13C RMN, microscopia eletrônica de varredura, porosimetria de sorção de nitrogênio e análise termogravimétrica. Os MIP foram empregados como fase estacionária em SPE para a determinação de diuréticos tiazídicos em urina por cromatografia líquida de alta eficiência e os mesmos apresentaram seletividade cruzada em relação aos análogos estruturais / Abstract: This work aimed to optimize and synthesize molecularly imprinted polymers (MIP) to be employed in processes of solid phase extraction (SPE), for the determination of thiazide diuretics in urine. Theoretical calculations of molecular modeling, using the Gaussian 09 software and the density functional theory and PCM methods, at the B3LYP/6-31G(d) level, were performed to select a the most appropriate functional monomer (FM) and porogenic solvent for the synthesis of the molecularly imprinted polymers (MIP). For the development of a water-compatible MIP chlorothiazide, hydrochlorothiazide or hydrfoflumethiazide were used as template, acrylamide as FM, ethyleneglycol dimethacrylate as cross-linker and tetrahydrofuran as porogenic solvent. Parameters that affect thepolymer efficiency, such as the amount of the monomer and nature of the cross-linker were evaluated. The adsorption isotherms for each of the synthesized polymers were constructed and the selectivities of the MIPs in relation to structural analogues of the templates were evaluated. The polymers were characterized by Fourier transform infrared, 13C NMR, scanning electron microscopy, nitrogen sorption porosimetry and thermogravimetric analysis. The MIPs were employed as stationary phase in SPE for the determination of thiazide diuretics in urine by high performance liquid chromatography and they showed cross-selectivity in relation to their structural analogues / Doutorado / Quimica Analitica / Doutor em Ciências

Human exposure to harmful compounds in the environment, from intake via food, occupational exposures or other sources, could have health implications. Exposure to reactive compounds/metabolites can be identified and quantified as hemoglobin (Hb) adducts by mass spectrometry. This thesis aimed at improved synthetic pathways for reference standards, and improved analytical methods for adducts to N-terminal valine in Hb from a range of reactive compounds; isocyanates, aldehydes, methyl vinyl ketone (MVK), and diepoxybutane (DEB). Isocyanates form urea adducts with N-terminal valine by carbamoylation, which are detachable as hydantoins by hydrolysis. A new synthetic pathway for reference standards of adducts from isocyanates and a method for their analysis by liquid chromatography/mass spectrometry (LC/MS) were developed. Aldehydes form reversible imines (Schiff bases) with N-termini in Hb. After stabilisation by reduction and detachment by isothiocyanates using modified Edman methods, these adducts could be analysed by gas chromatography/mass spectrometry (GC/MS) or LC/MS. 5-Hydroxymethylfurfural, its metabolites, and other aldehydes related to exposure via food, were studied with regard to analysis by these methods with synthesised standard references. A considerably improved analytical method for imines was developed. Many of the studied adducts are too short-lived in vivo or in vitro to be used for long-term biomonitoring. However, different approaches for the analysis were evaluated. Through synthesised reference standards, an observed unknown adduct in blood was verified as the adduct from MVK. There exist both natural and anthropogenic sources for MVK. DEB, metabolite of butadiene, forms a cyclic adduct to valine-N. A new approach using hydrazinolysis of protein and enrichment by molecularly imprinted solid-phase extraction was tested on synthesised reference DEB-adduct and gave promising results. Synthesised standards were characterized by NMR, LC/MS and GC/MS. / <p>At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 1: Submitted. Paper 3: Submitted. Paper 4: Submitted.</p>