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A method for traceable protein quantification using isotope dilution ICP-MS and its application on the tau proteinLemke, Nora 19 August 2022 (has links)
In dieser Arbeit wurde ein Verfahren zur rückführbaren Proteinquantifizierung unter Verwendung von Schwefelisotopenverdünnung mit induktiv gekoppelter Plasmamassenspektrometrie (ID-ICP-MS) entwickelt. Die Methode dient zur zuverlässigen Quantifizierung laborinterner Proteinstandards. Sie eignet sich nur zur Analyse reiner Proteine, deren Stöchiometrie bekannt ist, da die Proteinkonzentration aus dem Schwefelgehalt bestimmt wird. Nicht proteingebundener Schwefel wird durch Membranfiltration von der Proteinfraktion abgetrennt und mit ID-ICP-MS quantifiziert. Der Gesamtschwefelgehalt in der Probe wird ebenfalls mittels ID-ICP-MS quantifiziert und um die Menge an ungebundenem Schwefel korrigiert. Die Optimierung der Probenvorbereitung zeigte, dass ein Aufschluss die Unsicherheit des Ergebnisses verbessert.
Für die Methodenentwicklung wurden ein zertifiziertes Rinderserumalbumin-Referenzmaterial (BSA), sowie ein kommerzielles Avidin verwendet. Die Bestimmung der Proteinmassenfraktionen und Unsicherheitsbudgets erfolgte nach Korrektur für den ungebundenen Schwefel (0,4 % für BSA, 30 % für Avidin). Die Methode wurde auf das Tau-Protein angewendet, das ein Biomarker für die sogenannten „Tauopathien“ ist – eine Gruppe neurodegenerativer Krankheiten, die die Alzheimer-Krankheit und die frontotemporale Demenz einschließen. Durch Verwendung eines isotopenangereicherten Spikes, der an das SI-System angebunden ist, wurde die metrologische Rückführbarkeit für den Massenanteil des Tau-Proteins erreicht. Dieser Tau-Standard wurde zur absoluten Quantifizierung toxischer transgener Tau-Spezies in der löslichen Hirnfraktion transgener Mäuse verwendet.
Die entwickelte Methode ist für die rückführbare Quantifizierung von Proteinen zur Verwendung als Standards in der biologischen und medizinischen Forschung anwendbar. Sie zeigte eine ähnliche Präzision wie etablierte Verfahren, erforderte jedoch weniger Probenvorbereitung und keine spezies-spezifischen Standards. / In this work, a method for traceable protein quantification using sulphur isotope dilution inductively coupled plasma mass spectrometry (ID-ICP-MS) was developed. The method is intended for the reliable quantification of in-house protein standards. It is only suited for pure protein formulations for proteins of known stoichiometry because the protein concentration is determined from the sulphur content. Non-protein bound sulphur is separated from the protein fraction by membrane filtration and is quantified by ID-ICP-MS. The total sulphur content in the sample is as well quantified by ID-ICP-MS and corrected for the amount of non-protein bound sulphur. Optimisation of the sample preparation showed that digestion improves the uncertainty of the result.
For method development, a certified reference material bovine serum albumin (BSA) and a commercial avidin were used. The protein mass fractions with full uncertainty budgets were determined after correction for unbound sulphur. The developed procedure was applied to the tau protein, which is a biomarker fort he so-called „tauopathies“ – a group of neurodegenerative diseases including Alzheimer’s disease and Frontotemporal dementia. By employing an isotopically enriched spike, which is linked to the SI system, full metrological traceability was achieved for the tau mass fraction. The mass fraction of (0.328 ± 0.036) g kg-1 for tau was determined by ID-ICP-MS and confirmed by amino acid analysis. This tau standard was used for the absolute quantification of toxic transgenic tau species in the soluble brain fraction of transgenic mice.
The developed method is applicable for the traceable quantification of proteins for use as standards in biological and medical research. The precision of the method was similar to established absolute protein quantification procedures while requiring less sample preparation and no species-specific standards.
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ASSESSING THE ENVIRONMENTAL AND BIOLOGICAL IMPLICATIONS OF VARIOUS ELEMENTS THROUGH ELEMENTAL SPECIATION USING INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRYGRANT, TYRE D. 07 October 2004 (has links)
No description available.
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Chromium, DNA, and Soil Microbial CommunitiesMueller, Sabrina R. 03 April 2006 (has links)
No description available.
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Elemental Speciation Analysis of Arsenic, Selenium and Phosphorus: Exploring Foods and PlantsKubachka, Kevin M. 05 October 2007 (has links)
No description available.
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Small to large molecule speciation: Metallomics approaches stretch the horizonsKroening, Karolin January 2010 (has links)
No description available.
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Elemental speciation and trace metal analysis using chemical separations interfaced to inductively coupled plasma - mass spectrometryDay, Jason A. 11 October 2001 (has links)
No description available.
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Spéciation du mercure dans les produits de la pêche par double dilution isotopique et chromatographie en phase gazeuse couplée à un spectromètre de masse à plasma induit (GC-ICP-MS) / Mercury speciation in seafood by double isotope dilution and gas chromatography inductively coupled plasma mass spectrometry (GC-ICP-MS)Da fonseca Clemens, Stéphanie 15 September 2011 (has links)
Le mercure est un contaminant présent dans l'ensemble des compartiments de l'environnement et l'homme y est directement exposé via l'alimentation. Actuellement, les organismes gouvernementaux évaluent la sécurité des produits alimentaires en se basant essentiellement sur la concentration totale de cet élément. Cependant, la toxicité du mercure dépend, entre autre, de l'espèce absorbée (dont le méthylmercure, sa forme la plus toxique). Par conséquent, l'analyse de spéciation, c'est à dire la détection et quantification des différentes formes chimiques de cet élément, présente un intérêt croissant. Le principal objectif de ce projet a donc été de développer et de valider, sous assurance qualité, une méthode sensible et d'une grande exactitude, basée sur l'utilisation de la dilution isotopique. Elle sera par la suite appliquée comme méthode de référence par l'agence pour l'analyse en spéciation du mercure dans les produits de la pêche afin de permettre une meilleure évaluation des risques encourus par le consommateur. La première partie de ce travail a porté sur l'étude du cycle biogéochimique du mercure et de l'état de l'art des diverses méthodes de préparation de l'échantillon, de séparation et de quantification du Hg dans les matrices biologiques, afin d'émettre des choix analytiques. Ainsi, les principaux composés mercuriels susceptibles d'être retrouvés dans les produits de la pêche (le méthylmercure et le mercure inorganique) ont été déterminés par couplage GC-ICP-MS et une quantification par dilution isotopique. La seconde partie des travaux a été consacrée à l'optimisation de la méthode de préparation des échantillons et de la technique de quantification. Ces travaux sur différents matériaux de référence certifiés ont montré que des modifications de la distribution naturelle de l'échantillon pouvaient survenir dès l'étape d'extraction, préconisant un marquage isotopique avant extraction solide-liquide par digiPREP des espèces mercurielles et dérivation par propylation par le tétrapropylborate de sodium et agitation rotative. Les résultats expérimentaux ont été traités par dilution isotopique simple et multiple. Les teneurs obtenues ont été similaires, pour l'ensemble des matrices analysées, montrant que peu ou pas de transformation inter-espèces surviennent au cours de la procédure analytique. Une quantification par double marquage isotopique et dilution isotopique simple a donc été conservée. L'évaluation des critères analytique a démontré que la méthode est validée pour la spéciation du mercure dans les produits de la pêche, selon les normes françaises AFNOR NF V03-110 de 1998 et de 2010. La dernière partie des travaux a porté sur l'application de la méthode validée à la spéciation du mercure dans des échantillons biologiques réels, ainsi qu'à la participation à plusieurs essais interlaboratoires d'aptitudes organisés par le CSL-FAPAS sur un échantillon de thon en conserve et par l'IRMM sur le matériau IMEP-109 de homard. / Mercury is a contaminant which is found in all compartments of the environment and to which human beings are directly exposed when eating food. Government agencies assess the safety of food products by using total mercury concentrations. However, its toxicity depends on the species absorbed (among which methylmercury is its most toxic form). Therefore, the analysis of speciation, i.e. detection and quantification of different chemical forms of this element, is of high interest. The main objective of this project was to develop and validate, under quality assurance, a sensitive and highly accurate method, based on the use of isotope dilution. This method will then be applied as a reference method by the agency for speciation analysis of mercury in seafood, in order to better assess risks to the consumer. The first part of this work focused on the biogeochemical cycle of mercury and the state of art of the various methods of sample preparation, separation and quantification of Hg in biological matrices in order to make analytical choices. Thus, mercury compounds (methyl mercury and inorganic mercury) were determined by gas chromatography (GC) coupled with an inductively coupled plasma mass spectrometer (ICP-MS) and quantified by isotope dilution. The second part of the work was dedicated to the optimization of the method of sample preparation and the quantification technique. The work was made on different certified reference materials and showed that changes of the natural distribution of the sample could occur during the extraction step. Therefore, isotopic tracers had been added to the sample before this step. Mercury species were extracted by a solid-liquid extraction by using a digiPREP and derivated by propylation using tétrapropylborate the sodium and a rotary agitation. Data were treated by simple and multiple isotope dilution. Achieved concentrations were similar for all analyzed matrices. Results showed that inter-species transformation hardly occurred during the analytical procedure. This was the reason why the use of two isotopic tracers for quantification by simple isotope dilution was kept. To end, the method was validated for the speciation of mercury in seafood, in respect with the French norms AFNOR NF V03-110 of 1998 and 2010. Finally, the work ended with the applicability of the validated method for mercury speciation analysis in real biological samples and our participation in several inter-laboratory proficiency tests organized by the CSL-FAPAS on a sample of tuna and by the IRMM on the material IMEP-109 (lobster).
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[en] STUDIES ON THE ORIGIN AND TRANSFORMATION OF SELENIUM AND ITS CHEMICAL SPECIES ALONG THE PROCESS OF PETROLEUM REFINING / [pt] ESTUDOS SOBRE A ORIGEM E TRANSFORMAÇÃO DE SELÊNIO E DE SUAS ESPÉCIES QUÍMICAS AO LONGO DO PROCESSO DE REFINO DO PETRÓLEOCIBELE MARIA STIVANIN DE ALMEIDA 15 September 2008 (has links)
[pt] Diferentes métodos espectrométricos de análise, incluindo
ICP OES, ICP-DRCMS e Q-ICPMS com técnicas hifenadas
(geração de hidreto, vaporização eletrotérmica ou
cromatografia de íons), foram aplicados na caracterização
química de 16 óleos e 41 amostras de efluentes aquosos de
uma refinaria de petróleo. O objetivo específico
deste estudo foi o de entender o comportamento do selênio
(Se) e de suas espécies químicas ao longo do processo de
geração e tratamento dos efluentes desta unidade
industrial. A caracterização química multielementar das
amostras por ICP-MS revelou uma composição muito complexa
da maioria deles, com altas salinidades e potenciais
interferentes espectrais e não espectrais presentes. Por
isso, foi necessária uma reavaliação crítica das técnicas
analíticas para a determinação de Se e de suas
espécies. As técnicas de ICP-DRC-MS, utilizando CH4 como
gás de reação, e de ETVICPMS mostraram o seus potencial
para a determinação de Se com melhores limites
de detecção (cerca de 0,05 ug L-1 para ambas), mas também
as suas limitações na análise de efluentes com altas
salinidades. Nas 16 amostras de petróleo analisadas,
verificou-se uma grande variabilidade nas concentrações de
Se total, cobrindo uma faixa de < 10 ug kg-1 até 960 ug kg-
1, a qual poderia explicar também a carga muito
variável deste elemento nos efluentes das diferentes
unidades de tratamento. As maiores concentrações de Se
total foram encontradas nas águas ácidas, com
concentrações de até 1714 ug L-1. Confirmou-se a
predominância de SeCN - na maioria das amostras analisadas,
mas observaram-se também outras espécies com tempos de
retenção diferentes das espécies Se(IV), Se(VI) e SeCN-,
especialmente nos efluentes da estação de tratamento de
despejos industrais (E.T.D.I.). Em amostras ácidas,
identificou-se Se coloidal (Seº) formado pela decomposição
de SeCN-, ou de outras espécies pouco estáveis nestas
condições. Experiências de bancada com soluções de
SeCN- apoiaram esta hipótese. Foi constatada, que o perfil
de especiação de amostras coletadas num mesmo local de
processamento, mas em épocas diferentes, pode variar
significativamente, o que torna difícil a comparação de
dados obtidos neste trabalho com os de outros autores. / [en] Different spectrometric methods of analysis, including ICP
OES, ICP-DRC-MS and
Q-ICP-MS, the latter hyphenated to hydride generation,
eletrothermal vaporization or ion
chromatography have been appliesd to the chemical
characterization of 16 crude oils
and 41 effluents samples from a petroleum refinery. The
specific objective of this study
was to get information on the behavior of selenium (Se) and
its species along the
different processes of generation and treatment of the
effluents.Multielemental
characterization of effluents by ICP-MS revealed a complex
composition of most of them,
with high salinity and potential spectral and non spectral
interferents present. For this
reason, a critical reassessment of the analytical
techniques for the determination of total
Se and its species was necessary. DRC-ICP-MS and ETV-ICPMS,
using CH4 as cell
reaction gas, showed their potential for the determination
of Se with better detection
limits (about 0,05 ug L-1), but also their limitations for
the analysis of effluents with high
salinity. A large variability in the concentration of Se
was observed in the 16 analysed
crude oil samples (< 10 ug kg-1 Se until up to 960 ug kg-1),
which may explain also the
varying concentrations measured in the effluents. Highest
concentrations of selenium
were measured in samples from the treatment unit for acid
waters (up to 1.714 ug L-1).
The predominance of selenocyanate (SeCN-1) was confirmed in
most of the effluent
samples analysed, but also several other species with
retention times different from
Se(IV), Se(VI) e SeCN - were observed, especially in samples
from the treatment plant.
Colloidal Se (Seº) was identified in acid waters, probable
formed by decomposition of
SeCN - or other unstable species under these conditions.
Laboratory experiments with
selenocyanate solutions confirmed this hypothesis. The
speciation profile of samples
collected at the same point, but at different time
intervals, showed significant variations,
not allowing easy comparison of the results obtained in
this work with those of other
authors.
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Desenvolvimento de métodos rápidos de preparo de amostras para especiação química de arsênio em alimentos por LC-ICP-MS e avaliação das concentrações e do metabolismo em arroz / Development of rapid methods for sample preparation and chemical speciation of arsenic in foods by LC-ICP-MS and evaluation of metabolism and concentration in riceBatista, Bruno Lemos 27 June 2012 (has links)
O arsênio é um dos mais tóxicos elementos químicos e reconhecidamente carcinogênico. Ele pode ser encontrado em alimentos basicamente em 5 formas: arsenobetaína (AsB), dimetil-arsênio (DMA), monometil-arsênio (MMA), arsenato (As5+) e arsenito (As3+), sendo estas duas últimas (As-i) as mais tóxicas. Assim, é de suma importância a utilização da especiação química de As para avaliação dos reais riscos associados à ingestão de alimentos contaminados. Neste sentido, o presente trabalho teve como objetivos o desenvolvimento de um método para separação das espécies de As por LC e detecção por ICP-MS; extrações quantitativas das espécies de As de tecidos animais e em grãos de arroz; aplicação dos métodos em amostras de alimentos consumidos no Brasil; e estudo do metabolismo do As em diferentes cultivares de arroz. O método desenvolvido para a extração das espécies de As em tecidos animais (ovo, músculos de ave, peixe e boi, etc.) utilizou apenas metanol (10%v/v) e ácido nítrico (2%v/v) como extratores e 2 minutos de sonicação, mostrando recuperação quantitativa do analito (>88%, n=3) pela análise dos materiais de referência (CE278, DOLT-3, DORM-3 e SRM NIST 1577). No entanto, para a análise de arroz, apenas ácido nítrico 2%v/v foi utilizado como extrator, possibilitando uma recuperação quantitativa (>94%, n=6), quando da análise do material de referência (NIST Rice Flour 1568a). Para a separação cromatográfica foram avaliadas diversas colunas, das quais a troca aniônica (Hamilton PRP-X100®) foi utilizada em todos os experimentos. A aplicação dos métodos na análise de alimentos diversos consumidos no Brasil mostrou uma grande variação nas concentrações das diferentes espécies do arsênio em músculos, ovos e, especialmente, no arroz. Devido as altas concentrações de As encontradas em amostras de arroz comercializadas no Brasil (em vários casos com predominância das espécies mais tóxicas, As3+ e As5+) e ao grande consumo deste alimento no país e no mundo, foi também realizado um estudo de metabolismo do As em 6 diferentes cultivares. O foco deste estudo foi a síntese de fitoquelatinas (PCs), compostos não peptídicos produzidos por plantas expostas a elementos tóxicos, e sua influência no fator de transferência (TF) do As solo-grãos. O TF do As, assim como a concentração das PCs, variaram em relação aos cultivares (genótipos) estudados. Além disso, as PCs mostraram ter uma forte correlação positiva entre si e com a concentração de As-i nos grãos, bem como uma correlação negativa do TF do As raízes-grãos. Portanto, os métodos desenvolvidos demonstraram fácil aplicação em rotina para avaliação toxicológica dos alimentos em relação às espécies de As e, finalmente, o estudo de metabolismo do As pela planta do arroz pode contribuir para escolha de cultivares que o absorvam menos, reduzindo sua ingestão frente ao consumo de arroz. / Arsenic is one of the most toxic chemicals and known carcinogen. It can be found in food basically in 5 different forms: arsenobetaine (AsB), dimethyl arsenic (DMA), monomethyl arsenic (MMA), arsenate (As5+) and arsenite (As3+), the latter two forms (i-As) are the most toxic. Thus, it is of extreme importance the use of chemical speciation for the evaluation of the real risks associated to arsenic intake from contaminated food. In this sense, this study aimed develop a simple method for separation of arsenic species by LC and detection by ICP-MS, quantitative extraction of arsenic species from animal tissues and rice grains, the application of the proposed method in the analysis of food samples commercialized in Brazilian markets, and the study of arsenic metabolism in different rice cultivars. The method developed for the extraction of arsenic species in animal tissues (egg, muscle of chicken, fish and cattle, etc.) used only methanol (10%v/v) and nitric acid (2%v/v) as extractant and 2 minutes of sonication, showing quantitative recovery of the analyte (>88%, n=3) when analyzing reference materials (CE278, DOLT-3, DORM-3 e SRM NIST 1577). However, for the analysis of rice grains, only nitric acid (2%v/v) was used as extractant, allowing a quantitative recovery (>94%, n=6), when analyzing the reference material (NIST Rice Flour 1568a). For the chromatographic separation several columns were evaluated and an anion exchange column (Hamilton PRP X-100) was used in all experiments. The analysis of several foods consumed in Brazil, showed a wide variation in the concentrations of different arsenic species in muscle, eggs, and especially in rice. Due to the high concentrations of arsenic found in rice samples (in several cases with predominance of more toxic species, As3+ and As5+) and the large consumption of this food in the country and abroad, it was also carried out a study on arsenic metabolism in 6 different rice cultivars. The focus of this study was the synthesis of phytochelatins (PCs), non-peptide compounds produced by plants exposed to toxic elements, and its influence on the transfer factor (TF) soil-grains. The TF of arsenic as well as the concentration of PCs varied in relation to the cultivars (genotype) studied. Furthermore, the PCs have shown a strong positive correlation between themselves and with the concentration of i-As in the grains, and a negative correlation with TF roots-grains. Therefore, the developed method demonstrated feasibility for routine use in toxicological studies of arsenic species in food samples and, finally, the study of arsenic metabolism in rice plant can contribute to the selection of cultivars that absorb less arsenic, thereby reducing the intake of this toxic element by rice consumption.
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Desenvolvimento de método para determinação de Ag, As, Cd, Co, Mn, Ni, Pb e Se em sangue por espectrometria de massas com fonte de plasma acoplado indutivamente (ICP-MS) utilizando diluição das amostras em meio alcalino / Development of a high-throughput method for assessment of Ag, As, Cd, Co, Mn, Ni, Pb and Se in blood samples by inductively coupled plasma mass spectrometry (ICP-MS)Nunes, Juliana Andrade 07 August 2009 (has links)
A técnica analítica mais utilizada para o monitoramento de exposição a metais tóxicos ou para avaliação de deficiência a elementos essenciais é a espectrometria de absorção atômica chama (FAAS) ou com forno de grafite (GF AAS). Entretanto, cada vez mais os laboratórios de pesquisa na área clínica estão mudando seus métodos de análise, baseados nestas técnicas, para a utilização da espectrometria de massas com plasma acoplado (ICP-MS). Isso vem acontecendo porque o ICP-MS permite a determinação de elementos químicos, em diversas matrizes, numa ampla faixa de concentração (ng L-1 a mg L-1), além de possibilitar alta rapidez de análise, capacidade multielementar e limites de detecção menores que outras técnicas analíticas. Uma das principais características do método a ser utilizado para a análise de elementos químicos em rotina por ICP-MS é que ele seja rápido, com o mínimo de manipulação da amostra. Neste sentido, métodos que propõem a análise direta de amostra são mais atrativos. Todavia, ainda é limitado o número de métodos que propõem análise direta de fluidos biológicos por ICP-MS. Neste sentido, o presente trabalho teve como objetivo o desenvolvimento de um método para análise direta de sangue por ICP-MS para determinação de Ag, As, Cd, Co, Mn, Ni, Pb e Se. Para isso, amostras de sangue (200 µL) foram misturadas com 500 µL de hidróxido de tetrametilamônio (TMAH) (10% v/v) e incubadas por 10 minutos. Posteriormente, a solução resultante foi diluída para 10 mL com uma solução contendo 0,05% m/v EDTA; 0,005% v/v Triton® X-100. Em seguida, as amostras foram analisadas diretamente por ICP-MS (ELAN DRC II). Ródio (Rh) foi usado como padrão interno e a calibração das amostras foi feita por meio de ajuste de matriz com sangue base ovino. Os limites de detecção (LD) do método foram de 0,008; 0,02; 0,004; 0,009; 0,003; 0,09; 0,04; 0,1 µg L-1 para Ag, As, Cd, Co, Mn, Ni, Pb and Se, respectivamente. A validação dos resultados foi realizada com análise de um material de referência de sangue do Programa de Proficiência do Institut National de Santé Publique du Quebec, no Canadá. Validação adicional foi obtida pela comparação dos resultados obtidos pela análise de 20 amostras de sangue pelo método proposto e pela técnica de GF AAS. O método foi também comparado a outros dois existentes na literatura e comumente utilizados em laboratórios dos Estados Unidos e Suécia, apresentando limites de detecção comparáveis ou melhores e melhores exatidão e precisão. / The most used analytical technique for monitoring the exposure to toxic metals or for the assessment of the deficiency of essentials elements is the atomic absorption spectrometry with flame (FAAS) or graphite furnace (GF AAS). However, more and more clinical laboratories are changing their methods of analysis, based on this technique, to methods using inductively coupled plasma-mass spectrometry (ICP-MS). It occurs because ICP-MS allows the determination of chemical elements in various types of samples, at concentrations in a wide linear range (ng L-1 to mg L-1), providing high-throughput analysis with multielemental capability with lower detection limits. However, for routine porpuses the method of choice must be fast with minimal sample manipulation.On the other hand, the number of methods proposing direct introduction of biological fluids to the ICP-MS are still limited. This work aimed the development of a method for the direct analysis of blood samples by ICP-MS for the determination of Ag, As, Cd, Co, Mn, Ni, Pb and Se. For this, blood samples (200 L) were mixed with 500 L of tetramethylammonium hydroxide (TMAH) (10% v/v) and left at room temperature during 10 minutes. Subsequently, the resulting solution was diluted to 10 mL with a solution containing 0.05% m/v EDTA + 0005% v / v Triton ® X-100. Thus the samples were analyzed directly by ICP-MS (ELAN DRC II). Rhodium (Rh) was used as internal standard with matrix matching calibration. The method detection limits were: 0.008, 0.02, 0.004, 0.009, 0.003, 0.09, 0.04, 0.1 µg L-1 for Ag, As, Cd, Co, Mn, Ni , Pb, and Se respectively. Method validation was acquired with the analysis of blood reference material provided by the Institut National de Santé Publique du Quebec, Canada. Furthermore, for additional validation 20 ordinary blood samples were analyzed by the proposed method and by GF AAS. The method was also compared with two existing methods in the literature and commonly used in laboratories in the United States and Sweden where comparable or better detection limits and better accuracy and precision were obtained.
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