Gasoline is a complex mixture of hydrocarbons whose detailed study of its chemical profiles is a challenging task. This type of product of great commercial importance has its quality measured in Brazil from classical physical-chemical tests. Although robust, physical-chemical analyses generally require large amounts of assays, solvents, and samples, in addition to not being indicated for the detection of small compositional changes. In this work, NMR and chemometrics were used in the quantitative study of different samples of gasoline with varying ratings of octane and ethanol contents. The results demonstrated the usefulness of NMR spectroscopy both to characterize as well as to distinguish the chemical profiles of regular and premium gasoline. With the application of the ERETIC, the chemical profiles mentioned were quantitatively differentiated and the proportions between hydrocarbons were determined for both types of gasoline. The application of the ERETIC was also successful in the quantitative determination of ethanol contents in regular and premium gasoline. The aforementioned method, which dispenses with the use of quantification standards inserted directly into the sample of interest, was unequivocal in accounting for the volume of ethanol, in addition to showing excellent agreement with the method currently adopted by the Brazilian government. task physicalchemical physical tests robust assays solvents changes work interest government

Coffee is one of the most popular and consumed products in the world, with high nutritional value and economic importance. However, some factors can change the organoleptic properties of a coffee species, without causing significant damage such as loss of important components. The present study evaluated the chemical profile, via nuclear magnetic resonance (NMR), of the main biological properties and substances of the drink, verifying similarities in the composition of different types of arabica coffee made in different conditions, such as the roasting time and temperature. The main components were identified, using information from the literature and a database, and compared with the experimental data of 1D and 2D 1H NMR. The spectral data were analyzed and grouped via principal component analysis (PCA) using the Bruker Amix 3.9.14 software. 1H NMR was able to monitor the roasting process and qualify the intact bean and chemical profile of the coffee according to the roasting conditions. Due to the importance of the monitored components, the coffee species analyzed can be identified, along with the appearance of unwanted or adulterating compounds that are normally added to the product to reduce the cost of commercialization.

Brazilian gasoline type C can be purchased with octane number as the main difference. This quality parameter directly affects the price. Intermediate formulations may not be easily distinguished from conform samples due to similarity in visual appearance and physicochemical properties. The use of anhydrous ethanol as an additive also influences the octane values of the product. In this context, the present study describes the use of 1H nuclear magnetic resonance spectroscopy (1H NMR) associated with chemometrics in the characterization and distinction of gasolines by different octane number. Conform samples of common, premium and blends of common-premium were used. Models of NMR-PCA (principal component analysis) and NMR-SIMCA (soft independent modelling of class analogies) showed a good correlation with the values determined by the standard method. The octane values predicted by the NMR-PLS (partial least squares) model achieved a good correlation root mean square errors of prediction (RMSEP = 0.50), with the values determined by the standard method as well.

Foods with high lipid contents are susceptible to deterioration by oxidative processes that lead to the formation of food rancid. Determining the chemical nature of lipid oxidation products presents a nutritional and health interest due to the possibility of formation of compounds related to the development of degenerative diseases such as Parkinson’s and Alzheimer’s. In this context, the present study describes the use of nuclear magnetic resonance (NMR) spectroscopy and principal component analysis (PCA) to monitor the formation of oxidation products in Brazilian table margarines subjected to the heat treatment at 80, 100, 120, 140, 160 and 180 °C. Lipid profiles were characterized by 1H NMR experiments. Changes due to heat treatment were identified by NMR-PCA models, which indicated triacylglycerol (TAG) as the main descriptor from 160 °C. At this temperature, were identified signals evolution in 1H NMR spectra whose chemical shifts (δ) indicated the formation of aldehydes and dienes. The results were useful to highlight the need for efficient methods to maintain the oxidative stability of this type of food widely used in industrial and home cooking.

Chalcone-quinolinone hybrid compounds, as well as the synthesis of such compounds, have few reports in the literature. Such compounds may be quite useful in therapeutics, since various biological activities are reported for both chalcones and quinolinones. In the present work, several novel chalcone-quinolinone compounds have been synthesized. The reaction conditions developed allowed to obtain the compounds in a single step of synthesis from the chalcones. The products precipitated pure and were isolated by filtration. The yields of such reactions, from 45 to 94%, were promising. The product structures were confirmed by nuclear magnetic resonance (NMR) and electrospray ionization mass spectrometry (ESI-MS) techniques. Their antitumor activities were evaluated in HCT-116 (colon) cell lines by the 3-(4,5-dimethyl-2-thiazole)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) test. The half maximal inhibitory concentration (IC50) values obtained for the most active chalcones were between 2.9 and 7.5 and for active quinolinone was 19.3 mg L-1. The antitumor activities results suggest that the class of compounds studied has potential for use in cancer research.

This paper reports an optimized, simple, fast and inexpensive method for hydroxyapatite (HA) nanoparticle synthesis. Through a multivariate statistical analysis using a factorial design with 23 resolution, an empirical model was developed which allows control of the shape and size of the HA nanoparticles. This model was used to synthesize HA nanoparticles with sizes between 8 and 600 nm, formed by oriented attachment growth mechanism. The structure was confirmed by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images, which also showed that HA nanoparticles had well-defined nanorod forms and narrow size distributions. It was observed that the model is statistically significant and the main parameter for the growth of crystals in the hydrothermal process was temperature.

This work describes the potential of chemometric analyses applied to 1H high-resolution magic angle spinning nuclear magnetic resonance (1H HR-MAS NMR) data for the chemotaxonomic investigation of Hancornia speciosa (Apocynaceae) varieties. This plant, popularly known as mangaba, has a complex morphological differentiation and thus chemical analyses can be used for their taxonomic classification. In comparison to traditional techniques, 1H HR-MAS NMR allied with chemometrics provided a simple and low cost method for chemotaxonomy. Leaves of four varieties of H. speciosa from a common garden experiment was studied and demonstrated that H. speciosa var. speciosa differs from others due to its specific metabolic profile, and var. pubescens was discriminated based on its high phenolic compound content. The distinction between the latter variety and gardineri is important once it allows for the selection of samples with greater commercial value, once they produce the largest and heaviest fruits.

In this paper we investigated the ability of the GIAO-mPW1PW91/6-31G(d)//mPW1PW91/6-31G(d) level of theory to predict the 13C nuclear magnetic resonance (NMR) chemical shifts of the 2’-hydroxy-3,4,5-trimethoxy-chalcone molecule. Two different approaches were used. First: the absolute shieldings σ for all carbon atoms in each geometrically optimized conformers of the 2’-hydroxy-3,4,5-trimethoxy-chalcone molecule were calculated at the GIAO-mPW1PW91/6-31G(d)//mPW1PW91/6-31G(d) level of theory. This approach is further used to generate weighted average values for each atom considering the previously obtained conformational distribution. Second: only the σ for the lowest energetic conformer will be taken to account. The robustness of the method was evaluated for two other chalcones: (E)-1-(4-hydroxy-3-methoxyphenyl)-3-(3,5-di-tert-butyl-4-hydroxyphenyl)prop-2-en-1-one and (E)-1-(4-aminophenyl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one, corroborating the ability of the method in chemical shift prevision. Although, both approaches were able to reproduce the chemical shifts of the 2’-hydroxy-3,4,5-trimethoxy-chalcone, significant differences in the calculated values for C-4 and methoxy carbons were observed. The best results were obtained using the second approach (II).

A furanoditerpene-enriched fraction was obtained from the fruits of Pterodon emarginatus and submitted to semipreparative high performance liquid chromatography (HPLC). Two new furanoditerpenes, 6α,19β-diacetoxy-7β,14β-dihydroxyvouacapan and 6α-acetoxy-7β,14β-dihydroxyvouacapan, in addition to the known compound methyl 6α-acetoxy-7β-hydroxyvouacapan-17β-oate were obtained. Compound structures were determined by 1D and 2D nuclear magnetic resonance (NMR) experiments and electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS). The major compound methyl 6α-acetoxy-7β-hydroxyvouacapan-17β-oate was evaluated against promastigote forms of Leishmania amazonensis and L. braziliensis, presenting the concentration which causes lysis on 50% of parasites IC50 < 30 µg mL-1.

Illicit substances found in blotter papers and tablets seized by police are traditionally identified and characterized from extracts of these materials. However, the procedures involved in extraction stages can result in artifacts and even contamination of the samples to be analyzed. On the other hand, high-resolution magic angle spinning nuclear magnetic resonance (HR-MAS NMR) is a technique that requires no pretreatment steps, enabling direct analysis of the material, including the analysis of new illegal synthetic psychoactive substances. This study presents and discusses applications of the HR-MAS NMR in the analysis of tablets and blotter papers seized. Additional analysis in solution of the extracts of these materials was performed to compare the obtained spectral resolution signals. The results demonstrated that the HR-MAS NMR allowed the rapid identification of 3,4-methylenedioxy-N-methylcathinone (methylone), 4-methylmethcathinone (mephedrone), 2,5-dimethoxy-4-bromoamphetamine (DOB) and 2-(4-bromo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine (25B-NBOMe) in samples of tablets and blotter papers seized in Goiás State, Brazil.

The study of the Typha species has gained attention in tropical areas due to their rapid growth, nutrient release, and contribution to detritus in lakes. Analysis of the degradation of Typha angustifolia has shown that the first stage of decomposition is marked primarily by the release of soluble compounds, indicating that microorganisms have a minor influence at this stage. In subsequent stages, microorganisms act by degrading and consuming phenolic compounds and phosphorus. The remaining compounds form humic substances and are retained in the detritus. Thus, microorganisms significantly degrade organic matter, resulting in a two-fold increase in decomposition. Different forms of phosphorus could be detected in the remaining mass by 31P NMR (nuclear magnetic resonance). By comparing the 31P NMR data between the samples with and without the antibiotic, we can better understand the slow decomposition process of Typha angustifolia.

Ressonância magnética nuclear de ¹H de alta resolução com giro no ângulo mágico (HR-MAS NMR) é uma técnica empregada na avaliação de células e tecidos intactos. Entretanto, parâmetros bem estabelecidos de NMR são cruciais para a obtenção de resultados confiáveis. A fim de discutir as principais etapas envolvidas na otimização das análises de HR-MAS NMR, este artigo avaliou diferentes sequências de pulsos e parâmetros de NMR usando células de sarcoma 180 (S180). O completo assinalamento dos metabólitos de S180 é também apresentado para auxiliar estudos futuros.

High resolution magic angle spinning ¹H nuclear magnetic resonance spectroscopy (HR-MAS NMR) is a useful technique for evaluation of intact cells and tissues. However, optimal NMR parameters are crucial in obtaining reliable results. To identify the key steps for the optimization of HR-MAS NMR parameters, we assessed different pulse sequences and NMR parameters using sarcoma 180 (S180) cells. A complete assignment of the metabolites of S180 is given to assist future studies.

A bactéria Xanthomonas axonopodis (Xac) causa uma das mais temidas e incuráveis doenças da citricultura: o cancro cítrico. Para compreender o mecanismo de resposta das laranjeiras quando atacadas pela Xac, folhas e frutos de Citrus sinensis foram diretamente avaliados por espectroscopia de RMN HRMAS (ressonância magnética nuclear de alta resolução com giro no ângulo mágico). Esta técnica permite a análise de amostras sem as laboriosas etapas de pré-tratamento, acessando as informações importantes sobre a sua composição química. As folhas de laranjeira e cascas do fruto investigadas neste estudo demonstraram as alterações bioquímicas causadas pela Xac. Auxiliado pelas análises quimiométricas, os resultados de RMN HRMAS apresentaram alterações relevantes no conteúdo de aminoácidos, carboidratos, ácidos orgânicos e terpenóides.

Xanthomonas axonopodis (Xac) bacterium causes one of the most feared and untreatable diseases in citriculture: citrus canker. To understand the response mechanisms of orange trees when attacked by Xac, leaves and fruits of Citrus sinensis were directly evaluated by HRMAS NMR (high resolution magic angle spinning nuclear magnetic resonance) spectroscopy. This technique allows the analysis of samples without laborious pre-treatments and also allows access to important information about chemical composition of samples. The orange tree leaves and fruit peels investigated in this study demonstrated the biochemical changes caused by Xac. Aided by chemometric analysis, the HRMAS NMR results show relevant changes in amino acids, carbohydrates, organic acids and terpenoids content.

Várias tecnologias para o desenvolvimento de novas cultivares de cana-de-açúcar têm focado, principalmente, no aumento da produtividade e maior resistência à doença. Cultivares de cana-de-açúcar são, geralmente, identificadas pela organografia das folhas e caule, análise de peroxidase e atividade da isoenzima esterase, proteínas solúveis totais e teor de sólidos solúveis. A ressonância magnética nuclear (RMN) associada às análises quimiométricas provou ser uma técnica valiosa para avaliação de plantas. Assim, este trabalho descreve o potencial das análises quimiométricas aplicadas a RMN de ¹H de alta resolução com giro no ângulo mágico (HRMAS) e em solução para investigação de cultivares de cana-de-açúcar. Para esta proposta, folhas de oito diferentes cultivares de cana-de-açúcar foram analisadas por espectroscopia de RMN de ¹H aliada à quimiometria. As técnicas empregadas apresentaram-se como ferramentas úteis para a distinção e classificação das diferentes cultivares, bem como para acessar as diferenças na composição química das cultivares.

Several technologies for the development of new sugarcane cultivars have mainly focused on the increase in productivity and greater disease resistance. Sugarcane cultivars are usually identified by the organography of the leaves and stems, the analysis of peroxidase and esterase isoenzyme activities and the total soluble protein as well as soluble solid content. Nuclear magnetic resonance (NMR) associated with chemometric analysis has proven to be a valuable tool for cultivar assessment. Thus, this article describes the potential of chemometric analysis applied to ¹H high resolution magic angle spinning (HRMAS) and NMR in solution for the investigation of sugarcane cultivars. For this purpose, leaves from eight different cultivars of sugarcane were investigated by ¹H NMR spectroscopy in combination with chemometric analysis. The approach shows to be a useful tool for the distinction and classification of different sugarcane cultivars as well as to access the differences on its chemical composition.

Augusta tem sido tradicionalmente colocada na tribo Rondeletieae, Cinchonoideae subfamília. No entanto, recentes filogenias moleculares posicionou-a perto de Wendlandia, porém localizando A. longifolia perto do clado Ixoroidinae II. O estudo de A. longifolia resultou em duas cumarinas, cinco flavonoides, três triterpenoides e um derivado do ácido benzóico. Estes metabolitos reforçam a separação da Augusta como um gênero monoespecífico, e Lindenia como um gênero de três espécies, intimamente relacionada com Wendlandia.

Augusta has traditionally been placed in the tribe Rondeletieae, subfamily Cinchonoideae. However, recent molecular phylogenies positioned it near to Wendlandia (Ixoroideae), but locate A. longifolia near to the clade Ixoroidinae II. The study of A. longifolia afforded two coumarins, five flavonoids, three triterpenoids and one benzoic acid derivative. These metabolites reinforce the separation of Augusta as a monospecific genus, and Lindenia as a genus of three species, closely related to Wendlandia.