Croton zehntneri Pax et Hoffm. is a plant from Northeastern Brazil, whose main component of its essential oil is estragole. Its thermal instability and low aqueous solubility prevent its technological application. This study aimed to prepare and characterize the Croton zehntneri essential oil (CZEO) complexed with β-cyclodextrin (β-CD), and to evaluate antioxidant activity of free and complexed-CZEO in vitro systems by the elimination of 2,2-diphenyl-1-picrylhydrazyl radicals (DPPH•), 2,2’-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS•+), hydroxyl and nitric oxide, as well as their ability to transfer electrons by the reducing potential. The infrared spectroscopy and thermal techniques demonstrated the formation of the inclusion complex (Est/β-CD) obtained by spray drying method. The free CZEO and its Est/β-CD at 0.9, 1.8, 3.6, 7.2, 14.4 and 28.8 µg mL-1 showed the ability to remove DPPH• (EC50 (half maximal effective concentration) 26.06 and 9.46 µg mL-1, respectively) and ABTS•+ (EC50 22.73 and 4.47 µg mL-1, respectively), nitric oxide inhibition (EC50 17.65 and 2.68 µg mL-1, respectively), hydroxyl radical sequestration (EC50 23.42 and 2.34 µg mL-1, respectively) and reducing potential (EC50 46.48 and 12.47 µg mL-1, respectively). The formation of the inclusion complex significantly increases its antioxidant potential.

The Barreirinha Formation-Upper Devonian, is the main petroleum source rock of the Amazon Basin, deposited during the great Devonian Transgression, contributing to significant accumulations of organic matter (OM) in anoxic conditions, which allowed its preservation. The present work had the objective of characterizing the molecular composition of biomarkers in outcrops samples of the Barreirinha Formation, aiming to evaluate the paleoenvironment, thermal evolution, and the preservation of OM total organic carbon (TOC) and Rock-Eval pyrolysis indicate considerable amounts of immature OM deposited in a low oxygenation environment. Gas chromatography-mass spectrometry (GC-MS) and gas chromatography-tandem mass spectrometry (GC-MS/MS) data corroborate that the OM was deposited in a suboxic to the oxic environment and low salinity (absence or low relative abundance of β-carotane and gammacerane). 24-N-Propyl-cholestane was detected and identified by synthetic pattern co-injection. High concentrations of tetracyclic polyprenoids (TPPs) in ascending order from base to top, high hopane/sterane ratios, to suggest that the samples had a high molecular weight n-alkanes, C29 steranes, low thermal evolution, and anoxic depositional paleoenvironment.

In this paper, we have applied state-of-the-art technologies and new investigations were developed focusing on obtaining simple and inexpensive molecules for treating cardiovascular diseases, as they are considered the leading cause of death in the world. For the first time, the inclusion complex of sulcatone (SU) and β-cyclodextrin (β-CD) was achieved (using a spray drier) and characterized making use of spectroscopic, thermal and computational methods. In addition, the system was evaluated regarding its vasorelaxant properties. Evidence of the inclusion complex formation was provided using different techniques, such as X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier transform infrared (FTIR), and 1H nuclear magnetic resonance (NMR) spectroscopies and then deduced by pharmacological experiments, which showed significant changes in relation to the initial material.

Microalgae lipid-derived biofuels is considered promising candidates for substitution of petroleum-based energy sources. However, the lipid extraction from the algal biomass stands as a challenge due to its low yields and cost-intensive cell disruption procedures. In this study a multivariate optimization of the extraction conditions was suggested, aiming a maximization of the lipid extraction from Scenedesmus sp. microalgae grown using wastewater as a nutrient medium. The extraction method, extraction time, solvent mixture and pretreatment were considered between upper and lower levels in order to access their significance, including their interactions, on the experimental response, while using a reduced number of experiments. The studies were performed using low-cost extraction methods (magnetic stirring and ultrasonication). The optimal extraction condition was obtained using CHCl3:MeOH (2:1) solvent mixture, in a 2-hour extraction period using ultrasonication. Fatty acid profiles of extracted lipids were also evaluated.

Croton zehntneri (Euphorbiaceae) é uma planta aromática nativa da região Nordeste do Brasil. O monoterpenóide Estragol (ESL) foi isolado por métodos cromatográficos clássicos a partir do óleo essencial (OE) das folhas de C. zehntneri e caracterizado por CG-DIC e CG-EM, tendo seu potencial antimicrobiano e citotóxico avaliado. A análise do OE permitiu a identificação de 100% dos constituintes integrados, cujo rendimento foi cerca de 1.8%. Os principais componentes identificados foram: eucaliptol, estragol (84.7%) e espatulenol. A dosagem de 50 μg/disco de ESL apresentou halos de inibição bastante expressivos frente a bactérias gram positiva e fungos. O ESL apresentou toxicidade frente a Artemia salina com CL50 e CL90 de 4,54 e 8,47 μg mL-1. Entretanto, nos testes de inibição tumoral (células humanas), não houve inibição satisfatória em nenhuma das linhagens de células humanas cancerígenas (MCF-7, HEP-2 e NCIH292).

Croton zehntneri (Euphorbiaceae) is a native aromatic plant from Northeast region of Brazil. The monoterpenoid estragole (ESL) has been isolated by classical chromatographic methods from the essential oil (EO) of C. zehnteneri leaves and characterized by GC-FID and GC-MS, its antimicrobial and cytotoxic potentials being assessed. The analysis of the EO enabled the identification of 100% of the integrated constituents, of which yield was about 1.8%. The main components identified were: eucalyptol, estragole (84.7%) and spathulenol. The dosage of 50 μg/disk of ESL presented fairly significant zones of inhibition against Gram-positive bacteria and fungi. The ESL presented toxicity against Artemia salina with LC50 and LC90 of 4,54 and 8,47 μg mL-1. However, in tumor inhibition assays (human cells), there were no rewarding inhibition in any of the human cancer cell lines (MCF-7, HEP-2 and NCI-H292).

Croton zehntneri, a plant native to northeastern Brazil, is widely used in folk medicine to treat gastrointestinal problems and has rich essential oil content. The essential oil of C. Zehntneri was analyzed by GC-MS, and its inclusion complex with β-cyclodextrin (β-CD) was characterized by both vibrational spectroscopy and differential scanning calorimetry (DSC). Estragol was the major component identified in the essential oil by the study. IR spectra indicated an interaction of β-CD with essential oil from C. zehntneri, a finding corroborated by the stability constant and scanning calorimetry. Microencapsulation within β-CD has the potential to mask sensory attributes and increase aqueous solubility of oils, thereby improving their applicability as drugs.

The essential oil (EO) of aerial parts of Lantana camara L., Verbenaceae, from Simões, Piaui, Northeast of Brazil, were obtained by hydrodistillation and analyzed by GC-FID and GC-MS techniques. In total, 68 compounds were identified. The most representative compounds of the oil were mono and sesquiterpenes. The main compounds found in the oil of the leaves in different months were β-caryophyllene (10.5%, in June of 2009), sabinene (7.98%, in September of 2008), limonene (7.68%, in September of 2008), spathulenol (11.64%, in September of 2008). The oil from stems of L. camara was characterized by a largest amount of sesquiterpenoids, with spatulenol (15.9%) and caryophyllene oxide (17.1% in June of 2009), as main components. β-Gurjunene (32.7%, in September of 2008) was the most prominent compound in the stems oils, which was absent or at very low relative abundance in leaves. L. camara essential oils from leaves were cytotoxic to V79 mammalian cells and also to Artemia salina, showing 50% lethal concentration (LC50) values from 0.23 µg/mL. The in vitro data obtained in this study suggested that EO may also be effective treating yeast infection in patients infected with fluconazole and terbinafine resistant isolates, but its toxicity must be monitored carefully.

O óleo essencial de Schinus terebinthifolius foi analisado por CG e CG-EM. α-Fencheno, limoneno, β-pineno, α-felandreno e β-isosilvestreno representam aproximadamente 80% da composição do óleo. A toxicidade na reprodução de ratos Wistar machos foi avaliada. Não foram observadas mudanças na massa dos órgãos reprodutivos, no número e morfologia dos espermatozoides, nas taxas de reprodução e na massa corporal dos ratos machos após tratamento com o óleo essencial de S. terebinthifolius.

The essential oil of Schinus terebinthifolius (Anacardiaceae) was analyzed by GC and GC-MS. α-Fenchene, limonene, β-pinene, α-phellandrene, and β-isosylvestrene represent about 80% of the oil composition. The reproductive toxicity of the essential oil in Wistar male rats was evaluated. No changes were observed in the mass of the reproductive organs, number and morphology of spermatozoa, reproductive rates, and the body mass of offspring of male rats after treatment with the essential oil of S. terebinthifolius.

This work describes the phytochemical analysis of Croton adenocalyx Baill (Euphorbiaceae), a plant that is representative of the species from Ceará State (Brazil). The GC-MS analysis of the essential oil, obtained by hydrodistillation of the leaves from C. adenocalyx, allowed the identification of eleven volatile constituents; the main components were identified as α-pinene (32.63%); bicyclogermacrene (13.96%); trans-caryophyllene (10.23%); germacrene D (10.14%); β-pinene (10.11%) and β-elemene (8.31%). The chromatographic purification of the ethanolic extract from the trunk bark, allowed the isolation and identification of the 6-methoxy-7-hydroxycoumarin (1) and 3,5-dihydroxy-3,4,7-trimethoxyflavone (2).

Este trabajo describe el análisis fitoquímico de Croton adenocalyx Baill (Euphorbiaceae), una planta representativa de las especies del Estado de Ceará- Brasil. El análisis por CG-EM del aceite esencial, obtenido por hidrodestilación de las hojas de C. adenocalyx Baill, permitió la identificación de diez constituyentes volátiles. Los componentes mayoritarios fueron identificados como α-pineno (32.63%), biciclogermacreno (13.96%), trans-cariofileno (10.23%), germacreno D (10.14%), β-pineno (10.11%) y β-elemeno (8.31%). La purificación cromatográfica del extracto etanólico de la corteza del tronco, permitió aislar e identificar la coumarina 6-metoxi-7-hidroxicumarina (1) y el 3,5-dihidroxi-3,4,7-trimetoxiflavona (2).

Os óleos essenciais de Lantana camara L. e Lantana sp., Verbenaceae, foram obtidos por hidrodestilação e seus componentes analisados por CG/EM. Tal procedimento analítico revelou a predominância dos sesquiterpenos, biciclogermacreno (19,42%), isocariofileno (16,70%), valenceno (12,94%) e germacreno D (12,34%) no óleo de L. camara, enquanto o biciclogermacreno (13,93%), germancreno D (27,54 e β-cariofileno (31,50%), %) destacaram-se como majoritários no óleo de Lantana sp. Os dois óleos foram submetidos a avaliação de atividades antibacteriana e de toxicidade usando as larvas de Artemia salina. Os resultados mostraram considerável atividade antibacteriana do óleo de L. camara, principalmente para Proteus vulgaris (ATCC 13315) e Escherichia coli (ATCC 25922). O óleo de Lantana sp. mostrou-se mais significativo contra Sthaphylococcus aureus (ATCC 10390). As atividades de toxicidade CL50 revelaram resultados inferiores ao limite padrão de 1000 μg/mL.

The essential oils from Lantana camara L. and Lantana sp. Verbenaceae, were obtained by hydrodistillation and analyzed by GC/MS. This GC/MS analysis revealed the sesquiterpenoids bicyclogermacrene (19.42%), isocaryophyllene (16.70%), valencene (12.94%) and germacrene D (12.34%) as majoritaries in the essential oil of L. camara, and bicyclogermacrene (13.93%), germacrene D (27.54 and β-caryophyllene (31.50%) in the essential oil from Lantana sp. The two essential oils were evaluated to antibacterial activity and toxicity using Artemia salina. The results revealed considerable antibacterial activity for essential oil from L. camara, meanly for Proteus vulgaris (ATCC 13315) and Escherichia coli (ATCC 25922). The essential oil of Lantana sp. showed major activity for Sthaphylococcus aureus (ATCC 10390). The evaluation of toxicity CL50 revealed results with minor values to limit pattern of 1000 μg/mL.

In this study the volatile constituents from leaves and fruits of Julocroton triqueter (Lam.) Didr. (Euphorbiaceae), a medicinal plant from northwest Brazil, were investigated by GC/MS. Twenty one compounds, which represent about 96% of the total constituents of the essential oil, were identified. Caryophyllene oxide, humulene epoxide II, trans-caryophyllene, occidentalol, á-humulene in the fruit and CM-carvyl acetate, spathulenol, CM-carveol, trans-caryophyllene, trans-carvyl acetate and á-humulene in the leaves were the principal components. From one fraction of the hexane extract of the fruits a mixture of fatty acids were identified as: dodecanoic, tetradecanoic, hexadecanoic, 9-octadecenoic, eicosanoic, trieicosanoic and tetracosanoic acids. The partial analysis of the non-volatile constituents (hexanic fraction) from fruit allowed the isolation and characterization of tetracosan-1-ol (identify by ¹H and 13C NMR, FTIR).