ABSTRACT
Onion is rich in bioactive and volatile compounds with antioxidant activity. However, the pungent odor of volatile compounds (VOCs) released restricts its use. The encapsulation of red onion extract by electrospinning is an alternative to mask this odor and protect its bioactive compounds. The main objective of this study was to encapsulate red onion bulb extract (ROE) in different concentrations into zein nanofibers by electrospinning and evaluate their thermal, antioxidant, and hydrophilicity properties. The major VOC in ROE was 3(2H)-furanone, 2-hexyl-5-methyl. Incorporating ROE into the polymeric solutions increased electrical conductivity and decreased apparent viscosity, rendering nanofibers with a lower average diameter. The loading capacity of ROE on fibers was high, reaching 91.5% (10% ROE). The morphology of the nanofibers was random and continuous; however, it showed beads at the highest ROE concentration (40%). The addition of ROE to the nanofibers increased their hydrophilicity. The nanofibers' antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl, nitric oxide, and hydroxyl radicals ranged from 32.5% to 57.3%. The electrospun nanofibers have the potential to protect and mask VOCs. In addition, they offer a sustainable alternative to the synthetic antioxidants commonly employed in the food and packaging industry due to their antioxidant activities.
Subject(s)
Nanofibers , Zein , Onions , Antioxidants , Hydrophobic and Hydrophilic Interactions , Plant ExtractsABSTRACT
Electrospinning encapsulation is a highly viable method to protect bioactive compounds and prevent their degradation. Hence, this study produced ultrafine fibers based on yellow and white sweet potato starches and a red onion skin extract (ROSE; 0, 3, 6, and 9 %, w/w) using electrospinning. The fibers were evaluated for morphology, thermogravimetric properties, antioxidant, in vitro release simulation, thermal resistance (100 and 180 °C), and wettability. The fibers with ROSE presented 251-611 nm diameters, 67-78 % loading capacity, and 51.6-95.4 and 13.4-99.4 % thermal resistance (100 and 180 °C, respectively); apigenin presented the highest thermal protection. The phenolic compounds showed low release using 10 % ethanol and greater release with 50 % ethanol. The fibers with 9 % ROSE showed 2,2'-azino-bis(3-ethylbenzothiazoline) 6-sulfonic acid radical inhibition above 92 %. The ultrafine fibers and the unencapsulated ROSE showed inhibitory action against Escherichia coli and Staphylococcus aureus; only unencapsulated ROSE showed bactericidal activity.
Subject(s)
Ipomoea batatas , Starch , Flavonoids , Onions , Particulate Matter , Ethanol , Plant Extracts/pharmacologyABSTRACT
The aim of this work was to encapsulate curcumin at different concentrations in capsules and fibers of native potato starch by electrospraying and electrospinning. The best conditions for the production of capsules and fibers were obtained by varying the polymer concentration and resting time of the polymer solution. The best conditions were used for the encapsulation of curcumin. The curcumin-loaded capsules and fibers had an average diameter of 1373 nm to 1787 nm and 108 nm to 142 nm, respectively, and had a high curcumin loading capacity with values ranging from 79.01 % to 97.09 %. Curcumin encapsulated in starch capsules and fibers showed higher thermal stability at 180 °C for 2 h compared to unencapsulated curcumin. The antioxidant activity of starch fibers containing 1 % of curcumin had the greatest ability to inhibit the ABTS radical (45 % inhibition). These materials are promising for use in food or active packaging.
Subject(s)
Curcumin , Solanum tuberosum , Curcumin/pharmacology , Capsules , Antioxidants/pharmacology , Starch , PolymersABSTRACT
The yerba mate (Ilex paraguariensis A.St.-Hil.) is abundant on phenolic compounds and their preservation by encapsulation can promote increased stability. The objective was to produce mate extract with a high concentration of bioactive compounds, microencapsulate and characterize them. A commercial yerba mate was used to produce the extracts and select the best extraction solvent (ethanol, water, and ethanol:water (1:1). The ethanol:water extract was encapsulated at 1:1 (w/w) by fructooligosaccharide (FOS) and gum arabic (GA), in different combinations: FOS, GA:FOS (1:3), GA:FOS (1:1), GA:FOS (3:1) and GA. The encapsulation of chlorogenic acids was around 80%, considering the major phenolic compounds by HPLC. Thermal stability, by DSC, increased at treatments FOS, GA:FOS (1:3), and GA:FOS (1:1) compare to the unencapsulated extract, and changes were noticed in ATR-FTIR bands and antioxidant activity. The encapsulated phenolic compounds from I. paraguariensis can be stable in food under heat processing.
Subject(s)
Ilex paraguariensis/chemistry , Phenols/analysis , Plant Extracts/chemistry , Antioxidants/analysis , Chlorogenic Acid/chemistry , Gum Arabic/chemistry , Hot Temperature , Oligosaccharides/chemistry , Plant Leaves/chemistry , Spectroscopy, Fourier Transform InfraredABSTRACT
Foi estudada a extração simultânea de aflatoxinas (AFLAs) B1, B2, G1 e G2 em cebolas por meio de técnica de dispersão da matriz em fase sólida (MSPD), utilizando-se a casca de arroz como adsorvente. A identificação e quantificação das aflatoxinas foram realizadas empregando-se cromatografia em camada delgada de alta eficiência (CCDAE) e cromatografia líquida de alta eficiência acoplada ao detector de fluorescência (CLAE-FL). O melhor adsorvente foi constituído de mistura de casca de arroz: terra diatomácea (1:1)(p/p), empregado na proporção de 1:1 (p/p) com a massa de amostra e a mistura clorofórmio: metanol (5:25) (v/v) como eluente. A metodologia mostrou limites de detecção que variaram de 0,05 a 1 μg.kg-1,de exatidão entre 78 e 93 por cento, e coeficientes de variação compreendidos entre 11 e 14 por cento. Após a validação, a metodologia foi testada quanto à sua aplicabilidade para determinar a ocorrência das aflatoxinas em amostras de cebola, as quais foram classificadas segundo a norma do MAPA. A contaminação com aflatoxina foi verificada em 43 por cento das amostras analisadas com teor máximo de 90μg.kg-1 de AFLAB2.