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1.
J Sci Food Agric ; 103(6): 2914-2925, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-36507778

RESUMEN

BACKGROUND: Husk scald (HS) is a physiological disorder limiting the marketability of pomegranate fruit during long-term storage. Herein we propose that HS is triggered by water loss and mediated by ABA signaling. Therefore, pomegranate fruit were stored at three different storage temperatures (3.5, 7 and 11°C) and 96.5% ± 2.3% relative humidity (RH) evaluating weight loss (WL), abscisic acid (ABA), respiration rate (RR), total phenolics (TP), total anthocyanin (TA), antioxidant activity (AA), exocarp electrolyte leakage (EL), malondialdehyde (MDA), color attributes, browning index and visual quality of fruit. RESULTS: HS appeared after 3 months of storage at 11 °C, less at 7°C and non-present at 3.5°C. Incidence of HS occurred along with higher WL, RR, EL, MDA, and ABA content. Conversely, TP, TA and AA decreased significantly. WL increased with water vapor pressure deficit (VPD) at higher temperatures. After 93 days, 11 °C fruit reached ~10% WL while ABA increased to ~150 µg kg-1 . However, 3.5 and 7 °C fruit, reached 5 and 7% WL while ABA was ~31 and 75 µg kg-1 , respectively. CONCLUSION: Herein, we propose a mechanistic model of HS development where water stress induces ABA as a primary signaling molecule that triggers the HS response mediated by reactive oxygen species (ROS). Accumulation of ROS induces phenolic biosynthesis and oxidative stress promotes loss of membrane compartmentalization that induces phenolic degradation. Ultimately, husk scalding becomes visible due to the oxidation of phenolics into brown pigments. © 2022 Society of Chemical Industry.


Asunto(s)
Antioxidantes , Granada (Fruta) , Especies Reactivas de Oxígeno/metabolismo , Antioxidantes/análisis , Granada (Fruta)/metabolismo , Extractos Vegetales/análisis , Frutas/química , Ácido Abscísico/metabolismo
2.
Analyst ; 147(5): 819-827, 2022 Feb 28.
Artículo en Inglés | MEDLINE | ID: mdl-35044386

RESUMEN

A two-dimensional microscale carbon fiber/active carbon fiber system combined with a quadrupole time of flight high-resolution mass spectrometry (2DµCFs-QTOF-HRMS) system is proposed for the rapid putative identification of polar, medium-polar and weakly polar constituents in complex matrices while strongly mitigating ionic suppression effects. The capabilities of 2DµCFs-QTOF-HRMS have been proven by analysing the composition of Abelmoschus manihot flower extracts, allowing, in a single run, the detection of 41 known substances and the presence of 6 compounds never revealed before in these samples. 2DµCFs-QTOF-HRMS has been compared with traditional HPLC-MS, showing higher versatility and a significant reduction of both analysis time (70 min to 5 min) and solvent consumption (35 mL to 1.5 mL). A comparison with the results obtained by direct flow-injection MS analyses demonstrated that 2DµCFs-QTOF-HRMS leads to a more comprehensive analysis and to improved detection sensitivity. The proposed method can be considered suitable for the rapid and comprehensive analysis of food, environmental and pharmaceutical complex samples. 2DµCFs-QTOF-HRMS can thus be considered a rapid, versatile, reliable, high-throughput and economical technique that allows for the collection of information on polar, semipolar, and weakly polar components in complex matrices.


Asunto(s)
Abelmoschus , Abelmoschus/química , Carbono , Cromatografía Líquida de Alta Presión/métodos , Flores , Extractos Vegetales
3.
J Pharm Biomed Anal ; 187: 113339, 2020 Aug 05.
Artículo en Inglés | MEDLINE | ID: mdl-32480199

RESUMEN

In this work, a new an innovative micro liquid extraction technique named "gas purge micro solvent extraction" (GP-MSE) have been tested, hyphenated with gas chromatography-mass spectrometry (GC-MS), to evaluate its capability to extract volatile fractions from vegetal samples respect to classical steam distillation extraction procedure, by comparing essential oil fingerprints from three different Atractylodes species. GP-MSE showed higher extraction capabilities and sensitivities (in particular for semi-volatile components), obtaining more structured essential oil fingerprints with high reliabilities (relative standard deviation of the peak areas between 0.34% and 5.83%), requiring at the same time smaller sample amounts and reduced extraction times. Essential oil profile data were also submitted to principal component analysis and included cosine angle in order to highlight differences among the Atractylodes species under investigation. GP-MSE can be considered an alternative, simple, fast, sensitive and environmentally friendly extraction method, with high extraction efficiencies and reproducibility toward both volatile and semi-volatile compounds.


Asunto(s)
Atractylodes/química , Cromatografía de Gases y Espectrometría de Masas/métodos , Aceites Volátiles/química , Gases , Microextracción en Fase Líquida , Aceites Volátiles/análisis , Aceites Volátiles/aislamiento & purificación , Análisis de Componente Principal , Reproducibilidad de los Resultados , Solventes/química , Factores de Tiempo
4.
J Chromatogr A ; 1501: 1-9, 2017 Jun 09.
Artículo en Inglés | MEDLINE | ID: mdl-28460870

RESUMEN

A novel high-throughput, solvent saving and versatile integrated two-dimensional microscale carbon fiber/active carbon fiber system (2DµCFs) that allows a simply and rapid separation of compounds in low-polar, medium-polar and high-polar fractions, has been coupled with ambient ionization-mass spectrometry (ESI-Q-TOF-MS and ESI-QqQ-MS) for screening and quantitative analyses of real samples. 2DµCFs led to a substantial interference reduction and minimization of ionization suppression effects, thus increasing the sensitivity and the screening capabilities of the subsequent MS analysis. The method has been applied to the analysis of Schisandra Chinensis extracts, obtaining with a single injection a simultaneous determination of 33 compounds presenting different polarities, such as organic acids, lignans, and flavonoids in less than 7min, at low pressures and using small solvent amounts. The method was also validated using 10 model compounds, giving limit of detections (LODs) ranging from 0.3 to 30ngmL-1, satisfactory recoveries (from 75.8 to 93.2%) and reproducibilities (relative standard deviations, RSDs, from 1.40 to 8.06%).


Asunto(s)
Fraccionamiento Químico/métodos , Ensayos Analíticos de Alto Rendimiento/métodos , Espectrometría de Masas/métodos , Extractos Vegetales/química , Schisandra/química , Carbono/química , Fibra de Carbono , Fraccionamiento Químico/instrumentación , Flavonoides/química , Flavonoides/aislamiento & purificación , Ensayos Analíticos de Alto Rendimiento/instrumentación , Lignanos/química , Lignanos/aislamiento & purificación , Espectrometría de Masas/instrumentación , Extractos Vegetales/aislamiento & purificación
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