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1.
Int J Mol Sci ; 25(7)2024 Mar 27.
Article in English | MEDLINE | ID: mdl-38612532

ABSTRACT

Cherry stems, prized in traditional medicine for their potent antioxidant and anti-inflammatory properties, derive their efficacy from abundant polyphenols and anthocyanins. This makes them an ideal option for addressing skin aging and diseases. This study aimed to assess the antioxidant and anti-inflammatory effects of cherry stem extract for potential skincare use. To this end, the extract was first comprehensively characterized by HPLC-ESI-qTOF-MS. The extract's total phenolic content (TPC), antioxidant capacity, radical scavenging efficiency, and its ability to inhibit enzymes related to skin aging were determined. A total of 146 compounds were annotated in the cherry stem extract. The extract effectively fought against NO· and HOCl radicals with IC50 values of 2.32 and 5.4 mg/L. Additionally, it inhibited HYALase, collagenase, and XOD enzymes with IC50 values of 7.39, 111.92, and 10 mg/L, respectively. Based on the promising results that were obtained, the extract was subsequently gently integrated into a cosmetic gel at different concentrations and subjected to further stability evaluations. The accelerated stability was assessed through temperature ramping, heating-cooling cycles, and centrifugation, while the long-term stability was evaluated by storing the formulations under light and dark conditions for three months. The gel formulation enriched with cherry stem extract exhibited good stability and compatibility for topical application. Cherry stem extract may be a valuable ingredient for creating beneficial skincare cosmeceuticals.


Subject(s)
Anthocyanins , Cosmetics , Antioxidants/pharmacology , Anti-Inflammatory Agents/pharmacology , Plant Extracts/pharmacology
2.
J Sci Food Agric ; 100(13): 4688-4695, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32418224

ABSTRACT

BACKGROUND: The aromatic potential of mango by-products was evaluated to seek natural and cheap sources of odor-active compounds. Volatile compounds in mango peel and seed were chemically characterized and compared with those in mango pulp using headspace solid-phase microextraction coupled to gas chromatography-mass spectrometry (HS-SPME/GC-MS). RESULTS: More than 60 volatile compounds were detected in mango by-products, whose aromatic activity was estimated using odorant activity values (OAVs). The results indicated that mango peel was a valuable matrix of odor-active compounds, which were found in even larger quantities than in edible mango fractions. 3-Carene was the predominant compound, although other compounds such as decanal, 1-octen-3-one, nonanal, limonene, ß-damascenone, and 2-nonenal were the most odor-active compounds in mango peel. The greatest aromatic impact was obtained from mango peel, with sensorial features described as fresh / herbaceous, fruity, floral and resinous. CONCLUSION: The exceptional flavoring potential of mango peel by-product opens a door for its use and revalorization as a natural flavoring ingredient in the food and cosmetic industries. © 2020 Society of Chemical Industry.


Subject(s)
Flavoring Agents/chemistry , Mangifera/chemistry , Plant Extracts/chemistry , Waste Products/analysis , Flavoring Agents/analysis , Fruit/chemistry , Gas Chromatography-Mass Spectrometry , Odorants/analysis , Plant Extracts/isolation & purification , Solid Phase Microextraction , Volatile Organic Compounds/chemistry , Volatile Organic Compounds/isolation & purification
3.
Oxid Med Cell Longev ; 2016: 8915729, 2016.
Article in English | MEDLINE | ID: mdl-26904169

ABSTRACT

Grapefruit (Citrus paradisi Macf.) is an important cultivar of the Citrus genus which contains a number of nutrients beneficial to human health. The objective of the present study was to evaluate changes in bioactive flavonoids, antioxidant behaviour, and in vitro cytoprotective effect of processed white and pink peels after oven-drying (45°C-60°C) and freeze-drying treatments. Comparison with fresh grapefruit peels was also assessed. Significant increases in DPPH, FRAPS, and ABTS values were observed in dried grapefruit peel samples in comparison with fresh peels, indicating the suitability of the treatments for use as tools to greatly enhance the antioxidant potential of these natural byproducts. A total of thirteen flavonoids were quantified in grapefruit peel extracts by HPLC-MS/MS. It was found that naringin, followed by isonaringin, was the main flavonoid occurring in fresh, oven-dried, and freeze-dried grapefruit peels. In vivo assay revealed that fresh and oven-dried grapefruit peel extracts (45°C) exerted a strong cytoprotective effect on SH-SY5Y neuroblastoma cell lines at concentrations ranging within 0.1-0.25 mg/mL. Our data suggest that grapefruit (Citrus paradisi Macf.) peel has considerable potential as a source of natural bioactive flavonoids with outstanding antioxidant activity which can be used as agents in several therapeutic strategies.


Subject(s)
Antioxidants/pharmacology , Citrus paradisi/chemistry , Cytoprotection/drug effects , Desiccation , Flavonoids/pharmacology , Plant Extracts/pharmacology , Benzothiazoles/chemistry , Biphenyl Compounds/chemistry , Cell Line, Tumor , Cell Survival/drug effects , Chromatography, High Pressure Liquid , Freeze Drying , Glycosides/analysis , Humans , Iron/metabolism , Oxidation-Reduction/drug effects , Picrates/chemistry , Polyphenols/pharmacology , Principal Component Analysis , Sulfonic Acids/chemistry
4.
J Sci Food Agric ; 90(10): 1735-8, 2010 Aug 15.
Article in English | MEDLINE | ID: mdl-20564438

ABSTRACT

BACKGROUND: The carbohydrate profile of some woods used for aging wines and spirits has been recently studied using a pressurized liquid extraction method, the main differences found being related to cyclitol content. The aim of this study was to perform a detailed study of these compounds in woods of different Quercus species in order to identify two unknown compounds which appeared in the extracts and to verify whether the obtained profile was homogeneous for other Quercus species. RESULTS: Besides the known monosaccharides and five cyclitols previously described, three deoxy-inositols (epi-, vibo- and scyllo-quercitol) were identified. The presence of these eight cyclitols was confirmed in all subgenera and species of Quercus analyzed, allowing a characteristic cyclitol profile. CONCLUSIONS: Three deoxy-inositols (quercitols) have been identified in the carbohydrate profile of oak wood. All examined Quercus species displayed a common profile consisting of four inositols and four quercitols, which represent a good dataset for characterization of this genus.


Subject(s)
Cyclitols/analysis , Plant Extracts/chemistry , Quercus/chemistry , Wood/chemistry , Alcoholic Beverages , Food Industry/methods , Gas Chromatography-Mass Spectrometry , Species Specificity
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