scholarly journals Caftaric Acid Isolation from Unripe Grape: A “Green” Alternative for Hydroxycinnamic Acids Recovery

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1148
Author(s):  
Veronica Vendramin ◽  
Alessia Viel ◽  
Simone Vincenzi

Phenolic acids represent about one-third of the dietary phenols and are widespread in vegetable and fruits. Several plants belonging to both vegetables and medical herbs have been studied for their hydroxycinnamic acid content. Among them, Echinacea purpurea is preferentially used for caffeic acid-derivatives extraction. The wine industry is a source of by-products that are rich in phenolic compounds. This work demonstrates that unripe grape juice (verjuice) presents a simple high-pressure liquid chromatography (HPLC) profile for hydroxycinnamic acids (HCAs), with a great separation of the caffeic-derived acids and a low content of other phenolic compounds when compared to E. purpurea and other grape by-products. Here it is shown how this allows the recovery of pure hydroxycinnamic acids by a simple and fast method, fast protein liquid chromatography (FPLC). In addition, verjuice can be easily obtained by pressing grape berries and filtering, thus avoiding any extraction step as required for other vegetable sources. Overall, the proposed protocol could strongly reduce the engagement of solvent in industrial phenolic extraction.

Molecules ◽  
2021 ◽  
Vol 26 (16) ◽  
pp. 5037
Author(s):  
Julio Serna-Vázquez ◽  
Mohd Zamidi Ahmad ◽  
Grzegorz Boczkaj ◽  
Roberto Castro-Muñoz

Phenolic compounds have long been of great importance in the pharmaceutical, food, and cosmetic industries. Unfortunately, conventional extraction procedures have a high cost and are time consuming, and the solvents used can represent a safety risk for operators, consumers, and the environment. Deep eutectic solvents (DESs) are green alternatives for extraction processes, given their low or non-toxicity, biodegradability, and reusability. This review discusses the latest research (in the last two years) employing DESs for phenolic extraction, solvent components, extraction yields, extraction method characteristics, and reviewing the phenolic sources (natural products, by-products, wastes, etc.). This work also analyzes and discusses the most relevant DES-based studies for phenolic extraction from natural sources, their extraction strategies using DESs, their molecular mechanisms, and potential applications.


Author(s):  
М. С. Гарник

<p><strong>THE INVESTIGATION OF COMPOUNDS PHENOL ORIGIN GROUND IVY (GLECHOMA HEDERACEA L.)</strong></p><p><strong>M. S. Garnyk</strong></p><p>NationalPyrogovMemorialMedicalUniversity, Vinnytsia</p><p><strong>Summary:</strong> compounds of phenol origin have been quantified in ground ivy herb, they are hydroxycinnamic acids (4.20-6.47 %), flavonoids (0.77-1.35 %), oxidized phenols (7.75-8.51 %). Flavonoid groups (rutin, hyperozide, apigenin, luteolin, isoquercitrin), coumarines (scopoletin, umbelliferone) hydroxycinnamic acids (rosmarinic, chlorogenic, caffeic, p-coumaric) have been identified by the method of HPLC and their content has been identified.</p><p><strong>Key words</strong>: ground ivy, compounds of phenol origin, spectrophotometry, permanganatometry, high performance liquid chromatography.</p><p><strong>Introduction.</strong> The ability to synthesize and accumulate huge amount of phenolic compounds is a characteristic feature of the representatives of the plant world. Natural phenols exhibit high biological activity. They take part in various physiological processes: respiration, photosynthesis, growth, development and reproduction of plants; some polyphenols protect plants from pathogens and fungal diseases.</p><p>Medicinal products based on phenolic compounds are widely used as anti-microbial, anti-inflammatory, hemostatic, choleretic, diuretic, hypotensive, tonic, astringent and purgative means. Most of the phenolic compounds of plant origin have low toxicity and do not exhibit side effects.</p><p>Previous studies found that grass of ground ivy contains a number of phenolic compounds namely: hydroxycinnamic acids, flavonoids, tannins. Therefore the purpose of the study was to determine the quantitative content of phenolic compounds by spectrophotometric method and individual substances by high performance liquid chromatography.</p><p><strong>Methods.</strong> The determination of phenolic compounds recalculated to gallic acid has been performed by spectrophotometric method at a wavelength of 270 nm, the amount of hydroxycinnamic acids recalculated to chlorogenic acid – at a wavelength of 327 nm, the amount of flavonoids recalculated to rutin – at a wavelength of 410 nm; total oxidized amount of phenols has been determined by permanganatometrical titration. To separate the total amount of phenolic compounds into individual components high performance liquid chromatography was used.</p><p><strong>Results and discussion.</strong> The content of phenolic compounds in grass of ground ivy was 3.15-3.41% in the sample number 1 (raw materials harvested in Ternopil region) and 2.98-3.29 % in the sample number 2 (materials harvested in Vinnytsia region), the total content of oxidized phenols is 8.34-8.51 % and 7.75-8.14 %, the amount of flavonoids – 0.87-1.35% and 0.77-1.04 %, the amount hydroxycinnamic acids – 4.20-6.47 % and 4.84-6.36 % respectively for the objects number 1 and number 2.</p><p>Individual quantitative content of phenolic compounds in the grass of ground ivy was identified by the method of HPLC. Flavonoids (rutin, hyperozide, apigenin, luteolin, isoquercitrin) were identified in the studied objects, as well as coumarins (skopoletyn, umbelliferone), hydroxycinnamic acid (rosmary, chlorogenic, coffeic, p-coumaric), and their quantitative content was determined.</p><p>Among flavonoid compounds of ground ivy the greatest number falls to rutin – 0.40 and 0.23 % respectively in objects number 1 and 2. As for hydroxycinnamic acid the highest content of rosmarinic acid is observed in the sample number 2 – 1.13 %. The content of chlorogenic acid was also significant and made 0.84 % (№ 1) and 0.81 % (№ 2) in studied objects.</p><p><strong>Conclusions.</strong> 1. Quantitative content of phenolic compounds: total amount of oxidative phenols, total amount of hydroxycinnamic acids, total amount of flavonoids were detected in the studied samples of ground ivy.</p><p>2. Quantitative content of flavonoids (rutin – 0.23-0.40 %, hyperozide – 0.17-0.34 %, luteolin – 0.05-0.1% isoquercіtrіn – 0.02-0.03 %, apigenin – 0.06 %), hydroxycinnamic acids (chlorogenic – 0.81-0.84 %, rosmarinic – 0.2-1.13%, coffeic – 0.06 %, p-coumaric – traces) and coumarins (skopoletyn – 0.11-0.12 %, umbelliferonе – 0.02 %) was identified and defined by the method of HPLC.</p>


Food Control ◽  
2018 ◽  
Vol 92 ◽  
pp. 516-522 ◽  
Author(s):  
Vanessa Silva ◽  
Gilberto Igrejas ◽  
Virgílio Falco ◽  
Teresa P. Santos ◽  
Carmen Torres ◽  
...  

Processes ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 764 ◽  
Author(s):  
Danying Peng ◽  
Hafza Fasiha Zahid ◽  
Said Ajlouni ◽  
Frank R. Dunshea ◽  
Hafiz A. R. Suleria

Mango (Mangifera indica L.) is one of the most important fruits in the world. Mango peel is an important by-product that is rich in polyphenols and it could have high economic value if it is effectively utilized. Phenolic characterization is an essential step in the commercial utilization of mango peel by-products as food ingredients. Herein, qualitative and quantitative analyses of two Australian mango peel “Keitt” and “Kensington Pride” (K&P) by-products were conducted while using liquid chromatography coupled to electrospray ionisation and quadrupole time of flight mass spectrometry (LC-ESI-QTOF/MS) and high-performance liquid chromatography coupled to photodiode array detector (HPLC-PDA). A total of 98 polyphenols compounds were tentatively identified in both Keitt peel and K&P peel extracts, with greater concentrations of these compounds being detected in Keitt peel. The total phenolic content (TPC), total flavonoid content (TFC), and a total tannin content (TTC) were determined. The antioxidant activity of mango peel by-products was determined while using 2,2-diphenyl-1-picrylhydrazyl (DPPH) antioxidant assay, ferric reducing antioxidant power (FRAP) assay, and 2,2-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS) radical scavenging assay. Keitt peel contained higher concentrations of total phenolic compounds, flavonoids, and tannins and had higher antioxidant capacity in DPPH, FRAP, and ABTS assays as compared to K&P peel. In HPLC-PDA quantification, the predominant phenolic compounds in Keitt peel and K&P peel were catechin (62.32 ± 0.01 mg/gd.w.) and syringic acid (17.78 ± 0.01 mg/gd.w).


2020 ◽  
Vol 2 (3) ◽  
pp. 105-110
Author(s):  
Euzélia Lima de Souza1 ◽  
Talita Sousa Nascimento ◽  
Gabriele De Abreu Barreto ◽  
Ingrid Lessa Leal ◽  
Jeancarlo Pereira dos Anjos ◽  
...  

Grape bark from the wine industry still contains significant amounts of phenolic compounds. Specific characteristics of the applied solvents influence the extraction of phenolic compounds directly. This study aimed to evaluate the influence of different solvents obtaining phenolic compounds in Syrah grape barkextracts by High-Performance Liquid Chromatography (HPLC). Grape peel extracts were prepared with three different solvents (water, 50%, and 80% grain alcohol), and evaluated using standard curve with 15 phenolic compounds. It was not possible to quantify the phenolic compounds, but the chromatogramssuggest the presence of some of them. The solvent that provided the best interaction with grape peel was 50% grain alcohol.


2019 ◽  
Author(s):  
Buddhika Dorakumbura ◽  
Francesco Busetti ◽  
Simon Lewis

<p>Transformation of squalene and its by-products in fingermarks over time under different storage conditions (light, dark and underwater) was examined through ultrahigh-pressure liquid chromatography high resolution accurate mass Orbitrap™ mass spectrometry. Complications of assessing fingermark compositional variation over time using multiple samples with varying initial compositions were elucidated and a more rational approach was successfully demonstrated. Squalene was detected in all fresh natural fingermarks and the amount ranged between 0.20 to 11.32 μg/5 fingertips. A notable difference in the transformation of squalene was observed with different storage conditions, where a dark aquatic environment accelerated degradation of squalene compared to dark but dry conditions. Squalene monohydroperoxide was extremely short-lived in natural deposits while the amount of squalene epoxide was still increasing relative to the initial amount, after ageing under dark and aquatic conditions for up to 7 days. Some oxidation by-products of cholesterol were also tentatively identified, which exhibited a growth over time against their initial concentration under any of the storage condition tested. These by-products, therefore, show potential as biomarkers for targeted visualisation of aged deposits.</p>


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