scholarly journals Herbal Extract Decolourization Device Using Activated Carbon

2013 ◽  
Vol 61 (1) ◽  
Author(s):  
Teh Liam Chee ◽  
Rozilawati Abdul Gaffar ◽  
Fadzilah Adibah Abdul Majid ◽  
Mohammad Roji Sarmidi
Keyword(s):  
Activated Carbon ◽  
Phenolic Content ◽  
Radical Scavenging ◽  
Herbal Extract ◽  
Total Phenolic ◽  
Contact Period ◽  
Herbal Extracts ◽  
Leaf Extracts ◽  
Scavenging Capacity ◽  
Monolayer Coverage

Herbal extracts are known for their antioxidant, antimicrobial, and anti–inflammatory properties. However, the intense colour caused by their phenolic content and dark–coloured compounds may spoil the final product’s appearance. To remedy that, this study was undertaken to design a decolourization device to eliminate the intense colour of herbal extracts while retaining their beneficial properties. Batch experiments have been conducted to study decolourization and its effect on extract quality. From there, a decolourization device has been devised using activated carbon. Operating at optimum conditions, the device was able reduce 81 % of the total phenolic content of cashew leaf extracts while retaining 88 % of its radical scavenging capacity. Furthermore, the device is able to re–design the extract’s colour to fulfill the end–user’s needs by manipulating the contact period. The design of this device best fits Langmuir isotherm which demonstrates monolayer coverage of adsorbate at the outer surface of activated carbon.

Effect of 1-MCP on Bioavailability of Lingwu Long Jujube In Vitro Digestion

2012 ◽  
Vol 554-556 ◽  
pp. 1357-1360
Author(s):  
Zhong Li Jiang ◽  
Ai Li Wang ◽  
Xi Hong Li ◽  
Min Peng Zhu ◽  
Jun Wei Wang
Keyword(s):  
Free Radical ◽  
Total Phenolic Content ◽  
Phenolic Content ◽  
Radical Scavenging ◽  
Free Radical Scavenging ◽  
Total Phenolic ◽  
Radical Scavenging Capacity ◽  
Scavenging Capacity ◽  
Control Samples

The present study investigated the effect of 1-MCP on bioavailability of Lingwu long jujube stored at 0 °C for 60 days. At the end of the storage, compared with the control samples, Lingwu long jujube treated with 1-MCP exhibited higher Vc bioaccessibility, total phenolic content and free radical scavenging capacity, which demonstrated that 1-MCP treatment could provide a better effect on maintaining the bioavailability of Lingwu long jujube.

ANTIOXIDANT ACTIVITIES OF EXTRACTS FROM THE LEAVES AND STEM BARKS OF Artocarpus scortechinii KING

2015 ◽  
Vol 77 (2) ◽  
Author(s):  
Shajarahtunnur Jamil ◽  
Norazah Basar ◽  
Norzafneza Mohd Arriffin
Keyword(s):  
Ethyl Acetate ◽  
Gallic Acid ◽  
Phenolic Content ◽  
Ethyl Acetate Extract ◽  
Antioxidant Activities ◽  
Radical Scavenging ◽  
Dry Weight ◽  
Calibration Graph ◽  
Total Phenolic ◽  
Scavenging Capacity

The antioxidant activities of extracts (n-hexane, dichloromethane, ethyl acetate and methanol) from the leaves and stem barks of Artocarpus scortechinii were evaluated using various biochemical assays. The quantification of the Total Antioxidant Capacity was measured using ferric reducing antioxidant potential (FRAP) and 2,2'-azino-bis(3-ethyl-benzothiazoline-6-sulphonic acid) (ABTS) assays. While, the qualitative of The Total Phenolic Content (TPC) was determined via standard gallic acid calibration graph which was expressed as mg gallic acid equivalent (GAE)/g of dry weight (dw) using Folin Ciocalteau’s reagent. Among all the extracts tested, the methanolic extract of the stem barks showed the highest phenolic content with TPC value of 136.84 mg GAE/g dry weight (dw). FRAP results were expressed as mM equivalent to FeSO4.7H2O by calculating from the standard FeSO4.7H2O calibration graph. The ethyl acetate extract of the stem barks showed the most significant reducing potential in the range between 0.27-2.47 mM FRAP. ABTS+˙ radical scavenging capacity showed that the ethyl acetate extract of the stem barks had the highest scavenging capacity at concentration 1.0 mM with percentage of 90.9%.

scholarly journals Effect of Microwave Pretreatment of Seeds on the Quality and Antioxidant Capacity of Pomegranate Seed Oil

Foods ◽  
2020 ◽  
Vol 9 (9) ◽  
pp. 1287
Author(s):  
Tafadzwa Kaseke ◽  
Umezuruike Linus Opara ◽  
Olaniyi Amos Fawole
Keyword(s):  
Total Phenolic Content ◽  
Phenolic Content ◽  
Radical Scavenging ◽  
Oil Yield ◽  
Total Phenolic ◽  
Total Carotenoids ◽  
Yellowness Index ◽  
Microwave Pretreatment ◽  
Scavenging Capacity ◽  
Pomegranate Seeds

Microwave pretreatment of oilseeds is a novel technique used to enhance oil nutraceutical properties. In this study, the effect of microwave pretreatment of seeds was investigated on pomegranate seed oil quality attributes including oil yield, yellowness index, refractive index, peroxide value, ρ-anisidine value, total oxidation value, conjugated dienes, total phenolic content, total carotenoids content, phytosterol composition, fatty acid composition, 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging capacity, and ferric reducing antioxidant power (FRAP). The seeds of three different pomegranate cultivars (‘Acco’, ‘Herskawitz’, and ‘Wonderful’) were microwave heated at 261 W for 102 s. Pomegranate seeds microwave pretreatment enhanced oil yield, yellowness index, total carotenoids content, total phenolic content, FRAP and DPPH radical scavenging capacity, despite an increase in conjugated dienes, and peroxide value. Palmitic acid, oleic acid, linoleic acid, saturated, and monosaturated fatty acids were increased after pomegranate seeds microwave pretreatment, whilst the levels of punicic acid and β-sitosterol were reduced. Nevertheless, the refractive index, the ratio of unsaturated to saturated fatty acid of the extracted oil were not significantly (p > 0.05) affected by pomegranate seeds microwave pretreatment. Principal component analysis and agglomerative hierarchical clustering established that ‘Acco’ and ‘Wonderful’ oil extracts from microwave pretreated PS exhibited better oil yield, whilst ‘Herskawitz’ oil extracts showed higher total carotenoids content, total phenolic content, and antioxidant capacity.

scholarly journals Total Phenolic Content and Antioxidant Activity of Salvia spp. Exudates

2012 ◽  
Vol 7 (2) ◽  
pp. 1934578X1200700 ◽  
Author(s):  
Laura Giamperi ◽  
Anahi Bucchini ◽  
Angela Bisio ◽  
Emanuela Giacomelli ◽  
Giovanni Romussi ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Total Phenolic Content ◽  
Phenolic Content ◽  
Radical Scavenging ◽  
Natural Antioxidants ◽  
Total Phenolic ◽  
Dpph Radical ◽  
Radical Scavenging Capacity ◽  
Scavenging Capacity ◽  
Dpph Radical Scavenging

The total phenolic content and antioxidant activity of 6 Salvia spp. exudates were measured to find new potential sources of natural antioxidants. Total phenolic content was assessed by a modified Prussian blue method, and the antioxidant activity by two methods: 1,1- diphenyl-2-picryl- hydrazyl (DPPH) radical scavenging capacity assay and lipoxygenase inhibitory assay. The total phenolic content ranged between 1.3 μg/mg DW ( S. fallax) and 74.0 μg/mg DW ( S. cacaliaefolia). In the DPPH test, S. cacaliaefolia was more effective than BHT, while in the inhibition of lipid peroxidation all the extracts presented good antioxidant capacity.

scholarly journals Diversity in Accessions of Panicum miliaceum L. Based on Agro-Morphological, Antioxidative, and Genetic Traits

Molecules ◽  
2019 ◽  
Vol 24 (6) ◽  
pp. 1012 ◽  
Author(s):  
Bimal Ghimire ◽  
Chang Yu ◽  
Seung Kim ◽  
Ill-Min Chung
Keyword(s):  
Genetic Diversity ◽  
Total Phenolic Content ◽  
Phenolic Content ◽  
Radical Scavenging ◽  
Total Phenolic ◽  
Panicum Miliaceum ◽  
Expected Heterozygosity ◽  
Radical Scavenging Capacity ◽  
Bioactive Properties ◽  
Scavenging Capacity

The genetic diversity and antioxidant potential of Panicum miliaceum L. accessions collected from different geo-ecological regions of South Korea were evaluated and compared. Antioxidant potential of seeds was estimated by the 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulfonic acid (ABTS) radical scavenging assays and total phenolic content was determined by the Folin–Ciocalteu method. Total phenolic content (TPC) in 80% methanolic extracts ranged from 16.24 ± 0.86 to 58.04 ± 1.00 mg gallic acid equivalent (GAE)/g of the sample extracts and total flavonoid content (TFC) varied from 7.19 ± 1.05 to 52.56 ± 1.50 mg quercetin equivalents (QE) mg/g of the sample extracts. DPPH radical scavenging capacity of the extracts from the 15 accessions of P. miliaceum varied from 206.44 ± 7.72 to 2490.24 ± 4.641 mg GAE/g of the sample extracts and ABTS radical scavenging capacity ranged from 624.85 ± 13.1 to 1087. 77 ± 9.58 mg GAE/g of the sample extracts. A wide range of genetic variation was observed as measured by Shannon’s information index (I), number of effective alleles (Ne), number of observed alleles (Na), expected heterozygosity (He), unbiased expected heterozygosity (uHe). The observed variation in the bioactive properties, morphological traits, and genetic diversity among the accessions may provide useful information for breeding programs seeking to improve bioactive properties of P. miliaceum.

scholarly journals Assessment of total phenolic content and antioxidant potentiality of selected Indian folk medicinal plants by spectrophotometric method

2020 ◽  
Vol 7 (3) ◽  
pp. 383-390
Author(s):  
Satish Dubey ◽  
Kundan Ojha ◽  
Jagriti Chandrakar ◽  
Rashmi Dehariya ◽  
Shilpa Vinodia ◽  
...  
Keyword(s):  
Free Radical ◽  
Medicinal Plants ◽  
Spectrophotometric Method ◽  
Total Phenolic Content ◽  
Phenolic Content ◽  
Radical Scavenging ◽  
Dry Weight ◽  
Free Radical Scavenging ◽  
Total Phenolic ◽  
Leaf Extracts

Natural antioxidant capacity of five important folk medicinal plants measured in vitro. Total phenolic content (TPC), flavonoid content (FC) and free radical scavenging capacity of ethanolic, methanolic and aqueous leaf extracts of Lippia alba (LA), Annona squamosa (AS), Hyptis suaveolens (HS), Commiphora wightii (CW) and Milletia pinnata (MP) was assessed using spectrophotometric method. Folin ciocalteu and aluminium chloride method employed to optimise TPC and FC. Free radical scavenging potentiality of leaf extracts was assessed using Ferrous ion chelation (FIC), 2, 2'-diphenyl-1-picrylhydrazyl (DPPH•) scavenging, Hydroxyl (OH•) radical scavenging (HRS) and Superoxide (O- 2) radical scavenging (SRS) methods. Results revealed that the TPC (96.22±5.85 to 519.23±34.90 ?g GAE/gm dry weight) were found significant in aqueous extracts from all the plants except AS (p<0.05). For FC (?g QCE/gm dry weight), ethanol was found optimum for LA (463.94±6.49), CW (289.99±2.70) and MP (347.47±4.50) whereas, aqueous was found more appropriate for rest two plants were found significant instead of ethanol and methanol (all p<0.05). The lowest IC50 (?g/ml) were recorded from A. squamosa (27.72±8.95), H. suaveolens (27.78±0.88), C. wightii (27.18±0.16) and M. pinnata (27.30±0.03). All plants have reflected a high antioxidant capacity; however, the highest antioxidant activity was reported from ethanolic extract of H. suaveolens followed by L. alba, A. squamosa, C. wightii and M. pinnata. Hence, these studies show that all folk medicinal plants contain potential antioxidant bioactive compounds.

scholarly journals Evaluation of Phenolic and Flavonoid Content, Antioxidant and Radical Scavenging Capacity of Baru (Dipteryx alata Vog.) Almond

2021 ◽  
Vol 5 (Supplement_2) ◽  
pp. 326-326
Author(s):  
Deja Ivy ◽  
Rami Najjar ◽  
Maureen Meister ◽  
Maria Margareth Naves ◽  
Rafaela Feresin
Keyword(s):  
Phenolic Content ◽  
Radical Scavenging ◽  
Total Phenolic ◽  
Flavonoid Content ◽  
Radical Scavenging Capacity ◽  
Scavenging Capacity ◽  
Freeze Dried ◽  
Trolox Equivalent ◽  
Phenolic And Flavonoid ◽  
Dipteryx Alata

Abstract Objectives The legume plant species Dipteryx alata Vog., commonly known as baru, is a tree that grows in the Brazilian savanna. It produces drupe type of fruit and has an edible seed referred to as the baru nut. The baru nut is of interest as it possesses bioactive compounds useful in managing chronic diseases, yet little is known about its composition. Thus, the aim of this study was to determine the phenolic and flavonoid content, as well as antioxidant and radical scavenging capacity of the baru nut. Methods Baru nuts were roasted, pulverized, and freeze-dried prior to polyphenolic extractions, which were performed using 80% ethanol and ultrasonic bath. Baru crude extracts were then purified with chloroform, evaporated, and freeze-dried prior to being assayed. Total phenolic content and total flavonoid content of purified baru polyphenolic extracts were determined using Folin-Ciocalteu reagent and aluminum chloride colorimetric assay, respectively. Antioxidant capacity was measured using Trolox equivalent antioxidant capacity (TEAC) and ferric reducing antioxidant power (FRAP) while 2,2-diphenyl-1-picrylhydrazyl (DPPH) and oxygen radical absorbance capacity (ORAC) assays were used to determine radical scavenging capacity. Results Total phenolic content of purified baru nut extract was 58 ± 10 μmol gallic acid equivalent/L while total flavonoid content was 7 ± 0 μg quercetin equivalent/mL. The TEAC of purified baru nut extract was 161 ± 5 μmol trolox equivalent (TE)/L, which was higher than its FRAP, 55 ± 0.5 μmol TE/L. Radical scavenging capacity of baru nut extract was 17 ± 3 and 5 ± 7 μmol TE/L according to DPPH and ORAC, respectively. Conclusions Baru nut is rich in polyphenols and has high antioxidant activity. Further research is warranted to determine the antioxidant properties of baru nut in vitro and in vivo. Funding Sources No sources of funding.

scholarly journals Characterization and Uptake of Strawberry-Derived Exosome-Like Nanovesicles by Human Aortic Endothelial Cells

2021 ◽  
Vol 5 (Supplement_2) ◽  
pp. 310-310
Author(s):  
Jessica Danh ◽  
Brandon Canup ◽  
Rami Najjar ◽  
Maureen Meister ◽  
Hamed Laroui ◽  
...  
Keyword(s):  
Antioxidant Capacity ◽  
Phenolic Content ◽  
Radical Scavenging ◽  
Total Phenolic ◽  
Flavonoid Content ◽  
Aortic Endothelial Cells ◽  
Radical Scavenging Capacity ◽  
Scavenging Capacity ◽  
Human Aortic Endothelial Cells ◽  
Dpph Radical Scavenging

Abstract Objectives To characterize strawberry (SB)-derived exosome-like nanovesicles (ELNs), assess the total phenolic content, total flavonoid content, and total antioxidant capacity as well as its uptake by human aortic endothelial cells (HAECs). Methods SB ELNs were extracted using differential centrifugation. After final ultracentrifugation at 100,000 × g for 1 h, pellets were collected and washed in PBS. Characterization was performed using dynamic light scattering measurements. Total phenolic content (TPC) and flavonoid content (TFC) were determined using Folin-Ciocalteu and aluminum chloride, respectively. Antioxidant capacity was determined using the Trolox equivalent antioxidant capacity (TEAC) and ferric reducing ability of plasma (FRAP) assay while free radical scavenging power was measured using 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging capacity assay. Cell viability and uptake were assessed in HAECs. Cell viability was measured after 24-h incubation with SB ELNs using MTT reagent. Cell uptake was measured after 12-h incubation with 100 μg/mL coumarin-6 (C-6) labelled SB ELNs. Fluorescent microscopy and flow cytometry were used to detect cellular uptake of C-6 labelled SB ELNs on a LSR II. Results SB ELNs were sized at 119.4 ± 28.3 nm (PDI = 0.29 ± 0.06). TPC and TFC of SB ELNs were 158.9 ± 22.6 μmol GAE/L and 5.1 ± 0.4 μg QE/mL, respectively. Antioxidant capacity of SB ELNs was 211.38 ± 6.3 μmol TE/L and 118.0 ± 7.6 μmol Fe2+/L by TEAC and FRAP, respectively. DPPH radical scavenging capacity was 181.3 ± 2.5 μmol TE/L in SB ELNs. No cytotoxic effects were observed for SB ELNs in HAECs. Uptake of SB ELNs by HAECs was 15.3% higher compared to baseline levels. Conclusions We report, for the first time, the presence of phenolics and flavonoids in the cargo of SB ELNs, SB ELNs antioxidant capacity, and demonstrate their uptake by HAECs. Taken together, these findings support the need to further characterize and explore the antioxidant potential of SB ELNs in vitro and in vivo. Funding Sources None.

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