DPPH Free Radical Scavenging Potential Research Articles

Multi-frequency ultrasonic-assisted enzymatic extraction of coconut paring oil from coconut by-products: Impact on the yield, physicochemical properties, and emulsion stability

Extraction of coconut paring oil (CPO) from processing by-products adds value to the product and reduces resource wastage. This study aims to assess the impact of 20 kHz, 20/80 kHz and 20/40/80 kHz of multi-frequency ultrasonic-assisted enzymatic extraction (MFUAEE) on the yield, physicochemical properties, fatty acid composition, total phenolic content, antioxidant activity, and emulsion stability of CPO derived from wet coconut parings (WCP). Results revealed that the CPO extraction yield with MFUAEE was 32.58 % − 43.31 % higher compared to AEE. The tri-frequency 20/40/80 kHz mode of multi-frequency ultrasound pretreatment exhibited the highest CPO extraction yield (70.08 %). The oil extracted through MFUAEE displayed similar fatty acid profiles to AEE, but had lower peroxide value, K232 and K270 values. Particularly, MFUAEE oil contained higher total phenolic content and exhibited potent DPPH free radical scavenging capacity. Results observed by SEM indicated that the pretreatment with multi-frequency ultrasound more efficiently disrupts the cellular structure of the WCP. Additionally, MFUAEE enhanced emulsion stability through the cavitation effect of ultrasound. These findings suggest that MFUAEE is a valuable approach for method for obtaining CPO with elevated extraction yield and superior quality, thereby enhancing the utilization of coconut by-products.

Hybrid nanoparticles combining nanoselenium-mediated Carica papaya extract and trimethyl chitosan for combating clinical multidrug-resistant bacteria

Multidrug-resistant bacterial infections pose a significant threat to human health, prompting the exploration of innovative solutions. In this study, a new series of antibacterial hybrid nanoparticles (HNPs) were developed. The HNPs are based on a combination of selenium nanoparticles (SeNPs), synthesized using Carica papaya leaf extract, and chitosan (CS/SeHNPs) or trimethyl chitosan (TMC/SeHNPs), respectively. Comprehensive characterization using UV–Vis, FTIR, XRD, SEM-EDX, DLS, TEM, and DSC confirmed the structure and properties of the developed HNPs. SeNPs, CS/SeHNPs, and TMC/SeHNPs showed average hydrodynamic size of 78.8, 91.3, and 122 nm, and zeta potentials of −6.35 mV, +32.8 mV, and +54.8 mV, respectively. Biological assessments were conducted, including antibacterial and antibiofilm assays against clinical strains (E. coli, S. aureus, and K. pneumoniae), along with antioxidant activity. TMC/SeHNPs demonstrated superior performance compared to SeNPs and CS/SeHNPs with the lowest minimum inhibition concentrations (MIC) against S. aureus and K. pneumoniae (3.9 μg/mL) and 62.5 μg/mL against E. coli in addition to robust antibiofilm activity. Furthermore, the TMC/SeHNPs exhibited potent DPPH free radical scavenging ability and demonstrated good biocompatibility, as evidenced by cell viability assays on HFB4 cells. Overall, TMC/SeHNPs emerged as promising candidates in nanomedicine, offering high antioxidant, antibacterial, and antibiofilm activities alongside excellent biocompatibility.

Biogenic synthesis, characterization, and in vitro biological investigation of silver oxide nanoparticles (AgONPs) using Rhynchosia capitata

The current research aimed to study the green synthesis of silver oxide nanoparticles (AgONPs) using Rhynchosia capitata (RC) aqueous extract as a potent reducing and stabilizing agent. The obtained RC-AgONPs were characterized using UV, FT-IR, XRD, DLS, SEM, and EDX to investigate the morphology, size, and elemental composition. The size of the RC-AgONPs was found to be ~ 21.66 nm and an almost uniform distribution was executed by XRD analysis. In vitro studies were performed to reveal biological potential. The AgONPs exhibited efficient DPPH free radical scavenging potential (71.3%), reducing power (63.8 ± 1.77%), and total antioxidant capacity (88.5 ± 4.8%) to estimate their antioxidative power. Antibacterial and antifungal potentials were evaluated using the disc diffusion method against various bacterial and fungal strains, and the zones of inhibition (ZOI) were determined. A brine shrimp cytotoxicity assay was conducted to measure the cytotoxicity potential (LC50: 2.26 μg/mL). In addition, biocompatibility tests were performed to evaluate the biocompatible nature of RC-AgONPs using red blood cells, HEK, and VERO cell lines (< 200 μg/mL). An alpha-amylase inhibition assay was carried out with 67.6% inhibition. Moreover, In vitro, anticancer activity was performed against Hep-2 liver cancer cell lines, and an LC50 value of 45.94 μg/mL was achieved. Overall, the present study has demonstrated that the utilization of R. capitata extract for the biosynthesis of AgONPs offers a cost-effective, eco-friendly, and forthright alternative to traditional approaches for silver nanoparticle synthesis. The RC-AgONPs obtained exhibited significant bioactive properties, positioning them as promising candidates for diverse applications in the spheres of medicine and beyond.

Biochemical characterization of bioinspired nanosuspensions from Swertia chirayita extract and their therapeutic effects through nanotechnology approach.

Swertia chirayita is used as a traditional medicinal plant due to its pharmacological activities, including antioxidant, antidiabetic, antimicrobial, and cytotoxic. This study was aimed to evaluate the therapeutic efficacy of newly synthesized nanosuspensions from Swertia chirayita through nanotechnology for enhanced bioactivities. Biochemical characterization was carried out through spectroscopic analyses of HPLC and FTIR. Results revealed that extract contained higher TPCs (569.6 ± 7.8 mg GAE/100 g)) and TFCs (368.5 ± 9.39 mg CE/100 g) than S. chirayita nanosuspension, TPCs (500.6 ± 7.8 500.6 ± 7.8 mg GAE/100 g) and TFCs (229.5± 3.85 mg CE/100 g). Antioxidant activity was evaluated through DPPH scavenging assay, and nanosuspension exhibited a lower DPPH free radical scavenging potential (06 ±3.61) than extract (28.9± 3.85). Anti-dabetic potential was assessed throughα-amylase inhibition and anti-glycation assays. Extract showed higher (41.4%) antiglycation potential than 35.85% nanosuspension and 19.5% α-amylase inhibitory potential than 5% nanosuspension. Biofilm inhibition activity against E. coli was higher in nanosuspension (69.12%) than extract (62.08%). The extract showed high cytotoxicity potential (51.86%) than nanosuspension (33.63%). These nanosuspensions possessed enhanced bioactivities for therapeutic applications could be explored further for the development of new drugs.

Preliminary Assessment of Phytochemicals and Free Radical Scavenging Activity of Different Plants Collected from the Western Region of Nepal

Medicinal plants produce vital secondary metabolites in curing various diseases and pathological conditions. There are multiple tribes and communities where people are using plants from the medicinal aspect to cure different diseases. The aim of the present study was qualitative and quantitative phytochemical screening, determination of total phenol and total flavonoid content, and free radical scavenging activity of different parts of ethnomedicinally used plants collected from the western region of Nepal. The phytochemical screening of most of the extract showed the presence of phenols, carbohydrates, flavonoids, and glycosides. The ethanolic flower extract of Callicarpa macrophylla showed a higher phenolic content with a value of 195 ± 7.33 µg GAE/mg. Ethyl acetate extract of Elephantopus scaber root revealed the highest amount of flavonoid content with the value of 1692.31 ± 34.79 µg QE/mg of extract, followed by ethanolic flower extract of Callicarpa macrophylla. Ethanolic flower extract of Callicarpa macrophylla showed potent DPPH free radical scavenging activity with a half inhibitory concentration of 7.28 µg/ml. In contrast, Elephantopus scaber ethyl acetate root extract revealed the maximum free extreme scavenging properties among all the ethyl acetate extracts. From the experiment, the free radical scavenging potential of ethanolic flower extract of the Callicarpa macrophylla was comparable with ascorbic acid. This comparable activity may be attributed to higher phenols and flavonoid content in ethanolic extract. The result signifies that the ethanolic extract of Callicarpa macrophylla acts as an antioxidant and may contain a potent bioactive compound which, with further investigation, may lead to a novel compound.

Chitosan-based multifunctional films reinforced with cerium oxide nanoparticles for food packaging applications

The current study discusses the use of nanoceria as a multifunctional filler in food packaging biopolymer films for the first time. Nanoceria was synthesized using co-precipitation method. Chitosan-based food packaging films incorporated with 1 wt% and 2 wt% nanoceria were prepared and characterized. The FTIR absorption spectra confirms the presence of hydrogen bonding between nanoceria and chitosan structure. The nanocomposite films displayed strong UV-A and UV-B blocking properties besides being mechanically strong, thermally stable and possessing high moisture barrier properties. Further, due to the switching of oxidation states by cerium between Ce3+ and Ce4+, nanoceria shows high photocatalytic activity. This results in strong antimicrobial activity against E. coli and L. monocytogenes, especially under visible light. Further, the nanocomposite films displayed ∼1.25 times and ∼2.3 times higher ABTS and DPPH free radical scavenging potential, respectively, compared to pristine chitosan films, which indicate their high antioxidant potential. Moreover, the films depicted good biocompatibility towards L929 cells indicating their safety for food contact applications. With all these properties, the nanoceria-added chitosan films display strong potential for use in active food packaging, especially for high fat food products such as nuts and meats.

Screening of Antioxidant, Antibacterial, Anti-Adipogenic, and Anti-Inflammatory Activities of Five Selected Medicinal Plants of Nepal.

Herbal products have been widely used for the treatment of diseases throughout the ages. In this research, we investigated antioxidant, antibacterial, anti-adipogenic, and anti-inflammatory activities of methanolic extracts of five ethnomedicinally important plants; namely, Alnus nepalensis, Dryopteris sparsa, Artocarpus lacucha, Litsea monopetala, and Lyonia ovalifolia. We investigated the DPPH free radical scavenging potential, sensitivity of selected bacterial strains towards the extracts using a disc diffusion assay, anti-inflammatory activity in RAW-264.7 cells, and anti-adipogenic activity by the ORO assay in 3T3-L1 preadipocytes. The extract of A. nepalensis showed significant antioxidant activity (IC50=4.838 µg/mL), followed by A. lacucha, L. monopetala, and L. ovalifolia, exhibiting comparable IC50 values to that of ascorbic acid (IC50=5.063 µg/mL). Alnus nepalensis also showed good antibacterial activity in disc diffusion methods, with remarkable zones of inhibition in A. baumannii (14.66 mm) and P. mirabilis (15.50 mm) bacterial species. In addition, A. nepalensis was found to increase adipogenesis in 3T3-L1 cells, evidenced by increased lipid deposition in differentiated 3T3-L1 cells. A similar pattern of increased adipogenesis was observed on treatment with L. ovalifolia extracts. On the other hand, A. lacucha effectively reduced lipid deposition in 3T3-L1 cells at 100 µg/mL (75.18±6.42%) by inhibiting adipogenesis, showing its potential use in the management of obesity. Furthermore, A. lacucha 100 µg/mL (15.91±0.277 µM) and L. monopetala 75 µg/mL (12.52±0.05 µM) and 100 µg/mL (11.77±0.33 µM) significantly inhibited LPS-induced nitric oxide production in RAW 264.7 cells. Also, A. nepalensis and L. ovalifolia inhibited NO production significantly, endorsing their anti-inflammatory potential. The findings from these in-vitro studies suggest that the selected five plants possess remarkable antioxidant, antibacterial, anti-adipogenic, and anti-inflammatory activities. This study opens the door to conduct further advanced in-vivo experiments to find possible lead compounds for the development of valuable therapeutic agents for common health problems.

Physicochemical and nanomedicine applications of phyto-reduced erbium oxide (Er2O3) nanoparticles

Hyphaene thebaica fruits were used for the fabrication of spherical erbium oxide nanoparticles (HT-Er2O3 NPS) using a one-step simple bioreduction process. XRD pattern revealed a highly crystalline and pure phase with crystallite size of ~ 7.5 nm, whereas, the W–H plot revealed crystallite size of 11 nm. FTIR spectra revealed characteristic Er-O atomic vibrations in the fingerprint region. Bandgap was obtained as 5.25 eV using K-M function. The physicochemical and morphological nature was established using Raman spectroscopy, reflectance spectroscopy, SAED and HR-TEM. HT-Er2O3 NPS were further evaluated for antidiabetic potential in mice using in-vivo and in-vitro bioassays. The synthesized HT-Er2O3 NPS were screened for in vitro anti-diabetic potentials against α-glucosidase enzyme and α-amylase enzyme and their antioxidant potential was evaluated using DPPH free radical assay. A dose dependent inhibition was obtained against α-glucosidase (IC50 12 μg/mL) and α-amylase (IC50 78 μg/mL) while good DPPH free radical scavenging potential (IC50 78 μg mL−1) is reported. At 1000 μg/mL, the HT-Er2O3 NPS revealed 90.30% and 92.30% inhibition of α-amylase and α-glucosidase enzymes. HT-Er2O3 NPs treated groups were observed to have better glycemic control in diabetic animals (503.66 ± 5.92*** on day 0 and 185.66 ± 2.60*** on day 21) when compared with positive control glibenclamide treated group. Further, HT-Er2O3 NPS therapy for 21 days caused a considerable effect on serum total lipids, cholesterol, triglycerides, HDL and LDL as compared to untreated diabetic group. In conclusion, our preliminary findings on HT-Er2O3 NPS revealed considerable antidiabetic potential and thus can be an effective candidate for controlling the post-prandial hyperglycemia. However, further studies are encouraged especially taking into consideration the toxicity aspects of the nanomaterial.

Design, synthesis, in vitro anti-oxidant evaluation, α-amylase inhibition assay, and molecular docking analysis of 2-(2-benzylidenehydrazinyl)-4,4-diphenyl-1H-imidazol-5(4H)-ones

Reactive oxygen and nitrogen species (RONS) regulate physiological processes to ensure cellular integrity. However, overproduction of RONS leads to oxidative stresses which results in certain disorders like Diabetes Mellitus. In this connection, the design, synthesis, in vitro anti-oxidant, antidiabetic, and molecular docking (MD) analysis of a series of thiohydantoin-azomethine hybrids was carried out. Their oxidative potential was revealed from in vitro% DPPH quenching, phosphomolybdenum, and ferric (Fe3+) ion-reducing assays. Consequently, most of the screened compounds displayed excellent dose-dependent in vitro response as evident by their higher% DPPH free radical scavenging potential. The screened 2-hydrazinyl-4,4-diphenyl-1H-imidazol-5(4H)-one displayed the highest DPPH scavenging potential with IC50 values of 98.23 µg/mL and the associated DPPH free radical scavenging of 87.14%. Similarly, the screened compounds were found to have higher total anti-oxidant contents than their reducing contents. Moreover, the synthesized compounds were subjected to in vitro screening against the α-amylase enzyme. Most of the screened compounds lack pronounced dose-dependent responses, associated with lower% α-amylase inhibitory potential, and higher IC50 values. The most potent compound 2-(2-(4-(dimethylamino)benzylidene)hydrazinyl)-4,4-diphenyl-1H-imidazol-5(4H)-one displayed notable inhibition (65%) with IC50 value of 120.3 µg/mL using Acarbose as a reference standard. Furthermore, molecular docking analysis revealed that the screened compounds bind well within the active site of the α-amylase enzyme. The compounds bearing electron-withdrawing groups displayed better binding potential in comparison to those having electron-donating substituents.

PHYTOCHEMICAL SCREENING, In vitro ANTIOXIDANT AND GC-MS ANALYSIS OF Ziziphus mauritiana LEAVES EXTRACT

Ziziphus mauritiana (Z. mauritiana) is a plant known for its vast nutritional and pharmacological advantages. In the present investigation, leaf extracts of the plants with different solvents were analyzed by colorimetric methods for phytochemicals analysis, spectrophotometrically for the antioxidant activity by DPPH scavenging activity and gas chromatography-mass spectrometry (GC–MS) to identify the important functional groups and phytochemical constituents. The study observed the presence of some bioactive phytochemical constituents such as saponins, tannins, alkaloids, phenolics, terpenoids and flavonoids compounds. Colorimetric method suggested that, chloroform extract had the highest content of total phenolics (84.60 ± 0.92 μg GAE/mg of extract) while methanol extract contained higher content of total flavonoids (46.91±1.54 μg QE/mg of extract).Further, methanol extract exhibited higher DPPH free radical scavenging potential of 94.47% compared to ethyl acetate extract which showed the lowest activity of 70.34%.The GC– MS analysis detected the presence of 33 phytochemical compounds with diverse chemical structures from the different extracts. Major compounds identified in methanol, ethyl acetate, hexane and chloroform extracts were squalene (30.08%), salviolinic acid (12.55%), α-linolenic acid (26.42%) and palmitic acid (38.50%) respectively in addition to several other bioactive compounds.The results obtained in the present study suggest that leaves of Z. mauritiana can be used as a source for functional ingredients for pharmaceutical and food industries.

Qualitative and Quantitative Phytochemical Screening and Free Radical Scavenging Activity of Different Parts of Rubus ellipticus Sm.

Free radicals are molecules with reactive unpaired electrons which are produced during cell metabolism and create the oxidative stress inside tissue resulting in tissue damage. The aim of the present study was qualitative and quantitative phytochemical screening, determination of total phenolic and total flavonoid content, and free radical scavenging activity of different parts of ethnomedicinally used Rubus ellipticus Sm. plant. Root, stem, and leaves of Rubus ellipticus Sm. were collected from Annapurna Rural Municipality, Kaski, Western Nepal. Ethyl acetate and ethanol extracts of the plant parts were obtained by subsequent maceration process. The phytochemical screening of most of the extract showed the presence of phenols, carbohydrates, flavonoids, and glycosides. The ethanolic extract of stem showed the higher phenolic content with the value of 343.75 ± 2.21 µg GAE/mg. Ethanolic extract of stem had the highest amount of flavonoid content (1563.17 ± 10.79 µg QE/mg of extract), whereas all the ethyl acetate extracts of root, leaves and stem showed comparable flavonoid content. Ethanolic extracts of leaves showed potent DPPH free radical scavenging activity with IC50 value of 5.03µg/ml while ethyl acetate extract of stem showed the maximum free radical scavenging properties. The result depicted that the ethanolic extract of Rubus ellipticus Sm. showed the potent antioxidant activity by scavenging free radicals.

Phytochemical, Antioxidant, hair growth and wound healing property of Juniperus excelsa, Olea oleaster and Olea europaea

To study phytochemical screening, Antioxidant property, and wound healing and hair growth of Olives tree (wild and cultivars) and Juniperus excelsa are the most important natural sources used to treat many diseases around the sultanate of Oman. Preliminary phytochemical analysis and DPPH method of antioxidant assay was carried out invitro. The experimental plant materials were also used to test their effect on hair growth and wound healing on Swiss albino mice(n = 3). Results of phytochemical study showed that tannins, alkaloid, saponin, terpenes, phenolic were found at high concentration (+++), while the rest of the constituents were found at moderate (++) to low concentrations (+). DPPH free radical scavenging potential of water extract of juniperus excelsa was (50 µg/ml = 83.30 %) found to be more effective, at 200 µg/ml concentration be 64.62 % free radical scavenging percentage was noticed. In the wound healing study, it was observed that juniperus extract showed significant result on the recovery of linear wound. Against the hair growth study, it was observed that the wild and cultivar olive water extracts have the best effect on hair growth. From these findings it is clear that these traditional medicinal plant parts can be effectively used for pharmacological preparations.

Qualitative and quantitative phytoconstituent determination, DPPH free radical lowering effect and In-vitro hypoglycemic activity study by alpha amylase enzyme assay along with membrane diffusion technique.

Diabetes mellitus, a physiological disorder is characterized by low secretion of insulin due to the attack in insulin producing beta cell (Type I) or the body cell become insulin resistance (Type II). This study was designed to evaluate the DPPH lowering effect, in-vitro alpha amylase and glucose diffusion inhibition of the selected medicinal plants. Five different plant sample Amomum subulatum, Choerospondias axillaris, Musa sp, Myrica esculenta and Nephrolepis cordifolia were taken for the study. From the result it was revealed that the methanol extracts of Myrica esculenta stem bark and small branches showed potent DPPH free radical scavenging activity with the IC50 value of 4.23 µg/ml and 3.14 µg/ml respectively which is almost comparable to standard Ascorbic acid taken. Meanwhile, alpha-amylase inhibitory study showed that Myrica esculenta stem bark showed potent subsidiary effect on methanol extracts with IC50 value of 0.96 mg/ml which is comparable to standard volgibose taken. Lastly, membrane diffusion study with glucose and plant sample showed that Amomum subulatum seed and Choerospondias axillaris fruit have potent glucose diffusion inhibition with highest GDRI %. From the result, it could be correlated that the free radical scavenging activity and glucose lowering effect of these plant extracts is due to the presence of phytoconstituents like phenolics, flavonoids, alkaloids, terpenoids, glycosides saponins etc. as well as several other uncompetitive modes of inhibition.

Two new bibenzyls from Pleione grandiflora (Rolfe) Rolfe and their antioxidant activity

Two new bibenzyls (1 and 2) were isolated from the pseudobulbs of Pleione grandiflora (Rolfe) Rolfe along with six known compounds, including isoarundinin I (3), isoarundinin II (4), bulbocodin D (5), batatasin III (6), 5,3'-dihydroxy- 4-(p-hydroxybenzyl)-3-methoxybibenzyl (7) and shancigusin F (8). Their structures were established on the basis of spectroscopic methods. These compounds showed potent DPPH free radical scavenging effects with IC50 values ranging from 49.72 ± 0.35 μM to 65.41 ± 0.49 μM.

Antioxidant potential in the leaves of grape varieties (Vitis vinifera L.) grown in different soil compositions

Grape plant ( Vitis vinifera L.) is a species of the family Vitaceae. It is an economically important fruit plant abundantly grown all over the world. Vitaceae comprised of 900 species distributed across tropical, sub-tropical and partially temperate sorts of climatic zones. In the current study we aimed to evaluate the antioxidant activities of grape leaves extract from different Pakistani varieties. We have analyzed the crude methanolic extract from the leaves of Pakistani grape varieties (i.e. NARC Black, Sundar Khani, Shogran-1, Shogran-2, Haita, Sheghali, Perlette, and Sultania-C) cultivated in various soil compositions. Total phenolic contents (TPC) of the extract were determind by using Folin-ciocalteu reagent method. Total flavonoid contents (TFC) were determind by the Aluminum Chloride Calorimetric method. Antioxidant activities of the extracts of different concentration were evaluated using Phosphomolybdenum method, Reducing power and DPPH (2, 2-disphenyl-1-picryl-hydrazyl) assays. Assays performed for grape varieties showed great antioxidant potential. All varieties significantly depicted with variation in polyphenolic contents and antioxidant potential with changes in the soil conditions. The highest TPC and TFC were quantified in Shogran-1 97.58 ± 0.09 (GAE, g −1 ) and Sultania-C 97.47 ± 0.12 (µg QE/g DE) varieties respectively which were grown in (T6) and (T5), while lower were recorded in Sundar khani 5.16 ± 0.23 in (T6). Likewise, Shogran-1 128.26 ± 0.23 (µg AAE/g extract) variety grown in (T6) depicted highest total antioxidant capacity, NARC black 182.06 ± 0.24 (µg AAE/g extract) variety grown in (T6) resulted in maximum reducing power while DPPH free radical scavenging potential were determinded in Sultania-C 80.91 ± 0.10 (T4) equivalent µg/g. In the terms of bioassays, the promising results were showed by compost + sand + clay (T4), compost + clay + dung (T5) and sand + clay + dung (T6). Therefore, we conclude that variation in soil composition has a significant contribution in the quantity of phytochemicals and antioxidants expression. Our study further suggest that use of organic fertilizer (Compost) and loamy sort of soil enhance functioning of most of the varieties in terms of important phytochemicals.

Antioxidant Potential and GC-MS Analysis of Abrus precatorius Linn Leaves Ethanol Extract

Aims: The aim of present study to evaluate the antioxidant potential of Abrus precatorius Linn leaves ethanol extract containing bioactive compounds on free radical scavenger using DPPH. Ethanol extract of Abrus precatorius Linn leaves was subjected to preliminary phytochemical screening and fraction of extract was detected by Gas Chromatography-Mass Spectrometry analysis.&#x0D; Methodology and Results: GC-MS analysis of ethanol leaves extract was carried out on Shimadzu GC-MS model number QP 2010S and revealed the presence of 18 phytochemical compounds, with mome inositol as a dominant component. Antioxidant potential of leaves ethanol extract was evaluated using DPPH free radical scavenging assay at five different doses as 5, 10, 20, 30, 40 and 50 μg/mL and showed significant DPPH free radical scavenging potential with the IC50 value of 33.37 μg/mL. The bioautography of extract showed that fractions with the most prominent antioxidant potential tended to contain secondary metabolites reported in preliminary phytochemical screening such as alkaloids, carbohydrates, protein and amino acids, glycoside, tannins, flavonoids, triterpenoids and phenolic compounds. The results evaluate and justify the traditional relevance of Abrus precatorius Linn leaves ethanol extract for free radical scavenging potential as a antioxidant and can be used as a lead for the isolation of the antioxidant bioactive chemical constituents in further study.&#x0D; Conclusion: Preliminary phytochemical screening reported various bioactive compounds in the ethanol extract of Abrus precatorius Linn leaves and identified by GC-MS. The extract exhibited greater free radical scavenging activity i.e. antioxidant potential. The presence of various bioactive phytocompounds justifies the therapeutic use of the Abrus precatorius Linn plant leaves for various ailments by traditional practitioners.

Synthesis and Antioxidant Studies of Co(II), Ni(II) and Zn(II) Metal Complexes of 6-Pyridyl-5, 6-Dihydrobenzo[4,5]-Imidao[1,2-C] Quinazoline (N-N) Derivatives

The major class of organic molecules synthesis involved by the various atoms in their molecules, and they are joined in rings containing at least one atom in any synthesized compound of an element other than that of carbon atom (C). The current study aimed to synthesize the heterocyclic compound as one of the derivative N-heterocycle (I) using various complex materials and to determine their biological property in in vitro antioxidant study. Synthesis and antioxidant activities of novel Co(II), Ni(II) and Zn(II) Metal Complexes of 6-Pyridyl-5,6-Dihydrobenzo[4,5]- Imidao[1,2-C] Quinazoline (N-N) derivatives were undertaken employing a convenient and easily accessible procedure. The structures of all the synthesized compounds were confirmed with elemental analysis, IR, C13 NMR and H1NMR to know the probable structure of the molecules by stereochemistry. The synthesized five compounds were screened for in vitro antioxidant activity by 2, 2-Diphenyl-1-picrylhydrazyl (DPPH) method. In Antioxidant studies, compound C-2 exhibited maximum inhibition (77%) at 250μg/ml concentration showing satisfactory DPPH free radical scavenging potential with the IC50 concentration at 33.61μg/ml compared to the standard drug, ascorbic acid with 6ug/ml used for the study and other compounds were also exhibited minimum antioxidant property.

The Role of Allium subhirsutum L. in the Attenuation of Dermal Wounds by Modulating Oxidative Stress and Inflammation in Wistar Albino Rats.

In our study, Allium subhirsutum L. (AS) was investigated to assess its phenolic profile and bioactive molecules including flavonoids and organosulfur compounds. The antioxidant potential of AS and wound healing activity were addressed using skin wound healing and oxidative stress and inflammation marker estimation in rat models. Phytochemical and antiradical activities of AS extract (ASE) and oil (ASO) were studied. The rats were randomly assigned to four groups: group I served as a control and was treated with simple ointment base, group II was treated with ASE ointment, group III was treated with ASO ointment and group IV (reference group; Ref) was treated with a reference drug “Cytolcentella® cream”. Phytochemical screening showed that total phenols (215 ± 3.5 mg GAE/g) and flavonoids (172.4 ± 3.1 mg QE/g) were higher in the ASO than the ASE group. The results of the antioxidant properties showed that ASO exhibited the highest DPPH free radical scavenging potential (IC50 = 0.136 ± 0.07 mg/mL), FRAP test (IC50 = 0.013 ± 0.006 mg/mL), ABTS test (IC50 = 0.52 ± 0.03 mg/mL) and total antioxidant capacity (IC50 = 0.34 ± 0.06 mg/mL). In the wound healing study, topical application of ASO performed the fastest wound-repairing process estimated by a chromatic study, percentage wound closure, fibrinogen level and oxidative damage status, as compared to ASE, the Cytolcentella reference drug and the untreated rats. The use of AS extract and oil were also associated with the attenuation of oxidative stress damage in the wound-healing treated rats. Overall, the results provided that AS, particularly ASO, has a potential medicinal value to act as effective skin wound healing agent.

Antioxidant and Antibacterial Activities of Four Local Medicinal Plants

Potential antioxidant and antibacterial activity of methanolic, chloroformic and n-hexane leaf extracts of four local important medicinal plants like Ocimum americanum, O. basilicum, O. gratissimum and Centella asiatica was investigated. The methanolic leaf extracts of these plant species exhibited the potent DPPH free radical scavenging activity (IC50 value, 2.67 ± 0.01, 14.17 ± 0.11, 60.22 ± 0.01 and 2.39 ± 0.025 μg/ml, respectively). Methanolic leaf extract of C. asiatica showed strongest antioxidant activity. Chloroformic leaf extracts possessed moderate antioxidant activity (IC50 value of 79.44 ± 0.05, 110.56 ± 0.02, 54.95 ± 0.05, 101.0 ± 1.0 μg/ml, respectively) in all samples. The lowest antioxidant activity was recorded from n-hexane leaf extracts of O. americanum, O. gratissimum, C. asiatica and Ocimum basilicum (IC50 value 147.87 ± 0.06, 378.19 ± 2.65, 104.65 ± 0.39, 467.58 ± 0.52 μg/ml, respectively). Methanolic and chloro-formic leaf extracts showed antibacterial activity against both Gram-positive and Gram-negative pathogenic bacteria, namely Bacillus megaterium, Escherichia coli, Pseudomonas aeruginosa and Salmonella typhi. Methanolic leaf extract of O. americanum and chloroformic extract of C. asiatica showed excellent antimicrobial activity.&#x0D; Plant Tissue Cult. &amp; Biotech. 30(2): 179-187, 2020 (December)

Extraction kinetic of some phenolic compounds during Cabernet Sauvignon alcoholic fermentation and antioxidant properties of derived wines

In this study, we estimated the usage of Cabernet Sauvignon in microvinifications, obtaining wines with increased phenolic compound content. Kinetic extraction of phenolic compounds during alcoholic fermentation was affected by maceration time (3, 5, 7, 14 and 21 days) and the addition and kinetics of enzyme preparations (EP). The highest extraction rates were observed for catechin (EXV EP – EXV enzyme preparation and CP EP – Color plus enzyme preparation) and p-hydroxybenzoic acid (Car EP - Caractere enzyme preparation). According to extraction time of the analyzed phenolic compounds, maximal values (ellagic acid, ferulic acid, chlorogenic acid, caffeic acid, naringenin, p-hydroxybenzoic acid, p-coumaric acid, protocatechuic acid, trans-resveratrol, syringic acid, vanillin, and vanillic acid) were obtained on day 15 of maceration with addition of CP EP, with exceptions of gallic acid, catechin, and myricetin. Prolonged maceration times, up to 21 days, showed the most potent DPPH free radical scavenging activity with Car EP and the highest Ferric Reducing Ability of Plasma (FRAP) values with CP EP.