scholarly journals Oxygen radical antioxidant capacity (ORAC) and antibacterial properties of Melicope glabra bark extracts and isolated compounds

PLoS ONE ◽  
2021 ◽  
Vol 16 (5) ◽  
pp. e0251534
Author(s):  
Alexandra Quek ◽  
Hafizah Mohd Zaini ◽  
Nur Kartinee Kassim ◽  
Fadzil Sulaiman ◽  
Yaya Rukayadi ◽  
...  

Melicope glabra (Blume) T. G. Hartley from the Rutaceae family is one of the richest sources of plant secondary metabolites, including coumarins and flavanoids. This study investigates the free radical scavenging and antibacterial activities of M. glabra and its isolated compounds. M. glabra ethyl acetate and methanol extracts were prepared using the cold maceration technique. The isolation of compounds was performed with column chromatography. The free radical scavenging activity of the extracts and isolated compounds were evaluated based on their oxygen radical absorbance capacity (ORAC) activities. The extracts and compounds were also subjected to antibacterial evaluation using bio-autographic and minimal inhibitory concentration (MIC) techniques against two oral pathogens, Enterococcus faecalis and Streptococcus mutans. Isolation of phytoconstituents from ethyl acetate extract successfully yielded quercetin 3, 5, 3’-trimethyl ether (1) and kumatakenin (2), while the isolation of the methanol extract resulted in scoparone (3), 6, 7, 8-trimethoxycoumarin (4), marmesin (5), glabranin (6), umbelliferone (7), scopoletin (8), and sesamin (9). The study is the first to isolate compound (1) from Rutaceae plants, and also the first to report the isolation of compounds (2–5) from M. glabra. The ORAC evaluation showed that the methanol extract is stronger than the ethyl acetate extract, while umbelliferone (7) exhibited the highest ORAC value of 24 965 μmolTE/g followed by glabranin (6), sesamin (9) and scopoletin (8). Ethyl acetate extract showed stronger antibacterial activity towards E. faecalis and S. mutans than the methanol extract with MIC values of 4166.7 ± 1443.4 μg/ml and 8303.3 ± 360.8 μg/ml respectively. Ethyl acetate extract inhibited E. faecalis growth, as shown by the lowest optical density value of 0.046 at a concentration of 5.0 mg/mL with a percentage inhibition of 95%. Among the isolated compounds tested, umbelliferone (7) and sesamin (9) exhibited promising antibacterial activity against S. mutans with both exhibiting MIC values of 208.3 ± 90.6 μg/ml. Findings from this study suggests M. glabra as a natural source of potent antioxidant and antibacterial agents.

Author(s):  
Praptiwi Praptiwi ◽  
Ahmad Fathoni

Objective: The objectives of the study were to investigate phytochemical screening and gas chromatography-mass spectrometry (GC-MS) profiling of twigs and leaves of Exocarpos longifolius and its 2,2-diphenyl-1-picrylhydrazyl free radical scavenging activity.Methods: Phytochemical screening covering saponins, alkaloids, terpenoids, flavonoids, and tannins were carried out by standard methods. The free radical scavenging activity was performed by thin-layer chromatography - bioautography, followed by determining the IC50 values of active extracts. Chemical compounds of active extract were examined by gas chromatography/mass spectrometry.Results: The phytochemical screening revealed that all extracts have been shown to contain tannins and terpenoids, saponins were found in the methanol extract of twigs, and alkaloids were found in the ethyl acetate extracts of twigs and leaves, while flavonoids were found in the methanol extract and ethyl acetate extracts of twigs and leaves of E. longifolius. Ethyl acetate extract of twigs showed the best of IC50 value (15.65 μg/mL), while ethyl acetate extract of leaves and methanol extract of twigs have strong free radical scavenging activity which IC50 were 78.59 and 67.24 μg/mL, respectively. The GC-MS analysis of ethyl acetate extract of twigs has shown the presence of 12 identified compounds, and the main chemical compound is Stigmast-4-en-3-one (21.91%).Conclusions: The ethyl acetate extract of E. longifolius showed a very powerful free radical scavenging activity and revealed chemical compounds had been known to have biological activity. It might be used as a natural antioxidant.


Author(s):  
Sethupandian Geetha ◽  
Kokkaiah Irulandi ◽  
Palanichamy Mehalingam

Objective: This study was designed to determine the Total phenol, flavonoid content, antioxidant and free radical scavenging properties of different solvent extracts of Piper umbellatum.  Methods: Different solvent extracts evaluated with DPPH radical scavenging activity and Reducing power activity.Results: The presence of phenol and flavonoid showed highly in the methanol extracts than ethyl acetate and acetone extracts. All the extracts have various level of antioxidant activity. Methanol solvent extract have good extraction and show significant antioxidant activity. The effect of reducing power of methanol extract revealed good antioxidant activity compare with other tested extracts.Conclusion: On the basis of the above results we concluded that methanol extract of Piper umbellatum whole plant extracts shows significant antioxidant activity than ethyl acetate and acetone extracts.Keywords: Piper umbellatum, Antioxidant, DPPH, FRAP assay, Polar, Non polar solvents


2016 ◽  
Vol 19 (4) ◽  
pp. 76-83
Author(s):  
Trang Thi Xuan Dai ◽  
Anh Thi Tu Vo

This study was subjected to investigate antimicrobial and antioxidant properties of Eclipta alba extracts (methanol, hexane, chloroform and ethyl acetate extracts). The antioxidant property of the extract was assessed by 2,2- diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging method. Kirby-Bauer method was used to determine the antibacterial activity against Enterobacter cloacae of the extracts. The extracts of Eclipta alba were tested against E. cloacae. The highest antibacterial potentiality was exhibited by the ethyl acetate extract of E. alba leaves, means of zones of bacterial growth inhibition are 26.3 mm at a concentration of 32 μg/mL. DPPH free radical scavenging effect of the extracts was compared with standard antioxidant vitamin C. The highest antioxidant activity was exhibited by the ethyl acetate extract of E. alba leaves. The result also showed that the DPPH scavenging activity of ethyl acetate extract from leaves of E. alba was high (EC50 = 419.38 μg/mL). However, this result was 18.99 times lower than that of vitamin C (EC50 = 22.08 μg/mL).


Author(s):  
Adaikalam Raj ◽  
Saranya D ◽  
Sekar J

Objective: This study evaluated the antioxidant properties of petroleum ether, chloroform, ethyl acetate and methanol extracts of Abutilon indicum (L).Methods: The different extracts of A. indicum leaves, bark and roots  were antioxidant potential by using 1,1-diphenyl-2-picryl-hydrazyl (DPPH), 2, 2-Azino-bis-3-ethyl benzthiazoline-6-sulphonic acid (ABTS•+) , Hydrogen peroxide scavenging, Superoxide anions scavenging,  Hydroxyl radical scavenging, Ferric reducing antioxidant power, Total antioxidant activity (Phosphomolybdic acid) and total phenol and flavonoid contents.                      Results: The highest total phenol and flavonoid contents in leaves extracts of A. indicum. The total phenol (3.08 ± 0.06) mg/ml and flavonoid (7.16 ± 0.15) mg/ml were found to be higher in ethyl acetate extract of A. indicum and free radical scavenging activities IC50 values were calculated and compare to standard for L- ascorbic acid, (BHT) butylated hydroxytoluene and gallic acid    Conclusion:  The results of the study revealed that the ethyl acetate extract of A. indicum leaves can be used for the biological characterization and importance of the compounds identified and creates a platform to screen many bioactive compounds to treat many diseases.Keywords: Abutilon indicum, Free radical scavenging activity, 1,1-diphenyl-2-picryl-hydrazyl, 2-azino-bis-3-ethyl benzthiazoline-6-sulfonic acid,Ferric reducing antioxidant power.


Author(s):  
Gulnaaz Sabri ◽  
Vimala Y

 Objective: The aim of this study was to explicate antibacterial, antifungal, and antioxidant activities of Leucas aspera flowers.Methods: Antibacterial activity was done by agar diffusion method. The ethyl acetate extract of L. aspera flower was evaluated against both Gram-positive and Gram-negative bacteria. Antifungal activity was also done by agar diffusion method. The agar used for antifungal activity was Czapek Dox Agar. Nitric oxide scavenging assay and free radical scavenging assay were used for the antioxidant activity. Griess reagent was used in nitric oxide scavenging assay. 1,1-diphenyl-2-picryl hydrazyl was used in free radical scavenging assay.Results: L. aspera flower extract showed good antibacterial activity with the highest zone of inhibition against Vibrio cholera with 23 mm followed by Bacillus polymyxa showing 20 mm zone of inhibition. The ethyl acetate extract of L. aspera flower showed quite a good results with the highest inhibitory activity against Aspergillus niger with 13 mm zone of inhibition and lowest for Trichoderma viridae with 5 mm zone of inhibition. Antioxidant activity of L. aspera flower extract was done by free radical scavenging assay and nitric oxide scavenging assay. Nitric oxide scavenging assay showed prominent results almost performed equal to standard compound Butylated hydroxyl anisole (BHA) The values for 10 μl of L. aspera extract was 50.27, for the standard (BHA) showed 50.81. L. aspera extract values for 50 μl was 69.73 and for BHA, the values was 77.30. For 100 μl, the extract gave 82.70, and for standard BHA, the reading was 89.73.Conclusion: The results showed that L. aspera flower has broad-spectrum antibacterial activity ranging from 23 to 13 mm zone of inhibition. L. aspera flower has strong antioxidative power on nitric oxide radicals. The medicinal properties of plant species have made an outstanding contribution to the origin and evolution of many traditional herbal therapies.


Author(s):  
Renuka Saravanan ◽  
Brindha Pemaiah ◽  
Mahesh Narayanan ◽  
Sivakumar Ramalingam

  Objective: This study was aimed to assess the phytoconstituents, cytotoxic, and antioxidant efficacy of ethyl extract of Cleome gynandra leaves.Methods: Qualitative phytochemical analysis with different solvent extracts was performed. Quantitative and gas chromatography-mass spectrometry (GC-MS) analysis of the extract was performed with ethyl acetate extract. The cytotoxic effect of the ethyl acetate extract was determined by 3-[4,5-dimethylthiazol-2-yl]2,5-diphenyltetrazolium bromide (MTT) assay on Michigan Cancer Foundation-7 (MCF-7) cells using taxol as standard and free radical scavenging ability using 1,1-diphenyl-2-picrylhydrazyl (DPPH).Results: Leaves extracts with different solvents revealed the presence of alkaloids, cardiac glycosides, flavonoids, phenols, and tannins. GC-MS analysis of ethyl acetate of the plant leaves showed the presence of n-hexadecanoic acid. The IC50 value of the ethyl acetate extract was found to be 90.2 μg/ml on MCF-7 cell line, and the extract was found to possess significant DPPH free radical scavenging activity.Conclusion: From the results, we conclude that the C. gynandra extract possesses antioxidant and antiproliferating activity against MCF-7 cells.


2015 ◽  
Vol 18 (1) ◽  
pp. 25-29
Author(s):  
Faiza Tahia ◽  
Md Al Amin Sikder ◽  
Mohammad A Sayeed ◽  
Mohammad A Rashid

The present study was designed to evaluate the antioxidant, cytotoxic, thrombolytic, membrane stabilizing and antimicrobial activities of methanol extracts and different organic soluble partitionates of leaves of Murraya koenigii and bark of Adina cordifolia. In the DPPH free radical scavenging assay, the chloroform soluble fraction of methanol extracts of M. koenigii and A. cordifolia revealed the highest free radical scavenging activity with IC50 values of 6.9 ± 0.78 ?g/ml and 6.83 ± 0.29 ?g/ml, while the methanolic crude extract of M. koenigii and A. cordifolia displayed the highest cytotoxic potential having LC50 values of 1.94 ± 0.36 ?g/ml and 0.88 ± 0.64 ?g/ml, respectively as compared to standard vincristine sulphate (LC50 value of 0.45 ?g/ml). During assay for thrombolytic activity, the crude extracts of M. koenigii and A. cordifolia showed 8.6 ± 0.48 % and 9.25 ± 0.84% clot lysis, respectively. In the membrane stabilizing assay, the methanol extract of M. koenigii inhibited 62.80 ± 0.81 % and 21.23 ± 0.84 % hypotonic solution- and heat-induced haemolysis of RBCs as compared to 72.2 % and 42.2 % inhibition by acetyl salicylic acid (0.10 mg/ml), respectively. On the other hand, the methanol extract of A. cordifolia demonstrated 42.04 ± 0.57 % and 21.57 ± 0.22 % inhibition of hypotonic solution- and heat-induced hemolysis, respectively. The extractives of A. cordifolia exhibited antibacterial activity with zone of inhibition ranging from 8.0 to 26.0 mm against the test microorganisms with the highest zone of inhibition (26.0 mm) against Salmonella Typhi. Although the methanol extract of leaf of M. koenigii as well as its pet ether and aqueous soluble fractions demonstrated no antimicrobial activity, the carbon tetrachloride soluble fraction (CTC) revealed moderate antibacterial activity against Staphylococcus aureus (16.0 mm).Bangladesh Pharmaceutical Journal 18(1): 25-29, 2015


2020 ◽  
Vol 5 (1) ◽  
pp. 15-20
Author(s):  
Mohammad Emdadul Islam ◽  
Tofail Ahmed Chowdhury ◽  
Nasim Sultana ◽  
Abul Hasnat Muhammad Solaiman ◽  
SM Anamul Arefin

Biological activity was studied of the different solvent extracts such as n-hexane, ethyl acetate, n-butanol, and methanol extracts of the rhizomes of Sensevieria hyacinthoides. The cytotoxic potential were examined by using brine shrimp lethality bioassay. Ethyl acetate extract exhibited quite potent activity in brine shrimp lethality bioassay with LC50 1.95 μg/mL, respectively. These result suggested that it might contain antitumor or cytotoxic agent. The ethyl acetate extract showed significant free radical scavenging activity with IC50 10.51 μg/mL and demonstrated excellent antibacterial activity. The free radical scavenging activity of the solvent extracts (n-hexane, ethyl acetate and n-butanol) were assayed by using DPPH method. The IC50 for Vit-c (Ascorbic acid) and ethyl acetate extract were found to be 3.91 and 10.51 μg/mL, respectively. Asian Australas. J. Biosci. Biotechnol. 2020, 5 (1), 15-20


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