scholarly journals PHYTOCHEMICAL SCREENING, TOTAL FLAVONOID, ANTIOXIDANT ACTIVITY, AND TOXICITY OF ETHANOL EXTRACT Cleome gynandra L. HERB

2018 ◽  
Vol 3 (2) ◽  
pp. 41
Author(s):  
Agustinus Widodo ◽  
Ritha Pratiwi
Keyword(s):  
Antioxidant Activity ◽  
Ethanol Extract ◽  
Total Flavonoid ◽  
Phytochemical Screening ◽  
Food Ingredients ◽  
The People ◽  
Cleome Gynandra ◽  
Dpph Method ◽  
Central Sulawesi

<em>Cleome gynandra L. is one of the plants that the people of Palu, Central Sulawesi use as food ingredients. This plant is empirically used in traditional medicine. This study aims to determine phytochemical constituents, total flavonoid, antioxidant activity, and toxicity of 96% ethanol extract of C. gynandra herb. C. gynandra herb extract was obtained by maceration. Phytochemical screening of the ethanol extract was carried out qualitatively according to the standard methods. Determination of total flavonoid using AlCl<sub>3</sub> then determined by Spectrophotometric UV-Vis. Antioxidant activity using the DPPH method and determined IC<sub>50</sub> value. Toxicity test was assessed using shrimp lethality as an indicator of toxicity. Phytochemical screening showed 96% ethanol extract containing alkaloid compounds, flavonoids, saponins, steroids, and tannins. Total flavonoid of the 96% ethanol extract was 4,778 ± 0,522 mg QE/g extract. Antioxidant activity (IC<sub>50</sub>) of the ethanol 96% extract was 189,455 µg/ml. Lethal concentration 50% of the 96% ethanol extract was 472,648 mg/L (toxic). The results of this study indicate that 96% ethanol extract of C. gynandra herb has antioxidant activity and has the potential to be further tested as an anticancer activity.</em>

scholarly journals Determination of Quality Parameters and Antioxidant Activity of Cincau Hijau Leaves (Cyclea barbata L.Miers.)

2017 ◽  
Vol 15 (2) ◽  
pp. 236
Author(s):  
Erlindha Gangga ◽  
Rani Purwati ◽  
Yunahara Farida ◽  
Kartiningsih Kartiningsih
Keyword(s):  
Antioxidant Activity ◽  
Heavy Metal Contamination ◽  
Radical Scavenging ◽  
Ethanol Extract ◽  
Ash Content ◽  
Water Soluble ◽  
Phytochemical Screening ◽  
Water Soluble Compound ◽  
Dpph Method

Cincau Hijau leaves (Cyclea barbata L.Miers ) has been used empirically as a medicinal plant because it contains many potential compounds such as flavonoids. Cincau Hijau leaves has been known as antioxidant activity. Determination of pharmacognosy parameters and phytochemical screening of dry leaves and extracts have been carried out as well as determination of total fl avonoids content. Fresh leaves were extracts with water and Dry leaves were macerated with 96% ethanol and were then concentrated by rotavapor to obtain viscous extracts. Free radical scavenging activity of the extracts was evaluated using DPPH method. Afterwards, determination of specifi c and non-specifi c parameters were performed. Results of phytochemical screening of powder and 50% and 96% ethanol extract showed that tall the tested samples contained alkaloid, fl avonoids, saponins, tannins, steroids/ triterpenoids, coumarin. The examination of specifi c parameter showed that the extract has a thick consistency, tawny color, bitter taste, characteristic odor. In addition, water-soluble compound and 96% ethanol extract are 46.64 and 62.13% respectively whereas ethanol-soluble compounds are 39.22 and 74.72%, respectively. While the results of nonspecifi c parameters of 50% and 96 % ethanol extract displayed total ash content of 9.69 and 9.49%, respectively, acid insoluble ash content of 0.30 and 0.16%, respectively, content of water soluble ash of 9.17 and 4.30%, respectively, loss on drying of 9.35 and 8.9%, respectively, water content of 8.45 and 7.25%, respectively. Based on heavy metal contamination, Pb concentration in 50 and 96% ethanol extract are 0.0227 and 0.0333 mg/kg, respectively whereas Cd concentration are 0.1206 and 0.0022 mg/kg, respectively and total number of CFU of 4,22 x 103 and 2,30 x 103 colonies/g, respectively while molds and yeasts number of colony of 0,48 x 102 and 8,88 x 102 colonies/g, respectively. Moreover, the total flavonoid was 0,19 %. Result of DPPH inhibition test showed that IC50 96 % ethanol extract are 83,280 ppm and water extracts are 102,01 ppm

scholarly journals Phytochemical screening and in vitro antibacterial, antifungal, antioxidant and antitumor activities of the red propolis Alagoas

2019 ◽  
Vol 79 (3) ◽  
pp. 452-459 ◽  
Author(s):  
F. R. G. Silva ◽  
T. M. S. Matias ◽  
L. I. O. Souza ◽  
T. J. Matos-Rocha ◽  
S. A. Fonseca ◽  
...  
Keyword(s):  
Antimicrobial Activity ◽  
Antioxidant Activity ◽  
Phenolic Compounds ◽  
Gallic Acid ◽  
Bioactive Metabolites ◽  
Diffusion Method ◽  
Total Phenolic ◽  
Phytochemical Screening ◽  
Dpph Method

Abstract The study aimed to evaluate the antimicrobial activity, antioxidant, toxicity and phytochemical screening of the Red Propolis Alagoas. Antimicrobial activity was evaluated by disk diffusion method. Determination of antioxidant activity was performed using the DPPH assay (1.1-diphenyl-2-picrylhydrazyl), FTC (ferric thiocyanate) and determination of phenolic compounds by Follin method. Toxicity was performed by the method of Artemia salina and cytotoxicity by MTT method. The phytochemical screening for the detection of allelochemicals was performed. The ethanol extract of propolis of Alagoas showed significant results for antimicrobial activity, and inhibitory activity for Staphylococcus aureus and Candida krusei. The antioxidant activity of the FTC method was 80% to 108.3% hydrogen peroxide kidnapping, the DPPH method showed an EC50 3.97 mg/mL, the content of total phenolic compounds was determined by calibration curve gallic acid, resulting from 0.0005 mg/100 g of gallic acid equivalent. The extract was non-toxic by A. salina method. The propolis extract showed high activity with a higher percentage than 75% inhibition of tumor cells OVCAR-8, SF-295 and HCT116. Chemical constituents were observed as flavonones, xanthones, flavonols, and Chalcones Auronas, Catechins and leucoanthocyanidins. It is concluded that the extract can be tested is considered a potential source of bioactive metabolites.

scholarly journals THE QUALITY PARAMETERS, TOTAL FLAVONOIDS DETERMINATION AND ANTIOXIDANT ACTIVITY COMPOUND OF ANDALIMAN FRUIT ANDALIMAN FRUIT (ZANTHOXYLUM ACANTHOPODIUM DC.) EXTRACT

2021 ◽  
pp. 34-40
Author(s):  
YUNAHARA FARIDA ◽  
WIDI AZELA ◽  
MEGA ELOK LESTAR ◽  
DIAH KARTIKA PRATAMI
Keyword(s):  
Antioxidant Activity ◽  
Methyl Palmitate ◽  
Ethanol Extract ◽  
Quality Parameters ◽  
Total Flavonoid ◽  
Gas Chromatography Mass Spectrometry ◽  
Uv Spectrophotometry ◽  
Benzenedicarboxylic Acid ◽  
Ic50 Value ◽  
Dpph Method

Objective: The aim of this study was to investigate the chemical compound of the antioxidant activity of the extract from andaliman fruit (Zanthoxylum acanthopodium DC.) and the quality parameters and the total flavonoid determination of the highest antioxidant activity. Methods: The andaliman fruits were extracted using a solvent such as n-hexane, ethyl acetate and 70% ethanol obtained extracts, follow the antioxidant activity using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) method. The quality parameters and total flavonoid determination were performed from highest antioxidant activity. Fractionated was done using vacuum liquid chromatography (VLC) with the mobile phase chloroform-methanol (9:1 ~1:9). Purification with Thin Layer Chromatography (TLC) preparative, identification using UV-spectrophotometry, FTIR, Gas chromatography Mass Spectrometry (GCMS) analysis. Results: The 70% of ethanol has the highest antioxidant activity with IC50 value 84.11±0.47 ppm; the quality parameters in this study meet the quality requirements, both specific and nonspecific parameters. Total flavonoid content of the 70% ethanol extract was 2.37±0.02%. The results of the GCMS studies showed the presence of 1,2-benzenedicarboxylic acid, mono (2-ethylhexyl) ester; squalene, methyl palmitate, methyl isopalmitate, n-tetracosanol-1 and 4-isopropyl chalcone. Conclusion: The results indicate that the 70% ethanol extracts of andaliman fruits contains 1,2-benzenedicarboxylic acid, mono (2-ethylhexyl) ester; squalene, methyl palmitate, methyl isopalmitate, n-tetracosanol-1 and 4-isopropyl chalcone have antioxidant activity with IC50 value 51.35 ppm.

scholarly journals Determination of phenolic contents and antioxidant activity test of ethanol extract of Sirih merah (Piper crocatum Ruiz & Pav.) leaves using the DPPH method

2021 ◽  
Vol 13 (2) ◽  
pp. 137-142
Author(s):  
Kasta Gurning ◽  
◽  
Sifikal Lumbangaol ◽  
Risanti F. R. Situmorang ◽  
Saronom Silaban ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Total Phenolic Content ◽  
Phenolic Content ◽  
Ethanolic Extract ◽  
Ethanol Extract ◽  
Extraction Process ◽  
Total Phenolic ◽  
Betel Leaf ◽  
Dpph Method

The research objectives were to identify the secondary metabolite components, total phenolic content and determine the antioxidant activity of the ethanol extract of red betel leaf (Piper crocatum Ruiz & Pav.). The extraction process was carried out by materation using ethanol as a solvent. Determination of total phenolic content was carried out colorimetrically with Folin-Ciocalteu reagent measured at a maximum wavelength of 765 nm. Determination of antioxidant activity using the DPPH method measured by spectrophotometry at a maximum wavelength of 517 nm. The results of phytochemical screening of the ethanolic extract of red betel leaf contain secondary metabolites, including flavonoid, phenolic, tannin, alkaloids, steroids, and triterpenoids. The total phenolic content of the red betel leaf ethanol extract was 0.949±0.003 mg GAE/g d.w. and has antioxidant activity (IC50) 84,656 including strong category as an antioxidant. Keywords: Piper crocatum Ruiz & Pav., Antioxidant, Ethanol extract, Folin-Ciocalteu and DPPH

scholarly journals Antioxidant Activity of n-Hexane, Ethyl Acetate and Ethanol Extract from Lakoocha Leaves (Artocarpus lacucha Buch.-Ham) using DPPH Method

2018 ◽  
Vol 1 (2) ◽  
pp. 41-47
Author(s):  
Poppy Anjelisa Zaitun Hasibuan ◽  
Mardiana
Keyword(s):  
Antioxidant Activity ◽  
Ethyl Acetate ◽  
Ethyl Acetate Extract ◽  
Radical Scavenging ◽  
Ethanol Extract ◽  
Positive Control ◽  
Hexane Extract ◽  
Phytochemical Screening ◽  
Ic50 Value ◽  
Dpph Method

This study aimed to investigate phytochemical screening and antioxidant activity of n–hexane, ethyl acetate and ethanol extract from lakoocha leaves. The powdered simplicia was macerated with n–hexane, ethyl acetate and ethanol 96% successively, filtered, then concentrated using rotary evaporator to obtain n–hexane extract, ethyl acetate extract and ethanol extract. Phytochemical screening and antioxidant activity was performed against these extracts. Antioxidant activity was determined by DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging method using ultraviolet-visible spectrophotometer at wavelength of 516 nm after incubated for 60 minutes in dark place. Quercetin was used as positive control. The result of phytochemical screening showed n-hexane extract contains steroid, ethyl acetate extract contain steroid, tannin, glycoside, flavonoid and saponin, whereas ethanol extract contain tannin, glycoside, flavonoid and saponin. The IC50 value of n–hexane, ethyl acetate and ethanol extract was 1062.03±1.42 ppm, 323.18±0.02 ppm and 99.23±0.07 ppm respectively, whereas for quercetin was 2.32±0.01 ppm. This study showed that ethanol extract had antioxidant activity with strong category whereas n-hexane extract and ethyl acetate extract had inactive antioxidant activity with very weak categories.       Keyword: Antioxidant Activity, DPPH, Lakoocha leaf

scholarly journals UJI AKTIVITAS ANTIOKSIDAN DAUN BENALU KOPI (Loranthus Ferrugineus Roxb.) DENGAN METODE DPPH (1,1 – Difenil -2- Pikrilhidrazil)

2019 ◽  
Vol 6 (2) ◽  
pp. 192
Author(s):  
Muammar Yulian ◽  
Safrijal Safrijal
Keyword(s):  
Antioxidant Activity ◽  
Ascorbic Acid ◽  
Secondary Metabolites ◽  
Room Temperature ◽  
Ethanol Extract ◽  
Phytochemical Screening ◽  
Activity Test ◽  
Dpph Method ◽  
Ic50 Values ◽  
X 24

The study about antioxidant activity test of coffee parasite leaves (Loranthus ferrugineus Roxb.) by 1,1-diphenyl-2-pikrilhidrazyl (DPPH) method has been done. The aim of this study was to determine the content and activity of secondary metabolites, flavonoids and antioxidant, which found in the coffee parasite leaves. Dry powder of parasite coffee leaves (Loranthus ferrugineus Roxb.) as much as 0.5 kg were macerated by 2 L of ethanol solvent at room temperature for 4 x 24 hours, then mixed and filtered. Ethanol filtrate was evaporated at 30-40°C by using a rotary evaporator to obtain the crude extract of coffee parasite leaves. The results of the phytochemical screening showed positively that the extract was containing alkaloid, flavonoids, saponins, tannins and steroid compounds.The results of the antioxidant activity test by using DPPH method was obtained that the amount of antioxidant activity of the samples of ethanol extract had a very strong antioxidant activity against radical DPPH 0.05 mM, with IC50 values was obtained 6.063 ppm. Whereas, for comparison of ascorbic acid was about 3.127 ppm.

scholarly journals Determination of Total Phenolic, Total Flavonoid and Antioxidant Activity of Karamunting Leaves (Rhodomyrtus tomentosa (Aiton) Hassk) Extract and Fraction

2021 ◽  
Vol 9 (2) ◽  
pp. 72-78
Author(s):  
Rahma Dona
Keyword(s):  
Antioxidant Activity ◽  
Ethyl Acetate ◽  
Ethanol Extract ◽  
Ethyl Acetate Fraction ◽  
Total Flavonoid ◽  
Hexane Fraction ◽  
Total Phenolic ◽  
Water Fraction ◽  
Ic50 Value

Karamunting (Rhodomyrtus tomentosa (Aiton) Hassk) is a family of Myrtaceae which has been used by the community as traditional medicine. The purpose of this research is determine total phenolic and total flavonoid level and test antioxidant activity of Karamunting Leaves. Determination of total phenolic using gallic acid standard by the Folin Ciocalteu method. The results obtained total phenolic in water fraction of 99 mgGAE/g, ethanol extract 94,1 mgGAE/g, ethyl acetate fraction 83,3 mgGAE/g and n-hexane fraction 41,4 mgGAE/g. Determination of total flavonoid using standard quersetin with AlCL3 complex formation method, the results obtained total flavonoid in water fraction of 156,8 mgQE/g, ethanol extract 192,6 mgQE/g, ethyl acetate fraction 89,4 mgQE/g and n-hexane fraction 31,3 mgQE/g. Determination of antioxidant activity was determined by DPPH radical capture test (1,1-diphenyl-2-picrylhydrazyl), the results obtained in water fraction with IC50 value 15,02 µg/mL, ethanol extract 14,06 µg/mL, ethyl acetate fraction 14,48 µg/mL with very strong activity of antioxidant, whereas in the n-hexane fraction was categorized as weak antioxidant activity with an IC50 value of 264,02 µg/mL.

scholarly journals Penentuan Aktivitas Antioksidan dan Kandungan Flavonoid Total Ekstrak Daun Papasan (Coccinia grandis L.) Berdasarkan Perbedaan Pelarut Polar

KOVALEN ◽  
2021 ◽  
Vol 7 (1) ◽  
pp. 30-41
Author(s):  
Meliani Sari ◽  
Rani Nareza Ulfa ◽  
Mauritz Pandapotan Marpaung ◽  
Purnama
Keyword(s):  
Antioxidant Activity ◽  
Methanol Extract ◽  
Water Extract ◽  
Ethanol Extract ◽  
Total Flavonoid ◽  
Polar Solvents ◽  
Coccinia Grandis ◽  
Minor Metabolite ◽  
Ic50 Values

Papasan leaves have several properties, including antihyperglycemic, diabetes, antipyretic and antioxidant. Minor metabolite compounds that have the potential as antioxidants from this plant are flavonoids, alkaloids, saponins, and tannins. This study's purpose to determine the antioxidant activity and the flavonoid total contents of Papasan (Coccinia grandis L.) leaf extract based on the differences in polar solvents. The polar solvents used were ethanol, methanol, and water. Extraction used by maceration and dekokta. The antioxidant activity and the flavonoid total contents were established by UV-Vis spectrophotometry according to the decrease in absorbance at a maximum wavelength of 515 nm by the DPPH (2,2-diphenyl-1-picrylhydrazyl) method. Determination of antioxidant activity and the flavonoid total contents were excluded on quercetin comparisons. The values of  IC50 and the flavonoid total contents in the ethanol extract respectively were 287.92 ppm and 49.825 mg QE/g while the IC50 values and total flavonoid levels in the extract of methanol were 73.29 ppm and 50.415 mg QE/g. In the extract of the water, the value of IC50 was 39.80 ppm and the total flavonoid contents were 50.415 mg QE/g. The conclusions of these studies were that the most antioxidant activity was found in water extract, while water and methanol extract had the same and highest levels of total flavonoids.

scholarly journals Skirining fitokimia ekstrak etanol kulit buah sirsak (Annona muricata Linn) dan uji aktivitas antioksidan dengan metode DPPH

2021 ◽  
Vol 2 (2) ◽  
pp. 60-64
Author(s):  
Nur Alim ◽  
Nurul Jummah ◽  
Agus Sangka Pratama ◽  
Nurdiyanti Nurdiyanti
Keyword(s):  
Antioxidant Activity ◽  
Free Radicals ◽  
Ethanol Extract ◽  
Skin Extract ◽  
Annona Muricata ◽  
Phytochemical Screening ◽  
Fruit Skin ◽  
Ic50 Value ◽  
Dpph Method

Phytochemical screening research on the ethanol extract of soursop (Annona muricata Linn) peel and antioxidant activity was tested using the DPPH method. The purpose of this study was to determine several classes of compounds found in soursop rind and to determine the antioxidant activity of ethanol extract of soursop rind against DPPH free radicals. The results showed ethanol extract of positive soursop fruit skin containing flavonoids, tannins, and terpenoids. of soursop fruit skin extract was carried out by DPPH method results obtained IC50 value of 192.13 µg / mL ± 5.198137 which was categorized as weak.

scholarly journals UJI AKTIVITAS ANTIOKSIDAN DAUN GULMA SIAM (Chromoleana odorata L.) DENGAN METODE 1,1-DIFENIL-2-PIKRILHIDRAZIL

2017 ◽  
Vol 1 (2) ◽  
pp. 131-142
Author(s):  
Ajmi Saputra ◽  
Abdul Gani ◽  
Erlidawati Erlidawati
Keyword(s):  
Antioxidant Activity ◽  
Ascorbic Acid ◽  
Ethanol Extract ◽  
Complete Separation ◽  
Phytochemical Screening ◽  
Inhibitor Concentration ◽  
Methanol Fraction ◽  
Activity Test ◽  
Dpph Method ◽  
Function Group

Abstrak. Telah dilakukan penelitian uji aktivitas antioksidan daun gulma siam (Chromoleana odorata L.) dengan metode 1,1-difenil-2-pikrilhidrazil (DPPH). Tujuan penelitian ini untuk mengetahui kandungan senyawa metabolit sekunder, golongan flavonoid dan aktivitas antioksidan yang terdapat dalam daun gulma siam. Sebanyak 315 g daun gulma siam kering yang sudah dihaluskan, dimaserasi dengan etanol 95% diperoleh 100 g ekstrak kental etanol. Sebanyak 70 g ekstrak kental etanol difraksinasi dengan pelarut metanol dan n-heksana menghasilkan fraksi kental metanol 30,72 g dan n-heksana 14,62 g. Hasil skrining fitokimia ekstrak etanol menunjukkan positif mengandung senyawa alkaloid, flavonoid, saponin, tanin dan steroid. Fraksi metanol positif mengandung senyawa alkaloid, flavonoid, saponin, dan tanin. Fraksi metanol dilakukan isolasi dengan metode kromatografi kolom menggunakan eluen n-heksana : etil asetat : diklorometana (1:1:1) sebagai fase gerak pertama, kemudian ditingkatkan gradien kepolarannya untuk menghasilkan pemisahan secara sempurna. Hasil isolasi diperoleh 8 fraksi (A, B, C, D, E, F, G, H) dan hasil analisis secara KLT menunjukkan fraksi A dan B positif mengandung senyawa flavonoid. Senyawa flavonoid yang terkandung dalam fraksi A diperkirakan golongan isoflavon dan fraksi B diperkirakan golongan isoflavon, flavon, flavonol dan kalkon. Analisis FTIR menunjukkan fraksi A dan B mengandung gugus fungsi N-H, O-H (asam karboksilat), C=O (aldehid dan ester), C=C, C-H, C-X (flourida), C-O dan C-N. Hasil pengujian aktivitas antioksidan menggunakan metode DPPH, diperoleh Inhibitor concentrasi (IC50) untuk ekstrak etanol 15,5067 ppm, fraksi metanol 9,5671 ppm, fraksi A 82,7808 ppm dan fraksi B 16,2336 ppm, sedangkan untuk pembanding (asam askorbat) 0,8913 ppm. Dengan demikian, dapat disimpulkan aktivitas antioksidan yang paling kuat terdapat pada  fraksi metanol.Kata kunci: daun gulma siam, Chromoleana odorata L., flavonoid, DPPH. Abstract. The antioxidant activity of siam weed leaf (Chromoleana odorata L.) has been done with 1,1-diphenyl-2-picrilhidrazil (DPPH) method. This study is intended to know the the content of secondary metabolite compounds, the group of flavonoid and antioxidant activity that found in siam weed leaf. The 315 g dry siam weed leaf that was refined, macerated with ethanol 96% produced 100 g of ethanol viscous extract. The 70 of ethanol viscous extract was fractionated with methanol and n-hexane solvent produced 30,72 g of methanol viscous fraction and 14,62 g n-hexane. The results of phytochemical screening of ethanol extract showed positive that contained compound of alkaloids, flavonoids, saponins, tannins and steroids. Methanol fraction showed positive that contained compound of alkaloids, flavonoids, saponins and tannins. The isolation in methanol fraction was made by coloumn chomatography method using eluent n-hexene : acetate ethyl : dichloromethane (1:1:1) as first mation phase. Then the polarity gradient was increased to produce complete separation. The result of isolation produced 8 fractions (A, B, C, D, E, F, G, H) and the analysis results with TLC showed fraction of A and B was positive contain flavonoids compound. Flaconoids compound that was contained in fraction A was estimated isoflvone group and fraction B was estimated group os isoflavone, flavone, flavonol and chalcone. Analysis FTIR showed that the fraction of A and B containing function group N-H, O-H (carboxylic acid), C=O (aldehyde and ester), C=C, C-H, C-X (flouride), C-O and  C-N. The result of antioxidant activity test used DPPH method, obtained inhibitor concentration (IC50) for 15,5067 ppm of ethanol extract, 9,5671 of methanol fraction, 82,7808 ppm of fraction A and 16,2336 ppm of fraction B, while for comparison (ascorbic acid) is 0,8913 ppm. This, it can be concluded that strongert antioxidant activity was found in methanol fraction.Keywords: siam weed leaf, Chromoleana odorata L., DPPH.

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