In Vitro Antioxidant Activity of some Edibles Bearing Nutritional Value

Similar documents
Development and Validation of Stability Indicating HPTLC Method for Estimation of Seratrodast

Antioxidant Activity of the plant Andrographis paniculata (Invitro)

THIN LAYER CHROMATOGRAPHY

Chapter 2 Biochemical changes and antioxidant activity of elephant- foot yam corm during development

Determination of total phenolic, flavonoid content and free radical scavenging activities of common herbs and spices.

SUPPLEMENTARY MATERIAL Antiradical and antioxidant activity of flavones from Scutellariae baicalensis radix

Research Article GALLIC ACID AND FLAVONOID ACTIVITIES OF AMARANTHUS GANGETICUS

Comparative HPTLC Analysis of Leaves of Allium cepa L., Ficus carica L. and Ziziphus mauritiana L. with Standard Quercetin

Preparation and characterization of Aloe vera extract

Phytochemical and antioxidant properties of some Cassia species

This chapter deals with the evaluation of alpha amylase inhibitory

ARTESUNATE TABLETS: Final text for revision of The International Pharmacopoeia (December 2009) ARTESUNATI COMPRESSI ARTESUNATE TABLETS

Available online at Universal Research Publications. All rights reserved. Original Article

Phytochemical Analysis and Antioxidant property of Aegle marmelos Extracts

JPSBR: Volume 4, Issue 6: 2014 ( ) ISSN NO

Protein Cleavage Due to Pro-oxidative Activity in Some Spices

APPLICATION OF TLC METHOD WITH VIDEO SCANNING IN ESTIMATION OF DAILY DIETARY INTAKE OF SPECIFIC FLAVONOIDS ñ PRELIMINARY STUDIES

International Journal of Pharmacy and Pharmaceutical Sciences, Vol. 1, Issue 1, July-Sep. 2009

A HPTLC method for chemotaxonomic evaluation of some Curcuma Species and their commercial samples

Qualitative and quantitative determination of phenolic antioxidant compounds in red wine and fruit juice with the Agilent 1290 Infinity 2D-LC Solution

WORLD JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES. World Journal of Pharmacy and Pharmaceutical Sciences SJIF Impact Factor 6.

Vol-3, Issue-4, Suppl-1, Nov 2012 ISSN: Shingala et al PHARMA SCIENCE MONITOR

Examination of Chemicals in Trap Cases. (Phenolphthalein)

MATERIAL AND METHODS

Enzymatic Assay of PROTEASE (EC )

Development And Validation Of HPTLC Method For Simultaneous Estimation Of Rutin And Quercetin In Hydroalcoholic Extract Of Triphala Churna

ARTENIMOLUM ARTENIMOL. Adopted revised text for addition to The International Pharmacopoeia

ANTI-OXIDANTANT AND PHYTOCHEMICAL SCREENING OF ACALYPHA COMMUNIS (müll. arg.) BY HPTLC FINGER PRINTING METHOD

Title Revision n date

Analytical Method for 2, 4, 5-T (Targeted to Agricultural, Animal and Fishery Products)

TENOFOVIR TABLETS: Final text for addition to The International Pharmacopoeia (June 2010)

Vol-3, Issue-4, Suppl-1, Nov 2012 ISSN: Ghodasara et al PHARMA SCIENCE MONITOR

TOTAL ANTIOXIDANT ACTIVITY, TOTAL PHENOLIC CONTENT AND RADICAL SCAVENGING ACTIVITY BOTH FLESH AND PEEL OF RED PITAYA, WHITE PITAYA AND PAPAYA

An Investigative Study of Reactions Involving Glucosinolates and Isothiocyanates

Antioxidant Activity and Lipoxygenase Enzyme Inhibition Assay with Total Flavonoid Content from Garcinia hombroniana Pierre Leaves

STABILITY INDICATING ASSAY. differentiate an intact drug from its potential decomposition products 425.

Abs. tract. author: *Corresponding. Kumar Puspendra. Panchsakar Churna. HPTLC. efficient validated for tested in the. Group. India. and 50.

Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016.

International Journal of Research in Pharmacy and Science

ANTIOXIDANT ACTIVITIES OF FIVE WILD EDIBLE FRUITS OF MEGHALAYA STATE IN INDIA AND EFFECT OF SOLVENT EXTRACTION SYSTEM

Petrolatum. Stage 4, Revision 1. Petrolatum is a purified semi solid mixture of hydrocarbons obtained from petroleum.


REVISED DRAFT MONOGRAPH FOR THE INTERNATIONAL PHARMACOPOEIA RETINOL CONCENTRATE, OILY FORM. (August 2010)

Development and Validation of HPTLC Method for Quantification of Silodosin in Bulk and Pharmaceutical Dosage Form

Determination of Tanninoids. Analytical Pharmacognosy

Data sheet. TBARS Assay kit. (Colorimetric/Fluorometric) Kit Contents. MDA-TBA Adduct. 2-Thiobarbituric Acid. Cat. No: CA995.

Tenofovir disoproxil fumarate (Tenofoviri disoproxili fumaras)

Science & Technologies ANTIOXIDANT ACTIVITY AND SECONDARY METABOLITES IN DIFFERENT EXTRACTS OF EUPHRASIA OFFICINALIS L. GROWING IN BULGARIA

CYCLOSERINI CAPSULAE - CYCLOSERINE CAPSULES (AUGUST 2015)

Keywords: antioxidant; extraction; paper flower; phenolic compound

CONTENTS Determination of cholinesterase inhibitory activity High performance Thin Layer Chromatography

The Study of Antioxidant and Antibacterial Properties of Skin, Seeds and Leaves of The Sri Lankan Variety of Pumpkin.

Simultaneous Estimation and Validation of Tramadol and Paracetamol by HPTLC in Pure and Pharmaceutical Dosage Form

In vitro antioxidant activity of a flavonoid compound isolated from methanolic extract of Helianthus annuus leaves (Asteraceae)

Introduction. Cell Biology OLM

IJPRD, 2011; Vol 4(03): May-2012 ( ) International Standard Serial Number

Available Online through Research Article

RITONAVIRI COMPRESSI RITONAVIR TABLETS. Final text for addition to The International Pharmacopoeia (July 2012)

Pelagia Research Library. Study of antioxidant activity of ethanolic extract of fresh Eichhornia crassipes (Mart.)Solms

CAMAG TLC-MS INTERFACE

Supporting Information for. Boronic Acid Functionalized Aza-Bodipy (azabdpba) based Fluorescence Optodes for the. analysis of Glucose in Whole Blood

Determination of the Antioxidant Potentials of Two Different Varieties of Banana Peels in Two Different Solvents

E17 ETHYLCELLULOSE. Revision 3 Stage 4

INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH AND BIO-SCIENCE

Research Article Antioxidant and Free Radical Scavenging Activity of Anthocyanins from Two Forms of Brassica oleracea

TLC, HPTLC and Quantitative Estimation of Acetone, Methanolic and Hydro-Alcoholic Extract of Stem Bark of Bauhinia purpurea Linn.

6 CHAPTER-6 TOTAL PHENOLIC AND FLAVONOID CONTENT DETERMINATION

ANTIOXIDANT ACTIVITY STABILITY TEST OF CULTURING MEDIA FROM Pleurotus ostreatus VAR. BHUTAN IN COSMETIC PRODUCTS

AMERICAN SPIKENARD FOR HOMOEOPATHIC PREPARATIONS ARALIA RACEMOSA FOR HOMOEOPATHIC PREPARATIONS

DRAFT PROPOSAL FOR THE INTERNATIONAL PHARMACOPOEIA: CARBAMAZEPINI COMPRESSI - CARBAMAZEPINE TABLETS

Standardization of Milagathi Choornam

Available online at

Comparing Physicochemical Properties of Three Types Iranian Vinegars

SUPPLEMENTARY MATERIAL

Novel D-erythro N-Octanoyl Sphingosine Analogs As Chemo- and Endocrine. Resistant Breast Cancer Therapeutics

Antioxidative activities and phenolic compounds of pumpkin (Cucurbita pepo) seeds and amaranth (Amaranthus caudatus) grain extracts

Free radical scavenging activity of plant extracts of Chlorophytum tuberosum B

Validation of HPTLC Method for Quantification of Embelin from Embelia ribes Burm. F.

Nitrate/Nitrite Assay Kit Manual Catalog #

4. Determination of fat content (AOAC, 2000) Reagents

PRELIMINARY PHYTOCHEMICAL SCREENING AND IN-VITRO FREE RADICAL SCAVENGING ACTIVITY OF MELOCHIA CORCHORIFOLIA PLANT EXTRACTS

(Writing model for laboratory note book)

3. PRELIMINARY PHYTOCHEMICAL SCREENING

aspera & Asteracantha longifolia

Pharmacologyonline 2: (2009)

Stability indicating thin-layer chromatographic determination of eslicarbazepine acetate as bulk drug: Application to forced degradation study

Separation of Polyphenols by Comprehensive 2D-LC and Molecular Formula Determination by Coupling to Accurate Mass Measurement

Folin Ciocalteau Phenolic Content Quantification Assay Kit KB tests (96 well plate)

Β-FRUCTOFURANOSIDASE ENZYME

Determination of antioxidative potential of the compounds isolated from Sargassam wightii

7. NOOTROPIC AND ANTIOXIDANT ACTIVITY. 7.1 Introduction

DRAFT MONOGRAPH FOR THE INTERNATIONAL PHARMACOPOEIA PAEDIATRIC RETINOL ORAL SOLUTION (August 2010)

OLEANDER FOR HOMOEOPATHIC PREPARATIONS NERIUM OLEANDER FOR HOMOEOPATHIC PREPARATIONS

Journal of Chemical and Pharmaceutical Research

Detection of Antioxidants in the Development of an Effective Polyherbal Combination in the Management of Diabetes

CHEM104 Exp. 9 Phytochemical Antioxidants with Potential Benefits in Foods Part I. 1

Preliminary Phytochemical Evaluation and HPTLC Fingerprinting of Leaves of Azadirachta indica

Optimization of extraction method and profiling of plant phenolic compounds through RP-HPLC

(LM pages 91 98) Time Estimate for Entire Lab: 2.5 to 3.0 hours. Special Requirements

Phytochemical composition and in vitro antioxidant activity of methanolic and aqueous extracts of aerial part of Pentatropis nivalis (Asclepiadaceae)

Transcription:

International Journal of Biotechnology and Bioengineering Research. ISSN 2231-1238, Volume 4, Number 5 (2013), pp. 487-494 Research India Publications http://www.ripublication.com/ ijbbr.htm In Vitro Antioxidant Activity of some Edibles Bearing Nutritional Value Roopa Rani 1, Kiran Singh and M.M. Srivastava* 2 1,2 Department of Chemistry, Dayalbagh Educational Institute, Dayalbagh, Agra 282110, India. Abstract The present study deals with the estimation of antioxidant activity (DPPH and OH radical assay) and total phenolic contents in methanolic extract of peel and pulp of Aegle marmelose, Prunus persica and Prunus bokhrensis and quantification of total phenolic, most potent flavonoid (quercetin). The peel and pulp extracts, derived from the fruits were analyzed exhibiting an appreciable amount of DPPH free radical scavenging: Pulp- Aegle marmelose (80.07%, Prunus persica (41.07%) and Prunus bokhrensis (40.29%): Peel - Prunus persica (49.09%) and Prunus bokhrensis (66.90%). The peel and pulp extracts, derived from the fruits were also have an appreciable amount of Hydroxyl radical scavenging activity: Pulp- Aegle marmelose (54.03%), Prunus persica (38.05%) and Prunus bokhrensis (40.14%): Peel-Prunus persica (51.07%) and Prunus bokhrensis (40.56%). An appreciable amount of total phenolic has been found: Pulp- Aegle marmelose (80.54 mg GAE/g), Prunus persica (27.52mg GAE/g) and Prunus bokhrensis (57.25 mg GAE/g): Peel Prunus persica (49.32mg GAE/g) and Prunus bokhrensis (35.78mg GAE/g). HPTLC estimation of quercetin in the fruits under study has been carried out. The mobile phase used in this technique was toluene: ethyl acetate: formic acid (6:5:1, v/v/v). Quercetin estimation shows, pulp of Aegle marmelose - 601.58ng of quercetin while pulp of both Prunus bokherensis and Prunus persica have low amount of quercetin. Keywords: DPPH; Fenton assay; HPTLC, Total Phenolic content.

488 M.M. Srivastava et al 1. Introduction Antioxidants are electron deficient chemical species that have capacity to absorb electrons in its structural arrangement without undesirable effect. Destruction of free radicals may help to fight against cancer, heart disease and stroke (Stuart et al 2009; Lee et al, 2004). The biochemistry of free radicals is harmful and can produce deleterious and lethal effects over time, whereas natural antioxidants scavenge free radicals and prevent or minimize from the harmful effects of free radical biochemistry in the body. Antioxidants are prevalent in cruciferous vegetables, brightly colored berries, certain spices and herbs (Al-mamary, 2002). Quercetin belongs to a group of plant pigments called flavonoids. Quercetin is an antioxidant and scavenges damaging free radicals. Quercetin is basically an antioxidant that can easily reacts with the free radicals and stabilizes them by making itself a free radical (Boots et al, 2008). The free radical of quercetin is highly stable because of the resonance (Bjeldanes et al, 1997). Due to its stabilized nature, it is non reactive and causes less harm to the biomolecules. The present piece of work is carried out to estimate in-vitro antioxidant activity of peel and pulp of the fruits Prunus persica (Peach), Prunus bokherensis (Alu-bokhara) and Aegle marmelos (Bael) using DPPH and FENTON assay, estimation of total phenolic contents of the peel and pulp of the fruits (except Bael), against gallic acid as reference and HPTLC estimation of quercetin in peel and pulp of the fruits (being most important flavonoid exhibiting antioxidant activity). 2. Materials and Methods 2.1 Experimental The chemicals i.e. DPPH (2 2-Diphenyl-1-picrylhydrazyl), methanol, deoxyribose, H 2 O 2, EDTA, ascorbic acid, phosphate buffer, Folin-Ciocalteu reagent, sodium carbonate, AlCl 3, Gallic acid, Hydrogen peroxide, ferric chloride, thiobarbituric acid, trichloroacetic acid, acetic acid, Potassium iodide, ethyl acetate, formic acid, benzene, ethyl acetate, formic acid, sodium hydroxide, sodium chloride and sodium nitrite were purchased from Sigma Aldrich Pvt. Ltd., New Delhi. Appropriate amount of peel and pulp of each fruit have been extracted with methanol in soxhlet extractor for 48 hrs. The filtrate was used for the analysis. 2.3 DPPH (2 2-Diphenyl-1-picrylhydrazyl) and Fenton assay The reaction mixture of dilution series (10-100mg/ml) of extract/methanol mixture is incubated with 3 ml of 0.15 mm DPPH solutions in MeOH, allowed standing for about 30 min at room temperature. Extracts when reacted with DPPH, a stable purple coloured free radical converted into colorless compound α-α diphenyl-β-picryl hydrazine will be formed. The extent of decolouration indicates the amount of DPPH scavenged. The absorbance is measured at 517nm. And α- tocopherol is used as reference antioxidant. For Fenton assay, the reaction mixture containing different dilution series of extract is incubated with deoxyribose (3.75 mm), H O (1mM), FeCl 3 (100μM),

In Vitro Antioxidant Activity of some Edibles Bearing Nutritional Value 489 EDTA and ascorbic acid (100μM) in phosphate buffer (ph 7.4). The reaction is terminated by 1ml of thiobarbituric acid (1%w/v) and 1ml of trichloroacetic acid (2% w/v) and then the tubes are heated in a boiling water bath for about 15 min. The pink chromogen which has formed eventually results in the formation of thiobarbituric acid reactive substance (TBARS). The percent inhibition of DPPH and Fenton assay is calculated using the formula. [(C-T)/C] x100 Eq 1 Where, C is the absorbance of the control and T is for the test sample. 2.4 TOTAL PHENOLIC CONTENTS: TPC is a colorimetric method, based on Folin-Ciocalteu reagent, which is used to appraise the amount of total phenolics. The process involves the mixing of crude extract (50 mg) with Folin-Ciocalteu reagent (0.5 ml) and deionized water (7.5 ml). After waiting for 10 min, 20% aqueous sodium carbonate (w/v, 1.5 ml) is added and then the mixture is incubated at 40 C in a water bath for 20 min, followed by cooling in an ice bath. The absorbance of the final mixture is monitored at 755 nm (Lab India Spectrophotometer, DEI, Agra). For calculation of the TP amount, a standard gallic acid calibration curve, prepared by running solutions in the concentration range of 10 200 mg/l (R2 = 0.9980), is constructed. The amount of total phenolics is expressed as gallic acid equivalents (GAE) mg/100 g of dry matter. 2.5 HPTLC (HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHY) HPTLC analysis was performed on a computerized densitometer scanner 3 controlled by wincats planar chromatography manager version 1.4.4 (Camag, Switzerland). Different concentrations of the standard solution were loaded on the HPTLC (Silica gel F 254 ) plate using Linomat V with 100µl syringe (Hamilton, Switzerland). Plates were developed in twin trough chamber using optimized solvent system with no saturation time for the solvent chamber. Plates were visualized in UV-light at 254nm and 366nm. Qualitative and Quantitative assay was done by using TLC scanner 3 Camag HPTLC system at wavelength 282nm. 3. Results and Discussion 3.1 DPPH (2, 2-Diphenyl-1-picrylhydrazyl) and Fenton assay DPPH is a stable free radical with a deep violet color and accepts an electron to become a stable diamagnetic molecule. The effect of test samples under study has observed on reduction capability of DPPH in terms of the decrease in its absorbance at 517nm. In this test, the violet color of DPPH is reduced to a pale yellow color due to the abstraction of hydrogen atom from antioxidants

490 M.M. Srivastava et al percentage of inhibition(%) 100 80 60 40 20 0 DPPH radical scavenging activity 0 100 200 300 400 concentration (μg/ml) std.αtocopherol pulp of bael pulp of alucha peel of alucha pulp of peach peel of peach Hydroxyl radical scavenging activity % of OH radical scavenging 100 90 80 70 60 50 40 30 20 10 0 0 200 400 concentration (μg/ml) std.α-tocopherol pulp of bael pulp of alucha peel of alucha pulp of peach peel of peach Figure 1: DPPH radical scavenging activity of methanolic extract of samples against standard α-tocopherol using a) DPPH and b) Fenton assay. The increase in the concentration of the extract (peel and pulp) results into increase in the target antioxidant activity, finally attaining an optimum value which is considered its maximum antioxidant activity. Aegle marmelose (pulp) has been found to have the highest DPPH radical scavenging activity (80.07%) among the fruits studied. The Order of DPPH radical scavenging activity is Pulp of Aegle marmelose > peel of Prunus persica > peel of Prunus bokhrensis > pulp of Prunus bokhrensis > pulp of Prunus persica.

In Vitro Antioxidant Activity of some Edibles Bearing Nutritional Value 491 In in-vitro Fenton assay, Fe +2 -EDTA chelate was incubated with deoxyribose in phosphate buffer at ph 7.4 and resulting OH radicals were measured in terms of their ability to degrade the deoxyribose sugar into the fragments that react with thiobarbituric acid to form a pink chromogen. The test samples were found capable with deoxyribose for hydroxyl radical and decrease the rate of deoxyribose degradation. The hydroxyl radical scavenging activity of fruits (pulp & peel) show increase of concentration of the extract results into the increase in the target antioxidant activity, finally attaining an optimum value which is considered its maximum antioxidant activity and the Order of OH radical scavenging activity is Pulp of Aegle marmelose > Peel of Prunus persica > Peel of Prunus bokhrensis > Pulp of Prunus bokhrensis > Pulp of Prunus persica. 3.4 Total Phenolic Contents (TPC) TPC is a colorimetric method, based on Folin-Ciocalteu reagent, which is used to appraise the amount of total phenolics. The process involves the mixing of crude extract (50 mg) with Folin-Ciocalteu reagent (0.5 ml) and deionized water (7.5 ml). After waiting for 10 min, 20% aqueous sodium carbonate (w/v, 1.5 ml) were added and then the mixture was incubated at 40 C in a water bath for 20 min, followed by cooling in an ice bath. The absorbance of the final mixture was monitored at 755 nm (U-2001 Spectrophotometer, Hitachi Instruments Inc., and Tokyo, Japan). For calculation of the TP amount, a standard gallic acid calibration curve, prepared by running solutions in the concentration range of 10 200 mg/l (R2 = 0.9980), was constructed. The amount of total phenolics was expressed as gallic acid equivalents (GAE) mg/100 g of dry matter. Absorbance 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0-0.1 Calibration curve of Gallic acid y = 0.003x - 0.304 R² = 0.993 0 50 100 150 200 250 300 350 Concentration (ppm) Figure 2: Calibration curve of Gallic acid as standard.

492 M.M. Srivastava et al Aegle marmelose (bael) have the highest amount of total phenolics i.e. 80.54 mg GAE/g. The peel of Prunus bokhrensis (alucha) and Prunus persica (peach) have greater total phenolics than the pulps of these fruits. The order of total phenolics content is Pulp of Aegle marmelose > Peel of Prunus persica > Peel of Prunus bokhrensis > Pulp of Prunus bokhrensis > Pulp of Prunus persica. 3.5 Estimation of Quercetin Using Hptlc Quantitative estimation of quercetin is carried out by HPTLC using solvent systems. The mobile phase consisted of toluene: ethyl acetate: formic acid (6:5:1, v/v/v). Aluminum-backed TLC plates pre-coated with 0.2 mm layer of silica gel 60 F254 (20 cm 10 cm) was used as stationary phase. The bands were applied over the HPTLC plate with following settings: Band length 8mm, distance between track 14.0mm, slit dimension, 6.00 mm 0.30 mm, scanning speed, 20 mm/s; data resolution, 100 µm/step. Remaining parameters were left as default settings. Regression analysis and statistical data were automatically generated by the WinCATS software. The calibration curve was plotted and amount of quercetin was estimated in samples. Table 1: Amount of Quercetin estimated. Pulp of Pulp of Pulp of Peel of Peel of Aegle Prunus Prunus Prunus Prunus marmelose (ng) bokherensis (ng) Persica (ng) Bokherensis (ng) Persica (ng) 601.58 503.78 567.23 450.23 455.18 4. Conclusion Aegle marmelose (pulp) has been found to have the highest DPPH radical scavenging activity (80.07%) among the fruits studied. Aegle marmelose (pulp) has been found to have the highest hydroxyl radical scavenging activity (54.03%) among the fruits studied and pulp of peach has minimum among the fruits studied. Aegle marmelose (bael) have the highest amount of total phenolics i.e. 80.54 mg GAE/g. The peel of Prunus bokhrensis (alucha) and Prunus persica (peach) have greater total phenolics than the pulps of these fruits. The peel of Prunus bokhrensis (alucha) and Prunus persica (peach) have greater percentage of inhibition of DPPH radical, percentage of OH radical scavenging and total phenolics than the pulps of these fruits. Standardization of HPTLC method was done for the estimation of quercetin in fruit extracts. HPTLC method indicates that pulp of Aegle marmelose contains 601.58ng of quercetin, while pulp of P. bokherensis and P. persica have low quercetin content.

In Vitro Antioxidant Activity of some Edibles Bearing Nutritional Value 493 5. Acknowledgement The authors are thankful to Prof. Prem Kalra, Director, and Prof. L D Khemani, Head, Department of Chemistry, Dayalbagh Educational Institute, Agra. References [1] A Stuart, Rushworth, O Micheau (2009), Molecular crosstalk between trail and natural antioxidants in the treatment of cancer, Br. J. Pharmoco, 157, 7, pp. 1186-1188. [2] A W Boots, G R Haenen, A Bast (2008), Health effects of quercetin: from antioxidant to nutraceutical, Eur. J. Pharmacol, 582, 2-3, pp. 325-37. [3] J Lee, N Koo, D B Min (2004), Reactive oxygen species, aging, and antioxidative nutraceuticals Comprehensive Reviews, J. Food Sci. Food Saf, 3, 1, pp. 21-33. [4] L F Bjeldanes, G W Chang (1977), Mutagenic activity of quercetin and related compounds, J. Science, 197, pp. 577-578. [5] M Al-Mamary (2002), Antioxidant activity of commonly consumed vegetables in Yemen, Malaysia J.Nutr, 8, 2, pp. 79-189.

494 M.M. Srivastava et al