Ndpph method antioxidant activity pdf files

The correlation between antioxidant capacity and phenolic content of the four moroccan cupressaceae samples is described in table 3. Screening of brazilian plant extracts for antioxidant activity by the use of dpph free radical method luciana l. This method is easy and applies to measure the overall antioxidant capacity prakash 2001 and the free radical scavenging activity of fruit and. The first group was composed by five substances with higher values of antioxidant activity. The experiment consisted in the incubation of an ethanolic. Antioxidant activity of the leaf extract was assessed by dpph, cuprac and pfrap assays using lascorbic acid as standard. Aqueous extracts of 30 plants were investigated for their antioxidant properties using dpph and abts radical scavenging capacity assay, oxygen radical absorbance capacity orac assay, superoxide dismutase sod assay, and ferric reducing antioxidant potential frap assay. Evaluation of antioxidant activity of clitoria ternatea. Kradonbok, antioxidant activity, sample preparation methods, extraction time introduction. Being rapid, simple and independent of sample polarity, the dpph method is very convenient for the quick screening of many samples for radical scavenging activity.

In cells, there usually exists a balance between antioxidants elimination and free radical development. The objective of the present study were to determine the antioxidant activity, total phenolic content, reducing power activity, hydroxyl group reducing activity, estimation of ascorbic acid. A great number of plants worldwide showed a strong antioxidant activity10 and a powerful scavenger activity against free radicals. Studies on the antioxidant activity of pomegranate punica. Determination of dpph radical oxidation caused by methanolic. Mar 16, 2001 screening of brazilian plant extracts for antioxidant activity by the use of dpph free radical method luciana l. Pdf methods for determining the antioxidant activity. Is it possible to use the dpph and abts methods for. Antioxidant capacity is related with compounds capable of protecting a biological system against the potentially harmful effect of processes or reactions involving reactive oxygen and nitrogen species ros and rns. Review significance of antioxidant potential of plants and. Antioxidant activity and total polyphenol content of selected. Sc0334258 title antioxidant activity of seed extract and fractions of monodora tenuifolia annonaceae faculty medicine department pharmacology and toxicology date february, 2007 signature. Department of agriculture, arkansas childrens nutrition center, 1120 marshall street.

Cytotoxicity and apoptotic activity of ficus pseudopalma. In this study antioxidant activity was performed by dpph 1, 1diphenyl2picryl hydrazyl radical scavenging method for different extracts of aerial parts like leaves and flowers of ageratum. The method dpph is widely used for measurement of free radical scavenging ability of. Total carotenoids and antioxidant activity of fillets and. Effect of food preparation technique on antioxidant activity. Phenolic contents and antioxidant activity of various date. Analysis of antioxidant capacity and bioactive compounds. In this study antioxidant activity was performed by dpph 1, 1diphenyl2picryl hydrazyl radical scavenging method for different extracts of aerial parts like leaves and flowers of ageratum conyzoides linn. Synergistic and antimicrobial properties of commercial. The percentage of antioxidant activity aa% of 10% ascorbic acid. Screening of plant extracts for antioxidant activity. This could be due to the difference of the method that is used which involved boiling the sample. Free radicals scavenging activity and reducing power of two algerian sahara medicinal plants extracts abderrahim benslama and abdenassar harrar abstract the aim of this study is to evaluate antioxidant activity of aqueous aq.

The odd electron of nitrogen atom in dpph is reduced by receiving a hydrogen. The leaves extract from different solvents were tested for their scavenging activity against the stable free radical dpph 2, 2diphenyl1picryl hydrazyl in dot plot rapid screening assay method and quantified using a spectrophotometric assay. The substances can be divided in three main groups, as depicted in table 1. Objectives the outstanding antioxidant capacity of berry fruits is wellknown on the strength of data of several international literatures. The following antioxidant methods were used to evaluate the antioxidant properties of our test compounds. Extract dpph assay abts assay frap assay ic 50 gml ic 50 gml teac gml mol teg water ext. Screening of brazilian plant extracts for antioxidant. Assessment of antioxidant activity of spray dried extracts of.

Antioxidant and bactericidal activity of wild turmeric. Determining antioxidant activities of lactobacilli cellfree. Antioxidant and bactericidal activity of wild turmeric extracts. This method was developed by blois with the viewpoint to determine the antioxidant activity in a like manner by using a stable free radical. Genesis and development of dpph method of antioxidant assay. Radicalscavenging activity and ferric reducing ability of. Antioxidant activity by dpph assay of potential solutions to. The main mechanism of food antioxidant also is the free radical scavenging pokorny et al. This change in antioxidant activity was not detected by the abts method.

The antioxidant activity of the aerial part extract of m. The following assay procedure was modified from those described by blois 1958 and yamasaki, et al. The aim of this study was to assess, using the dpph assay, the antioxidant activity of several substances that could be proposed to immediately revert the problems caused by bleaching procedures. Total phenols were estimated by folinciocalteus method and flavonoids by. Standardized methods for the determination of antioxidant capacity and phenolics in foods and dietary supplements ronald l. Human body has multiple mechanisms especially enzymatic and non. The antioxidant activity of pomegranate peel and seed extracts was evaluated according to the method of jayaprakasha et al.

The imbalance in an antioxidant prooxidant is due to auto oxidation of glucose level in diabetes usually leads to high energy particle generation. Antiradical scavenging activity was tested by the dpph model table 5. Free radical scavenging activity was evaluated using 1,1diphenyl2picryl hydrazyl dpph free radical. Invitro antioxidant activity and total phenolic content of. The gradual increase in free radicals and diminishing antioxidant defense mechanism potential. Although slow, the hsgc method is preferable for assessing the antioxidant inhibitory properties on the formation of unwanted secondary volatile products. Biochemical evaluation of antioxidant activity in extracts. L of solutions of the concentrated extract and of the spray dried products were assayed at different concentrations 10, 20, 40, 50, 60, and 80. All the essential oils showed antioxidant activity. The antioxidant activities were high with values ranging from 63% inhibition breadfruit to 78% inhibition african mango pulp. Dpph free radical scavenging activity of the extracts of. The aim of this work is to study and compare the antioxidant properties and phenolic contents of aqueous leaf extracts of juniperus thurifera, juniperus oxycedrus, juniperus phoenicea, and tetraclinis articulata from morocco. Oct 03, 20 the antioxidant activity of plants is mainly contributed by the active compounds.

For validation of this method several well known antioxidants ascorbic acid6palmitate, gallic, chlorogenic, ferulic, caffeic, uric, gentisic and vanillic acids, catechin. Freezing led to losses in the total carotenoid content as well as in the antioxidant activity measured by the three methods in the extracts of shrimp shells with higher concentrations of carotenoids, probably due to oxidation of the compounds during the storage. According to above mentioned it is important and reasonable to get to know and to investigate the antioxidant characteristics of berry fruits grown in hungary and get to know the quality and. In this assay, kale seeds exhibited a strong concentrationdependent antioxidant potential ic 25 120. Evaluation of antioxidant activity of clitoria ternatea and. Antioxidant assay using acarotenelinoleate model system. There was a correlation between antioxidant activity and total phenol content. The yeast cells were isolated from the sugar factory effluents and isolated the yeast cell dna. The antioxidant activity of solvent extracts was investigated by dpph radical scavenging method. Cellular antioxidant activity caa assay was used in this study to. Among them, thyme and oregano exhibited the highest antioxidant activity, with i dpph values of 98.

Aiming at the exploration of herbal use by society, crude extracts of the seeds of some commonly used medicinal plants vitis vinifera, tamarindus indica and glycin max were screened for their free radical scavenging properties using ascorbic acid as standard antioxidant. Antioxidant activity by dpph assay of potential solutions. Screening of various botanical extracts for antioxidant. In this study, methanol and acetone were preferred as solvents for the extracts to be prepared. These protective effects of antioxidants have received increasing attention within biological, medical, nutritional, and agrochemical fields and resulted in the requirement of. Detection and activity evaluation of radical scavenging. There are currently approximately 19 in vitro and 10 in vivo methods of assessing antioxidant activity that are commonly applied for evaluation of the antioxidant activity of plant samples 6.

The antioxidant activity data obtained from the dpph method were highly correlated with the total phenolic contents and. Antioxidant and anticancer activities of brown and red. Dpph free radical scavenging assay is a rapid, simple, cheap and widely used methods to measure the capacity of a substance. The antiradical activity of crude extracts 80% methanol, 20% water of s. Antioxidant activities of the extracts were evaluated by 2,2diphenyl1picrylhydrazyl dpph free radicalscavenging ability, trolox equivalent. Effect of food preparation technique on antioxidant. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Antioxidant activity of polysaccharide fractions three seaweeds s. Ethanol extract exhibited the highest antioxidant activity compared to the other solvent buoh, etoac, me 2 cl 2 and pet. It is also possible to use screening methods to identify the class of antioxidant e. Review of methods to determine antioxidant capacities.

In its oxidized form, the dpph radical has an absorbance maximum centered at about 520 nm molyneux, 2004. Minimal inhibitory concentration mic of the extracts were determined by disc diffusion method. Pdf a novel amperometric method for antioxidant activity. Various plants have different free radical antioxidant activity which depends upon their different constituents. The assay is based on the measurement of the scavenging capacity of antioxidants towards it. In most of these in vitro assays plant samples showed potent antioxidant activity. University of nigeria research publications author njoku, ugochi olivia pgm. Effect of sample preparation methods and extraction time. Antioxidant activity of red algae kappaphycus alvarezii.

Conversely, the essential oil of anise in which the percentage of monoterpenes was as low as 2. Effect of food preparation technique on antioxidant activity and plant pigment content in broccoli, brussels sprouts, white cabbage, kale, chard, spinach and garden patience were studied. Hatbased methods measure the classical ability of an antioxidant to quench free radicals by hydrogen donation ah any h donor hence, many scientists feel these are most relevant to reactions where antioxidants typically act. Antioxidant activity and cytotoxicity of the leaf and bark extracts of. Free radical scavenging activity, total phenolic content. Extraction and determination of antioxidant activity of.

The antioxidant activity of the extract and the yield depends on the selected solvent gong et al. Antioxidant activity of commonly consumed cereals, millets. For example, tlc screening may be used10,11 to identify components in extracts that exhibit such activity. It was also found that the drying methods had significant impact on the antioxidant activity, total phenolic and flavonoid content of. The dpph assay provides an easy and rapid way to evaluate potential antioxidants. The synthesized test compounds were purified by recrystalization and characterized by uvvisble, infra red, nmr and mass spectroscopy. However, this malaysian herbs antioxidant activity and ability to retard lipid. Antioxidant activity and total polyphenol content of.

Pdf antioxidant activity by dpph radical scavenging. The antioxidant activity of the memq was evaluated by the phosphomolybdenum method according to the procedure of prieto et al. Brine shrimp lethality and mtt cytotoxicity tests were used to investigate the. Assessment of antioxidant activity of spray dried extracts. Antioxidant activities and total phenolic content of. Invitro antioxidant and antimicrobial activities of some. Antioxidant activity by dpph assay of potential solutions to be. A new method for the determination of antioxidant activity based on the amperometric reduction of 2,2diphenyl1picrylhydrazyl dpph at the glassy carbon electrode is proposed. The producers protocols for extracts or infusions and their medical use are listed in table 2. Comparative study of different methods to measure antioxidant.

Antioxidant activity, ferric reducing antioxidant power, diphenyl1picryl hydrazyl, total phenolic content, cereals, millets, pulses, legumes excessive free radical production and lipid peroxidation underlie the pathogenesis of diseases like atherosclerosis, carcinogenesis, diabetes, cataract and also ageing 1. In dpph radical scavenging method the free radicals, 2, 2 diphenyl 1 picrylhydroazyl dpph was used to find antioxidant scavenging activity of. Zygophyllaceae and arthrophytum scoparium chenpodiacea, two. Antioxidant and free radical scavenging activities of. The antioxidant ability of the aqueous lyophilized extract of kale seeds was screened by the dpph assay. Antioxidant activity of teucrium barbeyanum aschers 162 table 1. Comparative study of antioxidant properties and total. In brief, a mixture of 4 mg weight sample in 4 ml absolute. Some of the more meaningful tests will be utilized to evaluate a number of antioxidant systems for oxidation and deposit control capabilities in engine oils formulated with 470 ppm of zddpderived phosphorus. The highest content of chlorophyll a was detected in garden patience 0.

All experiments were done in threeelectrode electrochemical cell at. In general, the antioxidant activity was higher using dpph than bbm and abts. Chemical constituents and antioxidant activity of teucrium. Antioxidant activity and total polyphenol content of selected herbal medicinal products used in poland producers protocols of herbs preparation all analyzed herbs were prepared according to the procedure suggested by producer on the herb packaging. Correlation between total phenolic content, flavonoid content, and antioxidant activity. A number of methods and modifications have been proposed to determine antioxidant activity.

Even so, the abts assay is an easy and quick test that provides a comprehensive. Jan, 2009 antioxidant capacity is related with compounds capable of protecting a biological system against the potentially harmful effect of processes or reactions involving reactive oxygen and nitrogen species ros and rns. Dpph is a stable free radical in a methanolic solution. Free radical scavenging activity was evaluated using 1,1diphenyl2picrylhydrazyl dpph free radical. The dpph method is described as a simple, rapid and convenient method independent of sample polarity for screening of many samples for radical scavenging activity koleva et al. The 50% ethyl alcoholic extract of vitis vinifera seeds showed 85. Dpph free radical scavenging assay and teac assay because tpc act as free radical scavenger.

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