in vitro models for antioxidant activity evaluation in sri lanka

evaluation of in vitro antioxidant and brine shrimp

Evaluation of in vitro antioxidant and brine shrimp

China (Hainan, Yunnan), Sri-Lanka and Vietnam. The present study was designed to investigate antioxidant prop-erties (through in vitro method) as well as brine shrimp

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evaluation of antioxidant properties of 20 medicinal plant

Evaluation of antioxidant properties of 20 medicinal plant

total polyphenol content, in vitro antioxidant activities and to determine the relationship between polyphenol content and antioxidant activities of aqueous extracts of 20 medicinal plants traditionally used in Ayurvedic medicine in Sri Lanka. Materials and methods Plant material A total of 20 samples, representing 20 Sri Lankan

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in vitro and in vivo evaluation of antioxidant activity

in Vitro and in Vivo Evaluation of Antioxidant Activity

The present study was conducted to determine whether aerial parts of Trichosanthes cucumerina extracts can exert significant antioxidant activity. The antioxidant activity of a. hot water extract (HWE) and a. cold ethanolic extract (CEE) of T. cucumerina aerial parts was evaluated by assessing its (a) radical scavenging ability and prevention effect of lipid peroxidation in vitro, and (b) effects on lipid peroxidation and antioxidant enzyme activities, in vivo.

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evaluation of in vitro antioxidant potential of cordia retusa

Evaluation of In Vitro Antioxidant Potential of Cordia retusa

Evaluation of antioxidant activities by in vitro models: From the above three extracts, ethyl acetate and ethanol extract were selected for the determination of antioxidant activity by using different in vitro models. All the experiments were performed with different concentrations ranging from 125 to 1000 µg/ml (125,

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evaluation of the in vitro and in vivo antioxidant

Evaluation of the In Vitro and In Vivo Antioxidant

In Vitro Antioxidant Activity. The in vitro antioxidant free radical scavenging activity of SP was determined by using ABTS radical cation decolourization assay . In this assay, 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) or ABTS (C 18 H 18 N 4 O 6 S 4) is converted to its radical cation. This radical cation is dark green in colour and absorbs light at 734 nm.

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journal of the national science foundation of sri lanka

Journal of the National Science Foundation of Sri Lanka

BC model of the cosmosSee J.Natn.Sci. Foundation Sri Lanka 2019 47(3): 323– 331 ... which corresponded to the negative peak at 680 nm on-line HPLC-ABTS+ chromatogram was identified as an antioxidant compound. Antioxidant activity against 2,2-diphenyl-1- picrylhydrazyl (DPPH) was tested using radical scavenging activity with the electron spin ...

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evaluation of the in vitro antioxidant potential

Evaluation of the in vitro antioxidant potential

Antioxidant activity assays The antioxidant activity of the plant extracts was determined by in vitro methods: DPPH and ABTS radical scavenging activity assays and reducing power method. All assays were carried out in triplicate and the average values were considered and expressed as mean ± SD.

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evaluation of phenolic content and antioxidant property

Evaluation of phenolic content and antioxidant property

Six different in vitro antioxidant assays such as 1, 1’-diphenyl-2-picrylhydrazyl (DPPH), lipid peroxidation (LPO), nitric oxide, hydrogen perox- ide radical scavenging, reducing power of the extracts and total antioxidant capacity (values were

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evaluatİon of photoprotective and antioxidant activities

EVALUATİON OF PHOTOPROTECTIVE AND ANTIOXIDANT ACTIVITIES

present study focuses on evaluation of photo protective and antioxidant act ivities o f aqueous extracts ( 1 mg/ml) of eleven me dicinal plants in Sri Lanka. For t he determination

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bioprotective properties of seaweeds: in vitro evaluation

Bioprotective properties of seaweeds: In vitro evaluation

Hence it has been widely used for rapid evaluation of the antioxidant activity of plant and microbial extracts relative to other methods . DPPH is also considered as a good kinetic model for peroxyl radicals . The ability of seaweeds to scavenge DPPH radicals was determined by the decrease in its absorbance at 517 nm.

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in vitro models for antioxidant activity evaluation

In vitro models for antioxidant activity evaluation

Key words: Antioxidant assay, in vitro models, antioxidant medicinal plants.Evaluation of antioxidant activity A great number of in vitro methods have been developed to measure the efficiencyPhenolic and terpenoid constituents from the Sri Lankan medicinal plant Osbeckia aspera.

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in-vitro models for antioxidant activity evaluation: a review

In-Vitro Models For Antioxidant Activity Evaluation: A Review

In-vitro antioxidant activity was done by DPPH, ferrous chelating and reducing power assay method. The physicochemical parameter like a loss on dryingJoin ResearchGate to discover and stay up-to-date with the latest research from leading experts in In-vitro models and many other scientific topics.

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evaluation of the in vitro and in vivo antioxidant potentials

Evaluation of the In Vitro and In Vivo Antioxidant Potentials

The in vitro antioxidant activity of 0.5 μg of SP was equivalent to 14.45 μg of standard TROLOX. The percentage inhibition against the radical formationSudarshana powder (SP) is the most effective antipyretic Ayurvedic preparation, widely used in Sri Lanka as well as in India from the inception of

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in-vitro models for antioxidant activity evaluation: a review

In-Vitro Models For Antioxidant Activity Evaluation: A Review

ABSTRACT Antioxidants are gaining a lot of importance as a panacea for a large numberof life-style diseases like aging, cancer, diabetes, cardiovascular and otherdegenerative diseases etc. owing to our sedentary way of life and stressfulexistence. Added to these are the deleterious effects of pollution

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evaluation of antioxidant activities by in vitro models

Evaluation of antioxidant activities by in vitro models

Evaluation of In Vitro Antioxidant Potential of Cordia retusa. Murugesan Amudha* and Shanmugam Rani. Department of Pharmacy, AnnamalaiFrom the above three extracts, ethyl acetate and ethanol extract were selected for the determination of antioxidant activity by using different in vitro models.

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in-vitro and in-vivo models for antioxidant activity evaluation

In-vitro and in-vivo models for antioxidant activity evaluation

Antioxidants are gaining a lot of importance as a panacea for a large number of life-style diseases like aging, cancer, diabetes, cardiovascular and other degenerative diseases etc. owing to ourThe present article includes the detailed exploration of in-vitro and in-vivo models for antioxidant activity.

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in vitro and in vivo methods for anticancer activity

In vitro and in vivo Methods for Anticancer Activity

It lists various methods for evaluating anticancer activity so it will be easy for the experimenter. It emphasizes that in vitro anticancer assays have been carried out for most of27. Jagetia GC, Baliga MS. Evaluation of anticancer activity of the alkaloid fraction of Alstonia scholaris in vitro and in vivo.

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evaluation of in vitro antioxidant and antimicrobial activities

evaluation of in vitro antioxidant and antimicrobial activities

Evaluation of Antioxidant Activities of Various Solvent. In vitro Antioxidant and Antimicrobial Activities of anti-arthritic agent. It was used therapeutically in dentistry as an antiseptic for tooth-decay and gum swellings, as an antioxidant in tea form for relieving arthritis, fever, migraine

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evaluation of antioxidant and free radical scavenging activity

Evaluation of antioxidant and free radical scavenging activity

Conclusion: The evaluation of antioxidant activity of Samadera indica concludes that the plant extracts showed activity and this may be due to the presence of flavanoids. Hence, further work should be done on the isolation and identification of other antioxidant components of Samadera indica.

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in vitro models for calcification

In vitro models for calcification

In vitro models for calcification may refer to systems that have been developed in order to reproduce, in the best possible way, the calcification process that tissues or biomaterials undergo inside the body. The aim of these systems is to mimic the high levels of calcium and phosphate present in the blood

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