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Correlation between Anti-oxidant property and Total phenolic and flavonoid content of Azadirachta Indica A Juss Flowers

M Palanivelmurugan, Mary Saral A

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Abstract

Plants are the source of potential secondary metabolites which are the reasons for the antioxidant activity. Neem flowers also having higher amounts of antioxidants and phenolic substances [1]. We have investigated the antioxidant activity of shade dried neem flower powder extracts by 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging, phospomolybdenum assay, and ferric reducing antioxidant power assay (FRAP) methods respectively [2]. The antioxidant activity of different extracts of neem flower powder has been investigated and among them 80% hydroalcoholic extract displayed the highest scavenging activity with the IC50 value of 18 mg/L in phospomolybdenum assay, 29 mg/L in DPPH, 30 mg/L in FRAP assay. Whereas petroleum ether extract shows lowest antioxidant potential amongst the three extracts with the IC50­ value of 76 mg/L in FRAP, 37 mg/L DPPH, 28 mg/L in phospomolybdenum assay (Table 1). On examining the total Phenolic and flavonoid content of different extracts the 80% hydroalcoholic extract possesses the greatest phenolic content about 83.88 mg/L followed by methanol, acetone and petroleum ether about 62.05, 7.52, 3.56 mg/L respectively. The highest flavonoid content of 57.36 mg/L in 80% hydroalcoholic extract followed by methanol, acetone and petroleum ether about 20.56, 11.25, 1.56 mg/L respectively (Table 2) [3]. The order of total phenolic and flavonoid content of different extracts are found to be as; 80% hydroalcoholic > methanol > acetone > pet. ether respectively. The correlation between the antioxidant and total phenolic content, total flavonoid content was calculated using Prism Pad software and observed at 95% confidence interval level (Fig 1a & 1b). From the correlation graph, it is observed that there is a good correlation between antioxidant, total phenolic content (phospomolybdenum assay, R2 – 0.702) and total flavonoid content (DPPH assay, R2 – 0.665) and it is possible to suggest that total phenolic and flavonoid content of the plant extracts are the main reason for the antioxidant activity [4].

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What this paper is about

Plants are the source of potential secondary metabolites which are the reasons for the antioxidant activity. Neem flowers also having higher amounts of antioxidants and phenolic substances [1]. We have investigated the antioxidant activity of shade dried neem flower powder extracts by 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging, phospomolybdenum assay, and ferric reducing antioxidant power assay (FRAP) methods respectively [2]. The antioxidant activity of different extracts of neem flower powder has been investigated and among them 80% hydroalcoholic extract displayed the highest scavenging activity with the IC50 value of 18 mg/L in phospomolybdenum assay, 29 mg/L in DPPH, 30 mg/L in FRAP assay. Whereas petroleum ether extract shows lowest antioxidant potential amongst the three extracts with the IC50­ value of 76 mg/L in FRAP, 37 mg/L DPPH, 28 mg/L in phospomolybdenum assay (Table 1). On examining the total Phenolic and flavonoid content of different extracts the 80% hydroalcoholic extract possesses the greatest phenolic content about 83.88 mg/L followed by methanol, acetone and petroleum ether about 62.05, 7.52, 3.56 mg/L respectively. The highest flavonoid content of 57.36 mg/L in 80% hydroalcoholic extract followed by methanol, acetone and petroleum ether about 20.56, 11.25, 1.56 mg/L respectively (Table 2) [3]. The order of total phenolic and flavonoid content of different extracts are found to be as; 80% hydroalcoholic > methanol > acetone > pet. ether respectively. The correlation between the antioxidant and total phenolic content, total flavonoid content was calculated using Prism Pad software and observed at 95% confidence interval level (Fig 1a & 1b). From the correlation graph, it is observed that there is a good correlation between antioxidant, total phenolic content (phospomolybdenum assay, R2 – 0.702) and total flavonoid content (DPPH assay, R2 – 0.665) and it is possible to suggest that total phenolic and flavonoid content of the plant extracts are the main reason for the antioxidant activity [4].

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Available abstract

Plants are the source of potential secondary metabolites which are the reasons for the antioxidant activity. Neem flowers also having higher amounts of antioxidants and phenolic substances [1]. We have investigated the antioxidant activity of shade dried neem flower powder extracts by 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging, phospomolybdenum assay, and ferric reducing antioxidant power assay (FRAP) methods respectively [2]. The antioxidant activity of different extracts of neem flower powder has been investigated and among them 80% hydroalcoholic extract displayed the highest scavenging activity with the IC50 value of 18 mg/L in phospomolybdenum assay, 29 mg/L in DPPH, 30 mg/L in FRAP assay. Whereas petroleum ether extract shows lowest antioxidant potential amongst the three extracts with the IC50­ value of 76 mg/L in FRAP, 37 mg/L DPPH, 28 mg/L in phospomolybdenum assay (Table 1). On examining the total Phenolic and flavonoid content of different extracts the 80% hydroalcoholic extract possesses the greatest phenolic content about 83.88 mg/L followed by methanol, acetone and petroleum ether about 62.05, 7.52, 3.56 mg/L respectively. The highest flavonoid content of 57.36 mg/L in 80% hydroalcoholic extract followed by methanol, acetone and petroleum ether about 20.56, 11.25, 1.56 mg/L respectively (Table 2) [3]. The order of total phenolic and flavonoid content of different extracts are found to be as; 80% hydroalcoholic > methanol > acetone > pet. ether respectively. The correlation between the antioxidant and total phenolic content, total flavonoid content was calculated using Prism Pad software and observed at 95% confidence interval level (Fig 1a & 1b). From the correlation graph, it is observed that there is a good correlation between antioxidant, total phenolic content (phospomolybdenum assay, R2 – 0.702) and total flavonoid content (DPPH assay, R2 – 0.665) and it is possible to suggest that total phenolic and flavonoid content of the plant extracts are the main reason for the antioxidant activity [4].

Key concepts: Petroleum ether, Flavonoid, DPPH, Chemistry, Antioxidant, Food science, Acetone, Azadirachta

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Correlation between Anti-oxidant property and Total phenolic and flavonoid content of Azadirachta Indica A Juss Flowers — Research Paper | ScholarLens