Multidirectional insights into the phytochemical, biological, and multivariate analysis of the famine food plant (Calligonum polygonoides L).: A novel source of bioactive phytocompounds. (November 2020)
- Record Type:
- Journal Article
- Title:
- Multidirectional insights into the phytochemical, biological, and multivariate analysis of the famine food plant (Calligonum polygonoides L).: A novel source of bioactive phytocompounds. (November 2020)
- Main Title:
- Multidirectional insights into the phytochemical, biological, and multivariate analysis of the famine food plant (Calligonum polygonoides L).: A novel source of bioactive phytocompounds
- Authors:
- Pervaiz, Irfan
Saleem, Hammad
Sarfraz, Muhammad
Imran Tousif, Muhammad
Khurshid, Umair
Ahmad, Saeed
Zengin, Gokhan
Ibrahime Sinan, Kouadio
Locatelli, Marcello
Mahomoodally, Fawzi M.
Asnawi Zainal Abidin, Syafiq
Ahemad, Nafees - Abstract:
- Graphical abstract: Highlights: Phytochemical and biological profiling of different solvent extracts of Calligonum polygonoides were investigated. UHPLC-MS and HPLC-PDA analysis revealed different flavonoid, phenolic, alkaloid, and terpenoid derivatives. All the extracts presented varied antioxidant and enzyme inhibition potential. Univariate analysis showed that chloroform and n -hexane were suitable solvent to recover biomolecules with highest biological activities. Abstract: Calligonum polygonoides L. also known as famine food plant, is normally consumed in times of food scarcity in India and Pakistan and also used traditionally in the management of common diseases. The present design aims to provide an insight into the medicinal potential of four solvent extracts of C. polygonoides via an assessment of its phytochemical profile, antioxidant and enzyme inhibitory potential. Phytochemical composition was estimated by deducing total bioactive constituents, UHPLC-MS secondary metabolites profile, and HPLC phenolic quantification. Antioxidant potential was determined via six methods (radical scavenging (DPPH and ABTS), reducing power (FRAP and CUPRAC), phosphomolybdenum total antioxidant capacity and metal chelation activity). Enzyme inhibitory potential was assessed against clinical enzymes (acetylcholinesterase -AChE, butyrylcholinesterase -BChE, tyrosinase, and α-amylase). The highest amounts of phenolic contents were found in chloroform extract (76.59 mg GAE/g extract)Graphical abstract: Highlights: Phytochemical and biological profiling of different solvent extracts of Calligonum polygonoides were investigated. UHPLC-MS and HPLC-PDA analysis revealed different flavonoid, phenolic, alkaloid, and terpenoid derivatives. All the extracts presented varied antioxidant and enzyme inhibition potential. Univariate analysis showed that chloroform and n -hexane were suitable solvent to recover biomolecules with highest biological activities. Abstract: Calligonum polygonoides L. also known as famine food plant, is normally consumed in times of food scarcity in India and Pakistan and also used traditionally in the management of common diseases. The present design aims to provide an insight into the medicinal potential of four solvent extracts of C. polygonoides via an assessment of its phytochemical profile, antioxidant and enzyme inhibitory potential. Phytochemical composition was estimated by deducing total bioactive constituents, UHPLC-MS secondary metabolites profile, and HPLC phenolic quantification. Antioxidant potential was determined via six methods (radical scavenging (DPPH and ABTS), reducing power (FRAP and CUPRAC), phosphomolybdenum total antioxidant capacity and metal chelation activity). Enzyme inhibitory potential was assessed against clinical enzymes (acetylcholinesterase -AChE, butyrylcholinesterase -BChE, tyrosinase, and α-amylase). The highest amounts of phenolic contents were found in chloroform extract (76.59 mg GAE/g extract) which may be attributed to its higher radical scavenging, reducing power and tyrosinase inhibition potential. The n -butanol extract containing the maximum amount of flavonoids (55.84 mg RE/g extract) exhibited highest metal chelating capacity. Similarly, the n -hexane extract was found to be most active against AChE (4.65 mg GALAE/g extract), BChE (6.59 mg GALAE/g extract), and α-amylase (0.70 mmol ACAE/g extract) enzymes. Secondary metabolite assessment of the crude methanol extract as determined by UHPLC-MS analysis revealed the presence of 24 (negative ionization mode) and 15 (positive ionization mode) secondary metabolites, with most of them belonging to phenolic, flavonoids, terpene, and alkaloid groups. Moreover, gallic acid and naringenin were the main phenolics quantified by HPLC-PDA analysis in all the tested extracts (except n -butanol extract). PCA statistical analysis was also conducted to establish any possible relationship amongst bioactive contents and biological activities. Overall, the C. polygonoides extracts could be further considered to isolate bioactive enzyme inhibitory and antioxidant natural phytocompounds. … (more)
- Is Part Of:
- Food research international. Volume 137(2020)
- Journal:
- Food research international
- Issue:
- Volume 137(2020)
- Issue Display:
- Volume 137, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 137
- Issue:
- 2020
- Issue Sort Value:
- 2020-0137-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-11
- Subjects:
- Calligonum polygonoides -- Phytochemicals -- Antioxidants -- Enzyme inhibition -- Bioactive agents
Food -- Analysis -- Periodicals
Food industry and trade -- Periodicals
Food industry and trade -- Canada -- Periodicals
Food Technology -- Periodicals
Food -- Periodicals
Food-Processing Industry -- Periodicals
Aliments -- Industrie et commerce -- Périodiques
Aliments -- Industrie et commerce -- Canada -- Périodiques
Aliments -- Recherche -- Périodiques
Food industry and trade
Canada
Periodicals
Electronic journals
664.005 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09639969 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.foodres.2020.109606 ↗
- Languages:
- English
- ISSNs:
- 0963-9969
- Deposit Type:
- Legaldeposit
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