Journals / Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi / 2021 / Cilt: 11 - Sayı: 3

Determination of Chemical Compositions, Antioxidant and Enzyme Inhibitory Activities ofNaturally Growing Chenopodium album subsp. iranicum Aellen

Pages
2091–2101
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The obtained results indicated that the plant extract could be used as an easilyavailable natural antioxidants source for the food and pharmaceutical industry.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Chenopodium album has been used as folk medicine and nutrition for years by localpeople.
📊
Key Findings & Data:This study aimed to investigate the phenolic compounds by Reversed Phase-High PerformanceLiquid Chromatography-Diode Array Detector (RP-HPLC-DAD), total phenolic content (TPC), andbiological activities of the plant extracts prepared with three solvents (methanol, acetonitrile, and water)for the first time.
💡
Conclusion & Impact:The obtained results indicated that the plant extract could be used as an easilyavailable natural antioxidants source for the food and pharmaceutical industry.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Chenopodium album has been used as folk medicine and nutrition for years by localpeople. This study aimed to investigate the phenolic compounds by Reversed Phase-High PerformanceLiquid Chromatography-Diode Array Detector (RP-HPLC-DAD), total phenolic content (TPC), andbiological activities of the plant extracts prepared with three solvents (methanol, acetonitrile, and water)for the first time. Also, the chemical composition of essential oil and mineral content of the plant weredetermined by Gas Chromatography Mass-Spectrometry (GC-MS), and Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), respectively. The extracts of the plant were analyzed for thein vitro inhibitory activities against carbonic anhydrase (CA) and urease enzymes. The most abundantcompound in methanol extract was catechin (157.666 mg $L^{-1}$ ). Moreover, depending on the solvent usedin the extracts, varied levels of phenolic acids such as gallic, protocatechuic, p-OH benzoic, ferulic, andsyringic acids were identified. Thirty-four components were identified and methyl linolenate was foundto be the main constituents of the essential oil (11.28 %). The methanol extract of the plant exhibited the best antioxidant value given as TPC 65.41±5.20 µg $L^{-1}$ GAE, FRAP 113.54±1.57 µM TEAC,DPPH• 191.1±3.55 µg $L^{-1}$ $SC_50$, and ABTS•+ 74.7±1.55 µg $L^{-1}$ $SC_50$, respectively. According to themineral analyses, it was conducted that potassium and sodium were the most abundant minerals. Theextracts were found as inactive against CA and showed a moderate urease inhibition effect ($IC_50$:28.380±0.742 mg $L^{-1}$ ). The obtained results indicated that the plant extract could be used as an easilyavailable natural antioxidants source for the food and pharmaceutical industry.

🔖

Cite This Article

KARAÇELİK, A. A., ŞAHİN, H. (2022). Determination of Chemical Compositions, Antioxidant and Enzyme Inhibitory Activities ofNaturally Growing Chenopodium album subsp. iranicum Aellen. Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi, Cilt: 11 - Sayı: 3, 2091–2101. https://ajindex.com/articles/538511

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (8)

  1. Adedapo A, Jımoh F, Afolayan A, 2011. Comparison of the nutritive value and biological activities of the acetone, methanol and water extracts of the leaves of Bıdens pılosa and Chenopodıum album. Acta Poloniae Pharmaceutica- Drug Research, 68 (1): 83-92. Adams RP, 2007. Identification of Essential Oil Components by Gas Chromatography/Mass Spectrometry, 4th Edition.
  2. Allured Publ., Carol Stream, IL. Afolayan AJ, Jimoh FO, 2009. Nutritional quality of some wild leafy vegetables in South Africa. International Journal of Food Sciences and Nutrition, 60 (5): 424-431. Akpanyung EO, 2005. Proximate and mineral composition of bouillon cubes produces in Nigeria. Pakistan Journal of Nutrition, 4 (5): 327-329.
  3. Amic D, Davidovic-Amic D, Beslo D, Trinajstic N, 2003. Structure-radical scavenging activity relationship of flavonoids. Croatica Chemica Acta, 76 (1): 55-61.
  4. Benzie IFF, Strain JJ, 1999. Ferric reducing/antioxidant power assay: direct measure of total antioxidant activity of biological fluids and modified version for simultaneous measurement of total antioxidant power and ascorbic acid concentration. Methods in Enzymology, 299: 15-27.
  5. Brand-Williams W, Cuvelier ME, Berset C, 1995. Use of a free radical method to evaluate antioxidant activity. LWT - Food Science and Technology, 28 (1): 25-30.
  6. Che CT, Zhang H, 2019. Plant natural products for human health. International Journal of Molecular Sciences, 20(4): 830. Chigayo K, Mojapelo PEL, Mnyakeni-Moleele S, Misihairabgwi JM, 2016. Phytochemical and antioxidant properties of different solvent extracts of Kirkia wilmsii tubers. Asian Pacific Journal of Tropical Biomedicine, 6 (12): 1037-1043.
  7. Cutillo F, Dellagreca M, Gionti M, Previtera L, Zarrelli A, 2006. Phenols and lignans from Chenopodium album. Phytochemical Analysis, 17 (5): 344–349. Daur I, 2015. Chemical composition of selected Saudi medicinal plants. Arabian Journal of Chemistry, 8 (3): 329- 332. Efe D, 2020. Carbonic anhydrase enzyme inhibition and biological activities of Satureja hortensis L. essential oil. Industrial Crops and Products, 156: 112849. El-Sayed NH, Awaad AS, Hifnawy MS, Mabry TJ, 1999. A flavonol triglycoside from Chenopodium murale. Phytochemistry, 51 (4): 591-593.
  8. Guerrero JLG, Torija IME, 2009. Nutritional composition of leaves of Chenopodium species (C. album L., C. murale L. and C. opulifolium Shraeder). International Journal of Food Sciences and Nutrition, 48 (5): 321– 327. Guil JL, Torija ME, Giménez JJ, Rodríguez-García I, Giménez