IMPROVED HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY/MASS SPECTROSCOPY (HPLC/MS) METHOD FOR DETECTION OF ANTHRAQUINONES AND ANTIOXIDANT POTENTIAL DETERMINATION IN ALOE SINKATANA

  • Asim Halfawi Shargi Department of Pharmacogency, Pharmacy Program, Nile College, Khartoum , Sudan. Department of Pharmacogency, Faculty pharmacy, Sudan. International University, Department of Pharmacogency, Pharmacy Program, Al Yarmouk College, Khartoum
  • Mohammed Aboied Department of Chemistry, Faculty of Pharmacy, University of Khartoum, Khartoum, Sudan
  • Ibrahim ME Al-Ribat National University, Khartoum, Sudan, , Faculty of Pharmacy Khartoum, Sudan
  • Fatehalrahman F Magbool Department of Pharmaceutics, Khartoum University, P.O. Box 1998, Sudan
10.22270/ujpr.v5i2.381

Keywords:

Aloe sinkatana, anthraquinones, antioxidant, free radicals, HPLC/MS, medicinal plants

Abstract

Objectives:  Medicinal plants, either as an extract, pure compound or as a derivative, offer limitless opportunities for the discovery of new drugs. Sudan is a very rich source of medicinal plants which are used in the treatment of a wide range of diseases. Aloe sinkatana, has great potential to be developed as drug by pharmaceutical industries. The present study is undertaken to investigate the antioxidant potential of Aloe sinkatana by DPPH radical scavenging activity. In addition, the study also performed to explore the possibility of using HPLC-MS technique for the determination and analysis of Aloe sinkatana.

Methods:  The extracts of Aloe sinkatana were analyzed for antioxidant activity by using DPPH free radical scavenging activity. The results indicated that the extracts showed a high effective free radical scavenging in the DPPH assay, also these extracts exhibited a noticeable antioxidant effect at low concentrations.

Results:  During in vitro evaluation the antioxidant potential of methanolic extract was the highest, followed by aqueous extract  in DPPH radical scavenging activity. So the methanolic extract of the plant, exhibited a great antioxidant effect at 50 μg/ml which may be attributed to high phenolic content. Therefore, methanolic extract to be a more active radical scavenger than aqueous extract. The HPLC-MS analysis had shown the methanolic extract of Aloe sinkatana to be rich in the major anthraquinones and their glucosides, which revealed 9 compounds, and also UV spectroscopy detected the presence of two flavonoids.

Conclusion:  The results indicated that the extracts of Aloe sinkatana  is a potential source of natural antioxidants or nutraceuticals with potential application to reduce oxidative stress with consequent health benefits. Due to stronger antioxidant potential and phytochemical composition, Aloe sinkatana could be proved as a valuable prospect in pharmaceutical formulations by taking part in the antioxidant defense system against generation of free radicals.

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Peer Review History:

Received 5 February 2020; Revised 13 March; Accepted 27 April; Available online 15 May 2020

Academic Editor: Dr. Ali Abdullah Al-yahawiorcid22.jpg, Al-Razi university, Department of Pharmacy, Yemen, alyahawipharm@yahoo.com

Received file:blue_23983.gif                Reviewer's Comments:download_logo_r_29189.gif

Average Peer review marks at initial stage: 4.5/10

Average Peer review marks at publication stage: 7.0/10

Reviewer(s) detail:

Prof Cyprian Ogbonna ONYEJIorcid2.jpg, Obafemi Awolowo University, Ile-Ife, Nigeria, conyeji@oauife.edu.ng

Dr. Gehan Fawzy Abdel Raoof Kandeelorcid2.jpg, Pharmacognosy Department, National Research Centre, Dokki, 12622,  Giza, Egypt, gehankandeel9@yahoo.com 

Dr. Nyunaï Nyemborcid2.jpg, Ministry of Scientific Research and Innovation of Cameroon, nyunain@yahoo.fr

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Published

2020-05-15

How to Cite

Shargi, A. H., M. Aboied, I. ME, and F. F. Magbool. “IMPROVED HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY/MASS SPECTROSCOPY (HPLC/MS) METHOD FOR DETECTION OF ANTHRAQUINONES AND ANTIOXIDANT POTENTIAL DETERMINATION IN ALOE SINKATANA”. Universal Journal of Pharmaceutical Research, vol. 5, no. 2, May 2020, doi:10.22270/ujpr.v5i2.381.

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