In Vitro Antioxidant Capacity, Total Phenolic and Ascorbic Acid Contents of Crude Extracts from wild Fruits of Mimusops Caffra, Strychnos Madagascariensis and Vangueria infausta

Authors

  • Paulo Cumbane ISCTEM - Instituto Superior de Ciências e Tecnologia de Moçambique, Higher School of Health Sciences, Mozambique
  • Carvalho Madivate ISCTEM - Instituto Superior de Ciências e Tecnologia de Moçambique, Higher School of Health Sciences, Mozambique
  • Isabel Magaia ISCTEM - Instituto Superior de Ciências e Tecnologia de Moçambique, Higher School of Health Sciences, Mozambique
  • Shelsia Ibrahimo ISCTEM - Instituto Superior de Ciências e Tecnologia de Moçambique, Higher School of Health Sciences, Mozambique
  • Ananias Nharave ISCTEM - Instituto Superior de Ciências e Tecnologia de Moçambique, Higher School of Health Sciences, Mozambique
  • Raufa Jalá ISCTEM - Instituto Superior de Ciências e Tecnologia de Moçambique, Higher School of Health Sciences, Mozambique

Keywords:

Antioxidants; DPPH method; M. caffra; S. madagascariensis; V. infausta

Abstract

Ethnobotanical, phytochemical, ethnopharmacological and toxicological studies are being used by different authors to support indigenous knowledge and to provide scientific evidence of the benefic effects of native fruits and other natural products on health. In the present research, antioxidant capacity of hydroethanolic extracts of fruit pulp from Mimusops caffra (family Sapotaceae), Strychnos madagascariensis Poir. (family Loganiaceae) and Vangueria infausta Burch. subsp. infausta (Rubiaceae) was studied. The total phenolic compounds and total ascorbic acid were quantified by the spectrophotometric methods of Folin-Ciocalteu and 2,4-Dinitrophenyl Hydrazine respectively. The antioxidant capacity of the extracts was evaluated using reducing methods (phosphomolybdenum antioxidant assay, ferric reducing ability of plasma, metal chelating activity and ferric reducing power assay) and free radical scavenging method (DPPH and ABTS assay). The results showed significant differences (p <0.05) between the three samples analyzed. In the quantification of total phenols, the highest value (355.814 ± 4.167 mgEAG / gES) was found for the hydroethanolic extract of M. caffra while the hydroethanolic extract of V. infausta was the one that exhibited the highest content of ascorbic acid (120.146 ± 0.224). The highest total antioxidant activity was also exhibited by the fruit extract of M. caffra. The results found in the present study show that the fruits of the species of M. caffra and S. madagascariensis have secondary metabolites with a strong antioxidant activity, which suggests a beneficial effect on health, resulting from consumption of these fruits, especially in communities with limited resources. On the other hand, they can be used as an alternative to synthetic additives in the food processing industries or in pharmaceutical laboratories for the conservation of their formulations.

References

Amorim, E. L., Castro, V. T., Melo, J. G., Corrêa, A. J., & Sobrinho, T. J. (2012). Standard Operating Procedures (SOP) for the Spectrophotometric Determination of Phenolic Compounds Contained in Plant Samples. IntechOpen, 47-66. Retrieved from https://www.intechopen.com/books/latest-research-into-quality-control/standard-operating-procedures-sop-for-the-spectrophotometric-determination-of-phenolic-compounds-con.

Benzie, I. F., & Strain, J. (1996). The Ferric Reducing Ability of Plasma (FRAP) as a Measure of “Antioxidant Power”: The FRAP Assay. Analytical Biochemistry, 239, 70-76. Retrieved from https://booksc.xyz/book/1891961/a39b40

Botterweck, A., Verhagen, H., Goldbohm, R., & Kleinjans, J. (2000). Intake of butylated hydroxyanisole and butylated hydroxytoluene and stomach cancer risk: results from analyses in the Netherlands Cohort Study. Food and Chemical Toxicology, 38, 599-605. doi: https://doi.org/10.1016/S0278-6915(00)00042-9.

Chivandi, E., Mukonowenzou, N., & Berliner, D. (2016). The coastal red-milkwood (Mimusops caffra) seed: Proximate, mineral, amino acid and fatty acid composition. South African Journal of Botany, 102, 137-141. Retrieved fromhttps://www.sciencedirect.com/science/article/pii/S0254629915003403?via%3Dihub.

El-haskoury, R.; Al-Waili, N.; Kamoun, Z.; Makni, M.; Al-Waili, H. and Lyoussi, B. (2018). Antioxidant activity and protective effect of carob noney in CCl4-induced kidney and liver injury. Archives of Medical Research 49(5): 306-313. doi: 10.1016/j.arcmed.2018.09.011.

Floegela, A., Kim, D.-O., Chung, S.-J., Koo, S. I., & Chun, O. K. (2011). Comparison of ABTS/DPPH assays to measure antioxidant capacity in popular antioxidant-rich US foods. Journal of Food Composition and Analysis, 24, 1043-1048. doi: doi.org/10.1016/j.jfca.2011.01.008.

Fonseca, L. J., Nunes-Souza, V., Goulart, M. O., & Rabelo, L. A. (2019). Oxidative Stress in Rheumatoid Arthritis: What the Future Might Hold regarding Novel Biomarkers and Add-On Therapies. Oxidative Medicine and Cellular Longevity, 2019, 16 pages. doi: https://doi.org/10.1155/2019/7536805.

Gohari, A.R.; Hajimehdipoor, H.; Saeidnia, S.; Ajani, Y. and Hadliakhoondi, A. (2011). Antioxidant activity of some medicinal species using FRAP assay. Journal of Medicinal Plants 10(37): 54-60.

Hamid, A.A.; Aiyelaagbe, O.O.; Usman, L.A.; Ameen, O.M. and Lawai, A. (2010). Antioxidants: Its medicinal and pharmacological applications. African Journal of Pure and Applied Chemistry 4(8): 142-151.

Jan, S., Khan, M. R., Rashid, U., & Bokhari, J. (2013). Assessment of Antioxidant Potential, Total phenolics and Flavonoids of Different Solvent Fractions of Monotheca Buxifolia Fruit. Osong Public Health and Research Perspectives. 4, 246–254. doi: 10.1016/j.phrp.2013.09.003.

Jemli, M. E., Kamal, R., Marmouzi, I., Zerrouki, A., Cherrah, Y., & Alaoui, K. (2016). Radical-Scavenging Activity and Ferric Reducing Ability of Juniperus thurifera (L.), J. oxycedrus (L.), J. phoenicea (L.) and Tetraclinis articulata (L.). Advances in Pharmacological and Pharmaceutical Sciences, 2016, 6 pages. doi: https://doi.org/10.1155/2016/6392656.

Jeong, S.-H., Kim, B.-Y., Kang, H.-G., Ku, H.-O., & Cho, J.-H. (2005). Effects of butylated hydroxyanisole on the development and functions of reproductive system in rats. Toxicology, 208, 49-62. doi: 10.1016/j.tox.2004.11.014.

Joshi, A.; Bhobe, M. and Sattarkar, A. (2013). Phytochemical investigation of the roots of Grewia microcos Linn. Journal of Chemical and Pharmaceutical Research 5(7): 80-87.

Kapur, A., Haskovic, A., & Copra-Janicijevic, A. (2012). Spectrophotometric analysis of total ascorbic acid content in various fruits and vegetables. Bulletin of the Chemists and Technologists of Bosnia and Herzegovina, 38, 39-42

Kaska, A. and Mammadov, R. (2019). Antioxidant properties, proximate content and cytotoxic activity of Echinophora tournefortii Jaub. & Spach. Foor Science and Technology 39(4): 875-880. DOI: https://doi.org/10.1590/fst.09118.

Khaled-Khodja, N., Boulekbache-Makhlouf, L., & Madani, K. (2014). Phytochemical screening of antioxidant and antibacterial activities of methanolic extracts of some Lamiaceae. Industrial Crops and Products, 61, 41-48. doi: doi.org/10.1016/j.indcrop.2014.06.037.

Khan, M.M.R.; Rahman, M.M.; Islam, M.S. and Begun, S.A. (2006): A simple spectrophotometric method for the determination of vitamin C contents in various fruits and vegetables at Stylhet area in Bangladesh. Journal of Biological Sciences 6(2): 338-392.

Krishnaiah, D.; Sarbatly, R. and Nithyanandam, R. (2011). A review of antioxidant potential of medicinal plant species. Food and Bioproducts Processing 89: 217-233.

Leite, K.C. de S.; Garcia, L.F.; Lobón, G.S.; Thomaz, D.V.; Moreno, E.K.G.; de Carvalho, M.F.; Rocha, M.L.; dos Santos, W.T. and Gil, E.S. (2018). Antioxidant activity evaluation of dried herbal extracts: an electroanalytical approach. Brazilian Journal of Pharmacognosy 28: 325-332.

Lourenço, S. C., Moldão-Martins, M., & Alves, V. D. (2019). Antioxidants of Natural Plant Origins: From Sources to Food Industry Applications. Molecules, 24, 25 pages. doi:10.3390/molecules24224132.

Maroyi, A. (2018). Nutraceutical and Ethnopharmacological Properties of Vangueria infausta subsp. infausta. Molecules, 23, 19p. Retrieved from https://pubmed.ncbi.nlm.nih.gov/29734716/.

Mbukwa, E., Chacha, M., & Majinda, R. R. (2007). Phytochemical constituents of Vangueria infausta: their radical scavenging and antimicrobial activities. ARKIVOC, 2007, 104-112. Retrieved from https://quod.lib.umich.edu/a/ark/5550190.0008.912/1/--phytochemical-constituents-of-vangueria-infausta-their?page=root;size=150;view=pdf.

Newmann, D.J. and Cragg, G.M. (2007). Natural products as sources of new drugs over the last 25 years. Journal of Natural Products. Vol.70, 461-477.

Norscia, I., & Borgognini-Tarli, S. (2006). Ethnobotanical reputation of plant species from two forests of Madagascar: A preliminary investigation. South African Journal of Botany, 72, 656–660. Retrieved from http://www.ethnopharmacologia.org/prelude2020/pdf/biblio-hn-24-norscia.pdf.

Phuyal, N., Jha, P. K., Raturi, P. P., & Rajbhandary, S. (2020). Total Phenolic, Flavonoid Contents, and Antioxidant Activities of Fruit, Seed, and Bark Extracts of Zanthoxylum armatum DC. Scientific World Journal, 7 pages.

Pooja, V., & Sunita, M. (2004). Antioxidants and Disease Prevention. International Journal of Advanced Scientific and Technical Research, 2, 2249-9954. Retrieved from https://rspublication.com/ijst/2014/april14/80.pdf.

Prieto, P.; Pineda, M. and Aguilar, M. (1999). Spectrophotometric quantitation of antioxidant capacity through the formation of a phosphomolybdenum complex: Specific application to the determination of vitamin E. Analytical Biochemistry 269: 337-341.

Ramalingum, N., & Mahomoodally, M. F. (2014). Biologic Propensities and Phytochemical Profile of Vangueria madagascariensis J. F. Gmelin (Rubiaceae): An Underutilized Native Medicinal Food Plant from Africa. BioMed Research International, 2014, 15 pages. Retrieved from https://www.hindawi.com/journals/bmri/2014/681073/.

Rezaeian, S.; Pourianfar, H.R. and Janpoor, J. (2015). Antioxidant properties of several medicinal plants growing wild in northeastern Iran. Asian Journal of Plant Science and Research 5(2): 63-68.

Sariburun, E., Şahin, S., Demir, C., & Turkben, C. (2010). Phenolic Content and Antioxidant Activity of Raspberry and Blackberry Cultivars. Journal of Food Science, 75, 328-335. doi:10.1111/j.1750-3841.2010. 01571.x.

Sihem, D., Samia, D., Gaetano, P., Sara, L., Giovanni, M., Hassibaa, C., . . . Noureddine, H. A. (2015). In vitro antioxidant activities and phenolic content in crop residues of Tunisian globe artichoke. Scientia Horticulturae, 190, 128 - 136. doi: doi.org/10.1016/j.scienta.2015.04.014.

Sihema, D., Samia, D., Gaetano, P., Sara, L., Giovanni, M., Hassiba, C., . . . Noureddine, H. A. (2015). In vitro antioxidant activities and phenolic content in crop residues of Tunisian globe artichoke. Scientia Horticulturae, 190, 128-136. doi: doi.org/10.1016/j.scienta.2015.04.014.

Thabti, I., Elfalleh, W., Tlili, N., Ziadi, M., Campos, M. G., & Ferchichi, A. (2014). Phenols, Flavonoids, and Antioxidant and Antibacterial Activity of Leaves and Stem Bark of Morus Species. International Journal of Food Properties, 17, 842-854.

Wong, F.-C., Yong, A.-L., Ting, E. P.-S., Khoo, S.-C., Ong, H.-C., & Chaia, T.-T. (2014). Antioxidant, Metal Chelating, Anti-glucosidase Activities and Phytochemical Analysis of Selected Tropical Medicinal Plants. Iranian Journal of Pharmaceutical Research, 13, 1409–1415. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232808/.

Downloads

Published

2020-12-29

How to Cite

In Vitro Antioxidant Capacity, Total Phenolic and Ascorbic Acid Contents of Crude Extracts from wild Fruits of Mimusops Caffra, Strychnos Madagascariensis and Vangueria infausta. (2020). Asian Journal of Agriculture and Food Sciences, 8(6). https://ajouronline.com/index.php/AJAFS/article/view/6383

Similar Articles

11-20 of 58

You may also start an advanced similarity search for this article.