Evaluation of Mineral Elements Content of Senegal Fruits

Abstract

This study determined mineral value and antioxidant activity of Senegal fruits for contributing to improving healthy diet and preventing some chronic diseases. Mineral element contents of Dialium guineense, Landolphia heudelotti, Mangifera indica, Cyperus esculentus and Saba senegalensis, which are widely available and consumed, were studied. The results by ICP-OES spectrophotometry after acid mineralization showed highest levels of (per 100 g fruits), calcium (158 mg), potassium (1018 mg), magnesium (532 mg), zinc (26 mg) with juice of Landolphia heudelotti fruit pulp. Mangifera indica pulp is richer in sodium (89 mg), phosphorus (556 mg), sulphur (384 mg) and silicon (110 mg). Dialium senegalensis pulp is richer in iron (23 mg) and manganese (19 mg). Lyophilized Cyperus esculentus rhizomes analyzed by atomic absorption spectrophotometry gave highest concentrations of (per 100 g fruits), calcium (2550 mg), potassium (11,843 mg) and magnesium (7669 mg) but sodium content (22 mg) is lower. In vitro antioxidant activity evaluation with the DPPH radical showed for 10 mg/ml concentration, highest inhibition percentage for Saba senegalensis 4.03%, followed by Landolphia heudelotti and Dialium guineense, which were significantly similar 2.29% and 2.20% respectively, Mangifera indica 1.7% and finally Cyperus esculentus 0.5%, but much lower compared to the ascorbic acid equal to 96.32% used as a reference.

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Gueye, R. , Ledauphin, J. , Baraud, F. , Leleyter, L. , Lemoine, M. , Gueye, R. , Diedhiou, A. , Balde, M. , Gaye, N. , Seck, M. , Fall, D. and Wele, A. (2022) Evaluation of Mineral Elements Content of Senegal Fruits. Journal of Minerals and Materials Characterization and Engineering, 10, 163-173. doi: 10.4236/jmmce.2022.102013.

1. Introduction

Currently, non-transmissible diseases (NTDs), including cardiovascular disease, cancers, obesity and type 2 diabetes, cause more deaths each year. Poor diet, lack of physical activity, tobacco and alcohol are factors in the epidemiology of these diseases and are very important in public health [1] [2].

Fruits and vegetables are an important part of a healthy diet and, if consumed daily in sufficient quantities, they could help prevent serious diseases such as cardiovascular diseases and cancers [3] [4] [5] [6]. For example, according to the World Health Organization (WHO), low consumption of fruits and vegetables is the cause of about 31% of ischemic heart diseases and 11% of strokes worldwide. Indeed, globally, up to 2.7 million lives could be saved each year [1] by sufficient consumption of fruits and vegetables as dietary sources of fibers, vegetable proteins and protective micronutrients [7] [8] [9] [10] [11].

In this context, a minimum daily intake of 400 g of fruits and vegetables (excluding potatoes and other starchy tubers) is recommended to prevent chronic diseases such as heart diseases, cancers, diabetes, obesity [1] [12] [13] and to prevent or reduce several micronutrient deficiencies, particularly in the least developed countries [1].

In 2016, Senegal was among the least developed countries, ranked 165th in the world economy, 29th in Africa and 4th in the western part. It is characterized by low economic growth and high dependence on official development assistance. The prevalence rates of NTDs are more than 5.5% for diabetes and nearly 24% for high blood pressure [14]. Despite relatively low rainfall, a great diversity of local fruits is available in Senegal. The development of local resources and food self-sufficiency seem essential for sustainable development. Thus, the objective of this study is to determine the nutritional value, particularly mineral value, of 5 local fruits that are widely consumed in this country: Dialiumguineense, Landolphiaheudelotti, Mangiferaindica, Cyperusesculentus and Saba senegalensis.

Dialiumguineense Willd (Fabaceae) or Daliumnitidum or Black Tamarind corresponds to a tree 10 to 15 m high. The pulp surrounding the seed is acidic, it is sucked to quench thirst or macerated in cold water as a drink [8] [15] - [20]. The pulp is used, with other astringent drugs, for the treatment of diarrhoea, as well as the bark of the trunk [21] [22] and as an antimicrobial in wound healing [23]. In some localities, the consumption of fruit infusion is recommended against fever [8].

Landolphiaheudelotti (Apocynaceae) is a sarmentose shrub bushy presenting clumps from 2 to 5 cm high, or vine that can reach 15 m high. The fruits are spherical matte green berries that become orange-yellow when ripe; then a fine pulp sticks strongly to the seeds. Fruits are sold on local markets, the juice from the pulp is acidic and used as a seasoning. The decoction of leaves or roots has enteralgic properties without purgative effect [8]. The latex produced by the plant was used for rubber production for a long time before being replaced by rubber and synthesis [8].

Mangiferaindica L. (Anacardiaceae) or mango is a large fruit tree that can reach 10 to 25 meters in height. It has a stocky barrel and a dense shade foliage. The fleshy fruit is an oblong drupe attached to a long peduncle, of variable size depending on the variety. According to Pousset [14], all parts of mango are used in traditional medicine as an antidiarrheal. Some parts of the plant have been proven to be antidysenteric, antiamibiase, antioxidant, anti-inflammatory and can be used as analgesics [8] [24] [25].

Cyperusesculentus L. (Cyperaceae) or Tiger Nuts, an annual plant with tuberized rhizomes, is pantropical and cultivated in all dry regions of Africa. It is a perennial species that grows in small clumps, with a single flowering axis, but is connected to many son feet by spherical rhizomes, with a sweet taste. Depending on the locality, the leaves are used against migraines, the rhizome as a galactogen, stomachic, against headaches, diarrhoea, stomach aches, indigestion and bloating. This rhizome is an energy food [26] [27] [28] and is recommended in the prevention of heart attacks, thrombosis, colon cancer, diabetes and obesity [29] [30]. These properties are justified because of the high content of soluble glucose, vitamin E, fibers and minerals [29].

Saba senegalensis A. DC. Pichon (Apocynaceae) or guava vine, is a large woody vine, picked up on itself or climbing. It produces a milky sap and large fruits in the form of berries which contain a pulp sticking to the seeds. Leaves in boiling decoctions and inhalations could be anti-migraine and vapours could improve declining vision and rebellious coughs. Dry root bark powder is used as a healing agent on wounds and burns. Stem latex is hemostatic, coagulant, antitussive, antituberculous and emetic [8] [31]. Finally, the fruit is highly consumed because it is succulent, seasoned, in juice or marmalade, increasing the added value of the plant. Thus, Saba senegalensis has been the subject of domestication and planting studies [32].

In this study, the mineral contribution for these 5 fruits will be detailed along with the antioxidant activity of each.

2. Experimental

2.1. Material

2.1.1. Plant Material

Fruit samples of Dialiumguineense,Landolphia heudelotti were collected in Casamance region and Mangiferaindica was collected in Dakar. The rhizomes of Cyperusesculentus and the fruits of Saba senegalensis, were purchased at the Colobane market (Dakar). However, according to our surveys, most of these forest fruits sold in the markets would come from Casamance region.

The studied samples of these different fruits are mainly pulps and only rhizomes for Cyperusesculentus (Figure 1).

2.1.2. Reagents and Equipment

All reagents used were of purity for residue analysis. This study involved notably a lyophilization of samples with a Christ MartinTM alpha 1 - 2 LD Plus freeze-dryer, a mineralization with a Berghof microwave oven, a determination of the concentrations of elements using an inductively coupled plasma atomic

Figure 1. Studied fruits samples.

emission spectrometer (ICP-OES Agilent Technologies 5100, software ICP expert 7.4.1.0), a Varian SpectrAA 220 atomic absorption/emission spectrophotometer with air/acetylene flame for Cyperus samples and determinations of antioxidant activities with a UV-Visible spectrophotometer ATI Unicam.

2.2. Methods

2.2.1. Determination of the Concentrations of Elements

Frozen samples of fruits were lyophilized and a mass of 0.2 ± 0.01 g was weighed 3 times for each. They were then subjected to an acid mineralization consisting of a contact time of one hour with 10ml of mixture of HCl 37% (2 volumes) and HNO3 68% (1 volume) in Teflon bombs. The mineralization was performed during 50 minutes in the microwave oven (room temperature to 170?C (10 min), 170?C (10 min), 170?C to 100?C (10 min), 100?C (10 min), 100?C to 80?C (5 min), 80?C (5 min). Thus, mineralization was carried out in triplicate for each fruit sample. The mineralized samples were then collected in a volumetric flask and the volume adjusted precisely to 50 ml with ultrapure water and stored further in the refrigerator at +4?C. A filtration step using a syringe equipped with a microfilter (0.45 μm diameter) was performed before analysis with the ICP-OES spectrophotometer.

The following elements were specifically targeted using ICP-OES: Al (396,15 nm), As (188,980 nm), B (249,678 nm), Ca (422,673 nm), Cd (226,502 nm), Co (258,033 nm), Cr (267,716 nm), Cu (327,395 nm), Fe (238,204 nm), Ge (206,866 nm), K (766,491 nm), Li (670,783 nm), Mg (279,078 nm), Mn (257,610 nm), Mo (204,598 nm), Na (589,512 nm), Ni (216,555 nm), P (213,618 nm), Pb (217,000 nm), S (181,972 nm), Si (288,158 nm), Ti (344,188 nm), Zn (213,817 nm). Calibration was performed using nine points (2 decades) of dilution of a stock solution containing the whole elements at different concentrations. The stock solution was obtained by dilution of certified individual element or multi-element solutions at 1000 and 10,000 ppm.

2.2.2. Determination of the Antioxidant Activity

In this study, in vitro evaluation of antioxidant activity was performed by visible spectrophotometry with the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical according to the procedures described [33] [34]; the maximal absorption of the reduced DPPH radical is detected at 517 nm in ethanol. Antioxidant activity is defined by the index of the reduction of radical activity in percentage or percentage inhibition of oxidant activity noted PI. Thus, the absorbance of the reaction mixture, free radical and antioxidant sample (Abs sample), is related to the absorbance of the mixture without antioxidant (Abs witness) at a time t by the following relationship [34]:

PI % = ( ( Abs Witness ? Abs sample ) / Abs Witness ) × 100

A mixture of 0.5 g ± 0.01 of fruit samples with 25 ml of ethanol was stirred at room temperature one hour with ultrasound and macerated for 48h before being filtered and evaporated with rotavapor. The dry residue was taken back with 1 ml of ethanol and represented then the stock solution. 0.1 ml of this stock solution of ethanolic extract from fruit samples was added to 3.9 ml of 4% DPPH-. This mixture was placed in a dark place and the reading was taken after 30 minutes on a spectrophotometer at 517 nm. Each reading was repeated three times.

3. Results and Discussion

3.1. Concentrations of Minerals

The four targeted fruits (Dialiumguineense, Landolphiaheudelotti, Mangiferaindica, Saba senegalensis) and the dried rhizome of Cyperusesculentus are containing rather different concentrations of minerals (Figure 2).Comparing the fruits, the highest levels of calcium (158 mg/100g), potassium (1018 mg/100g), magnesium (532 mg/100g) and zinc (26 mg/100g) are obtained with the juice from the mechanical expression of the pulp of Landolphiaheudelotti fruit. Comparatively, Mango flesh pulp (Mangiferaindica) is richer in sodium (89 mg/100g), phosphorus (556 mg/100g), sulphur (384 mg/100g) and silicon (110 mg/100g) while the pulp ofDialium senegalensis is richer in iron (23 mg/100g) and manganese (19 mg/100g). Globally, the pulp of Saba senegalensis is poorer in quite all elements.

The levels of a dozen of elements: Al, As, B, Cd, Co, Cr, Cu, Ge, Li, Ni, Pb, Ti were also investigated in these fruits. However, the recorded absorbances using ICP-AES were systematically lower than the limits of detection of each element. With all the limits of detection measured between 25 and 175 μg/kg, it is possible to state that these elements are only present in the form of ultra-traces and that their concentrations never reach 175 μg/kg in the fruits.

Thecomposition in minerals of Cyperusesculentus was determined using atomic absorption and emission spectroscopy. The results obtained for this fruit are rather different from others because the dried rhizome part was analyzed. The concentrations of calcium (2550 mg/100g), potassium (11,843 mg/100g) and magnesium (7669 mg/100g) were very high compared to the levels observed in the other samples. However, the concentration in sodium (22 mg/100g) is in the

Figure 2. Fruits minerals concentrations.

same order and even a little lower.

According to the results, the various medicinal uses can be justified by the content of mineral elements, in particular calcium, iron, potassium, magnesium, manganese, phosphorus, sulphur and silicon.

3.2. Comparison of the Concentrations of Minerals in Studied Fruits with Other Fruits

The mineral composition of the studied fruits is compared with other fruits that also grow in Senegal. The data, from the literature, for these other fruits, which are known to be nutritious, are reported in Figure 3. They concern the fruit pulp of Adansoniadigitata (baobab) [8], banana or Musa spp, orange or Citrus sinensis, date or Phoenix reticulata and Detariumsenegalense [35] [36]. Some of these reference fruits are the most consumed in Senegal.

Firstly, Achoba et al. [16] already analyzed the pulp of Dialiumguineense in the early 1990s. The Nigerian species exhibited concentrations of 213 mg/100g, 42 mg/100g, 11 mg/100g and 98 mg/100g respectively for Ca, Mg, Na and K. In addition, we showed that Dialiumguineense has also a high content in Fe and Mn (23 mg/100g and 19 mg/100g respectively). These contents in Fe and Mn are the highest we found in the four studied juices (Figure 2). Studies led by Haddad [8], also for Dialiumguineense, have shown lower concentrations of Ca (104 mg/100g), P (71 mg/100g) and Fe (2.6 mg/100g). Dialium guineese, compared to the reference fruits (Figure 3),is richer in Fe than Adansonia (8.6 mg/100g),

Figure 3. Minerals concentrations according to bibliographic data of the fruits taken as reference.

in Mn than date (0.3 mg/100g), which have the highest levels of these elements among the reference fruits.

Landolphiaheudelotti could represent an important source of magnesium (532 mg/100g) if compared to other fruits of reference (Figure 3). It is twice that of Adansoniadigitata [8], more than 5 times that of Detariumsenegalense [35] [36] and more than 10 times that of banana, orange or date [37].

Among the four studied fruits, Mangiferaindica pulp has the highest Na, P, S and Si contents. This fruit could then represent a great intake of notably phosphorous as it is 5 times higher than that of Adansoniadigitata [8] which has the higher content in that element along the reference fruits (Figure 3). Moreover, this mango is a little richer in sodium than all reference fruits and notably Detariumsenegalensis [35] [36].

Saba senegalensis pulp exhibits relatively low contents of calcium (14 mg/100g) and potassium (110 mg/100g). However, if compared to other fruits of reference (Figure 3), it contains significant quantities of sodium (51 mg/100g) and iron (12 mg/100g).

The dried rhizome of Cyperusesculentus is containing very high contents of Ca (2550 mg/100g), K (11843 mg/100g) and Mg (7669 mg/100g) in comparison with other fruits (Figure 3). High quantities for this rhizome were already determined for species grown in Senegal by Ndiaye et al. [28] with 26 mg/100g of Ca, 896 mg/100g of K and 105 mg/100g of Mg. The level of potassium is then rather important in the studied rhizome; on another hand, the sodium content of the dried rhizome (22 mg/100g) is very low. Similarly, by comparing these results with other rhizomes [38], the levels found were as follows: Zingiberofficinale (Zingiberaceae) or ginger, for 100 g of raw root, 16 mg Ca, 0.6 mg Fe, 43 mg Mg, 34 mg P, 415 mg K, 13 mg Na, 0.34 Zn; Curcuma longa (Zingiberaceae) or turmeric, with: 183 mg of Ca, 41.42 mg of Fe, 193 mg of Mg, 2525 mg of K, 38 mg of Na, 4.35 of Zn, 0.6 mg of Cu, 7, 8 mg of Mn, 4.5 μg of Se. They are also significantly lower.

Thus, the recommended minimum daily intakes (Table 1), related to Directive 2008/100/EC, which are respectively 120 mg, 375 mg, 600 mg, 120 mg, 45 mg, 0.525 mg and 2.25 mg for Ca, Na, K, P, Mg, Mn and Zn could be largely covered by the consumption of the studied fruits according to the recommendation of the WHO.

3.3. Antioxidant Activity

Comparing the whole fruit studied,at a 10 mg/ml concentration, Saba had the highest PI at 4.03%, followed by LandolphiaandDialium, which exhibit similar PI values of 2.29% and 2.20% respectively. Value for Mangiferaindica was 1.7% and that of Cyperus was 0.5%. Global values obtained for all fruits are much lower compared to the PI (96.32%) of the ascorbic acid used as a reference. The IC50 of Landolphia (194 mg/ml) andSaba (150 mg/ml) could be determined for an IC50 equal to 0.147 mg/ml for ascorbic acid. These results, which are lowin vitro, can be increased in the human body. Indeed, some elements such as Mn, Zn, Cu and Zn are essential to the antioxidant activity of enzymes such as superoxide dismutase and glutathione peroxidase [9] [24] [39].

Table 1. Recommended Daily Intake (RDI) for minerals.

4. Conclusions

This study revealed interesting levels of essential or important mineral elements in local fruits, as well as their antioxidant activities. These fruits of forest origin, which are relatively easy to access and available in the markets, could contribute to improving the nutritional status of populations and thus the prevention of certain diseases.

In perspective, it is envisaged to extend this study to other local vegetable products in order to have its own mineral databases and furthermore elaborate diets adapted to our context of low income countries.

Acknowledgements

The authors wish to acknowledge the technical expertise of Mr Arnaud Dumartin, Mr Lamine Gueye and Mr Ibrahima Keita.

Conflicts of Interest

The author(s) declare(s) that there is no conflict of interest.

References

[1] Report of the Joint FAO/WHO (2004) Workshop Fruits and Vegetables for Health, Kobe, 1-3 September 2004.
[2] Zhang, C., et al. (2012) High Fruit Consumption before Pregnancy Does not Increase the Risk of Gestational Diabetes. Equation Nutrition, 125, 3.
[3] Carter, P., Gray, L.J., Troughton, J., Khunti, K. and Davies, M.J. (2011) Eating Green Leafy Vegetables May Reduce the Risk of Type 2 Diabetes. Equation Nutrition, 109, 2.
[4] Cooper, A.J. and Forouhi, N.G. (2012) Prevention of Type 2 Diabetes: Importance of the Quantity and Variety of Fruits and Vegetables. Equation Nutrition, 125, 2.
[5] Choi, S.H., Kim, D.S., Kozukue, N., Kim, H.J., Nishitani, Y., Mizuno, M., Levin, C.E. and Friedman, M. (2014) Protein, Free Amino Acid, Phenolic, β-Carotene, and Lycopene Content, and Antioxidative and Cancer Cell Inhibitory Effects of 12 Greenhouse-Grown Commercial Cherry Tomato Varieties. Journal of Food Composition and Analysis, 34, 115-127.
https://doi.org/10.1016/j.jfca.2014.03.005
[6] Dauchet, L. (2006) Fruits and Vegetables: Antihypertensive Foods? Equation Nutrition, 60, 4.
[7] Forouhi, N.G., et al. (2011) Fruits, Vegetables, and Risk of Type 2 Diabetes: Which Combination? Equation Nutrition, 109, 3.
[8] Haddad, C. (2000) Wild Fruit Trees from Senegal. Ph.D. Thesis, University of Montpellier, Montpellier.
[9] Koechlin-Ramonatxo, C. (2006) Oxygen, Oxidative Stress and Antioxidant Supplementation, or an Other Way for Nutrition in Respiratory Diseases. Nutrition Clinique et Métabolisme, 20, 165-177.
https://doi.org/10.1016/j.nupar.2006.10.178
[10] Meneton, P. (2006) Potassium and Its Role in Lowering Blood Pressure—The Place of Fruits and Vegetables. Equation Nutrition, 60, 2.
[11] Siegel, K.R. and Venkat Narayan, K.M. (2012) What Are the Social Factors Related to the Prevalence of Diabetes in 94 Countries? Equation Nutrition, 125, 4.
[12] Gibault, T. (2012) Fertility and Eating Habits: A Couple's Business. Equation Nutrition, 125, 5.
[13] Goya Wannamethee, S. (2011) Potential Protective Mechanisms of Dietary Fibre on the Risk of Type 2 Diabetes. Equation Nutrition, 109, 3.
[14] Pousset, J.L. (2004) Medicinal Plants from Africa. How to Recognize and Use Them? Aix en Provence, Edisud, 169-170.
[15] Abiodun, O.A., Dauda A.O., Adebisi, T.T. and Alonge, C.D. (2017) Physico-Chemical, Microbial and Sensory Properties of Kunu Zaki Beverage Sweetened with Black Velvet Tamarind (Dialium guineense). Croatian Journal of Food Science and Technology, 9, 46-56.
https://doi.org/10.17508/CJFST.2017.9.1.07
[16] Achoba, I.I., Elegbede, J.A. and Kagbu, J.A. (1993) Nutrient Composition of Black (African) Velvet Tamarind (Dialium guineense Wild) Seed and Pulp from Nigeria. Journal of Food Biochemistry, 16, 229-233.
https://doi.org/10.1111/j.1745-4514.1992.tb00448.x
[17] Adeniji, S.E. and Akindehinde, B.A. (2018) Comparative Analysis of Adsorption and Corrosion Inhibitive Properties of Ethanol Extract of Dialium guineense Leaves for Mild Steel in 0.5 M HCl. Journal of Electrochemical Science and Engineering, 8, 219-226.
https://doi.org/10.5599/jese.486
[18] Arogba, S.S., Ajiboro, A.A. and Odukwe, I.J. (1994) A Physico-Chemical Study of Nigerian Velvet Tamarind (Dialium guineense L) Fruit. Journal of the Science of Food and Agriculture, 66, 533-534.
https://doi.org/10.1002/jsfa.2740660417
[19] Assongba, Y.F., Djego, J.G. and Sinsin, B. (2013) Germination Capacity of Dialium guineense Willd (Fabaceae) an Agroforestry Species. Journal of Applied Biosciences, 62, 4566-4581.
https://doi.org/10.4314/jab.v62i0.86069
[20] Ayessou, N.C., Ndiaye, C., Cisse, M., Gueye, M., Sakho, M. and Dornier, M. (2014) Nutrient Composition and Nutritional Potential of Wild Fruit Dialium guineense. Journal of Food Composition and Analysis, 34, 186-191.
https://doi.org/10.1016/j.jfca.2014.01.002
[21] Olajubu, F.A., Akpan, I., Ojo, D.A. and Oluwalana, S.A. (2012) Antimicrobial Potential of Dialium guineense (Wild) Stem Bark on Some Clinical Isolates in Nigeria. International Journal of Applied and Basic Medical Research, 2, 58-62.
https://doi.org/10.4103/2229-516X.96811
[22] Ogu, G. and Amiebenomo, R. (2012) Phytochemical Analysis and in Vivo Anti-Diarrhoeal Potentials of Dialium guineense Stem Bark-Extract. Journal of Intercultural Ethnopharmacology, 1, 105-110.
https://doi.org/10.5455/jice.20120715061917
[23] Okeke, N.C., Udeani, T.K. and Onyebuchi, U.L. (2016) Wound-Healing and Antimicrobial Properties of Dichloromethane Fraction of Dialium guineense (Wild) Fruit Coat. Research in Pharmaceutical Sciences, 11, 219-226.
[24] Neve, J. (2000) Nutrition and Oxidative Stress. Modulation of Dietary Intake of Antioxidants. Nutrition Clinique et Métabolisme, 16, 292-300.
https://doi.org/10.1016/S0985-0562(02)00174-7
[25] Shi, S., Ma, X., Xu, W., Zhou, Y., Wu, H. and Wang, S. (2015) Evaluation of 28 Mango Genotypes for Physicochemical Characters, Antioxidant Capacity, and Mineral Content. Journal of Applied Botany and Food Quality, 88, 264-273.
[26] Abenaa, A., Okyere, A.C. and Odamtten, G.T. (2014) Physicochemical, Functional and Sensory Attributes of Milk Prepared from Irradiated Tiger Nut (Cyperus esculentus L.). Journal of Radiation Research and Applied Sciences, 7, 583-588.
https://doi.org/10.1016/j.jrras.2014.09.010
[27] Ndiaye, B., Ayessou, N.C., Balde, S., Niang, M., White, R., Cisse, M., Diop, C.M. and Sakho, M. (2018) Galactogenic Properties of Tigernut Cyperus esculentus. International Journal of Innovation and Scientific Research, 39, 1-6.
[28] Ndiaye, B., Ayessou, N.C., Cisse, O.I.K., Balde, S., Cisse, M., Diop, C.M. and Sakho, M. (2018) Technological Potential through the Biochemical Evaluation of the Flour of the Tubers of the Souchet Cyperus esculentus L. Afrique Science, 14, 209-214.
[29] Awonorin, S.O. and Udeozor, L.O. (2014) Chemical Properties of Tiger Nut-Soy Milk Extract. Journal of Environmental Science, Toxicology and Food Technology, 8, 87-98.
https://doi.org/10.9790/2402-08318798
[30] Bamishaiye, E.I. and Bamishaiye, O.M. (2011) Tiger Nut: As a Plant, Its Derivatives and Benefits. African Journal of Food Agriculture, Nutrition and Development, 5, 1-14.
https://doi.org/10.4314/ajfand.v11i5.70443
[31] Yougbare-Ziebrou, M.N., Ouedraogo, N., Lompo, M., Bationo, H., Yaro, B., Gnoula, C., Sawadogo, W.R. and Guissou, I.P. (2016) Anti-Inflammatory, Analgesic and Antioxidant Activities of the Aqueous Extract of the Leaf Stems of Saba senegalensis Pichon (Apocynaceae). Phytotherapie, 14, 213-219.
https://doi.org/10.1007/s10298-015-0992-5
[32] Danthu, P., Gueye, A., Boye, A., Bauwens, D. and Sarr, A. (2000) Seed Storage Behaviour of Four Sahelian and Sudanian Tree Species (Boscia senegalensis, Butyrospermum parkii, Cordyla pinnata and Saba senegalensis). Seed Science Research, 10, 183-187.
https://doi.org/10.1017/S0960258500000192
[33] Popovici, C., Saykova, I. and Tylkowski, B. (2009) Evaluation of the Antioxidant Activity of Phenolic Compounds by Reactivity with the Free Radical DPPH. Revue de Génie Industriel, l4, 25-39.
[34] Scherer, R. and Godoy, H.T. (2009) Antioxidant Activity Index (AAI) by the 2,2-Diphenyl-1-Picrylhydrazyl Method. Food Chemistry, 112, 654-658.
https://doi.org/10.1016/j.foodchem.2008.06.026
[35] Diop, N., Ndiaye, A., Cisse, M., Dieme, O., Dornier, M. and O. Sock. (2010) The Ditax (Detarium senegalense J. F. Gmel.): Main Characteristics and Uses in Senegal. Fruits, 65, 293-306.
https://doi.org/10.1051/fruits/2010025
[36] Diop, N., Dornier, M., Dhuique-Mayer, C., Prades, A., Pantel, M., Pelissier, Y., Laroque, M. and Sock, O. (2010) Characterization of a Wild Fruit from Senegal: Ditax (Detarium senegalense J. F. Gmel.). International and Interdisciplinary Symposium on Food, Medicinal and Cosmetic Plants in the Sahel Region, Dakar, Senegal, 20-22 October 2010.
[37] Favier, J.C., Ireland-Ripert, J., Laussucq, C. and Feinberg, M. (1993) Répertoire général des aliments: 3. Table de composition des fruits exotiques, fruits de cueillette d’Afrique [General Food Directory: 3. Composition Table of Exotic Fruits, Fruits Gathered in Africa]. ORSTOM, Lavoisier, INRA, Paris, 242 p.
[38] USDA (United States Department of Agriculture).
https://fdc.nal.usda.gov/fdc-app.html#/food-details/170926/nutrients
[39] Lecerf, J.M. (2006) The Protective Role of Folates and/or Antioxidants. Equation Nutrition, 60, 3.

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