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British Journal of Healthcare and Medical Research - Vol. 10, No. 6

Publication Date: December 25, 2023

DOI:10.14738/bjhmr.106.15314.

Nyam, M. A., Umaru, B. S., Wonang, D. L., Papi, D. Y., & Adolong, V. A. (2023). Comparative Studies on the Quality and Antimicrobial

Effect of the Fruit Oils of Canarium schweinfurthii Engl. (Atili), Dacryodes edulis H.J. Lam (Ube) and Persea americana Mill (Avocado).

British Journal of Healthcare and Medical Research, Vol - 10(6). 219-230.

Services for Science and Education – United Kingdom

Comparative Studies on the Quality and Antimicrobial Effect of

the Fruit Oils of Canarium schweinfurthii Engl. (Atili), Dacryodes

edulis H.J. Lam (Ube) and Persea americana Mill (Avocado)

Mary Azumi Nyam

Department of Plant Science and Biotechnology, University of Jos, Nigeria

Bethel S. Umaru

Department of Plant Science and Biotechnology, University of Jos, Nigeria

David Longwap Wonang

Department of Plant Science and Biotechnology, University of Jos, Nigeria

Danladi Yakubu Papi

Department of Plant Science and Biotechnology, University of Jos, Nigeria

Vincent Alfred Adolong

Department of Plant Science and Biotechnology, University of Jos, Nigeria

ABSTRACT

Increase in consumption of oils from plant origin has led to a wide debate regarding

their health effects. This study was undertaken to on three types of fruit oils,

Canarium schweinfuthii, Dacryodes edulis and Persea Americana to determine the

percentage yield, their phytochemical constituents, cholesterol levels and their

microbial effect on some selected fungi and bacteria species. Cold maceration

technique using n-Hexane was the extraction method used and the percentage yield

was determined. Phytochemical screening and cholesterol levels were determined

using standard methods. Antimicrobial activities were carried out on the clinical

isolates of the fungi (Aspergillus flavus, Aspergillus fumigatus and Aspergillus

terreus) and bacteria (Escherichia coli, Staphylococcus aureus and Pseudomonas

aeruginosa) using disk diffusion techniques. The results of the extraction showed

that 300g each of D. edulis had the highest percentage oil yield of 41.71%, followed

by C. schweinfuthii, 36.31% and P. Americana had the lowest amount with 18.37%.

The phytochemical screening also revealed the presence of secondary metabolites

such as steroids, anthraquinones, terpenes and cardiac glycosides, but alkaloids,

flavonoids, tannins and saponins were all absent in the oils. The cholesterol analysis

showed P. americana having the highest level of 3223.32 mg/ml (3.22%), followed

by D. edulis with 3108.69 mg/ml (3.11%) and C. schweinfurthii had the lowest,

2760.86 mg/ml (2.76%). It was observed that the oils had no antifungal activities

on the test organisms. The antibacterial activity was in a concentration-dependent

manner as S. aureus was the most susceptible to the oils with C. schweinfuthii having

the highest activities of 7.77±0.47-10.07±0.00 followed by D. edulis oil

6.67±0.35mm-9.00±0.00mm and P. americana oil which had no activity on the test

organism. D. edulis had the highest activity on E. coli 7.47±0.47-10.07±0.00 while C.

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British Journal of Healthcare and Medical Research (BJHMR) Vol 10, Issue 6, December- 2023

Services for Science and Education – United Kingdom

schweinfurthii and P. americana had no activity on the test organism. D. edulis also

had the highest activity of 6.67±0.33-10.33±0.33 which was significantly different

from C. schweinfurthii and P. americana which had no activity on the test organism,

therefore, at P<0.05, there was a significant difference in the antibacterial activities

of the oil. This implies from the study that the secondary metabolites found in the

oils possess healthy properties. The cholesterol levels of the oil samples showed

that the oils contain an acceptable amount of cholesterol and the antibacterial

activities of these oils showed that they have significant effects on the bacteria used

in the study; hence, the results of these findings support the use of these oils as

therapeutic agents.

Keywords: Fruit oils, cholesterol level, antifungal and antibacterial activities

INTRODUCTION

Vegetable oils are a group of fats that are derived from seeds, nuts, cereal grains, and fruits. It

is important to understand that not all of these vegetable oils are liquid oils at ambient

temperatures. In addition, not all of the vegetable oils produced in commercial quantities are

considered to be edible in the sense of being typical dietary components (Hammond, 2003).

Edible vegetable oils are mainly used in cooking, as salad dressings, in manufacture for

margarines, spreads, and bakery.

Olive oil is the oldest known edible oil used in humans’ diet. It is a main constituent of the

traditional Mediterranean diet, which has a protective role against a number of diseases

including cardiovascular disease and cancer (Savva et al., 2016). An important characteristic of

these sources of oil from plants is the high degree of unsaturation in their constituent fatty acids

which directly relates to their higher susceptibility to oxidative deterioration (Roxana and

Ovidiu, 2016). Vegetable oils and fats are principally used for human consumption but are also

used in animal feed, for medical purposes, and for certain technical applications. Oils are also

gotten from; soybean, rape, sunflower, peanut, cotton, corn, grape, fiberflax, safflower, rice,

perilla, oil palm, olive, walnut, hazelnut, pine, cocoa.

Edible vegetable oils form a vital part of the human diet and can provide the energy and fatty

acids needed by the body and promote the digestion and absorption of fat-soluble vitamins (Ma

et al., 2014). The content and proportion of oil intake are closely related to human health.

Consuming an appropriate amount of oil is conducive to the normal metabolism of fat, while

excessive ingestion leads to the deposition of fat in the body, resulting in hypertension,

hyperlipidemia and other diseases (Meng et al., 2009). Edible vegetable oils also contain certain

amounts of vitamin E and phytochemicals, such as phytosterols and sqaulene (Wu et al., 2019).

Furthermore, edible vegetable oils are rich in phytosterols, providing an excellent way for

humans to ingest these compounds (Gao et al., 2015).

There are issues of high cholesterol content in some fruit oils that are consumed by humans,

thus, posing a great challenge to the quality nature of such oils and also different health

challenges; furthermore, microorganisms are known to cause infections in humans and some

strains are resistant to the existing synthetic drugs, thereby posing great concern to health and

other commercial products. Hence, the need to find other sources of oils with low cholesterol

content which can inhibit the metabolic activities of certain microorganisms, especially

pathogenic microorganisms.

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Nyam, M. A., Umaru, B. S., Wonang, D. L., Papi, D. Y., & Adolong, V. A. (2023). Comparative Studies on the Quality and Antimicrobial Effect of the

Fruit Oils of Canarium schweinfurthii Engl. (Atili), Dacryodes edulis H.J. Lam (Ube) and Persea americana Mill (Avocado). British Journal of Healthcare

and Medical Research, Vol - 10(6). 219-230.

URL: http://dx.doi.org/10.14738/bjhmr.106.15314.

MATERIALS AND METHODS

Plant Materials

Fresh and ripened fruits of Canarium schweinfurthii, Dacryodes edulis and Persea americana

were collected from local marketers in Chobe and Farin gada markets of Jos north LGA, Plateau

state, in June 2021. The fruits collected were taken to the herbarium of the Department of Plant

Science and Biotechnology, University of Jos, Plateau State, for identification. The fruits were

sorted properly to remove any dirt or foreign materials and then they were weighed using a

weighing balance and 300g was gotten for each specimen. The fruits were then washed in cold

tap water to remove any dirt adhering to the surface of the fruits. A sterilized laboratory knife

was then used to separate the pulp from the seeds of the fruits of C. schweinfurthii, D. edulis and

P. americana.

The pulp was then cut into smaller pieces and oven dried at 600C for 24 hours to remove the

moisture content and get the dry matter of the fruits. After the fruits pulp were properly oven

dried, it was now pulverized using a laboratory mortar and pestle in order to get the granulated

form of the fruits pulp. Using a weighing balance, the granulated form of Canarium

schweinfurthii, Dacryodes edulis and Persea americana were weighed and recorded. The

powdered pulp of Canarium schweinfurthii, Dacryodes edulis and Persea americana were now

appropriately stored in sterile air-tight bottles and were properly labeled until when needed.

Extraction By Cold Maceration

The extraction method used in this study was maceration method as described by Abdulkadir

et al. (2015). The powdered plant samples (108.92g, 125.13g, and 55.11g) each of Canarium

schweinfurthii, Dacryodes edulis and Persea americana were soaked in 500ml of n- Hexane

solvent in separate 1 liter capacity conical flasks stopped and kept for 48 hours. The cold

extracts thus obtained were kept in a water bath for 1 hour at 69oC. After cooling, the extracts

were filtered successively through ordinary chesses cloth and Whatmann filter paper. The n- Hexane extracts of Canarium schweinfurthii, Dacryodes edulis and Persea americana were

evaporated in order to get the pure samples of the oil. The oils gotten were now stored in sterile

bottles, labeled appropriately and kept at 370C (room temperature) until needed.

Determination of the Percentage Yield of the Extract

This was done using the formula described by Falana and Nurudeen (2020). The yield of extract

(extractable components) expresses on dry weight basis of pulp was calculated from the

following equation: Yield (g/100g) = (W1x 100)/W2 where W1 is the weight of the extract

residue obtained after solvent removal and W2 is the weight of peel or pulp taken.

Phytochemical Analysis

Phytochemical analysis for qualitative detection of alkaloids, flavonoids, tannins, saponins,

terpenes, steroids, carbohydrates, cardiac glycosides and anthraquinones were carried out on

the extracts as described by Sofowora (2008).

Test for Alkaloids:

About 2ml of each plant extract was stirred with 3ml of 1% aqueous hydrochloric acid on

steams bath and filtered. 1ml of the filtrate was treated with a few drops of Mayer’s reagent and

a second 1ml portion was treated similarly with Dragedorffs reagent. Precipitation with either

of those reagents was taken as evidence for the presence of all alkaloids (Sofowora, 2008).

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Test for Saponins:

About 2ml of each plant extracts were added to 4.0ml of distilled water in a test tube and the

test tube was stopped and shaken vigorously for about 30 seconds. The test tube was allowed

to stand for half an hour. Frothing which persist on warming was taken as preliminary evidence

for the presence of Saponins (Sofowora, 2008).

Test for Flavonoids:

Lead sub-acetate test 2ml of each plant extract was dissolved in 5ml of distilled water, heated

for 5 minutes and filtered. The filtrate was allowed to stand for 5 minutes to cool and about 2-

3 drops of lead acetate solution was added to the filtrate. A yellow-colored precipitate indicated

the presence of flavonoids (Sofowora, 2008).

Test for Tannins:

About 2ml of each plant extract was stirred with 1ml of distilled water, filtered and few drop of

ferric chloride were added to the filtrate. A blue-black, green precipitate was taken as evidence

for the presence of tannins (Sofowora, 2008).

Tests for Anthraquinones:

About 2ml of each plant extract was taking into a test tube and 5ml of chloroform was added

and shaken for 5 minutes. The extract was filtered and the filtrate shaken with an equal volume

of 100% NH3 solution. A pink –violet color in the ammonical layer indicate the presence of free

anthraquinones (Sofowora, 2008).

Test for Cardiac Glycosides:

About 3ml of each plant extract was dissolved in 1 ml of glacial acetic acid containing one drop

of FeCl2(Ferric chloride) solution. It was then under-layered with 1 ml of concentrated H2SO4.

A brown ring was observed at the interphase, which is a positive reaction for the presence of a

deoxy-sugar characteristic of cardiac glycosides (Sofowora, 2008).

Test for Carbohydrates:

About 1ml of each plant extract was dissolved in 3ml of distilled water and mixed with a few

drops of Molisch reagent (10% solution of α- naphthol in alcohol). Then 1ml of concentrated

sulphuric acid was carefully added down the side of the inclined tube so that the acid forms a

layer beneath the aqueous solution without mixing it. A reddish or violet ring at the junction of

the liquids was observed indicating the presence of carbohydrate (Sofowora, 2008).

Cholesterol Screening

The cholesterol content test was carried out as described by Ojiako and Akubugwo (1997).

About 0.1ml of the sample oil extracts each and standard cholesterol dissolved in chloroform

in ratio 1:10 was evaporated to dryness in water bath at 500C. Glacial acetic acid (3.0mL) and

3.0mL of color reagent (a solution of ferric chloride/glacial acetic acid/sulphuric acid), was

added to each sample and the standard, then shaken vigorously to dissolve the oil. Blank

contained 2.0mL of chloroform, 3.0mL glacial acetic acid and 3.0mL of color reagent. After

cooling for 30mins at room temperature, absorbance of standard and samples were read at

560nm using JENWAY 6310 spectrophotometer.