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Household Essential Oils as Antimicrobial Agents for Health and Skin care

Haya Adel Alfassam1, Fadilah Sfouq Aleanizy2, Fulwah Yahya Alqahtani2, Alanoud Mohammed Altalal2 and Rawananwar Fitaihi2

1King Abdulaziz city for science and technology, Riyadh, Saudi Arabia.

2Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

Corresponding Author E-mail: halfassam@kacst.edu.sa

DOI : http://dx.doi.org/10.13005/ojc/330464

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ABSTRACT:

Essential oils have been traded and consumed in every house, for either beauty or food purposes. Essential Oils are volatile, concentrated, hydrophobic liquids containing aromatic compounds from plants. They are obtained via steam or hydro-distillation, it has been used as food remedies or beauty product and can be easily obtained from the local markets. The aim of this study is to investigate the antimicrobial effect of the most used commercial essential oils (Black seed, Lemongrass, Oregano, Marjoram) against selected microorganisms. Antimicrobial activity of the selected essential oils was investigated using agar diffusion method. Candida albicans (ATCC 10231) as fungus, Escherichia coli (ATCC 25922), Staphylococcus epidermidis (ATCC 14990) Pseudomonas aeruginosa (ATCC 27853) were used in this study and adjusted according to the Clinical and Laboratory Standards Institute (CLSI). The results showed that the Black seed oil has the most potential bactericidal effect.

KEYWORDS:

Essential oil; Black seed oil; Lemongrass oil; Oregano oil; Marjoram oil; home remedies; antimicrobial effect

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Alfassam H. A, Aleanizy F. S, Alqahtani F. Y, Altalal A. M, Fitaihi R. Household Essential Oils as Antimicrobial Agents for Health and Skin care. Orient J Chem 2017;33(4).


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Alfassam H. A, Aleanizy F. S, Alqahtani F. Y, Altalal A. M, Fitaihi R. Household Essential Oils as Antimicrobial Agents for Health and Skin care. Orient J Chem 2017;33(4). Available from: http://www.orientjchem.org/?p=35456


Introduction

Essential oils also called volatile oils are aromatic liquids retrieved from plant materials flowers, buds, seeds, leaves, twigs, bark, herbs, wood, fruits and roots. They can be obtained by different methods such as fermentation, expression or extraction and the most commonly commercial production method used is the steam distillation. Plant essential oils and extracts have been used for many millenniums(1), in the alternative medicine, food preservation and natural therapies. Essential oils have been traditionally used for pharmaceutical purposes as antibacterial and antifungal agents in different areas of the world (2). The chemical profile of each essential oil is different not just chemically but structurally as well, hence why they are extracted according to their purpose of use, e.g for perfume uses, extraction by carbon dioxide and lipophilic solvents are used rather than steam distillation. So that in order to obtain the quality and quantity of the oils they have to be extracted at the same conditions to reach the constant composition, from the same organ of the same plant, from the same soil, picked in the same season and under the same climate. (3,4).

3000 estimated essential oils are known, of that 300 have commercially importance in fragrance and beauty markets (3). Essential oils are lipid soluble and this feature helps themto pass through the cell membranes and leads to leakage of “macromolecules”, leading to celllysis(5). In the case of bacteria, this is associated with the damaging of the ion channel proton pumps, leading to a reduction in membrane potential. Damage to the proton pump will lead to a reduction of ATP being produced by the cell (6).

All previous studies focused on testing the in-vitro antimicrobial activity of pure essential oils such as; black seed, lemongrass, marjoram and oregano oils, but there are no studies revealed regarding the activity of the same oils intended for commercial use for hair and skin.

Aim of the Study

This study was conducted to investigate the antimicrobial activity of selected essential oils treated for commercial use for beauty and food, against different microorganisms.

Material and Methods

Essential oils were purchased from the local Saudi market, Tween 20 (Sigma), normal saline, Mueller Hinton medium (Oxoid),and sterilized discs (Whatman no. 5, 6 mm diameter) were purchased.

Preparation of the Essential Oils Samples

The oils were purchased from local markets and dissolved in normal saline with tween 20 then impregnated in sterilized discs with different concentrations (1:1, 1:5, 1:10,1:20) each disc had 25µL.

Microbial Preparation

Candida albicans (ATCC 10231), Escherichia coli (ATCC 25922), Staphylococcusepidermidis (ATCC 14990) Pseudomonasaeruginosa(ATCC 27853) were used in this study. The bacteria suspension was prepared and adjusted by comparison against 0.5 McFarlan turbidity standard (5×107 organisms/ml) in accordance with the Clinical and Laboratory Standards Institute (CLSI). (7)

Measuring the Antimicrobial Activity by Disc Diffusion Method

Mueller Hinton culture medium was distributed in Petri plates (100x20mm) forming a base layer of 10ml. After solidification of the medium, 10ml of medium containing microbial inoculums 1% in the range of approximately 105 CFU/ml were distributed over the base layer to form the seed layer. The selected essential oils were dissolved in normal saline with Tween 20 (0.5% v/v). Sterilized discs (Whatman no. 5, 6 mm diameter) were infused with (25μL) of different concentrations (1:1, 1:5, 1:10,1:20) of the relevant essential oils and placed on the agar surface. Gentamicin disc (25μg) was used as control. The plates were incubated at 37oC for 24 hours and the reading of the diameters of inhibition zones (mm) was performed. The studies were conducted in triplicate. The results were expressed as mean ± SD. P values <0.05 were considered as significant using ANOVA test (1,4).

Measuring the Minimum Inhibitory Concentration

A series of two fold dilution of each oil was prepared, ranging from 10 to 50 mg/ml. A final concentration of (0.5%v/v) Tween-20 (Sigma) was incorporated to enhance oil solubility. Aliquots of culture containing relatively 105 CFU/ml of each organism were incubated at 37oC for 24 hour.  Experiments were carried out in triplicate. Inhibition of bacterial growth in the test tubes containing tested oils was evaluated by comparison with growth in blank control tubes. The minimum inhibitory concentration were determined as the lowest concentration of oil inhibiting the visible growth of each tested organism (1,2,4,7).

Table 1: Antimicrobial activity of the selected essential oils against selected strains by disc diffusion method.

Table 1: Antimicrobial activity of the selected essential oils against selected strains by disc diffusion method.



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Figure 1: Antimicrobial activity of essential oils (B) black seed, (L) lemongrass, (O) oregano and (M) marjoram against bacteria and yeast, (A) Staphylococcus epidermidis, (D) Escherichia coli,  (E) Pseudomonas aeruginosa, (F) Candida albicans, using disc diffusion. Control antimicrobial agents (C) Gentamycin with the concentration of (25 µg).

Figure 1: Antimicrobial activity of essential oils (B) black seed, (L) lemongrass, (O) oregano and (M) marjoram against bacteria and yeast, (A) Staphylococcus epidermidis, (D) Escherichia coli,  (E) Pseudomonas aeruginosa, (F) Candida albicans, using disc diffusion. Control antimicrobial agents (C) Gentamycin with the concentration of (25 µg).



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Table 2: Minimum inhibitory concentration (MIC) of the selected essential oils (mg/ml) against selected strains by two-fold dilution method.

Table 2: Minimum inhibitory concentration (MIC) of the selected essential oils (mg/ml) against selected strains by two-fold dilution method.



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Results and Discussion

The antibacterial activity of the four selected oils against the selected species is summarized in table 1 and 2, also shown in figure 1. The results revealed that the selected essential oils showed antibacterial activity with varying magnitudes but there was no antifungal activity shown. The zone of inhibition for total diameter smaller than (8mm) was taken as non-sensitive (NI); for total diameter between (9-14mm) considered as sensitive; for total diameter between (15-19 mm) was taken as very sensitive and  for total diameter larger than (20mm) extremely sensitive. All selected oils showed activity against Escherichia coli and all oils except oregano showed activity against Staphylococcus epidermidis. Black seed and oregano oils revealed strong activity against Pseudomonas aeruginosa. Minimum inhibitory concentration of all tested oils was four to five-folds less as compared to the pure oils documented in literatures.

Conclusion

From this study it can be concluded that many commercially available essential oils possess antibacterial activity. Black seed oil has the most potential bactericidal properties against Gram-positive Staphylococcus epidermidisand Gram negative bacteria Escherichia coli and in particular pathogenic Pseudomonas aeruginosa, however, no antifungal activity was demonstrated. We believe that the present investigation combined with previous studies provide support to the antibacterial properties of commercially accessible oils specially those for hair and skin beauties and for food as well.

Acknowledgment

We express our gratitude to the Joint Center of Excellence Program at King Abdul Aziz City for Science and Technology, Riyadh, Saudi Arabia.

References

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