Chemical Composition Essential Oils Are Complex Biology Essay

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Essential oils are complex mixtures of many components, about 20-60 can be present at different concentrations depending on the oil Bakkali et al 2007.According to Bakkali et al(2008) they are characterized by components of the highest concentrations, there are usually 2 or 3 main components in each oil compared to some components in trace amounts. Major components of the oils determine the biological activity of the oils however the components in smaller amounts produce an additive effect(Bakkali et al, 2007). Chemical analysis of lemongrass and cinnamon oil distinguished several compounds. Terpenes are able to form structurally and functionally different classes. They are created from combinations of several 5 carbon units called isoprenes (Pichersky and Gershenzon,2009). According to Bakkali et al (2007) terpenes constitute 90% of essential oils. Tyagi and Malik (2010) found that phenols and aldehydes exhibited the highest vapour activity followed by alcohols, ketones and esters and lastly hydrocarbons.

Gas Chromatography Mass Spectrometry (GC MS) analysis found cinnamon oil contains high amounts of trans cinnamldehyde at 86.9% and eugenol at 6.2% as major components. Eugenol has been found to have antifungal activity (Cheng et al, 2008) as has Cinnamyl acetate, 4-terpineol, 1,8 cineole. The additive effects of the main components have been reported in one study, a mixture of cinnamaldehyde and eugenol inhibited growth of staphylococcus species whereas when they were applied individually they did not inhibit growth(Marei et al,2007).

Lemongrass exhibited a high concentration of citral, this has two isomers, geranial (trans citral) which presented at 51.3% and neral (cis citral) at 37.4% as major components of this oil. Usually one isomer does not occur without the other. In addition to the essential oil consists of small quantities of geraniol(alcohol) which often co exists with geranial and neral (Chen and Vilojen, 2010).,This study found strong activity of geraniol against Candida albicans (Chen and Vilojen, 2010). Geranyl acetate (Hanaa et al,2012)and limonene (Gehan et al 2012) have also been found to have antifungal properties. Similar concentration found in this analysis have been previously reported by Inouye et al (2003) A study also found lemongrass oil to show higher anticandidal activity against strains of superficial mycoses than citral suggesting additive effects of minor components (Kumar et al 2012)

http://www.sigmaaldrich.com/medium/structureimages/00/mfcd00007000.png

Fig.22 Structure of Trans Cinnamaldehyde (Sigma Aldrich 2012)

Fig23. Structures of cis(right) and trans (left) citral(Saddiq, monoterpenes)

.4.2 Vapour phase

Using the vapour phase has been a fairly recent advancement, Tyagi and Malik (2010) found that essential oils in the liquid medium form micelles and supress the essential oils attatching to the organism, however the vapour state allows for free attachment although studies have been carried out there is no standard assay to evaluate inhibition by vapour phase contact (Avila-Sosa et al,2012).A further study also stated that in liquid medium the diffusability and solubility of the essential oil whilst in vapour depends on the volatility of each compound and in a vapour form can facilitate the solubilisation of lipophilic monoterpenes better by inflicting higher cell damage on the cell membrane(Taweechaisupapong et al, 2012)

Rana (2012) found with Candida dublienesis ,where the essential oil is placed directly under the fungi the growth is completely inhibited as the vapours are the most volatile here .So growth is fungicidal until a certain point, as the volatile vapours spread out the concentration of the vapours is not high enough to inhibit growth so a fungistatic effect is produced. Although this effect was not produced with Candida albicans it demonstrates how the vapours work. Therefore a dispersal method would be more effective as there would be an even distribution of the oil. If volatile compounds retained less effectively therefore allowing more molecules in the vapour phase with increased antifungal activity promotes fungicidal effect at lower concentrations(Lopez et al ,2005) thought to be due to better penetration and contact(Tyagi and Malik, 2010).

4.3 Bonding and compounds

Essential oils cannot be used on their own as they are classed as irritants therefore a method is required where the oil is not as concentrated and can be used in application such as sprays where it is easier to distribute. If they are blended with a carrier oil which is unreactive this provides for a base in which they can be used. Essential oils are expensive so blended with a carrier oil is a cheaper option as well as them being more readily available.

The essential oils blended with carrier oils showed a significant difference in the results for example at 25µl (p<0.021). Vegetable oil produced the highest results with lemongrass oil (p<0.017) whereas sunflower oil produced the highest results with cinnamon oil (p<0.295) although no significance is shown there is a small difference between the control and the blend of cinnamon and sunflower oil demonstrating the effectiveness of the oil (85.9% inhibition).Interestingly sunflower oil produced the lowest zone of inhibition when blended with lemongrass oil (30.2% inhibition). Wheatgerm oil produced the lowest zone of inhibition when blended with cinnamon oil (32.7%) there was significance between the control and the blend of oil(p<0.002) however the difference was too large therefore this would not be an effective carrier oil for use. A varied difference is demonstrated between the cinnamon and lemongrass oil in the order of the results suggesting a difference in the way the carrier oils work with the two oils.

Carbon and oxygen form a polar bond (carbonyl group C=O) therefore if this bond is part of a molecule it affects how the molecule behaves making it more reactive. The greater the difference in electronegativity of molecules the greater the polarity of the bond. Polar molecules are hydrophilic(water loving)whilst most essential oil as are generally insoluble if a part of it has a polar molecule it will be slightly soluble to a certain extent .Polar bond have different electonegativities and therefore unequal sharing of the bonding electron pair. This results in a bond where the electron pair is displaced towards the more electronegative atom. The atom obtains a partial negative charge while less electron negative has a partial positive charge. Non polar molecules are hydrophobic (water hating) Non polar compounds share the same electronegativity therefore have equal sharing of the electron bonding pair. Because non polar molecules do not have a partially negative region it cannot take part in bonding therefore cannot mix with polar molecules .Essential oils are of mixed polarity ,with some polar and some non polar compounds in the oils(Pitman,2004).

4.4 Carrier oils

Carrier oils are non polar molecules (Pitman,2004) and has electrons equally distributed therefore will not be attracted to polar molecules . In carrier oils there is a mixture of short carbon structures made up of a fatty acid and glycerol which are non polar .The longer the carbon chain the compound becomes less soluble in water the molecule becomes more like a hydrocarbon chain (Bruice,2006).Therefore depending on the structures in the carrier oils affects how they interact with the essential oils. The length of the hydrocarbon varies according to the type of fatty acid this is hydrophobic whereas the carboxylic acid group is hydrophilic. The structure of the hydrocarbon is different for different fatty acids by length as well as the type of carbon to carbon bonding .Saturated chains contain single bonds whereas unsaturated ones contain one double bond known as monounsaturated or more than one double bond polyunsaturated(Pitman,2004).

The suggested theory is the polar molecules in the essential oil are likely to have an attraction for the polar molecules in the carrier oil for example palmitic acid(see table 7) contains a smaller hydrocarbon chain, as the chain size decreases hydrogen bonding becomes more important and Van der Waals less so. Hydrogen bonds are formed when hydrogen is bonded to the lone pair of electrons on the oxygen. This is the strongest type of interaction (Bruice, 2007). However the longer hydrocarbon chain will be non polar such as Arachidic acid (see table 7) as it has a longer chain therefore will not have an attraction for the polar molecules but will do for the non polar components forming weak Van der Waals. It is essential to find the structure of carrier oils as it may depend on how long the hydrocarbon chains are in working out which oil works best as a carrier oil. As the solubility of the carrier oils could be linked to the lipopholicity. Cinnamaldehyde contains a benzene ring which is non polar however the aldehyde is polar, overall the molecule is non polar. As the benzene ring is flat, Van der Waals forces can occur between the longer acids from the carrier oils with cinnamaldehyde. Citral is also non polar it also contains double bonds this cause less attraction which means fewer Van der Waals forces can occur between molecules. This molecule also contains an aldehyde group at the end. However it is less non polar than cinnamaldehyde as it contains fewer double bonds therefore is able to create more Van der Waals, so components more likely to be held and not released as a vapour. The shorter molecules of the carrier oil are likely to vaporise as normal as are the other polar molecules of the essential oil.

Table 7: Composition of carrier oils in order of zone of inhibitions with lemongrass oil

Palmitic

Palmitoleic

Heptadecanoic

Ginkgolic

Stearic

oleic

Linoleic

Linolenic

Arachidic

Gadoleic

Behenic

Erucic

Tetracosanoic

C16:0

C 16:1

C17.0

C17:1

C18:0

C18:1

C18:2

C18:3

C20:0

C20:1

C22.0

C22:1

C24:0

Sunflower oil

5.8

0.1

3.9

15.9

71.7

0.1

0.3

0.2

0.7

0.5

Extra virgin olive oil

14.9

1.84

0.04

0.09

2.00

69.6

10.1

0.59

0.35

0.23

0.11

0.04

Sweet almond oil

5.5

0.2

2.8

70.0

21

0.1

0.1

0.1

0.1

Groundnut oil

8.0

4.0

52.0

4.0

16.0

Grapeseed oil

6.5%

0.2

3.7

23.4

65.3

0.2

0.2

0.2

0.2

Parrafin oil

Walnut oil

6.0

0.1

4.0

29.8

58.5

0.4

0.3

0.2

Rapeseed oil

4.0

1.5

17.0

13.0

9.0

14.5

41.0

Wheatgerm oil

12.5

0.2

2.5

27.3

53.7

3.0

0.4

0.2

0.1

Palmitic

Palmitoleic

Heptadecanoic

Ginkgolic

Stearic

oleic

Linoleic

Linolenic

Arachidic

Gadoleic

Behenic

Erucic

Tetracosanoic

C16:0

C 16:1

C17.0

C17:1

C18:0

C18:1

C18:2

C18:3

C20:0

C20:1

C22.0

C22:1

C24:0

Groundnut oil

8.0

4.0%

52.0

4.0

16.0

Extra virgin olive oil

14.9

1.84

0.04

0.09

2.00

69.6

10.1

0.59

0.35

0.23

0.11

0.04

Rapeseed oil

4.0

1.5

17.0

13.0

9.0

14.5

41.0

Wheatgerm oil

12.5

0.2

2.5

27.3

53.7

3.0

0.4

0.2

0.1

Walnut oil

6.0

0.1

4.0

29.8

58.5

0.4

0.3

0.2

Sweet almond oil

5.5

0.2

2.8

70.0

21

0.1

0.1

0.1

0.1

Sunflower oil

5.8

0.1

3.9

15.9

71.7

0.1

0.3

0.2

0.7

0.5

Grapeseed oil

6.5%

0.2

3.7

23.4

65.3

0.2

0.2

0.2

0.2

Parrafin oil

Table 8: Composition of carrier oils in order of zones of inhibition with Cinnamon oil

The tables in order of how well they worked with lemongrass and cinnamon oil produced no clear link in terms of lipohilicity .However the composition of the oils was obtained from previous literature analysis. Consequently the oils tested against the species may not have the same composition as those tested in the literature. GC MS analysis was carried out on the carrier oils however they were not volatile enough to produce any results. To produce results esterification will be required.

A possibility is micelle formation this is a single layer of lipids. The hydrophobic tails pointing in and hydrophilic polar heads facing out in a sphere facing out the oil attaches to the hydrophobic tails inside the micelle and polar molecules attach to the heads on the outside the viscosity of the product help to emulsify small amounts of oils. However this requires more in depth research to consider it as a possibility.

4.6 Bandages

Natural textiles incorporated with essential oils to be used to stop infection is a possibility depending on how well the essential oils interact with the materials. They could be used in bandages and other materials so the bandages are working to stop infection as well as protecting the wound.

In natural textiles the essential oils can be fixed by Van der Waals forces (physical bonding or Covalent bonds (chemical bonding). As already established the essential oils are of mixed polarity therefore the affinity between the textile and the essential oil is mixed depending on the composition of the textile as each textile contains a different proportion of material although they may contain similar components. Textiles may be classified as two types. Non polar, synthetic polymers and polar natural textiles. This can be further divided into polymers from amino acids such as silk and wool or from cellulose such as cotton.

All fibres are made of polymers .Polymers are formed when hundreds and thousands of small molecules are covalently bonded into a linear chain. The backbone of most polymers for textile fibres contain covalently bonded carbon atoms.

http://www.tis-gdv.de/tis_e/ware/fasern/baumwoll/baumwoll.htm

http://textilefashionstudy.com/chemical-composition-of-flax-fiber-linen-fiber-composition/

Table 9: Composition of textiles

Bandage

Composition

Tubular

85% cotton, 10% latex, 5% polyester

Non woven bandage

100% viscose(medical textiles paper)

Stretch bandage

36%cotton, 36%viscose,28%polyamide

Crepe

Cotton mixed with wool

Cotton crepe

100% high twist cotton and rayon yarns

Gauze

100% hydrophilic cotton gauze

Cotton

Cotton 98% waxes 0.60%, fatty substances 0.40%

mineral salts 0.20%

non adherent

Porous polyethylene film and absorbent cotton pad.

Lint

92% cellulose 2% hemicellulose lignin 4% others 2%

4.7 Cinnamon oil and bandages

Lint produced the highest inhibition at 80%. Absorbent lint is composed of cotton.Cotton is the most common cellulosic fibre. Hydroxyl groups are mainly present in the structure of cellulose. They are hydrophilic, therefore any non polar(hydrophobic) molecules will not bind to the surface and will not be absorbed and released as a vapour due to its volatility . Gauze is also composed of 100% hydrophilic cotton gauze therefore this produced similar results to lint at 76.8% as it has the same effect.

However this is not shown by cotton which produced a low result of 33% although at 1µl it gave a result of 32.9% therefore not much difference between 25µl and 1µl however cotton contains a small amount of water which is highly polar it may retain components evwn more so components which may be slightly soluble will also frorm hydrogen bonds .Cotton crepe produced only a slightly better result than crepe at 25µl however it produced better results at all concentrations therefore reiterating the polarity effect . Cotton crepe contains 100% high twist cotton and rayon yarns .Rayon is viscose it has the same polymer structure as cellulosic fibres which is the same as cotton. Interestingly Viscose is a regenerated fibre from natural polymers therefore is not classed as a synthetic fibre although it is heavily processedso nor is it a natural product.it produced 51.6% inhibition in between the highest and lowest result in line with the theory

The results of the mixed synthetic and natural fibres show a significant reduction in inhibition(p<. Non woven fabric has a wide range of use in the medical field. They are disposable, sterile and cheap and are beneficial in prevention of cross infection. The material is 100% viscose highly prous alow air and water permeability unlike cotton crepe which comprises half viscose although inhibition was only slightly higher at 49.3%, however inhibition was lower at 10µl and 5µl.

Tubular bandages are composed of cellulose and elastic fibre such as latex blends in a knit structure. Cellulose is hydrophilic whereas the polyester is hydrophobic. Although there is a small amount of polyester the majority of the fibre is hydrophobic therefore the hydrophilic components attract the polar molecules in the essential oil whereas the non polar molecules in the bandage will cause some of the components to be released.

Stretch bandage contains 36% cotton therefore cellulosic and Polyamide usually present in bandages is nylon this is hydrophobic although it has the highest absorption capacity among synthetic fibres because of the polar amide group present. Viscose is hydrophilicSo in this fibre there are more hydrophilic groups than hydrophobic thereore inhibition 45.5%.

non adherent :porous polyethylene film and absorbent cotton pad. Polyethylene is non polar therefor th terpenes will bind to thisUsually used for burns.Hydrophobic polyethylene flm with absorbent cotton pad.

4.8 Lemongrass oil and natural textiles

With lemongrass oil Crepe produced a 100% inhibition. Crepe has high polarity as it is mix of wool and cotton. Wool has the highest capacity of water absorption and contains hydrophilic functional groups primary amine NH2 and carboxyl these structural features contribute to its ability to hold onto water molecules tightly. Therfore higher results produced because of the presence of the groups.

Cotton 90.5%.Cotton produced a much higher result with lemongrass oil than with cinnamon oil. This may be because of the polarity of the molecules or the difference in polarity of the molecules. Citral is less non polar than cinnamaldehyde because of the presence of the double bonds in the molecule. It maybe the effects of other components in the oil. Gauze and lint produced similar results with cinnamon oil producing zones of inhibition between 70 and 90%.

Tubular ,non adherent ,stretch and non woven bandage produced the lowest results .Showing the same general trend with cinnamon oil although in a slightly different order of reactivity. This is caused by the lower polarity of these fibres, as they are made of hydrophobic fibres. Van der Waals forces occur between the molecules and so the volatile molecules are not released as vapours. Although the textiles did produce inhibition with the mixed fibres ,the lowest being at 45% with the non woven bandage. This is suggestive of additive effects of other components in the oil. Suggests that the antifungal components are non polar and the major ones of this is citral and cinnamaldehyde. Other terpenes present in cinnamon and lemongrass oil are also non polar such as geraniol and cinnamyl acetate they also which have also been founf=d to have antifungal effects.

4.9 Biological effects

According to Bakkali et al (2007) essential oils are not thought to have any specific cellular targets as they have many constituents. They are able to pass through the cell wall and cytoplasmic membrane as they are lipophiles and disturb the structure of their different layers of polysaccahrides, fatty acids and phospholipids and make them permeable (Bakkali et al, 2007).This is mainly the effect of terpenes which are the major components of essential oils. They alter cell permeability, by penetrating between the fatty acyl chain making up the membrane lipid bilayers disrupting lipid packing and changing membrane fluidity .This leads to morphological alterations reducing adherence capacity of candida albicans (Taweechaisupapong et al,2012). Tyagi and Malik(2010)also found the same results with lemongrass oil vapours, components were able to enter and alter the permeability of the cell by disrupting the fatty acyl chain making up membrane lipid bilayers therefore properties of the membrane maybe changed. Which may affect the regulation and function of membrane bound enzymes and may alter the synthesis of components of the cell wall polysaccharides such as beta glucan, chitin and mannan and alter cell growth and morphogenesis.

Specifically essential oils can congeal the cytoplasm (Gustafson et al, 1998) as well as damage proteins and lipids. Cell wall and cell membrane damage can cause macromolecules to leak and to lysis. In eukaryotic cells essential oils can aggravate mitochondrial membranes to depolarize by decreasing the membrane potential affecting ionic Ca++ cycling .They are able to change membrane fluidity which become irregularly permeable causing leakage of radicals, calcium ions and proteins. Permeabilization of outer and inner mitochondria membranes leads to cell death by apoptosis and necrosis. Bakkali et al (2007) suggested a chain reaction occurs beginning from the cell wall or the outer cell membrane which invades the whole cell, entering through the membranes of different organelles like mitochondria and peroxisomes.

If the effects of essential oils are due to synergism or reflect only those of only the highest level which were shown by gas chromatography. The amplitude of their effect, being dependent on their concentration. It is possible the activity of the major constituents is moderated by minor components of the oils. It is suggested by Cal(2006) that several components of the essential oil play a role in defining the amount of cell penetration, hydrophilic or lipophilic attraction and fixation on cell wall and membranes as well as cellular distribution. Cellular distribution is an important feature because the how the oil is distributed in the cell determines the different types of radical reactions produced depending on the compartmentation in the cell (Bakkali et al 2007)

Very few studies have analysed sufficient numbers of essential oil to determine whether there is specificity for different effects according to different oils. It has been demonstrated by Bakkali et al. (2007) that there is a difference in the amplitude but not in the biological mode of action.

However one study specifically investigated the role of cinnamaldehyde by studying its effect on sterol biosynthesis and plasma membrane ATPase activity of fungi. ATPase is an important fungal pump it creates a membrane gradient which is used for transport of nutrient. The pump is activated in the presence of glucose which forces more H+ ions out. The Candida isolates which demonstrated susceptibility to cinnamaldehyde also showed inhibition of H+ ATPase mediated proton pumping the study suggested the two actions are linked. The study also found that cinnamaldeyde may have a similar mode of action to fluconazole as it inhibits ergosterol synthesis in sensitive strains. As the essential oil blocks the synthesis of ergosterol found that cinnamaldehyde acts in a dose dependent manner in decreasing ergosterol. Suggests that these are the primary target of cinnamaldeyde and could be a promising drug (Shreaz et al, 2011)

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