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Assessment of the Physicochemical Quality Indicators and Microbiological Effects of Brazilian Ozonized Vegetable Oils

Abstract

The study of quality indicators in the process of obtaining ozonized vegetable oils is useful for monitoring the ozonation reaction. The Brazilian oils “dendê”, soy, corn, rice and sunflower were studied, all of them were ozonated applying different doses of ozone. Ozonized oils were evaluated by determining the physicochemical indexes of peroxide, acidity, iodine and density in addition viscosity, fatty acid composition and microbiological activity were determined. The results showed that of the five ozonized oils evaluated, “dendê” oil exhibited a higher peroxide index, approximately 1746 mmol-equiv kg-1, using an applied ozone dose of 97 mg g-1, during an hour and a half of the ozonation reaction. This result could be explained by its chemical composition, rich in oleic acid that facilitates the reaction with ozone due to its spatial conformation. It was also demonstrated that “dendê” oil exhibits a greater antibacterial activity with minimum inhibitory concentration (MIC) values ranging from 1.9 to 4.75 mg mL-1 against Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli. It is suggested that the ozonated “dendê” oil presents greater possibilities to be used in the preparation of pharmaceutical or cosmetic formulations.

Keywords:
ozonized vegetable oils; “dendê” oil; physicochemical parameters; fatty acid composition; antibacterial activity


Introduction

Fats and oils are present in every single moment of our lives. We use them in our feeding, in our hygiene, in the preservation of our health, and in countless products we used and/or consume daily.11 Gunstone, F. D.; Structured and Modified Lipids; Marcel Dekker Inc.: New York, USA, 2001.,22 Durán, S. A.; Torres, J. G.; Sanhueza, J. C.; Nutr. Hosp. 2015, 32, 11. To obtain a vegetable oil with the required quality it is necessary to measure a group of characteristics and attributes both sensory and physical and chemical to establish its acceptance level.33 Soriano, N. U.; Migo, V. P.; Matsumura, M.; J. Am. Oil Chem. Soc. 2003, 80, 997.,44 Zanardi, I.; Travagli, V.; Gabbrielli, A.; Chiasserine, L.; Bocci, V.; Lipids 2008, 43, 877.

Since last century, it is a known fact that when a vegetable oil reacts with ozone it is formed a group of oxygenated compounds which provide antimicrobial effects to the oil, for that reason they have been used of the medicine and cosmetology fields.55 Díaz, M.; Sánchez, Y.; Gómez, M.; Hernández, F.; Veloso, M. C.; Pereira, P.; Mangrich, A. S.; Andrade, J. B.; Grasas Aceites 2012, 63, 466.,66 Menéndez, S.; González, R.; Ledea, O.; Hernández, F.; León, O. S.; Díaz, M. F.; Ozono, Aspectos Básicos y Aplicaciones Clínicas; CENIC: La Habana, Cuba, 2008. It should be noted that ozonated olive oil is the most widely used in Europe, while ozonated sunflower oil has been the most widely used in Cuba.77 Bocci, V.; A New Medical Drug, 2nd ed.; Springer Verlag: Dordrecht, The Netherland, 2005.,88 Díaz, M.; Gavin, J.; Ledea, O.; Hernández, F.; Alaiz, M.; Garcés, R.; Ozone: Sci. Eng. 2005, 27, 247.

Vegetable oils exhibit different physicochemical properties, which depend on the length of the carbon chain and the degree of unsaturation, so the search for other vegetable oils that can be studied by the ozonation reaction would provide new substrates for the study of the correlations between its physicochemical properties and its biological effects.99 Díaz, M. F.; Hernández, R.; Martínez, G.; Vidal, G.; Gómez, M.; Fernández, H.; Garcés, R.; J. Braz. Chem. Soc. 2006, 17, 403.,1010 Graciani, E.; Oils and Fats: Composition and Properties, 1sted.; Educación: Madrid, Spain, 2006.

An attractive substrate to be studied has been the “dendê” oil, manufactured and marketed in Brazil, which is obtained from the mesocarp of the fruit of the palm tree, and is used mainly in Bahian cuisine and for the manufacture of cosmetics.1111 Gunstone, F.; Haewood, L.; Padley, B.; The Lipid Handbook, 2nd ed.; Chapman & Hall: London, UK, 1994.,1212 Almeid, D. T.; Nunes, I. L.; Conde, P. L.; Rosa, R. P. S.; Rogério, W. F.; Machado, E. R.; Grasas Aceites 2013, 64, 38. In addition, Brazilian edible quality oils obtained from seeds such as soy, corn, rice and sunflower are also studied and compared.

It is known that, in order to follow an ozonation reaction of vegetable oils, several quality indexes such as acidity, iodine, density and viscosity must be taken into account, but mainly the peroxide index as a control of the reaction.66 Menéndez, S.; González, R.; Ledea, O.; Hernández, F.; León, O. S.; Díaz, M. F.; Ozono, Aspectos Básicos y Aplicaciones Clínicas; CENIC: La Habana, Cuba, 2008. Due to this, it is necessary to study them to homogenize, evaluate and compare these different quality indicators in ozonated oils.

The objective of this research is to study the compounds resulting from the ozonation reaction of the Brazilian vegetable oils “dendê”, soybean, corn, rice and sunflower which are evaluated by physical-chemical analysis such as peroxide, acidity, iodine, density and viscosity. Fatty acid composition will also be determined by gas chromatography and antimicrobial activity. This study aims to select the best substrate that could be used in pharmaceutical and cosmetic formulations.

Experimental

Solvents and reagents

Glacial acetic acid, chloroform, potassium iodide, sodium thiosulfate, starch, ethanol, ether, potassium hydroxide, phenolphthalein, iodine bromide, toluene, dimethoxypropane were purchase from Merck S.A. (representation in Havana, Cuba).

Edible oil of “dendê” was obtained from Tropicana Brazilian Industry (Salvador, Brazil) and soy, corn, rice and sunflower edible oils were obtained from especial oils Liza, São Paulo, Brazil.

Ozonation procedure

Five ozonation reactions were performed, one for each oil. Edible vegetable oil (50 mL) was placed into a bubbling reactor where ozone reaction took place in water bath, at room temperature (25 ºC).

The ozonation was allowed to continue for 90 min, employing medicinal oxygen as ozone source. Applied ozone dosages (AOD) 32; 65 and 97 mg g-1, were obtained through different bubbling times (0.5, 1 and 1.5 h). Applied ozone dosages were chosen to achieve peroxide values ranged between 400 and 1800 mmol-equiv kg-1. Three samples were taken in each ozonation procedure, respectively. Three replicates were carried out for each dosage. Replicates were pooled for each ozone dosage. Samples were stored at 2-8 ºC for 24 h before analysis.

Ozone generation

Ozone was generated passing oxygen through an Ozoney model SL-4M ozone generator (Cuba), at a fixed voltage (170 V), and a constant flow rate of 54 L h-1. The ozone initial concentration of the resulting stream medicinal oxygen 54 mg L-1 was determined by Anseros Ozomat equipment (Germany).

Physical chemical techniques

Peroxide index

Peroxide index (PI) is the number expressed as milliequivalents of active oxygen in 1 kg of the sample. 0.5 g of sample was weighed and mixed with a solution of glacial acetic acid-chloroform 3:2 v/v. 0.5 mL of a saturated potassium iodide solution was added. The mixture was allowed to stand for two minutes, then 30 mL of distilled water were added and it was slowly titrated with a solution of 0.1 mol L-1 sodium thiosulfate, stirring continuously until almost yellow disappearance. 5 mL of a starch indicator solution were added and titration was continued until the blue color disappeared. This determination was made in triplicate for each sample of ozonized vegetable oil.

The result was calculated by the expression:1313 United States Pharmacopeia and National Form, (USP-NF); Fats and Fixed Oils, 401 Peroxide Value, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.

(1) PI = M × V / Pm × 1000

where, M: sodium thiosulfate concentration (0.1 mol L-1), V: volume consumed of sodium thiosulfate in the titration (mL), Pm: sample weight.

Acidity index

Acidity index (AI) is expressed in milligrams of potassium hydroxide that are required to neutralize free acids in a gram of sample. 0.9 to 1.2 g of sample were weighed and mixed with 50 mL of a mixture of equal volumes of ethanol (96%) and ether. Subsequently, 0.5 mL of 1% m/v solution of phenolphthalein in ethanol (96%) was added. The mixture was titrated with a 0.1 M solution of potassium hydroxide, until the solution became weakly pink for at least 15 s. Three replications were made for each of the samples. The AI was calculated from the expression:1414 United States Pharmacopeia and National Form, (USP-NF); Fats and Fixed Oils, 401 Acid Value, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.

(2) AI = V × M / m × 56 . 1

where, V is the volume of potassium hydroxide consumed in mL, M is the molarity of the potassium hydroxide solution, m: is the mass in grams of the weighed sample.

Iodine index

Iodine index (II) represents the number of g of iodine absorbed, under the prescribed condition, by 100 g of the substance. 100 to 150 mg of oil sample were weighed and mixed with 15 mL of chloroform and stirred until dissolved. 25 mL of iodine bromide solution were added and let stand for 30 min, protected from light, stirring frequently. 10 mL of 10% m/v potassium iodide solution and 100 mL of purified water were added. The iodine released was titrated with 0.1 M sodium thiosulfate solution vigorously stirred until the yellow color almost disappeared. 5 mL of starch indicator solution were added. The titration continued by adding 0.1 M sodium thiosulfate solution dropwise until the bluish color completely disappears from the sample. The same method, exactly, was carried out, but without the substance to be examined (blank). Three replications were made for each of the samples. The II was calculated from the expression:1515 United States Pharmacopeia and National Form, (USP-NF); Fats and Fixed Oils, 401 Iodine Value, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.

(3) Iodine index II = B V M / PM × 12 . 69

where, B: volume in milliliters of 0.1 M sodium thiosulfate solution consumed by the blank, V: volume in milliliters of 0.1 M sodium thiosulfate solution consumed by the sample, M: molarity of the sodium thiosulfate solution, PM: weight in grams of the sample.

Density value

Density value represents the proportion between the mass of a substance and its volume at a determined temperature (g mL-1).1616 United States Pharmacopeia and National Form, (USP-NF); Physical Tests, 699 Density, 30th-25th ed.; Port City Press: Baltimore, USA, 2007. The density of the vegetable oil was determined with respect to water, for this, a pycnometer was used and the calculation was made by the ratio between the mass of a volume of the substance (ozonized vegetable oil) at 20 ºC and the mass of an equal volume of water at 4 ºC.1616 United States Pharmacopeia and National Form, (USP-NF); Physical Tests, 699 Density, 30th-25th ed.; Port City Press: Baltimore, USA, 2007. The determinations were made in triplicate.

Viscosity value

The increase in viscosity is a measure of the condensation polymerization of the peroxides that are formed during the ozonation of vegetable oil. The determination of this parameter is carried out using a UBBELOHDE Viscometer and is based on measuring the time required for a given sample volume to pass through a properly calibrated capillary, as a measure of the internal friction force of the product. The result is expressed in units of force viscosity per unit area, (mPa s).1717 United States Pharmacopeia and National Form, (USP-NF); Physical Tests, 911 Viscosity, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.

Gaseous chromatography (GC)

The ozonation effects on the fatty acids composition of different oils as “dendê”, soy, corn, rice and sunflower were analyzed. For gas chromatography analysis of esterified fatty acids, methyl ester derivatives were first prepared by transesterification as described by Garcés et al.1818 Garcés, R.; Mancha, M.; Anal Biochem. 1993, 211, 139.

Gas chromatography analyzes were performed in a high-resolution gas chromatography coupled to a quadrupole mass detector Shimadzu (GCMS-QP 2010), equipped with split/splitless type injector, automatic injector (AOC-20i auto-sampler). Analysis were performed in a HP-5-MS capillary column (30 m × 0.25 mm inner diameter), film thickness 1 μm. The carrier gas for esterified fatty acids analysis was hydrogen at a flow of 1 mL min-1 and a pressure of 50 kPa. For the analysis of the fatty acids the column temperature was programmed from 100 to 170 ºC with an increase of 8 ºC min-1and then up to 240 ºC with an increase of 2 ºC min-1, staying for 10 min to 240 ºC, (total time 51 min). Injections were done in duplicate using an injection volume of 1 μL. Fatty acid methyl esters were used as external standard C14-C22 (Sigma-Aldrich Chemical Company, Brazil) to identify components.

Antibacterial activity

Antibacterial activity of each edible quality vegetable oil and each ozonized oil obtained were determined. Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853 were chosen. Minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) by agar dilution and macro dilution methods were based on Clinical Laboratory Standards of the Clinical Laboratory Standards Institute (CLSI).1919 Clinical and Laboratory Standards Institute (CLSI); Methods for Dilution Antimicrobial, Susceptibility Testing of Bacteria that Grow Aerobically M07, 11th ed.; CLSI: Wayne, PA, USA, 2018. The spectrum of antibacterial activity was obtained for all samples.

Statistical analysis

Analyses were carried out in triplicate and were expressed as mean ± standard deviation (SD). Linear regression analysis was performed using the OriginPro 8 SRO statistical analysis.2020 OriginPro 8 SRO, Statistical Analysis; Origin Lab Corporation, Northampton, MA, USA, 2007.

Results

Five vegetable oils with different fatty acid composition have been ozonized, among which are “dendê”, soy, corn, rice and sunflower. Table 1 shows the physicochemical parameters quality indicators of the oils studied. It can be seen that ozonized vegetable oils have different behaviors in terms of their physicochemical properties.66 Menéndez, S.; González, R.; Ledea, O.; Hernández, F.; León, O. S.; Díaz, M. F.; Ozono, Aspectos Básicos y Aplicaciones Clínicas; CENIC: La Habana, Cuba, 2008.

Table 1
Physicochemical parameters of the ozonated oils studied

Regarding the peroxide index versus the ozone dose applied to the five oils studied, there is a linear correlation with a correlation (r) and determination coefficient (R2) greater than 0.99 and 98%, respectively, corresponding to a linear model adjustment.2121 Castillo, B.; González, R.; Rev. Cubana Farm. 1996, 30, 43. This result indicates the linear correspondence between the peroxide index and the ozone dose applied which is shown below:

(4) Ozonized " dend ê " oil ODO PI = 12 . 431 + 17 . 54 AOD r = 0 . 996 %; r 2 = 99 . 26 %
(5) Ozonized soy oil OSO PI = 43 . 038 + 10 . 695 AOD r = 0 . 995 %; r 2 = 99 . 01 %
(6) Ozonized corn oil OCO PI = 65 . 481 + 12 . 129 AOD r = 0 . 993 %; r 2 = 98 . 7 %
(7) Ozonized rice oil ORO PI = 37 . 414 + 10 . 971 AOD r = 0 . 997 %; r 2 = 99 . 42 %
(8) Ozonized sunflower oil OSFO PI = 42 . 956 + 13 . 526 AOD r = 0 . 997 %; r 2 = 99 . 38 %

In relation to the acidity index, an increase in this parameter was observed (Table 1) by increasing the dose of ozone applied (32, 65 and 97 mg g-1) in all the oils studied, presenting correlation (r) and determination coefficients (R2) from 0.95 and 91%, respectively, as shown below:

(9) Ozonized " dend ê " oil ODO AI = 0 . 241 + 0 . 222 AOD r = 0 . 997 %; r 2 = 99 . 39 %
(10) Ozonized soy oil OSO AI = 0 . 773 + 0 . 076 AOD r = 0 . 955 %; r 2 = 91 . 27 %
(11) Ozonized corn oil OCO AI = 29 . 55 + 0 . 642 AOD r = 0 . 983 %; r 2 = 96 . 68 %
(12) Ozonized rice oil ORO AI = 0 . 747 + 0 . 105 AOD r = 0 . 960 %; r 2 = 92 . 08 %
(13) Ozonized sunflower oil OSFO AI = 1 . 284 + 0 . 1868 AOD r = 0 . 980 %; r 2 = 96 . 06 %

During the ozonation reaction of the five vegetable oils studied in the three ozonation times applied (0.5; 1; 3 h) a gradual decrease of the double bonds can be observed (Figure 1) and the iodine index (Table 1). “Dendê” oil has a lower iodine index than the rest of the oils studied, however, it reacts more quickly consuming 94% of the moles of double bonds, while for the oils of soy, corn, rice and sunflower decreases at 55, 50, 60 and 55%, respectively.

Figure 1
Behavior of the moles number (moles) against ozonated time (T). ODO: ozonated “dendê” oil; OSO: ozonated soy oil; OCO: ozonated corn oil; ORO: ozonated rice oil; OSFO: ozonated sunflower oil.

Regarding the physical-chemical density, it is shown in Table 1 that when increasing the dose of ozone applied in “dendê”, soy, corn, rice and sunflower oils, they increase slightly by 4; 7; 6; 7 and 8%, respectively.

The viscosity (V) is a physical parameter that increases in all the oils studied, such as “dendê”, soy, corn, rice and sunflower by 91; 94; 91; 91 and 95%, respectively (Table 1). This magnitude meets an exponential correlation having a correlation and determination coefficient greater than 0.99 and 98% (Figure 2), respectively, which is shown below:

(14) Ozonized " dend ê " oil ODO V = 42 . 523 e 0 . 0257 DOA r = 0 . 994 %; r 2 = 98 . 81 %
(15) Ozonized soy oil OSO V = 37 . 184 e 0 . 0292 DOA r = 0 . 999 %; r 2 = 99 . 88 %
(16) Ozonized corn oil OCO V = 48 . 465 e 0 . 025 DOA r = 0 . 999 %; r 2 = 99 . 99 %
(17) Ozonized rice oil ORO V = 52 . 81 e 0 . 0248 DOA r = 0 . 999 %; r 2 = 99 . 99 %
(18) Ozonized sunflower oil OSFO V = 35 . 006 e 0 . 0306 DOA r = 0 . 995 %; r 2 = 99 . 01 %

Figure 2
Behavior of the viscosity (V) against the ozone dose applied (AOD). V: viscosity; ODO: ozonated “dendê” oil; OSO: ozonated soy oil; OCO: ozonated corn oil; ORO: ozonated rice oil; OSFO: ozonated sunflower oil.

Table 2 shows the percentages of the composition of unsaturated fatty acids C18:1 (oleic acid) and C18:2 (linoleic acid) of the five oils studied obtained by the gas chromatographic analytical technique. We can see that the oil “dendê” has a high percentage composition of C18:1 monounsaturated fatty acids and the lowest percentage composition of C18:2 polyunsaturated fatty acids, while the rest of the oils such as rice, soy, corn and sunflower contain a similar or lower percentage composition of C18:1 and a higher percentage composition of C18:2.2222 Firestone, D.; Physical and Chemical Characteristics of Oils, Fats and Waxes, 1st ed.; Champaign: Illinois, USA, 1999. We should note that the trans isomerism determines a linear structure around the double bond, unlike the cis isomerism, where the location of the substituent atoms on the same side of the molecule produces structures of high flexibility. In its natural form, unsaturated fatty acids present mostly cis isomerism (over 95%). All the structural functions of fatty acids are associated with cis isomerism.2323 Nakamura, M. T.; Nara, T. Y.; Annu. Rev. Nutr. 2004, 24, 345.,2424 Valenzuela, A.; Morgado, N.; Rev. Chil. Nutr. 2005, 32, 88.

Table 2
Percentage composition of unsaturated fatty acids in the five oils

Table 3 shows the antibacterial activity (mg mL-1) against the microorganisms Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli, of the five oils studied “dendê”, soy, corn, rice and sunflower, for the three doses of ozone applied (32, 65 and 97 mg g-1). The minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) are shown, reaching for the applied ozone dose of 97 mg g-1 better antibacterial activity values in all the oils studied.

Table 3
Antibacterial activity of the five ozonized oils

Discussion

It can be seen in Table 1 that as the dose of ozone applied in all the studied oils of “dendê”, soy, corn, rice and sunflower increased, higher levels of peroxides are reached. It should be noted that “dendê” oil reaches a higher peroxide index, which is 1.6 times higher than that achieved with soy oil, 1.4 times by corn oil, 1.6 times by rice oil and 1.3 times by oil sunflower. This increase in the peroxide index is due to the formation of oxygenated compounds during and after the ozonation reaction, which coincides with the facts described by Díaz et al.2525 Díaz, M. F.; Gavín, J. A.; Gómez, M.; Curtilles, V.; Hernández, F.; Ozone: Sci. Eng. 2006, 28, 59. and reported by the Criegee2626 Criegee, R.; Angew. Chem., Int. Ed. 1975, 14, 745. mechanism for the reaction of ozone with olefins.

The good linear correlation obtained between the behavior of the peroxides index and the applied ozone dose (0.99 for the correlation coefficient and 98% for the determination coefficient) predicts that the peroxides index parameter is considered the main indicator of quality in the process of ozonation of vegetable oils.

The linear correlation of the acidity index and the dose of ozone applied is not as good as we expected; this could be because carboxylic acids are not a direct product of the reaction, but an indirect result of the decomposition and oxidation of the oxygenated compounds derived from the reaction. Although the relationship between the dose of ozone applied and the acidity index is not as good, we can still say that there is a linear correlation, since the coefficients of correlation is greater than 0.95 and the determination is greater than 91%.

It should be noted that the ratio of the acidity index to the ozone dose applied for “dendê” reaches a high correlation and determination coefficient of 0.997 and 99.39%, respectively, which corresponds to the highest value of the index of acidity obtained for this oil (21 mg KOH g-1) (Table 1).

A progressive increase in the acidity index in all the oils studied (Table 1) could be due to the decomposition of peroxidic species, the oxidation of aldehydes in carboxylic acids and also the formation of acids during the ozonation reaction.2727 Moureu, S.; Violleau, F.; Haimoud-Lekhal, D. A.; Calmon, A.; Chem. Phys. Lipids 2015, 186, 79.

It is known that the reaction of ozone with unsaturated fatty acids occurs through the cleavage of double bonds.2828 Díaz, M.; Hernández, F.; Álvarez, I.; Vélez, H.; Ledea, O.; Molerio, J.; Rev. CENIC, Cienc. Quim. 1998, 29, 89.,2929 Martínez, G.; Pérez G.; Horwat, R.; Rev. Española Ozonoterapia 2012, 2, 121. So, it should be noted that “dendê” oil, despite having the lowest iodine value among all the oils studied, has a consumption of 94% moles of double bonds (Figure 1) reaching higher peroxide and acidity rates (Table 1).

Regarding density, it is shown in Table 1 that by increasing the dose of ozone applied in the oils of “dendê”, soy, corn, rice and sunflower, the mass increases due to the formation of oxygenated compounds such as ozonides, aldehydes, hydroperoxides, etc.3030 Hernández, R.; Martínez, G.; Díaz, M.; Rev. CENIC, Cienc. Quim. 2004, 35, 159.

When the concentration of peroxidic compounds increases, the viscosity of the medium increases in the applied ozone dosage (AOD) range from 32 to 97 mg g-1 (Table 1) for all the oils studied. This increase in viscosity could be a measure of the condensation polymerization that takes place from the peroxides that are formed during the ozonation of the vegetable oils or by the formation of compounds of greater molecular weight than the triglycerides originally present in the oil.3131 de Almeida, N. R.; Beatriz, A.; de Arruda, E. J.; de Lima, D. P.; de Oliveira, L. C. S.; Micheletti, A. C. In Vegetable Oil: Properties, Uses and Benefits, 1st ed.; Holt, B., ed.; Nova Science Publishers: New York, 2016, ch. 5.,3232 Díaz, M. F.; Ledea, O. E.; Regüeiferios, M. G.; Garcés, R. M.; Alaiz, M.; Martínez, F. E.; Quim. Nova 2009, 32, 2467. This physical parameter quality indicator that increases between 91 and 95% presenting an exponential correlation with a correlation coefficient greater than 0.99 and determination greater than 98% in all the oils studied.2121 Castillo, B.; González, R.; Rev. Cubana Farm. 1996, 30, 43. This result corresponds to one previously developed in ozonized sunflower oil by Hernández et al.3030 Hernández, R.; Martínez, G.; Díaz, M.; Rev. CENIC, Cienc. Quim. 2004, 35, 159. where the relationship between the peroxide index and the viscosity of the oil was reported as an exponential curve with an adequate coefficient of determination greater than 98%.

“Dendê” oil has a higher content of monounsaturated fatty acids such as C18:1 oleic acid and small amounts of polyunsaturated fatty acid (C18:2 linoleic acid) that differentiates it from soybean, corn, rice and sunflower oils, which contain higher amount of linoleic acid C18:2 than oleic C18:1.2222 Firestone, D.; Physical and Chemical Characteristics of Oils, Fats and Waxes, 1st ed.; Champaign: Illinois, USA, 1999. We should expect that these latter oils, due to their composition rich in double bonds in carbons 9 and 12, during the ozonation reaction have a higher oxidation that of “dendê” oil, which is rich in the double bonds of carbon 9. However, this does not happen, and we consider that it could be due to the non-linear spatial conformation showing an elbow that both acids adopt, with cis isomerism. On the other hand, due to the spatial conformation that both acids adopt, the double bond of oleic acid is more exposed to the ozonation reaction that the double bonds of linoleic acid that are more packed,2323 Nakamura, M. T.; Nara, T. Y.; Annu. Rev. Nutr. 2004, 24, 345. which could be the explanation for an ozonation reaction faster in the “dendê” oil.

Regarding the study of the percentage of the composition of unsaturated fatty acids (C18:1 and C18:2) by gas chromatography of the five vegetable oils “dendê”, soy, corn, rice and sunflower (Table 2), it can be observed that ozonation reaction is fast for fatty acids that are in high concentration, while the fatty acids at lower concentrations react more slowly. In this way the “dendê” oil, which has a high proportion of C18:1 oleic acid will react rapidly. This could explain the selectivity of the ozone at the time of reacting with the substrates99 Díaz, M. F.; Hernández, R.; Martínez, G.; Vidal, G.; Gómez, M.; Fernández, H.; Garcés, R.; J. Braz. Chem. Soc. 2006, 17, 403. and the rapid ozonation of “dendê” oil where 87% of the double bonds react.

The determinations of the content of unsaturated fatty acids made to the different oils such as “dendê”, soy, corn, rice and sunflower (Table 2), showed that the content of unsaturated fatty acids was decreasing and consequently increasing the peroxide index, the acidity index, the viscosity and the density. Both oleic acid and linoleic acid, which are the unsaturated fatty acids found in greater proportion in these oils,2323 Nakamura, M. T.; Nara, T. Y.; Annu. Rev. Nutr. 2004, 24, 345. are detected in all the samples analyzed, which indicates that not all double bonds of these two acids were attacked by ozone, leaving triglycerides modified in the reaction medium by the reaction with ozone and unmodified triglycerides, which could be subsequently oxidized by the oxygenated compounds formed.

It can be observed that ozonated oils, in general, have antibacterial activity against the microorganisms studied Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli, (Table 3). The MIC values for the applied ozone dose of 97 mg g-1 were for soy oil between 4.75 and 9.5 mg mL-1, corn oil between 19 and 22, rice oil between 9.5 and 14.25 mg mL-1, sunflower oil between 8.5 and 9.5, and “dendê” oil between 1.9 and 4.75 mg mL-1. While, the MBC values for applied ozone dose of 97 mg mL-1 were for soy oil between 14.83 and 29.6 mg mL-1, corn oil between 30.5 and 44.5 mg mL-1, rice oil between 14.83 and 29.6 mg mL-1, sunflower oil between 19.5 and 89.5 mg mL-1, and “dendê” oil between 14.83 and 22.26 mg mL-1. It should be noted that “dendê” oil has the best antibacterial activity of all the oils studied.

These results correspond to those reported by various researchers where the biological activity of ozonized oils is attributed to oxygenated species.3333 Díaz, M.; Lezcano, I.; Molerio, J.; Hernández, F.; Ozone: Sci. Eng. 2001, 23, 35.

34 Sechi, L. A.; Lezcano, I.; Nuñez, N.; Espim, M.; Dupre, I.; Pinna, A.; Molicotti, P.; Zanetti, S.; J. Appl. Microbiol. 2001, 90, 279.
-3535 Curtiellas, V.; Gómez, M.; Ledea, O.; Fernández, I.; Sánchez, E.; Rev. CENIC, Cienc. Biol. 2005, 36, 1. Currently, there are several hypotheses of the mechanism of action of ozonized oils on microorganisms, but given the nature of its main oxygenated compounds, damage occurs in the most sensitive biomolecules such as proteins and unsaturated lipids, due to the oxidative attack of these oxygenated compounds on the cell envelope of microorganisms.3636 Curtiellas, V.; Ledea, O.; Rodriguez, S.; Ancheta, O.; Echevarria, M.; Sánchez, E.; Fernández, I.; Rev. CENIC, Cienc. Biol. 2008, 39, 128.

37 Komanapalli, I. R.; Mudd, J. B.; Lau, B. H.; Toxicol. Lett. 1997, 90, 61.
-3838 Pryor, W. A.; Uppu, R. M.; J. Biol. Chem. 1993, 68, 3120. It should be noted that these ozonized oils do not pollute the atmosphere and there have been no reported cases of bacterial resistance to these substances, so the results of this study could be a contribution to their use in fighting various infections of microorganisms and the scientific development of the benefits of these oils in medicine and cosmetology.

Conclusions

The results showed that “dendê” oil has a better antimicrobial activity with an extraordinarily low MIC and MBC for the three microorganisms studied. In addition, with this oil a greater reaction of its moles of double bonds with ozone (94%) is obtained, reaching a high peroxide index of 1746 mmol-equiv kg-1, thus increasing the concentration of oxygenated compounds responsible for the antibacterial effects of oil. This could be due to its chemical composition, rich in oleic acid C18:1, which has a spatial conformation of high flexibility, less packaged that facilitates its ozonation reaction.

It was possible to verify the selectivity of the ozone gas by reacting with the double bonds of unsaturated fatty acids C18:1 and C18:2 of the 5 vegetable oils studied “dendê”, soy, corn, rice and sunflower through the technique of gas chromatography, showing that the ozonation reaction occurs rapidly for unsaturated fatty acid that is in greater proportion, while unsaturated fatty acid in smaller proportion reacts more slowly.

In conclusion, it is suggested that the ozonated oil “dendê” can be used in the preparation of pharmaceutical and cosmetic formulations.

Acknowledgments

The authors appreciate the financial support granted by the CITMA-CNPq project.

References

  • 1
    Gunstone, F. D.; Structured and Modified Lipids; Marcel Dekker Inc.: New York, USA, 2001.
  • 2
    Durán, S. A.; Torres, J. G.; Sanhueza, J. C.; Nutr. Hosp 2015, 32, 11.
  • 3
    Soriano, N. U.; Migo, V. P.; Matsumura, M.; J. Am. Oil Chem. Soc. 2003, 80, 997.
  • 4
    Zanardi, I.; Travagli, V.; Gabbrielli, A.; Chiasserine, L.; Bocci, V.; Lipids 2008, 43, 877.
  • 5
    Díaz, M.; Sánchez, Y.; Gómez, M.; Hernández, F.; Veloso, M. C.; Pereira, P.; Mangrich, A. S.; Andrade, J. B.; Grasas Aceites 2012, 63, 466.
  • 6
    Menéndez, S.; González, R.; Ledea, O.; Hernández, F.; León, O. S.; Díaz, M. F.; Ozono, Aspectos Básicos y Aplicaciones Clínicas; CENIC: La Habana, Cuba, 2008.
  • 7
    Bocci, V.; A New Medical Drug, 2nd ed.; Springer Verlag: Dordrecht, The Netherland, 2005.
  • 8
    Díaz, M.; Gavin, J.; Ledea, O.; Hernández, F.; Alaiz, M.; Garcés, R.; Ozone: Sci. Eng. 2005, 27, 247.
  • 9
    Díaz, M. F.; Hernández, R.; Martínez, G.; Vidal, G.; Gómez, M.; Fernández, H.; Garcés, R.; J. Braz. Chem. Soc. 2006, 17, 403.
  • 10
    Graciani, E.; Oils and Fats: Composition and Properties, 1sted.; Educación: Madrid, Spain, 2006.
  • 11
    Gunstone, F.; Haewood, L.; Padley, B.; The Lipid Handbook, 2nd ed.; Chapman & Hall: London, UK, 1994.
  • 12
    Almeid, D. T.; Nunes, I. L.; Conde, P. L.; Rosa, R. P. S.; Rogério, W. F.; Machado, E. R.; Grasas Aceites 2013, 64, 38.
  • 13
    United States Pharmacopeia and National Form, (USP-NF); Fats and Fixed Oils, 401 Peroxide Value, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.
  • 14
    United States Pharmacopeia and National Form, (USP-NF); Fats and Fixed Oils, 401 Acid Value, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.
  • 15
    United States Pharmacopeia and National Form, (USP-NF); Fats and Fixed Oils, 401 Iodine Value, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.
  • 16
    United States Pharmacopeia and National Form, (USP-NF); Physical Tests, 699 Density, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.
  • 17
    United States Pharmacopeia and National Form, (USP-NF); Physical Tests, 911 Viscosity, 30th-25th ed.; Port City Press: Baltimore, USA, 2007.
  • 18
    Garcés, R.; Mancha, M.; Anal Biochem 1993, 211, 139.
  • 19
    Clinical and Laboratory Standards Institute (CLSI); Methods for Dilution Antimicrobial, Susceptibility Testing of Bacteria that Grow Aerobically M07, 11th ed.; CLSI: Wayne, PA, USA, 2018.
  • 20
    OriginPro 8 SRO, Statistical Analysis; Origin Lab Corporation, Northampton, MA, USA, 2007.
  • 21
    Castillo, B.; González, R.; Rev. Cubana Farm. 1996, 30, 43.
  • 22
    Firestone, D.; Physical and Chemical Characteristics of Oils, Fats and Waxes, 1st ed.; Champaign: Illinois, USA, 1999.
  • 23
    Nakamura, M. T.; Nara, T. Y.; Annu. Rev. Nutr 2004, 24, 345.
  • 24
    Valenzuela, A.; Morgado, N.; Rev. Chil. Nutr. 2005, 32, 88.
  • 25
    Díaz, M. F.; Gavín, J. A.; Gómez, M.; Curtilles, V.; Hernández, F.; Ozone: Sci. Eng. 2006, 28, 59.
  • 26
    Criegee, R.; Angew. Chem., Int. Ed. 1975, 14, 745.
  • 27
    Moureu, S.; Violleau, F.; Haimoud-Lekhal, D. A.; Calmon, A.; Chem. Phys. Lipids 2015, 186, 79.
  • 28
    Díaz, M.; Hernández, F.; Álvarez, I.; Vélez, H.; Ledea, O.; Molerio, J.; Rev. CENIC, Cienc. Quim. 1998, 29, 89.
  • 29
    Martínez, G.; Pérez G.; Horwat, R.; Rev. Española Ozonoterapia 2012, 2, 121.
  • 30
    Hernández, R.; Martínez, G.; Díaz, M.; Rev. CENIC, Cienc. Quim. 2004, 35, 159.
  • 31
    de Almeida, N. R.; Beatriz, A.; de Arruda, E. J.; de Lima, D. P.; de Oliveira, L. C. S.; Micheletti, A. C. In Vegetable Oil: Properties, Uses and Benefits, 1st ed.; Holt, B., ed.; Nova Science Publishers: New York, 2016, ch. 5.
  • 32
    Díaz, M. F.; Ledea, O. E.; Regüeiferios, M. G.; Garcés, R. M.; Alaiz, M.; Martínez, F. E.; Quim. Nova 2009, 32, 2467.
  • 33
    Díaz, M.; Lezcano, I.; Molerio, J.; Hernández, F.; Ozone: Sci. Eng. 2001, 23, 35.
  • 34
    Sechi, L. A.; Lezcano, I.; Nuñez, N.; Espim, M.; Dupre, I.; Pinna, A.; Molicotti, P.; Zanetti, S.; J. Appl. Microbiol. 2001, 90, 279.
  • 35
    Curtiellas, V.; Gómez, M.; Ledea, O.; Fernández, I.; Sánchez, E.; Rev. CENIC, Cienc. Biol. 2005, 36, 1.
  • 36
    Curtiellas, V.; Ledea, O.; Rodriguez, S.; Ancheta, O.; Echevarria, M.; Sánchez, E.; Fernández, I.; Rev. CENIC, Cienc. Biol. 2008, 39, 128.
  • 37
    Komanapalli, I. R.; Mudd, J. B.; Lau, B. H.; Toxicol. Lett. 1997, 90, 61.
  • 38
    Pryor, W. A.; Uppu, R. M.; J. Biol. Chem. 1993, 68, 3120.

Publication Dates

  • Publication in this collection
    20 Jan 2021
  • Date of issue
    Jan 2021

History

  • Received
    27 Nov 2019
  • Accepted
    19 Aug 2020
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