- Original article
- Open Access
Antibacterial activities and antioxidant capacity of Aloe vera
© Nejatzadeh-Barandozi; licensee Springer. 2013
- Received: 6 February 2013
- Accepted: 3 June 2013
- Published: 19 July 2013
The aim of this study was to identify, quantify, and compare the phytochemical contents, antioxidant capacities, and antibacterial activities of Aloe vera lyophilized leaf gel (LGE) and 95% ethanol leaf gel extracts (ELGE) using GC-MS and spectrophotometric methods.
Analytically, 95% ethanol is less effective than ethyl acetate/diethyl ether or hexane (in the case of fatty acids) extractions in separating phytochemicals for characterization purposes. However, although fewer compounds are extracted in the ELGE, they are approximately 345 times more concentrated as compared to the LGE, hence justifying ELGE use in biological efficacy studies in vivo. Individual phytochemicals identified included various phenolic acids/polyphenols, phytosterols, fatty acids, indoles, alkanes, pyrimidines, alkaloids, organic acids, aldehydes, dicarboxylic acids, ketones, and alcohols. Due to the presence of the antioxidant polyphenols, indoles, and alkaloids, the A. vera leaf gel shows antioxidant capacity as confirmed by ORAC and FRAP analyses. Both analytical methods used show the non-flavonoid polyphenols to contribute to the majority of the total polyphenol content. Three different solvents such as aqueous, ethanol, and acetone were used to extract the bioactive compounds from the leaves of A. vera to screen the antibacterial activity selected human clinical pathogens by agar diffusion method. The maximum antibacterial activities were observed in acetone extracts (12 ± 0.45, 20 ± 0.35, 20 ± 0.57, and 15 ± 0.38 nm) other than aqueous and ethanol extracts.
Due to its phytochemical composition, A. vera leaf gel may show promise in alleviating symptoms associated with/or prevention of cardiovascular diseases, cancer, neurodegeneration, and diabetes.
- Aloe vera
- Antibacterial activities
- Antioxidant capacity
- Gas chromatography
- Mass spectrometry
Aloe vera (L.) Burm.f. (Aloe barbadensis Miller) is a perennial succulent xerophyte, which develops water storage tissue in the leaves to survive in dry areas of low or erratic rainfall. The innermost part of the leaf is a clear, soft, moist, and slippery tissue that consists of large thin-walled parenchyma cells in which water is held in the form of a viscous mucilage . Therefore, the thick fleshy leaves of aloe plants contain not only cell wall carbohydrates such as cellulose and hemicellulose but also storage carbohydrates such as acetylated mannans .
A. vera has been used for many centuries for its curative and therapeutic properties, and although over 75 active ingredients from the inner gel have been identified, therapeutic effects have not been correlated well with each individual component . Many of the medicinal effects of aloe leaf extracts have been attributed to the polysaccharides found in the inner leaf parenchymatous tissue [4, 5], but it is believed that these biological activities should be assigned to a synergistic action of the compounds contained therein rather than a single chemical substance . A. vera is the most commercialized aloe species, and processing of the leaf pulp has become a large worldwide industry. In the food industry, it has been used as a source of functional foods and as an ingredient in other food products, for the production of gel-containing health drinks and beverages. In the cosmetic and toiletry industry, it has been used as base material for the production of creams, lotions, soaps, shampoos, facial cleansers, and other products. In the pharmaceutical industry, it has been used for the manufacture of topical products such as ointments and gel preparations, as well as in the production of tablets and capsules [7, 8]. Important pharmaceutical properties that have recently been discovered for both the A. vera gel and whole leaf extract include the ability to improve the bioavailability of co-administered vitamins in human subjects . Due to its absorption enhancing effects, A. vera gel may be employed to effectively deliver poorly absorbable drugs through the oral route of drug administration. Furthermore, the dried powder obtained from A. vera gel was successfully used to manufacture directly compressible matrix-type tablets. These matrix-type tablets slowly released a model compound over an extended period of time and thereby showing potential to be used as an excipient in modified release dosage forms .
Apart from Aloe being used extensively in the cosmetic industry, it has been described for centuries for its laxative, anti-inflammatory, immunostimulant, antiseptic , wound and burn healing , antiulcer , antitumor , and antidiabetic  activities. These treatments are based on anecdotal evidence or research findings done almost exclusively on A. vera. Different Aloe species would have various phytochemical contents, health benefits, and possible toxicities. Hence, it is of relevance for scientists, industry, and rural communities not only to research the relevant medicinal uses of their indigenous Aloe species but also to determine the active components and their individual or combined mechanisms of biological function. The use of 95% ethanol extracts of various Aloe species is extensively described in the literature for determining biological activity in the treatment and prevention of a variety of health conditions [16, 17], in particular, diabetes [18, 19]. In this study, we determined and compared the phytochemical contents and antioxidant capacities, antibacterial activities of A. vera lyophilized leaf gel and 95% ethanol leaf gel extracts using gas chromatography–mass spectrometry (GC-MS) and spectrophotometric methods of analysis. This was done not only to describe A. vera leaf gel extracts with regard to phytochemical contents and possible health benefits but also to compare various extraction methods for both analytical efficacy and possible biological relevance.
Whole, freshly cut, A. vera leaves (100 kg) were harvested in the month of September from farms in the National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran of Iran. The inner leaf gel was removed, homogenized, freeze-dried, and stored at −20°C until analysis. This was termed the leaf gel extract (LGE) for the purpose of this study. Approximately half of the LGE was used for the preparation of a 95% ethanol extract as described previously . This was termed the 95% ethanol leaf gel extract (ELGE).
All analytical standards were purchased from Sigma-Aldrich (St. Louis, MO, USA), and phenol reagent and other reagent chemicals and all of the organic solvents used were of ultrahigh purity which were purchased from Merck (Darmstadt, Germany).
Ethyl acetate/diethyl ether extraction
The internal standard, 3-phenylbutyric acid (25 mg/50 mL), was added to 25 mg of finely ground LGE and ELGE, followed by the addition of 1 mL of sodium acetate buffer (0.125 M). β-Glucuronidase (30 μL) was added, and the sample was vortexed and incubated overnight at 37°C. The sample was extracted with 6 mL of ethyl acetate followed by 3 mL of diethyl ether. The organic phase was collected after each extraction via centrifugation. The organic phase from each extraction was pooled and dried under nitrogen. The dried extract was derivatized with bis(trimethylsilyl)trifluoroacetamide (BSTFA, 100 μL), trimethylchlorosilane (TMCS, 20 μL), and pyridine (20 μL) at 70°C for 30 min. After cooling, 0.1 μL of the extract was injected into the GC-MS via splitless injection.
Fatty acid extraction
Heptadecanoic acid (72 mM), as an internal standard, was added to 25 mg of LGE and ELGE followed by 100 μL of a 45-mM solution of butylated hydroxytoluene and 2 mL of methanolic HCl (3 N). The samples were then vortexed and incubated for 4 h at 90°C. After cooling to room temperature, the sample was extracted twice with 2 mL of hexane, dried under a nitrogen stream, and finally resuspended with 100 μL of hexane, 1 μL of which was injected onto the GC-MS via splitless injection.
Gas chromatography–mass spectrometry
An Agilent 6890 GC ported to a 5973 mass selective detector (Santa Clara, CA, USA) was used for the identification and quantification of individual fatty acids. For the acquisition of an electron ionization mass spectrum, an ion source temperature of 200°C and electron energy of 70 eV were used. The gas chromatograph was equipped with an SE-30 capillary column (Agilent), a split/splitless injection piece (250°C), and direct GC-MS coupling (260°C). Helium (1 mL/min) was used as the carrier gas. The oven temperature program for analyzing the ethyl acetate/diethyl ether extract was an initial oven temperature of 40°C and was maintained for 2 min, followed by a steady climb to 350°C at a rate of 5°C/min. For the fatty acid analysis, an initial oven temperature of 50°C was maintained for 1.5 min and then allowed to increase to 190°C at a rate of 30°C/min. The oven temperature was maintained at 190°C for 5 min and then allowed to increase to 220°C at a rate of 8°C/min. The oven temperature was again maintained for 2 min and finally ramped to 230°C at a rate of 3°C/min and maintained for 24 min at this temperature.
Total polyphenol assay
The total polyphenol content of the extracts were determined according to the Folin-Ciocalteu procedure . Briefly, 10 mg of finely ground LGE or ELGE was dissolved in 200 μL of H2O in a test tube followed by 1 mL of Folin-Ciocalteu's reagent. This was allowed to stand for 8 min at room temperature. Next, 0.8 mL of sodium carbonate (7.5%, w/v) was added, mixed, and allowed to stand for 30 min. Absorption was measured at 765 nm (Shimadzu UV-1601 spectrophotometer, Kyoto, Japan). The mean total phenolic content (n = 3) was expressed as milligrams of gallic acid (Sigma-Aldrich) equivalents per 100 g of wet and dry mass (mg of GAE/100 g) (standard deviation (SD)).
Total flavonoid assay
The total flavonoid content was measured using the AlCl3 colorimetric assay  with some modifications. Briefly, 10 mg of LGE or ELGE was dissolved in 1 mL of H2O, to which 60 μL of 5% (w/v) NaNO2 was added. After 5 min, 60 μL of a 10% (w/v) AlCl3 was added. In the sixth minute, 400 μL of 1 M NaOH was added, and the total volume was made up to 2 mL with H2O. The solution was mixed well, and the absorbance was measured at 510 nm against a reagent blank. Concentrations were determined using a catechin (Sigma-Aldrich) solution standard curve. The mean total flavonoid content (n = 3) was expressed as milligrams of catechin equivalents (CE) per 100 g of wet and dry mass (mg of CE/100 g) (SD).
Oxygen radical absorbance capacity
Oxygen radical absorbance capacity (ORAC) analyses of hydrophilic and lipophilic compounds in LGE and ELGE were performed as described previously . The analysis of lipophilic compounds was aided by the addition of randomly methylated β-cyclodextrin as a solubility enhancer as described before . Briefly, in a volume of 200 μL, the reaction contained 56-nM fluorescein (Sigma-Aldrich) as a target for free radical attack by 240-nM 2,2′-azobis(2-amidinopropane)dihydrochloride (Sigma-Aldrich). A BioTEK fluorescence plate reader (FL-600, Winooski, VT, USA) was used, and the decay of fluorescence of fluorescein (excitation, 485 nm; emission, 520 nm) was measured every 5 min for 2 h at 37°C. Costar black opaque (96 well) plates (Thermo Fisher Scientific, Waltham, MA, USA) were used in the assays. Trolox (Sigma-Aldrich) was used as standard at a range between 0 and 20 í M with a polynomial (second order) curve fit analysis. Mean values (n) 3) of antioxidant capacities were expressed as micromoles of Trolox equivalents (TE) per gram of wet and dry mass (SD).
Ferric reducing antioxidant power
Ferric reducing antioxidant power (FRAP) values were determined essentially as described previously . Briefly, the reduction of a Fe3+-2,3,5-triphenyltetrazolium (Sigma-Aldrich) complex in the assay by the antioxidants in the samples was monitored at 593 nm. As a standard, FeSO4 (Sigma-Aldrich) was used, and the FRAP activities of the samples were expressed as the mean (n = 3) micromoles of Fe2+ per gram of wet and dry mass (SD).
Antibacterial activity of Aloe vera
The antibacterial studies were carried out by disc diffusion technique . The sterile nutrient agar plates and potato dextrose agar plates were prepared. The bacterial test organisms like Staphylococcus aureus, Streptococcus pyogenes, Pseudomonas aeruginosa, and Escherichia coli were spread over the nutrient agar plates using separate sterile cotton buds. After the microbial lawn preparation, three different extracts (20 grams of powdered plant materials mixed with 100 ml of various solvents (distilled water, ethanol, and acetone solution)) of plant disc were placed on the organism-inoculated plates with equal distance; control discs were also prepared. All bacterial plates were incubated at 27°C for 24 h. The diameter of the minimum zone of inhibition was measured in millimeter. For each test, three replicates were performed.
Concentrations of GC-MS identified compounds from LGE and 95% ELGE
LGE (per dry mass LGE)
ELGE (per dry mass LGE
ELGE (per dry mass ELGE)
1.3 × 104
8.5 × 103
5.0 × 103
1.6 × 104
1.5 × 103
1.2 × 104
1.8 × 104
1.9 × 106
2.3 × 105
2.5 × 104
7.1 × 104
3.1 × 104
1.2 × 105
4.1 × 104
9.7 × 104
6.3 × 103
3.7 × 103
6.3 × 104
Linoleic (C18:2 n-6)
4.6 × 103
Concentrations of total polyphenols, flavonoids, and non-flavonoids as well as antioxidant capacity via ORAC and FRAP analyses
LGE (dry mass)
LGE (wet mass)
ELGE (expressed as dry mass ELGE)
ELGE (expressed as dry mass LGE)
ELGE (expressed as wet mass LGE)
Total polyphenols (mg of GAE/100 g ± SD)
78.2 ± 4.03
2.70 ± 0.14
413 ± 9.88
26.8 ± 0.63
0.93 ± 0.02
Total flavonoids (mg of CE/100 g ± SD)
5.3 ± 0.38
0.19 ± 0.01
33.6 ± 1.98
2.15 ± 0.13
0.08 ± 0.003
Total non-flavonoids (by calculation)
73.7 ± 0.43
2.55 ± 0.22
378 ± 6.78
24.5 ± 1.5
0.86 ± 0.02
ORAC, hydrophilic (í mol of TE/g)
53 ± 1.1
1.81 ± 0.04
136 ± 2.3
8.83 ± 0.16
0.30 ± 0.006
ORAC, lipophilic (í mol of TE/g)
ORAC, total (í mol of TE/g)
53 ± 1.1
1.81 ± 0.04
136 ± 2.3
8.83 ± 0.16
0.30 ± 0.006
FRAP (í mol/g)
4.9 ± 0.25
0.17 ± 0.07
19.0 ± 0.3
1.21 ± 0.02
0.05 ± 0.001
Over the past 10 years, there has been a growing interest in the value of polyphenols among researchers and food manufacturers. This is mainly because of their antioxidant properties, their abundance in our diet, and their role in the prevention of various diseases associated with oxidative stress such as cancer, cardiovascular disease, neurodegeneration , and diabetes . Polyphenols constitute a large class of molecules containing a number of phenolic hydroxyl groups attached to ring structures allowing for their antioxidant activities. These compounds are multifunctional and can act as reducing agents, hydrogen-donating antioxidants, and singlet oxygen quenchers . All of the individual A. vera leaf gel antioxidant polyphenols identified in Table 1 may contribute to the prevention of the above-mentioned diseases to a greater or lesser extent. The individual contributions of these to disease prevention would, however, depend on their concentrations, antioxidant capacities, bioavailabilities, and specific mechanisms of action. Although the individual phenolic acids/polyphenols occurring in the highest concentrations were benzoic acid, p-toluic acid, p-coumaric acid, p-salicylic acid, protocatechuic acid, hydroxyphenylacetic acid, ferulic acid, aloe emodin, and vanillic acid, it is well-known that the protective health benefits of polyphenols are mainly through a combination of additive and/or synergistic effects between the individual compounds . Consequently, those polyphenol/phenolic compounds identified in lower concentrations may also be of value. Due to the fact that the majority of the phenolic acids/polyphenols identified in A. vera leaf gel in Table 1 are antioxidants  and these compounds as a group occur in the highest concentrations, one would expect these to contribute to the majority of the antioxidant capacity measured in these extracts (Table 2). However, apart from these polyphenols, the indoles  and alkaloids identified  are also known to possess antioxidant activities and may consequently also contribute to the ORAC and FRAP values of these extracts. When interpreting the data of this nature, one should keep in mind that using the concentrations of these antioxidant compounds alone is insufficient criteria for making predictions of individual contributions to oxidative stress. As previously described, this is due to the fact that the concentrations of individual polyphenol antioxidants are not the only factor influencing antioxidant capacity; the structural arrangements (number and position of hydroxyl groups, double bonds, and aromatic rings) of these compounds also play a role . Additionally, their individual contributions to ORAC and FRAP may also differ. Due to the FRAP analysis being an indication of the ferric ion reducing power of a compound or mixture and the ORAC analysis indicating the ability of a compound or mixture to scavenge free radicals, the various individual polyphenol components of the mixture may have stronger free radical scavenging abilities than reducing power, or vice versa, dependent on their chemical structures . Phytosterols are another group of compounds that are well-known for their health benefits. Of the four phytosterols identified in Table 1, β-sitosterol occurred in by far the highest concentrations in the LGE, contributing to 93% of the total phytosterols identified.
Antibacterial activity of Aloe vera
Zone of inhibition (mm in diameter; mean ± SD; n= 3)
9 ± 0.53
7 ± 0.37
19 ± 0.36
14 ± 0.53
12 ± 0.45
20 ± 0.35
19 ± 0.57
14 ± 0.38
The ELGE was once again less effective in extracting these compounds, and only cholestanol was identified. However, the levels normalized to dry mass ELGE were not insignificant. Phytosterols are best described for their total cholesterol and low-density lipid cholesterol (LDL-C) lowering effects, consequently associated with reducing the risk for cardiovascular disease . As summarized by Devaraj and Jialal  evidence for this has been observed in hypercholesterolemic, diabetic, and healthy volunteers. The mechanism proposed by which phytosterols accomplish this is by lowering cholesterol absorption due to the structural similarities these compounds share with cholesterol [27, 29]. Apart from lowering cardiovascular risk factors associated with diabetes, phytosterols (â-sitosterol in particular) have been shown to positively affect diabetes by directly lowering fasting blood glucose levels by cortisol inhibition . Additionally, phytosterols have been shown to reduce biomarkers for oxidative stress and inflammation , as well as to reduce cancer development by enabling antitumor responses by increasing immune recognition of cancer, influencing hormonal-dependent growth of endocrine tumors, and altering sterol biosynthesis due to the structural similarities of the phytosterols with these compounds and their substrates . Phytosterols have also been shown to directly inhibit tumor growth by slowing cell cycle progression, by induction of apoptosis, and by the inhibition of tumor metastasis .
Long-chain polyunsaturated fatty acids (PUFAs) also have important biological functions noted to modulate risks of chronic degenerative and inflammatory diseases, of which the essential PUFAs, linolenic (C18:3 n-3) and linoleic (C18:2 n-6) acids, are best described [30, 33]. Both of these were present in the A. vera leaf gel extracts, with linoleic acid being the major fatty acid present. However, despite this, the concentrations of these are still very low in comparison to the other compounds identified with possible health benefits and were not even detectable in the lipophilic ORAC analysis. These fatty acids may probably be too low for the A. vera leaf gel to contribute to health through its fatty acid composition. In conclusion, the results of this study show that from an analytical perspective, 95% ethanol is a less efficient solvent for the extraction of the phytochemical components of A. vera leaf gel for descriptive purposes as compared to ethyl acetate/diethyl ether or hexane (in the case of fatty acids). Although the 95% ethanol extracts contain a smaller variety of extracted compounds, their concentrations are, however, approximately 345 times higher than those of the lyophilized A. vera leaf gel when quantified as dry mass ELGE extract. This justifies the popularity of the ELGE for applications testing biological efficacy in vivo and in vitro. For the purpose of determining possible biological application, A. vera leaf gel was characterized.
Various phenolic acids/polyphenols, phytosterols, fatty acids, indoles, alkanes, pyrimidines, alkaloids, organic acids, aldehydes, dicarboxylic acids, ketones, and alcohols were identified and quantified. Due to the presence of the antioxidant polyphenols, indoles, and alkaloids, the A. vera leaf gel shows antioxidant capacity as confirmed by ORAC and FRAP analyses. Both GC-MS and spectrophotometric analyses show the non-flavonoid polyphenols to contribute to the majority of the total polyphenol content. Due to the occurrence of the polyphenols, phytosterols, and perhaps the indoles present, A. vera leaf gel may show promise in alleviating or preventing the symptoms associated with cardiovascular diseases, cancer, neurodegeneration, and diabetes. This may be due to the well-documented lowering effects of these compounds on total cholesterol, LDL-C, and fasting blood glucose. These results support the current use of A. vera by both industry and traditional healers for the treatment of the above-mentioned diseases. However, further clinical trials regarding these claims are necessary before accurate conclusions regarding these heath benefits can be made.
The financial support of the National Institute of Genetic Engineering and Biotechnology (NIGEB), Iran, was greatly appreciated.
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