Dominant compounds of
Medicinal plants have a long tradition of use in folk and conventional medicine. In recent years numerous studies confirm various bioactivities of natural products, among them antibacterial activity. Natural antibacterial agents such are essential oils and isolated compounds now represent a notable source for pharmaceutical and food industry and are widely used in cosmetology. They meet standards of 'green consumerism' together with excellent antibacterial activity. Aromatic plants such is Thymus vulgaris L. are the major sources of essential oils. Thyme essential oil, as well as dominant compounds thymol and carvacrol are generally recognised as safe and have been registered by European Commission for use as flavouring agents in foodstuffs. However, essential oil is present in very low amount (0,8-2,6%) in thyme leaves. Thus, the majority of plant material remains unused after the isolation. Nowadays, the biological potential of various plant waste materials are in focus of numerous studies. These investigations also include the antimicrobial activity considering the fact that waste material extracts represent the valuable source of different phenolic compounds. Regarding all this, the aim of the present study was to determine antibacterial potential of chemically characterised extracts obtained from waste material remaining after the preparation of drug (stems) and isolation of thyme essential oil (deodorised leaves, postdistillation decoction) on selected bacterial strains. Also, in order to determine safety of waste extracts their cytotoxicity was investigated. All extracts were prepared with maceration using 45% or 75% ethanol (EtOH) for 24 h at room temperature (1:10 w/v). Total phenolic compounds and flavonoids were determined spectrophotometrically. Extracts were chemically characterized by HPLC/DAD analysis. Antibacerial testing was done with broth dilution method against several bacterial strains (Staphylococcus aureus, Bacillus cereus, Salmonella infantis, Escherichia coli and Campylobacter jejuni). Cytotoxicity and cytoprotection studies were performed by XTT assay. Result of HPLC analysis showed that investigated extracts, especially those obtained from deodorised leaves represent a valuable source of rosmarinic acid and luteolin 7-O-glucuronide. Antibacterial testing indicated that all waste material extracts, except the extract T2, possess similar or even stronger bacteriostatic activity than T1. No cytotoxicity nor cytoprotection were determined. In conclusion, results of this study confirmed antibacterial potential investigated thyme extracts. High concentrations of rosmarinic acid and luteolin 7-O-glucuronide, which both have numerous pharmacological activities, were determined. This indicates that thyme postdistillation waste material extracts could be used for isolation of dominant compounds or as addities in pharmaceutical and food industry.
- aromatic plants
- postdistillation waste
- antibacterial potential
Plants have been used as food, spice, and medicine since ancient time. Much before the discovery of the existence of microorganisms, plants were an integrated part of the traditional medicine of many communities used for the treatment of various infectious diseases. Likewise, the use of plants as spices, not only affected the organoleptic properties of food, but it was also one of the ways for its preservation . Today, modern consumers demand food that will be minimally processed and contain, as much as possible, additives of natural origin that unlike synthetic ones, will be safe and ecologically acceptable. Also, the approach in raising livestock and production of food of plant origin is shifting towards the use of traditional methods in protection against pests and diseases . In addition, the irrational use of antibiotics not only in human and veterinary medicine, but also to promote growth in agriculture, has led to more frequent occurrence of resistance to conventional antibiotics of some pathogenic microorganisms [3, 4, 5] such are
Aromatic plants such as
|γ-Terpinene||7.3–1.87||12, 16, 17|
|1, 8-Cineole||0.8–2.17||16, 17|
|Linalool||2.03–6.8||12, 16, 17|
|Carvacrol methyl ether||3.9||12|
|Thymol||35.51–47.9||12, 16, 17|
|Caryophyllene oxide||0.33–4.6||12, 17|
The percentage of the major constituents varies greatly, depending on numerous complex factors, both endogenous and exogenous such are: chemotype, ontogenesis, geographic and climatic conditions, methods used for plant material processing, and essential oil isolation . Also, similar to other medicinal plants, the drug could be adulterated or replaced with other representatives of the genus
||0.2–2.5||250–2000||125–280||12, 21, 22|
||0.45–20||250–3755||125–375||3, 12, 21|
||0.45–1.25||250–2000||125–560||12, 21, 22, 23|
Thyme essential oil, thymol, and carvacrol are generally recognised as safe (GRAS status) and have been registered by the European Commission for use as flavouring agents in foods . GRAS is a rigorous process that relies on common knowledge and expert consensus about the safety of the substance for its intended use. Well-conducted toxicology studies are one of the factors that are used to assess the safety of various natural products, for example, plant extracts or essential oils that are composed of a mixture of tens or hundreds of compounds .
In recent years, numerous studies confirm various bioactivities of thyme essential oil and isolated dominant monoterpenes, among them antibacterial and antifungal activity, together with the inhibition of mycotoxin production (Table 2) [3, 12, 16, 21, 23, 26, 27, 28]. Generally, most of the essential oils used in the pharmaceutical, cosmetic, and food industries possess strong antioxidant activity and represent a notable source of natural additives for different products [12, 29, 30]. What is more important is that they meet standards of 'green consumerism' . However, the essential oil is present in very low amounts (0.8%–2.6%) in thyme leaves. Thus, the majority of plant material remains unused after the isolation.
On the other hand, thyme leaves are found to be a rich source of various phenolic compounds, particularly phenolic acids, flavonoids, and other secondary metabolites that are expected to contribute to its biological activities (Table 3) .
Rosmarinic acid is an ester of caffeic acid and 3,4-dihydroxyphenyllactic acid (Figure 5) widely found in the plant kingdom and presumably accumulated as a defense compound. In the Lamiaceae family, the occurrence is mainly restricted to the subfamily Nepetoideae  and it is identified as one of the active components of several aromatic medicinal plants (e.g.,
|Butanol-soluble fraction||Acetophenone glycosides (Androsin, Picein, glycosides of 4-hydroxyacetophenone derivatives)|||
|Methanol, reflux, residue was extracted with distilled water at 100°C for 2 h||Acidic polysaccharide|||
|Acetone using a Polytron homogenizer for 1 min||Caffeic acid, Luteolin, Rosmarinic acid, Hispidulin|||
|CH2Cl2 soluble fraction||5,4`-Dihydroxy-6,7,8-trimethoxyflavone, 5,3`,4`-Trihydroxy-7-methoxyflavone, 5,4`-Dihydroxy-6,7,3`-trimethoxyflavone, 5,4`-Dihydroxy-6,7,8,3`-tetramethoxyflavone|||
|Extracted at 20°C with 1L of EtOH-H2O-HOAc (80:19:1) under N2 for 5 days; further fractionation||Rosmarinic acid, 3`-
|Methanol; 1 day at room temperature||biphenyl compounds (e.g. 3,4,3`,4`-tetrahydroxy-5,5`-diisopropyl-2,2`-dimethylbiphenyl)|||
|Deodorised aqueous extracts||Total phenolics (mg/g gallic acid equivalents)|||
|Methanol extract||Monoterpene glucosides (p-Cymenol-9-O-β-glucoside, 2- and 5-O-β-glucosides of thymoquinol, angelicoidenol-O-β-glucoside); Arbutin|||
|Ethanol/water (30:70, v/v) with the aid of sonication for 10 min||Rosmarinic acid, Caffeic acid|||
|methanol extract||compounds related to hydroxyjasmone (e.g. 5-hydroxyjasmone-5-O-ß-glucoside) and simple phenol glucosides (3-Hydroxy-4-methoxyphenethyl-3-O-ß-glucoside, eugenol-O-ß-glucoside, syringin)|||
|Methanol, 20 min, 60°C in a water bath with shaking||Luteolin-glucoside, Rosmarinic acid, Eriodictyol, Luteolin, Apigenin|||
|Methanol, 6 h, Soxhlet apparatus||Oleanolic acid, Ursolic acid|||
|aqueous extracts (boiling water), 30 min||Luteolin-7-O-glucuronide, Lithospermic acid, Rosmarinic acid, Caffeic acid|||
|Aquous, aq. methanolic, methanolic (1:100 or 1:200); infusion, hot methanolic, usage of ultrasonic bath for 15 or 30 min||Arbutin, Hydroquinone, Naringenin, Naringenin-7-O-ß-glucoside, Narirutin, Eriodictyol, Eriodictyol-7-O-ß-glucoside, Eriocitrin, Hesperidin, Luteolin, Luteolin-7-O-ß-glucuronide, Luteolin-7-O-ß-rutinoside, Rosmarinic acid, Methyl rosmarinate, Caffeic acid|||
|95% ethanol at 60°C for 2 h with stirring||Total phenolics (mg/g sinapic acid equivalents)|||
|Liquid nitrogen powdered samples were extracted with acidified methanol||Caffeic acid, Rosmarinic acid|||
Chlorogenic acid (5-O-caffeoylquinic acid) is a natural antioxidant that is produced in various plants as a response to pathogen microorganisms, different mechanical impairment, or excessive exposure to light (Figure 5) . Due to these characteristics, chlorogenic acid found its use in pharmaceutical and food industries, as well as in cosmetology . Gallic and ferulic acids are also proven antioxidant agents (Figure 3) .
Furthermore, many beneficial properties have been identified for flavonoids (e.g., quecetin and rutin as the most widely distributed in nature) (Figure 2), and one of the most popularly cited property is their antioxidant activity. Other actions that are proposed to contribute to their biological effects include chelating metal ions, stimulating phase II detoxifying enzyme activity, and inhibiting proliferation and inducing apoptosis. Also, for some of the flavonoids where anti-inflammatory activity has been confirmed, they decrease the vascular cell adhesion and molecule expression, increase endothelial nitric oxide synthase activity, as well as inhibit platelet aggregation .
Specifically, it is determined that luteolin (3',4',5,7-tetrahydroxyflavone) exhibit notable antioxidant, antimicrobial, and anti-inflammatory activities . Also, there is some evidence that apigenin and luteolin act as antimutagenic and anticarcinogenic agents (Figure 4) .
Since various plant extracts and isolated natural compounds are widely used and represent one of the major approaches in alternative and complementary medicine that are also accepted by conventional medicine, their quality, efficacy, and safety are of the utmost importance . Safety issues are especially significant due to increasing body of evidence on side effects and interactions between herbal remedies or/and food or conventional drugs. These interactions sometimes can be very serious. They may lead to increased or lack of action of conventional drugs and caution must be taken in the application of plant extracts .
Nowadays, the biological potential of various plant waste materials is the focus of numerous studies. This trend includes not only the examination of aromatic plants [43, 60, 61, 62], but also different fruits and plant products such as wine, olives, beetroot, tomato, garlic, and pomegranate [63, 64, 65, 66]. These investigations also include their antimicrobial activity, considering the fact that waste material extracts represent the valuable source of different phenolic compounds. These studies are important, both in terms of economy and ecology, in order to elucidate the way to exploit post-distillation waste material of aromatic plants and other plant waste materials more efficiently.
The aim of the present study was to determine the antibacterial potential of chemically well-characterised extracts obtained from waste material that remain after the preparation of the drug
2.1. Plant material and extract preparation
In July 2013, aboveground parts of thyme (
After the maceration, extracts were collected, filtered, and evaporated to dryness under vacuum. The quantities of dry extracts were determined gravimetrically. Residues were dissolved in water to make 10% (w/v) stock solutions for further investigation. For the high-performance liquid chromatography (HPLC analysis), residues were dissolved in methanol, 1% formic acid mixture (50:50 v/v) to make 2% (w/v) stock solutions.
2.2. Chemical composition
2.2.1. Determination of total phenolic compounds and total flavonoid content
The amount of total phenolic compounds in investigated extracts was determined spectrophotometrically with Folin-Ciocalteu (FC) reagent . The concentration of total phenolic compounds was expressed in mg of gallic acid equivalents (GAE) per g of dry extract (d.e.), using a standard curve of gallic acid (concentration range 0.08–0.24 mg/mL). Total flavonoid content was also determined spectrophotometrically using a method based on the formation of a flavonoid-aluminium complex with an absorptivity maximum at 430 nm . Flavonoid content was expressed in mg of quercetin equivalents (QE) per g of dry extract, using a standard curve of quercetin (concentration range 10–100 μg/mL). All measurements were done in triplicate.
2.2.2. HPLC/DAD analysis
Investigated thyme leaves extracts are rich in a wide range of phenolic compounds . Therefore, a method that allows simultaneous detection of various phenolics in a single run was developed. This decreases the time necessary for analysis and reduces the analysis costs . HPLC analysis was performed using a liquid chromatograph (Agilent 1200 series), equipped with diode array detector (DAD) and Eclipse XDB-C18, 1.8 μm, 4.6×50 mm column, at a flow-rate of 1 mL/min. Solvent gradient was performed by varying the proportion of solvent A (methanol) to solvent B (1% formic acid inwater (v/v)) . The total running time and post-running time were 45 and 10 min, respectively. The column temperature was 30ºC. The injected volume of samples and standards was 5 μL and it was done automatically using an autosampler. The spectra were acquired in the range of 210–400 nm and chromatograms plotted at 280, 330, and 350 nm with a bandwidth of 4 nm, and with reference wavelength/bandwidth of 500/100 nm. Quantification of selected phenolics: gallic acid, protocatechuic acid, caffeic acid, chlorogenic acid, syringic acid,
2.3. Antibacterial testing
2.3.1. Bacterial strains and growth conditions
Selected bacterial strains, namely
2.3.2. Broth microdilution method
Antimicrobial test systems should ideally be simple, reproducible, rapid, and inexpensive . Several methods are currently available to determine antimicobial activity of different plant extracts or isolated pure compounds. Since they are not based on the same principle, the obtained results are influenced not only by the selected method, but also by the microorganism used, as well as by the extraction procedure (polar or non-polar extracts, essential oils, etc.) or the solubility of the tested compound . In order to avoid overemphasizing the usefulness of various plant extracts or isolated compounds as antimicrobials, applied methods, both for extraction and antimicrobial testing, should be standardised to obtain comparable and reproducible results, prior to their
For the broth microdilution test, 50 μL of each bacterial suspension in suitable growth medium was added to the wells of a sterile 96-well microtitre plate already containing 50 μL of two-fold serially diluted standardised (T1) and post-distillation waste thyme extracts (T2, T3, T4, and T5) in proper growth medium. The final volume in each well was 100 μL. Control wells were prepared with culture medium, bacterial suspension only, plant extracts only, and ethanol in amounts corresponding to the highest quantity present. The contents of each well were mixed on a microplate shaker (Eppendorf, Hamburg, Germany) at 800 rpm for 1 min prior to incubation for 24 h in the cultivation conditions described above. The MIC was the lowest concentration where no viability was observed after 24 h on the basis of metabolic activity. To indicate respiratory activity, the presence of colour was determined after adding 10 μL/well of INT (Sigma) dissolved in water (INT 2 mg/mL) and incubated under appropriate cultivation conditions for 30 min in the dark . To determine the ATP activity, the bioluminescence signal was measured by a Microplate Reader (Tecan, Mannedorf/Zurich, Switzerland) after adding 100 μL/well of BacTiter-Glo™ reagent (Promega, Madison, USA) after 5 min of the incubation in the dark . Positive controls were wells with a bacterial suspension in an appropriate growth medium and a bacterial suspension in an appropriate growth medium with ethanol in amounts corresponding to the highest quantity present in the broth microdilution assay. Negative controls were wells with growth medium and plant extract. All measurements of MIC values were repeated in triplicate. Results are expressed in mg of total phenolics (TP).
2.4. Cytotoxicity studies
2.4.1. Cell culture
Human MRC-5 lung fibroblasts were grown in Minimum Essential Medium (MEM, Gibco, Invitrogen, Austria) supplemented with 2 mM of L-glutamine (Sigma, MO, USA), 10% of heat-inactivated fetal bovine serum (FBS, PAA laboratories, Austria), 100 units/mL of Penicillin (PAA laboratories), and 100 µg/mL of Streptomycin (PAA laboratories) (1% Pen/Strep). Cells were kept in a humidified 5% CO2 atmosphere at 37°C and passaged at 90% confluence. Passages P26 and P27 were used for the assays.
2.4.2. XTT assay for the determination of cytotoxicity
An automated microculture tetrazolium assay (MTA) has long been used for the
Cell proliferation kit II (XTT) (Cat. No. 11 465 015 001) was obtained from Roche Diagnostics (Mannheim, Germany). Aliquots (100 µL) of 1x105 cells/mL were seeded into 96 well plates (flat bottom) and grown for 24 h before the extracts were added. Afterwards, cells were incubated for 4 h or 24 h with investigated thyme extracts (20 µg/mL) before XTT solution was added. The XTT solution consisted of a XTT labeling reagent and an electron-coupling reagent and was always freshly prepared. XTT is a yellow tetrazolium salt and cleaved by metabolic active cells into an orange, water-soluble formazan dye. Since these color changes only occur in viable cells, it can be directly quantified using a scanning multiwell spectrophotometer . Numbers of viable cells were determined with the following formula and expressed as percentage of control :
Absorbance of treated cells/Absorbance of untreated cells x 100
Control cells represent vehicle-treated cells. Vehicle was 0.5% of DMSO (final concentration), which did not affect the cells as shown by control experiments.
2.4.3. Cytoprotection assay
Aliquots (100 µL) of 1x105 cells/mL were seeded into 96 well plates (flat bottom) and grown for 24 h before the extracts (20 µg/mL) were added for 4 h or 24 h. Afterwards, the medium with the extracts was removed and replaced by 100 µl of a H2O2 solution (50 µM, 100 µM, 200 µM or 500 µM) in MEM medium and further incubated for 2 h or 24 h. To finally determine the cell viability, XTT solution was added and analyzed as described above.
2.5. Statistical analysis
The data were reported as mean values ± standard deviation (SD) and processed using Microsoft Office Excel for Windows v. 2007.
3.1. The amount of dry extract
The amounts of dry extracts obtained by maceration of thyme leaves (T1), deodorised thyme leaves (T3 and T4), and thyme stems (T5) and post-distillation extract remaining after the evaporation of thyme decoction (T2) are shown in Table 4. Generally, the amount of dry extract T1 is in accordance with previously published data, considering the fact that numerous factors could influence the extraction yield [47, 83]. When the thyme waste extracts were analyzed, the highest amount was obtained in T2 . The difference in the extraction yield between T1 and T2 may be due to the mere extraction process since T2 is obtained after hydrodistillation of thyme leaves that favours extraction of polar substances, but also present carbohydrates genuine to the leaves or generated after hydrolysis of present glycosides. Deodorised leaves and stems yield a smaller amount of dry extracts when compared to T1.
3.2. Total phenolic compounds and flavonoid content
Spectrophotometric methods used are simple and reproducible for rough screening of total phenolic compounds and total flavonoids before detailed chemical analysis. The results are presented in Table 4. Total phenolic compounds in examined thyme leaves and stem extracts varied from 35.69 (T2) to 62.45 (T4) mg GAE/g d.e., while total flavonoids were in the 11.31 (T5)–52.89 (T3) mg QE/g d.e. range. Interestingly, deodorised leaves extracts (T3 and T4) have a relatively high content of total phenolic compounds and total flavonoids when compared to T1. The extract T2, for which the highest amount of dry extract was determined, is poor in total phenolic compounds and total flavonoids when compared to T1, but also to T3 and T4 [43, 51]. However, when absolute amounts (in plant material) are considered, T2 may also represent a valuable source of phenolic compounds and flavonoids. Stem extract (T5) have relatively high total phenolics, while are poor in total flavonoids.
3.3. HPLC analysis
The qualitative-quantitative data from the chromatographic analyses are presented in Table 5, with representative chromatograms for T1 and T3 (Figure 7). The following components: gallic, protocatechuic, caffeic, chlorogenic, syringic,
Regarding the hydroxybenzoic, hydroxycinnamic acids, and caffeic acid oligomers, rosmarinic acid was identified as the major component in all the investigated thyme extracts and was present within the range of 52.36 (T5) to 105.08 (T4) mg/g d.e, which is similar to the previously published data for officially prepared thyme extracts (T1) . Also, gallic, ferulic, and chlorogenic acids were present in considerable amounts. In general, 75% EtOH extract of the deodorised leaves (T4) abundant in rosmarinic, chlorogenic, and ferulic acid, whilst 45% EtOH contained higher amounts of gallic acid. In the flavonoid fraction, luteolin 7-O-glucuronide was the dominant and the second major identified component in all investigated extracts (from 11.01 (T5) to 87.11 (T4) mg/g d.e.). Similarly to the total phenolic content, the highest amounts of almost all quantified components, especially the dominant ones were determined in deodorised leaves extracts (T3 and T4). Also, although the stem is confirmed to be relatively poor in phenolic compounds, chlorogenic and ferulic acids are present in considerable amounts.
3.4. Antibacterial testing
Numerous studies have confirmed the use of herbs and spices as anti-infective agents . Among them, different essential oils and phenolic compounds, or plant extracts rich in phenolic compounds stand out for their antibacterial activity [85, 86]. This is particularly important, given that phenolic compounds possess a strong antioxidant potential. This joint action is significant for their usage in pharmaceutical and food industries, but also in all other fields where it is important to prevent both oxidation and contamination of certain products .
All investigated post-distillation thyme waste extracts exhibited relatively strong antimicrobial potential, against all tested bacterial strains, especially deodorised leaves extracts (T3 and T4) (Table 6) . Also, thyme stem extract (T5) expressed notable antibacterial action. What is more important, by comparing these results with the data obtained for butylhydroxytoluene (BHT), often used as a synthetic additive, antibacterial potential of thyme post-distillation waste material extracts becomes even more evident. Also, interestingly, all investigated thyme extracts showed lower minimal inhibitory concentration on all investigated bacterial strains when compared to isolated rosmarinic acid. This may indicate that phenolic compounds possess a synergistic antibacterial effect, which is important in terms of emerging occurrence of resistance.
Despite many recent technological advances in the food industry, which have contributed to increased safety in the food supply chain, we are still facing high incidence of foodborne illnesses. In 2011 alone, there were 69,553 human cases originating from foodborne zoonotic outbreaks in the EU . Ninety-three of them were fatal. In the same year,
Two selected extracts, T3 prepared from deodorised leaves and T1 as an officially prepared one, were tested against
3.5. Cytotoxicity studies
Cancer is a leading cause of death worldwide and sustained focus is on the discovery and development of newer and better-tolerated anti-cancer drugs, especially from plants. About 50% of all anti-cancer drugs approved internationally are either natural products or natural product mimics. They were developed on the basis of the knowledge obtained from small or macromolecules existing in nature .
The major challenges associated with currently available anti-cancer agents include selectivity, toxicity, resistance, and development of a secondary malignancy. These drawbacks have motivated the search for newer, more efficacious, and better tolerated anti-tumor drugs, with natural products, especially plants, offering an inexhaustible reservoir for new drug discovery and development. Also, molecular targeted agents are currently being studied in all treatment settings including that of chemoprevention, which is defined as the use of natural or synthetic nonessential dietary agents to interrupt the process of carcinogenesis and to prevent or delay tumor growth .
The effects of investigated post-distillation thyme waste extracts against human MRC-5 lung fibroblasts are presented in Figures 8–15. Cytotoxicity of the extracts, a possible reaction with the XTT solvent and a potential cytoprotective activity were evaluated. As shown in Figure 8, none of the investigated extracts at concentrations of 20 µg/ml exhibited cytotoxicity after 4 h or 24 h of incubation. To exclude a direct reaction of the extracts with the XTT solvent and, therefore, false-negative results, extracts and XTT solution were mixed in culture medium and incubated for 4 h or 24 h. There were no significant differences in the absorbance values of medium and XTT alone compared to DMSO (control) or extracts (20 µg/ml) in medium (Figure 9) that reveals that the extracts did not interact with the XTT solution.
Finally, a potential cytoprotective effect of the extracts was investigated. Cells were incubated with the extracts for 4 h or 24 h and cytoprotection was evaluated by adding different concentrations of H2O2, which is a well-known cell damaging agent causing oxidative stress.
The effects were compared to vehicle-treated (DMSO) cells (control) and to H2O2 treated cells (H2O2 control). As shown in Figures 10–15, none of the investigated extracts exhibited notable cytoprotective activity.
4. Further research
Results of microbiological tests indicate the possibility to use thyme postdistillation waste extracts primarily in the food or pharmaceutical industry as natural additives, regarding the relatively strong antibacterial activity on investigated bacterial strains.
Also, examined extracts represent a valuable source of phenolcarboxylic acids and flavonoids, which have numerous biological effects. Therefore thyme post-distillation waste material could be used for the isolation of rosmarinic acid and luteolin 7-O-glucuronide, as dominant compounds.
However, only limited data are presently available on the antimicrobial activity of plant extract in food systems and this indicates continuation of our study and the need for further work. Additionally, there is growing evidence on synergistic action of different plant products (extracts, essential oils, isolated compounds) with each other or with conventional antibiotics used in human and veterinary medicine . Besides, it would be very interesting to collect more data on the efficiency of both thyme essential oil and investigated thyme extracts as a dietary supplementation in animal feed on protective or prebiotic effects on the gut microflora. Also, it is important to test their influence on antioxidant and antimicrobial stability and shelf life of meat and meat products [93, 94, 95].
Furthermore, the results of our study recorded neither cytotoxicity, nor cytoprotection of examined extracts. Yet, detailed in vivo toxicology analyses are required in order to confirm the safety of usage of thyme postdistillation waste material.
The authors are thankful to the research agencies of Slovenia, Serbia, and Austria for financing the bilateral projects BI-034-SLO-SR-2010/2011 and WTZ SI 03/2011 and to the The Provincial Secretariat for Science and Technological Development of Vojvodina (grant number: 114-451-2056/2011-01).
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