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Article

Validation of Broth Macrodilution Volatilization Method for Testing of Essential Oils in Liquid and Vapor Phase: Chemical Composition, Cytotoxicity, and Antibacterial Effect of Indian Medicinal Plants against Pneumonia-Causing Pathogens

by
Aishwarya Chaure
1,
Marketa Houdkova
1,
Julien Antih
1,
Klara Urbanova
2,
Ivo Doskocil
3,
Mukund Lal Naik
4,
Khageshwar Singh Patel
5 and
Ladislav Kokoska
1,*
1
Department of Crop Sciences and Agroforestry, Faculty of Tropical AgriSciences, Czech University of Life Sciences Prague, 16500 Prague, Czech Republic
2
Department of Sustainable Technologies, Faculty of Tropical AgriSciences, Czech University of Life Sciences Prague, 16500 Prague, Czech Republic
3
Department of Microbiology, Nutrition and Dietetics, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, 16500 Prague, Czech Republic
4
National Center for Natural Resources, Pt. Ravishankar Shukla University, Raipur 492010, India
5
Department of Applied Sciences, Amity University, Manth (Kharora), State Highway 9, Raipur 493225, India
*
Author to whom correspondence should be addressed.
Molecules 2023, 28(12), 4625; https://doi.org/10.3390/molecules28124625
Submission received: 10 May 2023 / Revised: 2 June 2023 / Accepted: 5 June 2023 / Published: 7 June 2023
(This article belongs to the Special Issue Antimicrobial Activity of Plant Volatiles in Vapor Phase)
Browse Figure
Versions Notes

Abstract

:
Essential oils (EOs) have great potential in inhalation therapy for the treatment of respiratory infections. However, innovative methods for evaluation of antimicrobial activity of their vapors are still needed. The current study reports validation of the broth macrodilution volatilization method for assessment of the antibacterial properties of EOs and shows the growth-inhibitory effect of Indian medicinal plants against pneumonia-causing bacteria in liquid and vapor phase. Among all samples tested, Trachyspermum ammi EO exhibits the strongest antibacterial effect against Haemophilus influenzae, with minimum inhibitory concentrations of 128 and 256 µg/mL in the liquid and vapor phases, respectively. Furthermore, Cyperus scariosus EO is found to be nontoxic to normal lung fibroblasts assessed by modified thiazolyl blue tetrazolium bromide assay. Chemical analysis performed using gas chromatography–mass spectrometry identified α-citral, cyperotundone, and thymol as the main constituents of Cymbopogon citratus, C. scariosus, and T. ammi EOs, respectively. In addition, β-cymene is identified as the major compound of T. ammi EO vapors when analyzed using solid-phase microextraction and gas-tight syringe sampling techniques. This study demonstrates the validity of the broth macrodilution volatilization method for antimicrobial screening of volatile compounds in the vapor phase and suggests the therapeutic potential of Indian medicinal plants in inhalation therapy.

1. Introduction

Pneumonia is defined as acute infection of the lung parenchyma [1], typically caused by bacterial species including gram-positive Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, and gram-negative Haemophilus influenzae [2]. It is a major health problem associated with high morbidity and mortality, especially in developing countries, where vulnerable populations such as children of <5 years of age and older adults with prior chronic conditions are at great risk [3]. In the year 2020, India alone contributed 23% of the global pneumonia burden with case fatality rates between 14 and 30% [4]. The general approach in the treatment of pneumonia includes the timely administration of appropriate antibiotic therapy. Recently, nebulized antibiotics have become preferred over intravenous and oral therapies, as they allow high pulmonary efficacy and minimal systemic side effects [5]. Antibiotics currently marketed for inhalation treatment of chronic Pseudomonas aeruginosa infections include tobramycin, colistin, and aztreonam. Although both the U.S. Food and Drug Administration (FDA) and European Medicines Agency have approved their use for cystic fibrosis, they have not been approved in other disease areas because of a lack of supportive clinical trial evidence [6]. Moreover, other problems are associated with the distribution and deposition of aerosol particles, whose size plays a major role in efficient delivery. For example, larger particles preferably accumulate in the oropharyngeal area, while smaller particles deposit in the lower airways, which alters drug delivery, as small particles carry fewer active substances. In addition, patient-related factors such as age, physical capability, disease severity, and the cognitive ability of the patient to perform specific inhalation affect drug delivery [7].
Essential oils (EOs) can be promising sources for the development of new inhalation preparations, as the physical property of being volatile at room temperature enables them to freely distribute among the lung tissues [8]. Therefore, in contrast with nebulized antibiotics, EO vapors allow easy inhalation and uniform distribution of active substances in the upper and lower parts of the respiratory tract [9]. Furthermore, due to their antimicrobial and anti-inflammatory potency in the vapor phase, they offer effective treatment for various respiratory infections. In the last few years, several inhalation devices using a combination of different EOs have been developed and patented. For example, adhesive inhalation antiviral patches (Axogen Inc., Alachua, FL, USA), which contain safe and effective amounts of EOs obtained from plant species such as Cinnamomum verum J. Presl, Citrus limon (L.) Osbeck, Gaultheria procumbens L., Matricaria recutita L., Mentha × piperita L., Salvia sclarea L., Syzygium aromaticum (L.) Merr. & L.M. Perry, and Zingiber officinale Roscoe are usually placed near the nasal pathway with the application of an appropriate mask, which prevents the entry of various respiratory-infection-causing pathogens [10]. In addition, various herbal products based on EOs, e.g., GeloMyrtol (G. Pohl-Boskamp, Hohenlockstedt, Germany) and Bronchipret (Bionorica, Neumarkt, Germany), are recommended for the treatment of acute and chronic bronchitis [11]. EOs are very complex natural mixtures of compounds that work in synergy to provide various medicinal properties. They are mainly composed of aromatic and aliphatic compounds, hydrocarbon terpenes (isoprenes), and terpenoids (terpene hydrocarbons such as phenols, alcohols, ketones, aldehydes, acids, esters, and ethers) [12]. Especially the phenolic monoterpenoids, such as carvacrol and thymol, have been reported to exhibit a strong antibacterial effect in the vapor phase against pathogens that cause pneumonia [13]. The bioactivity of EOs depends greatly on their chemical composition, which makes the chemical characterization of volatile components an important work [14]. Nowadays, static headspace extraction, coupled with the gas chromatography–mass spectrometry (S-HS-GC/MS) technique, is commonly used to investigate EO vapors. It is a simple, rapid, and solventless technique that requires a small amount of sample and allows the analysis of highly volatile compounds [15]. Correspondingly, several studies have explored the chemical composition of EO vapors with the aim to find the most prominent volatile compounds responsible for antibacterial activity in the vapor phase using S-HS-GC/MS. For example, a study conducted by Schweitzer et al. [16] has explored the chemical composition of C. citratus EO vapors using solid-phase microextraction followed by GC/MS. Using this technique, citral, α-terpineol, γ-cadinene, and calamenene have been found to be the major components of EO vapors that are attributed to their antibacterial and antifungal activities. In another study, chemical investigation of T. ammi EO has been conducted using headspace–solid phase microextraction (HS-SPME) coupled with GC/MS, where γ-terpinene, p-cymene, and thymol were found to be major compounds [17].
In terms of plant diversity, 1500 species have been reported to have medicinal uses in India [18], many of which have not been phytochemically and pharmacologically explored [19]. Indian Ayurvedic medicine has a long tradition in the management of various respiratory diseases using poly-herbal preparations and multicomponent therapeutics. Several pharmaceutical companies are manufacturing and marketing different Ayurvedic formulations [20]. For example, Bresol-NS (Himalaya, Bengaluru, India), a nasal spray with a combination of Coleus aromaticus Benth., Eucalyptus globulus Labill., and Glycyrrhiza glabra L. extracts, helps relieve nasal congestion caused by upper respiratory tract infections. Administration of drugs through the nasal route is an integral part of Ayurvedic practices such as dhumpana (medicinal smoking), nasya (nasal administration of therapeutic oil), and dhupanartha (herbal fumigation). In addition, ethnobotanical evidence of using vapor-based medicines has been well-documented in northeast India. For example, in Manipur, the people of the Meitei community use leaves of Phlogacanthus thyrsiflorus Nees for steam inhalation in the treatment of pneumonia. Similarly, the stems of Clerodendrum indicum (L.) Kuntze and Rotheca serrata (L.) Steane & Mabb. are inhaled via smoke for treatment of acute bronchitis [21]. Among various plant species used in Indian traditional medicine for the treatment of respiratory infections, Cymbopogon citratus (DC.) Stapf and Trachyspermum ammi (L.) Sprague and certain species of genera Cyperus (e.g., Cyperus rotundus L.) are common ingredients for vapor-based medicines [22,23,24]. In correspondence with their traditional use, the antibacterial potential of EO vapors of the above-mentioned species has been previously reported in several in vitro experiments. For example, a study performed by Inouye et al. [25] assessed the growth-inhibitory effects of C. citratus EO vapors against respiratory tract pathogens such as H. influenzae, S. aureus, S. pneumoniae, and S. pyogenes using the airtight box disc volatilization method. In another study, T. ammi EO vapors exhibited a growth-inhibitory effect against bovine respiratory bacterial pathogens using an agar plug vapor-phase assay [26]. However, the antibacterial potential of T. ammi and Cyperus scariosus R.Br. EO vapors against pneumonia-causing bacteria has not been fully explored yet. Moreover, the methods used for examining the antimicrobial effect of the above-mentioned EO vapors provided mainly qualitative results, or in the case of quantitative methods, the results were expressed in different ways, e.g., as a concentration of volatile agent per volume of air [25], and interpretation of results, including minimum inhibitory concentration (MIC) values, was varying greatly [27]. Although EOs and their compounds are usually considered as safe, and they are registered as generally recognized as safe (GRAS) products by the U.S. FDA, toxicological evaluations are still necessary to know the risks associated with direct inhalation of EOs or their constituents on lung tissues [28]. There are several studies describing the low cytotoxicity of C. citratus EO when tested in vitro on human non-cancer fibroblasts [29]; however, there are no data on toxicity of T. ammi and C. scariosus EOs to lung cells.
The current study reports an assessment of the antibacterial properties of selected EOs from Indian medicinal plants, namely C. citratus, C. scariosus, and T. ammi, with the aim to validate the newly developed broth macrodilution volatilization method for simultaneous testing of EOs in liquid and vapor phase against the bacteria causing pneumonia. Additionally, their major chemical constituents responsible for growth-inhibitory effects were identified using GC/MS, and the chemical profile of EO vapors was determined by a time series of headspace analyses including both HS-SPME and headspace–gas-tight syringe (HS-GTS) sampling techniques. Moreover, the cytotoxicity of EOs against normal lung fibroblasts using a modified thiazolyl blue tetrazolium bromide (MTT) assay was evaluated in this study.

2. Results

2.1. Antibacterial Activity and Cytotoxicity

The results showed that all EOs produced a certain level of in vitro growth-inhibitory activity against the pneumonia-causing bacterial strains included in this study. The effectiveness of EOs varied substantially in the MIC values ranging from 128 to 1024 µg/mL in the liquid phase and being equal or greater than 256 µg/mL in the vapor phase. Among all samples tested, T. ammi EO was found to be the most active with respective MICs of 128 and 256 µg/mL in the liquid and vapor phases against H. influenzae, followed by C. citratus EO with growth-inhibitory effect against H. influenzae with MIC 256 µg/mL in both phases. The C. scariosus EO exhibited weak antibacterial effect with MIC 1024 µg/mL in the liquid phase against all bacteria tested, while vapors of this EO were active against H. influenzae (MIC 1024 µg/mL) only. In general, a higher activity was observed in the liquid than in the vapor phase, and H. influenzae was the most susceptible bacterium to the EOs assayed. Complete results on the antibacterial activity of Indian EOs against respiratory pathogens in both liquid and vapor phases are shown in Table 1.
The results of a cytotoxicity assay showed that the values of half maximal inhibitory concentration (IC50) varied substantially for all EOs tested. C. scariosus EO was evaluated as nontoxic (IC50 > 258 µg/mL), whereas both C. citratus and T. ammi EOs were found to be moderately toxic with respective IC50 values of 19.63 and 82.04 µg/mL. Similarly, the highest 80% inhibitory concentration of proliferation (IC80) values were calculated for C. scariosus (IC80 ≥ 258 µg/mL). According to the WHO [30], the EOs were classified as nontoxic (C. scariosus) and moderately toxic (C. citratus and T. ammi). The therapeutic index (TI) calculated for comparison of the antibacterial and cytotoxic effects indicates safety of the C. scariosus EO (TI > 0.252). The detailed results of the cytotoxicity of EOs to lung fibroblasts are shown in Table 2 with a graphical presentation in Figure 1.

2.2. Chemical Composition

Based on GC/MS analysis of EOs from C. citratus (aerial part), C. scariosus (rhizomes), and T. ammi (seeds), a total of 17, 28, and 9 components were identified using HP-5MS column, which represents 99.62, 91.48, and 99.47% of their total respective contents. Similarly, using the DB-HeavyWAX column, 15, 36, and 13 components were determined, which constituted 68.77, 77.17, and 84.26% of the EOs, respectively. In total, 21 compounds were identified in the C. citratus EO, 40 compounds in C. scariosus EO, and 15 in T. ammi EO. The analysis showed that in C. citratus and T. ammi EOs, monoterpene hydrocarbons and oxygenated monoterpenoids were the predominated groups of chemicals, whereas sesquiterpene hydrocarbons and oxygenated sesquiterpenoids were major classes of compounds in C. scariosus EO. For both the columns, in C. citratus EO, α- and β-citral were the most abundant compounds with peak areas of (HP-5MS = 48.9 and 35.8%) and (DB-HeavyWAX = 24.3 and 33.2%), respectively. Caryophyllene oxide was the third abundant compound in the EO (~3%). In the case of C. scariosus EO, cyperotundone was the major component with peak areas of (29.1 and 28.9%), followed by caryophyllene oxide (19.8 and 17.54%) and cyperene with (9.9 and 8.5%), when measured using HP-5MS/DB-HeavyWAX columns, respectively. Thymol was the most predominant substance reported for both the columns with 51.2 and 45.8% in T. ammi EO, followed by β-cymene (22.6 and 17.1%) and γ-terpinene (21.5 and 17.6%) for HP-5MS/DB-HeavyWAX columns, subsequently. The complete chemical profiles of C. citratus, C. scariosus, and T. ammi EOs are provided in Table 3, Table 4 and Table 5, respectively.

2.3. Chemical Composition of T. ammi EO Vapors

In the current study, the composition of headspace above the mixture of T. ammi EO and Mueller–Hinton broth (MHB) has been carried out using HS-SPME and HS-GTS in a time series every 3 h during a 12 h period using the HP-5MS column. Using HS-SPME extraction, a total of six volatile compounds were identified in the EO sample, which represented 97.25% of their respective total constituents. When using the HS-GTS extraction method, a lower number (five) of compounds was detected, which accounted for 93.4% of their total content. Regardless of the extraction method used, monoterpenes were the most predominant chemical groups of volatile compounds identified in the headspace. Using the HS-SPME extraction method, β-cymene was the most abundant constituent of the headspace of T. ammi EO. The content of β-cymene gradually decreased during the whole experiment with the peak area value ranging from 49% (time—0 h) to 43% (time—12 h). Similarly, a slight decrease in the concentration of γ-terpinene, the second-most abounding compound in the sample, was observed during overtime incubation from 39 to 31%. In contrast, the concentration of the thymol increased in the vapor over the time from 4.9 to 12%. In the case of HS-GTS extraction, β-cymene, γ-terpinene, and β-pinene were detected as the predominant compounds. For β-cymene and γ-terpinene, a steady decrease in the concentrations was observed during the experiment, ranging from 52 to 45% and 35 to 28%, respectively. Although the concentrations of both most-abundant compounds are nearly similar to those obtained using the HS-SPME method, the third-most abounding compound differed for the HS-GTS extraction method, β-pinene being detected with peak area values ranging from 2 to 6.5%. Interestingly, the chemical analysis showed that content of thymol detected by HS-SPME extraction was much higher in comparison with HS-GTS extraction (nearly 10%). Apart from this, no discrepancies for either sampling method were observed, and there were no significant changes in the chemical composition in the vapor of T. ammi EO over time. A complete chemical profile of T. ammi EO vapors is provided in Table 6.

3. Discussion

T. ammi is a medicinal plant highly valued in traditional Ayurvedic medicine [23]. Its EO has been reported to have pivotal antibacterial properties against foodborne and spoilage bacteria; however, only a few studies have reported its effect against pneumonia-causing pathogens [33,34]. The current study suggests the significant antibacterial activity of T. ammi EO against the targeted bacteria in both liquid and vapor phases. The observed endpoints for the liquid phase correspond well with a previously published study reporting the MIC of T. ammi EO against S. aureus at 500 µg/mL [35] and within a three-dilution MIC range for S. pneumoniae (MIC = 250 µg/mL) [36]. According to our best knowledge, the antibacterial activity of T. ammi EO vapors was described for the first time in this study. Considering the toxicity, the current study reports that T. ammi EO is moderately cytotoxic to lung fibroblasts. This result corresponds with an in vivo study published by Vazirian et al. [37], who observed mild oral toxicity of the EO in a rat model. Regarding inhalation toxicity, the sources of information on the safety of EO vapors are scarce. However, data on its predominant compound, thymol, might suggest its possible inhalation safety. The European Chemicals Agency reported thymol to be nontoxic to mice when they are exposed to the chemical via inhalation of its vapor for 2 h with a lethal dose 50% (LD50) of 7.57 mg/L [38]. Moreover, another study published by Xie et al. [39] reported no evidence of chronic toxicity of thymol through inhalation in a mouse model. Nevertheless, further experiments on their in vivo inhalation toxicity are necessary to determine the safety of T. ammi EO. The biological properties of T. ammi EO are attributed to its chemical composition, which has already been studied. The chromatographic profile obtained in the current study corresponds with previously published reports identifying thymol as the main component (ranging from 54.32 to 67.4%), β-cymene as the second-most abundant compound (ranging from 17.9 to 21.74%, respectively), and γ-terpinene as third-most abundant component (ranging from 11.3 to 19.38%) [35,40]. Moreover, research led by Modareskia et al. [41] investigated the bioactive potential of different populations of T. ammi EO in liquid phase and reported that the antibacterial effects are mainly due to the presence of phenolic and hydrocarbon monoterpenes such as thymol, p-cymene, and γ-terpinene. β-Cymene, γ-terpinene, and thymol were identified as the key constituents of vapors of T. ammi EO in the sample obtained using the HS-SPME technique. This is well-corresponding with the results of Liu et al. [17], who reported γ-terpinene (26.21%), p-cymene (23.58%), and thymol (20.02%) as the major components of T. ammi EO vapor analysis by HS-SPME. Because the EO samples for headspace analysis performed in this study were prepared by dissolving them in microbiological growth medium, variances in the concentration of γ-terpinene can be attributed to the different experimental conditions [42]. Our paper identifying β-cymene, γ-terpinene, and β-pinene as predominant components of T. ammi EO vapors is the first report on its analysis using the HS-GTS method. When comparing both sampling techniques, the present study reports disparities with thymol concentration. In comparison with the HS-SPME method, the analysis of the sample collected by the HS-GTS technique showed a lower amount of thymol. The possible explanation may be that it was due to the sensitivity and affinity of SPME fibers toward certain volatile components [43]. In contrast, the HS-GTS technique is less selective but provides a precise and, perhaps, closer assessment of the real distribution of volatile compounds in vials [44]. These findings are consistent with the data published by Antih et al. [42], who performed Thymus vulgaris L. EO headspace analysis using similar experimental conditions. The antibacterial potential of volatile monoterpene hydrocarbons (p-cymene and γ-terpinene) and phenolic monoterpene (thymol) are well-known; for instance, the bioactivity of thymol in the vapor phase against respiratory tract bacteria such as H. influenzae, S. aureus, and S. pneumoniae has been previously published [13]. As mentioned before, the antibacterial activity of T. ammi EO and its vapors is mostly due to its composition; particularly, the presence of hydrocarbon and phenolic monoterpenes in high concentrations are related to the growth-inhibitory effect. Moreover, the current study also reports higher activity in the broth medium as compared to the vapor phase. This can be related to data obtained from the headspace analysis, where thymol, which is regarded as the main antimicrobial constituent, was detected in lower amounts in the EO vapors. The hydrophobic nature of thymol worsening its solubility in water-based media and, subsequently, reducing its volatility, can be a possible reason of lower antimicrobial activity [45].
C. citratus EO is extensively used in Ayurvedic medicine as a folk remedy for coughs, flu, and pneumonia [46]. Previously published studies have reported the antibacterial and anti-fungal properties of C. citratus EO [47,48]. As a result of the modified agar dilution method, Inouye et al. [48] observed a moderate growth-inhibitory effect of C. citratus EO against S. pyogenes (MIC = 400 µg/mL), H. influenzae, and S. pneumoniae (MIC = 800 µg/mL). In addition, C. citratus EO vapors were reported to be more efficient against H. influenzae as compared to S. aureus, S. pneumoniae, and S. pyogenes. Despite certain variances in the MIC values caused probably by different bacterial strains and antimicrobial assays used, these results correspond well with our findings. Regarding cytotoxicity, the current study reports that C. citratus EO is moderately toxic (IC50 = 19.63 µg/mL) to the lung fibroblasts. A previous study reported a similar mild cytotoxic effect on human fibroblast cell line WI38 with an IC50 value of 49.39 μg/mL [29]. The minor variance in the IC50 values can be attributed to the modification of the cytotoxicity assay previously recommended for evaluation of biological properties of the volatile agents. The use of EVA Capmat protects microtiter plates against vapor transition and provides more reliable results [49]. The safety of C. citratus EO for potential inhalation use can be supported by a previously published study reporting a nontoxic effect of vapors of its predominant compound citral on Sprague–Dawley rats at concentrations up to 34 ppm [50]. Furthermore, other published data on the in vivo acute oral toxicity of C. citratus EO in mice and rabbit models have been reported to be nontoxic with an LD50 value > 2000 mg/kg [51]. Although C. citratus EO is classified as GRAS, further toxicological evaluation is necessary to confirm its nontoxicity for practical application in inhalation therapy. GC/MS analysis showed that the major constituents of C. citratus EO were α- and β-citral. These findings are consistent with those of several previously published studies. For instance, El-Kased and El-Kersh [52] and Hanaa et al. [53] reported α-citral (36.35 and 34.98%) and β-citral (34.99 and 40.72%) as the main components of hydrodistilled EO from this species. Citral has also been identified as the main antimicrobial compound of C. citratus EO [54].
The EO from rhizomes of C. scariosus is used as an ingredient in several Ayurvedic formulations as an anti-infective agent [55]. Previous studies have reported the growth-inhibitory effect of C. scariosus EO against carbapenem-resistant Klebsiella pneumoniae and methicillin-resistant S. aureus in liquid media [56]. In our study, we have observed only weak antibacterial activity of the EO. Considering cytotoxicity, the present research reports that C. scariosus EO is nontoxic to the human lung cells. According to our best knowledge, there are no studies reporting the toxicity of the EO from this species. In correspondence with results of our study, cyperene (20.1%) and cyperotundone (10.30%) have previously been identified as abundant components of C. scariosus EO [57]. Since a significant variability of chemical composition has been reported for C. scariosus EO extracted from plants grown in different geographical locations in India (e.g., content of caryophyllene oxide varied from 2.42 to 10.38%) [58], the geographical origin of plant material analyzed in this study can explain minor differences in the concentrations of detected compounds.
Despite the recent progress in evaluation of biological properties of volatile agents, development of new methodologies suitable for determination of antimicrobial effects in the vapor phase remains a challenge [27]. Recently, a broth macrodilution volatilization assay was developed by our team for evaluation of antimicrobial activity of volatile agents in liquid and vapor phases [59], which combines the principles of broth microdilution volatilization [13] and standard macrodilution methods [60]. The method is performed in commercially available microtubes, which can be tightly closed with a snap cap preventing loss of the active agents by evaporation. Another advantage is that appropriate amounts of media suitable for the cultivation of a broad spectrum of microorganisms (including slow growing fungi) can be applied in microtubes and their caps. However, our previous study assessed only several representatives of volatile phytochemicals. The results of experiments described in this paper clearly demonstrate the validity of a new assay for testing the susceptibility of bacterial pathogens causing respiratory infections to EOs and their vapors.

4. Materials and Methods

4.1. Chemicals

In biological assays, dimethyl sulfoxide (DMSO, CAS 67-68-5) and MTT dye (CAS 298-93-1) were used as solvent and indicator of cell viability, respectively. Amoxicillin (90%, CAS 26787-78-0), ampicillin (84.5%, CAS 69-52-3), oxacillin (86.3%, CAS 7240-38-2), and tetracycline (98–102%, CAS 60-54-8) were assayed as positive controls. Chemical standards, namely 3-carene (99%, CAS: 498-15-7), camphene (97.5%, CAS: 79-92-5), caryophyllene oxide (99%, CAS: 1139-30-6), citral (95%, CAS: 5392-40-5), linalool (97%, CAS: 78-70-6), m-cymene (99%, CAS: 535-77-3), thymol (99%, CAS: 89-83-8), α-pinene (99%, CAS: 7785-70-8), β-pinene (99.0%, CAS: 18172-67-3), γ-terpinene (97%, CAS: 99-85-4), and n-alkanes were used for GC-MS analyses. With the exception of n-hexane (CAS: 110-54-3) obtained from (Merck KGaA, Darmstadt, Germany), all other chemicals were purchased from Sigma-Aldrich (Prague, Czech Republic).

4.2. Plant Material and Sample Preparation

Plant materials were purchased from Bhagyashree Herbal Farms (Chhattisgarh, India). Dried aerial parts of C. citratus, rhizomes of C. scariosus, and seeds of T. ammi were homogenized using a Grindomix apparatus (GM 100 Retsch, Haan, Germany). The residual moisture contents of both samples were determined gravimetrically at 130 °C for 1 h by a Scaltec SMO 01 analyzer (Scaltec Instruments, Gottingen, Germany) in triplicate according to the Official Methods of Analysis of the Association of Official Agricultural Chemists [61]. EOs were extracted by hydrodistillation of 100 g of ground plant materials in 1 L of distilled water for 3 h using a Clevenger-type apparatus (Merci, Brno, Czech Republic) according to the procedure described in the European Pharmacopeia (2013) [62] and stored in sealed glass vials at +4 °C.

4.3. Bacterial Strains and Culture Media

The following four bacterial standard strains from the American Type Culture Collection (ATCC, Manassas, VA, USA) were used: H. influenzae ATCC 49247, S. aureus ATCC 29213, S. pneumoniae ATCC 49619, and S. pyogenes ATCC 19615. Cultivation and assay media (broth/agar) were Mueller–Hinton broth (MHB) complemented by Haemophilus test medium (H. influenzae), MHB (S. aureus), and brain–heart infusion (S. pneumoniae and S. pyogenes). The pH of the broths was adjusted to a final value of 7.6 using Trizma base (Sigma-Aldrich). All microbial strains and cultivation media were purchased from Oxoid (Basingstoke, UK). Stock cultures of bacterial strains were cultivated in broth medium at 37 °C for 24 h prior to testing in the incubator (Memmert GmbH & Co. KG, Buchenbach, Germany). For the preparation of inoculum, the turbidity of the bacterial suspension was adjusted to 0.5 McFarland standard using a Densi-La-Meter II (Lachema, Brno, Czech Republic) to obtain a final concentration of 108 colony-forming units per mL.

4.4. Antimicrobial Assay

EOs were tested for their in vitro antibacterial activity using the broth macrodilution volatilization method at various concentrations in the liquid and vapor phases [59] in standard 2 mL microtubes with snap covers (Eppendorf, Hamburg, Germany). Each EO was dissolved in DMSO, which was subsequently diluted in the appropriate broth medium. To make sufficient stock solutions and to prevent the loss of active chemicals by evaporation, six twofold serially diluted concentrations of samples were created in 15 mL test tubes (Gama Group, Ceske Budejovice, Czech Republic). The starting concentration of tested EOs was 1024 µg/mL. In the subsequent phase, 90 mL of melted agar was pipetted into the rims of the caps, and when the agar had solidified, 5 mL of bacterial suspension was added. Then, with a final volume of 1500 µL, the proper concentrations of each sample that had been prepared in test tubes were pipetted into microtubes. The microtubes were then sealed properly after being injected with 10 µL of bacterial solution. As growth and purity controls, microtubes with inoculated and non-inoculated medium were prepared, respectively. The experiment was incubated at 37 °C for 24 h. Thereafter, the MICs were determined by visual assessment of bacterial growth after coloring the metabolically active bacterial colonies with MTT dye. The respective volumes of 30 and 375 µL of MTT at a concentration of 600 µg/mL were pipetted into the caps and in the microtubes when the interface of color change from yellow to purple (relative to that of colors in control wells) was recorded in broth and agar. The MIC values were determined as the lowest concentrations that inhibited bacterial growth compared with the compound-free control, and they were expressed in µg/mL. DMSO, assayed as the negative control, did not inhibit any of the strains at the concentrations used in the assay (≤1%). The respective susceptibilities of H. influenzae, S. aureus, S. pneumoniae, and S. pyogenes to ampicillin, oxacillin, amoxicillin, and tetracycline were taken as positive antibiotic controls [63]. All tests were performed as three independent experiments, each carried out in triplicate, and the results were presented as median/modal values. According to the widely accepted norm in MIC testing, the mode and median were used for the final value calculation when triplicate endpoints were within the two- and three-dilution range, respectively.

4.5. Cell Cultures

Lung fibroblast cell line MRC-5, obtained from ATCC (Manassas, VA, USA), was propagated in Eagle’s minimum essential medium (EMEM) supplemented with 10% fetal bovine serum (FBS), 2 mM glutamine, 10 µL/mL nonessential amino acids, and 1% penicillin–streptomycin solution (10,000 units/mL of penicillin and 10 mg/mL of streptomycin); all these components were purchased from Sigma-Aldrich. The cells were pre-incubated in 96-well microtiter plates at a density of 2.5 × 103 cells per well for 24 h at 37 °C in a humidified incubator (Sanyo Electric Co, Ltd., Osaka, Japan) in an atmosphere of 5% CO2 in air. Vinorelbine (≥98%, CAS 125317-39-7), used as positive control, was also obtained from Sigma-Aldrich.

4.6. Cytotoxicity Assay

The modified MTT test, which is based on the metabolism of MTT to blue formazan by mitochondrial dehydrogenases in living lung cells, was used in the current investigation [64]. The evaluated EOs samples were applied to MRC-5 lung fibroblast cells grown in 96-well plates for 72 h. EOs were diluted in EMEM medium supplemented with 10% FBS after being dissolved in DMSO at a maximum concentration of 1%. The samples were then serially diluted eight times, yielding concentrations ranging from 256 to 2 µg/mL. The microtiter plates were incubated for 72 h at 37 °C in a humidified atmosphere of 5% CO2 in air with ethylene vinyl acetate EVA Capmats (USA Scientific Inc., Ocala, FL, USA). After that, MTT reagent (1 mg/mL) in EMEM solution was added to each well and the plates were incubated for an additional 2 h at 37 °C in a humidified atmosphere of 5% CO2 in air. Once the medium had been removed from the incubation, the intracellular formazan product had been dissolved in 100 µL of DMSO. The viability of the lung cells at the tested concentration (1%) was unaffected by the solvent utilized. The absorbance was measured at 555 nm using a Tecan Infinite M200 spectrometer (Tecan Group, Mannedorf, Switzerland), and the viability was computed in comparison to the untreated control. For each test, three independent experiments, each with two replicates, were conducted. Using the GraphPad Prism program (GraphPad Software, La Jolla, CA, USA), the results of the cytotoxicity effect were calculated and expressed as average IC50 with standard deviation in µg/mL. According to the Special Programme for Research and Training in Tropical Diseases (WHO-Tropical Diseases) [30], the levels of cytotoxic effects were categorized as cytotoxic (IC50 < 2 µg/mL), moderately cytotoxic (IC50 2–89 µg/mL), and nontoxic (IC50 > 90 µg/mL). Furthermore, for the purpose of comparing microbiological and toxicological data, IC80 was determined to be equal to the MIC endpoint [65]. To compare the quantity of toxic antibacterial agents with the amount of effective antibacterial agents, therapeutic indices (TIs) were defined as the ratio of IC80 and x-MIC values [66].

4.7. Chemical Analysis of EOs’ Liquid Phase

The dual-column/dual-detector gas chromatograph Agilent GC-7890B system (Agilent Technologies, Santa Clara, CA, USA) equipped with autosampler Agilent 7693, two columns, a fused-silica HP-5MS (30 m × 0.25 mm, film thick-ness 0.25 µm, Agilent 19091s-433), a DB-Heavy WAX (30 m × 0.25 mm, film thickness 0.25 µm, Agilent 122–7132), and a flame ionization detector (FID) coupled with single quadrupole mass selective detector Agilent MSD-5977B were used to characterize the chemical composition of the targeted EOs. Helium was used as the carrier gas at a rate of 1 mL/min, and the injector temperature for both columns was 250 °C. After 3 min, the oven temperature for both columns increased from 50 to 280 °C. Initially, the heating velocity was 3 °C/min until the system reached a temperature of 120 °C. Subsequently, the velocity increased to 5 °C/min until a temperature of 250 °C, and after 5 min holding time, the heating speed reached 15 °C/min until obtaining a temperature of 280 °C. Heating was followed by an isothermic period of 20 min. The EO samples were diluted in n-hexane for GC/MS at a concentration of 20 µL/mL. One microliter of the solution was injected in split mode in a split ratio of 1:30. The mass detector was set to the following conditions: ionization energy 70 eV, ion source temperature 230 °C, scan time 1 s, and mass range 40–600 m/z. Identification of constituents was based on a comparison of their retention indices (RI) and retention times (RT) and spectra with the National Institute of Standards and Technology Library ver. 2.0.f (NIST, Gaithersburg, MD, USA) [33], as well as with authentic standards. The RIs were calculated for compounds separated by the HP-5MS column using the retention times of n-alkanes series ranging from C8 to C40. For each EO analyzed, the final number of compounds was calculated as the sum of components simultaneously identified using both columns and the remaining constituents identified by individual columns only. Quantitative data were expressed as relative percentage content of constituents determined by the FID.

4.8. Chemical Analysis of EOs’ Vapor Phase

For the chemical analysis of EOs’ vapors, T. ammi was chosen, as it exhibited the highest antimicrobial potential. Similarly, like Antih et al. [43], two distinct sampling methods—HS-SPME and HS-GTS—were used to sample the headspace above a solution of MHB and EO at a concentration of 256 µg/mL, which was observed as the lowest MIC value of this EO in vapor phase. Five samples were made for each experiment (one for every three hours during the 12 h incubation period), and a volume of 2 mL of the combination was added to a 4 mL glass vial. Except for the first sample (t = 0 h), all the samples were incubated in the same way as the bacterial cultures at a temperature of 37 °C until they were analyzed at 3, 6, and 12 h. For the HS-SPME, a fiber assembly coated with a 50/30 m mixed layer of divinylbenzene/carboxen/polydimehylsiloxane (DVB/CAR/PDMS—SUPELCO, Bellefonte, PA, USA) was used. The coated fiber was exposed to the headspace for 15 min to allow the adsorption of the volatile chemicals above the mixture (EO and MHB) until the headspace had reached equilibrium. The fiber was then retained in the injector for the duration of the analysis until the next measurement, when the needle was removed and put into the GC injector port. The injection method was set at splitless mode and injector temperature was set at 250 °C. For the HS-GTS sampling technique, a 2.5 mL SampleLock gas-tight syringe (Hamilton Bonaduz AG, Bonaduz, Switzerland) was used, which has a twist valve lock and a positive rear plunger stop to prevent sample loss. At equilibrium, the needle was passed through the vial septum and inserted until reaching the middle of the headspace, and after collecting the headspace, the valve of the syringe was closed. Afterward, the syringe was removed from the vial and inserted into the GC injector at a similar temperature of 250 °C, but the injection mode was set as spitless mode. For both sampling methods, measurements were repeated every 3 h during a 12 h incubation period. Furthermore, analysis was performed on the HP-5MS column with similar operational parameters as described earlier for GC/MS analysis.
The chemical analysis of the all EO samples was performed in triplicate, including the chromatographic analysis of its liquid phase and the headspace analysis using both extraction techniques (HS-SPME and HS-GTS). Relative peak area percentages were expressed as mean average of these three measurements ± standard deviation.

5. Conclusions

In summary, this study reports validation of the broth macrodilution volatilization method for assessment of antibacterial properties of EOs and shows in vitro growth-inhibitory effect of EOs hydrodistilled from three Indian medicinal plants, namely C. citratus, C. scariosus, and T. ammi, against pneumonia-causing bacteria H. influenzae, S. aureus, S. pneumoniae, and S. pyogenes in liquid and vapor phase. Among all EOs tested, the strongest antibacterial effect was observed for T. ammi EO against H. influenzae with MIC 128 and 256 µg/mL in the liquid and vapor phases. The results of the cytotoxicity testing showed no toxicity of C. scariosus EO to the normal lung fibroblasts. The GC/MS analysis identified α-citral, cyperotundone, and thymol as the main constituents of C. citratus, C. scariosus, and T. ammi EOs, respectively. In a series of headspace experiments, β-cymene (52–49%), γ-terpinene (39–35%), thymol (12–2%), and β-pinene (6–2%) were identified as the major compounds of T. ammi EO vapors when analyzed using HS-GTS and HS-SPME sampling techniques. These compounds can be associated with imparting an antibacterial effect in the vapor phase. Furthermore, HS-SPME and HS-GTS have been proven to be complementary methods suitable for studying the qualitative and quantitative aspects of the volatile profiles of EO, subsequently. Overall, the broth macrodilution volatilization method can be recommended for testing the susceptibility of bacteria to EOs. In addition, T. ammi EO seems to be a promising antibacterial agent for further research in the area of inhalation therapies. However, further experiments focused on the safety and in vivo efficacy of EOs analyzed in this study are required to verify their practical applicability.

Author Contributions

Conceptualization, L.K.; formal analysis, A.C.; investigation, A.C.; plant material collection, M.L.N. and K.S.P.; performance of the cytotoxicity testing I.D.; supervision for chemical analysis L.K., K.U. and J.A.; supervision for microbiology experiments, M.H. and L.K.; writing—original draft, A.C.; writing—review and editing, M.H., J.A. and L.K. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Czech University of Life Sciences Prague (project IGA.20233109) and the METROFOOD-CZ research infrastructure project (MEYS Grant No: LM2023064), including access to its facilities.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Not available.

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Molecules 28 04625 g001 550
Figure 1. Cytotoxic activity of eight twofold serially diluted concentrations (2–256 µg/mL) of Cymbopogon citratus, Cyperus scariosus and Trachyspermum ammi EOs to lung fibroblast cells MRC-5 tested by MTT assay performed in microtiter plates sealed with vapor barrier EVA Capmat.
Figure 1. Cytotoxic activity of eight twofold serially diluted concentrations (2–256 µg/mL) of Cymbopogon citratus, Cyperus scariosus and Trachyspermum ammi EOs to lung fibroblast cells MRC-5 tested by MTT assay performed in microtiter plates sealed with vapor barrier EVA Capmat.
Molecules 28 04625 g001
Table
Table 1. In vitro growth-inhibitory effect of Indian essential oils in the liquid and vapor phases against respiratory pathogens.
Table 1. In vitro growth-inhibitory effect of Indian essential oils in the liquid and vapor phases against respiratory pathogens.
SampleBacterium/Growth Medium/Minimum Inhibitory Concentration (µg/mL)
Essential OilHaemophilus influenzaeStaphylococcus aureusStreptococcus pneumoniaeStreptococcus pyogenesx-MIC
BrothAgarBrothAgarBrothAgarBrothAgar
Cymbopogon citratus256256512102451210245121024448
Cyperus scariosus.102410241024>10241024>10241024>10241024
Trachyspermum ammi12825651251251210245121024416
Positive antibiotic control1 an.d.0.5 bn.d.0.25 cn.d.0.25 dn.d.-
x-MIC: mean value of minimal inhibitory concentrations in broth medium; positive antibiotic control: a ampicillin, b oxacillin, c amoxicillin, d tetracycline; n.d.: not detected.
Table
Table 2. Cytotoxicity of Indian essential oils to the normal lung fibroblast cell line MRC-5.
Table 2. Cytotoxicity of Indian essential oils to the normal lung fibroblast cell line MRC-5.
SampleIC50 ± SD (µg/mL)IC80 ± SD (µg/mL)TI
Essential oil
Cymbopogon citratus19.63 ± 1.0229.54 ± 2.180.065
Cyperus scariosus>258>258>0.252
Trachyspermum ammi82.04 ± 3.39156.57 ± 13.880.376
Positive control
vinorelbine0.54 ± 0.26>10n.a.
IC50: half maximal inhibitory concentration of proliferation in μg/mL; IC80: 80% inhibitory concentration of proliferation in μg/mL; SD: standard deviation; TI: therapeutic index (TI = IC80/x-MIC); n.a.: not applicable.
Table
Table 3. Chemical composition of Cymbopogon citratus essential oil.
Table 3. Chemical composition of Cymbopogon citratus essential oil.
RI aCompoundCl. bColumn
Content c (%)Identification f
Obs.Lit.HP-5MSDB-WAXHP-5MSDB-WAX
915926TricycleneMH0.26 ± 0.12tr. dRI, MS, Std,MS
927939α-PineneMH0.20 ± 0.04- eRI, MS, Std-
942953CampheneMH2.42 ± 0.791.62 ± 0.34RI, MS, StdMS
979985SulcatoneMO0.35 ± 0.18-RI, MS-
10231029D-LimoneneMH0.23 ± 0.03-RI, MS-
10291050trans-β-OcimeneMH0.31 ± 0.09-RI, MS-
103910113-CareneMH0.13 ± 0.02-RI, MS, Std-
106310304-NonanoneMO1.41 ± 0.381.55 ± 0.97RI, MSMS
10981098LinaloolMO0.46 ± 0.240.31 ± 0.07RI, MS, StdMS
11781184.7IsogeranialMO0.70 ± 0.010.55 ± 0.05RI, MSMS
11901189α-TerpineolMO0.39 ± 0.03-RI, MS-
12381240β-CitralMO35.8 ± 0.6124.3 ± 8.82RI, MS, StdMS
12681270α-CitralMO48.9 ± 0.5533.2 ± 11.2RI, MS, StdMS
13761381Geranyl acetateMO2.02 ± 0.20tr.RI, MSMS
14121418CaryophylleneSH0.45 ± 0.310.75 ± 0.05RI, MSMS
15101513γ-CadineneSH1.19 ± 0.331.20 ± 0.23RI, MSMS
g1797GeraniolMO-0.77 ± 0.07-MS
15821581Caryophyllene oxideSH3.0 ± 1.342.88 ± 1.40RI, MS, StdMS
g1430α-CyclocitralMO-0.45 ± 0.04-MS
gNAIsoneralMO-0.36 ± 0.02-MS
g1669IsoborneolMO-0.83 ± 0.01-MS
Total content (%)99.6268.77
a RI = retention indices; Obs. = retention indices determined relative to a homologous series of n-alkanes (C8–C40) on an HP-5MS column; Lit. = literature RI values [31,32], NA = RI values not available in the literature; b Cl = class; MH—monoterpene hydrocarbons, MO—oxygenated monoterpenoids, SH—sesquiterpene hydrocarbons; c relative peak area percentage as mean of three measurements ± standard deviation; d tr. = traces, relative peak area < 0.05%; e - = not detected; f identification method: MS = mass spectrum was identical to that of the National Institute of Standards and Technology Library (ver. 2.0.f), RI = the retention index was matching literature database; Std = constituent identity confirmed by co-injection of authentic standards; g retention indices were not calculated for compounds determined by DB-WAX column.
Table
Table 4. Chemical composition of Cyperus scariosus essential oil.
Table 4. Chemical composition of Cyperus scariosus essential oil.
RI aCompoundCl. bColumn
Content c (%)Identification f
Obs.Lit.HP-5MSDB-WAXHP-5MSDB-WAX
927939α-PineneMH1.34 ± 0.100.50 ± 0.01RI, MS, StdMS
970980β-PineneMH1.88 ± 0.330.06 ± 0.00RI, MS, StdMS
10251032EucalyptolMO0.24 ± 0.16- dRI, MS-
11371137PinocarveolMO1.85 ± 0.230.60 ± 0.01RI, MSMS
11581165PinocarvoneMO0.37 ± 0.320.09 ± 0.00RI, MSMS
11681193MyrtenalMO0.41 ± 0.270.13 ± 0.30RI, MSMS
13141327CyproteneSH0.16 ± 0.05tr.eRI, MSMS
13441349α-Terpinyl acetateMO1.65 ± 0.18tr.RI, MSMS
13711376CopaeneSH1.46 ± 0.47tr.RI, MSMS
13941398CypereneSH9.87 ± 0.598.5 ± 0.04RI, MSMS
14461477α-MuuroleneSH0.16 ± 0.04tr.RI, MSMS
14561461RotundeneSH1.94 ± 0.071.25 ± 0.01RI, MSMS
14831473.7γ-PatchouleneSH0.19 ± 0.05tr.RI, MSMS
14891491ValenceneSH0.63 ± 0.080.57 ± 0.60RI, MSMS
15181518β-CadineneSH0.31 ± 0.180.08 ± 0.40RI, MSMS
15281532Cyperene epoxideSO2.65 ± 0.261.50 ± 0.00RI, MSMS
15411542α-CalacoreneSH0.13 ± 0.05-RI, MS-
15651579Isoaromadendrene epoxideSO0.62 ± 0.071.03 ± 0.00RI, MSMS
15721627LongiverbenoneSO1.33 ± 0.151.20 ± 0.08RI, MSMS
15821581Caryophyllene oxideSH19.79 ± 0.5817.54 ± 0.12RI, MS, StdMS
1591NAβ-SantalolSO0.38 ± 0.12-RI, MS-
16091608Humulene epoxide 2SO1.69 ± 0.252.60 ± 0.10RI, MSMS
16561604GlobulolSO0.23 ± 0.040.39 ± 0.03RI, MSMS
16641663Patchouli alcoholSO0.50 ± 0.05-RI, MS-
16771676MustakoneSO6.26 ± 0.263.67 ± 0.30RI, MSMS
16971694CyperotundoneSO29.1 ± 1.1128.91 ± 0.72RI, MSMS
17501752AristoloneSO3.17 ± 0.773.73 ± 0.10RI, MSMS
18081807NootkatoneSO2.17 ± 0.492.03 ± 0.40RI, MSMS
gNAβ-PinoneMO-tr.-MS
g1586β-ElemeneSH-tr.-MS
g1652cis-VerbenolMO-tr.-MS
gNAAristolocheneSH-tr.-MS
g1680α-Terpineol tr.-MS
gNAα-MaalieneSH-tr.-MS
g1784MyrtenolMO-tr.-MS
g2063CubenolSO-0.49 ± 0.00-MS
g1978α-Cedrene epoxideSO-0.40 ± 0.10-MS
gNAAromadendrene oxide-(1)SO-1.35 ± 0.40-MS
gNACalarene epoxideSO-0.52 ± 0.02-MS
gNADiepicedrene-1-oxideSO-0.05 ± 0.00-MS
Total content (%)91.4877.17
a RI = retention indices; Obs. = retention indices determined relative to a homologous series of n-alkanes (C8–C40) on an HP-5MS column; Lit. = literature RI values [31,32], NA = RI values not available in the literature; b Cl = class; MH—monoterpene hydrocarbons, MO—oxygenated monoterpenoids, SH—sesquiterpene hydrocarbons, SO—oxygenated sesquiterpenoids; c relative peak area percentage as mean of three measurements ± standard deviation; d - = not detected; e tr. = traces, relative peak area < 0.05%; f identification method: MS = mass spectrum was identical to that of the National Institute of Standards and Technology Library (ver. 2.0.f), RI = the retention index was matching literature database; Std = constituent identity confirmed by co-injection of authentic standards; g retention indices were not calculated for compounds determined by DB-WAX column.
Table
Table 5. Chemical composition of Trachyspermum ammi essential oil.
Table 5. Chemical composition of Trachyspermum ammi essential oil.
RI aCompoundCl. bColumn
Content c (%)Identification e
Obs.Lit.HP-5MSDB-WAXHP-5MSDB-WAX
920917β-ThujeneMH0.30 ± 0.030.17 ± 0.02RI, MSMS
964925α-PineneMH0.19 ± 0.010.42 ± 0.13RI, MS, StdMS
981971β-PineneMH1.87 ± 0.252.13 ± 0.62RI, MS, StdMS
994984β-MyrceneMH0.21 ± 0.060.38 ± 0.03RI, MSMS
10079742-CareneMH0.20 ± 0.02- dRI, MSMS
10501031β-CymeneMH22.6 ± 0.8917.1 ± 3.99RI, MS, StdMS
10791065γ-TerpineneMH21.5 ± 0.8617.6 ± 0.99RI, MS, StdMS
11751086IsoterpinoleneMH0.08 ± 0.06-RI, MSMS
13151290ThymolMO51.2 ± 1.2545.8 ± 4.41RI, MS, StdMS
f1172α-TerpineneMH-0.12 ± 0.01-MS
f1244D-LimoneneMH-0.10 ± 0.01-MS
f1195β-PhellandreneMH-0.08 ± 0.03-MS
fNAtrans-2-Caren-4-olMO-0.18 ± 0.02-MS
f1680TerpineolMO-0.06 ± 0.01-MS
f1635Terpinen-4-olMO-0.20 ± 0.04-MS
Total content (%)99.4784.26
a RI = retention indices; Obs. = retention indices determined relative to a homologous series of n-alkanes (C8–C40) on an HP-5MS column; Lit. = literature RI values [31,32], NA = RI values not available in the literature; b Cl = class; MH—monoterpene hydrocarbons, MO—oxygenated monoterpenoids, SH—sesquiterpene hydrocarbons; c relative peak area percentage as mean of three measurements ± standard deviation; d - = not detected; e identification method: MS = mass spectrum was identical to that of the National Institute of Standards and Technology Library (ver. 2.0.f), RI = the retention index was matching literature database; Std = constituent identity confirmed by co-injection of authentic standards; f retention indices were not calculated for compounds determined by DB-WAX column.
Table
Table 6. Chemical composition of a headspace above a Trachyspermum ammi essential oil dissolved in Mueller–Hinton broth at a concentration of 256 µg/mL.
Table 6. Chemical composition of a headspace above a Trachyspermum ammi essential oil dissolved in Mueller–Hinton broth at a concentration of 256 µg/mL.
RI aCompoundExtraction Method/Time (h)/Content b (%)Ident. e
Solid Phase MicroextractionGas Tight Syringe Extraction
Obs.Lit.036912036912
925939α-Pinene1.27 ± 0.101.46 ± 0.001.42 ± 0.011.41 ± 0.001.25 ± 0.01tr. ctr.tr.tr.tr.RI, MS
96110112-Carene0.64 ± 0.000.44 ± 0.000.62 ± 0.010.65 ± 0.020.72. ±0.01- d----RI, MS
971980β-Pinene1.91 ± 0.012.80 ± 0.052.36 ± 0.002.31 ± 0.011.79 ± 0.206.57 ± 0.204.93 ± 0.403.89 ± 0.104.11 ± 0.012.02 ± 0.30RI, MS
10311030β-Cymene49.14 ± 1.0048.00 ± 1.1046.57 ± 0.8045.97 ± 1.8043.17 ± 0.9052.00 ± 3.5049.18 ± 2.9048.67 ± 2.5046.32 ± 1.4045.60 ± 0.60RI, MS
10651062γ-Terpinene39.36 ± 0.7035.41 ± 0.5035.11 ± 0.9033.26 ± 0.6031.01 ± 0.2035.00 ± 2.5032.23 ± 0.0931.60 ± 0.5032.22 ± 1.3028.20 ± 2.90RI, MS
13061290Thymol4.96 ± 0.015.66 ± 0.409.82 ± 0.0811.90 ± 0.9312.10 ± 0.80tr.1.23 ± 0.102.21 ± 0.202.07 ± 0.03tr.RI, MS
Total content (%)97.2594.2195.995.590.6693.4088.5787.9885.7279.05
a RI = retention indices; Obs. = retention indices determined relative to a homologous series of n-alkanes (C8–C40) on an HP-5MS column; Lit. = literature RI values [31,32]; b relative peak area percentage as mean of three measurements ± standard deviation; c tr. = traces, relative peak area < 0.05%; d - = not detected; e identification method: MS = mass spectrum was identical to that of the National Institute of Standards and Technology Library (ver. 2.0.f), RI = the retention index was matching literature database.
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MDPI and ACS Style

Chaure, A.; Houdkova, M.; Antih, J.; Urbanova, K.; Doskocil, I.; Naik, M.L.; Patel, K.S.; Kokoska, L. Validation of Broth Macrodilution Volatilization Method for Testing of Essential Oils in Liquid and Vapor Phase: Chemical Composition, Cytotoxicity, and Antibacterial Effect of Indian Medicinal Plants against Pneumonia-Causing Pathogens. Molecules 2023, 28, 4625. https://doi.org/10.3390/molecules28124625

AMA Style

Chaure A, Houdkova M, Antih J, Urbanova K, Doskocil I, Naik ML, Patel KS, Kokoska L. Validation of Broth Macrodilution Volatilization Method for Testing of Essential Oils in Liquid and Vapor Phase: Chemical Composition, Cytotoxicity, and Antibacterial Effect of Indian Medicinal Plants against Pneumonia-Causing Pathogens. Molecules. 2023; 28(12):4625. https://doi.org/10.3390/molecules28124625

Chicago/Turabian Style

Chaure, Aishwarya, Marketa Houdkova, Julien Antih, Klara Urbanova, Ivo Doskocil, Mukund Lal Naik, Khageshwar Singh Patel, and Ladislav Kokoska. 2023. "Validation of Broth Macrodilution Volatilization Method for Testing of Essential Oils in Liquid and Vapor Phase: Chemical Composition, Cytotoxicity, and Antibacterial Effect of Indian Medicinal Plants against Pneumonia-Causing Pathogens" Molecules 28, no. 12: 4625. https://doi.org/10.3390/molecules28124625

APA Style

Chaure, A., Houdkova, M., Antih, J., Urbanova, K., Doskocil, I., Naik, M. L., Patel, K. S., & Kokoska, L. (2023). Validation of Broth Macrodilution Volatilization Method for Testing of Essential Oils in Liquid and Vapor Phase: Chemical Composition, Cytotoxicity, and Antibacterial Effect of Indian Medicinal Plants against Pneumonia-Causing Pathogens. Molecules, 28(12), 4625. https://doi.org/10.3390/molecules28124625

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