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Article

Volatile Oil Chemical Composition of Wild, Edible Centaurea scabiosa L. and Its Cytotoxic Activity

by
Ivana Carev
1,2,3,*,
Anja Golemac
2,3,
Sonja Siljak-Yakovlev
4,
Francois Xavier Pellay
2,3 and
Olivera Politeo
1
1
Department of Biochemistry, Faculty of Chemistry and Technology, University of Split, Ruđera Boškovića 35, 21000 Split, Croatia
2
NAOS Institute of Life Science, 355, rue Pierre-Simon Laplace, 13290 Aix, France
3
Mediterranean Institute for Life Science, Meštrovićevo šetalište 45, 21000 Split, Croatia
4
Ecologie Systématique Evolution, CNRS, AgroParisTech, Université Paris-Saclay, 91190 Gif-sur-Yvette, France
*
Author to whom correspondence should be addressed.
Plants 2022, 11(23), 3267; https://doi.org/10.3390/plants11233267
Submission received: 2 November 2022 / Revised: 21 November 2022 / Accepted: 22 November 2022 / Published: 28 November 2022
(This article belongs to the Special Issue Phytochemistry of Aromatic and Medicinal Plants)

Abstract

:
Centaurea species are well known as a source of phytopharmaceuticals having both beneficial and harmful influences on human health. Centaurea scabiosa L. is a wild edible plant used in Mediterranean cuisine in the Dalmatian region of Croatia. We have assessed the volatile oil’s chemical composition using GC/MS chromatography and its cytotoxic activity on human fibroblasts using the MTT test. Data on chromosome number, obtained by classical karyological methods, and genome size, assessed by flow cytometry, of the same plant material of C. scabiosa, were also given. The major chemical compounds found in C. scabiosa volatile oil were heptacosane, caryophyllene oxide, alloaromadendrene epoxide, α-cyperone, and α-bisabolol. This volatile oil showed no cytotoxicity on human fibroblasts in a dose range of 0.01–1 g/L. The chromosome number of a C. scabiosa sample from Croatia showed 2n = 20 + 2B chromosomes. The total genome DNA amount of 2C = 3.3 ± 0.01 pg or 1 Cx = 1628 Mbp presents the first report on the genome size of this species from Croatia. The presented results support the idea of using this plant in the human diet. To our knowledge, this is the first report on edible C. scabiosa species in general and in particular from Croatia.

1. Introduction

The Centaurea L. genus (Asteracea family) comprises around 500–600 annual, biannual, and perennial herbaceous plants distributed around the world but only north of the equator, mostly in the Eastern Hemisphere with the diversification center in the Middle East. Many of these species have been used in traditional medicine for the treatment of various diseases and conditions [1].
Plants and their extracts can be valuable sources of pharmacologically active compounds such as antibiotics, anti-cancer agents, and neuroactive molecules. Centaurea species are known as a source of phytopharmaceuticals that could have both beneficial and harmful influences on human health. Among the many Centaurea species already known for their medicinal properties, only a few have been known for their use in human diets [2,3].
Harvesting wild plants and using them for medicinal purposes and in the diet is part of traditional plant use in the coastal Mediterranean area. Due to high biodiversity and ethnopharmacology practice, the people of Croatia and the Dalmatian region, as well as the south Herzegovina region in Bosnia and Herzegovina, use an unusually large number of wild plant species for medicinal purposes and diet. Centaurea scabiosa is well known in the Eastern and Western Mediterranean for its pharmacological properties and is a wild edible plant used in the Mediterranean cuisine of the Dalmatian region (Croatia). It is used as a raw food, and its volatile compounds from volatile oil are present in the diet [4,5,6].
Centaurea scabiosa has also been used for medical purposes, such as the treatment of scabies and other skin complaints, which is where the root of its scientific name, scabiosa, comes from. It is known that the roots and seeds of C. scabiosa are used in traditional medicine for wound healing, to treat kidney problems and mouth ulcers, as well as for tonic and diuretic purposes [7].
Centaurea scabiosa non-volatile extracts, studied so far, were assessed for the presence of phenolic components, flavonoids, and some sesquiterpene lactones. They were tested for antimicrobial and antioxidant activity [8,9].
The Centaurea genus is very difficult taxonomically due to its large morphological, karyological, and palynological diversity. Apart from the detailed morphological study, genome size and chromosome number assessments present additional approaches that assist in the identification of the studied plant material [10,11,12,13].
The aim of our study was to:
(a)
Assess the volatile oil chemical composition of C. scabiosa using the GC/MS technique;
(b)
Test C. scabiosa volatile oil cytotoxicity using the MTT assay on human fibroblasts at a concentration dose range of 0.01–1 g/L;
(c)
Determine genome size using flow cytometry and chromosome number using the classical karyological method.
Depending on the results obtained, this species could be proposed for use in human food.

2. Results and Discussion

The chemical composition of C. scabiosa hydro-distilled volatile oil was determined using the GC/MS chromatographic technique and is shown in Table 1.
The 32 detected volatile oil chemical compounds represent 90.21% of volatile oils. The chemical compounds are grouped in terpenes (43.73%), consisting of non-oxygenated sesquiterpenes (1.23%), oxygenated sesquiterpenes (41.09%), and diterpenes (1.41%); nonterpene compounds consisting of hydrocarbons (31.10%), aldehydes (3.67%), acids (7.00%), esters (4.03%), and other compounds (0.68%). The dominant chemical compounds in the studied volatile oils were heptacosane (19.62%), caryophyllene oxide (10.90%), alloaromadendrene epoxide (10.27%), α-cyperone (8.16%), and α-bisabolol (4.99%) (Table 1).
The common constituents of Centaurea species belong to a group of terpenes called sesquiterpenes, and they are usually dominant components in most of the Centaurea volatile oils [14,15,16,17,18,19,20,21,22,23,24,25]. Along with the sesquiterpenes, non-oxygenated hydrocarbon derivatives are dominantly present in most of the Centaurea species’ volatile oils, while oxygenated hydrocarbon derivatives are present in a smaller amount than non-oxygenated derivatives [14,15,16,17,18].
On the contrary, the studied C. scabiosa volatile oil demonstrated dominant compounds belonging to a group of oxygenated sesquiterpenes, while the non-oxygenated sesquiterpenes were present in a very small amount of 1.23% in total. While caryophyllene oxide can be found among the dominated compounds in Centaurea volatile oil, the presence of alloaromadendrene epoxide is rather exceptional, especially among dominant components, and this is the first report of this chemical compound as a dominant component of Centaurea volatile oil. It is also rare to find α-cyperone as a dominant compound in Centaurea volatile oils, as well as α-bisabolol [26]. Monoterpenes are usually present in amounts less than 1% in Centaurea species, and in the studied volatile oil of C. scabiosa, the monoterpenes were not present at all. Heptacosane was among the dominant components in C. scabiosa, which can also be found in some other Centaurea volatile oils [14,15,16,17,18,19,20,21,22,23,24,25].
It is interesting to point out that the name of the species scabiosa is derived from the skin disease scabies, and α-bisabolol, which is found in studied essential oils, is known for its effects on skin repair and wound healing [27].
The common constituents of Centaurea volatile oils, such as germacrene D and spathulenol, in our studied volatile oil were found in less than 1%. This is unusual for most of the Centaurea species, as these sesquiterpenes are commonly present as dominant constituents of Centaurea volatile oils. Hexadecanoic acid, another very common constituent of Centaurea volatile oils, was found in a small amount in the studied volatile oil [14,15,16,17,18,21,22,23].
The volatile oil of C. scabiosa studied revealed some distinct characteristics in the chemical composition of dominant components. It showed diversity in chemical composition compared to most of the Centaurea species, while showing some similarities with the chemical composition of volatile oils from the Lopholoma section, where C. scabiosa belongs [14,16,17,18,24]. Nonetheless, the dominant component combination is unique and first reported for this species, as is the presence of alloaromadendrene epoxide and α-cyperone as dominant components in Centaurea volatile oil.
Centaurea scabiosa volatile oil tested on primary human skin fibroblasts with the MTT assay showed no toxicity in a range of concentrations from 0.01 to 1 g/L with DMSO and water as controls (Figure 1). Centaurea scabiosa volatile oil tested on primary human skin fibroblasts with the MTT assay at five concentrations between 0.01 and 1 g/L showed there was no statistical difference from the control conditions, either water or DMSO, and therefore there is no toxicity. This has been supported by a test with propidium iodide that confirmed MTT results on the lack of toxicity of both tested extracts.
We compared the biological activity of the studied volatile oils to known volatile oils of edible Centaurea species because Centaurea species are very poorly known phytochemically and phytopharmacologically, on their chemical composition of volatiles or non-volatiles, and even less on their biological activity.
In the literature, some of the Centaurea species from Turkey and Italy have been mentioned as edible plants: Centaurea cheiranthifolia Willd. Var. cheiranthifolia; C. cheiranthifolia Willd. Var. purpurascens (DC.) Wagenitz, C. cyanus L., C. depressa Bieb., C. glastifolia L., C. iberica Trev. Ex Sprengel, C. solstitialis L. subsp. solstitialis, C. haradjianii, C. jacea, and C. calcitrapa. These species are mostly used in cooked or fresh salads, but no in-depth chemical analysis of the volatile oils of the mentioned species has been done in the cited literature [28,29].
Because there is a lack of data on the cytotoxic activity of the essential oils of the edible Centaurea plants mentioned, we used available literature data on the chemical composition of C. cyanus L., C. depressa Bieb., C. iberica Trev. Ex Sprengel, C. solstitialis L. subsp. solstitialis, C. jacea, and C. calcitrapa for discussion [21,22,30,31,32,33,34,35,36].
Centaurea cyanus L. and C. depressa Bieb., among their dominant components, had hexadecenoic acid, dodecanoic acid, and carvacrol, while C. depressa had tetradecanoic acid as well [26]. C. depressa was found to contain piperitone, elemol, β-eudesmol, and spathulenol as dominant components in another study [30]. The dominant components of C. iberica were arachidic acid, hexadecanoic acid, choleic acid, and isononane, while another record reported cyclosativene, dodecanoic acid, hexadecanoic acid, and tricosane as dominant components [31,32]. Centaurea jacea had two reports: one declared caryophyllene oxide, spathulenol, hexadecenoic acid, and 9-octadecanoic acid as dominant components, while the other listed germacrene D, hexahydrofarnesyl acetone, and ledol [21,33]. Centaurea solstitialis was the most studied, with four records on essential oil chemical composition, including bornyl acetate, limonene, and β-selinene in the first, hexadecenoic acid, heptacosane, and nonacosane in the second, and n-heneicosane, hexadecanoic acid, n-tricosane, n-pentacosane, and caryophyllene oxide in the third, and fourthly hexadecanoic acid, α-linolenic acid, germacrene D, and heptacosane [22,34,35,36]. As we can see, the dominant components of the essential oils from wild edible Centaurea species vary greatly, and only a few of the listed components overlap with those in C. scabiosa.
Previously reported essential oils that were tested for cytotoxic activity using the MTT test were isolated from C. cineraria, C. cyanus, C. behen, C. hajastana, and C. irritans. All of the mentioned essential oils showed cytotoxic activity on different cell lines: C. cineraria, with cyclosativene and tetracyclic sesquiterpene as dominant components in essential oil, was tested on neurons and neuroblastoma; C. cyanus with hexadecanoic and linoleic acid as dominant components in essential oil, was tested on the HT29 cell line; C. behen was tested on human blood cultures, but the essential oil and composition was not reported; C. hajastana with β eudesmol, β caryophyllene, germacrene D, and caryophyllene oxide as dominant components in essential oil were tested on human liver cancer cells (HepG2); and C. irritans with oxygenated monoterpenes as dominant components in essential oil was tested on breast lung cells (MCF 7). Tested essential oils showed high variability in their chemical composition. Comparing the studied essential oil with those previously studied and tested for cytotoxicity, we have found similar dominant components only with C. hajastana for caryophyllene oxide. [3,37,38,39,40].
The classical karyological method revealed 2n = 20 + 2B chromosomes in C. scabiosa. Genome size, assessed with flow cytometry, was 2C = 3.3 ± 0.01 pg or 1 Cx = 1628 Mbp and presents the first data on the DNA amount of this species from Croatia. The basic chromosome number in the Centaurea genus ranges from x = 7 to 16, and several ploidy levels, mainly diploid (2x) and tetraploid (4x), are presented. Previous data reported on the genome size of this species were 2.60 pg, 3.58 pg, and 3.54 pg [41,42]. Our data on chromosome number and genome size were in compliance with the previous data for diploid samples of this species and present data for easier authentication of plant material used for this phytochemical study [10,12].
Our study contributes to the body of knowledge on this plant genera by filling a gap in scientific data on phytochemistry and phytopharmacology. The presented data on the volatile oil chemical composition of C. scabiosa, a wild edible plant used in the Mediterranean human diet, may serve as a list of potentially bioactive chemical compounds presented as major and minor non-nutrient components of food. The absence of toxicity in human fibroblasts supports the idea of using this plant in the human diet.

3. Materials and Methods

3.1. Plant Material

Centaurea scabiosa L. plant material (leaves, stems, and flowers) was collected in July 2016 from wild growing populations in the coastal area of Croatia, in a village named Tijarica (X = 5,652,083; Y = 4,830,593), at an elevation of 645 m, growing on a dark brown soil type. The authentication of plant material was carried out by means of macroscopic traits. Centaurea scabiosa was additionally characterized by genome size estimation using flow cytometry and by chromosome number. Voucher specimens (2016_Cscabiosa_25_014) of plant materials used for this study have been deposited, with the date and location of collection, in the herbarium at the Department of Biochemistry, Faculty of Chemistry and Technology, Split, Croatia. On 4 May 2021, the plant name was checked with http://www.theplantlist.org for the last time. The leaves, stems, and a few flowers were used for aqueous and volatile oil extraction, while germinated seeds from the same individual plants were used for cytogenetic assessment and plant authentication.

3.2. Volatile Oil Extraction, Gas Chromatography (GC), and Gas Chromatography—Mass Spectrometry (GC–MS) Analyses

The volatile oil from extracted air-dried aerial parts of C. scabiosa was hydro-distilled using Clavenger apparatus for 3 h and stored in a sealed vial, under −20 °C until use. The gas chromatography analysis of EO was performed using a Varian Inc. gas chromatograph, model 3900, Lake Forest, CA, USA. The gas chromatograph was equipped with a flame ionization detector and mass detector, model 2100T, and a non-polar capillary column, VF-5MS (30 m × 0.25 mm i.d.; coating thickness 0.25 mm). The temperature program for the VF-5MS column was: 60 °C isothermal for 3 min, then increased to 246 °C at a rate of 3 °C min−1 and held isothermal for 25 min. The carrier gas was helium at a flow rate of 1 mL min−1, injector temperature was 250 °C, injected volume was 1 μL, split ratio was 1:20, and the FID detector temperature was 300 °C. Mass spectrometer ionization voltage was 70 eV, the mass scan range was 40–350 mass units, and the ion-source temperature was 200 °C. The percentages of components were calculated mathematically as mean values from the GC and GC-MS peak areas. Identification of EO chemical composition was based on comparison of compound mass spectra with databases (Wiley 7 library—Wiley, New York, NY, USA) and comparison of their retention indices, relative to a series of n-alkanes C9–C40, with an internal database created during previous analyses, and literature retention indices using NIST 2002 (National Institute of Standards and Technology, Gaithersburg, MD, USA) [43].

3.3. Toxicity on Human Primary Fibroblasts

The toxicity of C. scabiosa volatile oil was measured in primary fibroblasts through the MTT assay. To prepare a stock solution, essential oil was dissolved in dimethyl sulfoxide (DMSO) prior to cell treatment. Furthermore, when preparing working solutions for cell application, stock solutions were dissolved in cell culture growth medium. The concentrations used for biological activity testing were obtained through serial dilution in the 0.01–1 g/L range. Medium RPMI-1640 and Dulbecco’s phosphate-buffered saline were obtained from Sigma-Aldrich. Bovine serum, L-glutamine, the penicillin-streptomycin antibiotic, and trypsin-EDTA were obtained from Gibco by Life Technologies. Human skin primary fibroblasts were purchased from Axol Bioscience Ltd., GB. Cells were incubated with RMPI supplemented with 1% penicillin-streptomycin, 1% L-glutamine, and 10% fetal bovine serum in a 37 °C, humidified, 5% CO2 incubator. Fibroblasts were seeded on a 96-well plate for testing and incubated with Centaurea scabiosa volatile oil (VO) extract for 24 h (when tested on cells). After 24 h of incubation with plant extracts, the medium was removed and replaced with a fresh one, and MTT working solution of 5 mg/mL of Thiazolyl Blue-Tetrazolium Bromide was added to medium. Cells were incubated for 4 h at 37 °C in a 5% CO2 incubator. After incubation, the medium was removed, and samples of essential oil in a range of 8 serial dilutions in the range of 0.01–1 g/L, dissolved in DMSO (Sigma Aldrich, Co., St. Louis, MO, USA), as well as DMSO controls without essential oil in related concentrations, were added. The absorbance of samples in biological and technical triplicates of each sample was read at 595 nm with the EnSight multimode plate reader (PerkinElmer, Waltham, MA, USA). Since all the concentrations tested did not show a toxic effect, the final presentation of the result was made as the average of all the results for the technical triplicates for all concentrations used.

3.4. Chromosome Number and Genome Size Evaluation

Chromosome number was determined using the classical Feulgen technique from germinated seedlings of C. scabiosa. The cotyledons or first leaves were used for genome size assessment by flow cytometry, and Solanum lycopersicum L. ‘Montfavet 63–5′ (2C = 1.99 pg) was used as an internal standard [44]. Leaf samples and the internal standard were chopped together using a razor blade in a Petri dish with 600 μL of cold Gif Nuclear Isolation Buffer—GNB: 45 mM MgCl2, 30 mM sodium citrate, 60 mM MOPS (4-morpholine propane sulphonate, pH = 7), and 1% (w/v) polyvinylpyrrolidone 10,000, pH 7.2), containing 0.1% (w/v) Triton X–100, supplemented with 5 mM sodium metabisulphite and RNase (2.5 U/mL) [45]. The nuclei suspension was filtered through a nylon mesh (pore size 50 μm), to remove non-useful tissue fragments. The nuclei were stained with 50 μg/mL propidium iodide (Sigma Chemical Co., St. Louis, MO, USA) and flow cytometry was performed on a CytoFLEX S (Beckman Coulter- Life Science United States) with excitation at 561 nm, 30 mW; emission through a 610/20 nm band-pass filter. At least 5 individuals (biological replicates), measured in technical duplicates, with 5000–10,000 nuclei, were analyzed, and the average 2C DNA value was calculated using the linear relationship between the fluorescent signals from stained nuclei of known internal standards and the fluorescent signals from stained nuclei of the tested specimen.

3.5. Statistical Analysis

All statistical analyses were performed using the free software environment for statistical computing, the Microsoft Office package.

4. Conclusions

This study presents a multidisciplinary approach to volatile oil chemistry and some biological traits of C. scabiosa, a wild edible species used in the Mediterranean diet. This is the first study of C. scabiosa volatile oil’s chemical composition and biological activity, toxicity on human fibroblasts, as well as the first assessment of this species’ genome size in Croatia. The novelty in the chemical composition of the volatile oil was the dominance of oxygenated sesquiterpenes, which is unusual for Centaurea species. The presence of alloaromadendrene epoxide and α-cyperone as dominant chemical compounds in the volatile oil of C. scabiosa was first reported for the Centaurea genus. The presence of α-bisabolol as a dominant compound was also rather rare and first reported in this amount, as well as the presence of heptacosane, which had never been reported in such a high concentration. The cytotoxic activity of volatile oil on human fibroblasts was found to be non-existent. The presented results support the idea of using C. scabiosa species in the human diet, indicating their safety for dietary consumption.

Author Contributions

Experimental design, sample preparation and analysis, data analyses, and manuscript—preparation, I.C.; cytotoxic testing and manuscript—preparation, A.G.; designed cytogenetic plant studies and manuscript—preparation, S.S.-Y.; conceptualization of cytotoxic assessment experiments and manuscript—preparation, F.X.P.; performed volatile oil chemical analysis and manuscript—comments, O.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research has been supported in part by the Croatian Science Foundation under the project IP-2014-09-6897. This work was partially financially supported by the Ambassade de France en Croatie, the Service de Cooperation et d’Action Culturelle, the Agency for Mobility and EU Programs, the Centre National de la Recherche Scientifique de France (CNRS), and the Croatian Ministry of Science, Education, and Sport.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The work has been supported in part by the Croatian Science Foundation under the project IP-2014-09-6897. This work was partially a result of the project “Chemical and biological observation of selected plant species of Croatia”, which was financially supported by the Ambassade de France en Croatie, the Service de Cooperation et d’Action Culturelle, the Agency for Mobility and EU Programs, the Centre National de la Recherche Scientifique de France (CNRS), and the Croatian Ministry of Science, Education, and Sport. We would like to thank Spencer C. Brown for his assistance in cytometry at the Imagerie-Gif, Plateforme de Cytométrie CNRS-I2BC, Gif-sur-Yvette, France. We would also like to thank Mirko Ruščić for the botanical identification of the plant material.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

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Figure 1. Centaurea scabiosa volatile oil tested on primary human skin fibroblasts with the MTT assay in eight different concentrations in the range of 0.01–1 g/L (a) The result for essential oil presents the average of the results for eight different concentrations of C. scabiosa essential oils, in triplicates (b).
Figure 1. Centaurea scabiosa volatile oil tested on primary human skin fibroblasts with the MTT assay in eight different concentrations in the range of 0.01–1 g/L (a) The result for essential oil presents the average of the results for eight different concentrations of C. scabiosa essential oils, in triplicates (b).
Plants 11 03267 g001
Table 1. Chemical composition and chemical class distribution of the essential oil of Centaurea scabiosa L.
Table 1. Chemical composition and chemical class distribution of the essential oil of Centaurea scabiosa L.
Compound Name KIIdentification
Terpene Compounds
Non-oxygenated sesquiterpenes1.23
1Longifolene0.431409KI, MS
2Aromadendrene0.081421KI, MS
3γ-elemenetr1435KI, MS
4cis-ß-farnesenetr1443KI, MS
5α-hummulene0.181452KI, MS
6trans-ß-farnesenetr1478KI, MS
7Germacrene D0.541482KI, MS
Oxygenated sesquiterpenes41.09
8Spathulenol0.751568KI, MS
9Caryophyllene oxide10.901583KI, MS
10Aromadendrene oxide2.201626KI, MS
11Isospathulenol3.521639KI, MS
12Alloaromadendrene epoxide10.571655KI, MS
13α-bisabolol4.991692KI, MS
14α-cyperone8.161752KI, MS
Oxygenated diterpene1.41
15Phytol1.412119KI, MS
Non-terpene compounds
Hydrocarbons31.10
16Tricosane0.392300KI, MS
17Tetracosane0.212400KI, MS
18Pentacosane4.642500KI, MS
19Hexacosane0.942600KI, MS
20Heptacosane19.622700KI, MS
21Octacosane0.522800KI, MS
22Nonacosane4.782900KI, MS
Aldehydes3.67
23Benzene acetaldehyde0.351051KI, MS
24Longifolene aldehyde3.321609MS
Acids7.00
25Hexadecanoic acid4.031977KI, MS
26α-linolenic acid2.862165KI, MS
27Octadecanoic acid0.112197KI, MS
Esters4.03
28Benzoic acid methyl ester3.641091KI, MS
293,5-heptadienal-2-ethylidiene-6-methyl0.391345KI, MS
30Other compounds0.68
314-vinylguaiacol0.461330KI, MS
32Eugenol0.221363KI, MS
KI = Kovats retention index determined on a VF-5 MS column using the homologous series of n-alkanes (C9–C40); tr = traces (<0.1%); MS = mass spectra.
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Carev, I.; Golemac, A.; Siljak-Yakovlev, S.; Pellay, F.X.; Politeo, O. Volatile Oil Chemical Composition of Wild, Edible Centaurea scabiosa L. and Its Cytotoxic Activity. Plants 2022, 11, 3267. https://doi.org/10.3390/plants11233267

AMA Style

Carev I, Golemac A, Siljak-Yakovlev S, Pellay FX, Politeo O. Volatile Oil Chemical Composition of Wild, Edible Centaurea scabiosa L. and Its Cytotoxic Activity. Plants. 2022; 11(23):3267. https://doi.org/10.3390/plants11233267

Chicago/Turabian Style

Carev, Ivana, Anja Golemac, Sonja Siljak-Yakovlev, Francois Xavier Pellay, and Olivera Politeo. 2022. "Volatile Oil Chemical Composition of Wild, Edible Centaurea scabiosa L. and Its Cytotoxic Activity" Plants 11, no. 23: 3267. https://doi.org/10.3390/plants11233267

APA Style

Carev, I., Golemac, A., Siljak-Yakovlev, S., Pellay, F. X., & Politeo, O. (2022). Volatile Oil Chemical Composition of Wild, Edible Centaurea scabiosa L. and Its Cytotoxic Activity. Plants, 11(23), 3267. https://doi.org/10.3390/plants11233267

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