Methyl Isoeugenol Research Articles

Sedative-Hypnotic Effect and Mechanism of Carbon Nanofiber Loaded with Essential Oils of Ligusticum chuanxiong (Ligusticum chuanxiong Hort.) and Finger Citron (Citrus medica L. var. sarcodactylis) on Mice Models of Insomnia.

(1) Background: Insomnia is a neurological illness that poses a significant threat to both physical and mental health. It results in the activation of neuroglial cells, heightened neuroinflammation, oxidative stress, and disruptions in the Hypothalamic-Pituitary-Adrenal (HPA) axis. Ligusticum Chuanxiong (CX) and Finger citron (FC) are frequently utilized botanicals for addressing sleeplessness. Both herbs possess notable anti-inflammatory properties in their volatile oils. However, their effectiveness is hindered by the nasal mucosal irritation and instability they exhibit. (2) Methods: This study involved the preparation of a nanofiber composite system using carbon nanofiber (CNF) suspensions containing essential oils of Ligusticum chuanxiong-Finger citron (CXEO-FCEO-CNF). The effects and mechanisms of these essential oils in improving insomnia were investigated using an insomnia mouse model after encapsulation. (3) Results: The CXEO-FCEO-CNF had an average particle size of 103.19 ± 1.64 nm. The encapsulation rates of essential oils of Ligusticum chuanxiong (CXEO) and essential oils of Finger citron (FCEO) were 44.50% and 46.15%, respectively. This resulted in a considerable improvement in the stability of the essential oils over a period of 30 days. The essential oils effectively decreased the irritation of the nasal mucosa following encapsulation. Furthermore, CXEO-FCEO-CNF enhanced voluntary activity and sleep in mice with insomnia, notably boosted the activity of superoxide dismutase (SOD), reduced the concentration of lipoxidized malondialdehyde (MDA), decreased the levels of hormones associated with the HPA axis, and regulated the levels of neurotransmitters, resulting in a beneficial therapeutic outcome. CXEO-FCEO-CNF contains a total of 23 active ingredients, such as alpha-Asarone, (E)-methyl isoeugenol, and Senkyunolide. These ingredients primarily work by modulating the Janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling system to decrease oxidative stress and inflammatory reactions. (4) Conclusions: This study presented initial evidence that the combination of CXEO and FCEO in nanofiber formulations effectively reduces the nasal mucosal irritation and instability of essential oils. Furthermore, it demonstrated the potential anti-neuroinflammatory and therapeutic effects of these formulations in treating insomnia. Overall, this study provides a theoretical foundation for developing new essential oil formulations derived from herbs.

ITRAQ-based proteomics revealed the acaricidal mechanism of methyl isoeugenol against Dermatophagoides farinae

ABSTRACT Dermatophagoides farinae is a major source of allergens that are the cause of allergic diseases in humans. Methyl isoeugenol (MIE) is a naturally occurring compound in plants and its strong acaricidal toxicity has been established; however, the mechanism behind its acaricidal properties remains unclear. In this study, to investigate the action mechanism of MIE on D. farinae the isobaric tags for relative and absolute quantification (iTRAQ) proteomics method is used. Protein samples were extracted from D. farinae before and after 24 h of MIE treatment for iTRAQ technique analysis. Bioinformatics analysis revealed that most differentially expressed proteins were located in the cytoplasm, impacting cytoplasmic function. Additionally, Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses showed significant enrichment of the differential proteins in the cellular autophagy signalling pathway. The autophagy-related proteins Autophagy-Related Protein 3 (ATG3) and Cathepsin L (CTSL) were up-regulated, disrupting the autophagic process. We found that the main action mechanism of MIE against D. farinae might be cellular autophagy. The transcriptional validation of six differential proteins demonstrated consistent expression trends with the proteomics data. This study reveals the acaricidal mechanism of MIE for the first time and lays the foundation for further research on D. farinae control.

Antimicrobial properties of Clausena anisata (Rutaceae) essential oil from Bafou area against the pathogenic fungus Candida albicans and antioxidant activity

The aim of the present work was to determine the antimicrobial and antioxidant activities of Clausena anisata essential oil. The extraction of essential oils was performed by the hydro distillation method with a Clevenger apparatus. The determination of essential oils chemical composition was conducted by gas chromatography and gas chromatography coupled with mass spectrometry. Then the antimicrobial activity was assessed using disk diffusion method and micro titration. In order to determine the antioxidant activity 2 methods were carried out: the free radical scavenging assay was performed using the DPPH+ radical (2,2-diphenyl-1-picrylhydrazyl) and the method with ABTS radical reagents (acid2, 2'-azynobis-[3-ethylbenzothiazoline-6 ​​sulfonic acid]). The yield of extraction of the essential oil was 0.77%. The study of its chemical composition revealed E- anethol (70.77%), methyl iso eugenol (13.85) as major compounds. The anti-radical DPPH test revealed a SC50 of 1g/L; 0.265g/L respectively for DPPH and ABTS tests. The results also highlighted a potent antimicrobial property. An antimicrobial screening study revealed a susceptibility of Candida albicans isolates at a concentration of 8000 ppm. This activity was characterized by minimum inhibitory concentrations of 2000 ppm for all the tested pathogenic yeasts Sab1, Sab2, Sab3, Sab250, Sab2501, Sab256, Sab259 and Sab290. The essential oil minimum inhibitory concentration (MIC) was lower than the MIC of fluconazole. The same observations were resulted with the fungicidal effect. These data can be used as a starting point for subsequent studies to produce antifungal and antioxidant drugs to face the challenge of the antimicrobial resistance and oxidative stress.

Susceptibility Patterns in Staphylococcus and Klebsiella Causing Nosocomial Infections upon Treatment with E-Anethole-Rich Essential Oil from Clausena anisata

High rates of resistance to antibiotics are associated with healthcare-related infections, thus demonstrating the urgent need for effective antimicrobials against these maladies. The present study aims to determine the chemical composition of essential oil (EO) from Clausena anisata leaves and evaluate their antibacterial activity against selected nosocomial bacteria. To this end, one kilogram (1 kg) of fresh leaves of C. anisata was washed and boiled with 500 mL of distilled water for 2−4 h using a Clevenger apparatus. The oil was then collected in an Erlenmeyer, dried using anhydrous sodium sulfate, bottled in a tinted glass bottle and refrigerated at 4 °C before analysis. Next, the as-prepared oil was analyzed using gas chromatography-mass spectrometry (GC-MS). The essential oil was further tested against a panel of selected nosocomial bacteria, including Staphylococcus and Klebsiella species, among others, by microdilution using a resazurin assay to determine the minimum inhibitory and minimum bactericidal concentrations (MICs and MBCs, respectively). As a result, 0.77% of EO was extracted from fresh leaves of C. anisata. The GC-MS analysis revealed that the as-prepared essential oil contained E-anethole (70.77%), methyl isoeugenol (13.85%), estragole (4.10%), γ-terpinene (3.33%), myrcene (2.82%) and sabinene (0.77%), with E-anethole being the major constituent. Twenty-two compounds were identified in the EO of C. anisata leaves through gas chromatography. Upon antibacterial testing against selected nosocomial pathogens, the E-anethole-rich essential oil exhibited MIC and MBC values ranging from 3.91 to 125 µg/mL and 7.81 to 125 µg/mL, respectively, indicative of a bactericidal orientation of the plant’s essential oil (MIC/MBC ratio < 4). This novel contribution highlights the scientific validation of the use of C. anisata leaves in the traditional treatment of various infectious diseases. However, toxicity and pharmacokinetic studies, mechanistic bases of the antibacterial action, and in vivo antibacterial experiments of the E-anethole-rich EO of C. anisata should be investigated to successfully use this plant in the treatment of infectious diseases.

Highly efficient enrichment of eugenol anesthetics in aquatic products using magnetic nanospheres decorated covalent organic framework microflowers

Herein, uniform magnetic covalent organic framework (MCOF) microflowers were synthesized by facile inlaying aldehyde-functionalized Fe3O4 nanoparticles onto the COF under mechanical stirring at room temperature. The MCOF microflowers kept flower-shaped morphology with high crystallinity and magnetism. In addition, the good water dispersibility and reusability made the MCOF microflowers to be good magnetic solid phase extraction (MSPE) adsorbents for the high-efficiency enrichment of eugenol anesthetics from aquatic products. The MCOF microflowers showed fast adsorption rate (10 min) and high extraction efficiency (above 84.02%) for eugenol anesthetics under optimal conditions. The MCOF microflowers displayed maximum adsorption capacities of 6.67, 12.31, and 16.78 µg g−1 for eugenol, eugenol acetate, and methyl isoeugenol, respectively. The MCOF microflowers based MSPE coupled with high-performance liquid chromatography method was proposed for enrichment and analysis of eugenol anesthetics in tilapia, shrimp and crab samples. The method showed a wide linear of 5.0–500.0 µg kg−1 and low detection limits of 2.4–3.6 μg kg−1 for eugenol anesthetics. The recoveries of spiked eugenol anesthetics ranged from 80.0% to 118.8% with relative standard deviations no>9.2%. Results indicate the high potential of MCOF microflowers to be an adsorbent for efficient extraction and analysis of eugenol anesthetics from complex aquatic product samples.

Chemical Variation and Environmental Influence on Essential Oil of Cinnamomum camphora.

Cinnamomum camphora is a traditional aromatic plant used to produce linalool and borneol flavors in southern China; however, its leaves also contain many other unutilized essential oils. Herein, we report geographic relationships for the yield and compositional diversity of C. camphora essential oils. The essential oils of 974 individual trees from 35 populations in 13 provinces were extracted by hydrodistillation and analyzed qualitatively and quantitatively by gas chromatography-mass spectrometry and gas chromatography-flame ionization detection, respectively. Oil yields ranged from 0.01% to 3.46%, with a significantly positive correlation with latitude and a significantly negative correlation with longitude. In total, 41 compounds were identified, including 15 monoterpenoids, 24 sesquiterpenoids, and two phenylpropanoids. Essential oil compositions varied significantly among individuals and could be categorized into various chemotypes. The six main chemotypes were eucalyptol, nerolidol, camphor, linalool, selina, and mixed types. The other 17 individual plants were chemotypically rare and exhibited high levels of methyl isoeugenol, methyl eugenol, δ-selinene, or borneol. Eucalyptol-type plants had the highest average oil yield of 1.64%, followed in decreasing order by linalool-, camphor-, mixed-, selina-, and nerolidol-type plants. In addition, the five main compounds exhibited a clear geographic gradient. Eucalyptol and linalool showed a significantly positive correlation with latitude, while selina-6-en-4-ol was significantly and negatively correlated with latitude. trans-Nerolidol and selina-6-en-4-ol showed significantly positive correlations with longitude, whereas camphor was significantly and negatively correlated with longitude. Canonical correspondence analysis indicated that environmental factors could strong effect the oil yield and essential oil profile of C. camphora.

Fluorescent microsphere-based lateral-flow immunoassay for rapid and sensitive determination of eugenols

In this study, a sensitive monoclonal antibody (mAb) 1B5 against eugenols was prepared based on a novel hapten. Based on this mAb, a paper-based lateral-flow immunoassay (LFIA) was developed using Eu-fluorescent microspheres sensor, that could achieve qualitative and quantitative detection of eugenols within 10 min. Results showed colorimetric values observed by the naked eye were 12.3 µg/kg, 12.3 µg/kg, 37 µg/kg and 111 µg/kg for eugenol, isoeugenol, methyl eugenol, and methyl isoeugenol, respectively, in both water and fish samples. For quantitative detection of eugenol, isoeugenol, methyl eugenol and methyl isoeugenol, the detection ranges were 4.49–48.4 µg/kg, 6.02–66.8 µg/kg, 16.5–150 µg/kg and 47.9–710 µg/kg in water, and 3.9–30.9 µg/kg, 5.9–62.6 µg/kg, 16.7–255 µg/kg, and 44.5–890 µg/kg in fish, respectively. The recovery test and detection in fish demonstrated the reliability of the LFIA in real samples. Therefore, the developed LFIA produced a promising alternative tool for the rapid on-site detection of eugenols.

Masking effects on iso-valeric acid recognition by sub-threshold odor mixture.

Masking unpleasant odors with pleasant-smelling odorants has a long history and is utilized in various industries, including perfumery and consumer products. However, the effectiveness of odor masking is idiosyncratic and temporary. In this study, we employed Sniff olfactometry (SO) to investigate the psychophysics of masking using brief 70 ms stimulations with mixtures of the mal-odorant iso-valeric acid (IVA) and different masking agents. IVA is a component of human sweat that can overpower its smell and is often associated with unpleasant descriptors such as "gym locker," "smelly feet," "dirty clothes," and so on. Traditionally, high concentrations of pleasant-smelling odorants are used to mitigate the unpleasantness of IVA in situations involving clothing or environments contaminated with IVA. To examine the masking effects of sub-threshold levels of various masking agents (neohivernal, geraniol, florhydral, decanal, iso-longifolanone, methyl iso-eugenol, and s-limonene) on IVA, we conducted experiments using SO to measure the probability of recognizing IVA after 70 ms stimulations with headspaces containing mixtures of super-threshold concentrations of IVA and sub-threshold concentrations of IVA suppressors. The study involved nine subjects, and on average, a single masking agent was found to decrease IVA recognition probability by 14-72%. Moreover, a sub-threshold odor mixture consisting of 6 masking agents demonstrated a substantial decrease in IVA recognition, with a reduction of 96%.

Comparative Analysis Of Chemical Constituent And Antimicrobial Potential Of Acorus Calamus Linn (Sweet Flag) In The Different Geographical Regions Of North Himalayas

Sweet flag (Acorus calamus) is a well-known plant all over the world due to its specific bioactive components β- asarone in plants.The present study reports the quantitative estimation of rhizome oil of the sweet flag plant; obtain from the various district ofUttarakhand, and different geographical surroundings. GC-MS is used to estimate the quantity of rhizome oil. Although leaves areenriched by the several medicinal constituents revealed by the previous studies, rhizome, and the oil it is being investigated. The maincomponent which was identified was Cis-ocimene, Linalool, Trans methyl isoeugenol, β and α-asarone, and euasarone. β-asarone inthe different samples; showed a higher percentage as compared to another component. It was observed that the Gopeshwar regionsample had the 74.36 least percentage and the Pauri sample had the 92.22 highest percentage of β-Asarone. Meanwhile, the Gopeshwarregion sample had 17.25 highest percentage, and the Pauri sample had 1.57 least percentage of α-Asarone. Fungal infection is prevalentnowadays. The oil from all regions subjected to antifungal activity against the Aspirigilla fumigates, A. Parasiticus, MicrosporumCanis, M. gypsum, Cladosporium, Aspergillus niger. The inhibition zone diameter (IZD) against Aspirigilla fumigates, A. parasiticusand was a maximum of 10cm for the Gopeshwar sample,9cm for the Ramnagar sample as compared to the reference drug gentamicin.

Hydrophobic deep eutectic solvent-based ultrasonic-assisted liquid-liquid microextraction combined with GC for eugenol, isoeugenol, and methyl isoeugenol determination in aquatic products

The use of deep eutectic solvents (DESs) has great prospects because of the green and efficient characteristics, which can be used for developing analytical methods for foods. In this research, assisted by ultrasonic waves, a liquid-liquid microextraction detection method combined with gas chromatography was established for three anaesthetics (eugenol, isoeugenol, and methyl isoeugenol) in aquatic food. The processing conditions including the components, ratio of hydrogen bond acceptor and hydrogen bond donor, DES volume, ultrasonic time, and pH were evaluated and optimised to improve the extraction efficiency, which was based on the DES structures and properties. In-house method validation was carried out by applying to real samples. A Thymol: levulinic acid DES (with a molar ratio of 1:2) was used as the extractant and the recoveries were as high as 93–101% for eugenol, 90–100% for methyl isoeugenol, and 86–94% for isoeugenol with RSDs <5% under optimum conditions. The limit of detection and quantification of the eugenol compounds were 0.08–0.10 μg/mL and 0.26–0.33 μg/mL, respectively. The method has green credentials and comparable LOD to homologous apparatus, which can be used for the determination of eugenol components in aquatic food.

2-(4-Chlorophenyl)-4-(3,4-dimethoxy-phenyl)-6-methoxy-3-methylquinoline

A 2,4-diarylquinoline derivative, 2-(4-chlorophenyl)-4-(3,4-dimethoxyphenyl)-6-methoxy-3-methylquinoline, was synthesized in a conventional two-step procedure from p-anisidine, p-chlorobenzaldehyde and methyl isoeugenol as available starting reagents through a sequence of BF3·OEt2-catalyzed Povarov cycloaddition reaction/oxidative dehydrogenation aromatization processes under microwave irradiation conditions in the presence of a green oxidative I2-DMSO system. The structure of the compound was fully characterized by FT-IR, 1H and 13C-NMR, ESI-MS, and elemental analysis. Its physicochemical parameters (Lipinski’s descriptors) were also calculated using the Molinspiration Cheminformatics software. The diarylquinoline molecule obtained is an interesting model with increased lipophilicity and thus permeability, an important descriptor for quinoline-based drug design. Such types of derivatives are known for their anticancer, antitubercular, antifungal, and antiviral activities.

Effect of Salt (Sodium Chloride) Replacement With Potassium Chloride, High Pressure Processing, and Cold Storage at 4°C on Beef Sausage Volatile Compounds.

This study aimed to investigate the partial substitution of 0, 25 and 50% sodium chloride (NaCl) by potassium chloride (KCl) coupled with high-pressure processing (HPP) effects on volatile compounds and lipid oxidation of beef sausage at five (0, 3, 7, 14, and 21) different cold storage days (4°C). The odor activity values (OAV) of the various compounds were visualized by heat map analysis. Thiobarbituric acid reactive substances (TBARS) of the samples treated with 100% NaCl and HPP increased by an average of 0.52 ± 0.01 mg MDA/kg compared with the control (100% NaCl-no HPP) across the 21 storage days. In addition, 50% NaCl substitution with KCl in combinations with HPP treatments increased TBARS across the 21 storage days by an average of 0.40 ± 0.02 mg MDA/kg compared with no HPP treatment. However, on day 3, there was a sharp decrease in TBARS by an average of 0.10 ± 0.01 mg MDA/kg compared with days 0, 7, 14, and 21 in all treatments. At the end of 21 days of storage, a total of 227 volatile compounds were identified and quantified in the beef sausage, including 43 aldehydes, 46 phenols, 8 ketones, 30 alcohols, 14 acids, 12 esters, 27 terpenes, and 47 alkanes. However, no ketone compounds were detected on days 7, 14 and 21; esters on day 14 and acids on days 14 and 21 in the samples treated with or without HPP across the salts levels. However, high OAVs (OAV > 1) were obtained after partial substitution of NaCl with KCl at 25 and 50% with HPP treatment compared to the samples not treated with HPP. The aroma perceived in the beef sausage was due to compounds with the highest OAVs such as; pentadecanal, benzyl carbazate, anethole, myristicin, o-cresol, phenylacetaldehyde and (E)-methyl isoeugenol, pentadecanal, hexanoic acid, octanoic acid, eugenol, trans-2-nonenal, trans-2-octenal, trans-2-decenal, 2-butyl-1-octanol, 2,3-butanedione, ethyl hexanoate, ethyl octanoate, (-)-4-terpineol which had an OAV > 1 as compared to the other compounds with an OAV < 1. In conclusion, 25 and 50% NaCl partial replacement with KCl coupled with HPP technique can be considered in producing low-NaCl beef sausage in order to improve the flavor and decrease lipid oxidation during cold storage.

Dispersive solid-phase extraction combined with high-performance liquid chromatography for determination of seven anesthetics in aquatic products

随着麻醉剂广泛用于渔业生产过程和水产品运输等领域,建立水产品中麻醉剂残留的检测方法具有重要意义。由于水产品基质复杂且麻醉剂残留水平低,因此需要合适的前处理方法以提高检测灵敏度。该研究基于分散固相萃取-高效液相色谱,建立了一种同时检测水产品中普鲁卡因、丁氧卡因、三卡因、丁香酚、甲基丁香酚、异丁香酚、甲基异丁香酚7种麻醉剂的分析方法。前处理采用分散固相萃取;确定了1.0%甲酸乙腈为提取溶剂,20 mg苯乙烯-甲基丙烯酸缩水甘油酯聚合物微球(PS-GMA)、50 mg N-丙基乙二胺(PSA)和10 mg C18混合吸附剂为净化剂,二甲基亚砜(DMSO)辅助氮吹的前处理方法;优化了提取时间和DMSO用量等条件。7种麻醉剂采用Welch welchrom C18色谱柱(250 mm×4.6 mm, 5 μm)进行分离,以甲醇和0.05%甲酸-5 mmol/L乙酸铵水溶液为流动相进行梯度洗脱,检测波长为235、260和290 nm,以鱼肉和对虾两种基质匹配标准曲线进行定量分析。实验结果表明,在优化的实验条件下,7种目标麻醉剂在各自的浓度范围内具有良好的线性关系(相关系数R2>0.999),检出限(LOD)为0.011~0.043 mg/kg。在鱼肉样品中,3个水平的平均加标回收率为79.7%~109%,相对标准偏差(RSD)低于7.2%;在对虾样品中,平均回收率为78.0%~99.9%, RSD低于8.3%。该方法具有快捷简便、操作简单、灵敏度高等优点,可应用于水产品中3种氨基苯甲酸酯类和4种丁香酚类麻醉剂的检测。

Kinetic modeling for microwave-assisted green extraction: Effects of power on citronella oil from Cymbopogon nardus leaf

Cymbopogon nardus, known as a native plant to the subtropical and tropical areas, is widely cultivated and utilized for food flavoring and pharmaceutical purposes. Microwave-assisted hydrodistillation (MHD) was preferred as a greener method to extract essential oils. Kinetics of essential oil extraction from Cymbopogon nardus leaves were observed under different values of microwave irradiation power at atmospheric pressure. This method facilitated a high yield of citronella oil (3.68%–3.79%) at reduced time. Kinetic investigation of citronella oil extraction process was simulated using mathematic formulation such as pseudo-first and pseudo-second-order models. Results indicated that the studied models provided moderate fit for the experimental data, whereas the latter of the two kinetic models demonstrated better general fit, especially at low power levels. Moreover, GC-MS analysis of the citronella oil showed that the main compounds identified were geraniol and methyl isoeugenol. Other active compounds such as citronellal and β-citronellol were also present in considerable amount. These results suggested that the MHD method could be a prominent alternative to obtain essential oils in higher yields and deliver valuable chemical constituents upon shorter extraction time, compared to its conventional alternatives.

Hydrolyzation-Triggered Ultralong Room-Temperature Phosphorescence in Biobased Nonconjugated Polymers.

Amorphous nonconjugated room-temperature phosphorescent (RTP) polymers have aroused ever-increasing attention. However, the variety of such polymers is still rare due to limited preparation strategies. Herein, we report a facile strategy to achieve ultralong RTP emission in biobased nonconjugated polymers through a hydrolyzation process. The investigated polymers are synthesized by free radical solution copolymerization using biomass methyl isoeugenol and maleic anhydride as monomers. Noticeably, the obtained polymers carry no conventional fluorescent units but can exhibit blue fluorescence. More interestingly, after hydrolysis in sodium hydroxide aqueous solution, the resulting hydrolyzed polymers emit both enhanced blue emission and persistent RTP (up to 400 ms) under air conditions, with reversible emission performance switched via the uptake and removal of water. Also worthy to be highlighted is that the emission can be remarkably regulated by the cations in carboxylate or the substituents on the benzene ring. The as-obtained polymers demonstrate potential applications in anticounterfeiting and information encryption.

Preliminary Predictive Model of Termiticidal and Repellent Activities of Essential Oil Extracted from Ocotea quixos Leaves against Nasutitermes corniger (Isoptera: Termitidae) Using One-Factor Response Surface Methodology Design

Termites are one of the most challenging pests that agriculture and urban environments are faced with. They bring substantial losses in annual and perennial crops and damage wood components at construction sites. The development of natural products with biological activity for termite control is an ecological alternative in the search to replace conventional products. Hence, the aim of this research was to predict the termiticidal and repellent effects of the essential oil from Ocotea quixos leaves on Nasutitermes corniger using a one-factor response surface methodology design. The variable analysed was the concentration of essential oil in ethanol at an interval of 0.3–0.05% for anti-termite activity and between 0.12 and 0.01% for repellent action. A 100% mortality rate was found at concentrations higher than 0.12% and at the minimum concentration analysed, the effect was 22.2%. As for the repellent action, the concentration of 0.12% was able to repel 100% of the termites and at 0.01% it repelled 48.9%. The analysis of the essential oil from Ocotea quixos leaves by GC-MS resulted in the presence of 42 compounds, 39 of them elucidated. The main compounds were (E)-cinnamyl acetate (36.44%), (E)-cinnamaldehyde (27.03%), (E)-β-caryophyllene (5.21%) and (E)-methyl isoeugenol (4.18%).

Chemical composition of ocimum sanctum essential oil by GC-MS analysis

The essential oil from the dried leaves of Ocimum Sanctum was extracted by hydro distillation and after drying with sodium sulfate anhydrous it was analyzed by GC-MS. The oil was found to be a mixture of hydrocarbons (26.463%), alcohols (19.326%) and oxides (3.252%). Among the hydrocarbons caryophyllene (22.265%) was found to be a major component followed by α-caryophyllene (2.071%), α-pinene (0.125%), camphene (0.121%), α-cubebene (0.123%), copaene (1.637%) and α-bourboene (0.244%). Among the alcohols eugenol (15.906%) was found in large quantity followed by Borneol (0.468%) and Methyl iso-eugenol (2.952%). Caryophyllene oxide (3.252%) was also found in appreciable amount.

Albizia lebbeck and Albizia zygia volatile oils exhibit anti-nociceptive and anti-inflammatory properties in pain models

Ethnopharmacological relevanceAlbizia lebbeck and Albizia zygia are used in Nigeria, South Africa and other countries for the treatment of flu, fever, pain, epilepsy, and inflammation.Aim of the Study: Application of plant essence for treating ailments is common among local communities. This research was designed to characterize the volatile compounds and evaluate the toxicity, anti-inflammatory and anti-nociceptive properties of this plant species. Materials and methodsThe volatile oils were analysed comprehensively utilizing gas chromatography-flame ionization detector (GC-FID) and gas chromatography coupled with mass spectrometry (GC/MS) using the HP-5 column. The toxicity was evaluated using the toxicity assay. The anti-nociceptive and anti-inflammatory assays were analysed by a hot plate, Formalin, and carrageenan-induced edema assays, respectively. ResultsThe essential oils were obtained in a yield of 0.1% (v/w) calculated on a dry weight basis for both oils. The main compounds of A. lebbeck were 2-pentylfuran (16.4%), (E)-geranyl acetone (15.46%), (E)-α-ionone (15.45%) and 3-Octanone (11.61%), while the oil of A. zygia is mainly hexahydrofarnesyl acetone (33.14%), (E)-methyl isoeugenol (11.7%) and 2-methyl tetradecane (6.64%). The volatile oils are non-toxic to about 5000 mg/kg dose. Albizia zygia significantly (P < 0.001) suppressed the nociceptive afferent fibres in a non-dose dependent manner in comparison to A. lebbeck in the hot plate model. Both oils inhibited nociceptive mediators at both phases of the formalin-induced assay, with a maximum inhibition (100%) at the inflammatory stage. The volatile oils inhibited the Carrageenan-induced inflammation at all phases ranging from P < 0.05 to P < 0.001. The probable pro-inflammatory inhibitory mechanism might be the suppression of some pain biomarkers such as histamine, serotonin, bradykinin, and the Interleukins (ILs) induced by the edema. Volatile constituents such as ionones, eugenol derivatives and other compounds cause the anti-nociceptive and anti-inflammatory activities reported. ConclusionThis is the first report of the volatile oils and bioassays of Albizia zygia, while the study also confirms previous studies of A. lebbeck. Generally, the findings further prove the use of the plants as pain ameliorating agents.

Nematocidal Effects of a Coriander Essential Oil and Five Pure Principles on the Infective Larvae of Major Ovine Gastrointestinal Nematodes In Vitro.

The anthelmintic effects of extracted coriander oil and five pure essential oil constituents (geraniol, geranyl acetate, eugenol, methyl iso-eugenol, and linalool) were tested, using larval motility assay, on the third-stage larvae (L3s) of Haemonchus contortus, Trichostrongylus axei, Teladorsagia circumcincta, Trichostrongylus colubriformis, Trichostrongylus vitrinus and Cooperia oncophora. Coriander oil and linalool, a major component of tested coriander oil, showed a strong inhibitory efficacy against all species, except C. oncophora with a half maximal inhibitory concentration (IC50) that ranged from 0.56 to 1.41% for the coriander oil and 0.51 to 1.76% for linalool. The coriander oil and linalool combinations conferred a synergistic anthelmintic effect (combination index [CI] <1) on larval motility comparable to positive control (20 mg/mL levamisole) within 24 h (p < 0.05), reduced IC50 values to 0.11–0.49% and induced a considerable structural damage to L3s. Results of the combined treatment were validated by quantitative fluorometric microplate-based assays using Sytox green, propidium iodide and C12-resazurin, which successfully discriminated live/dead larvae. Only Sytox green staining achieved IC50 values comparable to that of the larval motility assay. The cytotoxicity of the combined coriander oil and linalool on Madin–Darby Canine Kidney cells was evaluated using sulforhodamine-B (SRB) assay and showed no significant cytotoxic effect at concentrations < 1%. These results indicate that testing essential oils and their main components may help to find new potential anthelmintic compounds, while at the same time reducing the reliance on synthetic anthelmintics.

Vapor Pressures and Thermodynamic Properties of Phenylpropanoid and Phenylbutanoid Attractants of Male Bactrocera, Dacus, and Zeugodacus Fruit Flies at Ambient Temperatures.

We report on the vapor pressures at ambient temperatures of seven attractants of Bactrocera, Dacus, and Zeugodacus fruit flies-raspberry ketone, cuelure, raspberry ketone trifluoroacetate, methyl eugenol, methyl isoeugenol, dihydroeugenol, and zingerone-by a vapor saturation method. Dry nitrogen was passed over each compound at well-controlled temperatures. Entrained vapor from the compounds was trapped on Tenax GR tubes and analyzed by thermal desorption-gas chromatography-mass spectrometry. The measured attractant amounts on the traps were converted to vapor pressures. Data were subsequently fitted by the Antoine equation. From the Antoine equation parameters, thermodynamic properties for each compound were calculated at 298K. The calculated vapor pressures were used to compare the volatility of the fruit fly attractants and to infer implications for field applications. Using ambient temperature readings yields far better estimates of vapor pressure values at temperatures relevant for insect control than do Antoine equation parameters derived from high-temperature readings.