Organ dependency variation of the chemical composition of Ziziphus lotus volatile fractions

The extended application fields of the essential oils keep them a subject of interest. In this study, we investigated the aerial part essential oil and the fruit essential oil of the wild plant Ziziphus lotus, collected from the southern region of Tunisia. These essential oils obtained by hydrodistillation using a Clevenger-type apparatus showed an extraction yield of 0.013% and 0.0046% respectively. The qualitative and quantitative analysis of the samples using GC-MS/GC-FID revealed two distinct compositions. Apocarotenoid derivatives characterized the essential oil of the aerial part; the major compound was hexahydrofarnesyl acetone (23.2%) followed by geranylacetone (12.5%) and cis-hexenyl-3-benzoate (11.1%). While the abundance of fatty acid marked the fruit essential oil. The noticed major compounds were 2-pentadecanone (16.9%), dodecanoic acid ethyl ester (14.5%) and n-hexadecanoic acid (13.0%). Such chemical composition may explain the traditional use of Ziziphus lotus as a drug to treat various pathologies. DOI: http://dx.doi.org/10.5281/zenodo.555296

GLC-MS profiling of non-polar extracts from Phlomis bucharica and P. salicifolia and their cytotoxicity

Phlomis species (Phlomis bucharica Regel and P. salicifolia Regel) have been traditionally used by Uzbek people as stimulant, tonic, diuretic, and in the treatment of ulcers, hemorrhoids, wounds and gynecological problems. In the present study, we characterized the chemical composition of non-polar extracts from P. bucharica and P. salicifolia by high resolution GLC-MS and evaluated their cytotoxicity. Concentrations of hexadecanoic acid in hexane and chloroform extracts were higher in P. bucharica than in P. salicifolia. 1,8- Cineol, camphor, borneol, α-terpinol, thymol, and isobornyl acetate were detected in P. bucharica but not in P. salicifolia. About 45 components were identified in P. bucharica and 40 in P. salicifolia. The chloroform extract from P. bucharica showed cytotoxicity in HeLa and HL-60 cells, with IC50 values of 26.07 and 29.42 μg/ml, respectively

Chemical investigation and screening of anti-proliferative activity on human cell lines of pure and nano-formulated lavandin essential oil

Lavandin essential oil (LEO), a natural sterile hybrid obtained by crossbreeding L. angustifolia × L. latifolia, is mainly composed by active components belonging to the family of terpenes endowed with relevant anti-proliferative activity, which can be enhanced by proper application of nanotechnology. In particular, this study reports the chemical characterization and the screening of the anti-proliferative activity on different human cell lines of pure and nano-formulated lavandin essential oil (EO). LEO and its formulation (NanoLEO) were analyzed by HS/GC-MS (Headspace/Gas Chromatography-Mass Spectrometry) to describe and compare their chemical volatile composition. The most abundant compounds were linalool and 1,8-cineole (LEO: 28.6%; 27.4%) (NanoLEO: 60.4%; 12.6%) followed by α-pinene (LEO: 9.6%; NanoLEO: 4.5%), camphor (LEO: 6.5%; NanoLEO: 7.0%) and linalyl acetate (LEO: 6.5%; NanoLEO: 3.6%). The cytotoxic effects of LEO and NanoLEO were investigated on human neuroblastoma cells (SHSY5Y), human breast adenocarcinoma cells (MCF-7), human lymphoblastic leukemia cells (CCRF CEM), human colorectal adenocarcinoma cells (Caco-2) and one normal breast epithelial cell (MCF10A) by the MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide)-assay. Caco-2, MCF7 and MCF10A normal cells resulted more resistant to the treatment with LEO, while CCRF-CEM and SHSY5Y cells were more sensitive. The antiproliferative effect of LEO resulted amplified when the essential oil was supplied as nanoformulation, mainly in Caco-2 cells. Scanning and transmission electron microscopy investigations were carried out on Caco-2 cells to outline at ultrastructural level possible affections induced by LEO and NanoLEO treatments

BIOLOGICAL PROPERTIES OF SALVIA SPECIES: AN OVERVIEW

In many Countries Salvia plant is used as common spice and added to food for a traditional longstanding culinary utilization. Many species of the genus Salvia are also widely used in folk medicine. Salvia plants are considered useful for numerous biological activities such as antioxidant, antibacterial, antiviral, antifungal, anticancer and for prevention of atherosclerotic plaque formation and blood circulation-improvement activity. In recent time attention was also focused on the possible use of salvia as anti-aging and neurodegenerative diseases counteracting agent. In the continuous searching for compounds potentially useful for the development of pharmaceuticals, the use of plants as pharmaceuticals has moved from an empirical-traditional knowledge and applications to more precise scientific uses. In this view in recent time species of salvia genus have been deeply investigated to identify compounds possibly responsible of the biological and pharmacological properties well established during time. In the present chapter an overview of recent findings on salvia compounds and their biological properties will be reported

GC-MS investigation and antiproliferative activities of extracts from male and female flowers of Schinus molle L

The aim of this study is to define chemical composition and antiproliferative activity of several compounds isolated from Schinus molle male and female flowers on human neuroblastoma (SH-SY5Y) and human leukemia (HL60) cell lines. Three extracts obtained by using solvents with different polarities (petroleum ether, diethyl ether and acetone) were characterized by GC/MS analysis revealing qualitative and quantitative differences in the chemical composition of male and female flowers. Nineteen components were identified and both flower extracts were dominated by the sesquiterpene hydrocarbons fraction, mainly elemol, followed by bicyclic sesquiterpenes and by a smaller amount of monoterpenes. The biological activities of the extracts were evaluated by dose-dependent viability assay on two different cell lines and HL60 cells resulted more sensitive to the treatment. The presence of compounds at low concentration with a well-established cytotoxic activity such as beta-elemene, beta-caryophyllene and gamma-eudesmol could exert a synergistic cytotoxic effect

Morphology, Anatomy and Secondary Metabolites Investigations of Premna odorata Blanco and Evaluation of Its Anti-Tuberculosis Activity Using In Vitro and In Silico Studies

In-depth botanical characterization was performed on Premna odorata Blanco (Lamiaceae) different organs for the first time. The leaves are opposite, hairy and green in color. Flowers possess fragrant aromatic odors and exist in inflorescences of 4-15 cm long corymbose cyme-type. In-depth morphological and anatomical characterization revealed the great resemblance to plants of the genus Premna and of the family Lamiaceae, such as the presence of glandular peltate trichomes and diacytic stomata. Additionally, most examined organs are characterized by non-glandular multicellular covering trichomes, acicular, and rhombic calcium oxalate crystals. P. odorata leaves n-hexane fraction revealed substantial anti-tuberculous potential versus Mycobacterium tuberculosis, showing a minimum inhibition concentration (MIC) of 100 μg/mL. Metabolic profiling of the n-hexane fraction using gas-chromatography coupled to mass spectrometry (GC/MS) analysis revealed 10 major compounds accounting for 93.01%, with trans-phytol constituting the major compound (24.06%). The virtual screening revealed that trans-phytol highly inhibited MTB C171Q receptor as M. tuberculosis KasA (β-ketoacyl synthases) with a high fitting score (∆G = -15.57 kcal/mol) approaching that of isoniazid and exceeding that of thiolactomycin, the co-crystallized ligand. Absorption, distribution, metabolism, excretion and toxicity predictions (ADME/TOPKAT) revealed that trans-phytol shows lower solubility and absorption levels when compared to thiolactomycin and isoniazid. Still, it is safer, causing no mutagenic or carcinogenic effects with higher lethal dose, which causes the death of 50% (LD50). Thus, it can be concluded that P. odorata can act as a source of lead entities to treat tuberculosis