The Effect of Post-Newtonian Spin Precessions on the Evolution of Exomoons’ Obliquity

Putative natural massive satellites (exomoons) have gained increasing attention when they orbit Jupiter-like planets within the habitable zone of their host main-sequence star S. An exomoon s is expected to move within the equatorial plane of its host planet p, with its spin S s aligned with its orbital angular momentum L , which, in turn, is parallel to the planetary spin S p. If, in particular, the common tilt ε of such angular momenta to the plane of the satellite–planet motion about the star, assumed fixed, has certain values, the stellar latitudinal irradiation experienced on the exomoon may allow it to sustain life as we know it, at least for certain orbital configurations. An Earth analog (similar in mass, radius, oblateness, and obliquity) is considered, which orbits within 5–10 planetary radii R p from its Jupiter-like host planet. The de Sitter and Lense–Thirring spin precessions due to the general relativistic post-Newtonian (pN) field of the host planet have an impact on an exomoon’s habitability for a variety of different initial spin–orbit configurations. Here I show it by identifying long-term variations in the satellite’s obliquity ε s, where variations can be ≲10°–100°, depending on the initial spin–orbit configuration, with a timescale of ≃0.1–1 million years. Also the satellite’s quadrupole mass moment J 2 s induces obliquity variations that are faster than the pN ones but do not cancel them. Tidal dissipations, which may potentially have a relevant impact on the outlined pattern, are not included in the present analysis.

Application of a Liquid-Liquid Microextraction Method Based on a Natural Hydrophobic Deep Eutectic Solvent for the Extraction of Plastic Migrants from Kombuchas

A vortex-assisted liquid-liquid microextraction, based on a natural hydrophobic deep eutectic solvent made from the monoterpene thymol and octanoic fatty acid, was employed for the analysis of 11 phthalate esters and one adipate in kombucha (a tea-based fermented beverage). Separation and determination were performed using an ultra-high performance liquid chromatography (UHPLC) system coupled to a single quadrupole mass spectrometer. Confirmatory analyses were carried out through UHPLC tandem mass spectrometry. The full method was validated in terms of matrix effect, matrix-matched calibration, sensitivity, recovery, limits of detection and quantification and repeatability. Satisfactory determination coefficients for quadratic calibration curves (≥0.9938), recovery values (67–120%) and limits of detection (0.07–5.45 µg/L) were obtained. Analysis of 26 kombucha samples reported concentrations for dibutyl phthalate and dimethyl phthalate in the range between the limit of quantification (LOQ) and 16.18 ± 1.14 µg/L, although these phthalates were also detected under the LOQ in some of the analyzed samples. Only one of the samples bottled in plastic containers (7) did not present residues while only five of the 19 samples in glass bottles contained any plasticizer. However, the highest concentration was found in a kombucha bottled in food-grade glass. This work represents the first application in which phthalates and adipates are analyzed in kombuchas.

Vitamin E Acetate Determination in Vaping Liquids and Non-targeted Analysis of Vaping Emissions of Diluents of Concern, Vitamin E Acetate and Medium-Chain Triglycerides Oil

During the summer of 2019, cases of lung injury associated with vaping emerged in North America, including among individuals who reported exclusive use of nicotine vaping liquids. Once vitamin E acetate was identified as a potential causative agent a quantitative method based on a simple sample dilution, separation by gas chromatography and analysis by triple quadrupole mass spectrometry (GC MSMS) was developed. Method detection limit (MDL) and limit of quantification (LOQ) were determined at 0.159 µg/mL and 0.505 µg/mL, respectively. The analysis was performed on a subset of 203 commercially sourced nicotine containing vaping liquids of various flavour profile and nicotine range (nicotine free-59 mg/mL) from an internal inventory. The target analyte, Vitamin E Acetate, was not detected in any samples analyzed, as expected, given the reported detection in literature and high association of the chemical with cannabis and not nicotine containing vaping products.

MASS SPECTROMETRIC STUDIES OF THE COMPOSITION OF VOLATILE ORGANIC COMPOUNDS RELEASED BY VARIOUS FUNGAL SPECIES OF GENUS LECANICILLIUM

For the first time, the quantitative and qualitative composition of volatile organic compounds (VOCs), released by strains of various species of entomopathogenic fungi (EF) of the genus Lecanicillium, was studied using a quadrupole mass spectrometer. Lecanicillium fungi are used as an alternative to chemical pesticides for plant protection. The main detected components of the gas phase over the EF mycelium on the 10th day of growing on the agar Czapek's medium were carbon dioxide (5–20%), oxygen (0.1–15%), acetone (0.2–12 ppm), pentane (up to 0.5 ppm), acetic acid (up to 0.15 ppm). Acetone and pentane were found in the VOCs of all studied strains, acetic acid — in 5 strains belonging to different species, in other strains it appeared after a longer period of time, or was absent completely. Among the VOCs of some strains, substances such as hexyl acetate, sulfur dioxide were found in small quantities. These substances may be responsible for the pathogenic and repellent properties of the studied fungi with respect to phytophages.

Quantification of 15 Antibiotics Widely Used in the Critical Care Unit with a LC-MS/MS System: An Easy Method to Perform a Daily Therapeutic Drug Monitoring

Potential under- or overdose of antibiotics may occur in intensive care units due to high variability in plasma concentrations. The risk is either treatment failure or toxicity. Thus, therapeutic drug monitoring of antibiotics may guide dosing adjustment, maximising antibacterial efficacy and minimising toxicity. The aim of this study was to develop and validate a method for the analysis of 15 antibiotics including beta-lactams, linezolid, fluoroquinolones, daptomycin, and clindamycin to have a complete panel in the management of infections. We proposed to develop a fast, sensitive, and quantitative method for the analysis of 15 antibiotics using ultra-performance liquid chromatography coupled with triple quadrupole mass spectrometer (UPLC-MS/MS) technology. this method required only 100 µL of plasma and consisted of a rapid liquid–liquid deproteinisation using methanol. Calibration curves ranged from 0.078 to 500 mg/L depending on the molecules, and were defined according to a therapeutic range. Inter- and intra-assay precisions values were less than 15%. This work described the development and the full validation of a precise, sensitive and accurate assay using UPLC-MS/MS technology. After validation, this new assay was successfully applied to routine therapeutic drug monitoring.