Le conte de fées parodique français du XVIIIe siècle : un discours antimerveilleux

À première vue inoffensif, le conte de fées parodique français du XVIIIe siècle dissimule, sous le couvert de la féérie, un discours anticontesque et antiromanesque. Qu'ils soient explicites ou non, ces propos prennent généralement forme dans les métalepses émises tant par les narrateurs que par les narrataires dans le texte lui-même ou dans le péritexte auctorial. L'élaboration d'une typologie, à partir de dix contes publiés entre 1730 et 1754, offre une vue d'ensemble de ce phénomène narratif épars et ouvre la voie à une analyse transversale des discours tenus dans ce trope. Loin d'être innocent, le contenu des métalepses contesques laisse poindre une nouvelle poétique du conte et du roman qui s'éloigne progressivement de l'idéal classique régissant toujours ces deux genres au XVIIIe siècle.

Assessment of Tandem Mass Spectrometry and High Resolution Mass Spectrometry for the Analysis of Bupivacaine in Plasma

Triple quadrupole mass spectrometers coupled with high performance liquid chromatography are workhorses in quantitative bioanalyses. It provides substantial benefits including reproducibility, sensitivity and selectivity for trace analysis. Selected Reaction Monitoring allows targeted assay development but data sets generated contain very limited information. Data mining and analysis of non-targeted high-resolution mass spectrometry profiles of biological samples offer the opportunity to perform more exhaustive assessments, including quantitative and qualitative analysis. The objectives of this study was to test method precision and accuracy, statistically compare bupivacaine drug concentration in real study samples and verify if high resolution and accurate mass data collected in scan mode can actually permit retrospective data analysis, more specifically, extract metabolite related information. The precision and accuracy data presented using both instruments provided equivalent results. Overall, the accuracy was ranging from 106.2 to 113.2% and the precision observed was from 1.0 to 3.7%. Statistical comparisons using a linear regression between both methods reveal a coefficient of determination (R2) of 0.9996 and a slope of 1.02 demonstrating a very strong correlation between both methods. Individual sample comparison showed differences from -4.5% to 1.6% well within the accepted analytical error. Moreover, post acquisition extracted ion chromatograms at m/z 233.1648 ± 5 ppm (M-56) and m/z 305.2224 ± 5 ppm (M+16) revealed the presence of desbutyl-bupivacaine and three distinct hydroxylated bupivacaine metabolites. Post acquisition analysis allowed us to produce semiquantitative evaluations of the concentration-time profiles for bupicavaine metabolites.