Keyword search (4,164 papers available)

"Skinner CD" Authored Publications:

Title Authors PubMed ID
1 Luminescent Electro-Spun Nanofibers Crosslinked with Boronic Esters Exhibiting Controlled Release of Carbon Dots for Detection of Wound pHs and Enhanced Antimicrobial Lokuge ND; Casillas-Popova SN; Singh P; Clermont-Paquette A; Skinner CD; Findlay BL; Naccache R; Oh JK; 40920389
BIOLOGY
2 Multi-stimuli-responsive degradable boronic ester-crosslinked e-spun nanofiber wound dressings Casillas-Popova SN; Lokuge ND; Singh P; Cirillo A; Thinphang-Nga A; Skinner CD; Vuckovic D; Findlay BL; Oh JK; 40557709
BIOLOGY
3 pH-Responsive Degradable Electro-Spun Nanofibers Crosslinked via Boronic Ester Chemistry for Smart Wound Dressings Casillas-Popova SN; Lokuge ND; Andrade-Gagnon B; Chowdhury FR; Skinner CD; Findlay BL; Oh JK; 38989606
BIOLOGY
4 A threshold LC-MS/MS method for 92 analytes in oral fluid collected with the Quantisal® device Desharnais B; Lajoie MJ; Laquerre J; Mireault P; Skinner CD; 33035929
CHEMBIOCHEM
5 The Key Role of Intrinsic Lifetime Dynamics from Upconverting Nanosystems in Multiemission Particle Velocimetry Tessitore G; Maurizio SL; Sabri T; Skinner CD; Capobianco JA; 32924221
CNSR
6 Qualitative threshold method validation and uncertainty evaluation: A theoretical framework and application to a 40 analytes liquid chromatography-tandem mass spectrometry method Camirand Lemyre F; Desharnais B; Laquerre J; Morel MA; Côté C; Mireault P; Skinner CD; 32476284
CHEMBIOCHEM
7 Capillary electrochromatography of peptides and proteins. Bandilla D, Skinner CD 15354432
CHEMBIOCHEM
8 Design and optimization of porous polymer enzymatic digestors for proteomics. Lin W, Skinner CD 19575382
CHEMBIOCHEM
9 Increased oxidative modifications of amniotic fluid albumin in pregnancies associated with gestational diabetes mellitus. Boisvert MR, Koski KG, Skinner CD 20063865
CHEMBIOCHEM
10 A case of fatal idiosyncratic reaction to the designer drug 3,4-methylenedioxypyrovalerone (MDPV) and review of the literature. Desharnais B, Dazé Y, Huppertz LM, Mireault P, Skinner CD 28668987
CHEMBIOCHEM
11 A Tool for Automatic Correction of Endogenous Concentrations: Application to BHB Analysis by LC-MS-MS and GC-MS Desharnais B; Lajoie MJ; Laquerre J; Savard S; Mireault P; Skinner CD; 31141151
CHEMBIOCHEM

 

Title:A Tool for Automatic Correction of Endogenous Concentrations: Application to BHB Analysis by LC-MS-MS and GC-MS
Authors:Desharnais BLajoie MJLaquerre JSavard SMireault PSkinner CD
Link:https://pubmed.ncbi.nlm.nih.gov/31141151/
DOI:10.1093/jat/bkz024
Publication:Journal of analytical toxicology
Keywords:
PMID:31141151 Category:J Anal Toxicol Date Added:2019-05-31
Dept Affiliation: CHEMBIOCHEM
1 Laboratoire de sciences judiciaires et de médecine légale, Department of Toxicology, 1701 Parthenais Street, Montréal, Québec, Canada.
2 Concordia University, Department of Chemistry & Biochemistry, 7141 Sherbrooke Street West, Montréal, Québec, Canada.

Description:

Several substances relevant for forensic toxicology purposes have an endogenous presence in biological matrices: beta-hydroxybutyric acid (BHB), gamma-hydroxybutyric acid (GHB), steroids and human insulin, to name only a few. The presence of significant amounts of these endogenous substances in the biological matrix used to prepare calibration standards and quality control samples (QCs) can compromise validation steps and quantitative analyses. Several approaches to overcome this problem have been suggested, including using an analog matrix or analyte, relying entirely on standard addition analyses for these analytes, or simply ignoring the endogenous contribution provided that it is small enough. Although these approaches side-step the issue of endogenous analyte presence in spiked matrix-matched samples, they create serious problems with regards to the accuracy of the analyses or production capacity. We present here a solution that addresses head-on the problem of endogenous concentrations in matrices used for calibration standards and quality control purposes. The endogenous analyte concentration is estimated via a standard-addition type process. This estimated concentration, plus the spiked concentration are then used as the de facto analyte concentration present in the sample. These de facto concentrations are then used in data analysis software (MultiQuant, Mass Hunter, etc.) as the sample's concentration. This yields an accurate quantification of the analyte, free from interference of the endogenous contribution. This de facto correction has been applied in a production setting on two BHB quantification methods (GC-MS and LC-MS-MS), allowing the rectification of BHB biases of up to 30 µg/mL. The additional error introduced by this correction procedure is minimal, although the exact amount will be highly method-dependent. The endogenous concentration correction process has been automated with an R script. The final procedure is therefore highly efficient, only adding four mouse clicks to the data analysis operations.





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