Francesco Della Valle , Fabiola Eugelio , Carmine Merola , Giulia Caioni , Federico Fanti , Marcello Mascini , Antonella Damiano , Michele Amorena , Michele Del Carlo , Manuel Sergi , Dario Compagnone
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Oxysterol fingerprinting via UPLC-APCI-MS/MS for monitoring developmental stages in the zebrafish model
Oxysterols, oxidized derivatives of cholesterol, play multifaceted roles in cholesterol homeostasis and cellular signalling. Despite their recognized biological relevance, the temporal dynamics of oxysterol profiles during vertebrate development remain poorly understood. In this study, we developed and validated a robust UHPLC-MS/MS method for the quantification of ten oxysterols in zebrafish (Danio rerio) embryos across five developmental stages (3-, 24-, 48-, 72-, and 96-hours post-fertilization). The method exhibited excellent performance in terms of sensitivity, recovery, and reproducibility, following EMA guidelines. A combination of hierarchical clustering analysis (HCA) and Random Forest classification revealed distinct stage-specific oxysterol profiles. Notably, 6α-hydroxycholesterol emerged as the most discriminative marker, followed by 24- and 27-hydroxycholesterol, indicating their potential involvement in neurodevelopmental and metabolic regulation processes. These findings provide new insights into the role of oxysterols during embryogenesis and establish a reliable platform for evaluating oxysterol dynamics in developmental, toxicological, and pharmacological studies using the zebrafish model.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.