Ítem


Avaluació de l’especificitat analítica en assajos diagnòstics in vitro

In vitro diagnostics is a cornerstone of modern medicine, providing essential information for early detection, monitoring, and management of a wide range of diseases. A significant proportion of clinical decisions rely on the results of these analytical tests, making the reliability and specificity of diagnostic methods crucial. This project was conducted in the laboratories of Linear Chemicals; a company specialized in in vitro diagnostic products. The main objective was to evaluate the analytical specificity of clinical chemistry assays (cholesterol, glucose, creatinine, uric acid, urea, and triglycerides) as part of the validation process for CE marking. The assays were performed using control serum samples (normal and pathological), supplemented with interfering compounds selected based on scientific literature. A deviation equal to or greater than ±10% compared to the non-supplemented control was considered a significant interference. The results show that most of the tested methods demonstrate good analytical specificity. However, relevant interferences were observed, such as ascorbic acid in glucose determination. In these cases, dose-response curves were performed to characterize the effect according to the concentration of the interferent. This study provides experimental validation of the analytical specificity of these methods and supports non-interference claims in the technical documentation required for CE certification

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Director: Vilanova i Brugués, Maria
Cano Masllorens, Lluís
Font Rifa, Maria
Altres contribucions: Universitat de Girona. Facultat de Ciències
Autor: Ramon i Ferrer, Pol
Data: juliol 2025
Resum: In vitro diagnostics is a cornerstone of modern medicine, providing essential information for early detection, monitoring, and management of a wide range of diseases. A significant proportion of clinical decisions rely on the results of these analytical tests, making the reliability and specificity of diagnostic methods crucial. This project was conducted in the laboratories of Linear Chemicals; a company specialized in in vitro diagnostic products. The main objective was to evaluate the analytical specificity of clinical chemistry assays (cholesterol, glucose, creatinine, uric acid, urea, and triglycerides) as part of the validation process for CE marking. The assays were performed using control serum samples (normal and pathological), supplemented with interfering compounds selected based on scientific literature. A deviation equal to or greater than ±10% compared to the non-supplemented control was considered a significant interference. The results show that most of the tested methods demonstrate good analytical specificity. However, relevant interferences were observed, such as ascorbic acid in glucose determination. In these cases, dose-response curves were performed to characterize the effect according to the concentration of the interferent. This study provides experimental validation of the analytical specificity of these methods and supports non-interference claims in the technical documentation required for CE certification
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Format: application/pdf
Accés al document: http://hdl.handle.net/10256/28679
Llenguatge: cat
Drets: Attribution-NonCommercial-NoDerivatives 4.0 International
URI Drets: http://creativecommons.org/licenses/by-nc-nd/4.0/
Matèria: Diagnòstic de laboratori
Diagnòstic in vitro
Diagnosis, Laboratory
In vitro diagnòstics
Títol: Avaluació de l’especificitat analítica en assajos diagnòstics in vitro
Tipus: info:eu-repo/semantics/bachelorThesis
Repositori: DUGiDocs

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