Evaluation of matrix effects in the analysis of volatile organic compounds in whole blood with solid phase microextraction
The complexity and matrix variability of biological samples requires an accurate evaluation of matrix effects. Dilution of the biological sample is the simplest way to reduce or avoid the matrix effect. In the present study, a set of volatile organic compounds with different volatilities was used to...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2013 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10256/19559 |
| Acceso en línea: | http://hdl.handle.net/10256/19559 |
| Access Level: | acceso abierto |
| Palabra clave: | Síntesi en fase sólida Compostos orgànics volàtils Sang -- Anàlisi Solid-phase synthesis Volatile organic compounds Blood -- Analysis |
| Sumario: | The complexity and matrix variability of biological samples requires an accurate evaluation of matrix effects. Dilution of the biological sample is the simplest way to reduce or avoid the matrix effect. In the present study, a set of volatile organic compounds with different volatilities was used to assess the effect of the dilution of blood samples on the extraction efficiency by headspace solid phase microextration. It was found that there was a significant matrix effect, but that this effect differs significantly depending on the volatility of the compound. A 1:2 (blood:water) dilution was enough to allow quantitative recoveries of those compounds VOCs with boiling points <100ºC. For compounds with boiling points between 100-150ºC, the matrix effect was stronger and a 1:5 dilution was required. The dilution of blood samples proved to be inefficient for quantitative recovery of compounds with boiling points >150ºC. A 1:5 dilution of the sample allowed detection limits in the range of of ng/L to be obtained. This was sufficient to detect the main volatile compounds present in blood and contamination after exposure |
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