Analytical method validation for determination of total mercury in human blood by zeeman mercury spectrometer ra-915+ with the pyrolysis module pyro-915+
This article describes the methodology of the validation about the identification of total mercury in blood samples by Zeeman atomic absorption spectrophotometry RA-915+ with the module of Pyrolysis PYRO-915+, suitable for the direct determination of total mercury concentrations in various matrices,...
- Autores:
-
Ramírez, Carolina
Olarte, Ermel
Tellez, Eliana
Palma, Marien
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2013
- Institución:
- Universidad Nacional de Colombia
- Repositorio:
- Universidad Nacional de Colombia
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unal.edu.co:unal/50024
- Acceso en línea:
- https://repositorio.unal.edu.co/handle/unal/50024
http://bdigital.unal.edu.co/43552/
- Palabra clave:
- mercurio
validación de métodos
espectrofotometría de absorción atómica
mercury
analytical methods validation
atomic absorption spectrophotometry
- Rights
- openAccess
- License
- Atribución-NoComercial 4.0 Internacional
Summary: | This article describes the methodology of the validation about the identification of total mercury in blood samples by Zeeman atomic absorption spectrophotometry RA-915+ with the module of Pyrolysis PYRO-915+, suitable for the direct determination of total mercury concentrations in various matrices, that unlike other atomization techniques (graphite furnace, cold vapor or hydride generator) does not require a sample pre-treatment. With the application of this validation, is provided the reliability in the results. Most of the validation parameters were subjected to analysis of variance ANOVA with a confidence level of 95%. It was obtained a detection limit of 2.16 µg/L, a quantitation limit of 5.54µg/L and linearity in the range of 5.54 µg/L to , in addition, the precision and accuracy was evaluated, obtaining favorable results in the analysis. The calculation of the expanded uncertainty for this method was 0.610 µg/L. |
---|