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Correction of creatine-creatinine conversion during serum creatinine quantification by two-dimensional liquid chromatography and double-spike isotope dilution tandem mass spectrometry.
Pineda-Cevallos, Daniela; Funes Menéndez, María; González-Gago, Adriana; Rodríguez-González, Pablo; Ignacio García Alonso, J.
Afiliación
  • Pineda-Cevallos D; Department of Physical and Analytical Chemistry, University of Oviedo, Avenida Julián Clavería, 8, 33006 Oviedo, Spain.
  • Funes Menéndez M; Department of Physical and Analytical Chemistry, University of Oviedo, Avenida Julián Clavería, 8, 33006 Oviedo, Spain.
  • González-Gago A; Department of Physical and Analytical Chemistry, University of Oviedo, Avenida Julián Clavería, 8, 33006 Oviedo, Spain.
  • Rodríguez-González P; Department of Physical and Analytical Chemistry, University of Oviedo, Avenida Julián Clavería, 8, 33006 Oviedo, Spain. Electronic address: rodriguezpablo@uniovi.es.
  • Ignacio García Alonso J; Department of Physical and Analytical Chemistry, University of Oviedo, Avenida Julián Clavería, 8, 33006 Oviedo, Spain.
Clin Chim Acta ; 554: 117778, 2024 Feb 01.
Article en En | MEDLINE | ID: mdl-38220136
ABSTRACT
BACKGROUND AND

AIMS:

Development of a candidate reference method based on bidimensional liquid chromatography coupled to ESI-MS/MS and double spike isotope dilution for serum creatinine quantification capable of correcting for creatinine-creatine interconversion during sample pretreatment. Study of the impact of the creatine-creatinine interconversion during the analysis of human serum samples. MATERIALS AND

METHODS:

13C1-creatinine and 13C2-creatine are added to the serum sample. Separation carried out by bidimensional liquid chromatography combining reversed phase and a strong cation exchange chromatography. The heart cut, containing creatine and creatinine, is automatically transferred to the second dimension. Quantification carried out by double spike isotope dilution tandem MS/MS.

RESULTS:

Minimization of spectral interferences and ion suppression due to matrix effects while increasing sample throughput compared to the direct coupling of cation exchange chromatography to the ESI source. Trueness of the method studied with the satisfactory analysis of two certified reference materials. Satisfactory intra- and inter-day precisions obtained analysing a serum pool and control sera. Analysis of 93 serum samples revealed negligible interconversions with no correlation with creatine levels.

CONCLUSIONS:

The method provides adequate analytical figures of merit for serum creatinine determination according to CSLI guidelines. Negligible creatine-creatinine interconversion is promoted with the applied sample preparation procedure.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Chim Acta Año: 2024 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Chim Acta Año: 2024 Tipo del documento: Article País de afiliación: España
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