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http://hdl.handle.net/10553/70033
Título: | Quantification of urinary derivatives of Phenylbutyric and Benzoic acids by LC-MS/MS as treatment compliance biomarkers in Urea Cycle disorders | Autores/as: | Andrade, Fernando Vitoria, Isidro Martín Hernández, Elena Pintos-Morell, Guillem Correcher, Patricia Puig-Piña, Rocío Quijada-Fraile, Pilar Peña Quintana, Luis Marquez, Ana Mª Villate, Olatz García Silva, Mª Teresa de las Heras, Javier Ceberio, Leticia Rodrigues, Esmeralda Almeida Campos, Teresa Yahyaoui, Raquel Blasco, Javier Vives-Piñera, Inmaculada Gil, David del Toro, Mireia Ruiz-Pons, Mónica Cañedo, Elvira Barba Romero, Miguel Angel García-Jiménez, Mª Concepción Aldámiz-Echevarría, Luis |
Clasificación UNESCO: | 32 Ciencias médicas | Palabras clave: | Benzoic Acid Hyperammonaemia Phenylbutyric Acid Stability Tandem Mass Spectrometry, et al. |
Fecha de publicación: | 2019 | Publicación seriada: | Journal of Pharmaceutical and Biomedical Analysis | Resumen: | Purpose: Salts of phenylacetic acid (PAA) and phenylbutyric acid (PBA) have been used for nitrogen elimination as a treatment for hyperammonaemia caused by urea cycle disorders (UCD). A new analytical method for PBA measurement in urine which helps to evaluate the drug adherence has been implemented. Methods: Urine specimens from UCD patients receiving PBA were analysed by tandem mass spectrometry to measure urine phenylacetylglutamine (PAGln). Some clinical and biochemical data for each patient were collected. Results: Our study included 87 samples from 40 UCD patients. The PAGln levels did not correlate with height, weight or age. However, the PAGln values showed correlation with PBA dose (r = 0.383, P = 0.015). Plasma glutamine and ammonia levels presented a positive correlation (r = 0.537, P < 0.001). The stability for PAGln in urine was determined at different storage temperatures. Conclusions: We have developed a simple method for the determination of PAGln in urine, which acts as useful biomarker of effective drug delivery. PAGln in urine is stable at room temperature at least for 15 days, and for several months when frozen at -20 °C. This procedure is useful for the optimization and monitorization of the drug dose allowing the use of spot urine samples. | URI: | http://hdl.handle.net/10553/70033 | ISSN: | 0731-7085 | DOI: | 10.1016/j.jpba.2019.112798 | Fuente: | Journal of Pharmaceutical and Biomedical Analysis [ISSN 0731-7085], v. 176 |
Colección: | Artículos |
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