Quantification of urinary derivatives of Phenylbutyric and Benzoicacids by LC-MS/MS as treatment compliance biomarkers in Urea Cycledisorders
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Date
2019-08-01Author
Andrade, Fernando
Vitoria, Isidro
Martín Hernandez, Elena
Pintos-Morell, Guillermo
Correcher, Patricia
Puig Piña, Rocío
Quijada Fraile, Pilar
Peña Quintana, Luis
Marquez, Ana M.
Villate, Olatz
García Silva, María Teresa
De las Heras Montero, Javier Adolfo
Ceberio, Leticia
Rodrigues, Esmeralda
Almeida Campos, Teresa
Yahyaoui, Raquel
Blasco, Javier
Vives Piñera, Inmaculada
Gil, David
Ruiz Pons, Mónica
Cañedo, Elvira
Barba Romero, Miguel Angel
García Jiménez, Mª Concepción
Aldámiz-Echevarría Azuara, Luis
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Journal of Pharmaceutical and Biomedical Analysis 176 : (2019) // Article ID 112798
Abstract
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.