Determination of synthetic cathinone "α-PVP" and its metabolite in urine using solid phase extraction and gas chromatography-mass spectrometry.

Rationale The presence of alpha-pyrrolidinovalerophenone (alpha-PVP) and its metabolites in urine is evidence of the administration of alpha-PVP. A toxicological challenge is that the metabolites of alpha-PVP exhibit amphoteric properties, which make them unsuitable for detection using gas chromatography-mass spectrometry (GC/MS). In the study reported, proper derivatization and sample extraction were essential for improving the sensitivity for GC/MS analysis. Methods An automated solid-phase extraction (SPE) method has been developed and optimized. The derivatization efficiency was tested using longer reaction time and the addition of polar pyridine into a mixture of N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) with 1% trimethylchlorosilane. Method validation, including linearity, limit of detection, precision, accuracy, and recovery, was evaluated using automatic SPE and GC/MS. Results The results suggested that adding pyridine to BSTFA (1:1, v/v) significantly improved derivatization efficiency and precision. After optimization, the linear range was from 25 to 1000 ng mL(-1) with R-2 > 0.9950. The limit of detection was 5 ng mL(-1) for alpha-PVP and 25 ng mL(-1) for OH-alpha-PVP. The recovery for SPE was over 88%. The inter-day and intra-day precisions were less than 15%. A forensic sample has been found containing alpha-PVP (67.3 ng mL(-1)) and OH-alpha-PVP (560.2 ng mL(-1)). Conclusions This study is the first to validate an auto-SPE-GC/MS method for the quantification and qualification of alpha-PVP and OH-alpha-PVP in urine. We have successfully improved the derivatization efficiency and developed a sensitive and semi-automatic approach. This approach is desirable for the detection of synthetic cathinone at trace levels in biological samples.