Only trace amounts of parent benzodiazepines are present in urine following extensive metabolism and conjugation. Thus, hydrolysis of glucuronides is necessary for improved detection. Enzyme hydrolysis is preferred to retain identification specificity, but can be costly and time-consuming. The assessment of a novel recombinant b-glucuronidase for rapid hydrolysis in benzodiazepine urinalysis is presented. Glucuronide controls for oxazepam, lorazepam and temazepam were treated with IMCSzymeTM recombinant b-glucuronidase. Hydrolysis efficiency was assessed at 558C and at room temperature (RT) using the recommended optimum pH. Hydrolysis efficiency for four other benzodiazepines was evaluated solely with positive patient samples. Maximum hydrolysis of glucuronide controls at 5 min at RT (mean analyte recovery 94% for oxazepam and lorazepam and 80% for temazepam) was observed. This was considerably faster than the optimized 30 min incubation time for the abalone b-glucuronidase at 658C. Mean analyte recovery increased at longer incubation times at 558C for temazepam only. Total analyte in patient samples compared well to targets from abalone hydrolysis after recombinant b-glucuronidase hydrolysis at RT with no incubation. Some matrix effect, differential reactivity, conjugation variability and transformation impacting total analyte recovery were indicated. The unique potential of the IMCSzymeTM recombinant b-glucuronidasewas demonstrated with fast benzodiazepine hydrolysis at RT leading to decreased processing time without the need for heat activation.

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