5 and 0 μM after mixing see more 100 μL of p-nitrophenol standard with 150 μL of stop solution) was added to the p-nitrophenol calibration curve

wells. The solutions were mixed for 30 s with a microplate shaker before reading the plate. Plates were read in a Molecular Devices SPECTRAmax plate reader using Softmax Pro software. The enzymatic reaction product (p-nitrophenol) was measured at the absorbance wavelength of 405 nm. Results of the test samples were expressed relative to the activity measured in velaglucerase alfa in the absence of serum sample and reported as percent inhibition: a sample with > 20% inhibition was considered to be “positive”, and a sample with ≤ 20% inhibition was considered to be “negative”. Serum samples that were positive for anti-velaglucerase alfa antibody were diluted in NAb sample diluent (20 mM citric acid/40 mM sodium phosphate/0.1% Triton X-100/1 mg/mL BSA, pH 5.5), and prepared for NAb quantification at 1/10, 1/20, 1/40, and 1/80 final dilutions. Serum from normal human donors was used as a negative control. The purified sheep anti-glucocerebrosidase polyclonal antibody was spiked in normal human serum at 250 μg/mL and used as a positive control. INCB024360 manufacturer A patient sample with > 30% inhibition was used as a second positive control. All assays were validated according to FDA and EMA guidelines (FDA,

2001 and EMEA, 2009). To assess assay repeatability, five independent assays were performed by a single analyst. Up to six determinations each of a minimum of three concentrations were tested in every assay. 4-Aminobutyrate aminotransferase Intra-assay precision was determined from up to six determinations per concentration per day and inter-assay precision was calculated from the determinations obtained from the five assays. Analyst and day effects were established from four

independent assays performed by two analysts on two different days (data not shown). Accuracy was determined from the precision data relative to the mean value of each concentration. The precision determined at each concentration level did not exceed 15% of the relative standard deviation (% RSD) as instructed in the FDA and EMA guidelines. Characterization of the mouse anti-glucocerebrosidase monoclonal antibody calibrator for the screening assay showed similar affinity and binding kinetics for velaglucerase alfa and imiglucerase. Furthermore, there was a negligible effect on the affinity and binding kinetics when these drugs were labeled with biotin (Table 1). Precision, accuracy, and sensitivity of this assay were determined according to FDA, EMA, and International Conference on Harmonisation (ICH) guidelines (FDA, 2001, ICH, 2005 and EMEA, 2009) and are reported in Table 2. The lowest limit of detection (LOD) and lowest limit of quantification (LOQ) were determined according to the following equations, as recommended by the ICH guidelines (ICH, 2005): LOD=[3.