TY - JOUR T1 - Validation of Isolated Metabolites from Drug Metabolism Studies as Analytical Standards by Quantitative NMR JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 433 LP - 440 DO - 10.1124/dmd.110.036343 VL - 39 IS - 3 AU - Gregory S. Walker AU - Tim F. Ryder AU - Raman Sharma AU - Evan B. Smith AU - Amy Freund Y1 - 2011/03/01 UR - http://dmd.aspetjournals.org/content/39/3/433.abstract N2 - In discovery and development, having a qualified metabolite standard is advantageous. Chemical synthesis of metabolite standards is often difficult and expensive. As an alternative, biological generation and isolation of metabolites in the nanomole range are readily feasible. However, without an accurately defined concentration, these isolates have limited utility as standards. There is a significant history of NMR as both a qualitative and a quantitative technique, and these concepts have been merged recently to provide both structural and quantitative information on biologically generated isolates from drug metabolism studies. Previous methodologies relied on either specialized equipment or the use of an internal standard to the isolate. We have developed a technique in which a mathematically generated signal can be inserted into a spectrum postacquisition and used as a quantitative reference: artificial signal insertion for calculation of concentration observed (aSICCO). This technique has several advantages over previous methodologies. Any region in the analyte spectra, free from interference, can be chosen for the reference signal. In addition, the magnitude of the inserted signal can be modified to appropriately match the intensity of the sample resonances. Because this is postacquisition quantification, no special equipment or pulse sequence is needed. Compared with quantitation via the addition of an internal standard (10 mM maleic acid), the signal insertion method produced similar results. For each method, precision and accuracy were within ±5%, stability of signal response over 8 days was ±5%, and the dynamic range was more than 3 orders of magnitude: 10 to 0.01 mM. ER -