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Improved Desmopressin Analysis of Clinical Samples

Scientific Expertise
Fast Turnaround Time

Need
  • A client required higher sensitivity at lower sample volume to conduct sampling for a bioequivalence study
  • The existing RIA method did not have the sensitivity to reduce the sample volume below 4mL to achieve a LLOQ of 2pg/mL
Approach
  • Developed and validated an LC-MS/MS method for Desmopressin using a four-fold reduced sample volume of 1mL
  • Performed a comparison between the RIA and the LC-MS/MS method by analyzing human samples using both methods
Benefits
  • With the new method the client successfully reduced the blood draw volume and increased the number of time points to support the bioequivalence study
  • As an additional benefit, the turnaround time was increased by a factor of four due to the faster sample preparation and analysis