Whole Blood Stability
This assay is used to determine the stability of a test article in whole blood from human, rat, mouse, dog, or monkey.
Required from Sponsor
- Either a minimum of 100 µL of test article at 10 mM in DMSO or 2 mg of powder
- Exact molecular mass of test article and its salt form
- MSDS or handling and storage information, e.g., light sensitive, store at -20°C, etc.
- A table of percent remaining of test article at each time point
- Half-life, as applicable
- Test article at 1 µM dissolved in whole blood collected with K2EDTA as the anticoagulant
- Whole blood from a species specified by the sponsor
- Human: mixed-gender, ≥ 3 donors pooled
- Rat: male Sprague-Dawley, ≥ 3 donors pooled
- Mouse: male CD-1, ≥ 3 donors pooled
- Dog: male Beagle, ≥ 3 donors pooled
- Monkey: male Cynomolgus, ≥ 3 donors pooled
- Adjust pH of whole blood to 7.4 prior to initiation of experiment
- Single incubation of test article (n=1) in whole blood at 37°C
- Sample a single replicate (n=1) at 0, 15, 30, 60, and 120 minutes
- Use LC-MS/MS to determine the peak area response ratio (peak area corresponding to test article divided by that of an analytical internal standard) without running a calibration curve
1. The results from this assay will be provided to the sponsor in the ExpressPlus report format, which may include graphical representations of data and comparison with historical data for reference articles.
2. This assay is often run to develop sample handling protocols for in vivo PK studies.
3. To distinguish effects of pH and ionic strength on test article stability from effects of the biological matrix, it is recommended that stability also be checked in phosphate-buffered saline.
- The sponsor must specify: the species of the blood donor—mouse, rat, dog, monkey or human