Sertraline and Desmethylsertraline, Serum/Plasma
Also known as: Zoloft®
Use
Quantitative measurement of sertraline (Zoloft®) and its metabolite desmethylsertraline in serum or plasma to support therapeutic drug monitoring, assessment of compliance, or evaluation of toxicity. Useful in clinical settings where monitoring drug levels is necessary for optimal dosing and patient safety.
Special Instructions
None provided in available sources.
Limitations
This test is a laboratory-developed test with performance characteristics determined by the performing laboratory and has not been cleared or approved by the U.S. Food and Drug Administration.
Methodology
Mass Spectrometry
Biomarkers
Result Turnaround Time
3-7 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.4 mL
Container
Plastic container (preservative-free)
Collection Instructions
Serum: Collect sample in Red top tube; Promptly centrifuge and separate Serum into a plastic screw capped vial.
Causes for Rejection
Polymer gel separation tube (SST or PST).
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 14 day(s) |
| Refrigerated | 1 month(s) |
| Frozen | 6 month(s) |