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HelpTest ID FCBDS Cannabidiol, Serum
Specimen Required
***Must submit one specimen per order. Specimens cannot be shared between multiple orders.***
Specimen Type: Serum
Collection Container/Tube: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Draw blood in a red-top tube(s). Serum gel tube is not acceptable.
2. Centrifuge and send 1 mL of serum refrigerated in a plastic, preservative-free vial.
Forms
If not ordering electronically, complete, print, and send a Therapeutics Test Request (T831) with the specimen.
Secondary ID
75527Method Name
High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS)
Reporting Name
Cannabidiol, SerumSpecimen Type
Serum RedSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | |
|---|---|---|---|
| Serum Red | Refrigerated (preferred) | 30 days | |
| Ambient | 14 days | ||
| Frozen | |||
Clinical Information
Mean peak CBD plasma concentrations at 3-4 hours post-dose with Sativex at a low dose (5.4 mg of Delta-9 THC and 5.0 mg of Cannabidiol) were 1.6 ± 0.4 ng/mL and at a high dose (16 mg of Delta-9 THC and 15 mg of Cannabidiol) were 6.7 ± 2.0 ng/mL.
Following high dose 400 and 800 mg oral synthetic CBD in corn oil administration, mean peak CBD plasma concentrations occurred within 1.5-3 hours post-dose and were 181.2 ± 39.8 and 221.1 ± 35.6 ng/mL, respectively.
The ratio of blood to serum or plasma concentration is unknown for this analyte.
Reference Values
Reporting limit determined each analysis
Units: ng/mL
Cautions
Known Interferences: Excessive amounts of oleamide from plastic tubes
Day(s) Performed
Monday-Sunday
Report Available
11 to 13 daysPerforming Laboratory
NMS LabsTest Classification
This test was developed and its performance characteristics determined by NMS Labs. It has not been cleared or approved by the U.S. Food and Drug Administration.CPT Code Information
80349
G0480, if appropriate