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Test Code FBUMT Bupropion and Metabolite, Serum


Specimen Required


***Must submit one specimen per order. Specimens cannot be shared between multiple orders.***

Collection Container/Tube: Red top (Serum gel/SST are not acceptable)

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL Serum

Collections Instructions:

1. Centrifuge and aliquot 1 mL of serum into a plastic vial.

2. Send refrigerated.


Secondary ID

75387

Method Name

High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)

Reporting Name

Bupropion and Metabolite, S

Specimen Type

Serum Red

Specimen Minimum Volume

Serum: 0.5 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Red Frozen 30 days

Reject Due To

Gross hemolysis Reject
Gross lipemia OK
Gross icterus OK
Polymer gel separation tube (SST or PST) Reject

Reference Values

Reporting limit determined each analysis.

None Detected

Interpretation

Bupropion:

Maximum antidepressant response was observed at trough plasma concentrations of 50 to 100 ng/mL bupropion with virtually no response below 25 ng/mL.

 

Reported average bupropion peak plasma concentrations:

Adults:

Males:

Single 100 mg IR: 120 ± 10 ng/mL

Single 200 mg IR:220 ±20 ng/mL

Single 150 mg SR - 140 ±20 ng/mL

 

Females:

Single 100 mg IR: 150 ±10 ng/mL

Single 200 mg IR: 270 ±20 ng/mL

Single 150 mg SR: 140 ±20 ng/mL

 

Juveniles:

100 mg/day SR for 2 weeks: 25 ±8 ng/mL

200 mg/day SR for 2 weeks: 53 ±22 ng/mL

 

Hydroxybupropion:

Oral dose (mg); peak plasma concentrations (ng/mL)

Adults:

Single 100 IR: 296 ±154 ng/mL

Single 150 SR: 311 ±168 ng/mL

Single 300 ER: 402 ±145 ng/mL

 

Juveniles:

Daily 100 SR for 2 weeks: 451 ±214 ng/mL

Daily 200 SR for 2 weeks: 712 ±349 ng/mL

Half-life: approximately 15-22 hr

Day(s) Performed

Monday through Sunday

Report Available

6 to 10 days

Performing Laboratory

NMS Labs

CPT Code Information

80338

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FBUMT Bupropion and Metabolite, S Not Provided

 

Result ID Test Result Name Result LOINC Value
Z3522 Bupropion 6706-6
Z3523 Hydroxybupropion 9418-5

Test 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.

Clinical Information

Refer to www.nmslabs.com/test-catalog.

Cautions

Specimens must be kept frozen. If specimens are not kept frozen, this may cause lower or negative values.