The EMIT® II Plus Buprenorphine Assay is intended for the qualitative and semiquantitative analysis of buprenorphine in human urine at a cutoff value of 5 ng/mL.
- Home
- Laboratory Diagnostics
- Drug Testing Diagnostics
- Drugs of Abuse Testing
- EMIT II Plus Buprenorphine Assay
EMIT II Plus Buprenorphine AssayNo cross-reactivity to commonly abused opiates
Features & Benefits
Buprenorphine is a semisynthetic opiate that has powerful analgesic capabilities and is approximately 25–40 times as potent as morphine. Buprenorphine is used as a substitution drug for opioid addiction treatment but has a high potential for abuse and addiction.
The EMIT II Plus Buprenorphine Assay provides:
- High specificity for buprenorphine and norbuprenorphine
- No cross-reactivity to buprenorphine glucuronide or norbuprenorphine glucuronide
- No cross-reactivity relative to common interferants such as riboflavin
- Ready-to-use liquid reagents, calibrators, and controls
- ≥90% agreement to LC-MS/MS
Applications are available for the Viva-Jr®, Viva-E®, Viva-ProE®, V-Twin® drug testing systems and AU® Series analyzers.
Technical Specifications
EMIT II Plus Buprenorphine Assay Performance
Assay Principle | Homogeneous Enzyme Multiplied Immonoassay (EMIT) |
Cut-off | 5 ng/mL |
Sample | Urine |
Reagent Stability | Unopened: until expiration date. Onboard instrument: up to 4 weeks |
Calibration Frequency | As indicated by control results |
Did this information help you?
Thank you.
Would you like to provide detailed feedback?
125 / 125