Sample: | Urine | Type: | Cassette |
---|---|---|---|
Certificate: | ISO, CE, FDA | Origin: | China |
Shelf Life: | 24 Months | Usage: | Professional Use |
Highlight: | Cassette Rapid Test Kit,BUP Rapid Test Kits,Buprenorphine Rapid Test Cassette |
BUP Rapid Test Kits Drug of Abuse Test
BUP Rapid Test is a rapid, screening test for the qualitative detection of BUP and metabolites in human urine at specified cut off levels.
For professional use only.
For in vitro diagnostic use only.
【INTENDED USE】
BUP Rapid Test is an immuno-chromatographic assay for the qualitative determination of the presence of BUP listed in the table below.
Drug(Identifier) |
Calibrator |
Cut-off level |
BUP |
BUP |
10 ng/mL |
This assay provides only a preliminary analytical test result. Gas Chromatography/Mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to BUP of abuse test result, particularly when preliminary positive results are indicated.
【SUMMARY】
BUP is a potent analgesic often used in the treatment of opioid addiction. The drug is sold under the trade names Subutex™, Buprenex™, Temgesic™ and Suboxone™, which contain BUP HCl alone or in combination with Naloxone HCl. Therapeutically, BUP is used as a substitution treatment for opioid addicts.Substitution treatment is a form of medical care offered to opiate addicts based on a similar or identical substance to the drug normally used. In substitution therapy, BUP is as effective as MTD but demonstrates a lower level of physical dependence. Concentrations of free BUP and Norbuprenorphine in urine may be less than 1 ng/ml after therapeutic administration, but can range up to 20 ng/ml in abuse situations.3 The plasma half life of BUP is 2-4 hours.3 While complete elimination of a single dose of the drug can take as long as 6 days, the window of detection for the parent drug in urine is thought to be approximately 3 days. Substantial abuse of BUP has also been reported in many countries where various forms of the drug are available. The drug has been diverted from legitimate channels through theft, doctor shopping, and fraudulent prescriptions, and been abused via intravenous, sublingual, intranasal and inhalation routes.
【PRINCIPLE】
BUP Rapid Test is a competitive immunoassay that is used to screen for the presence of BUP and metabolites in urine. It is chromatographic absorbent device in which, drugs within a urine sample, competitively combined to a limited number of drug monoclonal antibody (mouse) conjugate binding sites.
When the test is activated, the urine is absorbed into test by capillary action, mixes with the respective drug monoclonal antibody conjugate, and flows across a pre-coated membrane. When drug within the urine sample is below the detection level of the test, respective drug monoclonal antibody conjugate binds to the respective drug-protein conjugate immobilized in the Test Region (T) of the test . This produces a colored Test line in the Test Region (T) of the test, which, regardless of its intensity, indicates a negative test result.
When sample drug levels are at or above the detection level of the test, the free drug in the sample binds to the respective drug monoclonal antibody conjugate, preventing the respective drug monoclonal antibody conjugate from binding to the respective drug-protein conjugate immobilized in the Test Region (T) of the device. This prevents the development of a distinct colored band in the test region, indicating a preliminary positive result.
To serve as a procedure control, a colored line will appear at the Control Region (C) of test, if the test has been performed properly.
【WARNINGS AND PRECAUTIONS】
【CONTENTS】
【STORAGE AND STABILITY】
【OPERATION】
Test must be in room temperature (15ºC to 30ºC)
1. Donor collects urine specimen in a urine cup.
2. Open the sealed pouch by tearing along the notch. Remove the test from the pouch and place it on a level surface.
3. Hold the sample dropper vertically, and add exactly three drops of the urine specimen into the sample well.
4. The result should be read at 5 minutes. Do not interpret the result after 10 minutes. See the illustration below.
【INTERPRETATION OF RESULTS】
Preliminary positive (+)
Only one colored band appears, in the control region (C). No colored band appears in the test region (T).
Negative (-)
Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).
Invalid
Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.
For further operation or performance details, please refer to final instruction manual.