Format: | AllTest | Specimen: | Powder |
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Kit Size: | 40T/Kit | Storage: | 2-30℃ |
Color: | White | Certificate: | CE |
Highlight: | rapid diagnostic test kits,home drug test kits |
Powder Panel Tramadol Home Drug Abuse Test Kit Tramadol Diagnosis Kits of 100ng/ml
Application:
The Tramadol Rapid Test Panel is a rapid chromatographic immunoassay for the qualitative detection of Tramadol a cut-off 100ng/ml. This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated.
Description:
Tramadol(TML) is a quasi-narcotic analgesic used in the treatment of moderate to severe pain. It is a synthetic analog of codeine, but has a low binding affinity to the mu-opioid receptors. Large doses of tramadol can develop tolerance and physiological dependency and lead to its abuse. Tramadol is extensively metabolized after oral administration. The Tramadol contained within the TML Rapid Test Panel yields a positive result when the TML concentration exceeds 100ng/ml.
How to use?
INTERPRETATION OF RESULTS
(Please refer to the illustration above)
NEGATIVE:* A colored line appears in the Control region (C) and colored lines appear in the Test region (T). This negative result means that the concentrations in the sample are below the designated cut-off levels for a particular drug tested.
*NOTE: The shade of the colored lines(s) in the Test region (T) may vary. The result should be considered negative whenever there is even a faint line.
POSITIVE: A colored line appears in the Control region (C) and NO line appears in the Test region (T). The positive result means that the drug concentration in the sample is greater than the designated cut-off for a specific drug.
INVALID: No line appears in the Control region (C). Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for Control line failure. Read the directions again and repeat the test with a new test card. If the result is still invalid, contact your manufacturer.