A rapid test for the qualitative detection of Opiate (OPI) in human urine that can be performed with the use of AllTestTM LF Reader. For medical and other professional in vitro diagnostic use only.
The OPI Rapid Test Cassette (Urine) is a rapid chromatographic immunoassay for the detection of Morphine in human urine that can be performed with the use of AllTestTM LF Reader at the cut-off concentration of 2,000ng/mL. This test will detect other related compounds, please refer to the Analytical Specificity table in this package insert.
This assay provides only a qualitative, 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 used.
Opiate refers to any drug that is derived from the opium poppy, including the natural products, Morphine and Codeine, and the semi-synthetic drugs such as heroin. Opioid is more general, referring to any drug that acts on the opioid receptor.
Opioid analgesics comprise a large group of substance which control pain by depressing the central nervous system. Large doses of Morphine can produce higher tolerance levels and physiological dependency in users, and may lead to substance abuse. Morphine is excreted unmetabolized, and is also the major metabolic product of codeine and heroin. Morphine is detectable in the urine for several days after an opiate dose.1
The OPI Rapid Test Cassette (Urine) is a rapid urine screening test that can be performed with the use of LF Reader. The test utilizes a monoclonal antibody to selectively detect elevated levels of Morphine in urine. The OPI Rapid Test Cassette (Urine) yields a positive result when Morphine in urine exceeds 2,000ng/mL. This is the suggested screening cut-off for positive specimens set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA).
Allow the test, urine specimen, and/or controls to reach room temperature (15-30ºC) prior to testing.
1.Exact QR Code from the QR code card for specific information of the test. Use only QR code card provided inside the test kits.
2.Bring the pouch to room temperature before opening it. Remove the test Cassette from the sealed pouch and use it within one hour.
3.Place the test Cassette on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 120μL) to the specimen well (S) of the test Cassette, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See illustration below.
4.Wait for the colored line(s) to appear. The Results should be Read with AllTestTM LF Reader at 5 minutes.
5.Do not interpret test results visually.
INTERPRETATION OF RESULTS
Results read by AllTestTM LF Reader
The result of positive or negative for each analyte is determined by AllTestTM LF Reader.
Result may be exported to excel or PDF.
At this point the Test Cassette may be removed and appropriately discarded.
||Opiates (OPI) Rapid Test Cassette