Product Name: | SCOP Rapid Test Panel (Urine), Scopolamine Rapid Test For Drugs Of Abuset , High Accuracy | Principle: | Chromatographic Immunoassay |
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Format: | Panel | Specimen: | Urine |
Certificate: | CE/FDA | Reading Time: | 5 Minutes |
Pack: | 40T | Storage Temperature: | 2-30°C |
Shelf Life: | 2 Years | Sensitivity: | 93.5% |
Specificity: | 98.6% | Accuracy: | 97.0% |
Cut-Off: | 500 Ng/mL | PRODUCT FEATURES 1: | Fast Results In 5 Minutes |
PRODUCT FEATURES 2: | Simple Visual Interpretation | PRODUCT FEATURES 3: | Easy Urine Specimen Collection |
PRODUCT FEATURES 4: | Convenient Operation | PRODUCT FEATURES 5: | High Accuracy |
Highlight: | SCOP Rapid Test Panel,High Accuracy Scopolamine Rapid Test |
SCOP Rapid Test Panel (Urine), Scopolamine Rapid Test For Drugs of Abuset , High accuracy
The SCOP Rapid Test is a rapid chromatographic immunoassay for the detection of Scopol-amine in human urine at a cut-off concentration of 500ng/ ml.
Application
Scopolamine(SCOP), also known as hyoscine, or Devil's Breath, is a natural or synthetically produced tropane alkaloid and anticholinergic drug that is formallv used as a medication for treating motion sickness and postoperative nausea and vomiting. It may also be used orally and as a transdermal patch.
A travel advisory published by the Overseas Security Advisory Council (OSAC) in 2012 stated;One common and particularly dangerous method that criminals use in order to rob a victim is through the use of drugs, The most common lin Colombial has been scopolamine,Scopo-amine can render a victim unconscious for 24 hours or more. In large doses, it can cause respi-ratory failure and death.
Product Name: |
SCOP Rapid Test Panel (Urine), Scopolamine Rapid Test For Drugs of Abuset , High accuracy |
Format: | Panel |
Certificate: | CE/FDA |
Pack: | 40T |
Shelf Life: | 2 Years |
Specificity: | 98.60% |
Cut-Off: | 500 Ng/mL |
PRODUCT FEATURES 2: | Simple Visual Interpretation |
PRODUCT FEATURES 4: | Convenient Operation |
Principle: | Chromatographic Immunoassay |
Specimen: | Urine |
Reading Time: | 5 Minutes |
Storage Temperature: | 2-30℃ |
Sensitivity: | 93.50% |
Accuracy: | 97.00% |
PRODUCT FEATURES 1: | Fast Results In 5 Minutes |
PRODUCT FEATURES 3: | Easy Urine Specimen Collection |
PRODUCT FEATURES 5: | High Accuracy |
INTENDED USE
The SCOP Rapid Test Panel (Urine) is a rapid chromatographic immunoassay for the detection of Scopolamine in human urine at a cut-off concentration of 500ng/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. Clinicalconsideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.
SUMMARY
Scopolamine is a tertiary amine antifungal drug often used in sedative anesthesia, cough and asthma. It is a muscarinic acetylcholine receptor antagonist that has traditionally been used to treat motion sickness in humans.1,2 It is mainly derived from the Solanaceae plants Tianxian, mandola and so on. The drug has highly toxic and hallucinogenic effects and is used as a crime, even called the devil's breath.3 Therapeutically,
Scopolamine is used as a substitution treatment for Patients allergic to atropine. In alternative therapy, Scopolamine is as effective as atropine, and even more potent. The plasma half-life of Scopolamine is 1-3 hours. The SCOP Rapid Test Dipstick (Urine) is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes a monoclonal antibody to selectively detect elevated levels of Scopolamine in urine. The SCOP Rapid Test Dipstick (Urine) yields a positive result when Scopolamine in urine exceeds 500ng/ml.
PRINCIPLE
The SCOP Rapid Test Panel (Urine) is an immunoassay based on the principle of competitive binding. Drugs which may be present in the urine specimen compete against the drug conjugate for binding sites on the antibody. During testing, a urine specimen migrates upward by capillary action. Scopolamine, if present in the urine specimen below the cut-off level, will not saturate the binding sites of the antibody in the test. The antibody coated particles will then be captured by immobilized Scopolamine-protein conjugate and a visible colored line will show up in the test line region. The colored line will not form in the test line region if the Scopolamine level exceeds the cut-off level, because it will saturate all the binding sites of anti-scopolamine antibody.
A drug-positive urine specimen will not generate a colored line in the test line region because of drug competition, while a drug-negative urine specimen or a specimen containing a drug concentration less than the cut-off will generate a line in the test line region. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.
DIRECTIONS FOR USE
Allow the test, urine specimen, and/or controls to reach room temperature (15-30 ℃) prior to testing.
1. Remove the test panel from the sealed pouch and use it as soon as possible.
2. Remove the cap.
3. With the arrow pointing toward the urine specimen, immerse the test panel vertically in the urine specimen for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but do not touch the plastic device.
4. Replace the cap and place the test panel on a non-absorbent flat surface.
5. Start the timer and wait for the colored line(s) to appear.
6. The drug strip result should be read at 5 minutes. Do not interpret the result after 10 minutes.
QUALITY CONTROL
A procedural control is included in the test. A colored line appearing in the control line region (C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique.
Control standards are not supplied with this kit; however, it is recommended that positive and negative controls be tested as good laboratory testing practice to confirm the test procedure and to verify proper test performance.