Advantage

• 21 years experience
• Simple operation, reliable result
• High sensitivity and specificity,precision
• Drug of Abuse test kits

Introduction

Marijuana, or tetra-hydro-cannabinol (THC) is a hallucinogenic agent derived from the flowering portion of the hemp plant. Smoking is the primary method of use of marijuana. Higher doses used by abusers produce central nervous system effects, altered mood and sensory perceptions, loss of co-ordination, impaired short-term memory, anxiety, paranoia, depression, confusion, hallucinations and increased heart rate. A tolerance to the cardiac and psychotropic effects can occur, and withdrawal syndrome produces restlessness, insomnia, anorexia and nausea.

Intend to use

The THC Rapid Test Strip (Urine) is a rapid visual immunoassay for the qualitative presumptive detection of THC metabolites (11-nor-Δ⁹-THC-9-carboxylic acid) in human urine specimens.

Procedure

Bring tests, specimens, and/or controls to room temperature (15-30°C) before use.

1.Remove the test from its sealed pouch and use it as soon as possible. To obtain a best result, the assay should be performed within one hour.

2.Hold the strip at the handle with the product name imprints. Do not touch the membrane part of the strip to avoid contamination.

3.Dip the test strip vertically in the urine specimen for at least 10-15 seconds. Do not pass the maximum line (MAX) on the test strip when immersing the strip. As the test begins to work, you will see color move across the membrane.

4.Take the strip out of the specimen afterwards and place it on a non-absorbent flat surface. Start the timer and wait for the colored line(s) to appear. The result should be read at 5 minutes. Do not interpret the result after 20 minutes.

Interpretation of results

NOTE:

1. The intensity of the color in test region (T) may vary depending on the concentration of aimed substances present in the specimen. Therefore, any shade of color in the test region should be considered negative. Besides, the concentration level can not be determined by this qualitative test.
2. Insufficient specimen volume, incorrect operation procedure, or performing expired tests are the most likely reasons for control band failure.

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