MDMA- entertainment test kit

English abbreviation: MDMA
Contraband detection: MDMA, methylenedioxymethamphetamine MAMP
Test: urine
Clinical application: drug control system, drug rehabilitation center, a screening, quarantine and treatment, family etc.
Detection threshold: 500ng/ml
Detection principle: colloidal gold method (gold standard rapid detection method)
[packing specifications] 40T copies / boxes.
MDMA- entertainment test kit:
The MDMA assay kit uses a gold standard technique to detect the presence of MDMA and its metabolites in human urine by a single step, and is used for specific assisted diagnosis of patients who have taken MDMA, with a threshold of 500ng/ml. The kit is simple and quick to operate and provides visual and qualitative results for professional use only.
This product only provides preliminary test results, and untrained non professionals may be able to judge the results wrongly. The determination of the results must be obtained by precise chemical analysis. The preferred method of validation recommended by the National Institute for drug abuse is gas chromatography-mass spectrometry (GC / MS). When screening results are positive, it must be determined by this method and combined with clinical symptoms by professional physicians to make a judgement.
Overview of MDMA- entertainment testing kit:
The full name of MDMA, 3, 4-methlenedioxy-N-methamphetamine, also called Ectasy, Chinese called methylenedioxymethamphetamine MAMP, commonly known as "MDMA", MDMA composition is very complicated, its main component is MDMA. MDMA at the beginning of twentieth Century as a precursor of chemical drugs by pharmaceutical synthesis and apply for a patent, its chemical structure is similar to MAMP, and have similar central nervous stimulation, but its hallucinogenic effect is far greater than MAMP. It was not until twentieth Century 80s that MDMA was considered illegal. In 1985, the U. S. Bureau of drug control banned the drug as the first type of restricted drug (i.e., highly addictive and not used as a common drug). Although the drug has been included in the first category of controlled drugs, the current rate of illicit use of MDMA is very high, so an accurate and specific method is needed to detect and monitor it.
MDMA is usually made into tablets or capsules, at doses of 80-150mg. After oral administration, the drug can last for 3-6 hours and, like MAMP, can cause elevated blood pressure, elevated body temperature, confusion, anxiety, paranoia, sleep disorders and a range of symptoms. There are reports that the symptoms can last even weeks.
After taking MDMA, 65% excreted from the urine in the form of an agent, and nearly 7% were excreted from urine by demethylation in the form of MDA. Other forms of metabolism, including hydroxylation or hydroxylation, are excreted. Generally, MDMA can be detected from urine within 3 days after taking it.

Detection principle of MDMA- entertainment testing kit:

The MDMA test kit detected the presence of MDMA in the urine by an immune competitive inhibition assay, i.e., the banned substances (prohibited substances carriers) labeled by proteins compete with restricted substances in the urine to limit the antibody binding sites. A test paper is placed in the kit, and the MDMA carrier conjugate is coated in the test strip detection line area. One end of the detection area is provided with a dried MDMA antibody colloidal gold paper. If there is no contraband in the urine, prohibited antibodies, colloidal gold will run along the sample solution on the membrane to the test line, combined with MDMA carrier conjugates, showing a line visible to the naked eye, which is the negative result. If the urine contains contraband contraband or metabolites, and antibody binding sites they will be competing for the limited contraband carrier, when contraband concentration in the sample reaches a certain amount, it will occupy all with antibody colloidal gold antibody sites, thus preventing the combination of contraband carrier and antibody colloidal gold test strip area on the way, a wireless detection area, said the result is positive.
The quality control area on the test strip is coated with specific antibodies to indicate whether the reagent box reaction system is functioning properly. Quality control lines are not related to the presence of prohibited substances or prohibited substances. The appearance of the ribbon in the quality control area shows that: the amount of the sample is sufficient; the sample runs normally on the note.

Matters needing attention
For professional and in vitro diagnostic use only.
The urine sample should be compley free of contamination. The used samples and kits should be handled by infectious substances. Gloves and overalls should be worn during operation.
New collection containers and pipette should be used in each urine sample to prevent contamination of urine samples.
Self supplied articles: sample collection containers: timers: sample collection
This kit is for urine test only. It is recommended to use fresh urine without any special treatment. The urine sample can be stored at 2-8 DEG C for 2 days. It can be stored at -20 for 1-2 months. The frozen sample should be balanced to room temperature before testing, and the frozen sample should be compley dissolved and fully mixed before testing, otherwise it may affect the test result.
Test procedure
Read the instructions carefully, and then test the kit, patient sample and standard sample to room temperature (about 25 DEG C) before the test. Please don't open the packing bag before you are ready. Refrigerated packages should be placed at room temperature ahead of time so as to avoid moisture absorption.
Take out the kit from the sealed bag and mark the patient or standard number on the kit.
Suction the urine sample to the calibration line (approx. 0.2ml) and then drop all the sample holes. For each different sample and standard, use a different pipette and kit.
3-8 minutes after the drop of the sample, the result is invalid after 8 minutes.

Judgment of outcome
Negative: two ribbons should be observed in the window. The line (T line) of the inspection area appears to indicate that there is no contrabandThe line (C line) of the quality control area appears to indicate that the reagent box system is functioning properly.
Positive: only a ribbon appeared in the quality control area, and the T line did not appear, indicating the presence of prohibited substances in the sample.
Failure: no ribbon lines appear in the inspection area and quality control area. In any case, the C lines should be formed. C line does not appear, the test result is uncertain, should be redone.
Note: the detection zone in a very light bands indicated the detection threshold concentration methylenedioxymethamphetamine MDMA in urine and its metabolites to kit, should be re tested or determined by more sophisticated methods

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【公司名稱】 廣州健侖生物科技有限公司

【市場(chǎng)部】       楊永漢
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【騰訊 】
【公司地址】 廣州市清華科技園健新基地番禺石樓鎮(zhèn)健啟路63號(hào)二期2幢101-103室