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6 Panel Multiple Drug Abuse Test Kit Detecting Drug Metabolites In Human Urine

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6 Panel Multiple Drug Abuse Test Kit Detecting Drug Metabolites In Human Urine

6 Panel Multiple Drug Abuse Test Kit Detecting Drug Metabolites In Human Urine
6 Panel Multiple Drug Abuse Test Kit Detecting Drug Metabolites In Human Urine 6 Panel Multiple Drug Abuse Test Kit Detecting Drug Metabolites In Human Urine 6 Panel Multiple Drug Abuse Test Kit Detecting Drug Metabolites In Human Urine

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Product Details:
Place of Origin: China
Brand Name: New Life
Certification: ISO13485, CE
Model Number: 6 multiple panel
Payment & Shipping Terms:
Minimum Order Quantity: 5000pcs
Price: USD0.5-USD5
Packaging Details: 1pc/pouch, 25pcs/box
Delivery Time: 20-30days
Payment Terms: T/T, Western Union
Supply Ability: 2000000pcs/month
Detailed Product Description
Category: Drug Abuse TESGTING Format: 6 Multiple Panel
Specimen: Urine Testing Time: 5-15 Minu
Shelf Life: 24 Months Application: Multiple Drug Test
Cut-off: 1000ng, 500ng, Material: Membrane
High Light:

Human Urine Drug Abuse Test Kit


Multiple Drug Abuse Test Kit

6 Panel Multiple Drug Abuse Test Kit Detecting Drug Metabolites In Human Urine

Intended Use

The Multi-drug Rapid Test Panel (Urine) is rapid chromatographic immunoassays for the qualitative and simultaneous detection up to sixteen of the following drugs in human urine. The designed cutoff concentrations for these drugs are as follows:


Test Cut-off (ng/mL)
AMP(Amphetamine) 500
MOR(Morphine) 200
MET(Methamphetamine ) 500
MTD(Methadone) 300
BZO(Oxazepam) 200
FYL(Fentanyl) 100
OXY (Oxycodone) 100
PGB (Pregabalin) 500
Adulteration ( Oxidants,Specific Gravity,pH) /





The Multi-drug Rapid Test Panel (Urine) is one-step immunoassay in which chemically labeled drugs (drug-protein conjugates) compete for limited antibody binding sites with drugs which may be present in urine. The test panel contains membrane strips which are pre-coated with drug-protein conjugates on the test band(s). Each strip, the drug antibody-colloidal gold conjugate pad is placed at one end of the membrane. In the absence of drug in the urine, the solution of the colored antibody-colloidal gold conjugate move along with the sample solution upward chromatographically by capillary action across the membrane to the immobilized drug-protein conjugate zone on the test band region. The colored antibody-gold conjugate then attach to the drug-protein conjugates to form visible lines as the antibody complex with the drug conjugate. Therefore, the formation of the visible precipitant in the test zone occurs when the test urine is negative for the drug.When the drug is present in the urine, the drug/metabolite antigen competes with drug-protein conjugate on the test band region for the limited antibody. When a sufficient concentration of the drug is present, it will fill the limited antibody binding sites. This will prevent attachment of the colored antibody (drug-protein conjugate)-colloidal gold conjugate to the drug-protein conjugate zone on the test band region. Therefore, absence of the color band on the test region indicates a positive result.A control band with a different antigen/antibody reaction is added to the immunochromatographic membrane strip at the control region (C) to indicate that the test has performed properly. This control line should always appear regardless of the presence of drug or metabolite. If the control line does not appear the test panel should be discarded.




Store as packaged in the sealed pouch either at room temperature or refrigerated (2-30°C). The test is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.




1. The 6-MAM Rapid Test Cassette provides only a qualitative, preliminary analytical result. A secondary analytical method must be used to obtain a confirmed result. Gas chromatography/mass spectrophotometry (GC/MS) is the preferred confirmatory method2.3.

2. It is possible that technical or procedural errors, as well as other interfering substances in the urine specimen may cause erroneous results.

3. Adulterants, such as bleach and/or alum, in urine specimens may produce erroneous results regardless of the analytical method used. If adulteration is suspected, the test should be repeated with another urine specimen.

4. A positive result indicates presence of the drug or its metabolites but does not indicate level of intoxication, administration route or concentration in urine.

5. A negative result may not necessarily indicate drug-free urine. Negative results can be obtained when drug is present but below the cut-off level of the test.


performance characteristics


A side-by-side comparison was conducted using the Rapid Test Cassette (Urine) and GC/MS. The following results were tabulated:


Specimen Correlation


Method     GC/MS Total Results
ACL Rapid Test   Results Positive   Negative  
  Positive 23   2 25
Cassette (Urine)    
  Negative 2   68 70
Total Results     25   70 95
% Agreement   92.0%   97.1% 95.8%



Table 2: Specimen Correlation

AMP One Step Test Strip   + -
+ 132 9
- 4 155


Positive agreement with GC/MS: 132/(132+4) = 97%

Negative agreement with GC/MS: 155/(155+9) = 95%

Total agreement with GC/MS: (132+155)/(132+4+9+155) = 96%




Cross Reactivity


A study was conducted to determine the cross-reactivity of the test with compounds in either drug-free urine or drug positive urine containing, Amphetamine, Barbiturates, Benzodiazepines, Buprenorphine, Cocaine, Marijuana, Methadone, Methamphetamine, Methylenedioxymethamphetamine, Morphine, Tramadol , Methaqualone, Ketamine ,Phencyclidine, Propoxyphene or Tricyclic Antidepressants. The following compounds show no cross-reactivity when tested with the Multi-Drug Rapid Test Panel with Adulteration at a concentration of 100 µg/mL. Visual interpretations occurred at 5 minutes after specimen application. Results are presented in table below.

Table: Cross Reactivity

Acetophenetidin Cortisone Zomepirac d-Pseudoephedrine
N-Acetylprocainamide Creatinine Ketoprofen Quinidine
Acetylsalicylic acid Deoxycorticosterone Labetalol Quinine
Aminopyrine Dextromethorphan Loperamide Salicylic acid
Amoxicillin Diclofenac Meprobamate Serotonin
Ampicillin Diflunisal Methoxyphenamine Sulfamethazine
l-Ascorbic acid Digoxin Methylphenidate Sulindac
Apomorphine Diphenhydramine Nalidixic acid Tetracycline
Aspartame Ethyl-p-aminobenzoate Naproxen Tetrahydrocortisone,
Atropine b-Estradiol Niacinamide 3-acetate
Benzilic acid Estrone-3-sulfate Nifedipine Tetrahydrocortisone
Benzoic acid Erythromycin Norethindrone Tetrahydrozoline
Bilirubin Fenoprofen Noscapine Thiamine
d,l-Brompheniramine Furosemide d,l-Octopamine Thioridazine
Caffeine Gentisic acid Oxalic acid d,l-Tyrosine
Cannabidiol Hemoglobin Oxolinic acid Tolbutamide
Chloral hydrate Hydralazine Oxymetazoline Triamterene
Chloramphenicol Hydrochlorothiazide Papaverine Trifluoperazine
Chlorothiazide Hydrocortisone Penicillin-G Trimethoprim
d,l-Chlorpheniramine o-Hydroxyhippuric acid Perphenazine d,l-Tryptophan
Chlorpromazine 3-Hydroxytyramine Phenelzine Uric acid
Cholesterol d,l-Isoproterenol Prednisone Verapamil
Clonidine Isoxsuprine d,l-Propanolol  

Conclusion: The compounds listed in above table show no cross-reactivity when tested at a concentration of 100 mg/ml in 5 minutes.




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