Rapid DOA Test
Rapid DOA Panel Test Cup is an immunochromatography based one step in vitro test. It is designed for qualitative determination of drug substances in human urine specimens. This assay may be used in the point of care setting.
This assay provides only a preliminary analytical test result. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/ mass spectrometry (GC/MS) has been established as the preferred confirmatory method by the Substance Abuse Mental Health Services Administration (SAMHSA). Clinical consideration and professional judgement should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated. The optional built-in Adulteration Test is for validation of urine specimen’s integrity and must not be used for In Vitro diagnostic use.
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Product Description
Producer:
Xiamen Boson Biotech Co., Ltd
Country of production:
China
Article:
1L26K3, 1L22K3, 1L24K3
Brief description:
Rapid DOA Panel Test Cup is an immunochromatography based one step in vitro test. It is designed for qualitative determination of drug substances in human urine specimens. This assay may be used in the point of care setting.
This assay provides only a preliminary analytical test result. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/ mass spectrometry (GC/MS) has been established as the preferred confirmatory method by the Substance Abuse Mental Health Services Administration (SAMHSA). Clinical consideration and professional judgement should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated. The optional built-in Adulteration Test is for validation of urine specimen’s integrity and must not be used for In Vitro diagnostic use.
Appointment:
Qualitative determination of drug substances in human urine specimens.
Materials provided:
1. Rapid DOA Panel Test Cup. The amount of each coated antigen and/or antibody on the strip is less than 1.0 mg for antigen conjugate and is less than 1.0 mg for goat anti-rabbit IgG antibody. Test zone: contains drug bovine protein antigen conjugates Control zone: contains Goat anti-rabbit IgG antibody Conjugate pad: contains anti-drug antibody.
2. Instruction for use.
Materials required but not provided:
Timer or clock.
Amphetamine
500 ng/ml of d-amphetamine
Barbiturate
200 ng/ml of secobarbital
Benzodiazepine
300 ng/ml of oxazepam
Buprenorphine
10 ng/ml of Buprenorphine-3-β-d-glucoronide
Cocaine
300 ng/ml of benzoylecgonine
EDDP
100 ng/ml of EDDP
Ketamine
1000 ng/ml of Ketamine
MDMA (Ecstasy specific)
500 ng/ml of MDMA
Methadone
300 ng/ml of methadone
Methamphetamine
500 ng/ml of (+)methamphetamine
Opiate
300 ng/ml of morphine
Opiate ІІ
2000 ng/ml of morphine
Oxycodone
100 ng/ml of oxycodone
Phencyclidine
25 ng/ml of phencyclidine
Propoxyphene
300 ng/ml of Norpropoxyphene
Cannabinoid (THC)
50 ng/ml of 11-nor-△9-THC-9-COOH
Tramadol
200 ng/ml of Tramadol
Tricyclic antidepressant (TCA)
1000 ng/ml of Nortriptyline
Methylphenidate
300 ng/ml of methylphenidate
Fentanyl
10 ng/ml of fentanyl
Synthetic Cannabis (K2)
50 ng/ml of JWH-018 pentanoic acid and JWH73 butanoic acid
Clonazepam
300 ng/ml of 7-aminoclonazepam
Cotinine
100 ng/ml of cotinine
Sample Type:
urine
Delivery
Implemented by Nova Poshta. If the order is above 1500 UAH, the sender pays the shipping cost
Instructions for use (PDF) Declaration of Conformity (PDF)