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)