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Methylphenidate Ritalin Rapid Test Kits High Sensitivity For Human Urine

Product Details:

Place of Origin:China
Brand Name:AllTest
Certification:CE, ISO13485
Model Number:DMP-101/DMP-102/DMP-114

Payment & Shipping Terms:

Minimum Order Quantity:N/A
Price:Negotiation
Packaging Details:20cassette/box
Delivery Time:2-4 Weeks
Payment Terms:Ex works
Supply Ability:10 M tests/month
Detailed Product Description
Format: Cassette Color: Yellow
Certificate: CE Specimen: Urine
Cut-Off: 1000 Ng/mL* 300 Ng/mL Kit Size: 40T/Kit

Methylphenidate Ritalin Rapid Test Kits High Sensitivity For Human Urine 

 

 

Description: 

 

Methylphenidate (Ritalin) is a psychostimulant drug approved for treatment of ADHD orattention-deficit hyperactivity disorder, postural orthostatic tachycardia syndrome andnarcolepsy. Methylphenidate 

primarily acts as a norepinephrine-dopamine reuptakeinhibitor. Methylphenidate is most active at modulating levels of dopamine and to a

 lesserextent norepinephrine. Similar to cocaine, methylphenidate binds to and blocks dopaminetransporters

 and norepinephrine transporters. Methylphenidate has both dopaminetransporter and norepinephrine 

transporter binding affinity, with thedextromethylphenidate enantiomers displaying a prominent affinity for the

 norepinephrinetransporter. Methylphenidate may also exert a neuroprotective action against theneurotoxic

 effects of Parkinson's disease and methamphetamine abuse. Methylphenidatetaken orally has a bioavailability 

of 11-52% with a duration of action around 1-4 hours forinstant release, 3–8 hours for sustained release, and

 8–12 hours for extended release(Concerta). The half-life of methylphenidate is 2-3 hours, depending on the

 individual. Thepeak plasma time is achieved at about 2 hours.

The RIT Rapid Test Cassette (Urine) is a rapid urine-screening test that can be performed without the use of an instrument. The test utilizes the antibody to 

selectively detect elevated levels of Methylphenidate (Ritalin) in urine. The RIT Rapid Test Cassette (Urine)

 yields a positive result when the Methylphenidate (Ritalin) in urine exceeds the cut-off level. 

 

 

PRINCIPLE

 

The RIT Rapid Test Cassette (Urine) is an immunoassay based on the principle of competitive binding. Drugs

 which may be present in the urine specimen compete against the drug conjugate for binding sites on the 

antibody. 

During testing, a urine specimen migrates upward by capillary action. Methylphenidate (Ritalin), if present in

 the urine specimen below the cut-off level, will not saturate the binding sites of the antibody in the test. The 

antibody coated particles will then be captured by immobilized Methylphenidate (Ritalin)-protein conjugate and a visible colored line will show up in the test line region. The colored line will not form in

 the test line region if the Methylphenidate (Ritalin) level exceeds the cut-off level, because it will saturate all the

 binding sites of anti-Methylphenidate (Ritalin) antibody. 

A drug-positive urine specimen will not generate a colored line in the test line region because of drug 

competition, while a drug-negative urine specimen or a specimen containing a drug concentration less than the

 cut-off will generate a line in the test line region. To serve as a procedural control, a colored line will always 

appear at the control line region indicating that proper volume of specimen has been added and membrane 

wicking has occurred.

 

 

REAGENTS

 

The test contains mouse monoRITnal anti-Methylphenidate (Ritalin) antibody coupled particles and 

Methylphenidate (Ritalin)-protein conjugate. A goat antibody is employed in the control line system.

 

 

How to use? 

 

Methylphenidate Ritalin Rapid Test Kits High Sensitivity For Human Urine

 

 

Applications: 

 

The RIT Rapid Test Cassette (Urine) is a rapid chromatographic immunoassay for the detection of 

Methylphenidate (Ritalin) in urine at a cut-off concentration of 1000ng/ml. This test will detect other 

related compounds, please refer to the Analytical Specificity table in this package insert.

This assay provides only a qualitative, preliminary analytical test result. A more specific alternate 

chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass

 spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment

 should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

 

 

Specifications

 

Model

A rapid test for the diagnosis of Human Immunodeficiency Virus to

 detect antibodies to  RIT Rapid Test Cassette (Urine).

Format

Strip, Cassette, Uncut sheet

Accuracy

99.2%

Shelf life

24months

Component

Test cassettes, Droppers, Package insert, RIT buffer, Sample dilution tube

Specimen

Serum/Plasma/Blood

Storage

2-30°C

Read time

20 mins

Others

The kits can be made according to the customers' artwork or design

 

 

STORAGE AND STABILITY

 

Store as packaged 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.

 

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Tel:86-571-56267891

Fax:86-571-56267856

Contact Person: Mrs. Selina

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