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300Ng/ML Fast Reading Rdt Test Kit Diazepam DIA Human Urine Test Qualitative Detection

300Ng/ML Fast Reading Rdt Test Kit Diazepam DIA Human Urine Test Qualitative Detection

  • High Light

    300Ng/ML Fast Reading Rdt Test Kit

    ,

    Rdt Test Kit Diazepam DIA

    ,

    Diazepam DIA Human Urine Test

  • Product
    Fast Reading Rdt Kit For Qualitative Detection Of Diazepam DIA In Human Urine
  • Cat. No.
    DDI-102/101/114,DDI-X14
  • Principle
    Chromatographic Immunoassay
  • Format
    Dipstick, Cassette, Panel, Device, Cup
  • Specimen
    Urine, Powder
  • Certificate
    CE
  • Reading Time
    5 Minutes
  • Pack
    10T/25T/40T/50T
  • Storage Temperature
    2-30°C
  • Shelf Life
    2 Years
  • Sensitivity
    98.4%
  • Specificity
    99.2%
  • Accuracy
    98.8%
  • Cut-Off
    300 Ng/mL*
  • Place of Origin
    -
  • Brand Name
    Citest
  • Certification
    CE
  • Model Number
    DDI-102/101/114,DDI-X14
  • Minimum Order Quantity
    N/A
  • Price
    negotiation
  • Packaging Details
    10T/25T/40T/50T
  • Delivery Time
    2-4 Weeks
  • Supply Ability
    10 M tests/month

300Ng/ML Fast Reading Rdt Test Kit Diazepam DIA Human Urine Test Qualitative Detection

Fast Reading Rdt Kit For Qualitative Detection Of Dia/zepam DIA In Human Urine

 

 

Principle Chromatographic Immunoassay
Format Dipstick, Cassette, Panel, Cup
Specimen Urine, Powder
Certificate CE
Reading Time 5 minutes
Pack 25T/40T/50T
Storage Temperature 2-30°C
Shelf Life 2 Years
Sensitivity 98.40%
Specificity 99.20%
Accuracy 98.80%
Cut-Off 300 ng/mL*

 

 

A rapid test for the qualitative detection of Benzodia/zepines in human urine.For medical and other professional in vitro diagnostic use only.

 

Applications:  

 

The DIA Rapid Test (Urine) is a rapid chromatographic immunoassay for the detection of Dia/zepam in urine at a cut-off concentration of 300ng/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.

 

 

 

Description:  

 

Dia/zepam is a medication of the benzodia/zepine family that typically produces a calming effect. It has anticonvulsant properties. Dia/zepam has no effect on GABA levels and no effect on glutamate decarboxylase activity, but has a slight effect on gamma-amino butyric acid transaminase activity. Dia/zepam can be administered orally, intravenously intramuscularly (IM), or as a suppository.
 
When administered orally, it is rapidly absorbed and has a fast onset of action. The onset of action is one to five minutes for IV administration and 15–30 minutes for IM administration. The duration of dia/zepam's peak pharmacological effects is 15 minutes to one hour for both routes of administration.
 
The bioavailability after oral administration is 100% and 90% after rectal administration. Peak plasma levels occur between 30 and 90 minutes after oral administration and between 30 and 60 minutes after intramuscular administration; after rectal administration, peak plasma levels occur after 10 to 45 minutes. Dia/zepam is highly protein-bound, with 96 to 99% of the absorbed drug being protein-bound. The distribution half-life of dia/zepam is 2 to 13 minutes. When dia/zepam is administered IM, absorption is slow, erratic, and incomplete.

 

How to use? 

 

Allow the test, urine specimen, and/or controls to reach room temperature (15-30°C) prior to testing.


1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it within one hour.


2. Place the test cassette on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 120μL) to the specimen well (S) of the test cassette, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See the illustration below.


3. Wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10minutes.

300Ng/ML Fast Reading Rdt Test Kit Diazepam DIA Human Urine Test Qualitative Detection 0

 

DIRECTIONS FOR PANEL USE


Allow the test, urine specimen, and/or controls to reach room temperature (15-30ºC) prior to testing.


1. Bring the pouch to room temperature before opening it. Remove the test panel from the sealed pouch and use it within one hour.


2. Remove the cap.


3. With the arrow pointing toward the urine specimen, immerse the test panel vertically in the urine specimen for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but not above the arrow on the test panel.


4. Replace the cap and place the test panel on a non-absorbent flat surface.


5. Start the timer and wait for the colored line(s) to appear.
 

6. The result should be read at 5 minutes. Do not interpret the result after 10 minutes.

300Ng/ML Fast Reading Rdt Test Kit Diazepam DIA Human Urine Test Qualitative Detection 1

 

DIRECTIONS FOR DIPSTICK USE


Allow the test, urine specimen, and/or controls to reach room temperature (15-30ºC) prior to testing.


1. Bring the pouch to room temperature before opening it. Remove the test dipstick from the sealed pouch and use it within one hour.


2. With arrows pointing toward the urine specimen, immerse the test dipstick vertically in the urine specimen for at least 10-15 seconds. Do not pass the maximum line (MAX) on the Test Dipstick when immersing the strip. See the illustration below.


3. Place the test dipstick on a non-absorbent flat surface, start the timer and wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10 minutes.

 

300Ng/ML Fast Reading Rdt Test Kit Diazepam DIA Human Urine Test Qualitative Detection 2

 

 

 

INTERPRETATION OF RESULTS

 

(Please refer to the illustration above)

 

NEGATIVE:* Two lines appear. One color line should be in the control region (C), and another apparent color line should be in the test region (T). This negative result indicates that the Dia/zepam (DIA) concentration is below the detectable cutoff level.

*NOTE: The shade of color in the test region (T) may vary, but it should be considered negative whenever there is even a faint color line.

 

POSITIVE: One color line appears in the control region (C). No line appears in the test region (T). This positive result indicates that the Dia/zepam (DIA) concentration is above the detectable cutoff level.

 

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test Dipstick. If the problem persists, discontinue using the test Dipstick immediately and contact your local distributor.

 

Order Information

 

Cat. No. Product Specimen Pack
DDI-102 Dia/zepam (DIA) Rapid Test Cassette Urine 40T
DDI-114 Dia/zepam (DIA) Rapid Test Panel Urine 40T
DDI-101 Dia/zepam (DIA) Rapid Test Dipstick Urine 40T
DDI-X14 Dia/zepam (DIA) Rapid Test Panel Urine 40T