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4mm Dipcard Multi Drug Test Kit Detecting Benzodiazepines Oxazepam Calibrator

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4mm Dipcard Multi Drug Test Kit Detecting Benzodiazepines Oxazepam Calibrator

4mm Dipcard Multi Drug Test Kit  Detecting Benzodiazepines Oxazepam Calibrator
4mm Dipcard Multi Drug Test Kit  Detecting Benzodiazepines Oxazepam Calibrator 4mm Dipcard Multi Drug Test Kit  Detecting Benzodiazepines Oxazepam Calibrator

Large Image :  4mm Dipcard Multi Drug Test Kit Detecting Benzodiazepines Oxazepam Calibrator Get Best Price

Product Details:
Place of Origin: China
Brand Name: New Life
Certification: ISO13485, CE
Model Number: Dipcard/cassette/strip
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
Method: Gold Colloidal Width: 4mm DIPCARD
Specimen: Urine Testing Time: 5-15 Minutes
Shelf Life: 24 Months Application: Benzodiazepines
High Light:

drug test strips

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Drug test BZO Rapid test cassette ,4mm dipcard detecting Benzodiazepines in urine, Quick, Gold colloidal method

 

 

 

Intended Use

 

The BZO Rapid Test Device (Urine) is a rapid visual immunoassay for the qualitative, presumptive detection of Benzodiazepines in human urine specimens at the cut-off concentrations listed below:

 

Parameter Calibrator Cut-off(ng/mL)
BZO (Benzodiazepines) Oxazepam 300

 

 

Test Principle

 

 

The BZO Rapid Test Device (Urine) detects Benzodiazepines through visual interpretation of color development on the Device. Drug conjugates are immobilized on the test region of the membrane. During testing, the specimen reacts with antibodies conjugated to colored particles and precoated on the sample pad. The mixture then migrates through the membrane by capillary action, and interacts with reagents on the membrane. If there are insufficient drug molecules in the specimen, the antibody-colored particle conjugate will bind to the drug conjugates, forming a colored band at the test region of the membrane. Therefore, a colored band appears in the test region when the urine is negative for the drug. If drug molecules are present in the urine above the cut-off concentration of the test, they compete with the immobilized drug conjugate on the test region for limited antibody binding sites. This will prevent attachment of the antibody-colored particle conjugate to the test region. Therefore, the absence of a colored band at the test region indicates a positive result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.

 

 

DIRECTIONS FOR USE

 

Bring tests, specimens, and/or controls to room temperature (15-30°C) before use.

Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. For best results, the assay should be performed within one hour.

Using the provided disposable pipette, transfer 3 drops of specimen (approximately 120 µL) to the specimen well (S) of the device and start the timer.

Avoid trapping air bubbles in the specimen well (S), and do not add any solution to the result area.

As the test begins to work, color will migrate across the membrane.

Wait for the colored band(s) to appear. The result should be read at 5 minutes. Do not interpret the result after 8 minutes

 

INTERPRETATION OF RESULTS

 

(Please refer to the illustration above)

NEGATIVE:* A colored line appears in the Control region (C) and colored lines appears in the Test region (T). This negative result means that the concentrations in the urine sample are below the designated cut-off levels for a particular drug tested.

*NOTE: The shade of the colored lines(s) in the Test region (T) may vary. The result should be considered negative whenever there is even a faint line.

POSITIVE: A colored line appears in the Control region (C) and NO line appears in the Test region (T). The positive result means that the drug concentration in the urine sample is greater than the designated cut-off for a specific drug.

INVALID: No line appears in the Control region (C). Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for Control line failure. Read the directions again and repeat the test with a new test card. If the result is still invalid, contact your manufacturer.

 

 

QUALITY CONTROL

 

A procedural control is included in the test. A line appearing in the control region

(C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique.

Control standards are not supplied with this kit. However, it is recommended that positive and negative controls be tested as good laboratory practice to confirm the test procedure and to verify proper test performance.

 

Performance characteristics

 

The specimen correlation study was performed on 300 urine specimens. 135 positive urine specimens and 165 negative urine specimens were confirmed by GC/MS. These specimens were randomized and tested using the BZO One Step Benzodiazepines Test Strip (Urine). Specimens were rated as either positive or negative at 5minutes. The test results are shown in Table 1.

 

Table 1: Specimen Correlation

    GC/MS
BZO One Step Test Strip   + -
+ 131 8
- 4 157

 

Positive agreement with GC/MS: 131/(131+4) = 97%

Negative agreement with GC/MS: 157/(157+8) = 95%

                              Total agreement with GC/MS: (131+157)/(131+4+8+157) = 96%

 

ORIENT NEW LIFE MEDICAL CO., LTD.
Contact: Jerry Meng
Email: Jerry @ newlifebiotest .com
Tel. +86 18657312116
SKYPE enetjerry

Contact Details
Orient New Life Medical Co.,Ltd.

Contact Person: Jerry Meng

Tel: +8618657312116

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