|Sample:||Urine||Certificate:||ISO, CE, FDA|
|Usage:||Professional Use||Shelf Life:||24 Months|
Propoxyphene Rapid Test Kit,
PPX Rapid Test Kit,
Urine Sample Rapid Test Cassette
Propoxyphene (PPX) Rapid Test Kit Drug of Abuse Rapid Test Cassette for Urine Sample
Propoxyphene (PPX) Rapid Test is a rapid, screening test for the qualitative detection of Propoxyphene (PPX) and metabolites in human urine at specified cut oflevels.
For professional use only.
For in vitro diagnostic use only.
Propoxyphene (PPX) Rapid Tes is an immuno-chromatographic assay for the qualitative determination of the presence of drugs listed in the table below.
This assay provides only a preliminary analytical test result. Gas Chromatography/Mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to Propoxyphene (PPX) of abuse test result, particularly when preliminary positive results are indicated.
Propoxyphene is a prescription drug for the relief of pain. Overdose of propoxyphene can have the symptoms including analgesia, stupor, respiratory depression and coma . The half-life of propoxyphene is 8 to 24 hours. Propoxyphene reaches its peak in 1 to 2 hours after oral administration.
Propoxyphene (PPX) Rapid Test s a competitive immunoassay that is used to screen for the presence of Propoxyphene (PPX) and metabolites in urine. It is chromatographic absorbent device in which, drugs within a urine sample, competitively combined to a limited number of drug monoclonal antibody (mouse) conjugate binding sites.
When the test is activated, the urine is absorbed into each test strip by capillary action, mixes with the respective drug monoclonal antibody conjugate, and flows across a pre-coated membrane. When drug within the urine sample is below the detection level of the test, respective drug monoclonal antibody conjugate binds to the respective drug-protein conjugate immobilized in the Test Region (T) of the test strip. This produces a colored Test line in the Test Region (T) of the strip, which, regardless of its intensity, indicates a negative test result.
When sample drug levels are at or above the detection level of the test, the free drug in the sample binds to the respective drug monoclonal antibody conjugate, preventing the respective drug monoclonal antibody conjugate from binding to the respective drug-protein conjugate immobilized in the Test Region (T) of the device. This prevents the development of a distinct colored band in the test region, indicating a preliminary positive result.
To serve as a procedure control, a colored line will appear at the Control Region (C), of each strip, if the test has been performed properly.
【WARNINGS AND PRECAUTIONS】
【STORAGE AND STABILITY】
Test must be in room temperature ( 15ºC to 30ºC)
【INTERPRETATION OF RESULTS】
Preliminary positive (+)
Only one colored band appears, in the control region (C). No colored band appears in the test region (T).
Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).
Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.