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Sample Type
Human Serum / Plasma Sample
Specialty
Requires Refrigeration
Storage Requirements
Particle-enhanced Turbidimetric Immunoassay
Test Category
Lidocaine
Test Method
Therapeutic Drug Monitoring
Test Name
41116007
Test Type
R1: 2 X 18 mL
UNSPSC Code
R2: 2 X 9 mL
Volume
Features
The QMS® Lidocaine assay is intended for the quantitative determination of lidocaine in human serum or plasma on automated clinical chemistry analyzers; the results obtained are used in the diagnosis and treatment of lidocaine overdose and in monitoring levels of lidocaine to help ensure appropriate therapys
Significantly reduces labor
time
and expense compared to HPLC or LCMS and other technologies
Based on competitive inhibition immunoassay principle whereby free-drug in the sample competes for antibody binding sites with drug molecules coated onto uniform microparticles
Liquid stable and ready-to-use
Applicable to general chemistry analyzers
Validated parameters assure lab-to-lab reproducibility
Excellent correlation to reference methods
Optimal sensitivity
precision and dynamic range
Low cross-reactivity with metabolites and commonly co-administered drugs
Low interference from endogenous substances
