The cAMP Hunter™ Liraglutide Bioassay Kit provides a cell-based solution for liraglutide drug testing and quality control. This qualified bioassay enables precise liraglutide potency measurement and neutralizing antibody detection using CHO-K1 cells overexpressing human GLP-1 receptors. The assay leverages EFC technology for sensitive cAMP detection.
This bioassay kit serves companies developing GLP-1 receptor agonist therapies for diabetes and metabolic disorders. Applications include drug characterization, lot release testing, stability studies, and neutralizing antibody screening. The ready-to-use format accelerates results while ensuring consistency.
This kit has been optimized with Victoza® to meet regulatory requirements, providing validated parameters including accuracy, precision, linearity, and robustness for regulatory submissions and QC programs.
In the cAMP Hunter™ Liraglutide Bioassay Kit, CHO-K1 cells overexpressing human GLP-1R utilize the receptor's natural Gαs coupling to monitor activation. When activated by liraglutide, the receptor stimulates adenylyl cyclase, catalyzing ATP conversion to 3′-5′ cyclic adenosine monophosphate (cAMP). The resulting increase in intracellular cAMP is quantified using a homogeneous, gain-of-signal competitive immunoassay based on Enzyme Fragment Complementation (EFC) technology. Signal intensity correlates directly with cellular cAMP levels, higher GLP-1R activation produces greater cAMP concentrations and larger assay signals.
The Liraglutide qualification package demonstrates comprehensive validation of the cAMP Hunter™ Liraglutide Bioassay Kit across critical performance parameters. Validation studies include inter-plate precision assessment (8.6% RSD), accuracy evaluation (98.4% recovery), plate uniformity analysis (EC80 and IC80 across entire plate), plate-to-plate variability (three plates over three days), slope consistency, relative potency assessment (50-150% range), and parallelism testing with two operators. All studies were conducted with Victoza® and documented by designated assay developer and qualifier personnel.
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