ArticleACS omega2026
Application of Gyrolab, an Automated Microfluidic System, to Regulated Bioanalysis of a Therapeutic Antibody in Monkey Serum.
Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
3 authors.
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Abstract
A microfluidic ligand binding assay platform, Gyrolab, has been employed for the analysis of biotherapeutics due to its high-throughput capabilities and reduced assay development time. In this study, Gyrolab was utilized to quantify E6011, an anti-fractalkine monoclonal antibody, in monkey serum. During method development, the concentrations of critical reagents and the minimum required dilution (MRD) were optimized. A 10 μL aliquot of serum samples was subjected to an MRD of 1:100, and E6011 in naïve serum was quantified over a range of 0.1 to 100 μg/mL. Validation parametersincluding calibration curve, prozone effect, carryover, selectivity, assay reproducibility, dilution integrity, and the effect of the target proteinwere evaluated along with platform-specific parameters such as inter-disc variability and stability at the MRD. All validation criteria were met. The assay was subsequently applied to a pharmacokinetic (PK) study of E6011 in monkeys. PK data obtained using Gyrolab were compared with results from a previous study using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The PK parameters estimated by the Gyrolab assay were consistent with those obtained by LC-MS/MS, supporting the robustness of the Gyrolab platform and its viability as an alternative assay method for biotherapeutics.
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Registered trials
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