Evidence map›Paper›PMID 41552560›Full record

ArticleACS omega2026

Application of Gyrolab, an Automated Microfluidic System, to Regulated Bioanalysis of a Therapeutic Antibody in Monkey Serum.

Kei Nabeshima, Tomoko Kojima, Yuji Mano

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Kei NabeshimaDMPK & Bioanalysis Unit, Sunplanet Co., Ltd., Tokodai 5-1-3, Tsukuba, Ibaraki 300-2635, Japan.
Tomoko KojimaDMPK & Bioanalysis Unit, Sunplanet Co., Ltd., Tokodai 5-1-3, Tsukuba, Ibaraki 300-2635, Japan.
Yuji ManoGlobal Drug Metabolism and Pharmacokinetics, Eisai Co., Ltd., Tokodai 5-1-3, Tsukuba, Ibaraki 300-2635, Japan.ORCID https://orcid.org/0000-0002-8537-951X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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 parametersincluding calibration curve, prozone effect, carryover, selectivity, assay reproducibility, dilution integrity, and the effect of the target proteinwere 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.

Identifiers

PMID41552560
PMCPMC12809548

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.