Evidence map›Paper›PMID 42513002›Full record

ArticleMicromachines2026

Bovine Serum Albumin Enhances the Quantitative Performance of Polydimethylsiloxane-Based Chamber Digital PCR by Suppressing Surface Adsorption.

Eri Tsunoi, Kazuo Hosokawa, Hitoshi Ohmori, Kae Sato

Abstract read
In one paragraph

Article in Micromachines, 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

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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

4 authors.

Eri TsunoiDepartment of Chemical and Biological Sciences, Faculty of Science, Japan Women's University, 2-8-1 Mejirodai, Bunkyo, Tokyo 112-8681, Japan.
Kazuo HosokawaMaterials Fabrication Laboratory, RIKEN Pioneering Research Institute, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.ORCID 0000-0003-1249-2834
Hitoshi OhmoriMaterials Fabrication Laboratory, RIKEN Pioneering Research Institute, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Kae SatoDepartment of Chemical and Biological Sciences, Faculty of Science, Japan Women's University, 2-8-1 Mejirodai, Bunkyo, Tokyo 112-8681, Japan.ORCID 0000-0002-1618-2086

Funding

Japan Society for the Promotion of Science 24K15781
6 · The paper itself

Abstract

Polydimethylsiloxane (PDMS) surfaces are highly hydrophobic, and non-specific biomolecule adsorption is a well-known limitation in microfluidic PCR systems. Flow-based microfluidic PCR has been extensively studied, but the impact of surface adsorption on quantitative performance in closed-chamber digital PCR (dPCR) platforms remains poorly characterized. This adsorption may reduce the effective concentrations of key reaction components and compromise quantification accuracy. Therefore, in this study, we evaluated two approaches to prevent molecular adsorption in PDMS-based cdPCR systems: (i) the addition of chemical additives to the PCR reaction mixture and (ii) the incorporation of hydrophilizing agents into PDMS, with solution-phase additives proving more effective in this system. We investigated the effects of the reaction additives bovine serum albumin (BSA), Blocking One-P, and dextran on DNA quantification using a PDMS-based dPCR chip. A single-concentration comparison showed that 1.1% BSA produced the highest average DNA copy number (0.091 ± 0.010 copies/well), compared to the no-additive condition (0.039 ± 0.010 copies/well), corresponding to an approximately 2.3-fold increase, whereas Blocking One-P and dextran had no substantial effects. Dilution series experiments were then conducted under BSA-added and BSA-free conditions using plasmid DNA and cDNA derived from HSC4 cells as templates. In both cases, BSA improved quantitative linearity, as reflected by the increased slopes and coefficients of determination.

Indexed as

bovine serum albuminchamber-based dPCRdigital PCRnonspecific adsorptionPDMS device

Identifiers

PMID42513002
PMCPMC13413812

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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.