Evidence map›Paper›PMID 40861914›Full record

ArticleACS measurement science au2025

Microfluidic Determination of Cell-Derived ATP and Single Cell Pressure Mapping Confirms Benefits of Normoglycemic Stored Red Blood Cells.

Stephen A Branch, Yunong Wang, Samuel Azibere, Logan D Soule, Ashley R Davis, Timothy McMahon, R Scott Martin, Lane A Baker, Morgan K Geiger, Dana M Spence

Abstract read
In one paragraph

Article in ACS measurement science au, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

10 authors.

Stephen A BranchDepartments of Biomedical Engineering and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan 48824, United States.
Yunong WangDepartment of Chemistry, Texas A & M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0003-1327-4994
Samuel AzibereDepartment of Chemistry, Saint Louis University, St. Louis, Missouri 63103, United States.ORCID https://orcid.org/0000-0003-1302-7643
Logan D SouleDepartments of Biomedical Engineering and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan 48824, United States.
Ashley R DavisDepartments of Biomedical Engineering and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan 48824, United States.ORCID https://orcid.org/0009-0008-6031-020X
Timothy McMahonDepartment of Medicine, Duke University, Durham, North Carolina 27710, United States.ORCID https://orcid.org/0000-0002-3404-3223
R Scott MartinDepartment of Chemistry, Saint Louis University, St. Louis, Missouri 63103, United States.
Lane A BakerDepartment of Chemistry, Texas A & M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0001-5127-507X
Morgan K GeigerDepartments of Biomedical Engineering and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan 48824, United States.ORCID https://orcid.org/0000-0002-7862-4572
Dana M SpenceDepartments of Biomedical Engineering and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan 48824, United States.ORCID https://orcid.org/0000-0002-4754-6671

Funding

From single molecule to microfluidic 3D tissue platforms: novel multiscale tools to investigate hyper-stimulated immune cells in the circulationR01NS105888 · NINDS · MICHIGAN STATE UNIVERSITY · PI Lane A. Baker, ROBERT Scott MARTIN · 2018 to 2026
$4.0M
An Improved Red Blood Cell Storage Product and Extended Shelf Life using a Normoglycemic Additive SolutionR01HL156440 · NHLBI · MICHIGAN STATE UNIVERSITY · PI MCMAHON, TIMOTHY J, SPENCE, DANA M · 2021 to 2024
$2.0M
NHLBI NIH HHS R01 HL156440NINDS NIH HHS R01 NS105888
6 · The paper itself

Abstract

In the United States, ∼30,000 units of red blood cells (RBCs) are transfused daily to patient recipients. These RBCs are stored in one of multiple variations of media known as additive solutions, all of which contain glucose at concentrations well above physiological levels. Recently, strategies for storage of the RBCs in normoglycemic versions of the additive solutions whose glucose levels are maintained with periodic boluses of glucose were developed, resulting in benefits to the stored RBCs. Here, we describe a system capable of semiautonomous, Wi-Fi-enabled control of glucose delivery using a microperistaltic pump for maintenance of physiological concentrations of glucose in a closed RBC storage system. The RBCs stored in these normoglycemic conditions demonstrated reduced lysis and reduced hemoglobin glycation in comparison to those of the currently used hyperglycemic additive solutions. Furthermore, a novel single cell technique using pressure-induced conductivity mapping showed an improved Young's modulus for those RBCs stored in normoglycemic solutions. These quantitative measurements of the RBCs' chemical and physical properties coincide with improvements in cell functionality. Specifically, determinations of RBC-derived ATP using a 3D-printed microfluidic device show an increased release of ATP for RBCs stored in normoglycemic solutions in comparison to hyperglycemic storage, even for cells that were 2 weeks past a storage expiration of 42 days.

Indexed as

automatednormoglycemicoxidative stressRBCsstorage lesionstorage solution

Identifiers

PMID40861914
PMCPMC12371595

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.