Evidence map›Paper›PMID 41453424›Full record

ArticleActa biomaterialia2026

Rapidly dissolving biomaterials for high-efficiency viral transduction.

Christopher Moody, Pritha Agarwalla, Micah Mallory, Nidhi Rane, Treyvon W Davis, Israt Jahan Tulip, Sharda Pandit, Yevgeny Brudno

Abstract read
In one paragraph

Article in Acta biomaterialia, 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

8 authors.

Christopher MoodyJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA; Comparative Medicine Institute, North Carolina State University, Raleigh, NC, USA; Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Pritha AgarwallaJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA; Comparative Medicine Institute, North Carolina State University, Raleigh, NC, USA. Electronic address: Pritha@email.unc.edu.
Micah MalloryJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA; Comparative Medicine Institute, North Carolina State University, Raleigh, NC, USA.
Nidhi RaneJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA.
Treyvon W DavisDepartment of Biological Sciences, College of Veterinary Medicine, North Carolina State University, North Carolina, Raleigh, USA.
Israt Jahan TulipDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Sharda PanditJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA; Comparative Medicine Institute, North Carolina State University, Raleigh, NC, USA; Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Yevgeny BrudnoJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA; Comparative Medicine Institute, North Carolina State University, Raleigh, NC, USA; Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. Electronic address: ybrudno@email.unc.edu.

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Substrate Mediated siRNA Delivery from Scaffolds to Promote Wound RepairR01EB019409 · NIBIB · VANDERBILT UNIVERSITY · PI Craig Lewis Duvall · 2014 to 2026
$4.0M
Biomaterial Scaffolds for Ex Vivo and In Situ CAR-T Cell ProductionR37CA260223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Yevgeny Brudno · 2021 to 2026
$2.5M
MASTER Scaffolds for Rapid, Single-Step Manufacture and Prototyping of CAR-T cellsR33CA281875 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Yevgeny Brudno · 2023 to 2026
$1.3M
NCI NIH HHS P30 CA016086NCI NIH HHS R33 CA281875NCI NIH HHS R37 CA260223NIBIB NIH HHS R01 EB019409
6 · The paper itself

Abstract

Cell and gene therapy represent the frontier of genetic medicine for treating devastating diseases, yet they continue to face a critical bottleneck: inefficient genetic cell modification. While viral vectors remain our most powerful genetic delivery tools, their application suffers from significant transport insufficiencies with most viral particles wasted before reaching their cell targets. This fundamental challenge undermines the efficiency, safety, and economic viability of these potentially transformative therapies. Current transduction enhancers provide only partial solutions with significant drawbacks. RetroNectin works only with retroviruses and hematopoietic cells, spinoculation is time consuming and laborious, while polycationic polymers like polybrene pose toxicity concerns that preclude clinical applications. In this report, we introduce DUCTS (Dissolving Ultrafast Cell Transduction Sponges), a transduction enhancer based on uncrosslinked alginate cryogels that works within five minutes and completely dissolves, enabling rapid and easy workflows. DUCTS demonstrates broad versatility, boosting cell transduction across a variety of viral vectors (gamma retrovirus, lentivirus, and adeno-associated virus) in both suspension and adherent cells. Notably, DUCTS achieves comparable transduction efficiency while reducing viral concentration requirements by an order of magnitude compared to standard protocols. This cell- and virus-agnostic platform streamlines gene transfer procedures, reduces viral consumption and associated costs, and enhances the accessibility and scalability of cell and gene therapies. STATEMENT OF SIGNIFICANCE: In this report, we present DUCTS (Dissolving Ultrafast Cell Transduction Sponges), a major advance to improve transduction technology, addressing critical bottlenecks in cell therapy manufacturing. Unlike existing methods that require lengthy procedures, specialized equipment, or toxic additives, DUCTS achieves comparable transduction efficiency in just five minutes using a simple, dissolving alginate sponge. This platform works across multiple virus types (lentivirus, retrovirus, AAV) and cell types, dramatically reducing viral vector requirements by 10-fold while maintaining cell viability. A modified DUCTs can also simultaneously activate and transduce T cells in a single step to revolutionize CAR-T cell manufacturing. With exceptional shelf stability and GMP-compatible materials, DUCTS offers a practical solution to reduce costs, accelerate production timelines, and enhance accessibility of life-saving cell therapies for patients worldwide.

Indexed as

AlginateCAR T cellsCell therapycryogelMacroporousScaffoldsSpongesViral transduction

Identifiers

PMID41453424
PMCPMC13356821

What OpenQuestion holds

Textmetadata
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Read underepoch 390

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.