Evidence map›Paper›PMID 41668533›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Design and Characterization of DX-Tile DNA Nanostar-Based Hydrogels.

Dylan V Scarton, Alessandra B Coogan, Peter M Touma, Eray O Tulun, Katie A Harrison, Jack Buchen, Richard C Steiner, Christopher R Fellin, Hunter G Mason, Chih-Hsiang Hu and 4 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. 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. Review
  2. Article
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

14 authors.

Dylan V ScartonInterdisciplinary Program in Neuroscience, College of Science, George Mason University, Fairfax, Virginia, USA.
Alessandra B CooganInstitute for Advanced Biomedical Research, George Mason University, Manassas, Virginia, USA.
Peter M ToumaInstitute for Advanced Biomedical Research, George Mason University, Manassas, Virginia, USA.
Eray O TulunInstitute for Advanced Biomedical Research, George Mason University, Manassas, Virginia, USA.
Katie A HarrisonInstitute for Advanced Biomedical Research, George Mason University, Manassas, Virginia, USA.
Jack BuchenHenry Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, Maryland, USA.
Richard C SteinerHenry Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, Maryland, USA.
Christopher R FellinHenry Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, Maryland, USA.
Hunter G MasonSchool of System Biology, College of Science, George Mason University, Manassas, Virginia, USA.
Chih-Hsiang HuInstitute for Advanced Biomedical Research, George Mason University, Manassas, Virginia, USA.
Sally FaragInstitute for Advanced Biomedical Research, George Mason University, Manassas, Virginia, USA.
Xiaoning YuanDepartment of Physical Medicine and Rehabilitation, Center for Rehabilitation Sciences Research, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Shailly JariwalaHenry Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, Maryland, USA.
Remi VenezianoInstitute for Advanced Biomedical Research, George Mason University, Manassas, Virginia, USA.ORCID https://orcid.org/0000-0002-2726-3770

Funding

Cosmos Club FoundationUniformed Services University of the Health Sciences HU00012320007U.S. Army Medical Research Acquisition Activity HT9425-23-1-0037
6 · The paper itself

Abstract

Pure deoxyribonucleic acid (DNA) hydrogels synthesized via the hybridization of multi-arm DNA tiles (DNA nanostars) are uniquely programmable and functionalizable biomaterials, suitable for applications ranging from biosensing to cell-free protein production and soft tissue engineering. However, the full potential offered by DNA molecules in terms of design flexibility and functionalization has not yet been leveraged for pure DNA hydrogels, thus reducing their versatility and broader use. In this study, we introduce multi-arm double-crossover (DX)-tile motifs, often used in wireframe DNA nanoparticles assembly, to enable greater control over the hydrogel's mechanical properties and facilitate functionalization. Specifically, we demonstrate that modifying structural design parameters, such as the arm geometry, length, valency, and linker design, allows for fine control of the elastic modulus and viscoelastic properties of the hydrogels. We also show that their functionalization can be performed without compromising the hydrogels' physical properties and exhibit enhanced mechanical strength and tunable properties, compared to simple duplex-based DNA hydrogels. Furthermore, these DNA hydrogels demonstrated printability and scalability, which pave the way toward the development of novel formulations and bioinks for the rational design of soft tissue engineering scaffolds and broaden the use of DNA hydrogels for other biomedical applications.

Indexed as

Biocompatible MaterialsDNAHydrogelsTissue EngineeringDNA NanostructuresBiocompatible MaterialsDNAHydrogelsbioprintingDNA hydrogelsDNA nanotechnologydouble‐crossover (DX)‐tile

Identifiers

PMID41668533
PMCPMC13042906

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.