ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Design and Characterization of DX-Tile DNA Nanostar-Based Hydrogels.
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.
What it found
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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.
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Who cites it
2 citing papers in PubMed.
- Hydrogel microspheres for precision biomedicine: network engineering, microfabrication, and therapeutic applications.RSC advances · 2026Review
- DNA cross-over motifs-based, programmable supramolecular hydrogels for the mechanoregulatory effects of cellular behaviour and cytoskeleton reorganization.npj biomedical innovations · 2026Article
Corrections and comments
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Authors and funding
14 authors.
Funding
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.
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Registered trials
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