<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li Z</submitter><funding>Shaanxi Provincial Science and Technology Development Program</funding><funding>Project of Shaanxi Provincial Science and Technology New Star</funding><funding>National Natural Science Foundation of China</funding><funding>Shaanxi Provincial Key Research and Development Programme</funding><pagination>e02678</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12376516</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(30)</volume><pubmed_abstract>Constructing hydrogels with both remarkable mechanical and self-healing properties is highly desirable for soft electronics, yet remains challenging due to conflicting demands on chemical bonds and polymer chain mobility. Herein, a highly stretchable, self-healing, and conductive gelatin methacryloyl (GelMA) hydrogel is developed by incorporating polyvinyl alcohol, N-(2-amino-2-oxoethyl)-2-propenamide, sodium tetraborate, and sodium chloride into GelMA, followed by a two-step polymerization process. The introduced novel interpenetrating networks, hierarchical hydrogen bonds (weak and strong H-bonds), and borate ester bonds (BEBs) synergistically improve the mechanical strength, and concurrently function as sacrificial bonds for energy dissipation under deformation. Moreover, the constructed reversible BEBs and weak H-bonds enable autonomous self-healing at room temperature. The resulting hydrogel achieves remarkable stretchability (≈160%), tensile strength (≈130 kPa), and self-healing efficiency (86%), surpassing previously reported GelMA hydrogels. Importantly, a self-healing GelMA hydrogel strain sensor is demonstrated, featuring a high gauge factor (≈3.28), ultra-low detection limit (0.1%), and excellent recovery of sensitivity (≈100%) and detection range (≈75%) after damage. Successful monitoring of subtle and large-scale human motions with both original and healed sensors highlights the device's durability and longevity. This study provides a promising approach for the rational design and practical application of GelMA hydrogels in wearable bioelectronics.</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Highly Stretchable, Self-Healable, and Conductive Gelatin Methacryloyl Hydrogel for Long-Lasting Wearable Tactile Sensors.</pubmed_title><pmcid>PMC12376516</pmcid><funding_grant_id>52275570</funding_grant_id><funding_grant_id>2023KJXX-001</funding_grant_id><funding_grant_id>2024RS-CXTD-19</funding_grant_id><funding_grant_id>2023-LL-QY-35HZ01</funding_grant_id><funding_grant_id>52435010</funding_grant_id><pubmed_authors>Yu L</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Jia B</pubmed_authors><pubmed_authors>Lu D</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Qureshi MAK</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Xue Y</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Zhao L</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Han G</pubmed_authors><pubmed_authors>Yang P</pubmed_authors><pubmed_authors>Zhao K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Highly Stretchable, Self-Healable, and Conductive Gelatin Methacryloyl Hydrogel for Long-Lasting Wearable Tactile Sensors.</name><description>Constructing hydrogels with both remarkable mechanical and self-healing properties is highly desirable for soft electronics, yet remains challenging due to conflicting demands on chemical bonds and polymer chain mobility. Herein, a highly stretchable, self-healing, and conductive gelatin methacryloyl (GelMA) hydrogel is developed by incorporating polyvinyl alcohol, N-(2-amino-2-oxoethyl)-2-propenamide, sodium tetraborate, and sodium chloride into GelMA, followed by a two-step polymerization process. The introduced novel interpenetrating networks, hierarchical hydrogen bonds (weak and strong H-bonds), and borate ester bonds (BEBs) synergistically improve the mechanical strength, and concurrently function as sacrificial bonds for energy dissipation under deformation. Moreover, the constructed reversible BEBs and weak H-bonds enable autonomous self-healing at room temperature. The resulting hydrogel achieves remarkable stretchability (≈160%), tensile strength (≈130 kPa), and self-healing efficiency (86%), surpassing previously reported GelMA hydrogels. Importantly, a self-healing GelMA hydrogel strain sensor is demonstrated, featuring a high gauge factor (≈3.28), ultra-low detection limit (0.1%), and excellent recovery of sensitivity (≈100%) and detection range (≈75%) after damage. Successful monitoring of subtle and large-scale human motions with both original and healed sensors highlights the device's durability and longevity. This study provides a promising approach for the rational design and practical application of GelMA hydrogels in wearable bioelectronics.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-09T19:15:04.817Z</modification><creation>2026-04-08T01:11:01.361Z</creation></dates><accession>S-EPMC12376516</accession><cross_references><pubmed>40439485</pubmed><doi>10.1002/advs.202502678</doi></cross_references></HashMap>