Chlorophyll as a sustainable crosslinking strategy for engineering highly compressible hydrogels

Hydrogels are promising candidates for tissue repair. Non-invasive delivery of hydrogel patches involving high strains and deformations requires mechanical robustness and complex material design. Here we show chlorophyll, a sustainable plant-derived small molecule, functions as a universal physical crosslinker to significantly enhance hydrogels’ compressibility and resilience. Chlorophylls self-assemble in aqueous pre-polymer solution via hydrophobic interactions, leading to the nano-aggregations, acting as physical crosslinkers and anchoring points within hydrogels’ matrix. Additionally, the solvent exchange (SE) process promotes macroporous structure formation for high compressibility and resilience. With chlorophyll, the maximum compressive strains of gelatin methacrylate (GC) hydrogels increased from ~43% to ≥90%, allowing injection under 90.4% deformation while preserving structural integrity. This strategy enabled the fabrication of a single 36-mm diameter injectable conductive polypyrrole-deposited GC (GCP) cardiac patch for myocardial repair in minipigs. Moreover, chlorophyll functions as an intrinsic antioxidant reservoir, and improved ejection fraction (EF) by 11 % in porcine infarcted hearts. Hydrogels with high deformation and resilience are desirable for applications such as injectable cardiac patches. Here, authors provide a strategy using chlorophyll as a physical crosslinker to engineer highly compressible hydrogels.

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Publication Details

Journal
Nature Communications
Published
2026-09-29
DOI
https://doi.org/10.1038/s41467-026-77673-z
Primary Topic
Tissue Engineering and Regenerative Medicine
Type
article
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article

Chlorophyll as a sustainable crosslinking strategy for engineering highly compressible hydrogels

Xianglong Xing, Malcolm M. Q. Xing, Quan Wang, Yuqing Liu et al.
Nature Communications
Tissue Engineering and Regenerative Medicine
article

Chlorophyll as a sustainable crosslinking strategy for engineering highly compressible hydrogels

Xianglong Xing, Malcolm M. Q. Xing, Quan Wang, Yuqing Liu, Leyu Wang, Chaoran Zhao, Oluwaloba Wisdom Ojo, Kaige Xu, Mingsong Wu, Junjie Liu
article en

Abstract

Hydrogels are promising candidates for tissue repair. Non-invasive delivery of hydrogel patches involving high strains and deformations requires mechanical robustness and complex material design. Here we show chlorophyll, a sustainable plant-derived small molecule, functions as a universal physical crosslinker to significantly enhance hydrogels’ compressibility and resilience. Chlorophylls self-assemble in aqueous pre-polymer solution via hydrophobic interactions, leading to the nano-aggregations, acting as physical crosslinkers and anchoring points within hydrogels’ matrix. Additionally, the solvent exchange (SE) process promotes macroporous structure formation for high compressibility and resilience. With chlorophyll, the maximum compressive strains of gelatin methacrylate (GC) hydrogels increased from ~43% to ≥90%, allowing injection under 90.4% deformation while preserving structural integrity. This strategy enabled the fabrication of a single 36-mm diameter injectable conductive polypyrrole-deposited GC (GCP) cardiac patch for myocardial repair in minipigs. Moreover, chlorophyll functions as an intrinsic antioxidant reservoir, and improved ejection fraction (EF) by 11 % in porcine infarcted hearts. Hydrogels with high deformation and resilience are desirable for applications such as injectable cardiac patches. Here, authors provide a strategy using chlorophyll as a physical crosslinker to engineer highly compressible hydrogels.

Nature Communications
Southern Methodist University (US), Huzhou Normal University (CN), Shantou University (CN), Second Affiliated Hospital of Guangzhou Medical University (CN), University of Manitoba (CA), Southern Medical University (CN), Guangzhou Medical University (CN)
Responsible consumption and production
Openalex Percentile: Top 9%
Tissue Engineering and Regenerative Medicine
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