Chinese medicine-derived hydrogel attenuates traumatic brain injury by dual-antagonism of neuroinflammation and vasospasm

The malignant synergy between neuroinflammation and vasospasm is a core driving factor of secondary injury following traumatic brain injury (TBI), and self-assembling hydrogels for mechanical support and drug delivery have been extensively studied in therapeutic agents. Therefore, we utilized paeoniflorin (PF) and glycyrrhizic acid (GA) derived from Chinese medicine to synthesize a natural small-molecule self-assembling hydrogel (PG-gel, the PF/GA co-assembled hydrogel). Orchestrated via π-π stacking and hydrogen bonding interactions, as confirmed by X-ray Powder Diffraction, Fourier Transform Infrared Spectroscopy, ¹H Nuclear Magnetic Resonance and Mass Spectrometry. PG-gel exhibits a compliant mechanical modulus highly compatible with brain tissue modulus (~ 10 kPa) and achieving a cumulative drug release of 80% over 44 h. Mechanistically, PG-gel synergistically inhibits the dual pathological processes of neuroinflammation and vasospasm following TBI. Additionally, PG-gel demonstrates excellent biocompatibility and safety, with a hemolysis rate of less than 1%, meeting the application standards for green biomaterials. Taken together, this work not only describes a hydrogel that dually antagonizes neuroinflammation and vasospasm for effective intervention in TBI prognosis, but also provides new insights into strategies for neuroprotection and brain tissue repair.

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Publication Details

Journal
Journal of Nanobiotechnology
Published
2026-09-25
DOI
https://doi.org/10.1186/s12951-026-04840-1
Primary Topic
Nanoplatforms for cancer theranostics
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article
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article

Chinese medicine-derived hydrogel attenuates traumatic brain injury by dual-antagonism of neuroinflammation and vasospasm

罗杰坤, Tao Tang, Jun Zheng, Yang Wang et al.
Journal of Nanobiotechnology
Nanoplatforms for cancer theranostics
article

Chinese medicine-derived hydrogel attenuates traumatic brain injury by dual-antagonism of neuroinflammation and vasospasm

罗杰坤, Tao Tang, Jun Zheng, Yang Wang, Xudong Fan, Jiachen Sun, Yuqi Wu, Juewen Liu, Xin Guo, Ming Luo, Jingjing Liu, Weikang Luo
article en

Abstract

The malignant synergy between neuroinflammation and vasospasm is a core driving factor of secondary injury following traumatic brain injury (TBI), and self-assembling hydrogels for mechanical support and drug delivery have been extensively studied in therapeutic agents. Therefore, we utilized paeoniflorin (PF) and glycyrrhizic acid (GA) derived from Chinese medicine to synthesize a natural small-molecule self-assembling hydrogel (PG-gel, the PF/GA co-assembled hydrogel). Orchestrated via π-π stacking and hydrogen bonding interactions, as confirmed by X-ray Powder Diffraction, Fourier Transform Infrared Spectroscopy, ¹H Nuclear Magnetic Resonance and Mass Spectrometry. PG-gel exhibits a compliant mechanical modulus highly compatible with brain tissue modulus (~ 10 kPa) and achieving a cumulative drug release of 80% over 44 h. Mechanistically, PG-gel synergistically inhibits the dual pathological processes of neuroinflammation and vasospasm following TBI. Additionally, PG-gel demonstrates excellent biocompatibility and safety, with a hemolysis rate of less than 1%, meeting the application standards for green biomaterials. Taken together, this work not only describes a hydrogel that dually antagonizes neuroinflammation and vasospasm for effective intervention in TBI prognosis, but also provides new insights into strategies for neuroprotection and brain tissue repair.

Journal of Nanobiotechnology
Central South University (CN), University of Waterloo (CA), Peking University (CN), Peking University Third Hospital (CN), First Affiliated Hospital of University of South China (CN), Xiangya Hospital Central South University (CN), University of South China (CN)
Openalex Percentile: Top 21%
Nanoplatforms for cancer theranostics
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