A pH-responsive hyaluronic acid hydrogel delivering integrin α5β1-targeting peptides facilitated lesion-localized anti-fibrotic therapy for intrauterine adhesions by modulating macrophage polarization.
Smart delivery at disease siteThe hydrogel releases anti-fibrotic peptides only at inflamed, acidic adhesion sites — treating disease precisely where it occurs
What the researchers found
pH-responsive HA hydrogel delivers integrin α5β1-targeting peptides at acidic lesion sites, modulating macrophage M1→M2 polarization to reduce fibrosis and restore uterine tissue in IUA models.
Why it matters
IUA causes female infertility. A hydrogel that delivers anti-fibrotic peptides precisely at adhesion sites could restore fertility.
How the study worked
HA hydrogel design with pH-responsive release, integrin α5β1-targeting peptide incorporation, macrophage polarization studies, and IUA animal model evaluation.
What this study cannot tell us
Preclinical. Human uterine environment more complex. Hydrogel placement requires hysteroscopy.
How to read the evidence
Preclinical study with responsive delivery and mechanism characterization.
When this study was published
Published in 2025.
The bigger picture
Lesion-responsive peptide delivery represents precision medicine for fibrotic diseases — therapy activates only where needed.
Questions still open
- Could this approach treat other fibrotic conditions (liver, kidney)?
- How long does the hydrogel remain active in the uterine cavity?
- Would this improve IVF success rates in IUA patients?
Common questions
How does this treat infertility?
Why is pH-responsive delivery important?
Read the original research
A pH-responsive hyaluronic acid hydrogel facilitates lesion-localized integrin α5β1 agonism to attenuate osteopontin signaling and fibrosis in intrauterine adhesions.
Acta biomaterialia
Citation
Ji, Wanqing; Wen, Jiaming; Tong, Nian; Guo, Fang; Zheng, Jie; Wen, Xuejun; Liu, Jie; Zhang, Ning; Hou, Bo. (2026). A pH-responsive hyaluronic acid hydrogel facilitates lesion-localized integrin α5β1 agonism to attenuate osteopontin signaling and fibrosis in intrauterine adhesions.. Acta biomaterialia. https://doi.org/10.1016/j.actbio.2026.03.001