Postoperative
abdominal adhesions are a common problem after surgery
and can produce serious complications. Current antiadhesive strategies
focus mostly on physical barriers and are unsatisfactory and inefficient.
In this study, we designed and synthesized advanced injectable cream-like
hydrogels with multiple functionalities, including rapid gelation,
self-healing, antioxidation, anti-inflammation, and anti-cell adhesion.
The multifunctional hydrogels were facilely formed by the conjugation
reaction of epigallocatechin-3-gallate (EGCG) and hyaluronic acid
(HA)-based microgels and poly(vinyl alcohol) (PVA) based on the dynamic
boronic ester bond. The physicochemical properties of the hydrogels
including antioxidative and anti-inflammatory activities were systematically
characterized. A mouse cecum–abdominal wall adhesion model
was implemented to investigate the efficacy of our microgel-based
hydrogels in preventing postoperative abdominal adhesions. The hydrogels,
with a high molecular weight HA, significantly decreased the inflammation,
oxidative stress, and fibrosis and reduced the abdominal adhesion
formation, compared to the commercial Seprafilm group or Injury-only
group. Label-free quantitative proteomics analysis demonstrated that
S100A8 and S100A9 expressions were associated with adhesion formation;
the microgel-containing hydrogels inhibited these expressions. The
microgel-containing hydrogels with multifunctionality decreased the
formation of postoperative intra-abdominal adhesions in a murine model,
demonstrating promise for clinical applications.