Multifunctional Cu-doped Mn3O4 nanozyme hydrogel microspheres for oral targeted treatment of inflammatory bowel disease

TL;DR

Researchers developed a new oral treatment for inflammatory bowel disease using nanozyme hydrogel microspheres that target the colon and reduce inflammation.

Contribution

A colon-targeted hydrogel microsphere system with Cu-doped Mn3O4 nanozymes for oral IBD treatment was engineered.

Findings

HMCM effectively scavenges ROS and exhibits SOD, CAT, and GPx-like activities.

HMCM reduces inflammation, enhances antioxidant activity, and inhibits ferroptosis in colonic tissue.

HMCM restores gut microbiota balance and shows high biosafety and colon-specific retention.

Abstract

Oral drug therapy for inflammatory bowel disease (IBD) is often hindered by inadequate targeting, low bioavailability, and reactive oxygen species (ROS) accumulation. To address these challenges, we have developed hydrogel microspheres@Cu-Mn3O4 nanozymes (HMCM) by encapsulating hydrothermally synthesized Cu-doped Mn3O4 nanozymes (CM NZs) into calcium alginate hydrogel microspheres (HM) using microfluidics. These microspheres are designed for colon-targeted IBD treatment. The CM NZs exhibit exceptional superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) activities, effectively scavenging ROS such as H2O2, ·OH, and O2−·. The negatively charged HMCM promotes targeted accumulation in inflamed colon regions and facilitates specific nanozyme release. In a dextran sulfate sodium (DSS)-induced colitis mouse model, HMCM administration enhanced the expression of tight junction proteins (Claudin, ZO-1, Occludin) and repaired the damaged intestinal barrier. The oral HMCM group significantly reduced inflammation, enhanced antioxidant activity, and inhibited ferroptosis in colonic tissue through the upregulation of GPX4 and SLC7A11. It also restored gut microbiota balance by increasing probiotic populations and suppressing harmful bacteria. Systemic biosafety assessments confirmed HMCM's colon-specific retention and high biocompatibility. This research establishes HMCM as a precision-targeted colonic drug delivery platform, offering a promising therapeutic strategy for the treatment of inflammatory bowel disease.

Calcium alginate hydrogel microspheres @ Cu-Mn3O4 nanozymes (HMCM) were successfully synthesized. Due to their negatively charged surface, HMCM achieves site-specific enrichment in the colon and releases Cu-Mn3O4 nanozymes (CM NZs), which exhibit antioxidant enzyme-like activity and reactive oxygen species (ROS) scavenging capacity. In a DSS-induced colitis mouse model, HMCM effectively treated IBD through a triple synergistic mechanism: enhancing antioxidant and anti-inflammatory activities, inhibiting ferroptosis in colonic tissue cells, and regulating gut microbiota. This work presents an efficient, targeted strategy for IBD therapy.Image 1

•The synthesized Cu-Mn3O4 nanozymes (CM NZs) exhibit stronger multi-enzyme mimicking activities (SOD, CAT, GPx) and free radical scavenging ability compared to Mn3O4 NPs.•A colon-targeted composite of hydrogel microspheres@Cu-Mn3O4 nanozymes (HMCM) was engineered for precise oral nanozyme delivery.•HMCM treats IBD via a triple-synergistic mechanism. It simultaneously reduces inflammation and oxidative stress, inhibits ferroptosis by upregulating the GPX4/SLC7A11 pathway, and beneficially reshapes the gut microbiota, collectively restoring intestinal homeostasis.•HMCM demonstrates excellent systemic biosafety and colon-specific retention.

The synthesized Cu-Mn3O4 nanozymes (CM NZs) exhibit stronger multi-enzyme mimicking activities (SOD, CAT, GPx) and free radical scavenging ability compared to Mn3O4 NPs.

A colon-targeted composite of hydrogel microspheres@Cu-Mn3O4 nanozymes (HMCM) was engineered for precise oral nanozyme delivery.

HMCM treats IBD via a triple-synergistic mechanism. It simultaneously reduces inflammation and oxidative stress, inhibits ferroptosis by upregulating the GPX4/SLC7A11 pathway, and beneficially reshapes the gut microbiota, collectively restoring intestinal homeostasis.

HMCM demonstrates excellent systemic biosafety and colon-specific retention.

Figures