A nano-enzyme / deoxyribozyme synergistic anti-inflammatory complex targeting macrophages and application thereof in preparation of drugs for inflammatory diseases
By using a nanozyme/deoxyribonuclease synergistic anti-inflammatory complex, precise targeting and efficient anti-inflammatory effects are achieved at the site of inflammation, solving the problems of poor targeting and insufficient stability of existing anti-inflammatory drugs. This significantly improves the therapeutic effect and reduces side effects, making it suitable for the treatment of a variety of inflammatory diseases.
Patent Information
- Application Number
- CN202611013985.0
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2026-07-08
- Publication Date
- 2026-09-29
AI Technical Summary
Existing anti-inflammatory drugs have poor targeting, significant systemic side effects, are prone to relapse, and have poor long-term tolerance. Single nanozymes cannot block inflammatory signaling pathways, and deoxyribonucleases have poor stability and lack efficient targeted delivery systems, making it difficult to achieve efficient, safe, and precise anti-inflammatory treatment.
A nanozyme/deoxyribozyme synergistic anti-inflammatory complex was developed. The nanozyme and deoxyribozyme were constructed through self-assembly. The nanozyme and deoxyribozyme were combined through charge adsorption. The L-arginine-modified polymer material was used to achieve targeted delivery to the site of inflammation. The nanozyme cleared ROS, and the deoxyribozyme silenced the inflammatory signaling pathway, thus achieving a dual anti-inflammatory effect.
It significantly improves the treatment effect of inflammatory diseases, reduces side effects, achieves precise targeting and efficient anti-inflammatory effects at the site of inflammation, regulates the intestinal flora structure, repairs the intestinal mucosal barrier, and provides multi-dimensional treatment for a variety of inflammatory diseases.