Wang Dan, Wang Shuya, Liu Jinjin, Shi Xiaojing, Xiong Tingli, Li Ruishi, Wei Wei, Ji Liandong, Huang Qiong, Gong Xuejun, Ai Kelong
Department of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, 410008, China.
Adv Sci (Weinh). 2025 Apr;12(13):e2413925. doi: 10.1002/advs.202413925. Epub 2025 Feb 14.
Acute pancreatitis (AP) is a primary contributor to hospitalization and in-hospital mortality worldwide. Targeted elimination of mitochondrial reactive oxygen species (mtROS) within pancreatic acinar cells (PACs) represents an ideal strategy for treating AP. However, existing drugs fail to overcome the physiological barriers of the pancreas to effectively reach PACs mitochondria due to the trade-off between conventional positively charged mitochondrial-targeting groups and their inability to penetrate the blood-pancreas barrier (BPB). Here, a tungsten-based heteropolyacid nano-antioxidant (mTWNDs) is introduced, co-modified with tannic acid (TA) and melanin, enabling site-specific clearance of mtROS in PACs, offering a highly effective treatment for AP. TA exhibits a strong affinity for proline-rich type III collagen and the mitochondrial outer membrane protein TOM20. This unique property allows mTWNDs to traverse the damaged BPB-exposing type III collagen to reach PACs and subsequently penetrate mitochondria for targeted mtROS elimination. In cerulein-induced AP mice, mTWNDs reversed AP at 1/50th the dose of N-acetylcysteine, suppressing PACs apoptosis and inflammation by blocking the stimulator of the interferon genes pathway activation in macrophage. This study establishes a mitochondrial-targeting antioxidant nanomedicine strategy for AP treatment.
急性胰腺炎(AP)是全球范围内住院治疗和住院死亡率的主要原因。靶向清除胰腺腺泡细胞(PACs)内的线粒体活性氧(mtROS)是治疗AP的理想策略。然而,由于传统带正电的线粒体靶向基团与它们无法穿透血胰屏障(BPB)之间的权衡,现有药物无法克服胰腺的生理屏障以有效到达PACs的线粒体。在此,引入了一种基于钨的杂多酸纳米抗氧化剂(mTWNDs),其与单宁酸(TA)和黑色素共同修饰,能够在PACs中对mtROS进行位点特异性清除,为AP提供了一种高效的治疗方法。TA对富含脯氨酸的III型胶原蛋白和线粒体外膜蛋白TOM20具有很强的亲和力。这种独特的性质使mTWNDs能够穿过暴露III型胶原蛋白的受损BPB到达PACs,随后穿透线粒体以靶向清除mtROS。在雨蛙素诱导的AP小鼠中,mTWNDs以N-乙酰半胱氨酸剂量的1/50逆转了AP,通过阻断巨噬细胞中干扰素基因途径激活的刺激物来抑制PACs凋亡和炎症。本研究建立了一种用于AP治疗的线粒体靶向抗氧化纳米药物策略。