Aggregation‐Induced Emission Photosensitizer‐Armored Magnetic Nanoparticles for Sepsis Treatment: Combating Multidrug‐Resistant Bacteria and Alleviating Inflammation

败血症 光敏剂 炎症 金黄色葡萄球菌 细菌 抗菌剂 免疫系统 抗生素 多重耐药 活性氧 光动力疗法 微生物学 材料科学 医学 免疫学 化学 生物 光化学 生物化学 有机化学 遗传学
作者
Jiali Wang,Yuan Chen,Jia‐Xing Song,Bing‐Wei Guo,Feng‐Wei Xia,Yu Wan,Wan‐Xia Wu,Chungu Zhang,Shun Feng,Mingyu Wu
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:34 (10) 被引量:8
标识
DOI:10.1002/adfm.202312162
摘要

Abstract Sepsis, a life‐threatening condition stemming from an uncontrolled host immune response to bacterial infections, continues to impose a significant global burden with high morbidity and mortality. Addressing the challenges posed by antimicrobial resistance and uncontrollable inflammation remains a challenge in sepsis treatment. Moreover, traditional antibacterial materials have low bacterial trapping efficiency and inevitable prolonged circulation within the bloodstream, resulting in suboptimal antibacterial effects, metabolic complications, and undesirable side effects. In this study, an innovative solution is introduced through the development of Fe 3 O 4 @SH@TBTCP‐PMB, an aggregation‐induced emission (AIE) photosensitizer (PS)‐armored magnetic nanoparticles (NPs). It has high reactive oxygen species (ROS) generation efficiency and an exceptional ability to capture Gram‐positive bacteria with over 80% enrichment efficiency within just 1 h, even at low bacterial concentrations. Under white light illumination, 100 µg mL −1 of Fe 3 O 4 @SH@TBTCP‐PMB effectively eliminated more than 99.9% of methicillin‐resistant Staphylococcus aureus (MRSA). Furthermore, its magnetic separation properties efficiently prevent systemic blood circulation and associated side effects. Most importantly, Fe 3 O 4 @SH@TBTCP‐PMB demonstrates superior anti‐inflammatory effects by regulating cytokines, reducing adhesion molecule expression, and managing oxidative stress levels. This multifunctional approach significantly enhances sepsis survival rates, offering a promising strategy for combating multidrug‐resistant (MDR) bacterial infections in sepsis patients while addressing inflammation‐related complications.
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