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用于实时比率磁共振成像检测活性氧物种和体内缓解炎症的敏感活化纳米探针。

Sensitive Activatable Nanoprobes for Real-Time Ratiometric Magnetic Resonance Imaging of Reactive Oxygen Species and Ameliorating Inflammation In Vivo.

机构信息

Institute of Burn Research, Southwest Hospital, State Key Lab of Trauma, Burn and Combined Injury, Chongqing Key Laboratory for Disease Proteomics, Army Medical University, Chongqing, 400038, China.

Department of Radiology, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.

出版信息

Adv Mater. 2022 May;34(19):e2109004. doi: 10.1002/adma.202109004. Epub 2022 Apr 7.

DOI:10.1002/adma.202109004
PMID:35276751
Abstract

Imaging-guided real-time monitoring of the treatment process of inflammatory diseases is important for the timely adjustment of treatment planning to lower unnecessary side effects and improve treatment outcomes. However, it is difficult to reflect the dynamic changes of inflammation in vivo with enough tissue penetration depth. Here a novel nanotheranostic agent (denominated TMSN@PM) with platelet membrane (PM)-coated, tempol-grafted, manganese-doped, mesoporous silica nanoparticles is developed. The PM endows the TMSN@PM with the ability to target inflammation sites, which are verified by fluorescence imaging with Cyanine5 carboxylic acid (Cy5)-labeled TMSN@PM. Under the inflammatory environment (mild acidity and excess reactive oxygen species (ROS)), TMSN@PM can scavenge the excess ROS, thereby alleviating inflammation, degrade, and release manganese ions for enhanced magnetic resonance imaging (MRI). The relaxation changes (ΔR ) are almost linearly correlated with the concentration of H O , which can reflect the degree of inflammation. This method offers a non-invasive imaging-based strategy for early prediction of the therapeutic outcomes in inflammatory therapy, which may contribute to precision medicine in terms of prognostic stratification and therapeutic planning in future.

摘要

在炎症性疾病的治疗过程中进行成像引导的实时监测对于及时调整治疗计划以降低不必要的副作用和改善治疗结果非常重要。然而,用足够的组织穿透深度来反映体内炎症的动态变化是很困难的。在这里,开发了一种新型的纳米治疗剂(命名为 TMSN@PM),它具有血小板膜(PM)涂层、tempol 接枝、锰掺杂、介孔二氧化硅纳米粒子。PM 赋予 TMSN@PM 靶向炎症部位的能力,这通过用 Cy5 标记的 TMSN@PM 进行荧光成像得到了验证。在炎症环境(轻度酸度和过量的活性氧(ROS))下,TMSN@PM 可以清除过量的 ROS,从而减轻炎症,降解并释放锰离子以增强磁共振成像(MRI)。弛豫变化(ΔR )与 H O 的浓度几乎呈线性相关,可以反映炎症的程度。这种方法为炎症治疗中治疗效果的早期预测提供了一种基于非侵入性成像的策略,这可能有助于未来在预后分层和治疗计划方面实现精准医学。

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