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Near-Infrared Emitting PbS Quantum Dots for in Vivo Fluorescence Imaging of the Thrombotic State in Septic Mouse Brain

机译:脓毒症小鼠脑中血栓形成状态的体内荧光成像的近红外发射PbS量子点。

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Near-infrared (NIR) fluorescent imaging is a powerful tool for the non-invasive visualization of the inner structure of living organisms. Recently, NIR fluorescence imaging at 1000–1400 nm (second optical window) has been shown to offer better spatial resolution compared with conventional NIR fluorescence imaging at 700–900 nm (first optical window). Here we report lead sulfide (PbS) quantum dots (QDs) and their use for in vivo NIR fluorescence imaging of cerebral venous thrombosis in septic mice. Highly fluorescent PbS QDs with a 1100 nm emission peak (QD1100) were prepared from lead acetate and hexamethyldisilathiane, and the surface of QD1100 was coated with mercaptoundecanoic acid so as to be soluble in water. NIR fluorescence imaging of the cerebral vessels of living mice was performed after intravascular injection (200–300 μL) of QD1100 (3 μM) from a caudal vein. By detecting the NIR fluorescence of QD1100, we achieved non-invasive NIR fluorescence imaging of cerebral blood vessels through the scalp and skull. We also achieved NIR fluorescence imaging of cerebral venous thrombosis in septic mice induced by the administration of lipopolysaccharide (LPS). From the NIR fluorescence imaging, we found that the number of thrombi in septic mice was significantly increased by the administration of LPS. The formation of thrombi in cerebral blood vessels in septic mice was confirmed by enzyme-linked immunosorbent assay (ELISA). We also found that the number of thrombi significantly decreased after the administration of heparin, an inhibitor of blood coagulation. These results show that NIR fluorescence imaging with QD1100 is useful for the evaluation of the pathological state of cerebral blood vessels in septic mice. View Full-Text
机译:近红外(NIR)荧光成像是无害可视化活生物体内部结构的强大工具。最近,与传统的700-900 nm(第一光学窗口)NIR荧光成像相比,已显示1000-1400 nm(第二光学窗口)的NIR荧光成像具有更好的空间分辨率。在这里,我们报告硫化铅(PbS)量子点(QDs)及其用于化脓性小鼠脑静脉血栓形成的体内NIR荧光成像。由乙酸铅和六甲基二硅噻吩制备具有1100 nm发射峰的高荧光PbS QD(QD1100),并在QD1100的表面涂上巯基十一烷酸使其可溶于水。从尾静脉进行血管内注射(200–300μL)QD1100(3μM)后,对活体小鼠的脑血管进行NIR荧光成像。通过检测QD1100的NIR荧光,我们通过头皮和颅骨实现了脑血管的非侵入性NIR荧光成像。我们还实现了通过脂多糖(LPS)诱导感染的脓毒症小鼠脑静脉血栓形成的近红外荧光成像。从NIR荧光成像中,我们发现通过施用LPS,脓毒症小鼠中的血栓数量显着增加。通过酶联免疫吸附测定(ELISA)证实了败血症小鼠脑血管中血栓的形成。我们还发现,给予肝素(一种凝血抑制剂)后,血栓的数目显着减少。这些结果表明,使用QD1100进行的NIR荧光成像可用于评估败血性小鼠脑血管的病理状态。查看全文

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