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A Si-rhodamine-based near-infrared fluorescent probe for visualizing endogenous peroxynitrite in living cells, tissues, and animals†‡
Journal of Materials Chemistry B ( IF 7 ) Pub Date : 2018-06-16 00:00:00 , DOI: 10.1039/c8tb00987b Junfeng Miao 1, 2, 3, 4 , Yingying Huo 1, 2, 3, 4 , Hu Shi 1, 2, 3, 4, 5 , Junru Fang 1, 2, 3, 4 , Juanjuan Wang 2, 3, 4, 6 , Wei Guo 1, 2, 3, 4
Journal of Materials Chemistry B ( IF 7 ) Pub Date : 2018-06-16 00:00:00 , DOI: 10.1039/c8tb00987b Junfeng Miao 1, 2, 3, 4 , Yingying Huo 1, 2, 3, 4 , Hu Shi 1, 2, 3, 4, 5 , Junru Fang 1, 2, 3, 4 , Juanjuan Wang 2, 3, 4, 6 , Wei Guo 1, 2, 3, 4
Affiliation
Peroxynitrite (ONOO−) is an extremely powerful biological oxidant and it can react with a wide variety of molecular targets to result in a series of disease states, which has made ONOO− a central biological pathogenic factor. In order to disclose its various pathological events, a large number of fluorescent ONOO− probes have been developed in recent years. Nevertheless, some limitations still remain, such as short excitation and emission wavelengths, long fluorescence response times, and cross-interference caused by other reactive oxygen species (ROS). In this work, a new near-infrared (NIR) fluorescent probe, SiRTA, containing an aromatic tertiary amine functional group and a Si-rhodamine fluorophore, was developed for endogenous ONOO− detection and imaging. The probe exhibits not only a fast, sensitive, and specific fluorescence off–on response toward ONOO− in chemical systems but also excellent imaging ability for endogenous ONOO− in living cells. With the probe, the therapeutic effects of phenolic acid antioxidants in EA.hy926 endothelial cells suffering from ischemia–reperfusion injury and the pathogenesis of diabetes and diabetic nephropathy in pancreatic β-cells and diabetic rats have successfully been evaluated. These results indicate that SiRTA is a potentially outstanding imaging tool for studying the physiological and pathological events of ONOO− and relevant drug therapies.
中文翻译:
基于罗丹明的近红外荧光探针,用于观察活细胞,组织和动物中的内源性过氧亚硝酸盐† ‡
过氧亚硝酸盐(ONOO -导致一系列疾病状态,这已ONOO制成的是一个非常强大的生物氧化剂,它可以与各种各样的分子靶标反应)-中央生物的致病因子。为了揭示它的各种病理事件,大量荧光ONOO的-探测已经发展在最近几年。但是,仍然存在一些局限性,例如激发和发射波长短,荧光响应时间长以及其他活性氧(ROS)引起的交叉干扰。在这项工作中,一种新的近红外(NIR)荧光探针SiRTA含有芳香族叔胺官能团和Si-若丹明荧光团,被内源性ONOO开发-检测和成像。探针表现出不仅是一种快速,灵敏,和特异性荧光关-开响应朝向ONOO -在化学系统也为内源性ONOO极好的成像能力-在活细胞。用该探针成功地评估了酚酸抗氧化剂在EA.hy926内皮细胞缺血再灌注损伤以及胰腺β细胞和糖尿病大鼠中糖尿病和糖尿病肾病的发病机理中的治疗作用。这些结果表明,SiRTA是研究ONOO的生理和病理事件潜在的优秀成像工具-与相关的药物治疗。
更新日期:2018-06-16
中文翻译:
基于罗丹明的近红外荧光探针,用于观察活细胞,组织和动物中的内源性过氧亚硝酸盐† ‡
过氧亚硝酸盐(ONOO -导致一系列疾病状态,这已ONOO制成的是一个非常强大的生物氧化剂,它可以与各种各样的分子靶标反应)-中央生物的致病因子。为了揭示它的各种病理事件,大量荧光ONOO的-探测已经发展在最近几年。但是,仍然存在一些局限性,例如激发和发射波长短,荧光响应时间长以及其他活性氧(ROS)引起的交叉干扰。在这项工作中,一种新的近红外(NIR)荧光探针SiRTA含有芳香族叔胺官能团和Si-若丹明荧光团,被内源性ONOO开发-检测和成像。探针表现出不仅是一种快速,灵敏,和特异性荧光关-开响应朝向ONOO -在化学系统也为内源性ONOO极好的成像能力-在活细胞。用该探针成功地评估了酚酸抗氧化剂在EA.hy926内皮细胞缺血再灌注损伤以及胰腺β细胞和糖尿病大鼠中糖尿病和糖尿病肾病的发病机理中的治疗作用。这些结果表明,SiRTA是研究ONOO的生理和病理事件潜在的优秀成像工具-与相关的药物治疗。