Deng Zhiming, Bi Shenghui, Jiang Mingyang, Zeng Songjun
Synergetic Innovation Center for Quantum Effects and Application, Key Laboratory of Low-dimensional Quantum Structures and Quantum Control of Ministry of Education, Key Laboratory for Matter Microstructure and Function of Hunan Province, School of Physics and Electronics, Hunan Normal University, Changsha 410081, P.R. China.
ACS Nano. 2021 Feb 23;15(2):3201-3211. doi: 10.1021/acsnano.0c09799. Epub 2021 Jan 22.
Metformin as a hypoglycemic drug for antidiabetic treatment has emerged as a multipotential drug for many disease treatments such as cognitive disorders, cancers, promoting weight loss. However, overdose uptake may upregulate the hepatic HS level, subsequently leading to serious liver injury and toxicity. Therefore, developing intelligent second near-infrared (NIR-II) emitting nanoprobes by using endogenous HS as a smart trigger for noninvasive highly specific monitoring of the metformin-induced hepatotoxicity is highly desirable, which is rarely explored. Herein, an endogenous HS activated orthogonal NIR-II emitting myrica rubra-like nanoprobe based on NaYF:Gd/Yb/Er@NaYF:Yb@SiO coated with Ag nanodots was explored for highly specific ratiometrically monitoring of hepatotoxicity. The designed nanoprobes were mainly uptaken by the liver and subsequently converted to NaYF:Gd/Yb/Er@NaYF:Yb@SiO@AgS sulfuration reaction triggered by the overexpressed endogenous HS in the injured liver tissues, finally leading to a turn-on orthogonal emission centered at 1053 nm (irradiation by 808 nm laser) and 1525 nm (irradiation by 980 nm laser). The designed nanoprobe presents a high detection limit down to 0.7 nM of HS. More importantly, the highly specific ratiometric imaging of the metformin-induced hepatotoxicity was successfully achieved by using the activatable orthogonal NIR-II emitting probe. Our results provide an NIR-II ratiometric fluorescence imaging strategy for highly sensitive/specific diagnosis of hepatotoxicity levels induced by metformin.
二甲双胍作为一种用于抗糖尿病治疗的降血糖药物,已成为一种具有多种潜在用途的药物,可用于治疗多种疾病,如认知障碍、癌症、促进体重减轻。然而,过量摄入可能会上调肝脏中硫酸乙酰肝素(HS)的水平,随后导致严重的肝损伤和毒性。因此,利用内源性HS作为智能触发剂,开发用于无创、高特异性监测二甲双胍诱导的肝毒性的智能近红外二区(NIR-II)发射纳米探针是非常必要的,而这方面的研究很少。在此,我们探索了一种基于包覆银纳米点的NaYF:Gd/Yb/Er@NaYF:Yb@SiO的内源性HS激活的正交NIR-II发射杨梅状纳米探针,用于高特异性的比率法监测肝毒性。所设计的纳米探针主要被肝脏摄取,随后在受损肝组织中由过表达的内源性HS触发硫化反应,转化为NaYF:Gd/Yb/Er@NaYF:Yb@SiO@AgS,最终导致在1053 nm(808 nm激光照射)和1525 nm(980 nm激光照射)处开启正交发射。所设计的纳米探针具有低至0.7 nM的HS检测限。更重要的是,通过使用可激活的正交NIR-II发射探针,成功实现了二甲双胍诱导的肝毒性的高特异性比率成像。我们的结果为高灵敏度/特异性诊断二甲双胍诱导的肝毒性水平提供了一种NIR-II比率荧光成像策略。