Tang Huan, Yang Sheng-Tao, Ke Da-Ming, Yang Yi-Fan, Liu Jia-Hui, Chen Xing, Wang Haifang, Liu Yuanfang
Beijing National Laboratory for Molecular Sciences , Department of Chemical Biology , College of Chemistry and Molecular Engineering , Peking University , Beijing 100871 , China . Email:
College of Chemistry and Environment Protection Engineering , Southwest Minzu University , Chengdu 610041 , China . Email:
Toxicol Res (Camb). 2017 Jun 26;6(5):693-704. doi: 10.1039/c7tx00137a. eCollection 2017 Sep 1.
AgSe quantum dots (QDs) are novel fluorescent probes in the second near-infrared window with great imaging quality and biocompatibility. Surface modification is an essential step to disperse AgSe QDs into biological fluids, and endow AgSe QDs with diverse surface chemistry. However, the effect of surface chemistry on the biological behaviors and chemical fates of AgSe QDs has not been studied, which hinders the design of suitable AgSe QDs for biomedical applications. Here, the distribution, degradation, excretion and toxicity of 2-aminoethanethiol and mercaptopropionic acid coated AgSe QDs (denoted as QDs-MEA and QDs-MPA, respectively) were systematically investigated in mice for a 28-day observation period after a single intravenous injection. AgSe QDs with different surface chemistries displayed similar trends in all observations, such as fast blood clearance, main uptake in the liver and spleen, severe biotransformation, Ag excretion through feces, and low toxicity. The major different behaviors observed were the partially pulmonary deposition, the faster transformation at the initial stage, the lower excretion percentage, and the more obvious damage to the liver by QDs-MEA compared to QDs-MPA. The surface chemistry of AgSe QDs regulated their biological behaviors and chemical fates , and surface chemistry should be fully regarded when designing AgSe QDs for biomedical applications from the biosafety perspective.
AgSe量子点(QDs)是新型的第二近红外窗口荧光探针,具有出色的成像质量和生物相容性。表面修饰是将AgSe量子点分散到生物流体中并赋予其多样表面化学性质的关键步骤。然而,表面化学对AgSe量子点生物学行为和化学归宿的影响尚未得到研究,这阻碍了用于生物医学应用的合适AgSe量子点的设计。在此,在单次静脉注射后的28天观察期内,系统研究了2-氨基乙硫醇和巯基丙酸包覆的AgSe量子点(分别记为QDs-MEA和QDs-MPA)在小鼠体内的分布、降解、排泄和毒性。具有不同表面化学性质的AgSe量子点在所有观察中都呈现出相似的趋势,如快速的血液清除、主要在肝脏和脾脏中摄取、严重的生物转化、通过粪便排泄银以及低毒性。观察到的主要不同行为是部分肺沉积、初始阶段更快的转化、更低的排泄百分比以及与QDs-MPA相比,QDs-MEA对肝脏的损伤更明显。AgSe量子点的表面化学性质调节其生物学行为和化学归宿,从生物安全性角度设计用于生物医学应用的AgSe量子点时,应充分考虑表面化学性质。