Department of Nuclear Medicine, Chonbuk National University Medical School and Hospital, Jeonju, Jeonbuk 561-712, Republic of Korea.
Nanotechnology. 2010 Jul 16;21(28):285102. doi: 10.1088/0957-4484/21/28/285102. Epub 2010 Jun 18.
The aim of this study was to investigate the effect of gluconic acid (GA) conjugation on the biodistribution of cysteamine-capped quantum dots (amino-QDots) in vivo. Cadmium selenide/zinc sulfide (CdSe/ZnS) was capped with cysteamine through a thiol exchange method, and different amounts of GA were conjugated to the amine groups of cysteamine via the formation of an amide bond. The emission maxima of the synthesized QDots, the amino-QDots and the GA-conjugated amine-QDots (GA-QDots) were located at 720, 600 and 610 nm, respectively. In the cell viability studies, the GA-QDots showed very low toxicity against CHO cells as compared to the cytotoxicity of the amino-QDots. The QDots were next intravenously injected into normal mice and then we performed ex vivo optical imaging. The majority of the amino-QDots were accumulated in the lung. In contrast, the GA-QDots were cleared out of the body through the kidney. Therefore, we expect that the conjugation of GA onto the amino-QDots can create opportunities for using amino-QDots for in vivo imaging.
本研究旨在探讨葡萄糖酸(GA)缀合对半胱胺封端量子点(氨基-QDots)体内分布的影响。通过巯基交换法将硒化镉/硫化锌(CdSe/ZnS)用半胱胺封端,通过酰胺键的形成将不同量的 GA 缀合到半胱胺的氨基上。合成的 QDots、氨基-QDots 和 GA 缀合的氨基-QDots(GA-QDots)的发射最大值分别位于 720nm、600nm 和 610nm。在细胞活力研究中,与氨基-QDots 的细胞毒性相比,GA-QDots 对 CHO 细胞的毒性非常低。接下来,将 QDots 静脉注射到正常小鼠体内,然后进行离体光学成像。大部分氨基-QDots 积聚在肺部。相比之下,GA-QDots 通过肾脏被清除出体外。因此,我们期望将 GA 缀合到氨基-QDots 上可以为体内成像提供机会。