School of Pharmacy, Fudan University, Shanghai, China.
J Drug Target. 2011 Nov;19(9):814-20. doi: 10.3109/1061186X.2011.572975.
In this study, a small molecule, benzamide analogue, p-hydroxybenzoic acid (p-HA), was used as a novel ligand for brain-targeting gene delivery. p-HA was conjugated to polyethylenimine and further labeled with a near infrared dye, IR820, for in vivo and ex vivo imaging study. Significant fluorescent signal was detected in brain from 0.5 to 24 h after injection compared with unmodified PEI. Then nanoparticles were prepared with p-HA-PEI to encapsulate pEGFP and pGL2 as reporter genes and characterized on the cell level. In 5 y cells green fluorescent protein expression could be observed by fluorescent microscopy and significant higher expression of firefly luciferase was detected in p-HA-PEI/pGL2 group than in PEI/pGL2 group. For in vivo gene expression study, comparable high expression of green fluorescent protein in brain sections was confirmed using both confocal fluorescent microscopy and in vivo fluorescent imaging. All these results suggested that p-HA-PEI could be potentially used for brain targeted gene delivery.
在这项研究中,小分子苯甲酰胺类似物对羟基苯甲酸(p-HA)被用作新型脑靶向基因传递的配体。p-HA 与聚乙烯亚胺连接,并进一步用近红外染料 IR820 标记,用于体内和体外成像研究。与未修饰的 PEI 相比,注射后 0.5 至 24 小时,大脑中检测到明显的荧光信号。然后用 p-HA-PEI 制备纳米颗粒,封装 pEGFP 和 pGL2 作为报告基因,并在细胞水平上进行表征。在 5y 细胞中,可以通过荧光显微镜观察到绿色荧光蛋白的表达,并且在 p-HA-PEI/pGL2 组中检测到比 PEI/pGL2 组更高的萤火虫荧光素酶表达。为了进行体内基因表达研究,使用共聚焦荧光显微镜和体内荧光成像确认了脑切片中绿色荧光蛋白的表达水平相当高。所有这些结果表明,p-HA-PEI 可用于脑靶向基因传递。