Key Laboratory of Bioactive Materials, Ministry of Education, Nankai University, Tianjin 300071, People's Republic of China.
Nanotechnology. 2010 Apr 16;21(15):155602. doi: 10.1088/0957-4484/21/15/155602. Epub 2010 Mar 19.
In this study, we report the use of a phosphatase to catalyze the formation of nanospheres from a hydrophobic compound (Ada-GFFY-OMe, 2) via a unique mechanism. The nanospheres were stable in aqueous solutions for two weeks. Their size could be controlled by both concentrations of the precursor (Ada-GFFY(p)-OMe, 1) and the enzyme and the nanospheres were characterized by SEM and dynamic light scattering (DLS). We then demonstrated that nanospheres could help the cell-impermeable propidium iodine (PI) to penetrate the cells, which implied that the nanospheres have the potential to be developed into useful carriers for hydrophobic drugs. This study offers the first example of using an enzyme to control the formation of nanospheres from a hydrophobic compound. There is thus the potential that nanospheres can be developed into a carrier for hydrophobic drugs.
在这项研究中,我们报告了使用一种磷酸酶通过独特的机制催化疏水分子(Ada-GFFY-OMe,2)形成纳米球。纳米球在水溶液中稳定两周。它们的尺寸可以通过前体(Ada-GFFY(p)-OMe,1)和酶的浓度来控制,并且通过 SEM 和动态光散射(DLS)进行了表征。然后,我们证明了纳米球可以帮助不透细胞膜的碘化丙啶(PI)穿透细胞,这意味着纳米球有可能被开发为疏水性药物的有用载体。本研究首次提供了使用酶控制疏水分子形成纳米球的实例。因此,纳米球有可能被开发为疏水性药物的载体。