Karlsruhe Institute of Technology (KIT), Institute for Biological Interfaces (IBG 1), Hermann-von-Helmholtz-Platz, D-76344, Eggenstein-Leopoldshafen, Germany.
BASF SE, Dispersions & Colloidal Materials - B001, Carl-Bosch-Straße 38, 67056, Ludwigshafen, Germany.
Small. 2019 May;15(20):e1900083. doi: 10.1002/smll.201900083. Epub 2019 Apr 15.
The development of methods for colloidal self-assembly on solid surfaces is important for many applications in biomedical sciences. Toward this goal, described is a versatile class of mesoporous silica nanoparticles (MSN) that contain on their surface various types of DNA molecules to enable their self-assembly into micropatterned surface architectures useful for cell studies. Monodisperse dye-doped MSN are synthesized by biphase stratification and functionalized with an aptamer oligonucleotide that serves as gatekeeper for the triggered release of encapsulated molecular cargo, such as fluorescent dye rhodamine B or the anticancer drug doxorubicin. One or two additional types of oligonucleotides are installed on the MSN surface to enable DNA-directed immobilization on solid substrates bearing patterns of complementary capture oligonucleotides. It is demonstrated that this strategy can be used for efficient self-assembly of microstructured surface architectures, which not only promote the adhesion and guidance of cells but also are capable of affecting the fate of adhered cells through triggered release of their cargo. It is believed that this approach is useful for diverse applications in tissue engineering and nanobio sciences.
在生物医药科学的许多应用中,发展胶体在固体表面上自组装的方法非常重要。为此,本文介绍了一类多功能介孔硅纳米粒子(MSN),其表面含有各种类型的 DNA 分子,能够自组装成微图案表面结构,用于细胞研究。通过双相分层法合成单分散染料掺杂 MSN,并通过适体寡核苷酸进行功能化,该寡核苷酸作为触发封装分子货物(如荧光染料罗丹明 B 或抗癌药物阿霉素)释放的守门员。在 MSN 表面安装一种或两种额外类型的寡核苷酸,以实现 DNA 导向的固定在带有互补捕获寡核苷酸图案的固体基底上。结果表明,该策略可用于微结构化表面结构的有效自组装,不仅促进了细胞的粘附和导向,而且还能够通过触发货物的释放来影响粘附细胞的命运。相信这种方法在组织工程和纳米生物科学的各种应用中非常有用。