Kozielski Kristen L, Sitti Metin
Physical Intelligence Department, Max Planck Institute for Intelligent Systems, Stuttgart, Germany.
Curr Gene Ther. 2017;17(2):80-88. doi: 10.2174/1566523217666170510161120.
Successful gene delivery requires overcoming both systemic and intracellular obstacles before the nucleic acid cargo can successfully reach its tissue and subcellular target location. Materials & Methods: Non-viral mechanisms to enable targeting while avoiding off-target delivery have arisen via biological, chemical, and physical engineering strategies.
Herein we will discuss the physical parameters in particle design that promote tissue- and cell-targeted delivery of genetic cargo. We will discuss systemic concerns, such as circulation, tissue localization, and clearance, as well as cell-scale obstacles, such as cellular uptake and nucleic acid packaging.
In particular, we will focus on engineering particle shape and size in order to enhance delivery and promote precise targeting. We will also address methods to program or change particle shape in situ using environmentally triggered cues.
成功的基因递送需要克服全身和细胞内的障碍,核酸载体才能成功到达其组织和亚细胞靶点位置。材料与方法:通过生物、化学和物理工程策略,已出现了能够实现靶向同时避免脱靶递送的非病毒机制。
在此,我们将讨论颗粒设计中促进基因载体进行组织和细胞靶向递送的物理参数。我们将讨论全身相关问题,如循环、组织定位和清除,以及细胞层面的障碍,如细胞摄取和核酸包装。
特别是,我们将专注于设计颗粒形状和大小,以增强递送效果并促进精确靶向。我们还将探讨利用环境触发信号原位编程或改变颗粒形状的方法。