Department of Mechanical and Materials Engineering, Washington State University, Pullman, WA, 99164, USA.
Division of Physical Sciences, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Small. 2018 Dec;14(52):e1803544. doi: 10.1002/smll.201803544. Epub 2018 Nov 22.
The design and synthesis of biocompatible nanomaterials as cargoes for the intracellular delivery of therapeutic proteins or genes have attracted intense attention because of their potential for use in therapeutics. Despite the advances in this area, very few nanomaterials can be efficiently delivered to the cytosol. To address these challenges, crystalline nanoflower-like particles are designed and synthesized from fluorinated sequence-defined peptoids; the crystallinity and fluorination of these particles enable highly efficient cytosolic delivery with minimal cytotoxicity. A cytosol delivery rate of 80% has been achieved for the fluorinated peptoid nanoflowers. Furthermore, these nanocrystals can carry therapeutic genes, such as mRNA and effectively deliver the payload into the cytosol, demonstrating the universal delivery capability of the nanocrystals. The results indicate that self-assembly of crystalline nanomaterials from fluorinated peptoids paves a new way toward development of nanocargoes with efficient cytosolic gene delivery capability.
作为治疗性蛋白质或基因的细胞内递送载体,生物相容性纳米材料的设计和合成因其在治疗中的应用潜力而受到了极大关注。尽管在这一领域取得了进展,但只有很少的纳米材料能够有效地递送到细胞质中。为了解决这些挑战,设计并合成了由氟化序列定义的肽制备的类晶花状纳米颗粒;这些颗粒的结晶度和氟化度使其能够以最小的细胞毒性实现高效的细胞质递送。氟化肽纳米花的细胞质递送率达到了 80%。此外,这些纳米晶体可以携带治疗性基因,如 mRNA,并有效地将有效载荷递送到细胞质中,证明了纳米晶体的通用递送能力。结果表明,氟化肽自组装成结晶纳米材料为开发具有高效细胞质基因递送能力的纳米载体开辟了一条新途径。