Rudolf Boehm-Institute for Pharmacology and Toxicology, Clinical Pharmacology, University of Leipzig, Haertelstrasse 16 - 18, Leipzig, D-04107, Germany.
Department of Environmental Immunology, Helmholtz Centre for Environmental Research Leipzig - UFZ, Leipzig, D-04318, Germany.
Small. 2018 Mar;14(12):e1701810. doi: 10.1002/smll.201701810. Epub 2018 Feb 12.
Nucleic acid-based therapies rely on efficient formulations for nucleic acid protection and delivery. As nonviral strategies, polymeric and lipid-based nanoparticles have been introduced; however, biological efficacy and biocompatibility as well as poor storage properties due to colloidal instability and their unavailability as ready-to-use systems are still major issues. Polyethylenimine is the most widely explored and promising candidate for gene delivery. Polyethylenimine-based polyplexes and their combination with liposomes, lipopolyplexes, are efficient for DNA or siRNA delivery in vitro and in vivo. In this study, a highly potent spray-dried nanoparticle-in-microparticle delivery system is presented for the encapsulation of polyethylenimine-based polyplexes and lipopolyplexes into poly(vinyl alcohol) microparticles, without requiring additional stabilizing agents. This easy-to-handle gene delivery device allows prolonged nanoparticle storage and protection at ambient temperature. Biological analyses reveal further advantages regarding profoundly reduced cytotoxicity and enhanced transfection efficacies of polyethylenimine-based nanoparticles from the nanoparticle-in-microparticle delivery system over their freshly prepared counterparts, as determined in various cell lines. Importantly, this nanoparticle-in-microparticle delivery system is demonstrated as ready-to-use dry powder to be an efficient device for the inhalative delivery of polyethylenimine-based lipopolyplexes in vivo, as shown by transgene expression in mice after only one administration.
核酸基疗法依赖于高效的核酸保护和递送制剂。作为非病毒策略,已经引入了聚合物和基于脂质的纳米颗粒;然而,生物功效和生物相容性以及由于胶体不稳定性和无法作为即用型系统而导致的储存性能差仍然是主要问题。聚乙烯亚胺是最广泛探索和有前途的基因传递候选物。聚乙烯亚胺基的多聚物及其与脂质体的组合,对于 DNA 或 siRNA 的体外和体内递送是有效的。在这项研究中,提出了一种高效的喷雾干燥纳米颗粒-微颗粒递药系统,用于将聚乙烯亚胺基多聚物和脂质体多聚物包封到聚乙烯醇微颗粒中,而不需要额外的稳定剂。这种易于处理的基因传递装置允许在环境温度下长时间储存和保护纳米颗粒。生物学分析进一步揭示了关于纳米颗粒-微颗粒递药系统的显著优势,即与新鲜制备的多聚物相比,基于聚乙烯亚胺的纳米颗粒的细胞毒性显著降低,转染效率显著提高,这在各种细胞系中得到了证实。重要的是,该纳米颗粒-微颗粒递药系统被证明是一种即用型干粉,可作为吸入递送体内基于聚乙烯亚胺的脂质体多聚物的有效装置,如仅给药一次后在小鼠中观察到的转基因表达所示。