聚乙烯亚胺
材料科学
纳米颗粒
生物相容性
基因传递
转染
纳米医学
过滤(数学)
纳米技术
化学
生物化学
基因
数学
统计
冶金
作者
Heng-wen Liu,Yizong Hu,Yong Ren,Hwanhee Nam,José Luís Santos,Shirley Ng,Like Gong,Mary Brummet,Christine A. Carrington,Christopher G. Ullman,Martin G. Pomper,Il Minn,Hai‐Quan Mao
标识
DOI:10.1021/acsami.1c05750
摘要
Plasmid DNA (pDNA) nanoparticles synthesized by complexation with linear polyethylenimine (lPEI) are one of the most effective non-viral gene delivery vehicles. However, the lack of scalable and reproducible production methods and the high toxicity have hindered their clinical translation. Previously, we have developed a scalable flash nanocomplexation (FNC) technique to formulate pDNA/lPEI nanoparticles using a continuous flow process. Here, we report a tangential flow filtration (TFF)-based scalable purification method to reduce the uncomplexed lPEI concentration in the nanoparticle formulation and improve its biocompatibility. The optimized procedures achieved a 60% reduction of the uncomplexed lPEI with preservation of the nanoparticle size and morphology. Both in vitro and in vivo studies showed that the purified nanoparticles significantly reduced toxicity while maintaining transfection efficiency. TFF also allows for gradual exchange of solvents to isotonic solutions and further concentrating the nanoparticles for injection. Combining FNC production and TFF purification, we validated the purified pDNA/lPEI nanoparticles for future clinical translation of this gene nanomedicine.
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