聚乙烯亚胺
生物相容性
信使核糖核酸
化学
体外
转染
纳米颗粒
基因传递
药物输送
聚合物
纳米技术
全身给药
分子生物学
生物物理学
体内
输送系统
毒品携带者
丙烯酸酯
HEK 293细胞
体内分布
作者
Hongqian Zhang,Dongshan Chen,Song Xue,Zhengping Liu,Xuehua Yang,Cong Zhang,Dawei Li,Daizhou Zhang
标识
DOI:10.1021/acs.molpharmaceut.5c01272
摘要
Nonviral vectors hold great promise for mRNA (mRNA)-based therapeutics. However, achieving organ-selective mRNA delivery after systemic administration remains a major challenge. Herein, we engineered hydrophobized polymeric nanoparticles (PNPs) derived from arylated polyethylenimine (PEI) for efficient and organ-selective mRNA delivery. Nine new hydrophobized polymers were synthesized by grafting 2-phenylethyl acrylate (PA) onto PEI with three different molecular weights of PEI and three PA-to-PEI feeding molar ratios. The resulting PNPs were systematically evaluated for mRNA delivery both in vitro and in vivo. Through in vitro transfection screening, three optimal candidates (6PP3-PNP, 12PP6-PNP, and 24PP12-PNP) were selected for systemic mRNA delivery studies in mice. Remarkably, 6PP3-PNP preferentially delivered mRNA to the spleen, in contrast to the liver tropism observed with 12PP6-PNP and 24PP12-PNP. Moreover, 6PP3-PNP exhibited excellent biocompatibility both in vitro and in vivo. These findings elucidate the structure-function relationship of hydrophobized PEI in mRNA delivery and demonstrate a tunable strategy for developing organ-selective carriers, thereby expanding the potential of mRNA therapeutics for immunotherapy.
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