PEGylated pH-responsive peptide-mRNA nano self-assemblies enhance the pulmonary delivery efficiency and safety of aerosolized mRNA

被引:12
|
作者
Xu, Yingying [1 ,2 ]
Zheng, Yijing [1 ]
Ding, Xuqiu [3 ]
Wang, Chengyan [4 ]
Hua, Bin [1 ]
Hong, Shilian [1 ]
Huang, Xiaoman [1 ]
Lin, Jiali [1 ]
Zhang, Peng [5 ]
Chen, Wei [6 ]
机构
[1] Fujian Med Univ, Sch Pharm, Fuzhou, Peoples R China
[2] Xiamen Univ, State Key Lab Marine Environm Sci, Xiamen, Peoples R China
[3] Fujian Med Univ, Sch Clin Med, Fuzhou, Peoples R China
[4] Fujian Med Univ, Inst Lab Anim Ctr, Fuzhou, Peoples R China
[5] Shenzhen Univ, Affiliated Hosp 3, Affiliated Luohu Hosp, Dept Pharm, Shenzhen, Peoples R China
[6] Fujian Med Univ, Sch Pharm, Fujian Key Lab Drug Target Discovery & Struct & Fu, Fuzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Pulmonary mRNA delivery; pH-responsive peptide; PEGylated peptide gene vector; nano self-assemblies; inhalation safety; GENE DELIVERY; LIPID NANOPARTICLES; SIRNA DELIVERY; IN-VITRO; TRANSFECTION; DNA; OPTIMIZATION; COVID-19; VACCINES; VIVO;
D O I
10.1080/10717544.2023.2219870
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inhalable messenger RNA (mRNA) has demonstrated great potential in therapy and vaccine development to confront various lung diseases. However, few gene vectors could overcome the airway mucus and intracellular barriers for successful pulmonary mRNA delivery. Apart from the low pulmonary gene delivery efficiency, nonnegligible toxicity is another common problem that impedes the clinical application of many non-viral vectors. PEGylated cationic peptide-based mRNA delivery vector is a prospective approach to enhance the pulmonary delivery efficacy and safety of aerosolized mRNA by oral inhalation administration. In this study, different lengths of hydrophilic PEG chains were covalently linked to an amphiphilic, water-soluble pH-responsive peptide, and the peptide/mRNA nano self-assemblies were characterized by dynamic light scattering (DLS) and transmission electron microscopy ( TEM). The in vitro mRNA binding and release, cellular uptake, transfection, and cytotoxicity were studied, and finally, a proper PEGylated peptide with enhanced pulmonary mRNA delivery efficiency and improved safety in mice was identified. These results showed that a proper N-terminus PEGylation strategy using 12-monomer linear monodisperse PEG could significantly improve the mRNA transfection efficiency and biocompatibility of the non-PEGylated cationic peptide carrier, while a longer PEG chain modification adversely decreased the cellular uptake and transfection on A549 and HepG2 cells, emphasizing the importance of a proper PEG chain length selection. Moreover, the optimized PEGylated peptide showed a significantly enhanced mRNA pulmonary delivery efficiency and ameliorated safety profiles over the non-PEGylated peptide and LipofectamineTM 2000 in mice. Our results reveal that the PEGylated peptide could be a promising mRNA delivery vector candidate for inhaled mRNA vaccines and therapeutic applications for the prevention and treatment of different respiratory diseases in the future. [GRAPHICS] .
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页数:14
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