4.7 Article

Safe and Effective Delivery of mRNA Using Modified PEI-Based Lipopolymers

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PHARMACEUTICS
卷 15, 期 2, 页码 -

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MDPI
DOI: 10.3390/pharmaceutics15020410

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modRNA; lipopolymers; biocompatibility; lysosomal escape; effective transfection

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Chemically modified mRNA has shown potential as a versatile tool for treating cancers and infectious diseases, but a safe and effective delivery system is needed to overcome the complex barriers. Researchers have explored lipopolymers as novel transfection reagents, which demonstrated excellent biocompatibility, efficient delivery capabilities, and the ability to escape lysosomes, thus improving mRNA stability and promoting efficient gene translation in vitro and in vivo.
Chemically modified mRNA (modRNA) has proven to be a versatile tool for the treatment of various cancers and infectious diseases due to recent technological advancements. However, a safe and effective delivery system to overcome the complex extracellular and intracellular barriers is required in order to achieve higher therapeutic efficacy and broaden clinical applications. Here, we explored All-Fect and Leu-Fect C as novel transfection reagents derived from lipopolymers, which demonstrated excellent biocompatibility, efficient delivery capabilities, and a robust ability to escape the lysosomes. These properties directly increase mRNA stability by preventing mRNA degradation by nucleases and simultaneously promote efficient gene translation in vitro and in vivo. The modRNA delivered with lipopolymer vectors sustained effective transfection in mouse hearts following direct intramyocardial injection, as well as in major organs (liver and spleen) after systemic administration. No observable immune reactions or systemic toxicity were detected following the systemic administration of lipopolymer-mRNA complexes to additional solid organs. This study identified commercial reagents for the effective delivery of modRNA and may help facilitate the advancement of gene-based interventions involving the safe and effective delivery of nucleic acid drug substances.

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