囊性纤维化
粘液
粘蛋白
聚乙二醇
纳米技术
化学
计算生物学
细胞生物学
生物
遗传学
材料科学
生物化学
生态学
作者
Belal Tafech,Mohammad‐Reza Rokhforouz,Jerry Leung,Molly M. H. Sung,Paulo J.C. Lin,Don D. Sin,Daniel Lauster,Stephan Block,Bradley S. Quon,Ying K. Tam,Pieter R. Cullis,James J. Feng,Sarah Hedtrich
标识
DOI:10.1101/2024.01.18.575680
摘要
ABSTRACT Mucus forms the first defense line of human lungs, and as such hampers the efficient delivery of therapeutics to the underlying epithelium. This holds particularly true for genetic cargo such as CRISPR-based gene editing tools which cannot readily surmount the mucosal barrier. While lipid nanoparticles (LNPs) emerged as versatile non-viral gene delivery systems that could help overcome the delivery challenge, many knowledge gaps remain, especially for diseased states such as cystic fibrosis (CF). This study provides fundamental insights into Cas9 mRNA or ribonucleoprotein-loaded LNP-mucus interactions in healthy and diseased states by assessing the impact of the genetic cargo, mucin sialylation, mucin concentration, ionic strength, pH, and polyethylene glycol (PEG) concentration and nature on LNP diffusivity leveraging experimental approaches and Brownian dynamics simulations. Taken together, this study identifies key mucus and LNP characteristics that are critical to enabling a rational LNP design for transmucosal delivery. Graphical Abstract
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