纳米载体
分辨率(逻辑)
高分辨率
细胞生物学
神经科学
生物
人工智能
纳米技术
计算机科学
遥感
地质学
材料科学
纳米颗粒
作者
Jie Luo,Müge Molbay,Ying Chen,Izabela Horvath,Karoline Kadletz,Benjamin Kick,Shan Zhao,Rami Al-Maskari,Inderjeet Singh,Mayar Ali,Harsharan S. Bhatia,David‐Paul Minde,Moritz Negwer,Luciano Hoeher,Gian Marco Calandra,Bernhard Groschup,Jinpeng Su,Ceren Kımna,Zhouyi Rong,Nikolas F. B. Galensowske
标识
DOI:10.1038/s41587-024-02528-1
摘要
Abstract Efficient and accurate nanocarrier development for targeted drug delivery is hindered by a lack of methods to analyze its cell-level biodistribution across whole organisms. Here we present Single Cell Precision Nanocarrier Identification (SCP-Nano), an integrated experimental and deep learning pipeline to comprehensively quantify the targeting of nanocarriers throughout the whole mouse body at single-cell resolution. SCP-Nano reveals the tissue distribution patterns of lipid nanoparticles (LNPs) after different injection routes at doses as low as 0.0005 mg kg −1 —far below the detection limits of conventional whole body imaging techniques. We demonstrate that intramuscularly injected LNPs carrying SARS-CoV-2 spike mRNA reach heart tissue, leading to proteome changes, suggesting immune activation and blood vessel damage. SCP-Nano generalizes to various types of nanocarriers, including liposomes, polyplexes, DNA origami and adeno-associated viruses (AAVs), revealing that an AAV2 variant transduces adipocytes throughout the body. SCP-Nano enables comprehensive three-dimensional mapping of nanocarrier distribution throughout mouse bodies with high sensitivity and should accelerate the development of precise and safe nanocarrier-based therapeutics.
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