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Nanoscale · 2012 ·Vol. 5 ·期 2 ·744-752 · IF 5.914

Self-assembled magnetic theranostic nanoparticles for highly sensitive MRI of minicircle DNA delivery

Qian Wan,Lisi Xie,Lin Gao,Zhiyong Wang,Xiang Nan,Hulong Lei,Xiaojing Long,Zhi-Ying Chen,Cheng-Yi He,Gang Liu,Xin Liu,Bensheng Qiu

As a versatile gene vector, minicircle DNA (mcDNA) has a great potential for gene therapy. However, some serious challenges remain, such as to effectively deliver mcDNA into targeted cells/tissues and to non-invasively monitor the delivery of the mcDNA. Superparamagnetic iron oxide (SPIO) nanoparticles have been extensively used for both drug/gene delivery and diagnosis. In this study, an MRI visible gene delivery system was developed with a core of SPIO nanocrystals and a shell of biodegradable stearic acid-modified low molecular weight polyethyleneimine (Stearic–LWPEI) via self-assembly. The Stearic–LWPEI–SPIO nanoparticles possess a controlled clustering structure, narrow size distribution and ultrasensitive imaging capacity. Furthermore, the nanoparticle can effectively bind with mcDNA and protect it from enzymatic degradation. In conclusion, the nanoparticle shows synergistic advantages in the effective transfection of mcDNA and non-invasive MRI of gene delivery.

研究领域: 生物医学工程 · 分子生物学 · 影像医学
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JOURNAL OF NANOBIOTECHNOLOGY · 2024 ·Vol. 22 ·期 1 ·1-15 · IF 10.6

Short cell-penetration peptide conjugated bioreducible polymer enhances gene editing of CRISPR system

Wang Xiaobo,Cai Chengyuan,Lv Weiqi,Chen Kechen,Li Jiaxin,Liao Kaitong,Zhang Yanqun,Huang Hongxin,Lin Ying,Rong Zhili,Duan Xiaopin

CRISPR-based gene therapy offers precise targeting and specific editing of disease-related gene sequences, potentially yielding long-lasting treatment effects. However, efficient delivery remains a significant challenge for its widespread application. In this study, we design a novel short peptide-conjugated bioreducible polymer named TSPscp as a safe and effective delivery vector for the CRISPR system. Our results show that TSPscp markedly boosts transcriptional activation and genome editing activities of multiple CRISPR systems as confirmed by decomposition-seq and Deep-seq, which is resulted from its capability in facilitating delivery of plasmid DNA by promoting cellular uptake and lysosomal escape. Additionally, TSPscp further enhances genome editing of CRISPR by delivery of minicircle DNA, a condensed form of regular plasmid DNA. More importantly, TSPscp significantly improves delivery and genome editing of CRISPR system in vivo. In summary, our study highlights TSPscp as a promising delivery tool for CRISPR applications in vivo.Graphical Abstract

CAS / MDL: 1119-62-6 24424-99-5
研究领域: 基因治疗 · 分子生物学 · 生物技术
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