Highly compacted biodegradable DNA nanoparticles capable of overcoming the mucus barrier for inhaled lung gene therapy

被引:166
|
作者
Mastorakos, Panagiotis [1 ,2 ]
da Silva, Adriana L. [3 ]
Chisholm, Jane [1 ,4 ]
Song, Eric [1 ,5 ]
Choi, Won Kyu [1 ,4 ]
Boyle, Michael P. [6 ]
Morales, Marcelo M. [3 ]
Hanes, Justin [1 ,2 ,4 ]
Suk, Jung Soo [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Ctr Nanomed, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Dept Ophthalmol, Baltimore, MD 21297 USA
[3] Univ Fed Rio de Janeiro, Carlos Chagas Filho Inst Biophys, Lab Cellular & Mol Physiol, BR-21941902 Rio De Janeiro, RJ, Brazil
[4] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[5] Johns Hopkins Univ, Ctr Biotechnol Educ, Krieger Sch Arts & Sci, Baltimore, MD 21218 USA
[6] Johns Hopkins Univ, Sch Med, Div Pulm & Crit Care Med, Adult Cyst Fibrosis Program, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
lung gene therapy; mucus-penetrating particles; nanotechnology; biodegradable polymer; nonviral gene delivery; CYSTIC-FIBROSIS SPUTUM; MULTIPLE-PARTICLE TRACKING; IN-VITRO; POLY(BETA-AMINO ESTERS); POLYMERIC NANOPARTICLES; NONVIRAL VECTORS; DELIVERY; VIRUS; TRANSFECTION; DRUG;
D O I
10.1073/pnas.1502281112
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene therapy has emerged as an alternative for the treatment of diseases refractory to conventional therapeutics. Synthetic nanoparticle-based gene delivery systems offer highly tunable platforms for the delivery of therapeutic genes. However, the inability to achieve sustained, high-level transgene expression in vivo presents a significant hurdle. The respiratory system, although readily accessible, remains a challenging target, as effective gene therapy mandates colloidal stability in physiological fluids and the ability to overcome biological barriers found in the lung. We formulated highly stable DNA nanoparticles based on state-of-the-art biodegradable polymers, poly(beta-amino esters) (PBAEs), possessing a dense corona of polyethylene glycol. We found that these nanoparticles efficiently penetrated the nanoporous and highly adhesive human mucus gel layer that constitutes a primary barrier to reaching the underlying epithelium. We also discovered that these PBAE-based mucus-penetrating DNA nanoparticles (PBAE-MPPs) provided uniform and high-level transgene expression throughout the mouse lungs, superior to several gold standard gene delivery systems. PBAE-MPPs achieved robust transgene expression over at least 4 mo following a single administration, and their transfection efficiency was not attenuated by repeated administrations, underscoring their clinical relevance. Importantly, PBAE-MPPs demonstrated a favorable safety profile with no signs of toxicity following intratracheal administration.
引用
收藏
页码:8720 / 8725
页数:6
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