Department of Pharmaceutical Sciences, School of Pharmacy, Bouve College of Health Sciences, Northeastern University, Boston, Massachusetts 02115, United States.
Mol Pharm. 2020 Jun 1;17(6):1996-2005. doi: 10.1021/acs.molpharmaceut.0c00170. Epub 2020 May 19.
Nucleic acid-based therapeutics, including the use of messenger RNA (mRNA) as a drug molecule, has tremendous potential in the treatment of chronic diseases, such as age-related neurodegenerative diseases. In this study, we have developed a cationic liposomal formulation of mRNA and evaluated the potential of intranasal delivery to the brain in murine model. Preliminary studies in J774A.1 murine macrophages showed GFP expression up to 24 h and stably expressed GFP protein in the cytosol. Upon intranasal administration of GFP-mRNA/cationic liposomes (3 mg/kg dose) in mice, there was significantly higher GFP-mRNA expression in the brain post 24 h as compared to either naked mRNA or the vehicle-treated group. Luciferase mRNA encapsulated in cationic liposomes was used for quantification of mRNA expression distribution in the brain. The results showed increased luciferase activity in the whole brain in a dose-dependent manner. Specifically, the luciferase-mRNA/cationic liposome group (3 mg/kg dose) showed significantly higher luciferase activity in the cortex, striatum, and midbrain regions as compared with the control groups, with minimal systemic exposure. Overall, the results of this study demonstrate the feasibility of brain-specific, nonviral mRNA delivery for the treatment of various neurological disorders.
基于核酸的治疗方法,包括使用信使 RNA(mRNA)作为药物分子,在治疗慢性疾病方面具有巨大的潜力,如与年龄相关的神经退行性疾病。在这项研究中,我们开发了一种 mRNA 的阳离子脂质体制剂,并评估了其在小鼠模型中经鼻腔递送至大脑的潜力。初步研究表明,在 J774A.1 鼠巨噬细胞中,GFP 表达可持续至 24 小时,并且 GFP 蛋白在细胞质中稳定表达。在小鼠中经鼻腔给予 GFP-mRNA/阳离子脂质体(3mg/kg 剂量)后,与裸 mRNA 或载体处理组相比,24 小时后脑内 GFP-mRNA 表达显著增加。用阳离子脂质体包封的荧光素酶 mRNA 用于定量分析脑内 mRNA 表达分布。结果表明,整个脑内的荧光素酶活性呈剂量依赖性增加。具体而言,与对照组相比,3mg/kg 剂量的荧光素酶-mRNA/阳离子脂质体组在皮质、纹状体和中脑区域的荧光素酶活性显著更高,而全身暴露最小。总的来说,这项研究的结果表明,针对各种神经疾病的脑特异性、非病毒 mRNA 传递是可行的。