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聚焦超声/微泡辅助 BBB 开放增强了 LNP 介导的 mRNA 向脑内的递送。

Focused ultrasound/microbubbles-assisted BBB opening enhances LNP-mediated mRNA delivery to brain.

机构信息

Department of Pharmaceutical Informatics, Graduate School of Biomedical Sciences, Nagasaki University, 1-7-1 Sakamoto, Nagasaki-shi, Nagasaki, Japan.

Department of Neurosurgery, Nagasaki University, School of Medicine, Nagasaki University, 1-7-1 Sakamoto, Nagasaki-shi, Nagasaki, Japan.

出版信息

J Control Release. 2022 Aug;348:34-41. doi: 10.1016/j.jconrel.2022.05.042. Epub 2022 Jun 1.

Abstract

Messenger RNA (mRNA) medicine has become a new therapeutic approach owing to the progress in mRNA delivery technology, especially with lipid nanoparticles (LNP). However, mRNA encapsulated-LNP (mRNA-LNP) cannot spontaneously cross the blood-brain barrier (BBB) which prevents the expression of foreign proteins in the brain. Microbubble-assisted focused ultrasound (FUS) BBB opening is an emerging technology that can transiently enhance BBB permeability. In this study, FUS/microbubble-assisted BBB opening was investigated for the intravenous delivery of mRNA-LNP to the brain. The intensity of FUS irradiation was optimized to 1.5 kW/cm, at which BBB opening occurred efficiently without hemorrhage or edema. Exogenous protein (luciferase) expression by mRNA-LNP, specifically at the FUS-irradiated side of the brain, occurred only when FUS and microbubbles were applied. This exogenous protein expression was faster but shorter than that of plasmid DNA delivery. Furthermore, foreign protein expression was observed in the microglia, along with CD31-positive endothelial cells, whereas no expression was observed in astrocytes or neurons. These results support the addition of mRNA-LNP to the lineup of nanoparticles delivered by BBB opening.

摘要

信使 RNA(mRNA)医学由于 mRNA 递呈技术的进步,特别是脂质纳米颗粒(LNP)的进步,已成为一种新的治疗方法。然而,包裹在 mRNA 中的 LNP(mRNA-LNP)不能自发地穿过血脑屏障(BBB),这阻止了外源蛋白在大脑中的表达。微泡辅助聚焦超声(FUS)BBB 开放是一种新兴的技术,可以瞬时增强 BBB 的通透性。在这项研究中,研究了 FUS/微泡辅助 BBB 开放用于 mRNA-LNP 的静脉内递送至大脑。优化了 FUS 辐照强度为 1.5kW/cm,在此强度下,BBB 开放有效而不会发生出血或水肿。只有在应用 FUS 和微泡时,mRNA-LNP 中的外源蛋白(荧光素酶)才会在大脑的 FUS 辐照侧表达。这种外源蛋白的表达比质粒 DNA 递送更快但更短。此外,在外周蛋白表达在小胶质细胞中观察到,与 CD31 阳性内皮细胞,而在星形胶质细胞或神经元中未观察到表达。这些结果支持将 mRNA-LNP 添加到通过 BBB 开放递送至纳米颗粒的阵容中。

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