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通过微创鼻腔给药库(MIND)技术实现血脑屏障不通透性抗IL-1β抗体的有效鼻脑递送。

Effective Nose-to-Brain Delivery of Blood-Brain Barrier Impermeant Anti-IL-1β Antibody via the Minimally Invasive Nasal Depot (MIND) Technique.

作者信息

Di Francesco Valentina, Chua Andy J, Bleier Benjamin S, Amiji Mansoor M

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Northeastern University, 360 Huntington Avenue, 140 The Fenway Building, Boston, Massachusetts 02115, United States.

Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, 243 Charles Street, Boston, Massachusetts 02114, United States.

出版信息

ACS Appl Mater Interfaces. 2024 Dec 18;16(50):69103-69113. doi: 10.1021/acsami.4c18679. Epub 2024 Dec 10.

Abstract

Treatment of neuroinflammation and neurodegenerative diseases using biologic therapies is limited due to the blood-brain barrier (BBB). This study explores a clinically validated approach to bypass the BBB for the purposes of direct central nervous system (CNS) delivery of antibodies using the Minimally Invasive Nasal Depot (MIND) technique. Using a lipopolysaccharide (LPS)-induced mouse model of neuroinflammation, we evaluated the efficacy of MIND in delivering a BBB impermeant full-length anti-IL-1β antibody. The results demonstrated that MIND delivery resulted in a significant reduction in IL-1β levels and microglial activation in relevant brain regions, notably outperforming conventional intravenous (IV) administration. These results underscore the ability of the MIND approach to transform the treatment landscape for a range of neurodegenerative diseases by enabling the targeted delivery of otherwise BBB impermeant therapeutics.

摘要

由于血脑屏障(BBB)的存在,使用生物疗法治疗神经炎症和神经退行性疾病受到限制。本研究探索了一种经过临床验证的方法,即使用微创鼻腔给药系统(MIND)技术绕过血脑屏障,以便将抗体直接递送至中枢神经系统(CNS)。利用脂多糖(LPS)诱导的神经炎症小鼠模型,我们评估了MIND递送血脑屏障不透性全长抗IL-1β抗体的疗效。结果表明,MIND给药可显著降低相关脑区的IL-1β水平和小胶质细胞活化,明显优于传统的静脉内(IV)给药。这些结果强调了MIND方法通过实现对原本血脑屏障不透性治疗药物的靶向递送,改变一系列神经退行性疾病治疗格局的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0da6/11660045/b5580fb23bb0/am4c18679_0001.jpg

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