Nance Elizabeth, Timbie Kelsie, Miller G Wilson, Song Ji, Louttit Cameron, Klibanov Alexander L, Shih Ting-Yu, Swaminathan Ganesh, Tamargo Rafael J, Woodworth Graeme F, Hanes Justin, Price Richard J
Center for Nanomedicine at the Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21231 (USA).
Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD 21218 (USA).
J Control Release. 2014 Sep 10;189:123-132. doi: 10.1016/j.jconrel.2014.06.031. Epub 2014 Jun 28.
The blood-brain barrier (BBB) presents a significant obstacle for the treatment of many central nervous system (CNS) disorders, including invasive brain tumors, Alzheimer's, Parkinson's and stroke. Therapeutics must be capable of bypassing the BBB and also penetrate the brain parenchyma to achieve a desired effect within the brain. In this study, we test the unique combination of a non-invasive approach to BBB permeabilization with a therapeutically relevant polymeric nanoparticle platform capable of rapidly penetrating within the brain microenvironment. MR-guided focused ultrasound (FUS) with intravascular microbubbles (MBs) is able to locally and reversibly disrupt the BBB with submillimeter spatial accuracy. Densely poly(ethylene-co-glycol) (PEG) coated, brain-penetrating nanoparticles (BPNs) are long-circulating and diffuse 10-fold slower in normal rat brain tissue compared to diffusion in water. Following intravenous administration of model and biodegradable BPNs in normal healthy rats, we demonstrate safe, pressure-dependent delivery of 60nm BPNs to the brain parenchyma in regions where the BBB is disrupted by FUS and MBs. Delivery of BPNs with MR-guided FUS has the potential to improve efficacy of treatments for many CNS diseases, while reducing systemic side effects by providing sustained, well-dispersed drug delivery into select regions of the brain.
血脑屏障(BBB)对许多中枢神经系统(CNS)疾病的治疗构成了重大障碍,这些疾病包括侵袭性脑肿瘤、阿尔茨海默病、帕金森病和中风。治疗药物必须能够绕过血脑屏障,并穿透脑实质,才能在脑内达到预期效果。在本研究中,我们测试了一种非侵入性血脑屏障通透方法与一种具有治疗相关性的聚合物纳米颗粒平台的独特组合,该平台能够快速穿透脑微环境。带有血管内微泡(MBs)的磁共振引导聚焦超声(FUS)能够以亚毫米级的空间精度局部且可逆地破坏血脑屏障。与在水中的扩散相比,密集聚(乙二醇)(PEG)包被的脑穿透纳米颗粒(BPNs)具有较长的循环时间,并且在正常大鼠脑组织中的扩散速度慢10倍。在正常健康大鼠静脉注射模型纳米颗粒和可生物降解的BPNs后,我们证明了在血脑屏障被FUS和MBs破坏的区域,60nm的BPNs能够安全、压力依赖地递送至脑实质。通过磁共振引导FUS递送BPNs有潜力提高许多中枢神经系统疾病的治疗效果,同时通过向脑内特定区域提供持续、分散良好的药物递送,减少全身副作用。