Department of Neurosurgery, Yale University, New Haven, CT, 06511, USA.
Department of Biomedical Engineering, Yale University, New Haven, CT, 06511, USA.
Small. 2019 Aug;15(35):e1902011. doi: 10.1002/smll.201902011. Epub 2019 Jul 10.
Cell membrane coating has recently emerged as a promising biomimetic approach to engineering nanoparticles (NPs) for targeted drug delivery. However, simple cell membrane coating may not meet the need for efficient drug delivery to the brain. Here, a novel molecular engineering strategy to modify the surface of NPs with a cell membrane coating for enhanced brain penetration is reported. By using poly(lactic-co-glycolic) acid NPs as a model, it is shown that delivery of NPs to the ischemic brain is enhanced through surface coating with the membrane of neural stem cells (NSCs), and the delivery efficiency can be further increased using membrane isolated from NSCs engineered for overexpression of CXCR4. It is found that this enhancement is mediated by the chemotactic interaction of CXCR4 with SDF-1, which is enriched in the ischemic microenvironment. It is demonstrated that the resulting CXCR4-overexpressing membrane-coated NPs, termed CMNPs, significantly augment the efficacy of glyburide, an anti-edema agent, for stroke treatment. The study suggests a new approach to improving drug delivery to the ischemic brain and establishes a novel formulation of glyburide that can be potentially translated into clinical applications to improve management of human patients with stroke.
细胞膜包覆最近成为一种很有前途的仿生方法,可用于工程化纳米颗粒 (NPs) 以实现靶向药物递送。然而,简单的细胞膜包覆可能无法满足将药物高效递送到大脑的需求。在这里,报道了一种通过细胞膜包覆对 NPs 表面进行修饰以增强穿透大脑能力的新型分子工程策略。以聚(乳酸-共-乙醇酸) NPs 为模型,结果表明,通过用神经干细胞 (NSCs) 的细胞膜对 NPs 进行包覆,可增强 NPs 向缺血性脑的递送,并且使用过表达 CXCR4 的 NSCs 分离的膜进一步提高了递送效率。研究发现,这种增强是由 CXCR4 与 SDF-1 的趋化相互作用介导的,SDF-1 在缺血性微环境中富集。研究表明,由此产生的 CXCR4 过表达的细胞膜包覆的 NPs,称为 CMNPs,可显著提高抗水肿药物格列本脲治疗中风的疗效。该研究提出了一种改善缺血性脑内药物递送的新方法,并建立了一种新的格列本脲制剂,可能转化为临床应用,以改善人类中风患者的治疗。