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新型肽偶联纳米药物脑靶向:体内证据。

Novel peptide-conjugated nanomedicines for brain targeting: In vivo evidence.

机构信息

Nanotech Lab, Te.Far.T.I., Dept. Life Sciences, University of Modena and Reggio Emilia, Italy; Umberto Veronesi Foundation, Milan, Italy.

Nanotech Lab, Te.Far.T.I., Dept. Life Sciences, University of Modena and Reggio Emilia, Italy; Clinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, Modena, Italy.

出版信息

Nanomedicine. 2020 Aug;28:102226. doi: 10.1016/j.nano.2020.102226. Epub 2020 May 29.

Abstract

Central nervous system (CNS) compartments remain one of the most difficult districts for drug delivery. This is due to the presence of the blood-brain barrier (BBB) that hampers 90% of drug passage, dramatically requiring non-invasive treatment strategies. Here, for the first time, the use of opioid-derived deltorphin-derivative peptides to drive biodegradable and biocompatible polymeric (i.e. poly-lactide-co-glycolide, PLGA) nanomedicines delivery across the BBB was described. Opioid-derived peptides were covalently conjugated to furnish activated polymers which were further used for fluorescently tagged nanoformulations. Beyond reporting production, formulation methodology and full physico-chemical characterization, in vivo tests generated clear proof of BBB crossing and CNS targeting by engineered nanomedicines opening the research to further applications of drug delivery and targeting in CNS disease models.

摘要

中枢神经系统(CNS)仍然是药物输送最困难的区域之一。这是由于血脑屏障(BBB)的存在,阻碍了 90%的药物通过,这就迫切需要非侵入性的治疗策略。在这里,首次描述了使用阿片类衍生的德尔塔啡衍生肽来驱动生物可降解和生物相容的聚合物(即聚乳酸-共-羟基乙酸,PLGA)纳米药物穿越 BBB。阿片类衍生肽被共价连接以提供活化的聚合物,进一步用于荧光标记的纳米制剂。除了报告生产、制剂方法和全面的物理化学特性外,体内试验还提供了明确的证据,证明工程纳米药物可以穿越 BBB 并靶向 CNS,为药物输送和 CNS 疾病模型靶向的进一步应用开辟了研究途径。

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