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用于穿越血脑屏障的聚乳酸-羟基乙酸共聚物-聚乙二醇-血管生成素-2纳米颗粒:概念验证研究

PLGA-PEG-ANG-2 Nanoparticles for Blood-Brain Barrier Crossing: Proof-of-Concept Study.

作者信息

Hoyos-Ceballos Gina P, Ruozi Barbara, Ottonelli Ilaria, Da Ros Federica, Vandelli Maria Angela, Forni Flavio, Daini Eleonora, Vilella Antonietta, Zoli Michele, Tosi Giovanni, Duskey Jason T, López-Osorio Betty L

机构信息

Grupo de Investigación Ciencia de los Materiales, Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Calle 62 No. 52-59, Medellín 050015, Colombia.

Department of Life Sciences, University of Modena and Reggio Emilia, 41124 Modena, Italy.

出版信息

Pharmaceutics. 2020 Jan 17;12(1):72. doi: 10.3390/pharmaceutics12010072.

Abstract

The treatment of diseases that affect the central nervous system (CNS) represents a great research challenge due to the restriction imposed by the blood-brain barrier (BBB) to allow the passage of drugs into the brain. However, the use of modified nanomedicines engineered with different ligands that can be recognized by receptors expressed in the BBB offers a favorable alternative for this purpose. In this work, a BBB-penetrating peptide, angiopep-2 (Ang-2), was conjugated to poly(lactic--glycolic acid) (PLGA)-based nanoparticles through pre- and post-formulation strategies. Then, their ability to cross the BBB was qualitatively assessed on an animal model. Proof-of-concept studies with fluorescent and confocal microscopy studies highlighted that the brain-targeted PLGA nanoparticles were able to cross the BBB and accumulated in neuronal cells, thus showing a promising brain drug delivery system.

摘要

由于血脑屏障(BBB)对药物进入大脑的限制,影响中枢神经系统(CNS)疾病的治疗面临巨大的研究挑战。然而,使用经工程改造带有不同配体的纳米药物,这些配体可被血脑屏障中表达的受体识别,为此提供了一个有利的替代方案。在这项工作中,一种穿透血脑屏障的肽,血管活性肠肽-2(Ang-2),通过配方前和配方后策略与聚乳酸-乙醇酸共聚物(PLGA)纳米颗粒偶联。然后,在动物模型上定性评估了它们穿越血脑屏障的能力。荧光和共聚焦显微镜研究的概念验证研究突出表明,脑靶向PLGA纳米颗粒能够穿越血脑屏障并在神经元细胞中积累,从而显示出一种有前景的脑药物递送系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfa6/7023215/f80d198f236d/pharmaceutics-12-00072-g001.jpg

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