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使用用NFL-TBS.40-63肽功能化的脂质体作为靶向剂,以穿过体外血脑屏障并靶向胶质母细胞瘤细胞。

The use of liposomes functionalized with the NFL-TBS.40-63 peptide as a targeting agent to cross the in vitro blood-brain barrier and target glioblastoma cells.

作者信息

Mellinger Adélie, Lubitz Larissa J, Gazaille Claire, Leneweit Gero, Bastiat Guillaume, Lépinoux-Chambaud Claire, Eyer Joël

机构信息

GlioCure SA, Angers, France; Univ Angers, Inserm, CNRS, MINT, Angers, France.

Abnoba GmbH, 75223 Niefern-Oeschelbronn, Germany.

出版信息

Int J Pharm. 2023 Nov 5;646:123421. doi: 10.1016/j.ijpharm.2023.123421. Epub 2023 Sep 16.

DOI:10.1016/j.ijpharm.2023.123421
PMID:37722495
Abstract

Glioblastoma is the most common and aggressive brain tumor. Current treatments do not allow to cure the patients. This is partly due to the blood-brain barrier (BBB), which limits the delivery of drugs to the pathological site. To overcome this, we developed liposomes functionalized with a neurofilament-derived peptide, NFL-TBS.40-63 (NFL), known for its highly selective targeting of glioblastoma cells. First, in vitro BBB model was developed to check whether the NFL can also promote barrier crossing in addition to its active targeting capacity. Permeability experiments showed that the NFL peptide was able to cross the BBB. Moreover, when the BBB was in a pathological situation, i.e., an in vitro blood-brain tumor barrier (BBTB), the passage of the NFL peptide was greater while maintaining its glioblastoma targeting capacity. When the NFL peptide was associated to liposomes, it enhanced their ability to be internalized into glioblastoma cells after passage through the BBTB, compared to liposomes without NFL. The cellular uptake of liposomes was limited in the endothelial cell monolayer in comparison to the glioblastoma one. These data indicated that the NFL peptide is a promising cell-penetrating peptide tool when combined with drug delivery systems for the treatment of glioblastoma.

摘要

胶质母细胞瘤是最常见且侵袭性最强的脑肿瘤。目前的治疗方法无法治愈患者。部分原因在于血脑屏障(BBB),它限制了药物向病理部位的递送。为克服这一问题,我们开发了用神经丝衍生肽NFL-TBS.40-63(NFL)功能化的脂质体,该肽以对胶质母细胞瘤细胞具有高度选择性靶向作用而闻名。首先,建立了体外血脑屏障模型,以检查NFL除了其主动靶向能力外,是否还能促进跨越屏障。渗透性实验表明,NFL肽能够穿过血脑屏障。此外,当血脑屏障处于病理状态,即体外血脑肿瘤屏障(BBTB)时,NFL肽的通过量更大,同时保持其对胶质母细胞瘤的靶向能力。与不含NFL的脂质体相比,当NFL肽与脂质体结合时,它增强了脂质体在穿过BBTB后被胶质母细胞瘤细胞内化的能力。与胶质母细胞瘤细胞相比,脂质体在内皮细胞单层中的细胞摄取受到限制。这些数据表明,NFL肽与药物递送系统联合用于治疗胶质母细胞瘤时,是一种很有前景的细胞穿透肽工具。

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