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Bevacizumab loaded solid lipid nanoparticles prepared by the coacervation technique: preliminary in vitro studies

机译:通过凝聚技术制备的载有贝伐单抗的固体脂质纳米颗粒:体外初步研究

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摘要

Glioblastoma, the most common primary brain tumor in adults, has an inauspicious prognosis, given that overcoming the blood-brain barrier is the major obstacle to the pharmacological treatment of brain tumors. As neoangiogenesis plays a key role in glioblastoma growth, the US Food and Drug Administration approved bevacizumab ( BVZ), an antivascular endothelial growth factor antibody for the treatment of recurrent glioblastoma in patients whose the initial therapy has failed. In this experimental work, BVZ was entrapped in solid lipid nanoparticles ( SLNs) prepared by the fatty-acid coacervation technique, thanks to the formation of a hydrophobic ion pair. BVZ activity, which was evaluated by means of four different in vitro tests on HUVEC cells, increased by 100- to 200-fold when delivered in SLNs. Moreover, SLNs can enhance the permeation of fluorescently labelled BVZ through an hCMEC/D3 cell monolayeran in vitro model of the blood brain barrier. These results are promising, even if further in vivo studies are required to evaluate the effective potential of BVZ-loaded SLNs in glioblastoma treatment.
机译:胶质母细胞瘤是成人中最常见的原发性脑肿瘤,预后不佳,因为克服血脑屏障是药物治疗脑肿瘤的主要障碍。由于新血管生成在胶质母细胞瘤的生长中起着关键作用,因此美国食品药品监督管理局批准了贝伐单抗(BVZ),一种抗血管内皮生长因子抗体,用于治疗初始治疗失败的复发性胶质母细胞瘤。在这项实验工作中,由于疏水离子对的形成,BVZ被困在通过脂肪酸凝聚技术制备的固体脂质纳米颗粒(SLN)中。通过在HUVEC细胞上进行的四种不同的体外测试来评估BVZ活性,将其以SLN的形式递送时增加了100到200倍。此外,SLN可以通过血脑屏障的hCMEC / D3细胞单层体外模型增强荧光标记的BVZ的渗透。即使需要进一步的体内研究来评估BVZ负载的SLN在胶质母细胞瘤治疗中的有效潜力,这些结果也是有希望的。

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