Lockman Paul R, Koziara Joanna, Roder Karen E, Paulson Jennifer, Abbruscato Thomas J, Mumper Russell J, Allen David D
Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University HSC, 1300 So. Coulter Dr., Amarillo, Texas 79106-1712, USA.
Pharm Res. 2003 May;20(5):705-13. doi: 10.1023/a:1023492015851.
Nanoparticles have advantage as CNS drug delivery vehicles given they disguise drug permeation limiting characteristics. Conflicting toxicological data, however, is published with regard to blood-brain barrier integrity and gross mortality.
To address this issue two novel nanoparticle types: "emulsifying wax/Brij 78" and "Brij 72/Tween 80 nanoparticles were evaluated in vivo for effect on cerebral perfusion flow, barrier integrity, and permeability using the in situ brain perfusion technique. Additional evaluation was completed in vitro using bovine brain microvessel endothelial cells for effect on integrity, permeability, cationic transport interactions, and tight junction protein expression.
In the presence of either nanoparticle formulation, no overall significant differences were observed for cerebral perfusion flow in vivo. Furthermore, observed in vitro and in vivo data showed no statistical changes in barrier integrity, membrane permeability, or facilitated choline transport. Western blot analyses of occludin and claudin-1 confirmed no protein expression changes with incubation of either nanoparticle.
The nanoparticle formulations appear to have no effect on primary BBB parameters in established in vitro and in vivo blood-brain barrier models.
纳米颗粒作为中枢神经系统药物递送载体具有优势,因为它们可掩盖药物渗透限制特性。然而,关于血脑屏障完整性和总体死亡率,已发表了相互矛盾的毒理学数据。
为解决这一问题,使用原位脑灌注技术在体内评估了两种新型纳米颗粒类型:“乳化蜡/月桂醇聚醚78”和“月桂醇聚醚72/吐温80纳米颗粒”对脑灌注流量、屏障完整性和通透性的影响。使用牛脑微血管内皮细胞在体外完成了关于对完整性、通透性、阳离子转运相互作用和紧密连接蛋白表达影响的额外评估。
在存在任何一种纳米颗粒制剂的情况下,体内脑灌注流量未观察到总体显著差异。此外,体外和体内观察到的数据显示,屏障完整性、膜通透性或促进性胆碱转运均无统计学变化。对闭合蛋白和闭合蛋白-1的蛋白质印迹分析证实,两种纳米颗粒孵育后蛋白质表达均无变化。
在已建立的体外和体内血脑屏障模型中,纳米颗粒制剂似乎对主要的血脑屏障参数没有影响。