首页> 外文期刊>International Journal of Pharmaceutics >Targeted delivery of rosmarinic acid across the blood-brain barrier for neuronal rescue using polyacrylamide-chitosan-poly(lactide-co-glycolide) nanoparticles with surface cross-reacting material 197 and apolipoprotein E
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Targeted delivery of rosmarinic acid across the blood-brain barrier for neuronal rescue using polyacrylamide-chitosan-poly(lactide-co-glycolide) nanoparticles with surface cross-reacting material 197 and apolipoprotein E

机译:使用聚丙烯酰胺 - 壳聚糖 - 聚(丙交酯 - 共乙酰胺)纳米颗粒具有表面交叉反应材料197和载脂蛋白e的血脑屏蔽血脑屏蔽的血脑屏障的靶向尿液的递送

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Rosmarinic acid-loaded polyacrylamide-chitosan-poly(lactide-co-glycolide) nanoparticles (RA-PAAM-CH- PLGA NPs) were grafted with cross-reacting material 197 (CRM197) and apolipoprotein E (ApoE) for targeting of the blood-brain barrier (BBB) and rescuing degenerated neurons. The polymeric nanocarriers were prepared by microemulsion, solvent diffusion, grafting, and surface modification, and CRM197-ApoE-RA-PAAM-CH-PLGA NPs were used to treat human brain-microvascular endothelial cells, RWA264.7 cells, and A beta-insulted SK-N-MC cells. Experimental results revealed that an increase in the weight percentage of PAAM decreased the particle size, zeta potential, and grafting efficiency of CRM197 and ApoE. In addition, surface DSPE-PEG(2000) could protect CRM197-ApoE-RA-PAAM-CH-PLGA NPs against uptake by RWA264.7 cells. An increase in the concentration of CRM197 and ApoE decreased the transendothelial electrical resistance and increased the ability of propidium iodide and RA to cross the BBB. The order in the viability of apoptotic SK-N-MC cells was CRM197-ApoE-RA-PAAM-CH-PLGA NPs > CRM197-RA-PAAM-CH-PLGA NPs > RA. Thus, CRM197-ApoE-RA-PAAM-CH-PLGA NPs can be a promising formulation to deliver RA to A beta-insulted neurons in the pharmacotherapy of Alzheimer's disease. (C) 2017 Elsevier B.V. All rights reserved.
机译:迷迭香酸加载的聚丙烯酰胺 - 壳聚糖 - 聚(丙交酯 - 共 - 乙交酯)纳米颗粒(RA-PAAM-CH- PLGA NPS)与被移植交叉反应对血 - 靶向材料197(CRM197)和载脂蛋白E(载脂蛋白E)脑屏障(BBB)和拯救退化神经元。通过微乳液,溶剂扩散,接枝,和表面改性制备的聚合物纳米载体,和CRM197-的ApoE-RA-PAAM-CH-PLGA纳米颗粒被用于治疗人脑微血管内皮细胞,细胞RWA264.7,和β-侮辱性sk-n-mc细胞。实验结果表明,PAAM的重量百分比的增加降低了CRM197和ApoE的粒度,ζ电位和移植效率。此外,表面DSPE-PEG(2000)可以保护CRM197-APOE-RA-PAAM-CH-CH-PLGA NPS免受RWA264.7细胞的吸收。 CRM197和ApoE浓度的增加降低了颅内电阻并增加了碘化丙啶和Ra的能力。凋亡SK-N-MC细胞的可行性的顺序是CRM197-APOE-RA-PAAM-CH-PLGA NPS> CRM197-RA-PAAM-CH-PLGA NPS> Ra。因此,CRM197-APOE-RA-PAAM-CH-PLGA NPS可以是有希望的配方,以将RA递送到阿尔茨海默病的药物治疗中的β受损神经元。 (c)2017年Elsevier B.V.保留所有权利。

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