Department of Chemistry, via U. Schiff 6, 50519, Sesto Fiorentino, Florence, Italy.
Department of Health Sciences, Section of Clinical Pharmacology and Oncology, Viale Pieraccini 6, 50139 Florence, Italy.
Int J Biol Macromol. 2019 May 15;129:267-280. doi: 10.1016/j.ijbiomac.2019.02.005. Epub 2019 Feb 3.
The aim of the present study was the development of human serum albumin nanoparticles (HSA NPs) as nose-to-brain carrier. To strengthen, the efficacy of nanoparticles as drug delivery system, the influence of chitosan (CS) coating on the performance of HSA NPs was investigated for nasal application. HSA NPs were prepared by desolvation technique. CS coating was obtained adding the CS solution to HSA NPs. The mean particle sizes was 241 ± 18 nm and 261 ± 8 nm and the ζ-potential was -47 ± 3 mV and + 45 ± 1 mV for HSA NPs and CS-HSA NPs, respectively. The optimized formulations showed excellent stability upon storage both as suspension and as freeze-dried product after 3 months. The mucoadhesion properties were assessed by turbidimetric and indirect method. NPs were loaded with sulforhodamine B sodium salt as model drug and the effect of CS coating was investigated performing release studies, permeation and uptake experiments using Caco-2 and hCMEC/D3 cells as model of the nasal epithelium and blood-brain barrier, respectively. Furthermore, ex vivo diffusion experiments have been carried out using rabbit nasal mucosa. Finally, the ability of the formulations to reversibly open tight and gap junctions was explored by western blotting and RT-PCR analyzing in both Caco-2 and hCMEC/D3 cells.
本研究旨在开发人血清白蛋白纳米粒(HSA NPs)作为鼻腔递药载体。为了增强纳米粒作为药物传递系统的疗效,研究了壳聚糖(CS)包衣对 HSA NPs 鼻腔给药性能的影响。采用去溶剂化技术制备 HSA NPs,通过向 HSA NPs 中添加 CS 溶液获得 CS 包衣。HSA NPs 和 CS-HSA NPs 的平均粒径分别为 241±18nm 和 261±8nm,ζ-电位分别为-47±3mV 和+45±1mV。优化后的配方在 3 个月的储存期内,无论是作为混悬液还是冷冻干燥产品,均表现出良好的稳定性。通过浊度法和间接法评估了纳米粒的黏膜黏附性能。将磺基罗丹明 B 钠盐作为模型药物包载于 NPs 中,并通过 Caco-2 和 hCMEC/D3 细胞进行释放研究、渗透和摄取实验,分别作为鼻腔上皮和血脑屏障的模型,考察 CS 包衣的影响。此外,还使用兔鼻黏膜进行了离体扩散实验。最后,通过 Western blot 和 RT-PCR 分析,在 Caco-2 和 hCMEC/D3 细胞中研究了制剂可逆性开放紧密连接和缝隙连接的能力。