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壳聚糖纳米颗粒在体外与呼吸道上皮细胞具有相容性。

Chitosan nanoparticles are compatible with respiratory epithelial cells in vitro.

作者信息

Grenha Ana, Grainger Christopher I, Dailey Lea Ann, Seijo Begoña, Martin Gary P, Remuñán-López Carmen, Forbes Ben

机构信息

University of Santiago de Compostela, Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, 15782 Santiago de Compostela, Spain.

出版信息

Eur J Pharm Sci. 2007 Jun;31(2):73-84. doi: 10.1016/j.ejps.2007.02.008. Epub 2007 Feb 25.

Abstract

The aim of this work was to evaluate the biocompatibility of novel respirable powder formulations of nanoparticles (NP) entrapped in mannitol microspheres using human respiratory epithelial cell lines. Microspheres formulated at NP:mannitol ratios of 10:90, 20:80 and 40:60 were evaluated using the Calu-3 and A549 cell lines. The MTT cell viability assay revealed an absence of overt toxicity to Calu-3 or A549 cells following exposure to the formulations containing <1.3mg NP/ml (equivalent to 0.87 mg NP/cm(2)) for up to 48 h. Transepithelial electrical resistance (TER) and solute permeability in Calu-3 cell layers were determined following exposure of the cells to the NP:mannitol 20:80 formulation. After administration of the formulation dissolved in serum-free cell culture medium (1.3mg/ml NP suspension) to the cells, neither TER nor permeability were altered compared to untreated cell layers. Confocal microscopy did not reveal any NP internalisation under the conditions used in this study, although evidence of mucoadhesion was observed. All the data presented are encouraging with respect to the development of chitosan NP-containing microspheres for the pulmonary administration of therapeutic macromolecules. Not only do the formulations possess suitable aerodynamic characteristics and the capacity to encapsulate proteins as shown previously; they have now been shown to exhibit in vitro biocompatibility.

摘要

本研究的目的是使用人呼吸道上皮细胞系评估包裹在甘露醇微球中的新型可吸入纳米颗粒(NP)粉末制剂的生物相容性。使用Calu-3和A549细胞系对NP与甘露醇比例为10:90、20:80和40:60的微球进行评估。MTT细胞活力测定显示,暴露于含NP<1.3mg/ml(相当于0.87mg NP/cm²)的制剂长达48小时后,对Calu-3或A549细胞没有明显毒性。在Calu-3细胞层暴露于NP:甘露醇20:80制剂后,测定跨上皮电阻(TER)和溶质渗透性。将溶解于无血清细胞培养基中的制剂(1.3mg/ml NP悬浮液)给予细胞后,与未处理的细胞层相比,TER和渗透性均未改变。共聚焦显微镜检查在本研究使用的条件下未发现任何NP内化现象,尽管观察到了粘膜粘附的证据。就用于肺部给药治疗性大分子的含壳聚糖NP微球的开发而言,所有呈现的数据都令人鼓舞。这些制剂不仅具有合适的空气动力学特性和如前所示的包封蛋白质的能力;现在还已证明它们具有体外生物相容性。

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