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Calu-3 Model Under AIC and LCC Conditions and Application for Protein Permeability Studies

机译:AIC和LCC条件下的Calu-3模型及其在蛋白质渗透性研究中的应用

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Broad area of respiratory epithelium with mild surface conditions is an attractive possibility when trans-mucosal delivery of protein drugs is considered. A mucus and cellular barrier of respiratory epithelium can be modelled in vitro by Calu-3 cell line. We have monitored morphology and barrier properties of Calu-3 culture on permeable supports while developing into liquid covered or air interfaced and mucus lined cellular barrier. Besides morphological differences, cultures differed in electrical resistance and permeability to proteins as well. The accelerated permeability to proteins in these models, due to permeability modulator MP C16, was examined. The effect on electrical resistance of cellular layer was rapid in both cultures suggesting easy access of MP C16 to cells even though its overall impact on cell permeability was strongly reduced in mucus covered culture. Differences in properties of the two models enable better understanding of protein transmucosal permeability, suggesting route of transport and MP C16 modulator action.
机译:当考虑跨粘膜递送蛋白质药物时,具有轻度表面条件的大面积呼吸道上皮是有吸引力的可能性。可以通过Calu-3细胞系体外模拟呼吸道上皮的粘液和细胞屏障。我们已经监测了Calu-3培养物在可渗透支持物上的形态和屏障特性,同时发展成为液体覆盖或空气接触的和粘液衬里的细胞屏障。除了形态差异外,培养物的电阻和对蛋白质的渗透性也不同。在这些模型中,由于通透性调节剂MP C16,对蛋白质的通透性加快了。在两种培养物中,对细胞层电阻的影响都很快,这表明MP C16易于进入细胞,即使在粘液覆盖的培养物中,其对细胞通透性的总体影响已大大降低。两种模型的特性差异使人们能够更好地理解蛋白质的透粘膜通透性,提示其转运途径和MP C16调节剂的作用。

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