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首页> 外文期刊>Journal of Bioactive and Compatible Polymers >Effect of Chitosans and Other Excipients on the Permeation of Ketotifen,FITC-Dextran,and Rhodamine 123 through Caco-2 Cells
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Effect of Chitosans and Other Excipients on the Permeation of Ketotifen,FITC-Dextran,and Rhodamine 123 through Caco-2 Cells

机译:壳聚糖和其他赋形剂对酮康芬,FITC-右旋糖酐和若丹明123通过Caco-2细胞渗透的影响

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摘要

The determination of drug permeability is an important part of formulation,development,and studying the effect of excipients on drug delivery processes.Ketotifen,FITC-labeled dextran,and Rhodamine 123 permeation was evaluated across Caco-2 cells grown on permeable inserts in the presence of chitosan,N,O-carboxymethyl chitosan(NOCC),Carbopol 934P,Polysorbate 80,and Disodium edetate.Samples with chitosan decrease in transepithelial electrical resistance in a concentration dependent manner not seen with the other excipients used.This corresponds with significant improvement of paracellular permeation of FITC-dextran and Rhodamine 123 compared to the control(p<0.005)but Ketotifen permeation with chitosan does not show statistically significant improvement as compared to the control.Although Rhodamine 123 is a known p-glycoprotein substrate,this data would indicate that the p-glycoprotein transport system is not the rate limiting factor in Rhodamine 123 permeation.Ketotifen permeation is improved slightly in the presence of NOCC,Polysorbate 80,and Disodium edetate.These excipients have been associated with improved transcellular permeation.Carbopol 934P does not improve any of the drug models'permeation.These results clearly show the effectiveness of using Caco-2 cells for screening formulations and excipients for drug development.
机译:药物渗透性的测定是配制,开发和研究赋形剂对药物递送过程影响的重要部分。在存在的情况下,评估了可替芬,FITC标记的右旋糖酐和若丹明123对在可渗透插入物上生长的Caco-2细胞的渗透性壳聚糖,N,O-羧甲基壳聚糖(NOCC),Carbopol 934P,聚山梨酯80和乙二胺四乙酸二钠。具有壳聚糖的样品的上皮电阻呈浓度依赖的方式降低,这与其他所用赋形剂不同。 FITC-右旋糖酐和罗丹明123的细胞渗透率与对照组相比(p <0.005),但酮替芬与壳聚糖的渗透率与对照组相比无统计学意义的改善。尽管罗丹明123是已知的p-糖蛋白底物,但该数据表明p-糖蛋白转运系统不是若丹明123渗透的速率限制因素。在NOCC,聚山梨酯80和乙二胺四乙酸二钠的存在下得到了轻微的证明。这些赋形剂与改善的细胞渗透有关.Carbopol 934P不能改善任何药物模型的渗透。这些结果清楚地表明了使用Caco-2细胞的有效性用于筛选用于药物开发的制剂和赋形剂。

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