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口腔递送二甲双胍:评估使用生物粘附性壳聚糖盘增强药物渗透性的 TR146 细胞培养模型。

Buccal delivery of metformin: TR146 cell culture model evaluating the use of bioadhesive chitosan discs for drug permeability enhancement.

机构信息

Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark.

出版信息

Int J Pharm. 2013 Dec 31;458(2):254-61. doi: 10.1016/j.ijpharm.2013.10.026. Epub 2013 Oct 20.

Abstract

The oral cavity is considered an attractive site of drug administration. Metformin is currently, used in oral diabetes treatment. The aim of the current study was to study the feasibility of metformin, to permeate the buccal epithelium applying a bioadhesive and permeation enhancing drug delivery system. The in vitro TR146 cell culture model was used to study the effect of drug concentration (5-100mM) and the impact of a bioadhesive chitosan formulation (discs) and chitosan in solution (0-20mg/mL) acting as a permeation enhancer. The permeation of metformin occurred by passive diffusion via the paracellular pathway driven by the concentration gradient, yet with a possibility of increasing the metformin transport by using higher, donor concentrations. When using floating baskets, as a new application of the TR146 cell culture model, it was possible to observe a time-dependent effect of the bioadhesive metformin discs and, metformin permeation may be increased due to a combination of bioadhesion and permeation enhancement induced by chitosan, although the permeation enhancing effect of chitosan was not statistically significant. The limited apparent buccal permeability of metformin observed in vitro, suggest that in vivo absorption of therapeutic doses of metformin needs to take place as a combination of buccal and intestinal absorption as metformin therapy requires the use of high doses.

摘要

口腔被认为是药物给药的有吸引力的部位。二甲双胍目前用于口服糖尿病治疗。本研究的目的是研究将二甲双胍渗透颊上皮的可行性,应用生物粘附和渗透增强型药物传递系统。体外 TR146 细胞培养模型用于研究药物浓度(5-100mM)的影响以及生物粘附壳聚糖制剂(圆盘)和壳聚糖在溶液中的影响(0-20mg/mL)作为渗透增强剂。二甲双胍的渗透是通过浓度梯度驱动的细胞旁途径的被动扩散发生的,但通过使用更高的供体浓度,有可能增加二甲双胍的转运。当使用漂浮篮作为 TR146 细胞培养模型的新应用时,可以观察到生物粘附二甲双胍圆盘的时间依赖性作用,并且由于壳聚糖诱导的生物粘附和渗透增强的组合,二甲双胍的渗透可能增加,尽管壳聚糖的渗透增强作用没有统计学意义。在体外观察到的二甲双胍的有限表观颊部渗透性表明,治疗剂量的二甲双胍的体内吸收需要作为颊部和肠道吸收的组合发生,因为二甲双胍治疗需要使用高剂量。

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