Falavigna Margherita, Stein Paul C, Flaten Gøril Eide, di Cagno Massimiliano Pio
Drug Transport and Delivery Research Group, Department of Pharmacy, UiT The Arctic University of Norway, Universitetsvegen 57, 9037 Tromsø, Norway.
Department of Physics, Chemistry & Pharmacy, University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark.
Pharmaceutics. 2020 Feb 17;12(2):168. doi: 10.3390/pharmaceutics12020168.
Mucosal drug delivery accounts for various administration routes (i.e., oral, vaginal, ocular, pulmonary, etc.) and offers a vast surface for the permeation of drugs. However, the mucus layer which shields and lubricates all mucosal tissues can compromise drugs from reaching the epithelial site, thus affecting their absorption and therapeutic effect. Therefore, the effect of the mucus layer on drug absorption has to be evaluated early in the drug-development phase, prior to in vivo studies. For this reason, we developed a simple, cost-effective and reproducible method employing UV-visible localized spectroscopy for the assessment of the interaction between mucin and drugs with different physicochemical characteristics. The mucin-drug interaction was investigated by measuring the drug relative diffusivity (D) in the presence of mucin, and the method was validated by fitting experimental and mathematical data. In vitro permeability studies were also performed using the mucus-covered artificial permeation barrier (mucus-PVPA, Phospholipid Vesicle-based Permeation Assay) for comparison. The obtained results showed that the diffusion of drugs was hampered by the presence of mucin, especially at higher concentrations. This novel method proved to be suitable for the investigation on the extent of mucin-drug interaction and can be successfully used to assess the impact that the mucus layer has on drug absorption
黏膜给药涉及多种给药途径(即口服、阴道、眼部、肺部等),并为药物渗透提供了广阔的表面。然而,覆盖并润滑所有黏膜组织的黏液层会阻碍药物到达上皮部位,从而影响其吸收和治疗效果。因此,在药物研发阶段,必须在体内研究之前尽早评估黏液层对药物吸收的影响。出于这个原因,我们开发了一种简单、经济高效且可重复的方法,采用紫外可见局部光谱法来评估黏蛋白与具有不同理化特性的药物之间的相互作用。通过测量黏蛋白存在时药物的相对扩散系数(D)来研究黏蛋白 - 药物相互作用,并通过拟合实验数据和数学数据对该方法进行了验证。还使用覆盖黏液的人工渗透屏障(黏液 - PVPA,基于磷脂囊泡的渗透测定法)进行了体外渗透性研究以作比较。所得结果表明,黏蛋白的存在会阻碍药物扩散,尤其是在较高浓度时。这种新方法被证明适用于研究黏蛋白 - 药物相互作用的程度,并可成功用于评估黏液层对药物吸收的影响。