Abstract

Permeation assays are important for the development of topical formulations applied on buccal mucosa. Swine buccal and esophageal epithelia are usually used as barriers for these assays, while frozen epithelia have been used to optimize the experimental setup. However, there is no consensus on these methods. In transdermal studies, barrier integrity has been evaluated by measuring electrical resistance (ER) across the skin, which has been demonstrated to be a simple, fast, safe, and cost-effective method. Therefore, the aims here were to investigate whether ER might also be an effective method to evaluate buccal and esophageal epithelium mucosa integrity for in vitro permeation studies, and to establish a cut-off ER value for each epithelium mucosa model. We further investigated whether buccal epithelium could be substituted by esophageal epithelium in transbuccal permeation studies, and whether their permeability and integrity were affected by freezing at −20 °C for 3 weeks. Fresh and frozen swine buccal and esophageal epithelia were mounted in Franz diffusion cells and were then submitted to ER measurement. Permeation assays were performed using lidocaine hydrochloride as a hydrophilic drug model. ER was shown to be a reliable method for evaluating esophageal and buccal epithelia. The esophageal epithelium presented higher permeability compared to the buccal epithelium. For both epithelia, freezing and storage led to decreased electrical resistivity and increased permeability. We conclude that ER may be safely used to confirm tissue integrity when it is equal to or above 3 kΩ for fresh esophageal mucosa, but not for buccal epithelium mucosa. However, the use of esophageal epithelium in in vitro transmucosal studies could overestimate the absorption of hydrophilic drugs. In addition, fresh samples are recommended for these experiments, especially when hydrophilic drugs are involved.

Highlights

  • Oral administration is one of the most convenient forms of drug delivery, due to the ease of ingestion and convenience for the patient

  • The samples presented intact morphology and integrity, confirming the presence of a stratified squamous epithelium, with tightly attached cells arranged in layers

  • There was no difference between the electrical resistance (ER) values of the fresh esophageal and buccal epithelia (p = 0.4402)

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Summary

Introduction

Oral administration is one of the most convenient forms of drug delivery, due to the ease of ingestion and convenience for the patient. Transbuccal topical administration has some disadvantages, such as the limited area available for absorption (200 cm2 ) [4,5] and relatively low permeability, since the physiological function of the buccal mucosa is to act as a barrier [6]. This may require the use of permeation enhancers or even drug delivery systems, in order to increase drug permeation [1,7,8,9,10]. Formulations for buccal delivery should have a palatable taste and appropriate mucoadhesive characteristics [9]

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