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评估不同猪口腔黏膜部位作为药物渗透研究的渗透屏障模型。

Evaluation of different pig oral mucosa sites as permeability barrier models for drug permeation studies.

作者信息

Franz-Montan Michelle, Serpe Luciano, Martinelli Claudia Cristina Maia, da Silva Camila Batista, Santos Cleiton Pita Dos, Novaes Pedro Duarte, Volpato Maria Cristina, de Paula Eneida, Lopez Renata Fonseca Vianna, Groppo Francisco Carlos

机构信息

Department of Physiological Sciences, Piracicaba Dental School, University of Campinas - UNICAMP, Piracicaba, São Paulo, Brazil.

Department of Physiological Sciences, Piracicaba Dental School, University of Campinas - UNICAMP, Piracicaba, São Paulo, Brazil.

出版信息

Eur J Pharm Sci. 2016 Jan 1;81:52-9. doi: 10.1016/j.ejps.2015.09.021. Epub 2015 Oct 3.

Abstract

The objective of the present study was to investigate the influence of preparation and storage conditions on the histology and permeability of different parts of porcine oral mucosa used for in vitro studies of transbuccal formulations. Fresh and frozen (-20°C and -80°C, with or without cryoprotectant) epithelia of porcine palatal, gingival, dorsum of the tongue, and buccal mucosa were submitted for histological analyses to determine the effects of storage conditions on barrier integrity. Permeation of lidocaine hydrochloride (used as a hydrophilic model drug) across fresh and previously frozen oral epithelium was measured in order to evaluate the barrier function. Histological evaluation demonstrated that the oral epithelium was successfully separated from the connective tissue, except for gingival mucosa. After storage under different conditions, all tissues presented desquamation of superficial layers and spherical spaces induced by the freezing process. The permeability of lidocaine hydrochloride varied among the fresh oral mucosa and generally increased after freezing. In conclusion, fresh epithelium from the buccal and dorsum of the tongue mucosa should be used for in vitro studies investigating hydrophilic drug transport when these are the desired clinical application sites. However, when the palate is the target site, both fresh and frozen (for up to 4weeks, without addition of cryoprotectant) samples could be used. The addition of glycerol as a cryoprotectant should be avoided due to increased lidocaine hydrochloride permeability.

摘要

本研究的目的是调查制备和储存条件对用于经颊制剂体外研究的猪口腔黏膜不同部位的组织学和渗透性的影响。将新鲜的以及冷冻的(-20°C和-80°C,添加或不添加冷冻保护剂)猪腭黏膜、牙龈黏膜、舌背黏膜和颊黏膜上皮进行组织学分析,以确定储存条件对屏障完整性的影响。测量盐酸利多卡因(用作亲水性模型药物)在新鲜的和先前冷冻的口腔上皮中的渗透情况,以评估屏障功能。组织学评估表明,除牙龈黏膜外,口腔上皮已成功与结缔组织分离。在不同条件下储存后,所有组织均出现表层脱落以及由冷冻过程引起的球形间隙。盐酸利多卡因在新鲜口腔黏膜中的渗透性各不相同,且冷冻后通常会增加。总之,当颊黏膜和舌背黏膜是期望的临床应用部位时,应使用来自这些部位的新鲜上皮进行亲水性药物转运的体外研究。然而,当腭部是目标部位时,新鲜的和冷冻的(长达4周,不添加冷冻保护剂)样本均可使用。由于盐酸利多卡因渗透性增加,应避免添加甘油作为冷冻保护剂。

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