生物杀灭剂对粘膜的保护作用

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Cristina Alonso Merino, Luisa Coderch, Ana Cristina Calpena, Beatriz Clares, Anderson Ramos, Meritxell Martí
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引用次数: 0

摘要

背景杀菌剂与粘膜或皮肤接触后,能够穿透粘膜或皮肤,引起可能的局部病变,如刺激、过敏性接触性皮炎,甚至全身效应,如致癌。化合物在口腔或鼻腔粘膜的高渗透性是众所周知的,而在皮肤上的渗透性很差。因此,本工作的主要目的是生产一种能够增强粘膜的配方,增加其阻碍作用,从而减少或避免污染物和杀菌剂的渗透。结果配制并测定了几种成分;疏水配方F1,亲水配方F2和脂质体配方F3,其脂质和结构与皮肤角质组织中存在的脂质和结构相似。这些都诱导了脂质体配方F3的防水效果,特别是疏水配方F1诱导了最大程度的粘膜失水减少。测定三种杀菌剂真菌醇、丙环康唑和氯菊酯在皮肤及未处理和处理(F1、F2、F3)口腔粘膜中的渗透情况。这三种配方对所使用的每一种杀菌剂的影响是相当大的,达到与配方1对皮肤的影响显著相等的值。亲水性配方2大大增加了渗透性,疏水性配方1和脂质体配方3分别降低了大约90%和60%的渗透性,提供了几乎类似皮肤的屏障效果。因此,本研究提出了两种配方,通过减少三种模型杀菌剂的渗透来诱导粘膜不渗透性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protection of Mucous Membranes Against the Use of Biocides

Background

Biocides, in touch with the mucosa or skin, are capable of penetrating the mucosa or skin and causing possible local lesions, such as irritations, allergic contact dermatitis and even systemic effects such as carcinogenesis. The high permeability of compounds across the oral or nasal mucosa is widely known, in comparison to the poor penetration across the skin. Therefore, the main objective of this work is to produce a formulation that can strengthen the mucosa, increasing its hindering effect and thus decreasing or avoiding the penetration of contaminants and biocides.

Results

Several compositions have been formulated and assayed; the hydrophobic formulation F1, the hydrophilic formulation F2 and the liposomal formulations F3 with lipids and structure similar to those present in cutaneous keratinous tissues. These all induced a waterproofing effect with the liposomal formulation F3 and in particular the hydrophobic formulation F1 inducing the greatest decrease in Trans-mucosal water loss. Permeation of the three biocides Fungitrol, Propiconazole and Permethrin was evaluated in skin and in untreated and treated (F1, F2, F3) oral mucosal membranes. The influence of the three formulations on each of the biocides used is considerable, reaching values significantly equal to those of the skin for formulation 1. While hydrophilic formulation 2 greatly increases permeability, hydrophobic formulation 1 and liposomal formulation 3 reduce permeability, in approximately 90% and 60% respectively, providing an almost skin-like barrier effect.

Conclusions

Therefore, this work presents two formulations that induce mucosal impermeability by reducing the penetration of three model biocides.

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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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