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一种评估口腔用医疗器械和非处方产品潜在刺激性的体外方法的开发。

Development of an In Vitro Method for Assessing the Potential Irritation of Medical Devices and OTC Products Used in the Oral Cavity.

作者信息

Pellevoisin Christian, Puskar Marek, Molignano Jennifer, Coen Kaitlyn, Klausner Mitchell, Letasiova Silvia

机构信息

MatTek Corporation, Ashland, MA 01721, USA.

Urbilateria, 37540 Saint Cyr sur Loire, France.

出版信息

Toxics. 2025 Mar 22;13(4):233. doi: 10.3390/toxics13040233.

Abstract

The aim of this study was to evaluate an in vitro method using the EpiOral model, a three-dimensional cultured human buccal epithelium, for assessing the oral irritation potential of various products. We evaluated different concentrations of nine chemicals commonly found in over-the-counter (OTC) products and medical devices, including chlorhexidine digluconate, sodium hypochlorite, phosphoric acid, hydrogen peroxide, lactic acid, ethanol, sodium dodecyl sulfate, 1-decanol and methyl methacrylate. The method was able to identify the irritants with a clear dose-response relationship between cell viability and an increasing concentration of the chemicals in the tested solutions. Using three exposure times (1, 4 and 18 h) and calculating the ET-50 (time required to induce a 50% reduction in cell viability), the solutions were classified according to their irritant potency (strong, moderate, mild or non-irritant). The results showed excellent correlation with historical in vivo data by matching the potency classifications in most cases. This study highlighted the importance of multiple exposure times for accurate assessment, as some solutions with irritant chemicals require longer exposure to produce effects. By providing information on both the irritant potential and potency, this method proved useful for toxicologists in the risk assessment of OTC products and medical devices that come into contact with the oral cavity.

摘要

本研究的目的是评估一种使用EpiOral模型(一种三维培养的人颊黏膜上皮)的体外方法,用于评估各种产品的口腔刺激潜力。我们评估了非处方(OTC)产品和医疗器械中常见的九种化学物质的不同浓度,包括葡萄糖酸氯己定、次氯酸钠、磷酸、过氧化氢、乳酸、乙醇、十二烷基硫酸钠、1-癸醇和甲基丙烯酸甲酯。该方法能够识别出在所测试溶液中,细胞活力与化学物质浓度增加之间具有明确剂量反应关系的刺激物。使用三个暴露时间(1、4和18小时)并计算ET-50(诱导细胞活力降低50%所需的时间),根据其刺激强度(强、中、弱或无刺激)对溶液进行分类。结果表明,在大多数情况下,通过匹配强度分类,与历史体内数据具有良好的相关性。本研究强调了多次暴露时间对于准确评估的重要性,因为一些含有刺激性化学物质的溶液需要更长时间的暴露才能产生效果。通过提供有关刺激潜力和强度的信息,该方法被证明对毒理学家在评估与口腔接触的OTC产品和医疗器械的风险时有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3a/12031550/5cdf4ab0720c/toxics-13-00233-g001.jpg

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