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In Vitro Assessment of Skin Irritation Potential of Surfactant-based Formulations by Using a 3-D Skin Reconstructed Tissue Model and Cytokine Response

机译:通过使用3-D皮肤重建的组织模型和细胞因子反应体外评估基于表面活性剂的配方的皮肤刺激性

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The personal care industry is focused on developing safe, more efficacious, and increasingly milder products, that are routinely undergoing preclinical and clinical testing before becoming available for consumer use on skin. In vitro systems based on skin reconstructed equivalents are now established for the preclinical assessment of product irritation potential and as alternative testing methods to the classic Draize rabbit skin irritation test. We have used the 3-D EpiDerm (TM) model system to evaluate tissue viability and primary cytokine interleukin-1a release as a way to evaluate the potential dermal irritation of 224 nonionic, amphoteric and/or anionic surfactant-containing formulations, or individual raw materials. As part of our testing programme, two representative benchmark materials with known clinical skin irritation potential were qualified through repeated testing, for use as references for the skin irritation evaluation of formulations containing new surfactant ingredients. We have established a correlation between the in vitro screening approach and clinical testing, and are continually expanding our database to enhance this correlation. This testing programme integrates the efforts of global manufacturers of personal care products that focus on the development of increasingly milder formulations to be applied to the skin, without the use of animal testing.
机译:个人护理行业专注于开发安全,有效和日渐温和的产品,这些产品在供消费者在皮肤上使用之前,通常会经过临床前和临床测试。现在建立了基于皮肤重建等效物的体外系统,以对产品刺激性进行临床前评估,并作为经典Draize兔子皮肤刺激性试验的替代测试方法。我们已使用3-D EpiDerm(TM)模型系统评估组织活力和原发性细胞因子白细胞介素-1a释放,以此评估224种含非离子,两性和/或阴离子表面活性剂的配方或个别原料对皮肤的潜在刺激作用材料。作为我们测试计划的一部分,通过反复测试对两种具有已知临床皮肤刺激性的代表性基准材料进行了鉴定,以用作评估含有新的表面活性剂成分的皮肤刺激性的参考。我们已经建立了体外筛选方法和临床测试之间的关联,并且正在不断扩展数据库以增强这种关联。该测试计划整合了全球个人护理产品制造商的努力,这些开发人员专注于开发越来越温和的配方以应用于皮肤,而无需使用动物测试。

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