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皮肤致敏预测:?

Prediction of Skin Sensitization: ?

作者信息

Ta Giang Huong, Weng Ching-Feng, Leong Max K

机构信息

Department of Chemistry, National Dong Hwa University, Shoufeng, Taiwan.

Department of Basic Medical Science, Institute of Respiratory Disease, Xiamen Medical College, Xiamen, China.

出版信息

Front Pharmacol. 2021 May 4;12:655771. doi: 10.3389/fphar.2021.655771. eCollection 2021.

Abstract

Skin direct contact with chemical or physical substances is predisposed to allergic contact dermatitis (ACD), producing various allergic reactions, namely rash, blister, or itchy, in the contacted skin area. ACD can be triggered by various extremely complicated adverse outcome pathways (AOPs) remains to be causal for biosafety warrant. As such, commercial products such as ointments or cosmetics can fulfill the topically safe requirements in animal and non-animal models including allergy. Europe, nevertheless, has banned animal tests for the safety evaluations of cosmetic ingredients since 2013, followed by other countries. A variety of non-animal tests addressing different key events of the AOP, the direct peptide reactivity assay (DPRA), KeratinoSens™, LuSens and human cell line activation test h-CLAT and U-SENS™ have been developed and were adopted in OECD test guideline to identify the skin sensitizers. Other methods, such as the SENS-IS are not yet fully validated and regulatorily accepted. A broad spectrum of models, alternatively, to predict skin sensitization have emerged based on various animal and non-animal data using assorted modeling schemes. In this article, we extensively summarize a number of skin sensitization predictive models that can be used in the biopharmaceutics and cosmeceuticals industries as well as their future perspectives, and the underlined challenges are also discussed.

摘要

皮肤直接接触化学或物理物质易引发过敏性接触性皮炎(ACD),在接触的皮肤区域产生各种过敏反应,即皮疹、水泡或瘙痒。ACD可由各种极其复杂的不良结局途径(AOP)引发,这对生物安全保障而言仍是因果关系不明的问题。因此,诸如软膏或化妆品等商业产品可在包括过敏在内的动物和非动物模型中满足局部安全要求。然而,自2013年以来,欧洲已禁止对化妆品成分进行动物安全性评估测试,其他国家也纷纷效仿。针对AOP不同关键事件的多种非动物测试,如直接肽反应性测定(DPRA)、角质形成细胞传感试验(KeratinoSens™)、鲁米诺传感试验(LuSens)以及人细胞系激活试验(h-CLAT)和U-SENS™,已被开发出来并被纳入经合组织测试指南以识别皮肤致敏剂。其他方法,如SENS-IS尚未得到充分验证和监管部门认可。另外,基于各种动物和非动物数据,使用各种建模方案,出现了一系列预测皮肤致敏性的模型。在本文中,我们广泛总结了一些可用于生物制药和药妆品行业的皮肤致敏性预测模型及其未来前景,并讨论了其中突出的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d314/8129647/4403bd94ec74/fphar-12-655771-g001.jpg

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