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通过对局部淋巴结试验进行非放射性同位素修饰,根据皮肤致敏潜力对化学品进行分类的新方法。

Novel approach for classifying chemicals according to skin sensitizing potency by non-radioisotopic modification of the local lymph node assay.

作者信息

Takeyoshi Masahiro, Iida Kenji, Shiraishi Keiji, Hoshuyama Satsuki

机构信息

Hita Laboratory, Chemicals Evaluation and Research Institute, 3-822 Ishii-machi, Hita-shi, Oita 8770061, Japan.

出版信息

J Appl Toxicol. 2005 Mar-Apr;25(2):129-34. doi: 10.1002/jat.1045.

Abstract

The murine local lymph node assay (LLNA) is currently recognized as a stand-alone sensitization test for determining the sensitizing potential of chemicals, and it has the advantage of yielding a quantitative endpoint that can be used to predict the sensitization potency of chemicals. The EC3 has been proposed as a parameter for classifying chemicals according to the sensitization potency. We previously developed a non-radioisotopic endpoint for the LLNA based on 5-bromo-2'-deoxyuridine (BrdU) incorporation (non-RI LLNA), and we are proposing a new procedure to predict the sensitization potency of chemicals based on comparisons with known human contact allergens. Nine chemicals (i.e. diphencyclopropenone, p-phenylenediamine, glutaraldehyde, cinnamicaldehyde, citral, eugenol, isopropyl myristate, propyleneglycol and hexane) categorized as human contact allergen classes 1-5 were tested by the non-RI LLNA with the following reference allergens: 2,4-dinitrochlorobenzene (DNCB) as a class 1 human contact allergen, isoeugenol as a class 2 human contact allergen and alpha-hexylcinnamic aldehyde (HCA) as a class 3 human contact allergen. Consequently, nine test chemicals were almost assigned to their correct allergen class. The results suggested that the new procedure for non-RI LLNA can provide correct sensitization potency data. Sensitization potency data are useful for evaluating the sensitization risk to humans of exposure to new chemical products. Accordingly, this approach would be an effective modification of LLNA with regard to its experimental design. Moreover, this procedure can be applied also to the standard LLNA with radioisotopes and to other modifications of the LLNA.

摘要

小鼠局部淋巴结试验(LLNA)目前被公认为是一种用于确定化学物质致敏潜力的独立致敏试验,它具有产生定量终点的优势,该终点可用于预测化学物质的致敏效力。已提出将EC3作为根据致敏效力对化学物质进行分类的参数。我们之前基于5-溴-2'-脱氧尿苷(BrdU)掺入开发了一种用于LLNA的非放射性同位素终点(非RI LLNA),并且我们正在提出一种新程序,通过与已知人类接触性变应原进行比较来预测化学物质的致敏效力。通过非RI LLNA对九种被归类为人类接触性变应原1 - 5类的化学物质(即二苯环丙烯酮、对苯二胺、戊二醛、肉桂醛、柠檬醛、丁香酚、肉豆蔻酸异丙酯、丙二醇和己烷)进行了测试,并使用了以下参考变应原:作为1类人类接触性变应原的2,4-二硝基氯苯(DNCB)、作为2类人类接触性变应原的异丁香酚和作为3类人类接触性变应原的α-己基肉桂醛(HCA)。结果,九种受试化学物质几乎都被归入了正确的变应原类别。结果表明,非RI LLNA的新程序可以提供正确的致敏效力数据。致敏效力数据对于评估人类接触新化学产品的致敏风险很有用。因此,就其实验设计而言,这种方法将是对LLNA的有效改进。此外,该程序也可应用于使用放射性同位素的标准LLNA以及LLNA的其他改进方法。

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