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局部淋巴结试验在评估药物工艺中间体致敏潜力中的应用。

Use of the local lymph node assay in the evaluation of the sensitizing potential of pharmaceutical process intermediates.

作者信息

Durand Geneviève, de Burlet Georges, Virat Michel, Nauman Bruce D

机构信息

MSD-Chibret, Riom, France.

出版信息

Contact Dermatitis. 2003 Sep;49(3):148-54. doi: 10.1111/j.0105-1873.2003.00197.x.

Abstract

The murine local lymph node assay (LLNA) has recently been developed to determine the contact sensitization potential of chemicals. Since its original development, the LLNA results have been the subject of extensive comparisons with guinea pig and human data. The investigations described here were designed to explore the ability of the LLNA to identify accurately, pharmaceutical process intermediates (PIs) known to cause contact allergy in humans. To that end, 16 PIs previously tested in the guinea-pig maximization test (GPMT) were tested in the LLNA. Another PI known to be a contact sensitizer in humans was tested only in the LLNA. Cases of contact sensitization in humans were reported only for PIs that were extreme sensitizers in the GPMT and had low EC3 values (concentration of the test substance required to generate a threefold increase in lymph node cell proliferation) in the LLNA. These data provide additional evidence that the LLNA is able to discriminate skin sensitizers from chemicals that do not possess a significant skin sensitization potential and is thus a useful method for hazard identification. In addition, this method also offers important animal welfare benefits and may also be useful for risk assessment purposes.

摘要

小鼠局部淋巴结试验(LLNA)最近已被开发用于确定化学物质的接触致敏潜力。自最初开发以来,LLNA的结果一直是与豚鼠和人类数据进行广泛比较的主题。此处描述的研究旨在探索LLNA准确识别已知会在人类中引起接触性过敏的药物工艺中间体(PI)的能力。为此,在LLNA中对16种先前在豚鼠最大化试验(GPMT)中测试过的PI进行了测试。另一种已知在人类中为接触致敏剂的PI仅在LLNA中进行了测试。仅针对在GPMT中为极强致敏剂且在LLNA中具有低EC3值(使淋巴结细胞增殖增加三倍所需的测试物质浓度)的PI报告了人类接触致敏病例。这些数据提供了额外的证据,证明LLNA能够将皮肤致敏剂与不具有显著皮肤致敏潜力的化学物质区分开来,因此是一种用于危害识别的有用方法。此外,该方法还具有重要的动物福利益处,并且可能也可用于风险评估目的。

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