Bagley D M, Botham P A, Gardner J R, Holland G, Kreiling R, Lewis R W, Stringer D A, Walker A P
Colgate-Palmolive Co., 909 River Road, PO Box 1343, Piscataway, NJ 08855-1343, USA.
Toxicol In Vitro. 1992 Nov;6(6):487-91. doi: 10.1016/0887-2333(92)90059-z.
A list of 55 chemicals has been developed for which comprehensive in vivo rabbit eye irritation data are available. No new in vivo testing has been carried out to qualify a chemical for inclusion in the list. The 55 chemicals selected are available at high and consistent purity and are expected to be stable on storage. They have been tested undiluted in in vivo studies, except those chemicals where high concentrations of the substance could be expected to cause severe effects. The in vivo data have been generated since 1981 in studies carried out according to OECD Test Guideline 405 and following the principles of Good Laboratory Practice. The data were obtained from tests normally using at least three rabbits evaluated at the same time, involving instillation of 0.1 ml (or equivalent weight) into the conjunctival sac, and in which observations were made at least at 24, 48 and 72 hr after instillation. The chemicals represent a range of chemical classes (acetates, acids, alcohols, alkalis, aromatics, hydrocarbons, inorganics and surfactants) and different degrees of irritancy. They are ranked for eye irritation potential on the basis of a 'modified maximum average score'. The reference data bank should be of use in validation tests for promising alternatives to the in vivo rabbit eye irritation test. This is an essential step in the progression to regulatory acceptance of alternative procedures.
现已制定了一份包含55种化学品的清单,这些化学品均有全面的兔眼体内刺激数据。未开展新的体内试验来确定化学品是否符合列入该清单的条件。所选的55种化学品具有高纯度且纯度一致,预计在储存时稳定。除那些高浓度物质可能会导致严重影响的化学品外,它们在体内研究中均未稀释进行测试。自1981年以来,体内数据是根据经合组织测试指南405并遵循良好实验室规范原则开展的研究中生成的。数据通常来自至少同时对三只兔子进行评估的测试,包括向结膜囊中滴入0.1毫升(或等量重量),并在滴入后至少24、48和72小时进行观察。这些化学品代表了一系列化学类别(醋酸盐、酸、醇、碱、芳烃、碳氢化合物、无机物和表面活性剂)以及不同程度的刺激性。它们根据“修正后的最大平均得分”对眼刺激潜力进行排名。该参考数据库应可用于对有前景的兔眼体内刺激试验替代方法的验证测试。这是替代程序获得监管认可进程中的关键一步。