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两种体外试验用于筛选潜在发育毒性物质的评估。

Evaluation of two in vitro assays to screen for potential developmental toxicants.

作者信息

Steele V E, Morrissey R E, Elmore E L, Gurganus-Rocha D, Wilkinson B P, Curren R D, Schmetter B S, Louie A T, Lamb J C, Yang L L

机构信息

Northrop Services, Inc., Research Triangle Park, North Carolina 27709.

出版信息

Fundam Appl Toxicol. 1988 Nov;11(4):673-84. doi: 10.1016/0272-0590(88)90130-3.

Abstract

To evaluate two in vitro assays for their ability to detect known developmental toxicants and nontoxicants, a series of 44 coded compounds were assayed by two independent laboratories using standardized protocols. The two test systems were (1) the human embryonic palatal mesenchymal cell growth inhibition assay and (2) the mouse ovarian tumor cell attachment inhibition assay. After all compounds were tested, they were decoded and ranked according to the minimum IC50 value (the millimolar concentration of compound which inhibits growth or attachment by 50% compared to the solvent control) from either test. The in vitro test result concordance with established in vivo animal and human test results was examined over a wide range of concentration levels (above which the in vitro results were called positive and below which they were considered negative). A positive response from either test was defined as a positive in vitro response. Concordance was defined as the number of correct responses divided by the number of chemicals tested. At the 1 mM level, the concordance of data from the combined in vitro assays with the in vivo data was 66% in one laboratory and 58% in the other. The maximum agreement between the combined in vitro and in vivo data was reached at the 20 mM level, where there was a 73 and 74% concordance of results in the two laboratories. At that level there was a 16 and 10% incidence of false negative results, and a 54 and 77% incidence of false positive results. A portion of these false negative compounds may require metabolic activation. The use of either assay alone was not as accurate as using a positive result from either test. Agreement of the in vitro data at the 10 mM level with available human data was 71 and 75% for each laboratory. The data indicate that the two assays are complimentary and as such the combination of these assays could be useful as a preliminary screen to establish priorities for in vivo developmental toxicity testing.

摘要

为评估两种体外试验检测已知发育毒物和非毒物的能力,两个独立实验室使用标准化方案对一系列44种编码化合物进行了检测。这两种测试系统分别是:(1)人胚胎腭间充质细胞生长抑制试验;(2)小鼠卵巢肿瘤细胞附着抑制试验。所有化合物检测完毕后,对其进行解码,并根据任一试验的最低半数抑制浓度值(与溶剂对照相比,抑制生长或附着50%的化合物毫摩尔浓度)进行排序。在广泛的浓度水平范围内(高于此浓度水平体外试验结果判定为阳性,低于此浓度水平则判定为阴性),检查体外试验结果与既定的体内动物和人体试验结果的一致性。任一试验的阳性反应定义为体外阳性反应。一致性定义为正确反应数除以检测的化学物质数。在1毫摩尔水平时,一个实验室中体外联合试验数据与体内数据的一致性为66%,另一个实验室为58%。体外和体内联合数据之间的最大一致性在20毫摩尔水平达到,两个实验室的结果一致性分别为73%和74%。在该水平,假阴性结果的发生率分别为16%和10%,假阳性结果的发生率分别为54%和77%。这些假阴性化合物中有一部分可能需要代谢激活。单独使用任一试验都不如使用任一试验的阳性结果准确。在10毫摩尔水平时,每个实验室的体外数据与现有人体数据的一致性分别为71%和75%。数据表明这两种试验具有互补性,因此这些试验的组合可作为一种初步筛选方法,用于确定体内发育毒性试验的优先级。

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