Evaluation of two in vitro assays to screen for potential developmental toxicants
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 inhi...
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Veröffentlicht in: | Fundamental and applied toxicology 1988-11, Vol.11 (4), p.673-684 |
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Sprache: | eng |
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Zusammenfassung: | 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 m
m 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 m
m 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 m
m 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. |
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ISSN: | 0272-0590 1095-6832 |
DOI: | 10.1016/0272-0590(88)90130-3 |