1. Toxicity testing of human assisted reproduction devices using the mouse embryo assay.
- Author
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Punt-van der Zalm JP, Hendriks JC, Westphal JR, Kremer JA, Teerenstra S, and Wetzels AM
- Subjects
- Animals, Blastocyst, Catheterization adverse effects, Culture Media toxicity, Embryonic Development, Humans, Mice, Mineral Oil toxicity, Biological Assay methods, Models, Statistical, Reproductive Techniques instrumentation, Toxicity Tests methods
- Abstract
Systems to assess the toxicity of materials used in human assisted reproduction currently lack efficiency and/or sufficient discriminatory power. The development of 1-cell CBA/B6 F1 hybrid mouse embryos to blastocysts, expressed as blastocyst rate (BR), is used to measure toxicity. The embryos were divided into control and test groups, and were exposed to either control medium or to a potentially toxic test medium. Inferences on toxicity were based on differences in BR between the two groups. The mouse embryo assay followed a stratified (mouse), randomized (embryo), and balanced (equal number of embryos per group and per mouse) design. The number of embryos needed was calculated using power analysis. The basal BR of the hybrid strain was determined in a historical population. Sixty-nine mouse embryos per group were required to detect toxic materials with sufficient sensitivity and to account for the considerable inter-mouse variation in blastocyst development. Fifty-two samples, divided over batches of seven different products were tested before use in the study IVF centre and five of these were found to be toxic. This test system, presented as the Nijmegen mouse embryo assay (NMEA), can be used to detect embryo-toxic materials in daily IVF practice, and this report may provide a starting point for standardization.
- Published
- 2009
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