Abstract
A major consideration in assisted reproduction is providing a laboratory environment that is as similar to in vivo conditions as possible during embryo development. In vivo, the embryo is constantly in motion due to gross movement of the carrier or more localized forces from tubal fluid flow and kinetic forces exuded by tubal cilia. Laboratories worldwide currently use static culture systems; however, a dynamic system may more closely mimic in vivo conditions. Reported benefits to dynamic culture include improved blastulation and pregnancy rates (1,2).
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