73, and that in glycerol recovered

to 0.58. Even after 300 s, the cell OSI-744 price volume ratio was 0.80 in dimethyl sulfoxide, 0.75 in ethylene glycol, and 0.60 in glycerol, none of which exceeded 0.9. Furthermore, we attempted to calculate the volume change of the cells in response to changes in the molar concentration of the cryoprotectant. The amount of each cryoprotectant was: propylene glycol 2.6 mol, dimethyl sulfoxide 2.6 mol, ethylene glycol 3.2 mol, and glycerol 2.2 mol. We calculated the ratio of the molar concentration of each solution relative to that of propylene glycol (equation: Ratio of the molar concentration of each cryoprotectant = Molar concentration of each cryoprotectant/Molar concentration of propylene glycol). Next, we calculated

the expected volume of the cells based on the LDK378 molecular weight ratio of molar concentrations (equation: Volume of cells based on the molar concentration ratio of the cryoprotectant = Volume of the cell × Ratio of the molar concentration of each cryoprotectant). The change in volume of the cells based on the calculations was plotted as shown in Fig. 1, as measured by percent concentration (v/v). The results of the experiment in which embryos were exposed to CPS20 indicated that propylene glycol was the cryoprotectant with the fastest permeability into rat two-cell stage embryos. We then investigated the cytotoxicity of propylene glycol. All of the embryos exposed to CPS10 for 300 or 600 s survived (Table 2). The fetus development rate was 73.8% for the fresh embryos (control), 72.6% for those exposed to CPS10 for 300 s, and 82.5% mafosfamide for those exposed to CPS10 for 600 s. Implantation rate and fetus development were not significantly different among the groups. Based on the results of the vitrification experiment, CPS10 (hereafter referred to as P10) was used as the pretreatment solution and the exposure time was set to a maximum of 10 min at 25 ± 0.5 °C. When CPS containing a mixture of sucrose and cell-permeable cryoprotectant was cooled in liquid nitrogen, the color

of the solution was milky white in CPS-A and CPS-B and semitransparent in CPS-C and CPS-D (Table 3). CPS-E vitrified (transparent) but contained freeze fractures. Percoll was then added to CPS-E and the mixture was cooled in liquid nitrogen. CPS-F and CPS-G produced freeze fractures, but CPS-H did not. In addition, the P10 was first placed in a cryotube and cooled with liquid nitrogen with the addition of CPS-H. The solution was vitrified and contained no freeze fractures. Based on the experimental results, CPS-H (10% v/v propylene glycol, 30% v/v ethylene glycol, 0.3 mol sucrose, and 20% v/v Percoll; PEPeS) was added to the vitrification solution as the cryoprotectant for the embryo vitrification experiments. The survival rates of vitrified two-cell stage embryos after pretreatment were 95.9%, 98.3%, and 95.9% for those pretreated for 120, 300, and 600 s, respectively; these differences were not significant (Table 4).