ABSTRACT
Objective The effect of sieved particle size and equilibration time of soil samples on the measurement of radionuclides was studied to improve the accuracy of the specific activity of radionuclides in soil samples measured by gamma spectrometer. Methods The collected soil samples were dried and divided into four parts. After sieved with width of the mesh 2.0 mm, 1.0 mm, 0.5 mm and 0.25 mm respectively, they were filled into sample containers and sealed. The activity concentrations of 226Ra, 210Pb, 228Ra, 40K and 137Cs in different sieved soil samples were then measured at the sealed interval of 0, 4, 8, 12, 16, 21, 25 and 29 days by HPGe gamma-ray spectrometry respectively. Results The coefficients of variation ofthe specific activities of 226Ra, 210Pb, and 228Ra in soil samples measured at different equilibration intervals range from 0.9% to 4.3%. The coefficients of variation of the specific activities of 226Ra, 210Pb, 228Ra, 40K and 137Cs in soil samples with different sieved particle sizes range from 3.7% to 14.1%. Conclusion When the specific activities of radionuclides are determined by gamma-ray spectrometer, the effect of the sieved particle size on the measurement result must be considered, and its impact is higher than the equilibration time. This study is very useful for improving the accuracy of the determination of radionuclides in soil sample using gamma-ray spectrometer.
ABSTRACT
OBJECTIVE: One-cell human zygotes have been successfully frozen and thawed using 1,2-propanediol (PROH) during freezing and thawing. This study was performed to assess the effect of equilibration temperature and time on cryopreservation of 2-cell mouse embryos by investigating the equilibration temperature and time during initial PROH exposure prior to cryopreservation. MATERIALS AND METHODS: The late 2-cell mouse embryos were obtained from 5-6 week old ICR mice and were exposed to 1.5 M PROH in phosphate-buffered saline (PROH-PBS) at 37degrees C, room temperature (22- 24degrees C), and 4degrees C for 30 min. The PROH was washed off the 2-cell mouse embyos by incubating them for 5 min each in 1, 0.5, and then 0 M PROH-PBS in the order named. The 2-cell mouse embryos were subsequently cultured in Ham's F-10 medium and embryo development was assessed at 24, 48, and 96 hours. RESULTS: Incubation of 2-cell mouse embryos at 37degrees C for 30 min significantly impaired embryo development to blastocysts. Embryo development after exposure to PROH at 37degrees C for 10 min was 8.3% (P=0.047) and embryo development for 30 min was 5.4% (P=0.038). Incubation of 2-cell mouse embryos at room temperature or 4degrees C for up to 30 min did not significantly reduce embryo development. Cryosurvival of 2-cell mouse embryos exposed to PROH at room temperature or 4degrees C was similar. CONCLUSION: These findings suggested that pronanediol is toxic to 2-cell mouse embryos in a temperature- and time-dependent fashion. Cryopreservation of 2-cell mouse embryos after exposure at 4degrees C appears to be no better than after exposure at room temperature.