Table 2.
Results of in vitro development of separated oocytes by various methods followed by IVF.
| Method | Number of oocytes | Number of blastocysts | Developmental rate to blastocyst (% ± SEM) | ||||
|---|---|---|---|---|---|---|---|
| Early blastocyst | Blastocyst expansion | Hatched blastocyst | Total | ||||
| Microfluidic | Upper | 163 | 11 | 11 | 1 | 23 | 14.1 ± 1.3a |
| device | Lower | 197 | 18 | 43 | 10 | 71 | 36.0 ± 1.2b |
| BCB | BCB− | 143 | 12 | 9 | 1 | 22 | 15.4 ± 0.7ac |
| staining | BCB+ | 213 | 23 | 42 | 11 | 76 | 35.7 ± 1.2b |
| Conventional | A | 412 | 31 | 47 | 7 | 85 | 20.6 ± 1.1c |
| morphological | B | 375 | 38 | 86 | 6 | 130 | 34.7 ± 0.7b |
| evaluation | C | 300 | 30 | 44 | 11 | 85 | 28.3 ± 1.5d |
Oocytes collected from both upper and lower outlets were prepared for IVF and cultured, and their developmental rates to blastocyst stage were investigated on day 8. As a comparison method, BCB staining was performed to compare the separation capability between separation methods. The data were obtained from three replicates. Conventional morphological evaluation was performed by three different technicians (A, B, C) as a comparison method. COCs with a homogeneous spherical ooplasm and multilayered compact cumulus cells were selected by each technician and prepared for IVM and IVF. All technicians performed all procedures using the same protocols and materials. The data were obtained from six replicates. Values with different letters differ significantly, P < 0.01.