Table 4.
Treatment | System | No. of Embryos | Cell Number | ICM Ratio (%) | ACN | ACR (%) | ||
---|---|---|---|---|---|---|---|---|
TCN | TE | ICM | ||||||
Control | Group | 36 | 120.8 ± 49.60 a | 84.7 ± 40.93 a | 36.1 ± 14.81 a | 31.0 ± 10.50 a | 7.14 ± 4.00 a | 5.9 ± 2.39 a |
ControlA | Individual | 36 | 100.0 ± 26.72 b | 67.4 ± 29.28 b | 32.5 ± 6.31 a | 35.5 ± 13.96 a | 7.6 ± 4.28 a | 8.3 ± 5.69 b |
Control+PBS B | Individual | 40 | 109.9 ± 30.63 a | 77.7 ± 29.79 a | 32.1 ± 6.28 a | 30.9 ± 9.42 a | 8.7 ± 4.41 a | 8.2 ± 4.24 b |
EV supplementedC | Individual | 38 | 109.5 ± 33.30 a | 76.55 ± 32.66 a | 33.0 ± 5.65 a | 32.56 ± 10.32 a | 3.5 ± 2.91 b | 3.3 ± 2.90 a |
Data are represented as mean ± SD. A Control = SOF+ITS+BSA medium used in group culture system (25 presumed zygotes/50µL droplet); B Control = SOF+ITS+BSA medium used in individual culture system (1 presumed zygotes/20µL droplet); C Control+PBS = SOF+ITS+BSA medium with PBS (1:400); D EV supplemented = SOF+ITS+BSA medium supplemented with EVs in PBS with an EV concentration of 0.228µg/mL. Total cell number (TCN) which includes the sum of both trophectoderm (TE) and inner cell mass cells (ICM), apoptotic cell number (ACN), ICM ratio and, apoptotic cell ratio (ACR) of blastocyst collected at 8 dpi were calculated after differential apoptotic staining. a–c Within each column, values that differ significantly are indicated by different superscripts (p < 0.05).