EMBRION RIVOJLANISHI: GURUHLI KULTIVATSIYANING INDIVIDUAL TIME-LAPSE TIZIMIGA NISBATAN USTUNLIGI
The efficiency of embryo development in vitro is strongly influenced by the characteristics of the culture microenvironment, particularly medium volume, metabolic stability, and the presence of paracrine signaling between embryos. Group embryo culture provides a more physiologically supportive environment by preserving inter-embryonic communication and reducing metabolic stress, thereby enhancing developmental competence. In contrast, individual culture within time-lapse systems, despite offering continuous morphokinetic monitoring, is limited by small medium volume and the absence of paracrine interaction, which may restrict developmental potential. Analysis of 436 IVF cycles demonstrated that the proportion of good-quality Day-5 blastocysts was higher in group culture (40.8%) compared with individual time-lapse culture (35.4%), while fertilization rates and late
Natural sciencesblastocyst formation on Days 6–7 were comparable. These findings indicate that embryo development is determined primarily by the biological and metabolic properties of the microenvironment rather than imaging technology alone, positioning group culture as a more biologically advantageous approach in many laboratory settings.
1. Ebner, T., Moser, M., Sommergruber, M., & Tews, G. (2010). Group culture of human zygotes is superior to individual culture in terms of blastocyst development and implantation: a randomized controlled trial. Fertility and Sterility, 94(2), 678–681.
2. doi:10.1016/j.fertnstert.2009.04.007
3. Fancsovits, P., Pribenszky, C., Murber, Á., Kaszás, Z., & Urbancsek, J. (2022). Prospective-randomized study comparing clinical outcomes of IVF treatments where embryos were cultured individually or in a microwell group-culture dish. Journal of Assisted Reproduction and Genetics.
4. doi:10.1007/s10815-022-02600-w
5. Ciray, H. N., Campbell, A., Aguilar, J., et al. (2014). Proposed guidelines on the nomenclature and annotation of dynamic human embryo monitoring using time-lapse imaging. Human Reproduction, 29(12), 2650–2660.
6. doi:10.1093/humrep/deu278
7. Vajta, G., & Rienzi, L. (2020). Time-lapse culture: methodological considerations and clinical impact. Reproductive Biomedicine Online, 41(4), 663–675.
8. doi:10.1016/j.rbmo.2020.06.006
9. Lane, M., & Gardner, D. K. (2000). Regulation of embryonic development by amino acids. Human Reproduction Update, 6(4), 447–453.
10. doi:10.1093/humupd/6.4.447
11. Gardner, D. K., & Lane, M. (1997). Culture and selection of viable blastocysts: a feasible proposition for human IVF? Human Reproduction Update, 3(4), 367–382.
12. doi:10.1093/humupd/3.4.367
13. Morbeck, D. E., Paczkowski, M., et al. (2014). Composition of protein supplements used for human embryo culture. Journal of Assisted Reproduction and Genetics, 31, 1703–1711.
14. doi:10.1007/s10815-014-0335-7
15. Rijnders, P. M., & Jansen, C. A. (1998). Paracrine interactions between embryos: role in embryo development. Human Reproduction, 13(4), 1036–1042.
16. doi:10.1093/humrep/13.4.1036
17. Swain, J. E. (2014). Optimizing the culture environment in the IVF laboratory: impact of pH, osmolality, and oxygen tension. Reproductive Biomedicine Online, 28(4), 476–486.
18. doi:10.1016/j.rbmo.2013.12.005
19. Ciray, H. N., Karagenc, L., et al. (2012). Time-lapse embryo imaging improves embryo selection but may be limited by culture conditions. Fertility and Sterility, 98(4), 863–870.
20. doi:10.1016/j.fertnstert.2012.06.046
МUROTOV F. (2025). QUMBOSGAN GEOLOGIK MAYDONI TEKTONIK BUZILISH ZICHLIGI XARITASINI TUZISH METODIKASI. «ACTA NUUz», 3(3.2.1), 282–283. Retrieved from https://journals.nuu.uz/index.php/actanuuz/article/view/10117
JOVLIYEVA, U., & TURSUNOVA, S. (2025). SOME INDICATORS OF WATER EXCHANGE IN MENTHA PIPERITA L. AND MENTHA ARVENSIS L. SPECIES. «ACTA NUUz», 3(3.2.1), 82–84. Retrieved from https://journals.nuu.uz/index.php/actanuuz/article/view/10118
NORMATOVA, N., & AGZAMOVA, I. (2025). SHAHAR HUDUDLARIDA MUHANDISLIK-GEOLOGIK TADQIQOTLAR UCHUN MAHALLIY ME’YOR-TARTIBGA SOLISH ASOSINI RIVOJLANTIRISH TAHLILI. «ACTA NUUz», 3(3.2.1), 284–286. Retrieved from https://journals.nuu.uz/index.php/actanuuz/article/view/10119
JO‘RAQULOV, J., & MUSTAFAYEV, I. (2025). DATA ON THE DISTRIBUTION OF REPRESENTATIVES OF THE GENUS MONILINIA IN UZBEKISTAN. «ACTA NUUz», 3(3.2.1), 85–87. Retrieved from https://journals.nuu.uz/index.php/actanuuz/article/view/10122
ОРИНБАЕВ, Б., ХАЙИТОВ, О., САБУРОВ, Н., МАШАРИПОВА, Ш., & ДАВЛАТБОЕВ, Ж. (2025). ГЕОДИНАМИКА ЮРСКО-ПАЛЕОЗОЙСКИХ СТРУКТУРНЫХ ПЛАНОВ ЗОНЫ СОЧЛЕНЕНИЯ СУДОЧЬЕГО ПАЛЕОПРОГИБА И БЕРДАХСКОГО ВАЛА. «ACTA NUUz», 3(3.2.1), 294–297. Retrieved from https://journals.nuu.uz/index.php/actanuuz/article/view/10123
IBRAGIMOVA, S., & ALLAMURATOV, M. (2025). INSECTS AS AN ALTERNATIVE SOURCE OF PROTEIN: A REVIEW OF THE POTENTIAL USE OF LOCUSTS (DOCIOSTAURUS MAROCCANUS) AS A DIETARY COMPONENT FOR LABORATORY RATS. «ACTA NUUz», 3(3.2.1), 88–90. Retrieved from https://journals.nuu.uz/index.php/actanuuz/article/view/10124
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