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玻璃化冷冻保存人类胚胎的封闭系统支持其发育能力:人类胚胎的封闭玻璃化冷冻。

A closed system supports the developmental competence of human embryos after vitrification : Closed vitrification of human embryos.

机构信息

IVF Namba Clinic, Osaka, Japan.

出版信息

J Assist Reprod Genet. 2013 Mar;30(3):371-6. doi: 10.1007/s10815-012-9928-2. Epub 2013 Jan 12.

DOI:10.1007/s10815-012-9928-2
PMID:23315263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3607685/
Abstract

PURPOSE

Closed-system vitrification may enable the risk of contamination to be minimised. We performed three studies to compare the developmental competence of human embryos vitrified using either a closed vitrification system (CVS; Rapid-i®) or an open vitrification system (OVS; Cryo-top®).

METHODS

The first study was performed in vitro using 66 zygotes previously vitrified at pronuclear stage. These were warmed and randomised 1:1 to revitrification using either the OVS or the CVS. After re-warming, embryo development and blastocyst cell number were assessed. For the second study, also performed in vitro, 60 vitrified-warmed blastocysts were randomised 1:1:1 into three groups (OVS or CVS revitrification, or no revitrification). The proportion of dead cells was assessed by staining. The third study was performed in vivo, using 263 high-grade blastocysts randomly assigned to vitrification using either the CVS (n = 100) or the OVS (n = 163). After warming, single blastocyst transfer was performed.

RESULTS

There were no differences between the CVS and the OVS in survival rate (100 % vs. 97 %), blastulation rate (96 h: 50 % vs. 50 %; 120 h: 68 % vs. 56 %), proportion of good blastocysts (96 h: 32 % vs. 22 %, 120 h: 47 % vs. 41 %), or mean number of cells (137 vs. 138). The proportion of dead cells in blastocysts re-vitrified by CVS (31 %) was similar to that for OVS (38 %) and non-revitrification (32 %). In vivo, the implantation rate for blastocysts vitrified using the CVS (54 %) was similar to that with the OVS (53 %).

CONCLUSION

Our studies consistently indicate that human embryos may be vitrified using a CVS without impairment of developmental competence.

摘要

目的

封闭系统的玻璃化可能使污染风险最小化。我们进行了三项研究,比较了使用封闭系统(CVS;Rapid-i®)或开放系统(OVS;Cryo-top®)对人类胚胎进行玻璃化的胚胎发育能力。

方法

第一项研究在体外进行,使用 66 个先前在原核期进行玻璃化的受精卵。这些受精卵被解冻,并随机分为 1:1 比例,分别使用 OVS 或 CVS 进行再玻璃化。重新解冻后,评估胚胎发育和囊胚细胞数量。第二项研究也在体外进行,将 60 个玻璃化解冻的囊胚随机分为 1:1:1 三组(OVS 或 CVS 再玻璃化,或不进行再玻璃化)。通过染色评估死细胞的比例。第三项研究在体内进行,使用 263 个高等级囊胚随机分配使用 CVS(n=100)或 OVS(n=163)进行玻璃化。解冻后,进行单个囊胚转移。

结果

CVS 和 OVS 之间在存活率(100%与 97%)、囊胚形成率(96 小时:50%与 50%;120 小时:68%与 56%)、优质囊胚比例(96 小时:32%与 22%,120 小时:47%与 41%)或平均细胞数(137 与 138)方面均无差异。CVS 再玻璃化的囊胚中的死细胞比例(31%)与 OVS(38%)和不进行再玻璃化(32%)相似。在体内,使用 CVS 进行玻璃化的囊胚的着床率(54%)与使用 OVS 的相似(53%)。

结论

我们的研究一致表明,人类胚胎可以使用 CVS 进行玻璃化,而不会损害其发育能力。

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