Lee Jung-Woo, Cha Jeong-Ho, Shin Sun-Hee, Kim Yun-Jeong, Lee Seul-Ki, Cha Hye-Jin, Kim Ji-Hae, Ahn Ji-Hyun, Kim Hye-Young, Pak Kyung-Ah, Yoon Ji-Sung, Park Seo-Young, Park Choon-Keun
1Agaon Fertility Clinic, Seoul 08391, Korea; College of Animal Life Science, Kangwon National University, Chuncheon 24341, Korea.
1Agaon Fertility Clinic, Seoul 08391, Korea.
Dev Reprod. 2016 Sep;20(3):219-225. doi: 10.12717/DR.2016.20.3.219.
Most of the commercial devices for vitrification are directly immersed into the warming solution (WS) for increasing of warming rate. However, the previous modified cut standard straw (MCS) which has reported is difficult to immerse into the WS. The aim of this study was to investigate whether the long cut straw (LCS) could be useful as a stable tool for vitrified-warmed human blastocysts. A total of 138 vitrified-warmed cycles were performed between November 2013 and November 2014 (exclusion criteria: women ≥38 years old, poor responder, surgical retrieval sperm, and severe male factor). The artificial shrinkage was conducted using 29-gauge needles. Ethylene glycol and dimethyl sulfoxide (7.5% and 15% (v/v)) were used as cryoprotectants. Freezing and warming were conducted using the LCS tool. The cap of LCS was removed using the forceps in the liquid nitrogen (LN) and then directly immersed into the first WS for 1 min at 37℃ (1 M sucrose). Only re-expanded blastocysts were transferred after it was cultured in sequential media for 18-20 h. A total of 294 blastocysts were warmed, and all were recovered (100%). Two hundred eighty-five embryos were survived (96.9%). The vitrifiedwarmed blastocysts of all patients were transferred without any cancellation. We were able to achieve a reasonable implantation (24.2%), following by clinical pregnancy (36.2%), which then continued to ongoing pregnancy (36.2%), and live birth (31.2%). Using LCS is achieved the acceptable rates of survival, pregnancy and live birth. Therefore, the LCS could be considered as a stable and simple tool for human embryo vitrificaton.
大多数用于玻璃化的商业设备直接浸入解冻液(WS)中以提高解冻速率。然而,先前报道的改良切割标准吸管(MCS)很难浸入WS中。本研究的目的是调查长切割吸管(LCS)是否可作为玻璃化-解冻人类囊胚的稳定工具。2013年11月至2014年11月期间共进行了138个玻璃化-解冻周期(排除标准:年龄≥38岁的女性、反应不良者、手术取精、严重男性因素)。使用29号针进行人工收缩。乙二醇和二甲基亚砜(7.5%和15%(v/v))用作冷冻保护剂。使用LCS工具进行冷冻和解冻。在液氮(LN)中用镊子取下LCS的帽,然后直接浸入37℃的第一种WS中1分钟(1M蔗糖)。只有再膨胀的囊胚在序贯培养基中培养18-20小时后才进行移植。共解冻294个囊胚,全部回收(100%)。285个胚胎存活(96.9%)。所有患者的玻璃化-解冻囊胚均顺利移植。我们能够获得合理的着床率(24.2%),随后是临床妊娠率(36.2%),然后持续到持续妊娠率(36.2%)和活产率(31.2%)。使用LCS可实现可接受的存活率、妊娠率和活产率。因此,LCS可被视为一种稳定且简单的人类胚胎玻璃化工具。