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Development of Cheaper Embryo Vitrification Device Using the Minimum Volume Method

机译:使用最小体积方法开发便宜的胚胎玻璃化装置

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摘要

This study was designed to compare the efficiency of the Cryotop and Calibrated plastic inoculation loop (CPIL) devices for vitrification of rabbit embryos on in vitro development and implantation rate, offspring rate at birth and embryonic and fetal losses. CPIL is a simple tool used mainly by microbiologists to retrieve an inoculum from a culture of microorganisms. In experiment 1, embryos were vitrified using a Cryotop device and a CPIL device. There were no significant differences in hatched/hatching blastocyst stage rates after 48 h of culture among the vitrified groups (62±4.7% and 62±4.9%, respectively); however, the rates were significantly lower (P<0.05) than those of the fresh group (95±3.4%). In experiment 2, vitrified embryos were transferred using laparoscopic technique. The number of implanted embryos was estimated by laparoscopy as number of implantation sites at day 14 of gestation. At birth, total offspring were recorded. Embryonic and fetal losses were calculated as the difference between implanted embryos and embryos transferred and total born at birth and implanted embryos, respectively. The rate of implantation and development to term was similar between both vitrification devices (56±7.2% and 50±6.8% for implantation rate and 40±7.1% and 35±6.5% for offspring rate at birth); but significantly lower than in the fresh group (78±6.6% for implantation rate and 70±7.2% for offspring rate at birth, P<0.05). Likewise, embryonic losses were similar between both vitrification devices (44±7.2% and 50±6.8%), but significantly higher than in the fresh group (23±6.6%, P < 0.05). However, fetal losses were similar between groups (10±4.4%, 15±4.8% and 8±4.2%, for vitrified, Cryotop or CPIL and fresh, respectively). These results indicate that the CPIL device is as effective as the Cryotop device for vitrification of rabbit embryos, but at a cost of €0.05 per device.
机译:本研究旨在比较冷冻冷冻和校准塑料接种环(CPIL)设备对兔胚胎进行玻璃化的效率,包括体外发育和着床率,出生时的后代率以及胚胎和胎儿的流失。 CPIL是一种简单的工具,主要供微生物学家用于从微生物培养物中获取接种物。在实验1中,使用Cryotop设备和CPIL设备将胚胎玻璃化。在玻璃化组中培养48 h后的孵化/孵化胚泡阶段率没有显着差异(分别为62±4.7%和62±4.9%);但是,该比率显着低于新鲜组(95±3.4%)(P <0.05)。在实验2中,使用腹腔镜技术转移玻璃化的胚胎。通过腹腔镜估计植入的胚胎的数目作为妊娠第14天的植入部位的数目。出生时,记录了全部后代。胚胎损失和胎儿损失的计算方法分别是植入的胚胎与移植的胚胎和出生时的总出生人数以及植入的胚胎之间的差异。两种玻璃化装置的足月植入和发育率相似(植入率分别为56±7.2%和50±6.8%,出生时的后代率为40±7.1%和35±6.5%);但显着低于新鲜组(出生时植入率为78±6.6%,后代出生率为70±7.2%,P <0.05)。同样,两个玻璃化装置之间的胚胎损失相似(44±7.2%和50±6.8%),但明显高于新鲜组(23±6.6%,P <0.05)。然而,两组之间的胎儿损失相似(玻璃化,Cryotop或CPIL和新鲜的分别为10±4.4%,15±4.8%和8±4.2%)。这些结果表明,CPIL装置与Cryotop装置对兔胚胎玻璃化的效果相同,但每个装置的成本为€0.05。

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