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首页> 外文期刊>Reproductive biomedicine online >In-vitro development of vitrified-warmed bovine oocytes after activation may be predicted based on mathematical modelling of cooling and warming rates during vitrification, storage and sample removal
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In-vitro development of vitrified-warmed bovine oocytes after activation may be predicted based on mathematical modelling of cooling and warming rates during vitrification, storage and sample removal

机译:在激活后,可以基于玻璃化,储存和样品去除期间的冷却和温暖速率的数学建模来预测活化后玻璃化牛卵母细胞的体外发育

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Heat transfer during cooling and warming is difficult to measure in cryo-devices; mathematical modelling is an alternative method that can describe these processes. In this study, we tested the validity of one such model by assessing in-vitro development of vitrified and warmed bovine oocytes after parthenogenetic activation and culture. The viability of oocytes vitrified in four different cryo-devices was assessed. Consistent with modelling predictions, oocytes vitrified using cryo-devices with the highest modelled cooling rates had significantly (P 0.05) better cleavage and blastocyst formation rates. We then evaluated a two-step sample removal process, in which oocytes were held in nitrogen vapour for 15 s to simulate sample identification during clinical application, before being removed completely and warmed. Oocytes exposed to this procedure showed reduced developmental potential, according to the model, owing to thermodynamic instability and devitrification at relatively low temperatures. These findings suggest that cryodevice selection and handling, including method of removal from nitrogen storage, are critical to survival of vitrified oocytes. Limitations of the study include use of parthenogenetically activated rather than fertilized ova and lack of physical measurement of recrystallization. We suggest mathematical modelling could be used to predict the effect of critical steps in cryopreservation. (C) 2018 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
机译:冷却和变暖过程中的热传递难以测量冷冻装置;数学建模是一种可以描述这些过程的替代方法。在这项研究中,我们通过评估单性激活和培养后的玻璃化和温热的牛卵母细胞的体外发育来测试一种这种模型的有效性。评估了四种不同冷冻装置中玻璃化的卵母细胞的可行性。与建模预测,使用具有最高建模冷却率的冷冻装置玻璃化的卵母细胞显着(P <0.05)更好的切割和胚泡形成率。然后,我们评估了两步样品去除过程,其中卵母细胞在氮气中保持为15秒,以模拟临床应用期间的样品鉴定,然后被完全和温热。根据该模型,暴露于该程序的卵母细胞显示出在相对低温下的热力学不稳定性和透过的透明度,发育潜力降低。这些研究结果表明,低温视察选择和处理,包括从氮气储存中去除的方法,对玻璃化卵母细胞的存活至关重要。该研究的局限性包括使用单性激活而不是受精卵,缺乏重结晶的物理测量。我们建议数学建模可用于预测临界步骤在冷冻保存中的效果。 (c)2018年Elsevier Ltd.出版的Everyver Ltd.保留所有权利。

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