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In Vitro Fertilization on a Single-Oocyte Positioning System Integrated with Motile Sperm Selection and Early Embryo Development

机译:单卵母细胞定位系统与能动精子选择和早期胚胎发育相结合的体外受精

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摘要

In vitro fertilization (IVF) technology has been broadly applied to solve human infertility in recent years. However, the physical tools for IVF remain unchanged over several decades before microfluidic technology was introduced in this field. Here, we report a novel microdevice that integrates each step of IVF, including oocyte positioning, sperm screening, fertilization, medium replacement, and embryo culture. Oocytes can be singly positioned in a 4 X 4 array of octacolumn units. The four symmetrical straight channels, crossing at the oocyte positioning region, allowed efficient motile sperm selection and facilitated rapid medium replacement. The fertilization process and early embryonic development of the individual zygote was traced with microscopic recording and analyzed by in situ fluorescent staining. The murine sperm motility was increased from 60.8 +- 3.4percent to 96.1 +- 1.9percent through the screening channels. The embryo growth rate and blastocyst formation were similar between the routine Petri dish group and the microdevice group. The healthy blastocysts developed in the microdevice could be conveniently retrieved through a routine pipetting operation and used for further embryo transfer.
机译:近年来,体外受精(IVF)技术已广泛应用于解决人类不育症。然而,在将微流体技术引入该领域之前,体外受精的物理工具在过去的几十年中一直保持不变。在这里,我们报告了一种新颖的微型设备,该设备整合了IVF的每​​个步骤,包括卵母细胞定位,精子筛选,受精,培养基置换和胚胎培养。卵母细胞可以单独放置在4 X 4八格单位的阵列中。在卵母细胞定位区域交叉的四个对称的直通道允许有效的运动精子选择并促进快速的培养基置换。通过显微镜记录追踪单个合子的受精过程和早期胚胎发育,并通过原位荧光染色进行分析。通过筛选通道,鼠的精子活力从60.8%-3.4%增加到96.1%-1.9%。常规培养皿组和微器械组之间的胚胎生长速率和胚泡形成相似。可以通过常规移液操作方便地取出微设备中发育的健康胚泡,并将其用于进一步的胚胎移植。

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