首页> 外文期刊>The Journal of Urology >A noninvasive, motility independent, sperm sorting method and technology to identify and retrieve individual viable nonmotile sperm for intracytoplasmic sperm injection.
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A noninvasive, motility independent, sperm sorting method and technology to identify and retrieve individual viable nonmotile sperm for intracytoplasmic sperm injection.

机译:一种非侵入性,与运动无关的精子分选方法和技术,用于识别和检索用于细胞质内精子注射的单个可行非活动性精子。

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PURPOSE: For intracytoplasmic sperm injection in the absence of sperm motility it can be virtually impossible to distinguish viable from nonviable sperm. A reliable means to identify viable nonmotile sperm is needed and would likely improve the intracytoplasmic sperm injection success rate. Optoelectronic tweezers are a new technology that uses light induced dielectrophoresis fields to distinguish individual live cells from dead cells. We assessed the ability of optoelectronic tweezers to distinguish viable from nonviable individual nonmotile human sperm. MATERIALS AND METHODS: Fresh semen specimens from 6 healthy men were suspended in an isotonic sucrose/dextrose solution and incubated with 0.4% trypan blue dye (Sigma-Aldrich(R)). Within 15 minutes we randomly selected 5 motile and 50 nonmotile sperm, including 25 trypan negative, followed by 25 trypan positive sperm, under 200x magnification for optoelectronic tweezers assay. We recorded the individual sperm response (attraction or repulsion) to the optoelectronic tweezer field and trypan staining status. RESULTS: From each subject 55 unwashed sperm were individually assayed for a total of 330. All motile sperm were attracted to optoelectronic tweezers. Of 150 trypan negative (viable) sperm 132 (88%) were attracted to the optoelectronic tweezer field with 0.88 sensitivity (95% CI 0.82-0.93) vs that of the trypan blue assay. All 150 trypan positive (nonviable) sperm were repulsed by or neutral to the optoelectronic tweezer field with 1.0 specificity (95% CI 0.98-1.00) vs that of the trypan blue assay. Type I error equaled 0 and overall assay agreement was 94%. CONCLUSIONS: The optoelectronic tweezer assay can distinguish viable from nonviable nonmotile viable sperm with sensitivity comparable to that of the trypan blue assay and equal specificity. Optoelectronic tweezers are a promising means of selecting sperm for intracytoplasmic sperm injection.
机译:目的:对于在没有精子活动力的情况下进行胞浆内精子注射,实际上不可能将有活力和无活力的精子区分开。需要一种可靠的方法来鉴定存活的非活动性精子,这可能会提高胞浆内精子注射的成功率。光电镊子是一种新技术,它利用光诱导介电电泳场来区分单个活细胞和死细胞。我们评估了光电镊子区分存活和不存活的个体非活动性人类精子的能力。材料与方法:将来自6名健康男性的新鲜精液标本悬浮在等渗蔗糖/葡萄糖溶液中,并与0.4%台盼蓝染料(Sigma-Aldrich®)孵育。在15分钟内,我们在200倍放大倍率下随机选择5个活动精子和50个非活动精子,包括25个锥虫阴性精子,然后选择25个锥虫阳性精子进行光电镊子测定。我们记录了单个精子对光电镊子场和锥虫染色状态的反应(吸引或排斥)。结果:每个受试者分别对55个未清洗的精子进行了总含量为330的分析。所有活动精子都被光电镊子吸引。与锥虫蓝测定法相比,在150个锥虫阴性(活菌)精子场中,有132个(88%)精子以0.88灵敏度(95%CI 0.82-0.93)被吸引到光电镊子场中。相对于锥虫蓝测定法,1.0特异性(95%CI 0.98-1.00)将所有150个锥虫阳性(不活菌)精子排斥或中性至光电镊子场。 I型错误等于0,总分析一致性为94%。结论:光镊法可将活精子与不活精子区分开,其灵敏度与锥虫蓝法相当,且特异性相同。光电镊子是选择用于细胞质内精子注射的精子的有前途的手段。

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