首页> 外国专利> METHOD OF MICROSCOPIC DIAGNOSTICS OF SPERM QUALITY AFTER EJACULATE SEDIMENTATION

METHOD OF MICROSCOPIC DIAGNOSTICS OF SPERM QUALITY AFTER EJACULATE SEDIMENTATION

机译:精子沉积后精子质量的显微诊断方法

摘要

FIELD: medicine.;SUBSTANCE: invention relates to the field of medicine and medical diagnostics. Method of microscopic diagnosis of the quality of sperm after sedimentation of the ejaculate, including the selection of cells from the sediment of ejaculate (SE), the preparation of cytological preparations from selected SE cells with placement on slides, is disclosed, drying and staining of preparations, the subsequent count of the number, evaluation of various cell types and comparison with the data of the control group to obtain a conclusion. At the same time, before taking a diagnostic material, they provoke an inflammatory process for the subsequent detection of an infectious agent; SE is obtained by sedimentation of ejaculate; for this purpose, ejaculate is incubated for 20–30 minutes in a thermostat at a temperature of 37 °C until complete liquefaction, the portion is transferred to a graduated centrifuge tube; centrifugation is carried out at 1,000–1,500 rpm for 15–20 minutes; using a pipette, the supernatant is separated without trapping sediment from the bottom; the preparation is prepared using an automatic dosing pipette, which is taken 10 mcl of the prepared SE in such a way that the smear covers an area of 1/3–2/3 of the glass slide, while using slides with high adhesion; drying of the preparation is carried out in a thermostat for 15–20 minutes in conditions of high humidity and at a temperature of 37 °C. Cells are counted and evaluated using a microscope, adjusting its optical magnification.;EFFECT: invention makes it possible to identify malignant findings, to increase the diagnostic value of the biomaterial, to conduct a comprehensive microscopic study and to improve the accuracy of the study.;4 cl, 25 dwg
机译:技术领域本发明涉及医学和医学诊断领域。显微诊断精子沉淀后精子质量的方法,包括从精子沉淀物中选择细胞(SE),从选定的SE细胞上放置载玻片制备细胞学制剂,并进行干燥和染色准备,随后的计数,评估各种细胞类型并与对照组数据进行比较以获得结论。同时,在服用诊断材料之前,它们会引发炎症过程,随后检测出传染源。 SE通过射精的沉淀获得;为此,将射精在温度为37°C的恒温器中孵育20–30分钟,直到完全液化,然后将其转移到带刻度的离心管中;在1,000–1,500 rpm下离心15–20分钟;使用移液器分离上清液,而不会从底部捕获沉淀物。使用自动定量移液器制备制剂,该移液器以准备好的SE的10毫升作为剂量,以使涂片覆盖载玻片的1 / 3–2 / 3区域,同时使用具有高附着力的载玻片;在高湿度和37°C的温度下,将制剂在恒温器中干燥15至20分钟。使用显微镜对细胞进行计数和评估,调整其光学放大倍数。效果:本发明使识别恶性发现,增加生物材料的诊断价值,进行全面的显微镜研究和提高研究准确性成为可能。 ; 4 cl,25载重吨

著录项

  • 公开/公告号RU2686685C1

    专利类型

  • 公开/公告日2019-04-30

    原文格式PDF

  • 申请/专利权人 SAPOZHKOVA ZHANNA YUREVNA;

    申请/专利号RU20180106318

  • 发明设计人 SAPOZHKOVA ZHANNA YUREVNA (RU);

    申请日2018-02-20

  • 分类号G01N33/48;C12Q1/06;G01N1/28;

  • 国家 RU

  • 入库时间 2022-08-21 11:46:14

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