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Turbidity test for endotoxins - useful for quantitative tests with e.g. biological fluids, drugs and parental compsns

机译:内毒素的浊度测试-用于定量测试,例如生物体液,药物和父母药

摘要

Endotoxin content of an aq. liquid is determined by mixing the liquid with aq. lysate of washed amoebocyte cells from the blood of the horseshoe crab (the lysate is obtd. by water lysing washed amoebocyte cells and is buffered at pH 6.5-6.8). The lysate is of such concn. that u ml. is reactive with 0.1 ml. endotoxin contg. 1 ng/ml to develop, after 60 mins. at 37 degrees C, turbidity that imparts an absorbency between 0.07-0.2 at 360 nm. The mixture is incubated and the absorbence is determined. Qualitative and quantitative test suitable for screening drugs, biological fluids, water samples, parenteral prepns., medical equipment etc. for pyrogens by a simple, effective and reliable method, even with low levels of endotoxins.
机译:水溶液的内毒素含量。通过将液体与水溶液混合来确定液体。 washed血液中洗涤的变形细胞细胞的裂解物(裂解物通过水裂解洗涤的变形细胞细胞而被溶解,并缓冲在pH 6.5-6.8中)。裂解物就是这样的。那你毫升。与0.1毫升反应。内毒素控制60分钟后显影至1 ng / ml。在37摄氏度下,浊度在360 nm下赋予0.07-0.2之间的吸收率。将混合物孵育并测定吸光度。定性和定量测试适用于通过简单,有效和可靠的方法筛查药物,生物液体,水样品,肠胃外制剂,医疗设备等中的热原,即使内毒素水平较低。

著录项

  • 公开/公告号FR2396298B1

    专利类型

  • 公开/公告日1981-06-19

    原文格式PDF

  • 申请/专利权人 WORTHINGTON BIOCHEMICAL CORP;

    申请/专利号FR19770019986

  • 发明设计人

    申请日1977-06-29

  • 分类号G01N33/16;

  • 国家 FR

  • 入库时间 2022-08-22 15:06:20

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