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利用血小板聚集仪计算血浆纤维蛋白纤维的质量-长度比

Calculation of plasma fibrin fiber mass-length ratios utilizing platelet aggregometers.

作者信息

Carr M E, Zekert S L

机构信息

Department of Medicine, Medical College of Virginia, Richmond 23298.

出版信息

Thromb Res. 1990 Jul 1;59(1):183-94. doi: 10.1016/0049-3848(90)90283-i.

DOI:10.1016/0049-3848(90)90283-i
PMID:2399528
Abstract

We report a technique for measuring plasma gel fiber size utilizing optical platelet aggregometers. Three aggregometers were used to measure gelation kinetics and final gel turbidity: Sienco Model DP247E, Bio-Data Model PAP-2A, and Chrono-log Model 500-VS aggregometer. Each aggregometer was calibrated using dilutions of latex microspheres. Optical densities of microsphere solutions were measured at 626, 670 and 945 nm. Calibration curves were plots of aggregometer readings versus absorbance. Gels of various fiber size were prepared by varying thrombin concentrations and ionic strength. Fiber mass-length ratios were calculated from the wavelength dependence of gel turbidity. Gel optical densities at 640 nm and 945 nm were shown to be linear functions of fiber mass-length ratio. Aggregometer study gels were formed directly in aggregometer cuvettes. Gel formation kinetics were easily measured in the Sienco and Chrono-log instruments. Gelation kinetics in the Bio-Data instrument did not allow measurement of maximum turbidity. The latter value could be measured, however, once gelation was complete. Final aggregometer readings were made one hour after thrombin addition, and were converted to absorbance values using calibration curves. Absorbencies were then converted to mass-length ratios using the optical density versus mass-length ratio plots. Fiber mass-length ratios measured with aggregometers were in good agreement with those measured spectrophotometrically. This technique may allow routine quantification of plasma clot structure utilizing equipment ordinarily available in clinical laboratories.

摘要

我们报告了一种利用光学血小板凝集仪测量血浆凝胶纤维大小的技术。使用三台凝集仪来测量凝胶化动力学和最终凝胶浊度:Sienco 型号 DP247E、Bio-Data 型号 PAP-2A 和 Chrono-log 型号 500-VS 凝集仪。每台凝集仪都使用乳胶微球稀释液进行校准。在 626、670 和 945 nm 处测量微球溶液的光密度。校准曲线是凝集仪读数与吸光度的关系图。通过改变凝血酶浓度和离子强度制备了各种纤维大小的凝胶。根据凝胶浊度的波长依赖性计算纤维质量-长度比。结果表明,640 nm 和 945 nm 处的凝胶光密度是纤维质量-长度比的线性函数。凝集仪研究用的凝胶直接在凝集仪比色皿中形成。在 Sienco 和 Chrono-log 仪器中很容易测量凝胶形成动力学。Bio-Data 仪器中的凝胶化动力学不允许测量最大浊度。然而,一旦凝胶化完成,就可以测量该值。在加入凝血酶一小时后读取最终凝集仪读数,并使用校准曲线将其转换为吸光度值。然后使用光密度与质量-长度比的关系图将吸光度转换为质量-长度比。用凝集仪测量的纤维质量-长度比与用分光光度法测量的结果非常一致。该技术可能允许利用临床实验室通常可用的设备对血浆凝块结构进行常规定量。

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