1972
DOI: 10.1159/000213739
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A Simple Device for Measuring Diameters of Fibrinolysis Zones on Fibrin Plates

Abstract: The fibrinolytic activity of a solution is frequently determined by the fibrin plate method, lytic activities of drops being related to the lysed areas in a fibrin layer. A simple device was designed to measure the diameters of fibrinolysis zones. Using the principle of light scattering by the fibrin layer, we could clearly distinguish lysis zones from non-lysed substrate, even from very transparent fibrin. Application of this principle offers the great advantage that zone diameters can be read off directly, r… Show more

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Cited by 5 publications
(4 citation statements)
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“…From each euglobulin fraction, 3 drops of 30 pi each were placed on the different fibrin plates. After incubation at 37 °C for 18 h, two perpendicular diameters of each lysed zone were measured with H averkate's [11] special device. The mean diameters of the lysed zones were used to represent the fibrinolytic activity of the euglobulin fraction.…”
Section: Methodsmentioning
confidence: 99%
“…From each euglobulin fraction, 3 drops of 30 pi each were placed on the different fibrin plates. After incubation at 37 °C for 18 h, two perpendicular diameters of each lysed zone were measured with H averkate's [11] special device. The mean diameters of the lysed zones were used to represent the fibrinolytic activity of the euglobulin fraction.…”
Section: Methodsmentioning
confidence: 99%
“…From each euglobulin fraction, three drops of 30//I each were placed onto the surface of fibrin plates [12]. After incubation of the plates at 37 °C for 18 h on carefully leveled shelves in a Heraeus incubator, type FB 420 (vibratory motions of the incubator being avoided), two perpendicular diameters of each lysed zone were determined with a device especially designed for this purpose [11], The mean of the dia meters was taken as the diameter of the zone. Noncircular zones seldom appeared and were excluded.…”
Section: Introductionmentioning
confidence: 99%
“…Fibrin plates were freshly made each day and left for a few hours before application of the euglobulin solutions, from each of which 30 pi were placed in triplicate on the surface of the fibrin by an adjustable pipette with disposable tips (Finnpipette®, Helsinki). After incubation for 17 h at 37 °C on a level glass plate in a moist incubator (Heraeus B 5060), the activity was determined using as a measure the amount of dissolved fibrin expressed arbitrarily by the product (in mm2) of two perpendicular diameters of the lyzed zones conveniently read by the device described elsewhere [ 17] with a precision of ± 0.5 mm and calculating the mean of the triplicates. Duplicate euglobulin precipitations and assays were made from each plasma sample and the mean was recorded as the final value.…”
Section: Methodsmentioning
confidence: 99%