Avtor/Urednik		Blinc, Aleš; Francis, Charles W; Trudnowski, Janet L; Carstensen, Edwin L
Naslov		Characterization of ultrasound-potentiated fibrinolysis in vitro
Tip		članek
Vir		Blood
Vol. in št.		Letnik 81, št. 10
Leto izdaje		1993
Obseg		str. 2636-43
Jezik		eng
Abstrakt		We have characterized the effects of ultrasound on fibrinolysis in vitro to investigate the mechanism of ultrasonic potentiation of fibrinolysis and to identify potentially useful ultrasound parameters for therapeutic application. Radiolabeled clots in thin walled tubes were exposed to ultrasound fields in a water bath at 37 degrees C, and lysis was measured by solubilization of radiolabel. Ultrasound accelerated lysis of plasma, whole blood, and purified fibrin clots mediated by recombinant tissue-type plasminogen activator (rt-PA), urokinase, or streptokinase, but ultrasound by itself caused no clot solubilization. The degree of ultrasonic potentiation was dependent on plasminogen activator concentration, increasing from 2.2-fold at a streptokinase concentration of 75 U/mL to 5.5-fold at 250 U/mL in a 1 MHz ultrasound field at 4 W/cm2. Ultrasound exposure resulted in heating due to absorption by the plastic tube, but the temperature increase was insufficient to account for the increase in clot lysis rate, indicating that the primary effect was nonthermal. Ultrasound did not accelerate hydrolysis of a peptide substrate by rt-PA and did not alter the rate of plasmic degradation of fibrinogen, indicating that the augmentation of enzymatic fibrinolysis required the presence of a fibrin gel. The acceleration of fibrinolysis by ultrasound was greater at higher intensities and duty cycles and was maximum at frequencies between 1 and 2.2 MHz, but decreased at 3.4 MHz. These findings suggest that ultrasound accelerates enzymatic fibrinolysis by increasing transport of reactants through a cavitation-related mechanism.
Deskriptorji		BLOOD COAGULATION FIBRINOLYSIS ULTRASONICS UROKINASE ALTEPLASE CHROMOGENIC COMPOUNDS KINETICS OLIGOPEPTIDES RECOMBINANT PROTEINS STREPTOKINASE SUBSTRATE SPECIFICITY THERMODYNAMICS TIME FACTORS