Erythrocyte aggregability from human, horse, and rat blood by ultrasound backscattering measurements
A pulse-echo system was used in a cylindrical chamber with a stirring magnet and a 5-MHz focused transducer for studying erythrocyte aggregation from human, horse, and rat blood. The highest backscattering power was measured from horse blood and followed by human and rat blood both at stasis and und...
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Veröffentlicht in: | The Journal of the Acoustical Society of America 2006-11, Vol.120 (5_Supplement), p.3112-3113 |
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creator | Nam, Kwon-Ho Paeng, Dong-Guk Bok, Tae-Hoon Choi, Min Joo |
description | A pulse-echo system was used in a cylindrical chamber with a stirring magnet and a 5-MHz focused transducer for studying erythrocyte aggregation from human, horse, and rat blood. The highest backscattering power was measured from horse blood and followed by human and rat blood both at stasis and under shear forces. In human and horse blood, the backscattered power (BP) was decreased with stirring speed and saturated within 1 min. The BP was increased to 20 dB when blood flow was stopped. Since the aggregation of rat erythrocytes in autologous plasma is very low and barely detectable by the ultrasound BP, rat plasma was replaced by phosphate buffered saline containing polyvinylpyrrolidone 360 in order to enhance the aggregation. In conclusion, this simple in vitro ultrasound measurement system requires a small amount of blood, which may provide an alternative method to investigate the mechanisms and physiological roles of erythrocyte aggregation. Furthermore, the rat erythrocytes in polymer solution may be useful for an automatic measurement system to examine the bioactive materials that affect aggregation in preclinical studies. |
doi_str_mv | 10.1121/1.4787608 |
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The highest backscattering power was measured from horse blood and followed by human and rat blood both at stasis and under shear forces. In human and horse blood, the backscattered power (BP) was decreased with stirring speed and saturated within 1 min. The BP was increased to 20 dB when blood flow was stopped. Since the aggregation of rat erythrocytes in autologous plasma is very low and barely detectable by the ultrasound BP, rat plasma was replaced by phosphate buffered saline containing polyvinylpyrrolidone 360 in order to enhance the aggregation. In conclusion, this simple in vitro ultrasound measurement system requires a small amount of blood, which may provide an alternative method to investigate the mechanisms and physiological roles of erythrocyte aggregation. 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title | Erythrocyte aggregability from human, horse, and rat blood by ultrasound backscattering measurements |
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