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Platelet aggregation using a microfluidics device

A technology of platelet aggregation and microfluidics, applied in the direction of using thermal variables to measure fluid velocity, applying thermal effects to detect fluid flow, fluid controllers, etc.

Inactive Publication Date: 2012-02-08
MONASH UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the exact mechanism by which rheology accelerates the atherosclerotic process is still not fully understood

Method used

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  • Platelet aggregation using a microfluidics device
  • Platelet aggregation using a microfluidics device
  • Platelet aggregation using a microfluidics device

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0232] Example 1 Blood Perfusion Through Step Geometry

[0233] Figure 11 a A series of representative photomicrographs (40× magnification) of human (hirudin-anticoagulated) blood perfusion through a microshear gradient device consisting of 100 μm inflow (entrance) width, 90° constriction angle θ c , 10μm gap height, 60° expansion angle θ e , 700μm expansion / exit width composition. The gray arrows indicate the initial aggregation point [t=12sec], and the black arrows indicate the extent of thrombus growth in the expanded area (n=3 experiments).

[0234] Figure 11 b is the result (velocity v displacement (displacement) diagram) obtained from the computational fluid dynamics (CFD) simulation, showing that the platelet (particle) moves 1 μm (1 / 2 the disc platelet diameter) from the surface of the microchannel wall geometry in (a) ) changes in speed. For linear microchannel part (1,800.s -1 In laminar flow), the platelets move at a uniform velocity throughout their path le...

example 2

[0239] Example 2 The flow rate dependency of the interaction of two step geometries

[0240] Figure 12a Included are representative aggregation records depending on flow rate (Q = 2, 4, 6, 8 μl / min) through a microshear gradient device consisting of 100 μm inflow / inlet width, 90° constriction angle (θ c ), 20μm gap height, 30° expansion angle (θ e ), 700 μm expansion / exit width composition.

[0241] Figure 12b For representative aggregation recordings, depending on flow rate (Q = 2, 4, 6, 8 μl / min) through a microshear gradient device consisting of 100 μm inflow width and 90° constriction angle θ c , 20μm gap height, 90° expansion angle θ e , consisting of 700 μm expansion width.

[0242] Analysis of the dependence of flow rate (Q = 2, 4, 6, 8 μl / min) was detected in two step geometry configurations with divergence angles of 30° and 90° (see respectively Figure 12a and Figure 12b ). In both geometry configurations, the size of the aggregates decreased significantly...

example 3

[0243] Example 3 spherical geometry

[0244] Figure 13a includes a DIC image box, showing the use of 10,000.s -1 γ Nature and extent of discoid platelet aggregation on the downstream side of the VWF-coated spherical geometry after perfusion of human whole blood (pretreated with 100 μM MRS2179, 10 μM 2-MeSAMP, and 10 μM indomethacin) (n=5).

[0245] Figure 13b shows the size of the average discoid platelet aggregate (surface area in μm 2 denoted), depending on the downstream low τ x,y Pit (surface area of ​​zone 3 in μm 2 Indicates), showing τ≤30.4Pa (n=3).

[0246] Figure 13c is using 10,000.s -1 γ, size of disc-shaped platelet aggregates on the downstream face of the spherical geometry coated with 5 μm VWF; control, hirudin anticoagulated whole blood; anti-α IIb beta 3 , hirudin anticoagulated whole blood treated with 30 μg / ml c7E3Fab for 10 minutes before blood perfusion; anti-GPIb, hirudin anticoagulated whole blood treated with 50 μg / ml anti-GPIb blocking IgGALMA12 f...

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Abstract

A microfluidics device to provide real time monitoring of platelet aggregation of a biological sample obtained from a subject. The device comprises a channel configured for passage of the biological sample, the channel comprising a protrusion configured to induce an upstream region of shear acceleration coupled to a downstream region of shear deceleration and defining there-between a region of peak rate of shear, the downstream region of shear deceleration defining a zone of platelet aggregation. The device further comprises a platelet detection means for detecting aggregation of platelets in the zone of aggregation as a result of passage of the biological sample through the channel. Methods to assess real time platelet aggregation of a biological sample obtained from a subject are further described.

Description

[0001] Cross References to Related Applications [0002] This application claims priority to Australian Provisional Patent Application No 2009901033, filed 10 March 2009, and Provisional Australian Patent Application No 2009905303, filed 29 October 2009, the contents of which are incorporated herein by reference. technical field [0003] The present invention relates to a device that facilitates the analysis of aggregation of platelets or their progenitors in biological samples. The device induces disturbances in the local control of blood flow leading to spatially controlled platelet aggregation. The present invention also relates to a method of aggregating platelets at known sites for diagnosis of platelet function and activity. The present invention also relates to a method of controllably modulating the rate and extent of platelet aggregation. The method of the present invention is particularly useful for assessing whether there is abnormality in platelet function of a s...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01L3/00B81B1/00
CPCB01L3/502707B01L3/502746B01L3/502761B01L3/502776B01L2300/0654B01L2300/1827B01L2400/0457B01L2400/0475B01L2400/086G01N21/82
Inventor A·D·米切尔F·J·托瓦尔洛佩斯S·P·杰克逊W·S·内斯比特J·卡伯里
Owner MONASH UNIV