1. Field of the Invention
The present invention relates to a cell separation device and a cell separation method.
This application is based on Japanese Patent Application Nos. 2007-213922, and 2008-197043, the content of which is incorporated herein by reference.
2. Description of Related Art
Heretofore, techniques for separating particles using differences in their dielectrophoretic properties have been known (for example, see PCT International Publications Nos. WO1997/34689 Pamphlet, WO2001/5512 Pamphlet, WO2001/5513 Pamphlet, and WO2001/5514 Pamphlet).
According to a technique disclosed in PCT International Publication No. WO1997/34689 Pamphlet, a plurality of traps formed of flat electrodes is disposed in a flow path, beads covered with antibodies which particularly adsorb certain bacteria are supported on the electrodes, and an effluent to be analyzed is made to flow through the flow path, so that bacteria approaching the vicinities of the electrodes are collected by the beads using dielectrophoretic properties.
According to a technique disclosed in PCT International Publication No. WO2001/5512 Pamphlet, a flow path is formed in which a plurality of wave-shaped electrodes is arranged, and plural types of particles are made to flow in the electrode arrangement direction, so that the particles are separated using the difference in dielectrophoretic properties.
According to a technique disclosed in PCT International Publication No. WO2001/5513 Pamphlet, after particles are transferred by application of ultrasonic waves, an electric field is applied so as to separate the particles by means of dielectrophoresis.
According to a technique disclosed in PCT International Publication No. WO2001/5514 Pamphlet, particles are separated by applying an electric field having at least two wavelengths so that a plurality of dielectrophoretic forces acts on the particles.
According to the technique disclosed in PCT International Publication No. WO1997/34689 Pamphlet, bacteria are quantitatively measured by the steps of preparing an analytical chamber at a downstream side in a flow path, measuring dielectrophoretic properties of beads before the bacteria are collected, separating beads that collect certain bacteria from the electrodes, and sending the beads thus separated into an analytical chamber for measurement to determine the difference in properties from beads that collect no bacteria; hence the process of this technique is disadvantageously complicated.
In addition, according to the technique disclosed in PCT International Publication No. WO 2001/5512 Pamphlet, in order to separate the particles flowing in the electrode arrangement direction, the wave-shaped electrodes must be used; hence, the device is complicated and expensive, and in addition, inconveniently, the separation cannot be efficiently performed.
In addition, the technique disclosed in PCT International Publication No. WO 2001/5513 Pamphlet disadvantageously requires additional energy such as ultrasonic waves.
Furthermore, the technique disclosed in PCT International Publication No. WO 2001/5514 Pamphlet is disadvantageously complicated since an electric field having two wavelengths is used.
The present invention has been conceived in consideration of the above-described situation, and an object of the present invention is to provide a cell separation device and a cell separation method that can efficiently separate plural types of cells having different dielectrophoretic properties using a simple structure.
In order to accomplish the above object, the present invention provides the following solutions.
According to a first aspect of the present invention, there is provided a cell separation device comprising: a flow path through which a cell suspension flows, the cell suspension containing plural types of cells which have different dielectrophoretic properties; electrodes disposed to face each other in a direction intersecting a flow direction of the cell suspension flowing in the flow path; an electric field gradient forming portion which generates an electric field strength gradient between the electrodes; and a power supply applying an alternating voltage having a direct current component across the electrodes.
According to the first aspect of the present invention, when an alternating voltage having a direct current component is applied across the electrodes by operation of the power source, an electric field having an electric field strength gradient is formed between the electrode by the operation of the electric field gradient forming portion, and in addition, charges are unevenly distributed at one electrode side due to the direct current component included in the alternating voltage. That is, the plural types of cells contained in the cell suspension all receive an electrophoretic force caused by the uneven distribution of charges. On the other hand, cells having negative dielectrophoretic properties contained in the cell suspension receive a dielectrophoretic force in the direction along which the electric field strength decreases, and cells having positive dielectrophoretic properties receive a dielectrophoretic force in the direction along which the electric field strength increases. In addition, a dielectrophoretic force is not applied to cells having no dielectrophoretic properties, such as dead cells, but only the electrophoretic force is applied thereto.
Accordingly, dielectrophoretic forces having different directions and an electrophoretic force can be applied to cells having different dielectrophoretic properties, and by maintaining an appropriate balance therebetween, the cells having different dielectrophoretic properties can be effectively separated from each other.
That is, for example, when the direction in which a negative dielectrophoretic force acts is set opposite to the direction in which an electrophoretic force acts, a relatively small force obtained by counteraction between the dielectrophoretic force and the electrophoretic force can be applied to cells having negative dielectrophoretic properties, and on the other hand, a relatively large force formed of only the electrophoretic force can be applied to cells having no dielectrophoretic properties. Hence, cells having no dielectrophoretic properties are attracted by the electrophoretic force, and cells having negative dielectrophoretic properties are made to flow along the flow direction, so that the cell separation can be performed.
In the above first aspect of the present invention, the electric field gradient forming portion may be an insulating member which has at least one opening and which is disposed between the electrodes.
With the above structure, the electric lines of force formed between the electrodes can be squeezed by the insulating member so as to pass through the opening, and an electric field having an electric field strength gradient can be easily formed between the electrodes.
In addition, in the above first aspect of the present invention, the electrodes may be parallel plate electrodes which form an electric field having an approximately uniform electric field strength.
With the above structure, according to the combination between the electrodes having a simple structure and the insulating plate, an electric field having an electric field strength gradient can be more easily formed between the electrodes.
In addition, in the above first aspect of the present invention, the electric field gradient forming portion may be constructed by forming one of the electrodes smaller than that of the other electrode.
With the above structure, by changing the density of the electric lines of force from the large electrode to the small electrode, an electric field having an electric field strength gradient can be easily formed.
In addition, according to a second aspect of the present invention, there is provided a cell separation method comprising the steps of: making a cell suspension containing plural types of cells having different dielectrophoretic properties flow in a flow path; and applying an alternating voltage including a direct current component across electrodes which faces each other in a direction intersecting a flow direction of the cell suspension flowing in the flow path to form an electric field having an electric field strength gradient between the electrodes.
According to the above second aspect of the present invention, when an alternating voltage including a direct current component is applied across the electrodes, an electric field having an electric field strength gradient is formed between the electrodes, and at the same time, charges are unevenly distributed at one electrode side due to the direct current component included in the alternating voltage. That is, all types of cells contained in the cell suspension receive an electrophoretic force caused by the uneven distribution of charges. On the other hand, cells having negative dielectrophoretic properties contained in the cell suspension receive a dielectrophoretic force in the direction along which the electric field strength decreases, and cells having positive dielectrophoretic properties receive a dielectrophoretic force in the direction along which the electric field strength increases. In addition, to cells having no dielectrophoretic properties, such as dead cells, a dielectrophoretic force is not applied, but only the electrophoretic force is applied.
Accordingly, dielectrophoretic forces having different directions and an electrophoretic force can be applied to cells having different dielectrophoretic properties, and by maintaining an appropriate balance therebetween, the cells having different dielectrophoretic properties can be effectively separated from each other.
The present invention provides an advantage in that plural types of cells having different dielectrophoretic properties can be effectively separated with a simple structure.
A cell separation device 1 according to one embodiment of the present invention will be described with reference to
The cell separation device 1 according to this embodiment includes, as shown in
The flow path 2 is divided by the electrically insulating plate 4 into a first flow path 2a and a second flow path 2b, both of which extend in a flowing direction.
The electrodes 3a and 3b are, for example, parallel plate electrodes and are disposed on facing wall surfaces of the flow path 2 to face each other in the direction perpendicular to a flow direction L.
In addition, the insulating plate 4 is formed to have a flat plate shape, is disposed at a central position of a space formed between the electrodes 3a and 3b, and has at least one through-hole (opening) 4a.
Hence, the first flow path 2a and the second flow path 2b communicate with each other via the through-hole 4a formed in the insulating plate 4.
Accordingly, since electric lines of force C generated from one side to the other side between the electrodes 3a and 3b by operating the power source 5 are blocked by the insulating plate 4, the electric lines of force C pass only through the through-hole 4a formed in the insulating plate 4, as shown in
The power source 5 is, as shown in
A cell separation method using the cell separation device 1 according to this embodiment, having the structure as described above, will now be described.
In order to separate the plural types of cells A and B having different dielectrophoretic properties using the cell separation device 1 according to this embodiment, an alternating voltage is applied across the electrodes 3a and 3b by operating the power source 5 to form the electric lines of force C, as shown in
In the state described above, a cell-suspension liquid containing the plural types of cells A and B having different dielectrophoretic properties is made to flow in the first flow path 2a. In this case, for example, the cell-suspension liquid is made to flow through the first flow path 2a between the minus (−) side electrode 3a and the insulating plate 4, and a medium containing no cells A and B is made to flow through the second flow path 2b between the plus (+) side electrode 3b and the insulating plate 4. The flow velocities of the cell-suspension liquid and the medium are set sufficiently slow.
Once the cells A having negative dielectrophoretic properties reach an area between the electrodes 3a and 3b, due to an electric field having an electric field strength gradient formed between the electrodes 3a and 3b, the cells A receive a dielectrophoretic force f1 in the direction along which the electric field strength decreases, as shown in
On the other hand, since the dielectrophoretic force f1 is not applied to the cells B having no dielectrophoretic properties, the electrophoretic force f2 is only applied to the cells B. As a result, due to the electrophoretic force f2, the cells B are attracted by the plus (+) side electrode 3b and flow into the second flow path 2b through the through-hole 4a formed in the insulating plate 4.
That is, by operating the power source 5, the amplitude and frequency of the alternating voltage applied across the electrodes 3a and 3b are adjusted so as to adjust the dielectrophoretic force f1 applied to the cells A having dielectrophoretic properties, and the absolute value of the direct current component included in the alternating voltage is adjusted so as to adjust the electrophoretic force f2 applied to the cells A and B. Accordingly, when the sum of the dielectrophoretic force f1 and the electrophoretic force f2 applied to the cells A, and the electrophoretic force f2 applied to the cells B are appropriately adjusted, it is possible to form a flow of the cells A flowing in the first flow path 2a without being interrupted and a flow of the cells B introduced into the second flow path 2b by being attracted by the electrode 3b, as shown in
As described above, according to the cell separation device 1 and the cell separation method of this embodiment, by adopting the structure in which only the parallel plate electrodes 3a and 3b and the insulating plate 4 are disposed in the flow path 2 through which the cell-suspension liquid flows, it is possible to obtain an advantage in that the plural types of cells A and B having different dielectrophoretic properties can be efficiently separated from each other.
In this embodiment, although at least one through-hole 4a is provided in the insulating plate 4 which is disposed between the electrodes 3a and 3b, the number of the through-holes 4a is not particularly limited. In addition, the shape, arrangement, and intervals of the through-holes 4a may be arbitrarily determined as long as a sufficient electric field gradient can be formed.
In addition, although the insulating plate 4 is disposed at the central position of the space formed between the parallel plate electrodes 3a and 3b, instead of this arrangement, as shown in
Hereinafter, an Example using the cell separation device 1 shown in
As the electrodes 3a and 3b, a pair of flat plate-shaped electrodes 3a and 3b made of titanium having a thickness of 1 mm was used. The space between the electrodes 3a and 3b was set to approximately 1 mm. In addition, as the insulating plate 4, a Kapton film having a thickness of 50 μm was used. In addition, as the through-hole 4a formed in the insulating plate 4, a hole having a diameter of approximately 100 μm was formed.
In addition, instead of the cells A and B having different dielectrophoretic properties, particles D made of polystyrene beads having a diameter of approximately 10 μm were used.
As the alternating voltage, sine waveform voltages having amplitudes of 1, 1.2, and 1.5 V, a direct current component of 0 to 3 V, and frequencies of 10 kHz, 100 kHz, 500 kHz, 1 MHz, 5 MHz, and 10 MHz were used.
The results are shown in
At all amplitudes, since the value of a necessary direct current component was maximized in the vicinity of a frequency of 1 MHz, it was understood that a large electrophoretic force f2 was applied to the particles D. Hence, in the vicinity of a frequency of 1 MHz, it was understood that a large dielectrophoretic force f1 counteracting the large electrophoretic force f2 was exerted.
As a result, by adjusting the amplitude and the direct current component of the alternating voltage, the particles D are made to migrate toward the electrode 3a by the electrophoretic force f2, and particles D to which the dielectrophoretic force f1 is applied continue to flow in the same way or are made to migrate in the opposite direction, so that separation can be performed.
In addition, in the above embodiment, by covering the surface of the electrode 3a with the insulating plate 4, only the portion exposed through the through-hole 4a was used as the electrode 3a; however, an electrode (not shown) having a small area similar to that of the through-hole 4a may be employed from the beginning.
Next, another Example using the cell separation device 1 shown in
As the device conditions, the distance between the electrodes 3a and 3b was set to approximately 1.2 mm, and as the insulating plate 4, a plate having a thickness of 0.2 mm was used. The width of the flow path 2 was set to 0.5 mm (the width of the flow path 2a and that of the flow path 2b were each set to 0.5 mm), and as the through-hole 4a formed in the insulating plate 4, a hole having a diameter of approximately 0.2 mm was used.
As living cells and dead cells, 3-2H3 cells on the second day of culture were used, and as a bulk liquid, a mixture of an aqueous solution containing 8.5 percent by weight of sucrose and an aqueous solution containing 0.3 percent by weight of glucose was used.
In addition, still another Example using a cell separation device 111 shown in
As the device conditions, in the cell separation device 111 having a width of 12 mm, a length of 90 mm, and a height of 30 mm, the distance between the electrodes 3a and 3b was set to approximately 1.2 mm, and as the insulating plate 4, a plate having a thickness of 0.2 mm was used. The number of holes was set to approximately 1,000, and as the through-hole 4a formed in the insulating plate 4, a hole having a diameter of approximately 0.2 mm was used. In the arrangement shown in
As shown in
The flow rates of the cell-suspension liquid, bulk liquid, retention liquid, and transmission liquid were set to 0.3, 0.3, 0.2, and 0.4 ml/minute, respectively.
As the living cells and the dead cells, 3-2H3 cells on the second day after culture at a concentration of 5.0×105 cells/ml were each used, and as the bulk liquid, a mixture of an aqueous solution containing 8.5 percent by weight of sucrose and an aqueous solution containing 0.3 percent by weight of glucose was used.
As shown in
Number | Date | Country | Kind |
---|---|---|---|
2007-213922 | Aug 2007 | JP | national |
2008-197043 | Jul 2008 | JP | national |