FLUID SEPARATION SYSTEM AND METHOD WHICH USES MAGNETIC PARTICLES

Abstract

One embodiment relates to a system and method by which the magnetic susceptibility of a fluid is changed to separate the fluid according to differences in magnetic susceptibility. According to one embodiment, a fluid separation system and method can efficiently separate materials contained in a fluid according to magnetic susceptibility, without damage such as hemolysis or without changes in the types or concentrations of marker proteins in plasma.

Claims

1. A fluid separation system comprising: a channel in which fluid is able to flow; one or more inlets; two or more outlets; magnetic particles for imparting paramagnetism to the fluid; a magnet for creating a magnetic field in the channel, wherein fluid flows through the channel to pass through a domain where the magnetic field is created, to thereby separate and discharge the materials contained in the fluid through the two or more outlets according to differences in paramagnetism.

2. The fluid separation system of claim 1, wherein at least one of the two or more outlets comprises a magnetic structure for separating the magnetic particles.

3. The fluid separation system of claim 1, wherein the magnetic particles have attached thereto a detection material capable of specifically binding to a target material contained in the fluid.

4. A fluid separation method comprising: mixing a fluid and magnetic particles to change magnetic susceptibility of the fluid; injecting the fluid into a channel having one or more inlets and two or more outlets; passing the fluid through a domain where a magnetic field is created; and separating the fluid according to difference in magnetic susceptibility to be discharged through the two or more outlets.

5. The fluid separation method of claim 4, wherein the fluid is blood containing blood cells and plasma, and blood cells and plasma are separated by the method.

6. The fluid separation method of claim 4, wherein the channel further has comprised of a magnetic structure for removing the magnetic particles.

7. The fluid separation method of claim 4, wherein the magnetic particles have attached thereto a detection material capable of specifically binding to a target material contained in the fluid.

8. A fluid separation method comprising: mixing a fluid and magnetic particles having attached thereto a detection material capable of specifically binding to a target material contained in the fluid, to thereby change magnetic susceptibility of the fluid; injecting the fluid into a channel having one or more inlets and two or more outlets; passing the fluid through a domain where a magnetic field is created; separating materials contained in the fluid according to difference in magnetic susceptibility to be discharged through the two or more outlets; and separating the magnetic particles from the separated fluid.

9. The fluid separation method of claim 8, wherein the fluid is blood containing blood cells and plasma, blood cells and magnetic particles are separated from the plasma by the method.

10. A method of detecting a target material contained in fluid, the method comprising: mixing a fluid and magnetic particles having attached thereto a detection material capable of specifically binding to a target material contained in the fluid, to thereby change magnetic susceptibility of the fluid; injecting the fluid into a channel having one or more inlets and two or more outlets; passing the fluid through a domain where a magnetic field is created; separating materials contained in the fluid according to difference in magnetic susceptibility to be discharged through the two or more outlets; separating the magnetic particles from the separated fluid; and detecting the target material from the separated magnetic particles.

11. The fluid separation method of claim 9, wherein the fluid is blood.

12. The fluid separation method of claim 10, wherein the target material is at least one biomarker selected from nucleic acids, peptides, cells, viruses, cell-derived materials, and proteins.

13. The fluid separation method of claim 1, wherein the magnetic particles enter into the materials contained in the fluid.

14. The fluid separation method of claim 4 or 8, wherein the magnetic particles enter into the materials contained in the fluid.

15. The fluid separation method of claim 13, wherein the material contained in the fluid is a cell or a microorganism.

16. The fluid separation method of claim 15, wherein the cell or the microorganism included in the fluid is a cell or a microorganism in which at least one of a cell membrane and a cell wall is damaged, or at least one of a cell membrane and a cell wall is highly permeable.

17. The fluid separation method of claim 14, wherein the material contained in the fluid is a cell or a microorganism.

18. The fluid separation method of claim 17, wherein the cell or the microorganism included in the fluid is a cell or a microorganism in which at least one of a cell membrane and a cell wall is damaged, or at least one of a cell membrane and a cell wall is highly permeable.

19. The fluid separation method of claim 13, wherein the fluid separation system is used to diagnose infectious disease.

20. The fluid separation method of claim 14, wherein the method is used to diagnose infectious disease.

21. A fluid separation and target material detection system comprising: a channel in which fluid is able to flow; one or more inlets; one or more outlets; magnetic particles for imparting paramagnetism to the fluid; and a magnet for creating a magnetic field in the channel, wherein a material capable of binding to a target material is immobilized on at least a portion of the wall of the channel inside the channel adjacent to the magnet, and the fluid containing the magnetic particles is guided to flow through the channel to a domain in which a magnetic field is created, and thus, by using the difference in magnetic susceptibility between the fluid and one or more materials other than the target material included in the fluid, the contact between materials other than the target material and the material capable of binding to the target material is prevented.

22. The fluid separation and target material detection system of claim 21, wherein the material capable of binding to the target material is beads.

23. A fluid separation and target material detection method comprising: mixing a fluid containing a target material with magnetic particles to change magnetic susceptibility of the fluid; injecting the fluid into a channel having one or more inlets and one or more outlets; passing the fluid through a domain where a magnetic field is created; allowing the target material to bind to the material capable of binding to the target material immobilized on at least a portion of the wall of the channel inside the channel near a magnet for creating a magnetic field inside the channel; and separating materials included in the fluid according to the difference in magnetic susceptibility to be discharged through one or more outlets.

24. The fluid separation and target material detection method of claim 23, wherein the material capable of binding to the target material is beads.

25. The fluid separation and target material detection method of claim 23, further comprising binding, to a material labeled with fluorescence, the target material that binds to the material capable of binding to the target material.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0037] FIG. 1 illustrates a method of separating materials in a fluid according to magnetic susceptibility.

[0038] FIG. 2 illustrates a method of separating materials in a fluid according to magnetic susceptibility using a channel having two or more inlets and three or more outlets.

[0039] FIG. 3 illustrates a method of separating blood cells according to magnetic susceptibility and attaching antibodies to magnetic particles to detect a biomarker included in the blood.

[0040] FIG. 4 shows images of plasma separated from blood using magnetic susceptibility differences according to an embodiment.

[0041] FIG. 5 illustrates an image (left) of a 1:200 dilution of blood and an image (right) of separated plasma according to an embodiment.

[0042] FIG. 6 illustrates the results of absorbance measurement of hemoglobin in separated plasma according to an embodiment.

[0043] FIGS. 7A-B shows a graph (A) of absorbance measured at different wavelengths to observe hemolysis in separated plasma and a graph (B) of absorbance at 540 nm, according to an embodiment.

[0044] FIG. 8 is an image showing the results of sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) performed to identify the types of proteins in separated plasma according to an embodiment.

[0045] FIG. 9 is a graph illustrating the results of a bicinchoninic acid (BCA) protein assay performed to determine a protein concentration in separated plasma according to an embodiment (Centrifugation denotes a negative control group and Device denotes plasma separated using paramagnetic particles, according to an embodiment).

[0046] FIGS. 10A-C illustrates the target protein detection using paramagnetic particles:

[0047] FIG. 10A is a schematic side view of an apparatus for detecting proteins in plasma using whole blood without centrifugation; FIG. 10B is an image of fluorescence attached on secondary antibodies bound to beads which have been treated with primary and secondary antibodies after the mixture including blood and 4 ng/mL PSA is allow to flow in a channel with the beads, with which anti-PSA antibody binds, located at the bottom thereof (Whole blood, top), an image of fluorescence attached on secondary antibodies bound to beads which have been treated with primary and secondary antibodies after the blood including 10 nm paramagnetic particles (SPIONs) is mixed with 4 ng/mL PSA and the mixture is allowed to flow in the channel including a magnet located on the surface of the channel on which beads are immobilized (Whole blood supplemented with SPIONs, middle), and an image of fluorescence attached on secondary antibodies bound to beads which have been treated with primary and secondary antibodies after 4 ng/mL PSA is mixed with blood and then plasma obtained by centrifugation is allowed to flow in the channel (Plasma, bottom); FIG. 10C shows results obtained by mixing various concentrations of PSA with blood using the methods.

[0048] FIGS. 11A-D illustrates the nucleic acid separation using paramagnetic particles:

[0049] FIG. 11A is a schematic view of an apparatus for detecting a nucleic acid in plasma using whole blood without centrifugation; FIG. 11B shows diagrams showing that when 10 nm paramagnetic particles (SPIONs) are mixed with bacteria-containing blood, in the case of bacteria in which a cell membrane and a cell wall are damaged, 10 nm-size paramagnetic particles (SPIONs) enter into the bacteria cell through the damaged cell membrane and cell wall, and thus, blood cells showing paramagnetic or diamagnetic properties in the magnetic field are pushed away from the magnet, and in the case of bacteria in which a cell membrane and a cell wall are damaged, the concentrations of paramagnetic particles contained inside/outside liquid of cells are similar to each other and thus, the cells are not effectively pushed away.

[0050] FIG. 11C shows the case in which plasma is obtained using the channel according to the present disclosure (left), and the case in which although a nucleic acid attached on a bacteria in which a cell membrane and a cell wall are damaged and a nucleic acid released from bacteria existing in plasma may be obtained, when plasma is obtained by centrifugation (right), a nucleic acid attached on bacteria is separated together with blood cells from plasma in a centrifugation process, and thus, only a nucleic acid released from the bacterial body remains in the plasma.

[0051] FIG. 11D shows quantitative results obtained by a real-time polymerase chain reaction of bacterial nucleic acid in a plasma obtained by each of a method according to the present disclosure in which the bacteria of which the cell membrane is destroyed is added to blood (graph: Diamagnetic) and a centrifugation method (graph: Centrifugation)

MODE OF DISCLOSURE

[0052] One or more embodiments of the present disclosure will now be described in detail with reference to the following examples. However, these examples are only for illustrative purposes and are not intended to limit the scope of the one or more embodiments of the present disclosure.

EXAMPLE 1

Plasma Separation using Paramagnetic Particles

[0053] The whole blood taken from 8-week-old Wistar rats was mixed with magnetic nanoparticles (carboxylated iron oxide, 10 nm, Ocean NanoTech, US, paramagnetic nanoparticles, 1 mg/mL), and then injected into a channel having a width of about 1 mm and a height of about 100 m. A permanent magnet was arranged about 500 m away from the bottom of the channel to create a magnetic field. A negative pressure was applied to an outlet portion of the channel with a micropump to allow the whole blood to flow (2 L/min).

[0054] As a result, as shown in FIG. 4, the separation of the plasma from the whole blood was clearly observed. The dark red portion is the area where blood cells such as red blood cells and white blood cells are concentrated, and the remaining transparent portion is the plasma.

[0055] In addition, as a result of experiments with a channel having a width of about 5 mm and a height of about 700 m in which the location of a magnetic field creation domain is varied, it was found that plasma can be separated at 5 L/min, indicating that the plasma separation rate can be increased by widening the channel.

EXAMPLE 2

Purity Measurement on Plasma Separated using Paramagnetic Particles

[0056] The plasma separated in Example 1 was subjected to purity measurement. A 1:200 dilution of the blood and the plasma separated in Example 1 were comparatively observed using a microscope (Olympus CKX53, 20 Object lens). As shown in FIG. 5, a large number of blood cells which were observed in the diluted blood were not observed in the plasma separated in Example 1.

[0057] FIG. 6 illustrates the results of absorbance measurement of hemoglobin in the separated plasma using a NanoDrop (ThermoFisher Scientific, USA). The value at a wavelength of 540 nm wavelength is interpreted as a hemoglobin absorbance value. In FIG. 6, the yellow line at the bottom represents the absorbance of the plasma separated in Example 1, which was found to have a hemoglobin level lower than that of the plasma obtained by centrifugation (the blue middle line) or the plasma obtained by hemolysis of the blood cells with Triton-X(X-100) (1%) and then centrifugation (the red uppermost line).

[0058] As a result of calculating a hemolysis percentage on the basis of the data of FIG. 6, the hemolysis percentage was about 5.76%, indicating less hemolysis than with existing centrifugation technology. According to existing technologies, since plasma is separated from blood cells using pressure difference or size difference, hemolysis may occur easily. However, it was found that using difference in magnetic field density and paramagnetic materials may cause less hemolysis than in existing centrifugation, since the external force applied to cells is so weak as not to cause hemolysis.

EXAMPLE 3

Observation of Hemolysis in Plasma Separated using Paramagnetic Particles

[0059] Hemolysis refers to the destruction of red blood cells leading to dissolution of red blood cell contents in plasma, and is a cause of an incorrect test result in the diagnosis of a disease with plasma. Thus, in Example 1, the hemolysis of blood cells which may occur in the process of separation was observed.

[0060] In particular, to check a hemolysis rate of the plasma obtained using paramagnetic particles, absorbances of a positive control group, a negative control group, and the plasma obtained using paramagnetic particles were measured using a Nanodrop (ThermoFisher Scientific, USA). To prepare the positive control group, the blood taken from 8-week-old Wistar rats was mixed with 1% Triton X-100 (Sigma Aldrich) and then reacted at about 36 C. for about 30 minutes to hemolyze the blood cells. Subsequently, the resulting blood was centrifuged at about 4 C. at 500g for about 13 minutes to obtain the supernatant, which was used as a sample of the positive control group. To prepare the negative control group, the blood taken from the rats was centrifuged at about 4 C. at 500g for about 13 minutes to obtain the supernatant, which was used as the negative control group. Next, absorbances of the positive control group, the negative control group, and the plasma obtained using paramagnetic particles were measured using a Nanodrop (ThermoFisher Scientific, USA). The results are shown in FIGS. 7A-B.

[0061] Referring to FIGS. 7A-B, it was found that the plasma obtained using paramagnetic particles had no difference in absorbance from the negative control group. This means that separating plasma using paramagnetic particles, according to an embodiment, does not cause hemolysis.

EXAMPLE 4

Verification of Protein Pattern in Plasma Separated using Paramagnetic Particles

[0062] Proteins in plasma are available as a biomarker in the diagnosis of a disease. Accordingly, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was used to verify whether the various proteins in plasma were well maintained after the separation of the plasma using paramagnetic particles. The plasma prepared as the negative control group in Example 3 was used, and the markers from Precision Plus Protein Dual Color Standards (BIO-RAD, CA, USA) were used, and it was identified that there were albumin (65 kDa), 1-globulin (44 kDa), 2-globulin (85 kDa), and fibrinogen (up to 340 kDa), which are plasma proteins. In particular, to perform SDS-PAGE, after 2 Laemmli Sample Buffer (available from BIO-RAD) and 2-mercaptoethanol (available from BIO-RAD) were mixed in a 9:1 ratio, the thus obtained mixture was mixed with the plasma in a 1:1 ratio. Then, the sample was immersed in boiling water for 3 minutes and then spun down. The Mini-PROTEAN TGX Precast Gel (available from BIO-RAD) was assembled in an electrophoresis chamber (available from BIO-RAD). Next, after the electrophoresis chamber was filled with Tris/Glycine/SDS buffer (available from BIO-RAD), the sample and Precision Plus Protein Dual Color Standards (available from BIO-RAD) were added, and the electrophoresis system was operated. After staining with a Coomassie brilliant blue R-250 staining solution (BIO-RAD) for 2 to 3 hours, destaining was performed using a Coomassie Brilliant blue R-250 destaining solution (BIO-RAD). The results of the SDS-PAGE are shown in FIG. 8.

[0063] Referring to FIG. 8, in the case of the plasma obtained using paramagnetic particles, it was found that the types of proteins in the plasma were not different from the protein in the plasma (Control) obtained by centrifugation. This means that separating plasma using paramagnetic particles, according to an embodiment, ensures that the various types of proteins in the plasma were well maintained after the separation.

EXAMPLE 5

Determination of Protein Concentration in Plasma Separated using Paramagnetic Particles

[0064] Following Example 4, a bicinchoninic acid (BCA) protein assay was performed to determine the quantitative concentrations of the proteins in the plasma separated in Example 1.

[0065] In particular, the negative control group of Example 4 was used. The total protein concentrations in the plasma separated using paramagnetic particles and in the plasma of the negative control group were compared according to the manufacturer's instructions using a Pierce BCA Protein Assay Kit (ThermoFisher Scientific, USA). The results are shown in FIG. 9.

[0066] Referring to FIG. 9, the plasma separated using paramagnetic particles was found not to be different in total protein concentration from the plasma (control group) separated using centrifugation. Accordingly, it was found that in separating plasma using paramagnetic particles, according to an embodiment, the plasma may be separated well without loss in total protein, and with no influence on future assays using protein.

[0067] As a result, it was found that a plasma separation method using paramagnetic particles, according to an embodiment, ensures separation of the plasma without affecting the types and concentration of plasma proteins.

EXAMPLE 6

Target Protein Detection using Paramagnetic Particles

[0068] Anti-PSA antibody (Sino Biological, China) with biotin immobilized thereon was reacted with Streptavidin-immobilized magnetic beads (diameter of 18 m; Spherotech, CA, USA) for 40 minutes at room temperature to prepare anti-PSA antibody immobilized magnetic beads. The magnetic beads were then washed three times with a washing buffer solution (tris-buffered saline with 0.05% Tween 20 (TBST; Biosesang, Korea)), and then, reacted with biotin-polyethylene glycol (PEG; Nanocs, NY, USA) for 30 minutes at room temperature to prevent non-specific reactions. The beads were placed in a channel provided with a magnet located at the bottom surface thereof (0.1 mm32.65 mm0.08 mm; widthlengthheight) (FIGS. 10A-C) at a speed of 60 L/h for 5 minutes to immobilize the beads on microgrooves (30 m30 m; diameterdepth) at the bottom surface of the channel due to the magnet located at the bottom surface of the channel, and then, flushed with a washing buffer solution (TBST) at the speed of 200 L/h for 6 minutes to remove the beads that are not immobilized. To the channel provided with the beads at the bottom surface thereof (the magnet is located at the bottom surface of the channel), blood including 10 nm-size paramagnetic particles and various concentrations of PSA (0, 2, 4, 10 ng/mL; BiosPacific, CA, USA) was provided at the speed of 3 L/h for 45 minutes. In this process, the beads placed on the bottom surface of the channel only come into contact with plasma or the components contained in the plasma. Then, the washing buffer solution (TBST) was provided thereto to proceed with a washing process for 6 minutes at the speed of 200 L/h. To detect the captured PSA, a primary antibody (anti-PSA rabbit IgG antibody; Abcam, UK) was provided at 30 L/h for 30 minutes and a washing buffer solution was provided at the speed of 200 L/h for 6 minutes. Fluorescence-labeled secondary antibodies capable of binding to the primary antibody (Alexa Fluor 488 labeled goat anti rabbit IgG antibody; Abcam, UK) was provided thereto at the speed of 30 L/h for 30 minutes. After washing with a washing buffer solution provided at the speed of 200 L/h for 6 minutes, the intensity of fluorescence of 18 m-size beads located on the bottom surface of the channel was measured by using a fluorescence microscope (Alexa Fluor 488).

[0069] Like the results of FIG. 10B, when the present disclosure is applied to the channel-based immunoassay, even when plasma was not isolated prior to the assay, the same result as obtained with the case in which the isolated plasma was used for the assay may be obtained. Accordingly, it can be seen that even without expensive centrifugation devices and experts required therewith, the same level of measurements as obtainable in the conventional case may be obtained (see FIGS. 10B and 10C). The PSA detection limit of this system is 2.5 ng/mL, which is lower than the cut off value for diagnosing prostate cancer, which is 4 ng/mL. This shows that the present disclosure provides outstanding performance in providing information about the diagnosis of prostate cancer.

[0070] FIG. 10A is a schematic side view of an apparatus for detecting proteins in plasma using whole blood without centrifugation. The apparatus includes a channel in which blood flows (0.1 mm32.65 mm0.08 mm; widthlengthheight) and cylindrical microgrooves (30 m30 m; diameterdepth) for immobilizing 18 m-size beads on which antibodies are attached and which are located at the bottom surface of the channel (diameter of 18 m). Anti-PSA antibodies are immobilized on the surfaces of the beads immobilized in the microgrooves, and proteins captured by antibodies (for example: prostate specific antigen (PSA)) are detected by the reaction occurring when other antibodies (primary antibody and fluorescence-labeled secondary antibodies) are sequentially provided into the channel after blood is provided to the channel, and fluorescent immunoassay.

[0071] As described above, when beads on which antibodies, which are capable of detecting proteins, attached, are placed at the bottom of the channel thereto and blood mixed with 10 nm paramagnetic particles (SPIONs) is provided thereto, due to the magnet at the bottom of the channel, blood cells are pushed away from the antibodies-attached beads, and thus, only plasma and components included in plasma are brought into contact with the antibodies-attached beads. This is because the magnetic susceptibility of the fluid (plasma) changes when the 10 nm-sized paramagnetic particles are mixed in the blood, so that the diamagnetic or weak paramagnetic blood cells are pushed away from a region having a strong magnetic field (magnet side, near the beads) to a region having a weak magnetic field (upwards the channel). Eventually, the same effect as obtainable when only plasma components are isolated and provided, may be obtained (FIG. 10B).

[0072] FIG. 10B is an image of fluorescence attached on secondary antibodies bound to beads which have been treated with primary and secondary antibodies after the mixture including blood and 4 ng/mL PSA is allow to flow in a channel with the beads, with which anti-PSA antibody bonds, located at the bottom thereof (Whole blood, top), an image of fluorescence attached on secondary antibodies bound to beads which have been treated with primary and secondary antibodies after the blood including 10 nm paramagnetic particles (SPIONs) is mixed with 4 ng/mL PSA and the mixture is allowed to flow in the channel (Whole blood supplemented with SPIONs, middle), and an image of fluorescence attached on secondary antibodies bound to beads which have been treated with primary and secondary antibodies after 4 ng/mL PSA is mixed with blood and then plasma obtained by centrifugation is allowed to flow in the channel (Plasma, bottom).

[0073] FIG. 10C shows results obtained by mixing various concentrations of PSA with blood using the methods. It was confirmed that the intensity of fluorescence obtained from blood supplemented with SPIONs (graph: Blood+SPIONs) was higher than the intensity of fluorescence obtained from blood without SPIONs (graph: Blood) at all concentrations of PSA, and all fluorescence values were similar to those obtained using plasma (graph: Plasma) obtained by centrifugation.

EXAMPLE 6

Nucleic Acid Separation using Paramagnetic Particles

[0074] After mixing the bacteria in which a cell membrane and a cell wall were artificially damaged in blood, plasma was obtained by centrifugation and the method according to the present invention, and then, through real-time polymerase chain reaction, the amount of the nucleic acid of bacteria obtained by centrifugation was compared with that obtained using the present disclosure.

[0075] 10.sup.6 CFU/mL E. coli K12 species (KCTC No.: 2223) was sonicated for 1 hour (50 W, 35 C.), and E. coli K12 was mixed with whole blood containing 10 nm-size paramagnetic particles at a ratio of 1(saline containing sonicated E. coli):10(whole blood containing paramagnetic particles). The resulting blood was allowed to flow into the channel and then, plasma was obtained through a plasma outlet (outlet 2) at the speed of 2 L/min. The blood thus obtained was centrifuged (800 g, 4 C., and 10 minutes) to obtain plasma from the supernatant. Using the DNeasy Blood & Tissue Kit (Qiagen, Germany), nucleic acids were extracted from the two plasmas according to the manufacturers instructions, and the nucleic acids were stored in a 20 C. freezer until the polymerase chain reaction. Nucleic acids were detected using a real-time polymerase chain reaction based on SYBR Green (LightCycler 480 system (Roche, Switzerland) using E. coli K12 species-specific primer (Macrogen, Korea) and LightCycler 480 SYBR Green I Master (Roche, Switzerland). Then, the amount of nucleic acid was analyzed using Delta crossing point (C.sub.p) method.

[0076] As shown in FIG. 11D, considering that the amount of E. coli nucleic acids obtained according to the present disclosure is about 2.3 times greater than the amount of nucleic acids obtained through centrifugation, it is expected that when the present disclosure is applied to the polymerase chain reaction, a faster and more accurate sepsis diagnostics can be developed.

[0077] FIG. 11A is a schematic view of an apparatus for detecting a nucleic acid in plasma using whole blood without centrifugation. The apparatus (channel size: 4 mm50 mm0.18 mm; widthlengthheight) includes an inlet blood enters, and outlet 1 through which blood cells are discharged and outlet 2 through which plasma is discharged.

[0078] FIG. 11B shows diagrams showing that when 10 nm paramagnetic particles (SPIONs) are mixed with bacteria-containing blood, in the case of bacteria in which a cell membrane and a cell wall are damaged, 10 nm-size paramagnetic particles (SPIONs) enter into the bacteria cell through the cell membrane and cell wall, and thus, blood cells showing paramagnetic or diamagnetic properties in the magnetic field are pushed away from the magnet, and in the case of bacteria in which a cell membrane and a cell wall are damaged, the concentrations of paramagnetic particles contained inside/outside liquid of cells are similar to each other and thus, the cells are not effectively pushed away.

[0079] FIG. 11C shows the case in which plasma is obtained using the channel according to the present disclosure (left), and the case in which although a nucleic acid attached on a bacteria in which a cell membrane and a cell wall are damaged and a nucleic acid released from bacteria existing in plasma may be obtained, when plasma is obtained by centrifugation (right), a nucleic acid attached on bacteria is separated together with blood cells from plasma in a centrifugation process, and thus, only a nucleic acid released from the bacterial body remains in the plasma.

[0080] FIG. 11D shows quantitative results obtained by a real-time polymerase chain reaction of bacterial nucleic acid in a plasma obtained by each of a method according to the present disclosure in which the bacteria of which the cell membrane and the cell wall is destroyed is added to blood (graph: Diamagnetic) and a centrifugation method (graph: Centrifugation) The amount of the bacterial nucleic acid obtained by the method of the present disclosure is about 2.3 times greater than the amount of the nucleic acid obtained by the centrifugation method.