The present invention relates to a detector and a detecting method and particularly relates to a detector and a detecting method which use the hysteresis loss of a magnetic particle.
In immunization analysis, the following technique is mainly used. First, marker particles such as a phosphor material are diffused into a test sample. A secondary target material trap reacting only with a specific target material is coupled to the marker particle. The test sample is injected to a reaction field to which a primary target material trap reacting only with the target material is coupled. Then, in the presence of a desired target material, the marker particle is fixed to the reaction field via coupling between the target material and the secondary target material trap, unreacted marker particles are removed from the reaction field, and then the target material is detected. For example, this method includes radioimmunoassay (RIA) or immunoradiometric assay (IRMA) in which a competitive antigen or antibody is labeled with a radionuclide and an antigen is quantitatively measured from measurement results of the activity. An advantage of this method is a high sensitivity but a special facility or apparatus is necessary in view of the safety of radionuclides. As compared with radioimmunoassay, the enzyme-labeled antibody method (EIA) using an enzyme for modifying an antibody can be handled more easily and satisfies a practical sensitivity. However, it is necessary to further improve sensitivity and ease of handling.
The target material is a material handled in conventional immunoassay. For example, the target material is selected from the group consisting of an antibody, an antigen, protein, carbohydrate, lipid, nucleotider nucleic acid, and a cell. The target material trap is a material specifically coupled to the target material.
Japanese Patent Application Laid-Open No. S63-108264 discloses a magnetic immunoassay technique using a magnetic ultrafine particle.
However, higher sensitivity and more ease of handling are demanded in the above method. In the method of the application, a predetermined output waveform can be obtained by detecting the magnetization of magnetic ultrafine particles. However, the output waveform is obtained according to. the amount of magnetization of all magnetic ultrafine particles in a given region of a test sample. Thus, it is impossible to quantitatively treat, as digital data, the amount of an antigen or antibody in a specimen according to the detected waveform.
Therefore, in the currently used detecting method, quantitative detection cannot be made with ease. Detecting methods satisfying these needs are demanded.
The present invention relates to a detecting method using the hysteresis loss of a magnetic particle. In view of the problem, a magnetic particle is used as a marker particle. For example, an alternating magnetic field is applied to magnetic particles which remain due to specific coupling such as a biochemical reaction and amount of heat is generated on the particles, so that a temperature change corresponding to the number of magnetic particles or a change in physical quantity due to the change is detected and quantitative detection can be made on a detected material such as an antigen.
Other features and advantages of the present invention will be apparent from the following description taken in conjunction with the accompanying drawings, in which like reference characters designate the same or similar parts throughout the figures thereof.
The accompanying drawings, which are incorporated in and constitute apart of the specification, illustrate embodiments of the invention and, together with the description, serve to explain the principles of the invention.
The present invention relates to a method of detecting a sample in a sample solution by using a magnetic particle. The magnetic particle is heated by applying an alternating magnetic field to the magnetic particle, and a temperature change or a change in physical quantity due to the temperature change is detected on at least one of the magnetic particle or the peripheral area of the magnetic particle, so that the sample contained in the sample solution is detected. First, samples and magnetic particles are fixed by an antigen-antibody reaction or the like, and the magnetic particles are trapped according to the number of samples. Thereafter, the magnetic particles are heated by applying an alternating magnetic field to the magnetic particles, and a temperature change or a change in physical quantity due to the temperature change is detected. The change in physical quantity includes a change in index of refraction and a change in the magnetization of the magnetic particle. The change in physical quantity may be detected from the magnetic particle. When the magnetic particle is dispersed in a solution, a temperature change and a change in physical quantity due to the temperature change is detected in the solution, a container (channel) of the solution, and so on.
A conventionally used target material trap is applicable to the present invention. When the target material trap is fixed to a reaction field, a material which is readily coupled to the target material trap is chemically or physically carried on the inner wall of the reaction field. Thereafter, the target material trap can be injected and coupled to the reaction field. Various target material traps are available.
Similarly, various target material traps can act as a secondary target material trap to be fixed to a magnetic particle.
For example, the reaction field is a part of a channel where the sample solution flows. It is preferable that the reaction field be made of a material from which no heat is generated by the application of an alternating magnetic field. In order to prevent amount of heat generated from a magnetic particle from escaping, it is preferable that the reaction field be made of a material of low thermal conductivity or a heat shield be disposed around the reaction field.
For efficient heat generation, it is preferable that a magnetic particle used as a marker particle be made of a material of high hysteresis loss.
Any means can be used for a method of applying an alternating magnetic field to the magnetic particle. For example, a coil is disposed near or in the reaction field and an alternating current is applied to the coil. By filling the coil with a material such as an iron core of high magnetic permeability, a magnetic field can be generated more efficiently. Further, an alternating magnetic field can be applied to the magnetic particle also by causing a magnet to rotate on its axis or around the magnetic particle. When an alternating magnetic field is applied, generated amount of heat is kept in the reaction field, e.g., an inlet/outlet of a specimen in the reaction field is closed, so that quantitative detection can be made with higher-accuracy.
As a detecting method, an electrical detection is available which uses a thermocouple varied in electromotive force according to a temperature change, a thermistor varied in resistance value, and so on. A thermocouple and a thermistor available in the present invention can be used around room temperature. For example, the thermocouple is selected from the group consisting of chloroalumel-alumel, copper-constantan, chromel-constantan and platinrhodium-platinum. The thermomistor is an oxide of a transition metal selected from the group consisting of nickel-barium titanate, manganese, cobalt and iron. Further, a temperature change can be detected by an infrared radiometer. Moreover, optical detection can be made on surface plasmon resonance and a thermal lens using a change in the index of refraction of a solvent in the reaction field. The specific configurations of the present invention will be described in detail in the following embodiments.
With this detector, a prostate-specific antigen (PSA) known as a marker of a prostate cancer can be detected according to the protocol below the primary antibody 501 for identifying a PSA is fixed on the inner wall of the channel.
(1) Phosphate buffered saline (sample solution) containing a PSA, which is an antigen (sample), is introduced into the channel and incubation is carried out for five minutes.
(2) An unreacted PSA is cleaned with phosphate buffered saline.
(3) An anti-PSA antibody (secondary antibody) solution labeled with a magnetite bead (magnetic particle) is introduced into the channel and incubation is carried out for five minutes.
(4) The unreacted and labeled antibody is cleaned with phosphate buffered saline and the channel is filled with the phosphate buffered saline.
With this protocol, the magnetic particle is fixed to the reaction field via the primary antibody, the antigen and the secondary antibody. In this case, the average diameter of the magnetic particle is about 400 nm and superparamagnetism is observed. In
Thereafter, laser light 305 is launched into the prism 104 and reflected light is measured by a photodetector 304. In a range including the angles of total reflection on the surface of the thin metal film 105, an incident angle is scanned by an automatic gonio stage having a high angle resolution while an angle between incident light and reflected light has a constant value all the time, and a reflectivity is measured. Then, a high-frequency current of 500 kHz is applied to a coil 401 by an alternating-current power supply 402, so that an alternating magnetic field is applied to the channel. Heat is generated on the magnetic particle by the alternating magnetic field and thus liquid in the channel 201 is heated. When a desired antigen is present in a specimen, the magnetic particle carried by the antigen-antibody reaction is heated and thus the liquid in the channel 201 changes its index of refraction and has a different reflectivity from that before the application of the magnetic field. Thus, an antigen in the specimen can be detected. For example, when the liquid is water, a decrease in plasmon resonance angle is confirmed by making measurements with SPR (surface plasmon resonance) of a Kretschmann configuration in which a gonio stage has an angular resolution of 0.0025°.
The angle change is converted into an index of refraction and further converted into a temperature change. The temperature change is converted into an antigen concentration according to a predetermined calibration curve, so that the antigen concentration of the PSA can be detected.
The present embodiment described the measuring method of surface plasmon resonance, in which the prism 104 is used. As shown in
Further, thermal conductivity is reduced by providing the casing 101 with a dual structure and producing a vacuum between two casings, thereby achieving detection with higher sensitivity.
Thereafter, a high-frequency current of 500 kHz is applied to a coil 401 by an alternating-current power supply 402, and an alternating magnetic field is applied to the channel 201. A magnetic particle carried in the channel 201 by an antigen-antibody reaction is heated by the alternating magnetic field and thus the thermocouple is heated. At this point, the electrodes are both kept at a fiducial temperature of 0° C. The electrodes are respectively composed of the copper 306 and the constantan 307, protrude from the channel 201, and are formed on a lid 102 of the casing 101. Then, electromotive force is induced in the thermocouple according to a temperature difference from the junction of the copper 306 and the constantan 307. As the number of magnetic particles increases, a temperature increases in the channel 201. As the temperature increases, the thermocouple has higher electromotive force. Thus, the concentration of an antigen contained in the specimen can be detected by measuring the electromotive force.
The present embodiment described the method of measuring a temperature in the channel 201 with the thermocouple. A thermistor 308 may be used to measure a temperature.
The present embodiment will describe an example in which a porous is used for a reaction region. In
According to the methods of Embodiments 1 and 2, a PSA specimen in a specimen is reacted and a magnetic particle 603 is fixed via an antigen 604. Thereafter, a high-frequency current of 500 kHz is applied to a coil 401 by an alternating-current power supply 402, so that an alternating magnetic field is applied to a channel 201. The magnetic particle 603 carried in the channel 201 by an antigen-antibody reaction is heated by the high-frequency magnetic field. A temperature change caused by the heat generation is detected by a thermistor 308, so that the amount of antigen in the specimen is quantified.
The detecting method and the detection device of the present invention described in these embodiments are used particularly for a method of detecting a biological material. In this method, a magnetic particle is used as a marker particle, a change in physical quantity corresponding to the number of magnetic particles is detected, and a material contained in a sample solution is detected. A target material such as an antigen can be quantitatively detected with ease.
This application claims priority from Japanese Patent Application No. 2004-132604 filed Apr. 28, 2004, which is hereby incorporated by reference herein.
Number | Date | Country | Kind |
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2004-132604 | Apr 2004 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP05/08265 | 4/22/2005 | WO | 9/6/2005 |