Patent Application
20200386778
The present invention relates to a liquid delivery system which supplies liquid to an inspection chip including a side wall member or recovering the liquid from the inspection chip. The present invention also relates to an inspection system using the inspection chip including the side wall member.
In biochemical inspection, biochemical reactions such as antigen-antibody reactions are used. For example, in fluoroimmunoassay (FIA), a labeling substance containing a fluorescent substance is bound to a substance to be detected (antigen), and the substance to be detected is labeled with fluorescence. Thereafter, the substance to be detected labeled with the fluorescence is irradiated with excitation light, fluorescence emitted from the fluorescent substance is detected, and an amount of the substance to be detected and the like is specified from intensity of the fluorescence. Among such FIAs, surface plasmon-field enhanced fluorescence spectroscopy (SPFS) is known as a method capable of detecting the substance to be detected with an especially high degree of sensitivity.
In the SPFS, a first capturing body (for example, a primary antibody) which specifically binds to the substance to be detected is immobilized on a metal film to form a reaction site for capturing the substance to be detected. For example, Patent Literature 1 discloses an SPFS device provided with a well-type inspection chip (sensor structure 22) in which a reaction site is arranged on a bottom surface of a well (a bottomed concave portion for accommodating liquid). In the inspection chip, the well is formed by fixing a well member having a through hole on a metal film formed on a light transmissive dielectric member, and the reaction site is arranged on the metal film forming the bottom surface of the well. Then, by introducing a specimen (sample and the like) which may contain the substance to be detected into this well, the substance to be detected is bound to the first capturing body immobilized on the metal film and forming the reaction site. Then, a second capturing body is further bound to the substance to be detected bound to the first capturing body by introducing the second capturing body labeled with fluorescence (for example, a secondary antibody) into the well. That is, the substance to be detected is indirectly labeled with fluorescence. When the metal film is irradiated with the excitation light from a side of a dielectric nienibet in this state, the fluorescent substance is excited by an electric field enhanced by surface plasmon resonance (SPR) to emit fluorescence. In the SPFS device disclosed in Patent Literature 1, the fluorescence emitted from the fluorescent substance passes through a liquid surface of the liquid in the well and is detected by a detection unit arranged above the well.
Patent Literature 1: WO 2012/157403 A
As described above, in the inspection chip disclosed in Patent Literature 1, since the metal film is formed on the bottom surface of the well and the reaction site is arranged, a tip end of a liquid delivery tool might be in contact with the metal film or the reaction site to break them when removing liquid such as reagent in the well. Therefore, the tip end of the liquid delivery tool cannot be pressed against the bottom surface of the well, and it is difficult to sufficiently remove the liquid in the well. Then, if the liquid such as the reagent is not removed sufficiently and remains in the well, various reactions do not proceed properly, and detection accuracy is lowered.
In addition, as described above, in the SPFS device disclosed in Patent Literature 1, a detection unit is arranged above the well and detects fluorescence which passes through the liquid surface of the liquid in the well, so that a detection result of the fluorescence might be affected by meniscus, air bubbles or the like present on the liquid surface. If the detection result of the fluorescence is affected by the meniscus, the air bubbles or the like, the detection accuracy is lowered.
That is, in the inspection chip in which the reaction site is provided on the bottom surface of the well as in the conventional art, there is a problem that the detection accuracy is lowered.
In order to solve the above-described problem that the detection accuracy is lowered occurring when the inspection chip provided with the reaction site on the bottom of the well is used, it is conceivable that the reaction site, the dielectric member and the like are provided on a position other than the bottom surface of the well, for example, the side surface of the well.
As described above, in the biochemical inspection, the liquid such as the reagent is supplied into the well and the liquid such as the reagent supplied into the well is recovered; when supplying the liquid into the well or recovering the liquid in the well, in a case where the liquid delivery tool such as a pipette chip passes through a region on a side on which the side wall member 62y is provided of the inspection chip 60y as indicated by any one of arrows Px1, Px2. and Px3 as illustrated in
That is, providing the reaction site, the dielectric member or the like on the side surface of the well solves the problem that the detection accuracy is lowered according to the conventional art in which the reaction site is provided on the bottom surface of the well, but there is concern that the unexpected contamination might occur in the reaction site, dielectric member or the like provided on the side surface of the well.
A liquid delivery system of the present invention is a liquid delivery system which supplies liquid to an inspection chip formed of a well main body for accommodating the liquid and a side wall member arranged on a side surface of the well main body or recovers the liquid present in the inspection chip via a liquid delivery tool, the liquid delivery system including a conveyance unit which conveys the liquid delivery tool. and a control unit which controls the conveyance unit such that the liquid delivery tool does not pass through a region on a side on which the side wall member is arranged of the inspection chip.
An inspection system of the present invention includes a light source which irradiates an inspection chip formed of a well main body for accommodating liquid and a side wall member arranged on a side surface of the well main body with light, a detection unit which detects light to be measured emitted from the inspection chip, a first conveyance unit which conveys a liquid delivery tool, and a control unit which controls the first conveyance unit such that the liquid delivery tool does not pass through a region on a side on which the side wall member is arranged of the inspection chip when supplying the liquid to the inspection chip or recovering the liquid present in the inspection chip via the liquid delivery tool.
A liquid delivery method of the present invention is a liquid delivery method for supplying liquid to an inspection chip formed of a well main body for accommodating the liquid and a side wall member arranged on a side surface of the well main body or recovering the liquid present in the inspection chip via a liquid delivery tool, the method including a conveying step of conveying the liquid delivery tool so as not to pass through a region on a side on which the side wall member is arranged of the inspection chip.
According to the present invention, the detection accuracy of the substance to he detected is further improved, and it becomes possible to prevent the occurrence of the unexpected contamination on the member used for the inspection.
Hereinafter, a mode for carrying out the present invention is described with reference to the drawings. This embodiment is a biochemical inspection system adopting a continuous mode in which a plurality of measurement units for performing respective steps forming one inspection is sequentially arranged in a production line, capable of substantially simultaneously performing a plurality of inspections by sequentially introducing a plurality of inspection chips while the respective steps are sequentially performed and the inspection progresses by progress of the inspection chip along the production line. However, the present invention is not limited to the continuous mode. For example, it is also possible to adopt a non-continuous mode in which the respective steps forming one inspection are performed in the same position, and the progress of the inspection is not dependent on the progress of the inspection chip.
Meanwhile, although a method using SPFS as a biochemical inspection is adopted in this embodiment, the present invention is not limited to the method using the SPFS. For example, methods such as surface plasmon resonance (SPR), general fluorescence immunoassay and the like may also be adopted. A type and a mode of the inspection are not limited, and in a case where it is necessary to use an asymmetric inspection chip, an effect of simultaneously realizing further improvement in detection accuracy of a substance to be detected and stable and efficient stirring may be obtained.
(Biochemical Inspection System)
As illustrated in
(Vibration Unit)
The vibration unit 10 is provided with stirring devices not illustrated which stir liquid accommodated in inspection chips 60a, 60c, and 60d by rotary vibration in positions 10a, 10c, and 10d corresponding to the inspection chips 60a, 60c, and 60d. The stirring device is arranged in apposition not interfering with an optical path of the excitation light, fluorescence, plasmon scattered light and the like and includes an eccentric rotating body. The rotating body performs the rotary vibration in a contacting state with the inspection chip, thereby applying rotary vibration in a circumferential direction to the inspection chip to stir the liquid accommodated in the inspection chip. However, the stirring device is not limited to that including the eccentric rotating body as long as this may stir the liquid accommodated in the inspection chip by applying the rotary vibration to the inspection chip.
By stirring the liquid accommodated in the inspection chip by the stirring device, reaction, cleaning and the like at each step in the biochemical inspection may be performed efficiently. From the viewpoint of efficiently stirring the liquid in the inspection chip, the stirring device preferably applies the rotary vibration to the inspection chip at an inherent frequency of the inspection chip accommodating the liquid, or at vibration frequencies around the same. It is also possible to apply the rotary vibration to the inspection chip while sequentially switching different inherent frequencies (n-th order inherent frequency and m-th order inherent frequency, n and in being positive integers). Meanwhile, the position in which the stirring device is provided is not limited to the above-described position, and it is also possible to change the installation position or the number as needed or to provide the stirring devices so as to correspond to all the inspection chips according to operational contents and the like at each step.
(Light Projection Unit)
The light projection unit 20 formed of a light source unit and a first angle adjustment unit (both are not illustrated) irradiates the inspection chip with the excitation light.
The light source unit formed of a light source, a beam shaping optical system, an APC mechanism, and a temperature adjusting mechanism irradiates the inspection chip with the excitation light.
A type of the light source is not especially limited, and is, for example, a laser diode (LD). Other examples of the light source include a light emitting diode, a mercury lamp, and other laser light sources. In a case where the light emitted from the light source is not a beam, the light emitted from the light source is converted into the beam by a lens, a mirror, a slit and the like. Also, in a case where the light emitted from the light source is not monochromatic light, the light emitted from the light source is converted into the monochromatic light by a diffraction grating and the like. Furthermore, in a case where the light emitted from the light source is not linear polarized light, the light emitted from the light source is converted into the linear polarized light by a polarizer and the like.
The beam shaping optical system is formed of, for example, a collimator, a band pass filter, a linear polarization filter, a half wavelength plate, a slit, a zoom means and the like. However, the beam shaping optical system may also be formed to include only a part of them. The collimator collimates the excitation light emitted from the light source. The band pass filter makes the excitation light emitted from the light source narrow band light having only a central wavelength. This is because the excitation light emitted from the light source has a slight wavelength distribution width. The linear polarization filter makes the excitation light emitted from the light source completely linear polarized light. The half wavelength plate adjusts a polarization direction of the excitation light so that a P wave component is incident on the reflective surface 73. The slit and zoom means adjust a beam diameter, a contour shape and the like of the excitation light so that the shape of the irradiation spot on the reflective surface 73 becomes a circle of a predetermined size.
The APC mechanism controls the light source so that an output of the light source is constant. Specifically, the APC mechanism detects a light amount of light branched from the excitation light by a photodiode or the like, and controls input energy by a recurrent circuit to control the output of the light source constant.
The temperature adjusting mechanism is, for example, a heater, a Peltier element and the like. The wavelength and energy of the light emitted from the light source might fluctuate depending on temperature, so that the temperature adjusting mechanism maintains the temperature of the light source constant, thereby controlling the wavelength and energy of the light emitted from the light source constant.
The first angle adjustment unit relatively rotates an optical axis of the excitation light 91 and the inspection chip 60 to adjust an incident angle α of the excitation light 91 on the reflective surface 73.
For example, the first angle adjustment unit rotates the light source unit about an axis in the height direction of the inspection chip 60 (an axis perpendicular to a paper surface in
As described above, when the first angle adjustment unit scans the incident angle α of the excitation light 91, an enhancement angle is specified in the detection unit 40 to be described later. The enhancement angle is an angle being an incident angle when an amount of plasmon scattered light 94 having the same wavelength as that of the excitation light 91 passing through the reflective surface 73 to be emitted on a side of the well main body 61 of the inspection chip 60 is the maximum in a case where the reflective surface 73 is irradiated with the excitation light 91. The enhancement angle is set as the incident angle α of the excitation light 91 at the time of optical blank measurement and fluorescence value measurement to be described later. Meanwhile, an incident condition of the excitation light 91 such as the enhancement angle is roughly determined by design elements of the inspection chip 60 (for example, a material and a shape of the prism 71, a film thickness of the metal film 75, a wavelength of the excitation light 91 and the like), a refractive index of the liquid accommodated in the inspection chip 60 and the like, but this might fluctuate depending on an error in shape of the prism 71, a composition of the liquid accommodated in the inspection chip 60 (for example, a type and an amount of fluorescent substance and the like), so that it is preferable to specify an optimum enhancement angle for each inspection.
(Detection Unit)
The detection unit 40 is formed of a first lens, an optical filter, a second lens, a position switching unit, and a light receiving sensor (all are not illustrated) and detects fluorescence 93 and the plasmon scattered light 94 emitted from the inspection chip 60.
The first lens is, for example, a condensing lens, and condenses light emitted from the vicinity of the reaction site 77. The second lens is, for example, an image forming lens, and forms an image of the light condensed by the first lens on a light receiving surface of the light receiving sensor. An optical path between the first lens and the second lens is a substantially parallel optical path.
The optical filter is arranged on the optical path between the first lens and the second lens by a position switching unit in a case of detecting the fluorescence 93. The optical filter is, for example, a filter including a multilayer film which reflects a predetermined light component, or a color glass filter which absorbs a predetermined light component, and removes an excitation light component such as the excitation light 91 and the plasmon scattered light 94 out of the light condensed by the first lens and guides only the fluorescence 93 to the light receiving sensor. As a result, in the light receiving sensor, the fluorescence 93 may be detected at a high signal (S)/noise (N) ratio. Examples of the optical filter include an excitation light reflecting filter, a short wavelength cutting filter, and a band pass filter.
In a case where the plasmon scattered light 94 is detected, the optical filter is arranged outside the optical path between the first lens and the second lens. In this case, the enhancement angle which is the incident angle when the light amount of the plasmon scattered light 94 is the maximum is specified.
The position switching unit arranges the optical filter on the optical path between the first lens and the second lens or outside the same as needed. Specifically, in a case of detecting the fluorescence 93, the optical filter is arranged on the optical path, and in a case of detecting the plasmon scattered light 94, the optical filter is arranged outside the optical path.
The light receiving sensor detects the fluorescence 93 and the plasmon scattered light 94. The light receiving sensor is, for example, a photomultiplier tube (PMT), an avalanche photodiode (APD) or the like. However; the light receiving sensor is not limited to them, and may be any sensor capable of detecting weak fluorescence 93 and having high sensitivity.
The detection unit 40 may also be configured to detect reflected light 92 of the excitation light 91 instead of detecting the plasmon scattered light 94. For example, this may be configured to detect the reflected light 92 by the above-described light receiving sensor or by a light receiving sensor (for example, a photodiode) for detecting the reflected light separately provided. In this case, when the first angle adjustment unit of the light projection unit 20 scans the incident angle α of the excitation light 91, the detection unit 40 specifies a resonance angle in place of the enhancement angle, and this is set as the incident angle α of the excitation light 91 at the time of the optical blank measurement and the fluorescence value measurement to be described later. The resonance angle is an angle which is the incident angle when the light amount of the reflected light 92 of the excitation light 91 reflected by the reflective surface 73 is the minimum in a case where the reflective surface 73 is irradiated with the excitation light 91. Meanwhile, the resonance angle is in the close vicinity of the enhancement angle.
Also, the light projection unit 20 and the light receiving sensor are arranged at the same height as the inspection chip 60. As a result, the biochemical inspection system may be made compact. However, the light projection unit 20 and the light receiving sensor are not necessarily arranged at the same height as the inspection chip 60. For example, it is also possible to freely change positions of the light projection unit 20 and the light receiving sensor using a mirror or the like.
(Liquid Delivery/Conveyance Unit)
The liquid delivery/conveyance unit 30 is formed of a liquid delivery means and a conveyance means (both are not illustrated). The liquid delivery means supplies liquid such as a reagent to the inspection chip, and recovers the liquid accommodated in the inspection chip as needed. The conveyance means moves the inspection chip to arrange in an appropriate position as needed.
The liquid delivery means is formed of a reagent chip, a pipette unit, and a first moving mechanism (all are not illustrated).
The reagent chip is a container capable of accommodating a sample, a sample diluting solution, a measuring buffer solution, a cleaning solution, a labeling solution for assigning a fluorescent label to the substance to be detected and the like. Types of the sample and the substance to be detected are not especially limited. Examples of sample include body fluid such as blood, serum, plasma, cerebrospinal fluid, urine, nostril fluid, saliva, and semen and tissue extracts. Examples of the substance to be detected include nucleic acids (DNA and RNA), proteins (polypeptides, oligopeptides and the like), amino acids, carbohydrates, lipids and modified molecules thereof The sample diluting solution includes, for example, bovine serum albumin (BSA), Antifoam SI, NaN3, carboxymethyl-dextran (CMD), human anti-mouse antibodies (HAMA) inhibitor, phosphate buffered saline with Tween 20 (PBST) and the like. The measuring buffer solution includes, for example, BSA, Antifoam SI, NaN3, and PBST. The cleaning solution includes, for example, Antifoam SI, NaN3, and PBST. The labeling solution includes, for example, a secondary antibody labeled with a fluorescent substance and PBST. The reagent chip is usually such that a plurality of containers is arranged according to the type of liquid, or a plurality of containers is integrated.
The pipette unit is formed of a syringe pump and a nozzle. The syringe pump includes a syringe, a plunger capable of reciprocating in the syringe, and a drive mechanism, and sucks or discharges the liquid quantitatively by reciprocating movement of the plunger. The drive mechanism is a means for reciprocating the plunger and is formed of for example, a stepping motor. One end of the nozzle is connected to the syringe pump. A pipette chip is mounted on the other end of the nozzle not connected to the syringe pump. However; it is also possible to supply the liquid such as the reagent directly into the inspection chip by the nozzle, or to directly recover the liquid accommodated in the inspection chip by the nozzle without using the nozzle.
The first moving mechanism moves the nozzle and arranges the same in a predetermined position. For example, the first moving mechanism freely moves the nozzle in two directions: vertical and horizontal directions. Examples of the first moving mechanism include one formed of a robot arm and a biaxial stage or a turntable which may move up and down.
The conveyance means is formed of an inspection chip holding unit and a second moving mechanism (both are not illustrated).
The inspection chip holding unit is for holding the inspection chip 60, and is fixed to the second moving mechanism or configured to be removable. The second moving mechanism moves the inspection chip holding unit to arrange the inspection chip 60 held by the inspection chip holding unit to appropriate positions as needed such as the positions 10a to 10e corresponding to the respective measurement units which perform the individual steps forming the inspection. Examples of the second moving mechanism include a conveyor and a rotating stage. However, it is not necessary to provide the second moving mechanism in a case of adopting the non-continuous mode to perform the respective steps forming one inspection in the same position without adopting the continuous mode in which a plurality of inspections may be substantially simultaneously performed. For example, it is also possible to configure such that the second moving mechanism is omitted and only the inspection chip holding unit is provided to hold the inspection chip 60. Also, even in a case of adopting the continuous mode, if it is not necessary to move the inspection chip 60 in accordance with the prowess of the inspection, it is also possible to provide a plurality of inspection chips 60 corresponding to the measurement units performing the respective steps forming one inspection and transfer the liquid such as the reagent in the inspection chip 60 to the inspection chip 60 corresponding to a next measurement unit by the liquid delivery means and the like instead of moving the inspection chip 60 after operation in one measurement unit is completed. In this case also, the second moving mechanism may be omitted, and only the inspection chip holding unit is provided to hold each inspection chip 60.
(Control Arithmetic Unit)
The CPU 51 controls entire measurement and allows each control unit or arithmetic unit to be described later to operate as needed. The light projection control unit 52 controls the light projection unit 20 and applies the excitation light to a predetermined position. The liquid delivery drive control unit 53 controls the pipette unit of the liquid delivery means of the liquid delivery/conveyance unit 30, and sucks or discharges predetermined liquid by a predetermined amount. The liquid delivery movement control unit 54 controls the first moving mechanism of the liquid delivery means of the liquid delivery/conveyance unit 30 and arranges the nozzle in a predetermined position. The conveyance control unit 55 controls the conveyance means of the liquid delivery/conveyance unit 30, and arranges the inspection chip in an appropriate position as needed. The detection control unit 56 controls the detection unit 40, and detects the plasmon scattered light or fluorescence as needed. The arithmetic unit 57 specifies the enhancement angle on the basis of the light amount of the plasmon scattered light, performs quantitative measurement such as calculation of concentration of the substance to be detected on the basis of the light amount of fluorescence, and performs other correction processing of data and the like.
(Inspection Chip)
(Well Main Body)
The well main body 61 is formed of a material transparent to light having the wavelength of the excitation light 91 and light having the wavelength of the fluorescence 93, and is formed of, for example, a resin or glass. However, a part of the well main body 61 may be formed of a material opaque to the light having the wavelength of the excitation light 91 and the light having the wavelength of the fluorescence 93 as long as measurement by an inspection method to be described later is not interfered.
The bottom surface structure 66 is a curved surface in which a tip end 66a leans toward the side wall member 62.
As described above, when the inspection chip 60 may perform the stable circular movement, the inspection chip 60 does not fall from the stirring device, so that it becomes possible to efficiently stir the liquid such as the reagent accommodated in the inspection chip 60 by the circular movement and sufficiently supply the liquid such as the reagent to the reaction site to be described later.
The bottom surface structure 66 is not limited to the curved surface, and may be, for example, a pyramid having a tip end at the tip end position x or a flat surface having a protrusion at the tip end position x. That is, it is sufficient that the bottom surface structure 66 is configured to be in contact with the rotating body 99 of the stirring device at the tip end position x to receive the circular movement. Also, from the viewpoint of stability when being mounted on the rotating body 99, the bottom surface structure 66 preferably has the same shape as that of the surface of the rotating body 99 which is in contact.
Also, in this embodiment, the tip end position x and the center of gravity G2 of the inspection chip 60 are located on the same axis in the length direction of the inspection chip 60, but the tip end position x is not limited thereto, and it is sufficient that this inclines toward the side wall member 62 from the center position (in this embodiment, the symmetry center c) of the cross-section of the well main body 61. For example, due to a weight and the like of the side wall member 62, it is sometimes impossible to arrange the tip end position x and the center of gravity G2 of the inspection chip 60 on the same axis in the length direction of the inspection chip 60 because of the structure of the inspection chip 60. In such a case, it is not necessary that the tip end position x and the center of gravity G2 of the inspection chip 60 be located on the same axis in the length direction of the inspection chip 60, and if the tip end position xis arranged to incline toward the side of the side wall member 62. it is possible to obtain an effect of making the circular movement of the inspection chip 60 stable and efficiently stirring the liquid such as the reagent accommodated in the inspection chip 60.
Also, as described above, the center of gravity of the inspection chip 60 is exactly the center of gravity of the inspection chip 60 in a state of accommodating the liquid such as the reagent, but it is also possible that the center of gravity of the inspection chip 60 is the center of gravity of the inspection chip 60 itself for the convenience of the manufacture and the like.
Also, in this embodiment, as the inspection chip 60, that in which the well main body 61 includes the bottom surface structure 66 in which the tip end 66a leans toward the side wall member 62 is used as described above, but the present invention is not limited to this. For example, the well main body 61 may be configured such that the tip end 66a is located at the symmetry center c of the cross-section of the well main body 61.
(Side wall Member)
The prism 71 is an optical element made of a dielectric transparent to the excitation light 91 and has not a little birefringence characteristic. The material of the prism 71 includes the resin and glass and this is preferably the resin having a refractive index of 1.4 to 1.6 and small birefringence.
Also, in a case where the light source of the excitation light 91 is a laser diode (LD), when the excitation light 91 returns to the LD, an excited state of the LD is disturbed, and the wavelength and output of the excitation light 91 fluctuate, so that the incident surface 72 is formed so that the excitation light 91 does not return to the light projection unit 20, and an angle with the reflective surface 73 is set so that the excitation light 91 is not perpendicularly incident on the incident surface 72. In this embodiment, the angle between the incident surface 72 and the reflective surface 73 and the angle between the reflective surface 73 and the emitting surface 74 are both about 80 degrees.
The metal film 75 is formed on the reflective surface 73 of the prism 71. A material of the metal film 75 is not especially limited as long as this is metal capable of causing the surface plasmon resonance. Examples of the material of the metal film 75 include gold, silver, copper, aluminum, and alloys thereof. A method of forming the metal film 75 is not especially limited. Examples of the method of forming the metal film 75 include sputtering, vapor deposition, and plating. Although a thickness of the metal film 75 is not especially limited, this is preferably within a range of 30 to 70 nm.
The capturing film 76 is a region in which the first capturing body which specifically binds to the substance to be detected is immobilized on the metal film 75. A type of the first capturing body is not especially limited as long as this may specifically bind to the substance to be detected. Examples of the first capturing body include an antibody (primary antibody) capable of specifically binding to the substance to be detected or a fragment thereof, a nucleic acid, an enzyme and the like.
The reaction site 77 is a region of the capturing film 76 exposed to the liquid accommodation unit 65 of the well main body 61 in the second opening 64. In the reaction site 77, the first capturing body which is immobilized on the metal film 75 and forms the capturing film 76 specifically binds to the substance to be detected present in the sample to selectively capture the substance to he detected. From the viewpoint of detection accuracy, it is preferable that the surface on which the reaction site 77 is formed, that is, the surface of the region of the metal film 75 corresponding to the reaction site 77 in this embodiment is a flat surface. It is also possible to apply a protective layer for maintaining a capturing ability of the first capturing body for a long time on the reaction site 77.
A size of the reaction site 77 is not especially limited. In a case where the capturing film 76 has such a size to close the second opening 64, the size of the reaction site 77 is defined by the second opening 64. As a result, the size of the reaction site 77 may be adjusted easily with a high degree of accuracy. On the other hand, in a case where the capturing film 76 is smaller than the second opening 64, the size of the capturing film 76 directly becomes the size of the reaction site 77.
Also, it is preferable that the reaction site 77 be arranged in a position away from the bottom surface on the bottom surface structure 66 side of the well main body 61. As a result, the liquid such as the reagent in the liquid accommodation unit 65 may be supplied to the reaction site 77 to perform the reaction efficiently. Also, when detecting the fluorescence 93, it is possible to prevent the detection accuracy from being lowered by noise caused by the bottom surface on the bottom surface structure 66 side of the well main body 61.
(Operation of Biochemical Inspection System)
First, preparation for measurement is performed (step S10). Specifically, by control of the control arithmetic unit 50, the liquid delivery/conveyance unit 30 moves a target inspection chip 60 to the position 10a of the biochemical inspection system A (refer to
Next, the inspection chip 60 is irradiated with the excitation light, and enhancement measurement for specifying the enhancement angle and optical blank value measurement for measuring an optical blank value are performed (step S20). Specifically, by the control of the control arithmetic unit 50, the liquid delivery/conveyance unit 30 arranges the target inspection chip 60 in the position 10b (refer to
Thereafter, by the control of the control arithmetic unit 50, the light projection unit 10 irradiates the region of the reflective surface 73 corresponding to the reaction site 77 of the inspection chip 60 with the excitation light 91 at the incident angle α set to the enhancement angle. At the same time, the detection unit 40 detects the amount of light of the same wavelength as that of the fluorescence 93. The control arithmetic unit 50 records the light amount of the light measured by the detection unit 40 as the optical blank value.
Thereafter, the measuring buffer solution in the inspection chip 60 is recovered by the liquid delivery/conveyance unit 30, and a sample to be measured is newly supplied into the inspection chip 60. Meanwhile, as the sample to be measured, a sample collected directly from an inspection subject may be used, or a sample obtained by diluting the sample directly collected from the inspection subject with the sample diluting solution may be used.
Next, a primary reaction for allowing the substance to be detected present in the sample to bind to the first capturing body exposed to the reaction site 77 is performed (step S30). Specifically, by control of the control arithmetic unit 50, the liquid delivery/conveyance unit 30 moves the target inspection chip 60 to the position 10c (refer to
After a sufficient time for the reaction elapses, in order to clean the inside of the inspection chip 60, the sample to be measured in the inspection chip 60 is recovered by the liquid delivery/conveyance unit 30, and the cleaning solution is newly supplied into the inspection chip 60. At that time, since the liquid in the inspection chip 60 is continuously stirred by the vibration unit 10, the substance to be detected, impurities and the like which are nonspecifically adsorbed in the inspection chip 60 are removed.
Thereafter, the cleaning solution in the inspection chip 60 is recovered by the liquid delivery/conveyance unit 30, and the labeling solution is newly supplied into the inspection chip 60.
Next, a secondary reaction for assigning the fluorescent label to the substance to be detected captured by the first capturing body is performed (step S40). Specifically, by control of the control arithmetic unit 50, the liquid delivery/conveyance unit 30 moves the target inspection chip 60 to the position 10d (refer to
After a sufficient time for the reaction elapses, in order to clean the inside of the inspection chip 60, the labeling solution in the inspection chip 60 is recovered by the liquid delivery/conveyance unit 30, and the cleaning solution is newly supplied into the inspection chip 60. At that time, since the liquid in the inspection chip 60 is continuously stirred by the vibration unit 10, the second capturing body, impurities and the like which are nonspecifically adsorbed in the inspection chip 60 are removed.
Thereafter, the cleaning solution in the inspection chip 60 is recovered by the liquid delivery/couveyance unit 30, and the measuring buffer solution is newly supplied into the inspection chip 60.
Next, the fluorescence value measurement for measuring the fluorescence value from the substance to be detected labeled with the fluorescence is performed (step S50). Specifically; by the control of the control arithmetic unit 50, the liquid delivery/conveyance unit 30 arranges the target inspection chip 60 in the position 10e (refer to
Thereafter, the inspection chip 60 is disposed by the control of the control arithmetic unit 50, and the control arithmetic unit 50 subtracts the optical blank value obtained at step S20 from the obtained fluorescence value to calculate a signal value correlated with the amount of the substance to be detected. The control arithmetic unit 50 may also further convert the signal value into the amount, concentration and the like of the substance to be detected on the basis of a calibration curve created in advance.
After that, the inspection ends. At above-described steps, the biochemical inspection system A may measure the presence or amount of the substance to be detected in the sample.
Meanwhile, at step S20 described above, the incident angle α of the excitation light 91 is set to the enhancement angle, but the incident angle a, of the excitation light 91 may be set to the resonance angle in place of the enhancement angle. In this case, at step S20, the light projection unit 10 irradiates the region of the reflective surface 73 corresponding to the reaction site 77 of the inspection chip 60 with the excitation light 91 while scanning the incident angle α At the same time, the detection unit 40 detects the light amount of the reflected light 92. The control arithmetic unit 50 obtains data including a relationship between the incident angle α of the excitation light 91 and the light amount of the reflected light 92, specifies the incident angle α when the light amount of the reflected light 92 becomes minimum as the resonance angle on the basis of the data, and sets the incident angle α of the excitation light 91 as the resonance angle.
(Liquid Delivery and Recovery by Liquid Delivery/Conveyance Unit)
Similarly, also when the liquid in the well main body 61 is recovered at each process described above, the first moving mechanism of the liquid delivery/conveyance unit 30 may move the nozzle so as not to pass the region on which the side wall member 62 is arranged of the inspection chip 60 by the control of the control arithmetic unit 50. For example, after the pipette unit sucks the liquid present in the well main body 61, the first moving mechanism of the liquid delivery/conveyance unit 30 may move the nozzle so as move away from the inspection chip 60 from the side on which the side wall member 62 is not arranged of the inspection chip 60 in any direction opposite to the direction indicated by any one of arrows P1, P2, P3, and P4. As a result, it is possible to prevent the inspection result from being adversely affected due to the unexpected contamination on the side wall member 62 used for the biochemical inspection in a case where liquid leakage occurs or a droplet drips from the pipette chip also in a course of recovering the liquid in the well main body 61.
Also, when the liquid in the well main body 61 is recovered at each step described above, the first moving mechanism of the liquid delivery/conveyance unit 30 may move the nozzle so as to extract the pipette chip after removing liquid remaining in the pipette chip or around the pipette chip by allowing the same to creep on an inner wall of the inspection chip 60 on the side on which the side wall member 62 is not arranged by the control of the control arithmetic unit 50. This further reduces a risk of occurrence of the unexpected contamination on the side wall member 62.
The present application claims priority based on JP 2017-025826 A filed on Feb. 15, 2017. The contents described in the specification and drawings of the application are entirely incorporated herein by reference.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2017-025826 | Feb 2017 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2018/003962 | 2/6/2018 | WO | 00 |
