JP2006112790A - Liquid droplet spectroscopic system and spectroscopic method - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an infinitesimal spectroscopic system in order not only to respond to needs of the conversion of measurement to a micro-amount system and a cuvette system but also to solve the point at issue accompanied by the conversion of measurement to the micro-amount system, and also provide a spectroscopic method. <P>SOLUTION: Liquid droplets are formed on a hydrophobic substrate and a hydrophilic line for guiding the movement of the liquid droplets is provided to successively feed the liquid droplets on the line. A detection system is constituted so as to cross the hydrophilic line and, when the liquid droplets traverse the detection system, absorbancy or the intensity of fluorescence is measured. The liquid droplets on the hydrophilic line are irradiated with white light or exciting light to spectrally diffract the transmitted light or to detect fluorescence. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention utilizes the phenomenon that when a very small amount of a sample containing water as a solvent is dropped on a water-repellent substrate, it becomes a droplet on the water-repellent substrate, and a measurement and apparatus for measuring a spectral solute with a very small amount of liquid. About the system.

  As a method for measuring the amount of solute contained in a solvent, there is a method using optical measurement such as a spectrophotometer or a fluorometer. In a spectrophotometer, light having a wavelength at which a solute contained in a solvent absorbs light is irradiated, and the amount of light absorbed by the solute and reduced is measured as absorbance. In a fluorimeter, light of a specific wavelength is absorbed by a solute to bring the solute molecule into an excited state, and the intensity of light emitted when the electronic state changes from the excited state to the ground state is detected. In any case, the sample solution is put into a cuvette having a certain optical path length and measurement is performed. Since the amount of light absorption changes when the optical path length varies, it is important to ensure a constant optical path length in absorbance measurement and fluorescence measurement. In measuring absorbance in a solution using a spectrophotometer, a cuvette having an optical path length of 1 cm is generally used.

  Recently, in order to cope with the miniaturization of the sample solution, a micro cuvette capable of measuring the absorbance with 5 μl of the sample solution is already on the market. A trace amount cuvette is used as a foil layer having an optical path length of about 0.5 mm, but there are problems such as difficulty in cleaning the cuvette, poor operability, and the time taken to measure multiple specimens. In order to increase the throughput, there is a method in which a sample is continuously input using a flow cell and measurement is performed. However, if the cuvette is not sufficiently washed, a carry-over in which the previous sample affects the next sample occurs. In addition, since the sample is measured serially, the throughput does not increase so much.

  As a technique for increasing throughput by parallel processing, a technique using a microplate has been established. This uses 96 wells and 384 wells as cuvettes. Since a certain amount of sample solution is put into each of these wells and the absorbance is measured, this is an excellent technique from the viewpoint of throughput.

  In the fluorometer, the situation is the same as the absorbance measurement.

  Regardless of whether it is absorbance measurement or fluorescence intensity measurement, it is an important issue to cope with a small amount of sample and high throughput. In recent years, in the field of biochemistry, the reaction has been miniaturized, and most enzyme reactions have been performed in several to several tens of microliters at most. In the biochemical field, there are a wide variety of combinations of samples to be reacted, and the mainstream is the miniaturization of reactions and high throughput by multiple simultaneous reactions.

  Furthermore, the problem is that the ratio of the surface area of the cuvette to the volume of the sample increases as the amount is reduced. When the surface area of the cuvette is increased, the phenomenon that the solute is adsorbed on the wall often becomes remarkable. In some cases, scattering of light between the solution and the wall affects the measurement as scattered light. In general, the spectroscopic measurement and the fluorescence measurement are performed by transferring the various reactions in different containers before the measurement to a measurement cuvette. When the number of specimens increases, it is difficult to perform the transfer operation alone, and the fact that human error such as transfer mistakes cannot be eliminated is a problem particularly in medical biomaterial testing. Although this is a problem that can be solved by automation using a robot, the apparatus becomes large and expensive.

  The present invention proposes an extremely small amount of spectroscopic system and spectroscopic method in order to meet the needs of micro measurement and cuvette measurement, and to solve the problems associated with micro measurement as described above.

  The present invention utilizes a phenomenon in which a solvent mainly composed of water becomes droplets that are almost perfect circles on a water-repellent substrate. Droplets are generated on a hydrophobic substrate, a hydrophilic line for guiding the movement of the droplets is provided, and the droplets are sequentially conveyed on the lines. The detection system is configured to intersect with the hydrophilic line, and the absorbance and fluorescence intensity are measured when the droplet crosses the detection system. The liquid droplets on the hydrophilic line are irradiated with white light or excitation light, and the transmitted light is dispersed to measure the absorbance, or the fluorescence is detected. Regarding the optical path length required for absorbance measurement and fluorescence measurement, the optical path length is derived by measuring the size of the droplet.

  It enables high-throughput absorbance measurement and fluorescence intensity measurement on the order of submicroliters, which is essential in modern biochemistry. Since the amount of sample liquid is extremely small, the amount of valuable sample used can be reduced. Furthermore, the tip can be made disposable, the droplet can be rolled along the hydrophilic line, and a recovery area can be provided at the end point of the line, whereby the valuable sample liquid can be recovered.

Example 1
An example of measuring protein concentration will be described. Here, protein quantification is attempted at a wavelength of 280 nm, which is a general protein absorption band. The protein is chicken egg white lysozyme and the molecular extinction coefficient is E ^1% ₂₈₀ = 26.6. The concentration is used in advance as a dilution series prepared from 0.05 mg / ml to 10 mg / ml.

  1A is a plan view of a measurement substrate 100 suitable for the first embodiment and a conceptual diagram of a measurement system configured based on the measurement substrate. FIG. 1B is an AA view of the plan view of the measurement substrate 100. FIG. It is sectional drawing of the measurement board | substrate 100 when it sees in the arrow direction at a position. Reference numeral 1 denotes a silicon substrate, which has a thickness of 1 mm and a size of 40 mm × 40 mm, for example. The surface of the silicon substrate 1 is a hydrophobic region 2 in which a hydrophilic line 4 is provided. The length of the hydrophilic line 4 is, for example, 20 mm and the width is 0.1 mm. A liquid reservoir 3 is formed at the end point of the hydrophilic line 4. Reference numeral 5 denotes a positioning marker, which is formed on one surface of the silicon substrate 1. As will be described later, a droplet is formed at the left end of the hydrophilic line 4, and the droplet is moved to the liquid reservoir 3 on the hydrophilic line 4 at a predetermined speed. The size of the drawings is deformed for explanation.

  A measurement system 50 is provided at a substantially central position of the hydrophilic line 4 so as to intersect the hydrophilic line 4. The measurement system 50 includes the wide-area light source 10 that emits light from the ultraviolet region to the visible region, and the white light parallel to the surface of the measurement substrate 100 in the vicinity of a droplet that guides the white light of the wide-area light source 10 and moves on the hydrophilic line 4. An optical fiber 11 that irradiates the droplet with light, an optical fiber 12 that is provided opposite to the optical fiber 11 with the hydrophilic line 4 interposed therebetween, receives white light transmitted through the droplet, and transmits a droplet guided by the optical fiber 12. The detector 13 includes white light as an input. Here, it goes without saying that the tips of the optical fibers 11 and 12 that are arranged to face each other across the hydrophilic line 4 are arranged so as not to come into contact with the liquid droplets moving on the hydrophilic line 4. The detector 13 includes a spectroscope 14 and a CCD line sensor 15.

  On the left side of the measurement system 50, the laser beam 20 is irradiated in parallel with the surface of the measurement substrate 100 so as to intersect the hydrophilic line 4. 21 is a laser source, 22 and 23 are reflection mirrors of the laser beam 20, and 24 is a detector of the laser beam 20. This laser beam 20 is for measuring the diameter of a droplet moving on the hydrophilic line 4. Therefore, the irradiation of the laser beam 20 may be performed on the right side of the measurement system 50.

  In FIG. 1B, since the cross-sectional position is the position of the hydrophilic line 4, the entire central portion of the substrate 1 is a hydrophilic region. A liquid reservoir 3 is provided at the right end of the hydrophilic line 4.

For example, the hydrophilic line 4 (hydrophilic region) and the hydrophobic region are created by oxidizing the upper surface of the hydrophobic silicon substrate 1 to temporarily form the entire region as a hydrophilic SiO ₂ thin film. Thereafter, the hydrophobic region may be created by dissolving and removing the SiO ₂ thin film in the region to be made hydrophobic with hydrofluoric acid. Alternatively, if the hydrophilic surface material of the substrate 1 is the surface is previously SiO ₂ film formation, fluorine-based resin, a hydrophobic material such as silicon-based resin, by disposing thereon, forming a hydrophobic region Just do it. In this case, the hydrophilic region present in the hydrophobic region is reduced by the thickness of the hydrophobic material. The example of FIG. 1 is an example in which the hydrophobic region 3 and the hydrophilic line 4 are formed by the latter method.

  In Example 1, a liquid droplet to be measured is formed in advance on the left end of the hydrophilic line 4 and moved to the right side at a predetermined speed on the hydrophilic line 4. Measure the size and analyze the droplet.

  FIG. 2 is a conceptual diagram illustrating an example of a system configuration in which droplets are formed at the left end of the hydrophilic line 4 of the measurement substrate 100 suitable for the implementation of the present invention and measured.

  First, an operation for forming a liquid droplet 36 to be measured at the left end of the hydrophilic line 4 of the measurement substrate 100 will be described below. When the system is activated, the user pays attention to the marker 5 described with reference to FIG. 1A and gives an operation signal 28 to the personal computer 26 so that the measurement board 100 is at a predetermined activation position, and the drive device 27, the stage 19 is operated and positioned. The stage 19 is driven in the XY directions according to the signal. Next, an operation signal 28 is given to the personal computer 26 so that the mounting position of the liquid droplet 36 to be measured (the left end of the hydrophilic line 4) is a position corresponding to the tip of the pipette 33, and driving. The stage 27 is operated by the device 27 and positioned. At this time, if necessary, the position signal can be fed back to the personal computer 26 and accurately matched while monitoring the tip of the pipette 33 with an optical system. Note that the liquid to be measured is sucked into the pipette 33 in advance.

  When the measurement substrate 100 comes to a predetermined position, that is, when the left end of the hydrophilic line 4 and the tip of the pipette 33 are in a corresponding position, this is detected, or by the operator's instruction from the personal computer 26, the drive device 32 Is sent a signal for discharging the liquid 34 to be measured, and the syringe pump 31 is driven to discharge the liquid to be measured in the pipette 33 and form a droplet 36 at the tip of the pipette 33. The size of the droplet 36 formed at the tip of the pipette 33 is determined by the density and specific gravity of the liquid to be measured, the size of the tip of the pipette 33, and the like. Since it falls, the stop of the syringe pump 31 is merely programmed in the personal computer and does not necessarily need to be controlled.

  If it is better to control, the droplet 36 formed at the tip of the pipette 33 is monitored by an optical system, and the drive device 32 is controlled according to the signal given thereto. Or by the operator's instruction to stop the syringe pump 31 and push down the pipette 33 (not shown, but for this purpose, a drive device similar to the drive device 37 for controlling the rod 41 described later) The droplet 36 formed on the tip of the pipette 33 may be brought into contact with the left end of the hydrophilic line 4 of the measurement substrate 100 and transferred onto the hydrophilic line 4. The reason why the base of the pipette 33 and the connection portion of the tube 30 are separated is that the pipette 33 is enlarged and displayed.

  Next, measurement of the liquid droplet 35 to be measured placed on the left end of the hydrophilic line 4 of the measurement substrate 100 will be described. Here, 1 μl of the solution containing the protein (solvent: 50 mM phosphate buffer solution of pH 7.4 containing 150 mM NaCl) is used as the solution to be measured. Next, a rod 41 made of glass having a diameter of 0.1 mm and having a hydrophilic tip and a hydrophobic polyimide on the side is brought into contact with the top of the droplet 35. Here, the rod 41 is assumed to be linked to a drive device 37 that moves the rod 41 up and down and moves horizontally on the hydrophilic line 4. When the rod 41 is positioned at the left end of the hydrophilic line 4 and a signal is given to the personal computer 26 to lower the rod 41 by the user, the rod 41 is moved downward by the dynamic drive device 37. When the tip of the rod 41 comes into contact with the droplet 35, the dynamic drive device 37 is stopped, and then the rod 41 is moved horizontally on the hydrophilic line 4 to the right at a predetermined speed. Accordingly, the droplet 35 on the hydrophilic line 4 of the measurement substrate 100 moves along the hydrophilic line 4 horizontally to the right at a predetermined speed and falls into the liquid reservoir 3.

  The droplet 35 passes through the laser beam 20 in the process of moving horizontally on the hydrophilic line 4 to the right at a predetermined speed, and the diameter of the droplet 35 is measured. For example, when the rod 41 is moved at a speed of 2 mm / second, the droplet 35 is clung to the tip of the rod 41 and moved at the same speed. That is, the droplet 35 also moves at 2 mm / second at the moving speed of the rod 41. When the droplet 35 crosses the laser beam 20, light is refracted at the interface of the droplet 35, and the amount of light reaching the detector 24 changes. When the droplet 35 passes the laser beam 20, the light amount reaching the detector 24 returns to the original light amount. If the time traversing the laser beam is 1.22 seconds, the diameter of the droplet 35 is calculated as 0.61 (= 1.22 / 2) mm at the position traversing the laser beam. In this case, it is assumed that the height of the laser beam 20 from the measurement substrate 100 is half the diameter of the droplet 35. Therefore, when the diameter of the droplet 35 changes greatly, it is necessary to adjust the height of the laser beam 20 from the measurement substrate 100 accordingly.

  The droplet 35 then passes through a position where the optical fibers 11 and 12 of the detector system face each other. In this case, since the heights of the optical fibers 11 and 12 from the measurement substrate 100 are also set equal to the height of the laser beam 20 from the measurement substrate 100, the optical path length of the liquid to be measured is also 0.61 mm. The maximum absorbance when passing between the optical fibers 11 and 12 of the detector system is measured, and converted to a value when the optical path length is 1 cm.

  FIG. 3 is a characteristic diagram when the measured absorbance according to Example 1 is plotted. The characteristic which consists of the linear part 21 and the non-linear part 22 as shown in a figure is acquired. The non-linear portion 22 is a phenomenon that generally occurs because the lysozyme concentration is too high. The measurement results are in good agreement when compared with known values for known protein concentrations.

  In the measurement of the first embodiment, the droplet 35 that has fallen into the liquid reservoir 3 is only transmitted through the laser beam 20 and white light irradiated from the optical fiber 11 of the detector system. No operation involving Therefore, the droplet 35 that has fallen into the liquid reservoir 3 can be sucked and used for other measurements.

  Furthermore, in the measurement of Example 1, only the hydrophilic line 4 of the measurement substrate 100 is contaminated by the measurement. Therefore, even if a new sample droplet is dropped on the left end of the hydrophilic line 4 and the measurement is repeated, the new sample droplet is not contaminated by the previous measurement sample. Can be successively dropped onto the hydrophilic line 4 of the measurement substrate 100 to perform measurement, and the throughput can be increased.

  The measurement according to the present invention is capable of instantaneously measuring the spectrum, and the applied light only needs to have no change in the intensity of the wavelength component over time, and can be measured in an open space. Of course, a conventional spectroscopic optical system that measures the absorbance by irradiating the droplets with light split to a single wavelength may be employed. In this case, it cannot be used in an open space and is measured in a dark box.

  In addition, since no cuvette is used, only the droplets and air are exposed to light. For this reason, there is an advantage that spectroscopic measurement can be performed even at a wavelength at which the cuvette absorbs light. For example, when trying to measure the amount of protein with light absorption at 210 nm, a normal glass cuvette or plastic cuvette cannot be used. Although a cuvette made of expensive fused quartz may be used, the expensive fused quartz cuvette can be eliminated by using the present invention.

(Example 2)
Example 2 is an example in which fluorescence measurement is performed. This is an example including a pretreatment in which a reagent is mixed with a liquid to be measured before measurement and a reaction is performed.

  4A is a plan view of a measurement board 200 suitable for the second embodiment and a conceptual diagram of a measurement system configured based on the measurement board. FIG. 4B is a plan view of the measurement board 200 taken along line AA. It is sectional drawing of the measurement board | substrate 100 when it sees in the arrow direction at a position. The size of the drawings is deformed for explanation.

  The measurement substrate 200 is the same as the measurement substrate 100 of the first embodiment, and 1 is a silicon substrate, and has a thickness of 1 mm and a size of 40 mm × 40 mm, for example. The surface of the silicon substrate 1 is a hydrophobic region 2, and a hydrophilic region 52-54 and a hydrophilic line 56-59 for holding droplets are provided therein. A liquid reservoir 3 is formed at the end (right end) of the hydrophilic line 59. The size of the hydrophilic region 52-55 is determined by the size of the droplet held in this region, and is about 400 μm × 400 μm, for example. The width of the hydrophilic line 56-59 is about 0.1 mm. Reference numeral 5 denotes a positioning marker, which is formed on one surface of the silicon substrate 1. Reference numeral 8 denotes a temperature control plate, which is provided on the back surface of the silicon substrate 1. The size of the drawings is deformed for explanation.

  A measurement system 51 is provided so as to intersect the hydrophilic line 59. The measurement system 51 irradiates the laser beam in parallel with the surface of the measurement substrate 100 in the vicinity of the droplet that moves on the hydrophilic line 59 by guiding the laser beam of the fluorescence excitation laser source 21 ′ and the laser source 21 ′. An optical fiber 11 that irradiates the droplet, an optical fiber 12 that faces the optical fiber 11 across the hydrophilic line 59, receives fluorescence emitted by the droplet, and detection that uses fluorescence emitted by the droplet guided by the optical fiber 12 as input. It is composed of a container 13 '. The optical fiber 12 is installed so as to form an angle of 120 degrees with the optical fiber 11 so that the reflected light of the surface of the laser beam irradiated to the droplet does not enter. Again, the optical fiber 12 provided opposite to the optical fiber 11 is provided at a distance such that the tip of the optical fiber 12 does not contact the droplet moving on the hydrophilic line 59.

  In Example 1, as described with reference to FIG. 2, droplets are formed in the hydrophilic regions 52-54. The hydrophilic region 54 is a droplet containing a single-stranded cDNA mixture reversely transcribed from mRNA, the hydrophilic region 53 is a droplet consisting of a 60-base probe solution that hybridizes to a specific cDNA, and the hydrophilic region 52 is a droplet. Each form a droplet consisting of a Cyber Green I solution that specifically intercalates into two strands. Each droplet is 0.5 μl. Here, as a model system, a cDNA probe of 0.2 pmol / μl is examined with a 5 pmol / μl complementary probe and a specific complementary probe. The solvent is 10 mM Tris-HCl (pH 8.0) containing 50 mM NaCl.

  First, the droplets formed in the hydrophilic region 54 and the droplets formed in the hydrophilic region 53 are moved to the hydrophilic region 55 by the same method as in the first embodiment, and mixed here. Mixing can be performed by rotating the rod 41 used for transporting the droplets in the axial direction. Of course, a piezoelectric element is provided on the back surface of the silicon substrate 1 at the position where the hydrophilic region 55 is formed, and the ultrasonic wave generated by this is applied to the droplet placed in the hydrophilic region 55 to stir by specific contact. May be. After stirring for 30 seconds, the droplet formed in the hydrophilic region 52 is added to the droplet stirred in the hydrophilic region 55 and stirred again. After stirring for 30 seconds, the three droplets stirred in the hydrophilic region 55 are moved on the hydrophilic line 59 at a predetermined speed, for example, 2 mm / second. When the droplet moving on the hydrophilic line 59 passes between the tips of the optical fiber 12 provided opposite to the optical fiber 11, it receives the laser beam of the laser source 21 'and emits fluorescence. The fluorescence intensity at this time is measured by the detector 13 ′ via the optical fiber 12.

  When cDNA complementary to the probe is present in the sample solution, fluorescence with an intensity corresponding to the amount is obtained. In the absence of complementary cDNA, the fluorescence intensity is less than 1/20.

In the second embodiment, it is better to manage the size of the droplets more strictly than in the first embodiment. Therefore, when the droplets described with reference to FIG. 2 are formed, measurement is performed with a CCD camera using an optical system (not shown). Then, it is preferable to control the drive device 32 of the syringe pump 31 by inputting it into the personal computer 26 and performing a predetermined process. In short, this optical system only needs to monitor the tip of the pipette 33. In addition, the temperature control plate 8 provided on the back surface of the measurement substrate 200 may be controlled so that the measurement substrate 200 is operated in a wet state at a temperature of 42 ° C. to 46 ° C. and an atmosphere of 45 ° C. When the droplet size changes while monitoring the droplet size after movement and stirring with the optical CCD camera, feedback control is applied to the temperature control plate 8 so that the droplet size is 10% or more. It is better to control so that it does not fluctuate. (In Example 2, I think it is better to touch briefly why it is better to strictly control the droplet diameter.)
In Example 2, the droplet formed in the hydrophilic region 54 and the droplet formed in the hydrophilic region 53 are moved to the hydrophilic region 55 in the same manner as in Example 1 and mixed to react. The pretreatment is performed, and then the mixed droplets are reacted with the droplets formed in the hydrophilic region 52, whereby the treatment can be integrated, so that the above-described artificial mistake can be prevented. In addition, since this process is performed on one measurement substrate 200, in order to prevent contamination, it is preferable to use a single-use chip that is measured immediately after the reaction.

  It can be used for the purpose of detecting reaction products in combination with various reactions, and can be solved by using a system-on-chip that integrates sample reaction and detection. The reaction precursor is divided into several droplets, and each droplet is collided in a predetermined order on the hydrophilic line to carry out the reaction. The reaction time may be, for example, that a hydrophilic region having a diameter of about 2 to 4 times the line width is provided on the hydrophilic line so that the droplet stays there, or a slightly recessed portion is provided. This can be solved by allowing the droplets to stay there for a predetermined time.

(Other examples)
The present invention is not limited to the configuration of the above-described embodiment, and can be implemented in various forms.

  For example, the movement of the liquid droplet by the rod 41 described with reference to FIG. 2 can be replaced by gas injection. For example, a gas injection nozzle is disposed on the extension line of the hydrophilic line 4, and a tube connected to a gas pressure tank and a valve are provided in the gas injection nozzle. The movement of 35 may be controlled. If gas jetting is performed in consideration of the size and mass of the droplet, the droplet 35 is guided by the hydrophilic line 4, moves on the hydrophilic line 4 at a predetermined speed, and falls into the liquid reservoir 3. Also in Example 2, the movement from the hydrophilic region 55 to the liquid reservoir 3 can be performed in the same manner. When gas injection is performed in this way, the number of structures that move on the upper surface of the measurement substrate 200 is reduced, and the configuration of the apparatus is simplified.

  Surface acoustic waves can be used to move the droplets. FIG. 5 is a conceptual diagram illustrating an example of a system configuration in which a droplet is formed at the left end of the hydrophilic line 4 and is measured by moving the droplet using a surface acoustic wave. A surface acoustic wave generator including a piezoelectric element 205 and a comb-shaped electrode 206 is disposed under the hydrophobic line 4 on which the droplets on the substrate 1 move. As the comb electrode, a lithium compound such as lithium tetraborate, lithium tantalate, or lithium niobate can be used. As described in the first embodiment, the surfaces of the piezoelectric element 205 and the electrode 206 are subjected to a hydrophobic coating, and the hydrophilic line 4 is provided in the droplet transport direction. By applying a voltage between the counter electrodes of the comb-shaped electrode 206, surface-aligned surface acoustic waves can be generated along the hydrophilic line 4. The droplet 202 moves on the surface acoustic wave. Here, the comb-type device is installed in the upstream portion of the hydrophilic line 4 for creating a droplet. The piezoelectric substrate portion may be installed in the entire hydrophilic line of the substrate 1 or may be installed only in the vicinity of a portion where the droplet 202 is dropped as shown in FIG. By applying a voltage between the comb electrodes, a surface acoustic wave is generated, and a droplet is ejected in the direction of arrow 204 and moves.

  Generally, the sample used for the conventional absorbance measurement is discarded as it is. For this reason, if the amount of liquid used for measurement is large, the sample is wasted.

  For example, a plurality of systems of the hydrophilic line 4 and the liquid reservoir 3 described in FIG. 1 are provided in parallel, and a solution of a sample to be measured is disposed as a droplet at the left end of each hydrophilic line 4, and this is gas. High throughput can be achieved by performing measurement by sequentially rolling to the detection unit by injection. In this case, it is practical to use one gas injection system and move the stage 19.

  As another force for moving the droplet, it is possible to move the droplet by putting one micro magnet into the droplet and moving the micro magnet with a magnetic field from the back of the substrate. In this case, the micro magnets are hydrophilic so that the droplets cling. The micro magnet can be made to be less than half the diameter of the droplet so as not to interfere with the subsequent absorbance measurement.

(A) is a plan view of a measurement substrate 100 suitable for Example 1, and a conceptual diagram of a measurement system configured based on this measurement substrate, (B) is an AA position of the plan view of the measurement substrate 100. It is sectional drawing of the measurement board | substrate 100 when it sees in the arrow direction. It is a conceptual diagram explaining the example of the system structure which comprises a droplet at the left end of the hydrophilic line 4 of the measurement board | substrate 100 suitable for implementation of this invention, and measures this. It is a characteristic view when the measured light absorbency by Example 1 is plotted. (A) is a plan view of a measurement board 200 suitable for the second embodiment and a conceptual diagram of a measurement system configured based on the measurement board, and (B) is a position AA in the plan view of the measurement board 200. It is sectional drawing of the measurement board | substrate 100 when it sees in the arrow direction. It is a conceptual diagram explaining the example of the system structure which comprises a droplet at the left end of the hydrophilic line 4, and moves and measures this using a surface acoustic wave.

Explanation of symbols

  DESCRIPTION OF SYMBOLS 1 ... Silicon substrate, 2 ... Hydrophobic area | region, 3 ... Liquid reservoir, 4 ... Hydrophilic line, 5 ... Positioning marker, 8 ... Temperature control board, 10 ... Wide-area light source, 10 '... Laser source, 11, 12 ... Optical fiber, 13, 13 '... detector, 14 ... spectroscope, 15 ... CCD line sensor, 20 ... laser beam, 21 ... laser source, 22, 23 ... reflection mirror, 26 ... personal computer, 27, 32, 37 ... drive device , 28 ... Operation signal, 33 ... Pipette, 34 ... Liquid to be measured, 31 ... Syringe pump, 35, 36, 202 ... Droplet, 52-55 ... Hydrophilic region, 56-59 ... Hydrophilic line, 50, DESCRIPTION OF SYMBOLS 51 ... Measurement system, 100, 200 ... Measurement board | substrate, 205 ... Piezoelectric element, 206 ... Comb-type electrode.

Claims (10)

  Means for forming a droplet containing a solute on the substrate; means for moving the droplet across the light beam; and a light source for the light beam and a photodetector for detecting a signal obtained when the droplet crosses the light beam. Absorption spectroscopic system.   Absorption having means for forming droplets containing a solute on the substrate, means for condensing the light rays on the droplets, and a photodetector for detecting the intensity of light incident on the droplets and passing through the droplets. Spectroscopic system.   Means for forming a droplet containing a solute on the substrate; means for moving the droplet across the light beam; and a light source for the light beam and a photodetector for detecting a signal obtained when the droplet crosses the light beam. Fluorescence spectroscopy system.   A substrate having a hydrophilic pattern for holding droplets on a water-repellent surface, means for moving droplets formed on the substrate across the beam on the hydrophilic pattern, the light source of the beam and the droplet An absorption spectroscopic system having a photodetector for detecting a signal obtained by crossing a light beam, and measuring means for measuring the size of a droplet moving across the light beam on the hydrophilic pattern, An absorption spectroscopic system having an arithmetic unit that calculates an optical path length based on a droplet size.   A substrate provided with a hydrophilic pattern for holding droplets on a water-repellent surface; means for moving droplets formed on the substrate across the hydrophilic pattern using surface acoustic waves; Absorption spectroscopy system having a light source and a photodetector for detecting a signal obtained when the droplet crosses the light beam, an arithmetic unit for estimating the size of the droplet from time variation of the position of the droplet and calculating the optical path length And a spectroscopic system.   6. The spectroscopic system according to claim 5, wherein the means for generating the surface acoustic wave is a piezoelectric substrate disposed in the droplet conveyance path and a comb-shaped electrode of lithium tetraborate, lithium tantalate, or lithium niobate.   The absorption spectroscopy system according to claim 4, wherein the substrate includes a temperature adjustment plate in contact with the substrate.   Drops are placed on a substrate line with a hydrophilic line pattern that holds the droplets on the water-repellent surface, and the droplets are moved according to the hydrophilic line pattern. A signal including droplet information is detected by a light detector by traversing the detected light, and the size of the droplet is measured from the signal, and the droplet passes through the droplet based on the measured droplet size. Spectroscopy that calculates the optical path length of light and measures the light absorption or fluorescence of the droplet.   The hydrophilic line pattern has a pattern in which a plurality of hydrophilic lines merge together, and the respective droplets held in the plurality of hydrophilic lines are mixed at a pattern merge point. 6. A spectroscopic system for measuring light absorption or fluorescence of a droplet according to 5.   The plurality of hydrophilic lines have a pattern of merging into one, and a further merging point is on the downstream side of the merging point, at the merging point of each droplet held in the plurality of hydrophilic lines. The spectroscopic method for measuring light absorption or fluorescence of a droplet according to claim 6, which has a pattern in which mixing can be performed a plurality of times in time series.

Images