JP2005147957A - Microchip for mass spectrometry and mass spectrometer using the same - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a component for mass spectrometry capable of measuring the mass of a trace amount of a sample. <P>SOLUTION: This microchip 1 is provided with a sample inlet part 12; a sample cutting part 20, formed in a channel communicating with the sample inlet part for cutting out parts of the sample; branch channels 22 for feeding cutout samples to different channels; branch channel opening and closing valves VC, each provided for the branch channels; sample storage parts 24 each formed downstream of the branch channel opening and closing valves VC; and extraction channels 28 communicating with the sample storage parts 24 for extracting the stored sample. The microchip 1 is used for fractionating the trace amount of the sample required for the sample storage parts 24 and delivering it into a mass spectrometer. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to a mass analysis microchip for preparing an analysis sample to be supplied to a mass spectrometer, and more particularly to a microchip ionization component used when ionizing an analysis sample. The present invention also relates to a mass spectrometer that performs mass spectrometry using a microchip for mass spectrometry.

Various methods have been devised for the ion source of the mass spectrometer.
When a sample on a solid or semi-solid is measured by TOFMS (time-of-flight mass spectrometer), a MALDI method in which the sample is scattered and ionized by laser irradiation is frequently used. This has the feature that the MALDI method can softly ionize the polymer ions in the sample while leaving the features as polymer ions, and the ionization by pulsed laser irradiation is intermittently measured. It is because it is suitable for.

  However, in the measurement by the MALDI method, after separating and purifying the sample in a separate process in advance, the sample is dispensed to the micro cell plate for MALDI irradiation, and the micro cell plate into which the sample is injected is attached to the mass spectrometer. I do. These operations are discontinuous operations involving a plurality of processes processed independently, and are difficult to automate. Of course, it is not impossible to proceed with automation using a robot mechanism, but even if it is automated, discontinuous work is likely to contain contaminants in the sample during the work. Causes uncertainty in the measurement results.

In LCMS (liquid chromatograph mass spectrometer) that combines a mass spectrometer using atmospheric pressure ionization method such as ESI (electrospray ionization) and a liquid chromatograph, a liquid sample separated by a column. Is continuously sent to the ion source, and the liquid sample sent to the ion source is sequentially ionized to detect a mass spectrometer detector (in this case, an ion trap detector, a quadrupole detector) Used) and continuous measurement is performed.
However, when an atmospheric pressure ionization method such as ESI is combined as an ion source for TOFMS or an ion trap mass spectrometer, the TOFMS or ion trap mass spectrometer performs measurement intermittently, so that ions are measured in addition to the measurement timing. The sample introduced into the source is discarded without being measured, and the utilization efficiency of the sample is never good.

In recent years, as the importance of mass spectrometry in the bio field dealing with biological samples has increased, opportunities for mass analysis of trace samples such as proteins have increased. On the mass spectrometer side, the use efficiency of trace samples has been increased, There is a need to make effective measurements.
In particular, in an ion trap mass spectrometer using an ion trap detector, there is a strong demand for effective use of a sample, and a pulsed ion source capable of measuring with a very small amount of sample is required.
JP 9-320515 A JP 2003-16992 A

Therefore, an object of the present invention is to provide a mass spectrometer capable of performing mass spectrometry by effectively using a trace amount sample and a new ionization component suitable for mass analysis of the trace amount sample.
Another object of the present invention is to provide an ionization component suitable for ionization of a mass spectrometer that is intermittently measured, such as a TOFMS or an ion trap mass spectrometer.

  A first invention made to solve the above-mentioned problems is a microchip for mass spectrometry for preparing a sample for mass spectrometry, which is formed on a sample introduction part and a channel communicating with the sample introduction part The sample cutting unit that sequentially cuts a part of the sample flowing from the sample introduction unit, the plurality of sample storage units, the sample cutting unit, and each sample storage unit are connected to each other through the flow path, and the sample cutting unit cuts the sample. A branch channel for sending a part of the sample to any one of the sample storage units, a branch channel opening / closing valve provided in each of the branch channels, and a sample stored in the sample storage unit in communication with the sample storage unit And an extraction flow path for taking out the liquid.

  According to the present invention, the sample injected from the sample introduction part is sent to the sample cutting part and cut out by a certain amount. Each micro sample cut out is sent to one of the branch channels selected by the branch channel open / close valve, and stored in a sample storage section provided in each branch channel. Thus, each micro sample cut by the sample cutting part is stored independently in a separate sample storage part. And when measuring with a mass spectrometer, the trace sample of a measuring object is selected and it introduce | transduces into a mass spectrometer through a extraction flow path from a sample storage part. Thus, mass spectrometry is performed by sequentially taking out the samples stored in the sample storage unit at a necessary timing.

  In the microchip for mass spectrometry of the second invention, the take-out flow path communicates with a discharge nozzle formed on the outer wall of the microchip. According to the present invention, mass analysis is performed by sending the sample discharged from the nozzle on the outer wall of the chip to the mass spectrometer.

  Moreover, the microchip for mass spectrometry of the third invention further includes a sample separation unit for separating the sample introduced from the sample introduction unit for each component in the flow path between the sample introduction unit and the sample cutting unit. I have to. According to the present invention, since the injected sample is separated for each component in the sample separation unit, the micro sample separated for each component is stored in each sample storage unit.

  In the microchip for mass spectrometry of the fourth invention, a chromatography column or an electrophoresis column for separating each component is formed in the sample separation unit. According to this invention, the column material for chromatography or the column material for electrophoresis is formed in the flow path formed on the chip, whereby the sample is separated for each component.

Further, the microchip for mass spectrometry according to the fifth aspect of the present invention has a sample cutting part that branches from the cut-off channel sandwiched between the front-side channel switching unit and the rear-side channel switching unit and the front-side channel switching unit and vents. A vent flow path connected to the port and a discharge flow path branched from the rear flow path switching portion and connected to the discharge port are configured. According to the present invention, the rear flow channel switching unit flows from the sample introduction unit side until the sample portion to be cut flows between the front flow channel switching unit and the rear flow channel switching unit. The sample is driven downstream to become a discharge port. When the sample portion to be cut is between the front channel switching unit and the rear channel switching unit, the rear channel switching unit switches the channel to the branch channel. Then, the front side channel switching unit is switched to the vent channel side, and the sample is driven so as to be sent to the sample storage unit via one branch channel opening / closing valve selected from the vent channel. When the sample is stored in the sample storage unit, the rear channel switching unit switches to the discharge channel side again, and waits until the next sample to be cut comes. Thereafter, the sample portions to be sequentially cut out in the same procedure are stored in the sample introduction portion.
A detection mechanism for confirming the sample position to be cut out may be provided. For example, a sensor such as a photodetector or a fluorescence sensor can be provided in front of the bulb. Moreover, you may position by the sample amount introduce | transduced from the sample separation part.

  In the microchip for mass spectrometry of the sixth invention, the front flow path switching unit and the rear flow path switching unit are formed by a three-way valve. According to this invention, the switching of the vent flow path and the switching of the discharge flow path can be easily performed by the three-way valve.

Moreover, the microchip for mass spectrometry of the seventh invention is further provided with a reagent solvent introduction part for injecting a reagent or a solvent between the sample cutting part and the branch channel.
According to the present invention, various pretreatments can be performed before mass spectrometry by diluting or reacting the sample by injecting a reagent or a solvent from the reagent solvent introduction part.

In the mass spectrometry microchip according to the eighth aspect of the present invention, an ionization opening for ionization by laser irradiation is further formed, and the take-out flow path communicates with the opening.
According to this invention, the microchip for mass spectrometry is directly attached to the ionization part of the mass spectrometer main body. Then, a small amount of sample is sent from one selected sample storage section to the ionization opening through a sample extraction open / close valve, and ionization is performed by performing laser irradiation from the laser light source of the mass spectrometer.

The microchip for mass spectrometry of the ninth invention further forms a waveguide for guiding laser light to the ionization opening.
According to the present invention, the laser light is accurately and efficiently guided to the ionization opening through the waveguide.

According to a tenth aspect of the present invention, there is provided a mass spectrometry microchip having the above-described ejection nozzle, a mass spectrometer main body having a mass spectrometry unit for performing mass analysis of a sample, and a mass spectrometry microchip. And an interface unit for introducing the sample discharged from the discharge nozzle of the chip into the mass analyzing unit.
According to the present invention, the sample discharged from the discharge nozzle is introduced from the interface unit to the mass analyzing unit, and the sample is subjected to mass analysis.

According to an eleventh aspect of the present invention, a mass spectrometer according to an eleventh aspect of the present invention is arranged in the interface section of the mass spectrometer described above at a position facing the discharge nozzle of the microchip for mass analysis. A small hole for introduction is formed.
According to the present invention, the discharge nozzle of the microchip for mass spectrometry placed under atmospheric pressure faces the small hole of the interface unit. Since the mass spectrometer is maintained in a vacuum, a differential pressure is formed by the small holes. When a small amount of sample is discharged from the discharge nozzle, the sample passes through the small hole and is introduced into the mass analyzing unit, and mass analysis is performed.

A mass spectrometer according to a twelfth aspect of the invention includes a mass spectrometry microchip having the ionization opening described above, and a mass spectrometry unit that performs mass analysis of a sample ionized by the ionization unit and the ionization unit. The ionization unit has a laser light source, and ionization is performed by irradiating the ionization opening on the microchip for mass spectrometry with laser light.
According to this invention, the mass analysis microchip is attached to the ionization part of the mass spectrometer, the ionization opening is irradiated with a laser from the laser light source to ionize, and the ionized sample is guided to the mass analysis part to perform mass analysis. I do.

  According to the microchip for mass spectrometry of the first invention, since only a part of the introduced sample necessary for analysis can be cut out and stored in the sample storage part, only the minimum necessary sample can be stored. What is necessary is just to supply. In addition, since only the necessary sample can be sent to the mass spectrometer when the sample is necessary, it is not necessary to prepare a large amount of samples in anticipation of the discarded samples, and the samples are not wasted.

  According to the microchip for mass spectrometry of the second invention, the sample is discharged from the discharge nozzle on the outer wall of the microchip. Therefore, if the pipe is connected to the discharge nozzle and sent to the mass spectrometer, the sample storage unit A small amount of sample stored in can be easily sent to the mass spectrometer when necessary.

According to the microchip for mass spectrometry of the third aspect of the present invention, the microchip for mass spectrometry further includes a sample separation unit that separates the sample introduced into the flow path between the sample introduction unit and the sample cutting unit for each component.
According to the present invention, since the injected sample can be stored in the sample storage unit after being separated for each component in the sample separation unit, it is not necessary to supply a sample in which the components are separated in advance.

  According to the microchip for mass spectrometry of the fourth aspect of the invention, since the column for chromatography or the column for electrophoresis is formed in the sample separation unit, the component separated by chromatography or electrophoresis is sampled for each component. In addition, the stored trace amount sample can be sent to the mass spectrometer main body at a necessary time.

  According to the microchip for mass spectrometry of the fifth aspect of the present invention, only the necessary trace sample portion can be sent to the sample storage unit and stored by switching the channel between the front channel switching unit and the rear channel switching unit. Since other solvents and unnecessary sample components can be discarded from the discharge port using the vent port and discharge port without being sent to the mass spectrometer, unnecessary measurement can be avoided and piping can be performed. Cleaning can also be reduced.

  According to the microchip for mass spectrometry of the sixth invention, the front side channel switching unit and the rear side channel switching unit can perform channel switching more easily than the three-way valve.

  According to the microchip for mass spectrometry of the seventh invention, various pretreatments are performed before mass spectrometry by diluting or reacting the sample by injecting a reagent or solvent from the reagent solvent introduction part. Can be. In addition, by adjusting the storage time in the sample storage unit and sending it to the mass spectrometer, it is possible to analyze the change over time after the reaction.

  According to the microchip for mass spectrometry of the eighth invention, the necessary trace sample can be easily ionized when necessary by attaching the chip directly to the ionization part of the mass spectrometer main body and irradiating with laser. . In particular, it is possible to perform efficient analysis by synchronizing intermittent analysis in TOFMS or ion trap mass spectrometer with the timing of laser irradiation.

  According to the microchip for mass spectrometry of the ninth aspect of the invention, the laser light is guided to the ionization opening through the waveguide formed in the chip, so that the optical path of the laser light source is simply guided to the waveguide. The optical system can be easily aligned.

  According to the mass spectrometer of the tenth aspect of the invention, only the necessary sample is temporarily stored in the sample storage part of the microchip for mass spectrometry, and the stored micro sample is massed through the interface part at an appropriate time. Since it can send to the analyzer main body, even if the sample amount which can be prepared is very small, it can analyze reliably.

  Further, according to the mass spectrometer of the eleventh aspect, when a small amount of sample is discharged from the discharge nozzle, almost all of the sample passes through this small hole and is introduced into the mass analyzing unit. It can be performed.

  According to the mass spectrometer of the twelfth invention, the mass analysis microchip is directly attached to the ionization section of the mass spectrometer main body, and the ionized opening is irradiated with laser to perform mass analysis of the ionized sample. Therefore, the laser irradiation and the mass analysis by the mass analyzer can be easily synchronized and analyzed. In particular, when intermittent measurement is performed with a TOFMS or an ion trap mass spectrometer, it is possible to easily synchronize with the measurement timing.

  The best mode for carrying out the present invention will be described below with reference to the drawings. The embodiment described below is only an example, and modifications can be made without departing from the gist of the present invention.

Configuration of Microchip FIG. 1 is a plan view showing the configuration of a microchip for mass spectrometry as one embodiment of the present invention, and FIG. 2 is a perspective view thereof.
The microchip 1 for mass spectrometry is formed by bonding two pieces of quartz glass composed of a base plate and a cover plate subjected to necessary hole processing and groove processing.
Three openings of a sample introduction port 12, a vent port 14, and a discharge port 16 serving as a sample introduction portion are formed on the upper surface of the microchip 1, and each port supplies a sample solution and a solvent solution from an external channel (not shown). And can be discharged.

Inside the microchip 1, in order from the upstream side, the separation channel 18 communicating with the sample introduction port 12 is connected to the separation channel 18 via a three-way valve VA (front channel switching unit). The cut flow channel 20 is connected to the cut flow channel 20 via a three-way valve VB (rear flow channel switching unit), and the branch flow channel 22 is branched at the end side (each branch portion is a branch flow channel 22). -1, 22-2, 22-3), a sample storage unit 24 that communicates with the end of the branch flow path 22 and stores a sample (each sample storage unit is 24-1, 24-2, 24- 3) is formed. Further, a branch channel opening / closing valve VC (each branch channel opening / closing valve is VC-1, VC-2, VC-3) is formed in the middle of the branch channel 22, and each branch channel 22-1. , 22-2 and 22-3 can be opened and closed. On the downstream side of the sample storage unit 24, extraction channels 28 (each extraction channel is 28-1, 28-2, 28-3) communicating with the nozzles 26 provided on the outer wall of the microchip are formed.
The open / close valve and three-way valve used in the microchip 1 are not limited to valves that move mechanically like a diaphragm valve, but use EWOD (electro wetting on dielectric) to control the wettability of the inner surface of the flow path. It is also possible to use a valve that does not have a movable part, such as a valve that switches the direction of the fluid, or a passive valve that switches the direction of the fluid using the difference in wettability of the material constituting the inner surface of the flow path and the pressure applied to the fluid. In short, it is only necessary that the flow path can be switched.

  In addition, a vent channel 30 branched from the three-way valve VA is formed and communicates with the vent port 14. Similarly, a discharge flow path 32 branched from the three-way valve VB is formed and communicates with the discharge port 16.

  The separation channel 18 is a channel part for separating the introduced sample for each component in the microchip 1, and a chromatography column agent or an electrophoresis column is used depending on the sample. To do. In addition, when introducing the sample separated in advance in the previous step to be introduced into the sample introduction unit 12, it is not necessary to perform separation in this flow path portion, and therefore, it is used as a simple connection flow path. Further, the sample separated in the previous step may be further separated by the separation channel 18 in the microchip 1.

  The three-way valve VA is switched so as to selectively connect either the separation channel 18 and the cut channel 20 or the vent channel 30 and the cut channel 20. The three-way valve VB is switched so as to selectively connect either the cutoff channel 20 and the discharge channel 32 or between the cutoff channel 20 and the branch channel 22.

  The cut-off channel 20 is a channel sandwiched between two three-way valves VA and VB. By switching the flow direction on the downstream side of the sample portion confined between the two valves VA and VB by the valve operation, Cut out the sample part.

  The branch flow path 22 branches downstream of the three-way valve VB, and one of the branch flow path opening / closing valves VC-1, VC-2, and VC-3 among the branch flow paths 22-1, 22-2, and 22-3. When one is selectively opened, the sample is sent to the corresponding branch channel 22.

  Each sample storage unit 24-1, 24-2, 24-3 is subjected to hole processing, and an opening is formed at the bottom thereof. A plastic bottom member is attached so as to block the opening at the bottom of each sample storage section, and a discharge actuator 34 (each discharge actuator) comprising a piezoelectric element for raising and lowering the bottom member below the bottom member. Are referred to as 34-1, 34-2, 34-3) (see FIGS. 1 and 4). When the discharge actuator 34 is energized, the bottom member rises and the liquid in the sample storage unit 24 is pressurized, flows through the extraction flow path 28 and is discharged from the nozzle 26.

Configuration of Mass Spectrometer Next, a mass spectrometer for performing mass analysis using the microchip 1 will be described with reference to the drawings. FIG. 3 is a schematic plan view showing the configuration of a mass spectrometer which is an embodiment of the present invention.

  The mass spectrometer 50 includes a microchip 1, an interface unit 60 located at a position facing the discharge nozzle 26 (see FIG. 1) of the microchip 1, and a mass that is connected to the interface unit 60 through a flow path and performs mass analysis of a sample It comprises an analyzer main body 70. In the present embodiment, the mass spectrometer main body 70 is configured by combining an ion guide portion 71 having an ion guide 73 and a mass analysis portion 72 having an ion trap 75. Note that the interface unit 60 and the mass analysis unit 72 are not limited to these.

The interface unit 60 is a sealed space, and a sample introduction unit 62 in which a small hole 61 is formed is provided in a part of the wall surface of the interface unit 60, and mass spectrometry is performed through the small hole 61. It communicates with the ion guide part 71 of the apparatus main body 70. A gas supply system (not shown) is formed between the microchip 1 and the sample introduction unit 62 so that a dry gas (for example, heated nitrogen gas) flows around the flow of the sample discharged from the microchip 1. . Furthermore, the sample introduction part 62 having the small holes 61 may be partially heated in some cases, and a heating mechanism is incorporated.
A high voltage power supply 80 is connected between the microchip 1 and the sample introduction unit 62 so that a voltage can be applied.

In the mass spectrometer main body 70, an ion guide 71 and a mass analyzer 72 are partitioned by a partition, the mass analyzer 72 is in a high vacuum (approximately 10 ⁻⁴ Pa), and the ion guide 71 is in a medium vacuum (approximately 10 ⁻¹ to 10 ⁻² Pa). The interface unit 60 is approximately atmospheric pressure.

  The mass spectrometer 50 also includes a control unit 82 that controls the entire system including the microchip 1, the interface unit 60, and the mass spectrometer main body 70 during mass analysis. That is, for the microchip 1, the flow direction control of the three-way valves VA, VB, the opening / closing control of the branch flow path opening / closing valve VC, the discharge control of the sample liquid by the piezoelectric element 34, and the bottom of the microchip 1 are attached. A sample monitor (for example, an absorbance detector) (not shown) for monitoring the sample position is controlled, application control of a high voltage power supply 80 is performed for the interface unit 60, and The ion guide 73 and the ion trap 75 are controlled.

Preparative storage process of the sample by the microchip will be described with reference to the drawings procedure for storing the sample using the microchip 1. Here, for the sake of convenience, the description will be made assuming that the sample supplied from the flow path (not shown) in the preceding stage of the microchip 1 is already sent in a component-separated state, but it may be a component that is supplied in the separation flow path 18. Absent. In addition, the sample liquid is pressurized before the microchip 1 and flows into the downstream microchip 1 with the pressure difference as a driving force. For example, a case where a liquid chromatograph apparatus is connected to the previous stage is given as an example, but the present invention is not limited to this.

  FIG. 4 is a diagram for explaining a process of separating and storing a trace amount sample by switching operation of the three-way valves VA and VB, and a necessary trace amount by sequentially executing the following steps (a) to (h). Each sample component is stored separately in the sample storage.

(A) Step The three-way valve VA that functions as a front channel switching unit is placed in a state where the separation channel 18 and the cut channel 20 are in communication (referred to as a separation channel side state), and functions as a rear channel switching unit. The three-way valve VB is placed in a state where the cut-off channel 20 and the separation channel 32 communicate with each other (referred to as a discharge channel side state).
The sample liquid introduced from the front stage of the microchip 1 to the sample introduction port 12 and flowing through the separation channel 18 sequentially flows to the downstream side. At this time, it is monitored by a sample monitor (not shown) provided at the bottom of the separation channel 18. This state is maintained until the first component 1 reaches the cut-off channel 20. Therefore, unnecessary solvents and unnecessary components flowing before component 1 are discarded in the discharge port.

(B) Process When the component 1 reaches the cut-off channel 20, the branch channel opening / closing valve VC-1 is opened to introduce the component 1 to the sample storage unit 24-1, which is the first storage unit, and another branch flow With the road opening / closing valves VC-2 and VC-3 closed, the three-way valve VB is switched to a state where the cut-off flow path 20 and the branch flow path 22 communicate with each other (referred to as a branch flow path side state).

(C) Process In order to introduce the component 1 to the sample storage unit 24-1, which is the first storage unit, the branch flow path opening / closing valve VC-1 is opened, and the other branch flow path opening / closing valves VC-2, VC-3 are opened. In a state of being closed, the three-way valve VA is switched to a state where the vent channel 30 and the cutout channel 20 communicate with each other (referred to as a vent channel side state). And before the component 2 reaches the three-way valve VA, the component 1 is pumped so as to reach the sample reservoir 24-1.

(D) Process When the component 1 reaches the sample storage unit 24-1, the three-way valve VA is switched to the separation channel side state, the three-way valve VB is switched to the discharge channel side state, and the sample is flowed. And it waits until the component 2 reaches the cut-off channel 20.
When the component 2 reaches the cut-off channel 20, the branch channel opening / closing valve VC-2 is opened to introduce the component 2 to the sample storage unit 24-2 as the second storage unit, and another branch channel opening / closing valve is opened. With the VC-1 and VC-3 closed, the three-way valve VB is switched to the branch channel side state.

(E) Process In order to introduce the component 2 to the sample storage section 24-2 as the second storage section, the branch flow path opening / closing valve VC-2 is opened, and the other branch flow path opening / closing valves VC-1 and VC-3 are opened. In the state where it is closed, the three-way valve VA is switched to the vent flow path side state. Then, before the component 3 reaches the three-way valve VA, the component 2 is pumped to the sample storage unit 24-2.

(F) Process When the component 2 reaches the sample storage unit 24-2, the three-way valve VA is switched to the separation channel side state, the three-way valve VB is switched to the discharge channel side state, and the sample flows. And it waits until the component 3 reaches the cut-off channel 20.
When the component 3 reaches the cut-off channel 20, the branch channel opening / closing valve VC-3 is opened to introduce the component 3 to the sample storage unit 24-3 as the third storage unit, and another branch channel opening / closing valve is opened. With VC-1 and VC-2 closed, the three-way valve VB is switched to the branch flow path side state.

(G) Process In order to introduce the component 3 to the sample storage section 24-3 as the third storage section, the branch flow path opening / closing valve VC-3 is opened and the other branch flow path opening / closing valves VC-1 and VC-2 are opened. In the state where it is closed, the three-way valve VA is switched to the vent flow path side state. And the component 3 is pumped to the sample storage part 24-3.

(H) Process When component 1 to component 3 are stored in separate sample storage units 24-1, 24-2, and 24-3, respectively, three-way valve VA is in the separation channel side state, and three-way valve VB is in the discharge channel side state. And the branch flow path opening / closing valves VC1 to VC3 are closed. As a result, unnecessary samples and solvents that flow later are discarded in the discharge port.

Analysis Step by Mass Spectrometer Next, the operation of sending and analyzing a small amount of sample collected and stored on the microchip to the mass spectrometer main body will be described. Here, it is assumed that trace samples stored in the sample storage units 24-1, 24-2, and 24-3 are measured in this order. In the analysis, the following steps (i) to (h) are sequentially executed to analyze a small amount of sample separately at a desired timing.

(I) Process In advance, the mass spectrometer main body 70 is started up to a standby state where measurement is possible at any time, and waits for the sample to be supplied.

(J) Process The branch flow path opening / closing valves VC-1 to VC-3 are closed, and the inside of the sample storage unit 24-1 in which the component 1 is stored is pressurized by the discharge actuator 34-1 to form a certain amount of sample. The sample droplet is discharged into the space of the interface unit 60 to which a high electric field is applied.

Step (k) The discharged trace sample of component 1 is ionized and passes through the small hole 61 (capillary) of the interface unit 60. The trace sample is desolvated and refined while passing through the small hole 61 and enters the ion guide unit 71, and is guided by the ion guide 73 and enters the mass analysis unit 72. In the mass analyzer 72, mass analysis is performed while the incoming ions are electromagnetically processed by the ion trap detector 75.

(L) Process When the mass analysis of component 1 is completed, the inside of the sample storage unit 24-2 in which the component 2 is stored is pressurized by the discharge actuator 34-2, and a sample droplet that becomes a certain amount of sample is subjected to a high electric field. Is discharged into the space of the interface unit 60 to which is applied. Thereafter, mass spectrometry is performed in the same process.

Step (m) When mass analysis of component 2 is completed, the inside of the sample storage unit 24-3 in which component 3 is stored is pressurized by the discharge actuator 34-3, and a sample droplet that becomes a certain amount of sample is applied to a high electric field. Is discharged into the space of the interface unit 60 to which is applied. Thereafter, mass spectrometry is performed in the same process.

Modification of the microchip Next, FIG. 1, illustrating a modified embodiment of a microchip shown in Fig.
FIG. 5 is a diagram showing a schematic configuration of a microchip for mass spectrometry which is another embodiment of the present invention. 5, the same components as those in FIGS. 1 and 2 are denoted by the same reference numerals, and the description thereof is omitted.
In the microchip 2 of FIG. 5, the open / close valves 25-1, 25-2, and 25-3 are further provided in the extraction channels on the downstream side of the sample storage units 24-1, 24-2, and 24-3. Different from the embodiment of FIGS.
According to the microchip 2, by closing the open / close valves on both sides of the sample storage unit 24, the sample in the sample storage unit 24 can be stored in a sealed state. It can be made difficult to receive.

FIG. 6 is a diagram showing a schematic configuration of a microchip for mass spectrometry which is another embodiment of the present invention. In FIG. 6, the same components as those in FIGS. 1 and 2 are denoted by the same reference numerals, and the description thereof is omitted. In this embodiment, the sample is separated into components by electrophoresis in a microchip, the sample is stored, and then mass spectrometry is performed.
In the microchip 3 of this embodiment, the sample introduction channel 13 is formed so as to intersect the separation channel 18 at the intersection X, and the sample introduction port 12a and the second electrode port 12b are formed at both ends thereof. Further, the third electrode port 12c is formed at the upstream end of the separation channel 18 (that is, in this embodiment, the sample introduction port 12 in FIG. 1 becomes the third electrode port 12c). The separation channel 18 is an electrophoresis column.

  These sample introduction port 12a, second electrode port 12b, third electrode port 12c, and discharge port 16a are formed with electrodes so that a voltage can be applied from the outside to the sample solution in each port.

In the microchip 3 of the present embodiment, the migration phenomenon caused by the potential gradient is used for the movement of the sample from the sample introduction port 12a to the cut-off channel 20. That is, the sample introduced from the sample introduction port 12a migrates toward the intersection X due to the potential difference between the sample introduction port 12a and the second electrode port 12b. When a part of the sample to be measured reaches the intersection X, the voltage is adjusted so that a potential difference is applied between the third electrode port 12c and the discharge port 16a.
As a result, a part of the sample migrates to the separation channel 18 side, and flows toward the three-way valve VA while separating each component in the separation channel 18. When the first separated component reaches the cut-off channel 20, compressed air is introduced from the vent port 14 by the same procedure as in the first embodiment, and the sample is guided to the sample storage unit 24-1 by the pressure difference. Thereafter, the components are sequentially stored in separate sample storage units in the same procedure as in Example 1.

FIG. 7 is a diagram showing a schematic configuration of a microchip for mass spectrometry which is another embodiment of the present invention. 7, the same components as those in FIGS. 1 and 2 are denoted by the same reference numerals, and the description thereof is omitted. In the present embodiment, the flow direction of the sample in the branch channel 22 is switched by changing the hydrophilicity within the microchip.
The microchip 4 of this embodiment forms constricted portions Y1, Y2, and Y3 at the positions of the branch channels 22-1, 22-2, and 22-3 immediately after the branch point Y0 in the branch channel 22, and this portion. The voltage can be applied to. Then, the voltage applied to the narrowed portions Y1, Y2, and Y3 when the trace sample cut out in the cut-off channel 20 approaches the branch point is controlled (the flow property is changed by changing the zeta potential of the sample surface). As a result, the flow proceeds to one of the branch flow paths. This makes it possible to switch the flow path accurately at the branch point Y0.

FIG. 8 is a diagram showing a schematic configuration of a microchip for mass spectrometry which is another embodiment of the present invention. 8, the same components as those in FIGS. 1 and 2 are denoted by the same reference numerals, and the description thereof is omitted. In this embodiment, a sample can be mixed with a reagent and a solvent in a microchip.
In the microchip 5 of the present embodiment, a reagent / solvent introduction part including a reagent / solvent introduction port 40 for supplying a reagent and a solvent and a reagent solvent flow path 42 is formed, and immediately before the branch point Y0 in the branch flow path 22. To communicate with. Then, if necessary, a reagent or solvent is supplied to the sample storage unit 24, and a chemical reaction is caused or diluted in the sample storage unit 24 before being sent to the mass spectrometer.

  Although some modifications have been described above, these are only examples. Needless to say, the number and shape of the sample storage portions formed on the microchip may be modified as necessary.

FIG. 9 is a plan view of a microchip for mass spectrometry as another embodiment of the present invention, and FIG. 10 is a perspective view thereof.
Unlike the microchips 1 to 5 connected to the mass spectrometer via the interface unit 60 as described in the first embodiment, the microchip 6 for mass spectrometry is directly used as an ionization unit of the mass spectrometer. It is to be used. The same components as those in FIGS. 1 and 2 are denoted by the same reference numerals, and the description thereof is omitted.

  In the microchip 6, a bottomed opening 44 for irradiating the sample with laser is formed, and the extraction channels 28-1, 28 on the downstream side of the sample storage units 24-1, 24-2, 24-3 are formed. -2 and 28-3 are formed to communicate with the opening 44. In addition, open / close valves 25-1, 25-2, and 25-3 are provided in the middle of the extraction channels 28-1, 28-2, and 28-3. Further, a waveguide 46 extending from the side wall surface of the microchip 6 to the opening 44 is formed, and by irradiating laser light from the waveguide portion on the side wall surface, the sample in the opening 44 is irradiated with laser so that the sample can be ionized. It has become.

FIG. 11 is a diagram showing a schematic configuration of a mass spectrometer for performing mass spectrometry using the above-described microchip 6 (FIG. 9).
The mass spectrometer 90 includes a time-of-flight (TOF) detector 92, a laser light source 94 for irradiating laser light to the opening 44 of the microchip 6, and ions ejected from the opening 44 by being excited by the laser light. And an ion lens 96 for advancing in a desired direction. Control of the detector 92, laser light source 94, ion lens 96 and valve control of the microchip 6 are controlled by the control unit 98.

Next, the operation of mass spectrometry using this apparatus will be described. Here, it is assumed that a small amount of sample is already stored in the sample storage units 24-1, 24-2, and 24-3 of the microchip 6 by the same procedure as in the first embodiment.
The branch flow path opening / closing valves VC1 to VC3 are closed, the opening / closing valve 25-1 is opened, and the opening / closing valves 25-2 and 25-3 are closed to drive the discharge actuator 34-1 of the sample storage unit 24-1. The trace amount sample of component 1 stored in the storage unit 24-1 is sent out to the opening 44.

When the detector 92 is in a measurable state, by irradiating the laser from the laser light source 94 to the opening 44 of the microchip, the sample in the opening 44 is excited and ionized, and jumps out into the space. The jumped out ions are sent to the detector 92 by the ion lens 96 and subjected to mass analysis.
After the first mass analysis, when the detector 92 becomes measurable after a while, the laser light source 94 irradiates the laser again and the second mass analysis is performed. Thus, the measurement is repeated intermittently.
When the measurement of the component 1 is completed, the open / close valve 25-2 is opened, the other open / close valves are closed, and the discharge actuator 34-2 is driven to open the trace sample of the component 2 stored in the sample storage unit 24-2. The same mass analysis is performed. Thereafter, mass analysis of a small amount of sample is sequentially performed by repeating the same operation.

  INDUSTRIAL APPLICABILITY Since the amount of sample consumed in the ionization process of the mass spectrometer can be made very small, the present invention is useful for a rare sample mass spectrometer. Moreover, it is useful for ionization in a mass spectrometer that performs analysis intermittently, such as TOF or an ion trap mass spectrometer.

The plane block diagram of the microchip for mass spectrometry which is one Example of this invention. The perspective view of the microchip for mass spectrometry which is one Example of this invention. The figure explaining schematic structure of the mass spectrometer which is one Example of this invention. The figure explaining the preparative storage process of the sample by the microchip for mass spectrometry which is one Example of this invention. The plane block diagram of the microchip for mass spectrometry which is another Example of this invention. The plane block diagram of the microchip for mass spectrometry which is another Example of this invention. The plane block diagram of the microchip for mass spectrometry which is another Example of this invention. The plane block diagram of the microchip for mass spectrometry which is another Example of this invention. The plane block diagram of the microchip for mass spectrometry which is another Example of this invention. The perspective view of the microchip for mass spectrometry which is another Example of this invention. The figure explaining schematic structure of the mass spectrometer which is another Example of this invention.

Explanation of symbols

1-6: Microchip 12: Sample introduction port (sample introduction part)
14: Vent port 16: Discharge port 18: Separation channel 20: Cut-off channel 22: Branch channel 24: Sample storage unit 26: Discharge nozzle 28: Extraction channel 30: Vent channel 32: Discharge channel 34: Discharge actuator 40: Reagent solvent port 42: Reagent solvent flow path 44: Opening 46: Waveguide 50: Mass spectrometer 60: Interface unit 61: Small hole 62: Sample introduction unit 70: Mass spectrometer main body 72: Mass analysis unit 90: Mass spectrometer 92: Detector (TOF)
94: Laser light source VA: Three-way valve (front flow path switching unit)
VB: Three-way valve (rear flow path switching part)
VC: Branch channel open / close valve

Claims (12)

A mass spectrometry microchip for preparing a sample for mass spectrometry,
A sample introduction unit;
A sample cutting section formed on a flow path communicating with the sample introduction section, and sequentially cutting a part of the sample flowing from the sample introduction section;
A plurality of sample storage units;
A branch channel for connecting a sample cutting part and each sample storage part to each other and sending a part of the sample cut by the sample cutting part to any one of the sample storage parts;
A branch channel opening / closing valve provided in each of the branch channels;
A microchip for mass spectrometry, comprising: an extraction flow path that communicates with a sample storage unit and extracts a sample stored in the sample storage unit. 2. The microchip for mass spectrometry according to claim 1, wherein the take-out flow path communicates with a discharge nozzle formed on the outer wall of the microchip. 2. The mass spectrometric analysis device according to claim 1, further comprising a sample separation unit that separates the sample introduced from the sample introduction unit for each component in a flow path between the sample introduction unit and the sample cutting unit. Microchip. The microchip for mass spectrometry according to claim 3, wherein a column for chromatography or a column for electrophoresis is formed in the sample separation unit for separating each component. The sample cutting unit includes a cutting channel sandwiched between the front channel switching unit and the rear channel switching unit, a vent channel branched from the front channel switching unit and connected to the vent port, and a rear channel The microchip for mass spectrometry according to claim 1, comprising a discharge flow path branched from the switching section and connected to a discharge port. The microchip for mass spectrometry according to claim 5, wherein the front side flow path switching unit and the rear side flow path switching unit are formed by a three-way valve. 2. The microchip for mass spectrometry according to claim 1, further comprising a reagent solvent introduction unit for injecting a reagent or a solvent between the sample cutting unit and the branch channel. 2. The microchip for mass spectrometry according to claim 1, wherein the microchip for mass spectrometry is further formed with an opening for ionization by laser irradiation, and the extraction channel communicates with the opening. 9. The microchip for mass spectrometry according to claim 8, further comprising a waveguide for guiding laser light to the opening for ionization. 3. The mass analysis microchip according to claim 2, a mass spectrometer main body having a mass analysis unit for performing mass analysis of the sample, and a sample discharged from a discharge nozzle of the mass analysis microchip are introduced into the mass analysis unit. And a mass spectrometer. 11. The interface portion is formed with a small hole for introducing a sample discharged from the discharge nozzle to the mass analysis portion, which is disposed at a position facing the discharge nozzle of the microchip for mass analysis. The mass spectrometer described in 1. 9. A mass analysis microchip according to claim 8, and a mass spectrometer main body having an ionization unit and a mass analysis unit for performing mass analysis of a sample ionized by the ionization unit, wherein the ionization unit has a laser light source. A mass spectrometer characterized in that ionization is performed by irradiating a laser beam to an ionization opening on a mass spectrometry microchip.

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