JP2013005809A - Detection object collection implement, and method for using the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a detection object collection implement which allows more accurate analysis of a detection object when a carrier with the detection object being collected thereon is subjected to a plurality of analyses such as qualitative analysis and quantitative analysis, and a method for using the same.SOLUTION: The detection object collection implement 1 includes a carrier 5 for collecting the detection object (microorganism), which is divided to a plurality of pieces; and a collection dish 4 which holds the carrier 5, the carrier 5 being disposed on one surface side of the collection dish 4. The carrier 5 includes a carrier 5a for enumerative analysis and a carrier 5b for identification analysis, which are separately disposed on a first dish half body 4a (separated body) and a second dish half body 4b (separated body) of the collection dish 4 respectively.

Description

  The present invention relates to an object collecting tool for collecting an object to be detected such as microorganisms and chemical substances, and a method of using the same.

  2. Description of the Related Art Conventionally, as a technique for collecting an object to be detected such as a microorganism or a chemical substance floating in the air, a technique for sucking air through a filter and separating the object to be detected by a filter is widely known. In addition, as a collecting device for collecting microorganisms floating in the air, a device in which a carrier that undergoes a phase transition from gel to sol by raising the temperature from room temperature is arranged on a collecting dish is known (for example, Patent Document 1). This collector is used by being assembled to an impactor type air sampler, and when the air sucked by the air sampler collides with the carrier, it collects microorganisms accompanying the air on the gel carrier. It has become. The collected microorganisms are taken out from the collection dish together with the sol-formed carrier by raising the temperature, and counted according to a predetermined counting method.

  On the other hand, as a method for counting microorganisms, a so-called ATP method is known in which microorganisms are indirectly counted by quantifying ATP (adenosine triphosphate) extracted from the microorganisms (see, for example, Patent Document 2). In this ATP method, an ATP extraction reagent is brought into contact with a collected microorganism to extract ATP contained in the microorganism, and the microorganism is counted based on the luminescence intensity when the ATP is reacted with the luminescent reagent. .

According to this ATP method, for example, a counting method that counts microorganisms collected by the number of colonies of microorganisms cultured on a plate medium requires several days. It can be drastically shortened to about several hours.
However, since this ATP method counts microorganisms based on weak luminescence intensity, it is necessary to reduce as much as possible the possibility of substances that cause disturbances in the sample to be counted.

JP 2009-131186 A JP-A-11-137293

By the way, in the conventional collection tool (for example, refer patent document 1), since the support | carrier on a collection dish is exposed, after collecting microorganisms on a support | carrier with an air sampler, this is used for the count of microorganisms. During this time, for example, extra microorganisms that are not subject to inspection and other substances that cause disturbance may be mixed into the carrier. In particular, when the inspection place where the microorganisms are collected and the microorganism counting facility are separated from each other, the risk of contamination is further increased.
That is, in the conventional collection tool (for example, refer patent document 1), after removing from an air sampler, a carrier is contaminated by the time until the count of microorganisms, so that microorganisms collected at an inspection place can be accurately detected. There is a possibility that it cannot be counted.

Therefore, prior to this application, the present applicant, after performing the collection operation of the detected object with the carrier of the collection dish facing upward, detects the detected object with the carrier facing downward. An application has already been filed for an object collecting tool configured to do so (unpublished Japanese Patent Application No. 2009-295655).
According to this detection object collecting tool, the carrier after the collection operation of the detection object is arranged in a downward direction, so that the collection dish itself serves as a cover of the carrier, and the disturbance It is possible to prevent the factor substance from being mixed into the carrier.

On the other hand, in such an object collecting tool, there is a demand for performing quantitative analysis and qualitative analysis of the object collected by the carrier in parallel. For example, when the object to be detected is a microorganism, there is a demand for performing counting of microorganisms and identification of microorganisms in parallel.
Since the carrier (sample) used for the quantitative analysis of the object to be detected and the carrier (sample) used for the qualitative analysis need to be collected at the same time and at the same place, One carrier that collects the detected substance may be used separately for, for example, quantitative analysis and qualitative analysis.
However, when the carrier is separated and used, when performing the separation operation or weighing the separated carrier for quantitative analysis, a substance that causes disturbance may be mixed into the carrier for accurate analysis. There is a fear that it cannot be done.

  Therefore, the problem of the present invention is that when a carrier that collects the detection object is subjected to a plurality of analyzes such as quantitative analysis or qualitative analysis of the detection object, the analysis can be performed more accurately. An object of the present invention is to provide an object collecting tool and a method of using the same.

  The present invention that solves the above-mentioned problem is provided with a collection dish that divides a carrier for collecting an object to be detected into a plurality of pieces and holds the carrier, and the carrier is arranged on one side of the collection dish. This is a detected object collecting tool.

  Further, the present invention for solving the above-mentioned problems is a method of using a detection object collecting tool in which a carrier for collecting a detection object is divided and arranged in a plurality of sections, and is one side of a collection dish After collecting the detected object with the carrier arranged in the area, the carrier is divided according to the section, and a part of the divided carrier is used as a first of the detected object. It is a method for using a detection object collecting tool, characterized in that it is subjected to a detection operation and the remainder of the divided carrier is subjected to a second detection operation of the detection object.

  According to the present invention, when a carrier that has collected a detection object is subjected to a plurality of analyzes such as quantitative analysis or qualitative analysis of the detection object, the detection can be performed more accurately. An object collector and a method of using the same can be provided.

It is composition explanatory drawing of the microorganisms counter which attaches the to-be-detected object collection tool which concerns on 1st Embodiment of this invention. It is a perspective view which shows the mode of the mounting part vicinity of the to-be-detected object collector in the microorganisms counting apparatus of FIG. It is sectional drawing which shows a mode that the to-be-detected object collector is mounted in the mounting part of the to-be-detected object collector in the microorganisms counting apparatus of FIG. It is a flowchart which shows the process in which a microbe counting device operate | moves based on the instruction | command of a control part. It is a perspective view of the to-be-detected object collection tool which concerns on 1st Embodiment of this invention. It is a disassembled perspective view of the to-be-detected object collection tool of FIG. 5, (a) is an exploded perspective view at the time of looking down from diagonally upward, (b) is an exploded perspective view at the time of looking up from diagonally downward. It is VII-VII sectional drawing of FIG. It is a perspective view for demonstrating the method to collect microorganisms with the to-be-detected object collection tool which concerns on 1st Embodiment of this invention. It is a perspective view which shows a mode that a support | carrier is divided | segmented in the to-be-detected object collection tool which concerns on 1st Embodiment of this invention. (A-1) to (a-4) are cross-sectional views of an object collecting tool for explaining a method of using the object collecting tool in the microorganism counting apparatus, and (b-1) to ( b-4) is a schematic diagram showing an enlarged view of the vicinity of the filter in the scenes corresponding to (a-1) to (a-4). It is a decomposition | disassembly top view of a collection dish for demonstrating the structure of the modification of a collection dish. It is a disassembled perspective view of the to-be-detected object collection tool which concerns on 2nd Embodiment of this invention, (a) is an exploded perspective view at the time of looking down from diagonally upward, (b) is when looking up from diagonally downward It is a disassembled perspective view. It is sectional drawing of the to-be-detected object collection tool which concerns on 2nd Embodiment in the cross section corresponding to the VII-VII cross section of FIG. It is a perspective view which shows a mode that a support | carrier is divided | segmented in the to-be-detected object collection tool which concerns on 2nd Embodiment of this invention.

  Next, an embodiment of the detected object collector of the present invention will be described in detail with reference to the drawings as appropriate. Here, although the detection object collecting tool which collects microorganisms (bacteria, fungi, etc.) floating in the air as the detection object will be described, the detection object collection tool of the present invention is used as the detection object. It may be one that collects fine particles of metals or chemical substances, and the object to be detected is not limited to a solid but may be a mist.

(First embodiment)
Below, the whole structure of the microorganisms counter which mounts the to-be-detected object collection tool which concerns on 1st Embodiment of this invention, and the counting principle of the microorganisms in the microorganisms counter are demonstrated, and it concerns on 1st Embodiment after that. The detection object collecting tool and the method of using the same will be described.

<Overall configuration of microbe counting apparatus>
As shown in FIG. 1, the microorganism counting device 10 is a device that counts microorganisms contained in a sample in accordance with the ATP method, and is a detection object collecting tool 1 having a sample in a housing 101. (See FIG. 2), a mounting unit 102, a liquid tank 105, a hot water supply unit 103, a suction unit 104, a reagent cartridge 2 in which a plurality of reagents R are arranged, a dispensing unit 106, and a luminescence intensity measurement A unit 107 and a control unit 108 are provided.
In FIG. 1, the casing 101 and the reagent cartridge 2 are indicated by phantom lines for convenience of drawing, and the detection object collecting tool 1 is not shown.

  As shown in FIG. 2, the mounting portion 102 has a concave portion 102 a that houses the detection object collecting tool 1 (housing 6), and the mounting portion 102 is provided with an engagement ring 102 b. . Further, a heater 102c (see FIG. 3) is embedded in an aluminum material arranged around the recess 102a, in other words, forming the recess 102a, as will be described later. In addition, in order to form the recessed part 102a, you may use another heat conductive material instead of this aluminum material.

The engagement ring 102b is disposed at the opening edge of the recess 102a. As will be described in detail later, the engagement ring 102b engages with a first engagement claw 62a provided on the housing 6 of the detection object collecting tool 1, thereby supporting the housing 6 on the mounting portion 102. It is like that. Incidentally, the engagement ring 102b has a notch 102d having a planar shape in which the first engagement claw 62a of the housing 6 can be accommodated, and the first engagement claw 62a between the device main body 10a in which the recess 102a is formed. The gap G is formed with a thickness capable of accepting.
In other words, when the housing 6 is fitted into the recess 102a, the first engagement claw 62a is inserted into the recess 102a through the notch 102d, and the housing 6 is rotated so that the first engagement claw 62a is separated from the gap G. The housing 6 is engaged with the engagement ring 102b.

As shown in FIG. 3, the cover 3 of the detected object collecting tool 1 is removed from the detected object collecting tool 1 arranged in the recess 102a. As will be described in detail later, among the first dish half 4a and the second dish half 4b constituting the collection dish 4, the carrier for counting analysis of the first dish half 4a disposed in the housing 6 is used. 5a is arranged so as to be exposed in the internal space 66 of the housing 6.
In the scene shown in FIG. 3, the second dish half 4 b and the carrier for identification analysis 5 b constituting the carrier 5 do not exist in the housing 6, and are represented by virtual lines.

  In FIG. 3, reference numeral 64 a is a discharge opening of the housing 6, reference numeral 7 is a filter provided in the discharge opening 64 a, reference numeral 102 b is an engagement ring, and reference numeral 104 a is connected to the housing 6. This is a suction head of the suction unit 104 (see FIG. 1). The internal space 66 of the housing 6 corresponds to a “space” in the claims.

  The heater 102c may be any means as long as it can warm the concave portion 102a (aluminum material) surrounding the housing 6 of the detection object collecting tool 1 supported by the mounting portion 102 to a predetermined temperature, but a cartridge heater or the like is preferable.

  The liquid tank 105 shown in FIG. 1 stores liquid such as sterilized distilled water. For example, this liquid is added into the housing 6 (see FIG. 3) for the purpose of improving the filtration speed of the counting analysis carrier 5a (see FIG. 3) of the detection object collecting tool 1 to be described later, and for cleaning. Is filled in the piping system of the syringe pump 106c of the dispensing unit 106 described later. The liquid tank 105 can store a buffer solution.

  The hot water supply unit 103 heats and supplies sterilized distilled water supplied from the liquid tank 105. More specifically, the hot water supply unit 103 injects hot water into the internal space 66 (see FIG. 3) of the housing 6, and is not shown in the figure. What discharges through the nozzle formed by this is mentioned. Incidentally, this nozzle is inserted into the internal space 66 (see FIG. 3) of the housing 6 as necessary by providing means for moving in the horizontal and vertical directions.

The suction unit 104 shown in FIG. 1 sucks hot water injected into the internal space 66 (see FIG. 3) of the housing 6 and a reagent R, which will be described later, through the filter 7 (see FIG. 3). Are discharged. The suction unit 104 can be composed of, for example, the above-described suction head 104a (see FIG. 3), a suction pump (not shown) connected to the suction head 104a via a predetermined pipe, a waste liquid tank, and the like.
Incidentally, the suction unit 104 in this embodiment is configured so that the suction head 104a (see FIG. 3) can be connected to and separated from the housing 6 (see FIG. 3) supported by the mounting portion 102. An elevating device (not shown) for moving the 104a up and down is further provided.

  The reagent cartridge 2 shown in FIG. 1 collectively arranges a plurality of reagents R necessary for the ATP method. The reagent cartridge 2 is disposed at a predetermined position in the vicinity of the mounting portion 102. In the reagent cartridge 2, a dispensing nozzle 106 a of a dispensing unit 106 described below can dispense the reagent R into the housing 6 of the detection object collecting tool 1 in a predetermined order. Thus, the reagent R is positioned. That is, the position (coordinates) of the reagent R is stored in the control unit 108 that controls the dispensing unit 106, as will be described later.

Examples of the reagent R necessary for the ATP method include an ATP erasing reagent for erasing ATP existing outside the collected microorganism, an ATP extraction reagent for extracting ATP resident in the microorganism, and the like.
Examples of the ATP elimination reagent include ATP degrading enzyme.
Examples of the ATP extraction reagent include benzalkonium chloride, trichloroacetic acid, Tris buffer, and the like.
Note that the reagent R can include a correction reagent of the luminescence intensity measurement unit 107, sterilized pure water, and the like. However, since the ATP luminescent reagent for emitting ATP extracted from the microorganism is prepared separately as described later, the luminescent tube 107a (see FIG. 1) preliminarily filled with the ATP luminescent reagent of the specified concentration is prepared. The reagent cartridge 2 in this embodiment is not arranged.
Examples of the ATP luminescent reagent include a luciferase / luciferin reagent.

  The dispensing unit 106 shown in FIG. 1 dispenses the reagent R described above into the housing 6 of the detection object collecting tool 1. In addition, the dispensing unit 106 is arranged on the light detection unit main body 107b with ATP (ATP extract containing ATP) extracted from the microorganism by the ATP extract in the reagent R and the housing 6 (see FIG. 3). This is dispensed into the light emitting tube 107a.

  The dispensing unit 106 includes a dispensing nozzle 106a formed of a thin tube, an actuator 106b that moves the dispensing nozzle 106a in three axial directions, and a syringe pump 106c connected to the dispensing nozzle 106a by a predetermined flexible pipe. In addition, it can be configured by a pipe or the like (not shown) for supplying sterilized distilled water or the like from the liquid tank 105 to the dispensing nozzle 106a via the syringe pump 106c.

  The luminescence intensity measuring unit 107 shown in FIG. 1 includes a luminescent tube 107a containing an ATP luminescent reagent that receives an ATP extract containing ATP dispensed from within the housing 6 (see FIG. 3) and emits light. And a photodetection unit main body 107b having a photomultiplier tube for detecting the emission intensity.

  The control unit 108 shown in FIG. 1 generally controls the microorganism counting apparatus 10 as a whole, and after mounting the detection object collector 1 (see FIG. 3) on the mounting unit 102, the hot water supply unit 103, The suction unit 104, the dispensing unit 106, and the light emission intensity measuring unit 107 are configured to be controlled by the procedure described below. Such a control unit 108 includes a CPU, a ROM, a RAM, various interfaces, an electronic circuit, and the like.

<Operation of microbe counting apparatus and microbe counting principle>
Next, the operation of the microorganism counting apparatus 10 and the principle of counting microorganisms will be described mainly with reference to FIG. 4 while explaining the procedure executed by the control unit 108. FIG. 4 is a flowchart showing a process in which the microorganism counting device operates based on a command from the control unit.

  In the microorganism counting apparatus 10 shown in FIG. 1, the control unit 108 executes the following procedure by turning on a start switch (not shown) after the detection object collector 1 (see FIG. 3) is mounted on the mounting unit 102. To do.

  The control unit 108 outputs a command to a predetermined inverter or the like so as to energize the heater 102c (see FIG. 3), and causes the heater 102c to generate heat. That is, as shown in FIG. 4, the control unit 108 raises the temperature of the counting analysis carrier 5a (see FIG. 3) of the detection object collecting tool 1 with the heater 102c (step S201). As a result, the carrier for counting analysis 5a is made into a sol and peeled off from the first dish half 4a (see FIG. 3) to the bottom of the housing 6 (see FIG. 3).

  Next, the control unit 108 outputs a command to the hot water supply unit 103 (see FIG. 1) to inject the hot water into the housing 6 (see FIG. 3) (step S202). As a result, the sol-formation of the counting / analysis support 5a (see FIG. 3) is promoted, and the counting / analysis support 5a is diluted with warm water.

  Next, the control unit 108 outputs a command to the suction unit 104 (see FIG. 1) to connect the suction head 104a (see FIG. 3) to the housing 6 (see FIG. 3) and suck the housing 6 (see FIG. 3). The contents of FIG. 3) are filtered (step S203). As a result, the microorganisms collected on the counting analysis carrier 5a are separated and held by the filter 7 (see FIG. 3), and the diluted counting analysis carrier 5a is filtered and discharged out of the housing 6. Is done.

  Next, the control unit 108 outputs a command to the hot water supply unit 103 again, and dispenses the hot water into the housing 6 (see FIG. 3) (step S204). Thereafter, the warm water is filtered again (step S205). Thereby, the inside of the housing 6 is washed, and the microorganism recovery rate in the filter 7 is improved.

  Next, the control unit 108 outputs a command to the dispensing unit 106 (see FIG. 1) to dispense the ATP erasing reagent of the reagent cartridge 2 into the housing 6 (see FIG. 3) (step S206). As a result, ATP present outside the cells of the microorganism on the filter 7 is erased.

  Next, the control unit 108 outputs a command to the suction unit 104 (see FIG. 1) to cause the suction unit 104 (see FIG. 1) to suck and filter the contents of the housing 6 (see FIG. 3) (step S207). As a result, the microorganisms are separated and held by the filter 7 (see FIG. 3), and the ATP elimination reagent is filtered and discharged out of the housing 6.

  Next, the control unit 108 outputs a command to the emission intensity measurement unit 107 (see FIG. 1) to turn on the light detection unit main body 107b (see FIG. 1) (step S208). As a result, the background of the luminescent tube 107a containing the ATP luminescent reagent, which is previously disposed above the light detection unit main body 107b, is measured.

  Next, the control unit 108 outputs a command to the dispensing unit 106 (see FIG. 1) to dispense the ATP extract from the reagent cartridge 2 into the housing 6 (see FIG. 3) (step S209). As a result, ATP is extracted from the microorganisms held in the filter 7 and a sample solution is prepared on the filter 7.

  Next, the control unit 108 outputs a command to the dispensing unit 106 (see FIG. 1), and dispenses the ATP extract containing ATP in the housing 6 to the luminescent tube 107a on which the background measurement was performed. (Step S210). As a result, in the luminescence tube 107a, light is emitted by the reaction between ATP in the ATP extract and the ATP luminescence reagent.

  Next, the control unit 108 digitally processes the signal output by the light detection unit main body 107b (see FIG. 1) detecting the emission of ATP, and measures the emission intensity based on the single photon counting method (step S211). ). And the control part 108 is ATP contained in the ATP extract liquid dispensed to the tube 107a for light emission based on the calibration curve which shows the relationship between the amount of ATP (amol) memorize | stored beforehand, and light emission intensity (CPS). Calculate the amount (amol) and count the microorganism as an ATP equivalent value of the amount of microorganisms contained in the carrier 5 based on the amount of ATP (amol) and the amount of ATP extract in the sample solution prepared in step S209. Is performed (step S212).

<Detection object collector>
The detected object collecting tool 1 (see FIG. 2) according to the first embodiment of the present invention mainly includes a carrier that collects microorganisms, which are detected objects in the air, divided and arranged in a split manner. Features.
This collected object collector 1 is used by collecting and collecting microorganisms, which are detected objects in the air, placed on an impactor-type air sampler 50 (see FIG. 8). Is counted and used in the microorganism counting apparatus 10 described above. By the way, as will be described in detail later, the detection object collecting tool 1 is used so that the top and bottom (top and bottom) are reversed when collecting microorganisms and counting.

  Next, FIG. 5 referred to is a perspective view of the detection object collecting tool according to the first embodiment of the present invention. 6 is an exploded perspective view of the detection object collecting tool of FIG. 5, (a) is an exploded perspective view when looking down obliquely from above, and (b) is an exploded perspective view when looking up from obliquely below. FIG. 7 is a sectional view taken along line VII-VII in FIG. In the following description, the vertical direction of the detection object collecting tool 1 is based on the vertical direction shown in FIG.

  As shown in FIG. 5, the detection object collecting tool 1 according to the first embodiment is formed in a substantially conical shape whose upper part is formed in a substantially cylindrical shape and whose lower part is reduced in diameter downward. ing. Then, as will be described in detail later, the upper part of the detection object collector 1 is engaged with an air sampler 50 (see FIG. 8) to collect microorganisms, and the lower part thereof is a microorganism counter 10 (FIG. 1). The microorganisms collected by engaging with (see) are used for the counting.

  In FIG. 5, reference numeral 3 denotes a lid, reference numeral 6 denotes a housing, reference numeral 31 denotes a second engagement claw that engages with an air sampler 50 (see FIG. 8) described later, and reference numeral 62a denotes a microorganism. A first engaging claw that engages with the counting device 10.

  As shown in FIGS. 6 (a) and 6 (b), the detection object collecting tool 1 includes a lid 3, a collection dish 4, a carrier 5, a housing 6, a filter 7, The filter fixing rings 8 are assembled to each other in the order.

  The lid 3 is disposed so as to close an upper opening of the housing 6 to be described later, and has a bottomed cylindrical shape opened upward. And the above-mentioned 2nd engagement nail | claw 31 is formed in the upper end edge of the surrounding surface of the cover body 3 along with the circumferential direction so that it might extend outside in radial direction. Incidentally, three second engaging claws 31 in the present embodiment are formed in accordance with the number of recesses 53 (see FIG. 8) of the air sampler 50 described later.

  At the lower end edge of the peripheral surface of the lid 3, three third engaging claws 32 are formed side by side along the circumferential direction so as to extend outward in the radial direction. The third engaging claw 32 is fitted into a first L-shaped groove 61a of the housing 6 described later, and the lid 3 is detachably connected to the housing 6. Further, the third engaging claw 32 may be fitted into a third L-shaped groove 35a (see FIG. 9) of the first cover body 35 to be described later, and the lid 3 is detachably connected to the first cover body 35. is there.

  As shown in FIG. 6B, the outer surface of the bottom portion of the lid 3 is formed as an uneven surface in which a plurality of strips protruding downward are arranged in parallel. The outer surface (lower surface) of the bottom portion was formed as an uneven surface when arranged so as to be in contact with the upper surface of the collection dish 4 (first dish half 4a and second dish half 4b) described below. The contact area is reduced. This uneven surface leaves the collection dish 4 on the housing 6 side when the lid 3 is removed from the housing 6 so that it is easily separated from the collection dish 4. Further, as described later, after the microorganisms are collected by the air sampler 50 (see FIG. 8), the microorganisms are collected as necessary up to the microorganism counting facility (for example, the facility for arranging the microorganism counting device 10 (see FIG. 1)). When transported while being kept cold, condensation may rarely occur between the lid 3 and the collection dish 4. Even in this case, the uneven surface is easily separated from the collection dish 4. Yes. In addition, this uneven surface is not limited to the above-described stripes, and can be formed by a plurality of protrusions, and can be formed by, for example, a texture such as satin or cloth.

  Moreover, as shown in FIG.6 (b), the cylindrical protrusion 33 which protrudes below is formed in the outer surface (lower surface) of the bottom part of the cover body 3. As shown in FIG. The outer diameter of the projection 33 is slightly smaller than the inner diameter of a through hole 41 (see FIG. 7) of the collection dish 4 described below. Further, the height of the protrusion 33 is equal to the length of the through hole 41.

As shown in FIGS. 6A and 6B, the collection dish 4 is formed of a first dish half 4a and a second dish half 4b.
The first dish half 4a and the second dish half 4b correspond to “divided bodies” in the claims.
Each of the first dish half 4a and the second dish half 4b has a semicircular shape in plan view, and the collection dish 4 has a circular shape in plan view by being combined with each other.
Further, when the first dish half 4a and the second dish half 4b are combined so as to form the collection dish 4, the above-described through hole 41 (see FIG. 7) is formed at the center thereof. Thus, semi-cylindrical depressions 41a and 41b are provided.

The top surfaces of the first dish half 4a and the second dish half 4b are flat surfaces so as to be in contact with the outer surface of the bottom of the lid 3 as shown in FIG.
Further, the lower surface of the first dish half 4a and the second dish half 4b accommodates a carrier so that a semi-disc-shaped carrier for counting analysis 5a and a carrier for identification analysis 5b described below can be accommodated respectively. Ribs 42a and 42b are erected.

  Incidentally, the outer diameter of the collection dish 4 is set within the range of the inner diameter of the lower cylindrical portion 62 of the housing 6 to be described later and not more than the inner diameter of the upper cylindrical portion 61, but is substantially the same as the inner diameter of the upper cylindrical portion 61. It is desirable to set to.

  As will be described later, the carrier 5 is arranged in an air sampler 50 (see FIG. 8), receives an air flow when the air sampler 50 sucks air, and collects microorganisms accompanying the air. is there.

As described above, the carrier 5 includes the count analysis carrier 5a and the identification analysis carrier 5b. The count analysis carrier 5a and the identification analysis carrier 5b are accommodated in the carrier accommodating ribs 42a and 42b, respectively. It will be divided and arranged.
The carrier 5 composed of the carrier for counting analysis 5a and the carrier for identification analysis 5b is arranged on one side of the collection dish 4, and the carrier for counting analysis 5a and the carrier for identification analysis 5b are the first carrier. The dish half 4a and the second dish half 4b can be divided.
The carrier 5 is formed of a material that undergoes a phase transition from gel to sol when the temperature is raised from room temperature. The material of the carrier 5 is preferably one that undergoes a phase transition to sol at 30 ° C. or higher, and more preferably one that liquefies at 37 to 40 ° C. Among these, gelatin, a mixture of gelatin and glycerol, and a 10: 1 copolymer of N-acryloylglycinamide and N-methacryloyl-N′-biotinylpropylenediamine are desirable.

  As shown in FIGS. 6A and 6B, the housing 6 includes an upper cylindrical portion 61 having an inner diameter substantially the same as the outer diameter of the lid body 3 from the upper side to the lower side, and the upper cylindrical portion. A lower cylindrical portion 62 having an inner diameter further reduced than the inner diameter of 61, an inverted conical funnel portion 64 having an inner diameter gradually reduced from the inner diameter of the lower cylindrical portion 62, and the funnel portion 64. The filter mounting portion 65 provided around the outlet of the discharge opening 64a formed at the lowermost portion is configured to be integrated in this order.

  As described above, the first L-shaped groove 61a into which the third engagement claw 32 of the lid 3 is fitted corresponds to the third engagement claw 32 along the inner circumference on the inner peripheral surface of the upper cylindrical portion 61. Three positions are formed at the position.

The lower cylindrical portion 62 is connected to the upper cylindrical portion 61 via the shelf portion 63.
A first engagement claw 62 a that engages with the engagement ring 102 b (see FIG. 2) of the microorganism counting device 10 is formed on the outer peripheral surface of the lower cylindrical portion 62. The first engaging claws 62 a are formed at equal intervals along the circumferential direction so as to extend outward in the radial direction of the lower cylindrical portion 62. Incidentally, four first engaging claws 62a in the present embodiment are formed.

  The funnel portion 64 has an inner diameter that gradually decreases downward, so that the contents can easily flow toward the lowermost discharge opening 64a (see FIG. 6B).

  The filter mounting portion 65 is a filter housing portion 65a (see FIG. 6 (FIG. 6)) that forms a thin disk-like space in accordance with the shape of the filter 7 arranged so as to close the outlet of the discharge opening 64a (see FIG. 6 (b)). b) and a cylindrical ring support portion 65b for supporting the filter fixing ring 8 are integrally formed.

  A second L-shaped groove 65c into which a fourth engagement claw 82a formed in the filter fixing ring 8 to be described later is fitted is formed on the inner peripheral surface of the ring support portion 65b. Four second L-shaped grooves 65c are formed along the circumferential direction at equal intervals.

  The filter 7 in the present embodiment is a membrane filter, and as described above, the filter 7 is arranged outside the discharge opening 64a so as to close the outlet of the discharge opening 64a, and sequentially from the discharge opening 64a side, A hydrophilic filter 7a and a hydrophobic filter 7b are overlaid.

Commercially available products can be used for the hydrophilic filter 7a and the hydrophobic filter 7b. Examples of the hydrophilic filter 7a include MF-Millipore (Nippon Millipore), Durapore (Nippon Millipore), Isopore (Nippon Millipore).
Examples of the hydrophobic filter 7b include Mytex (manufactured by Nihon Millipore) and polypropylene prefilter (manufactured by Nihon Millipore).
Needless to say, those filters 7 having an outer diameter larger than the inner diameter of the discharge opening 64a are used.

  As shown in FIGS. 6A and 6B, the filter fixing ring 8 fixes the filter 7 to the housing 6 (the funnel portion 64). The filter fixing ring 8 passes through the discharge opening 64a of the funnel portion 64 and the filter 7. And a through hole 81 at a position where they communicate with each other.

  The filter fixing ring 8 is formed below the ring body 82 and has a ring body 82 having an outer shape substantially the same as the inner diameter of the ring support portion 65b of the filter mounting portion 65, and is larger than the outer diameter of the ring body 82. And a flange portion 83 having a diameter.

  Further, as shown in FIG. 6A, the filter fixing ring 8 is integrally formed on the upper surface of the ring main body 82, and is fitted into the filter accommodating portion 65a of the housing 6, and the fitting portion And an annular rib 85 erected around the opening of the through hole 81 at 84. Incidentally, the filter 7 is pressed around the outlet of the discharge opening 64a (see FIG. 6B) by the annular rib 85.

  Then, on the peripheral surface of the ring main body 82, four fourth engaging claws 82a are formed at equal intervals along the circumferential direction so as to extend outward in the radial direction. The fourth engagement claw 82a is formed at a position corresponding to the second L-shaped groove 65c of the ring support portion 65b described above, and the filter fixing ring 8 can be detachably attached to the housing 6 by being fitted into the second L-shaped groove 65c. To be linked.

As shown in FIG. 7, the first object half 4a and the second dish half 4b are combined with each other to form the disk-shaped collection dish 4, as shown in FIG. At the same time, the collection dish 4 is placed on the shelf 63 of the housing 6, and the housing 6 and the lid 3 are interposed between the first L-shaped groove 61 a and the collection dish 4. And the third engaging claw 32. At this time, the through hole 41 of the collection dish 4 is sealed by the protrusion 33 of the lid 3.
The housing 6 and the lid 3 can be disconnected from each other by rotating the housing 6 and the lid 3 relative to each other and extracting the third engaging claw 32 from the first L-shaped groove 61a.

  The filter 7 is disposed in the filter housing portion 65a so as to close the outlet of the discharge opening 64a of the funnel portion 64, and the filter mounting portion 65 and the filter fixing ring 8 are provided with the second L-shaped groove 65c and By being connected by the fourth engagement claw 82 a, the discharge opening 64 a of the funnel portion 64 and the through hole 81 of the filter fixing ring 8 communicate with each other via the filter 7. At this time, as described above, the filter 7 is pressed firmly around the outlet of the discharge opening 64a by the annular rib 85 of the filter fixing ring 8, and is firmly fixed.

In such an object collecting tool 1, the projection 33 of the lid 3 seals the through hole 41 as shown in FIG. 7. Further, the outlet of the discharge opening 64a of the funnel portion 64 is closed with a filter 7 that separates microorganisms. As a result, the internal space 66 becomes a space (closed space) separated from the external environment at least for microorganisms. Then, the carrier for counting analysis 5a held in the first dish half 4a and the carrier for identification analysis 5b held in the second dish half 4b are arranged in this closed space.
The detection object collecting tool 1 as described above can be formed of a moldable resin except for the filter 7. Of these, polypropylene is preferable.

<Usage of detection object collector>
Next, the usage method of the to-be-detected object collector 1 which concerns on 1st Embodiment is demonstrated.
Here, a method for collecting microorganisms with the detection object collecting tool 1 will be described first. Next, FIG. 8 to be referred to is a perspective view for explaining a method of collecting microorganisms with the detection object collecting tool of the present invention, and FIG. 9 is a carrier in the detection object collecting tool according to the present embodiment. It is a perspective view which shows a mode that is divided | segmented.

  When collecting the microorganisms in the air using the detection object collector 1 (see FIG. 7), as shown in FIG. 8, the first dish half 4a holding the counting analysis carrier 5a, The second dish half 4b holding the identification analysis carrier 5b is combined with each other to form the collection dish 4, and the collection dish 4 placed on the lid 3 is used. . That is, in the detection object collecting tool 1 shown in FIG. 7, the housing 6 and the filter fixing ring are turned upside down, leaving the first dish half 4a and the second dish half 4b on the lid 3 side. The one with 8 removed is used. Incidentally, the removal of the housing 6 from the lid 3 is performed by positioning the lid 3 on the pedestal 52 of the air sampler 50 and arranging the housing 6 and the lid 3 as described above, as will be described below. The third engagement claw 32 (see FIG. 6 (a)) is extracted from the first L-shaped groove 61a (see FIG. 6 (a)) by rotating it relatively, and the connection is released.

  The detected object collecting tool 1 is placed on a circular pedestal 52 in a plan view formed above the main body 51 of the air sampler 50. As described above, the pedestal 52 is formed with the recess 53 for receiving the second engagement claw 31 of the lid 3, and the detection object collecting tool 1 is positioned at the center of the pedestal 52. It is like that.

  Incidentally, in FIG. 8, reference numeral 54 is a suction port of the main body 51, reference numeral 55 is a nozzle head of the air sampler 50, and reference numeral 55 a is a nozzle arranged in the nozzle head 55. The nozzle 55a is obtained by forming a plurality of fine nozzle holes in a disk-shaped plate.

  That is, in this method for collecting microorganisms, the object collecting tool 1 with the carrier 5 exposed is mounted on the pedestal 52 by removing the housing 6 and the filter fixing ring 8 together as shown in FIG. The nozzle head 55 is arranged so as to cover the pedestal 52.

  Then, when a fan (not shown) disposed in the main body 51 is driven and air is sucked from the suction port 54, the air flow is transferred from the plurality of nozzle holes of the nozzle 55 a provided in the nozzle head 55. Is injected into. As a result, the microorganisms accompanying the air jetted onto the carrier 5 are collected in the carrier for counting analysis 5a and the carrier for identification analysis 5b. That is, the microorganisms are collected with the carrier 5 facing upward.

At this time, as shown in FIG. 8, the through-hole 41 (see FIG. 7) of the collection dish 4 is sealed by the projection 33 of the lid 3, so the surface of the collection dish 4 on the carrier 5 side is The turbulence of the received air flow is suppressed. As a result, the carrier 5 can efficiently collect microorganisms.
When the air sampler 50 sucks a predetermined amount of air, the microorganism collecting process by the detection object collecting tool 1 is completed.
When this collection process is completed, the housing 6 and the filter fixing ring 8 are once attached to the lid body 3 again, and the state returns to the state of the detection object collecting tool 1 shown in FIG.

Next, the usage method of the to-be-detected object collector 1 in the microorganisms counter 10 which counts the collected microorganisms is demonstrated.
After the above-described collection step is completed, the detection object collecting tool 1 that has returned to the state shown in FIG. 7 is transported by the user to the installation location of the microorganism counting device 10 (see FIG. 1) as it is. .
Next, the housing 6 is removed from the lid 3 by the user.
The first dish half 4a holding the counting analysis carrier 5a is removed from the lid 3 as shown in FIG. 9, and then disposed on the mounting portion 102 together with the housing 6 as shown in FIG.
On the other hand, as shown in FIG. 9, the first cover 35 covers the identification analysis carrier 5b on the lid 3 on which the second dish half 4b holding the identification analysis carrier 5b is left. It is attached.
The first cover body 35 has a bottomed cylindrical shape, and has a third L-shaped groove 35a on the inner peripheral surface of an opening having substantially the same inner diameter as the upper cylindrical portion 61 (see FIG. 6A) of the housing 6. Is formed. The third L-shaped groove 35a has a structure similar to the first L-shaped groove 61a of the housing 6 (see FIG. 6A).
The first cover body 35 and the lid body 3 are connected by fitting the third engagement claw 32 of the lid body 3 into the third L-shaped groove 35 a of the first cover body 35. As a result, the first cover body 35 seals the identification analysis carrier 5 b with the lid body 3.
Incidentally, the carrier for identification analysis 5b is subjected to identification analysis in order to specify the type of microorganism. The counting analysis corresponds to the “first detection operation of the detection object” in the claims, and the identification analysis is the “second detection operation of the detection objects” in the claims. Equivalent to.

Next, the usage method of the to-be-detected object collector 1 in the microorganisms counter 10 which counts the collected microorganisms is demonstrated.
Next, FIGS. 10 (a-1) to 10 (a-4) to be referred to are cross-sectional views and drawings of the detected object collecting tool for explaining a method of using the detected object collecting tool in the microorganism counting apparatus. 10 (b-1) to (b-4) are schematic diagrams showing an enlarged view of the vicinity of the filter in the scene corresponding to FIGS. 10 (a-1) to (a-4).
10 (b-1) to (b-4), the microorganism indicated by the symbol B is actually a micrometer size, and ATP is actually a molecular level size, FIGS. 10 (b-1) to (b-4) do not show their relative sizes.

  When the carrier 5 is heated in step S201 (see FIG. 4), as shown in FIG. 10 (a-1), the counting analysis carrier 5a held in the first dish half 4a is solated. To peel off the funnel 64 of the housing 6. At this time, as shown in FIG. 10 (b-1), the microorganism B collected by the air sampler 50 (see FIG. 8) stays on the filter 7 together with the counting analysis support 5 a.

  Next, when the hot water HW is injected into the housing 6 in the above-described step S202 (see FIG. 4), the sol-formation of the counting analysis support 5a is further promoted and diluted with the hot water. At this time, as shown in FIG. 10 (a-2), the lower side of the filter 7 is composed of the hydrophobic filter 7b, so that the hot water HW including the count analysis carrier 5a diluted is contained in the housing 6. Stays on. The microorganism B stays with the hot water HW on the filter 7. In FIG. 10A-2, reference numeral 4a denotes a first dish half, and reference numeral 64 denotes a funnel (the same applies to the reference numerals in the following drawings).

  Next, in step S203 (see FIG. 4), when the contents in the housing 6 are filtered, the hot water HW in the housing 6 (see FIG. 10 (a-2)) is changed to FIG. 10 (a-3). ) As shown. At this time, the microorganisms B in the hot water HW are separated and held by the filter 7 as shown in FIG. 10 (b-3).

  Incidentally, as shown in FIG. 10 (b-3), the filter 7 in this embodiment has a double structure of a hydrophilic filter 7a and a hydrophobic filter 7b, and is therefore used in the conventional ATP method. Unlike those formed with only hydrophilic filters, the hydrophobic filter 7b allows the liquid to be retained at the top unless suction or pressure filtration is applied, so that reagent reactions such as ATP extraction Processing can take place on the filter 7.

In step S206 (see FIG. 4), the ATP elimination reagent is dispensed in the housing 6, and then in step S209 (see FIG. 4), the ATP extraction reagent is dispensed in the housing 6.
These reagent dispensing steps correspond to the “fourth step of injecting the reagent into the housing” in the claims.

  In step S209 (see FIG. 4), as shown in FIG. 10 (a-4), the ATP extract EX stays in the housing 6 into which the ATP extraction reagent has been injected. At this time, as shown in FIG. 10 (b-4), ATP is present in the ATP extract EX in an amount corresponding to the number of microorganisms B.

In step S210 (see FIG. 4), the ATP extract EX shown in FIG. 10 (b-4) is dispensed into the light emission tube 107a (see FIG. 1). Thereafter, the microorganisms are counted through the above-described step S211 and step S212 (see FIG. 4).
When the presence of microorganisms in the counting analysis carrier 5a is confirmed, the identification analysis carrier 5b held in the second dish half 4b left on the lid 3 side shown in FIG. 9 is used for identification analysis. This identifies the type of microorganism.

  According to the detection object collecting tool 1 and the method of using the same as described above, the carrier 5 including the counting analysis carrier 5a and the identification analysis carrier 5b is disposed on one surface side of the collection dish 4. Therefore, when the collection dish 4 is arranged on the air sampler 50 (see FIG. 8) and the carrier 5 receives the air flow when the air sampler 50 sucks, the carrier for counting analysis 5a and the carrier for identification analysis 5b. The microorganisms can be collected so that the number of microorganisms per unit area (exposed area) is substantially equal to each other.

  In addition, according to the detection object collecting tool 1 and the method of using the same, the carrier 5 is divided and arranged as a counting analysis carrier 5a and an identification analysis carrier 5b so that the carrier 5 is integrated. Unlike the above, it is not necessary to cut the carrier 5 after collecting the microorganisms and weigh it. Therefore, according to this to-be-detected object collector 1 and its usage method, it can prevent that the substance used as a disturbance factor mixes in the support | carrier 5 when performing a cutting operation or weighing. As a result, according to the detected object collecting tool 1 and the method of using the same, when the carrier 5 after collecting the microorganisms is subjected to a plurality of analyzes such as quantitative analysis and qualitative analysis of the detected object. You can do their analysis more accurately.

Moreover, according to the to-be-detected object collector 1 and its usage method, after performing the operation of collecting microorganisms with the carrier 5 facing upward, the reagent is brought into contact with the microorganisms with the carrier 5 directed downward. .
Therefore, according to the detected object collecting tool 1 and the method of using the same, the carrier 5 is directed upward to facilitate the collection of microorganisms, and when the reagent is brought into contact with the microorganisms, that is, the microorganisms are detected. In this case, the collection dish 4 functions as a lid of the carrier 5 by directing the carrier 5 downward. As a result, for example, the carrier 5 is prevented from being contaminated by dust or bacteria falling from above.

In addition, the carrier 5 is attached to the housing 6 before the detection object collecting tool 1 is attached to the air sampler 50 and before the microorganisms are collected by the air sampler 50 and before being transported into the microorganism counting device 10. Unlike the conventional collector (for example, see Patent Document 1), the carrier 5 is contaminated with a substance that causes disturbance of the count of microorganisms. Can be prevented.
As a result, according to the detected object collecting tool 1 and the method of using the same, the microorganisms collected at the inspection place can be counted more accurately.

  Moreover, according to the to-be-detected object collector 1 and its usage, it has the discharge opening 64a which discharges the contents of the housing 6, and the filter which isolate | separates and hold | maintains microorganisms is arrange | positioned at this discharge opening 64a. Therefore, the microorganism and the reagent R can be brought into contact with each other in the housing 6. As a result, unlike the conventional collector (see, for example, Patent Document 1), the disturbance factor of the count of microorganisms is dramatically different from the one in which a reagent is brought into contact with the microorganisms taken out from the collector and the microorganisms are counted. Decrease.

  Moreover, according to the to-be-detected object collector 1 and its usage method, since the filter 7 has a double structure of the hydrophilic filter 7a and the hydrophobic filter 7b, the hydrophilicity used in the conventional ATP method is used. The reagent reaction process for the collected microorganisms can be performed on the filter 7.

  Moreover, according to the to-be-detected object collector 1 and its usage, the lid 3 is provided with the second engaging claw 31 that engages with the air sampler 50 on the opposite side of the housing 6, as shown in FIG. As shown in FIG. 8, after the lid 3 and the housing 6 are integrated with each other, the housing 6 side is gripped with fingers and the lid 3 is placed on the air sampler 50 as shown in FIG. By removing the housing 6 from the carrier 5, the carrier 5 can be exposed. That is, when the carrier 5 is exposed, it is possible to avoid fingers from touching the collection dish 4 holding the carrier 5. Therefore, according to the detected object collecting tool 1 and the method of using the same, it is possible to more reliably prevent the carrier 5 from being contaminated with a substance that causes disturbance of the counting of microorganisms.

  Moreover, according to the to-be-detected object collection tool 1 and its usage method, when the lid 3 is removed from the housing 6 by the user, the first dish half of the collection dish 4 is disposed on the mounting portion 102. 4a is upside down (upside down), and the count analysis carrier 5a faces the inner space 66, so that contamination of the count analysis carrier 5a can be more reliably prevented.

Although the first embodiment of the present invention has been described above, the present invention is not limited to the above-described embodiment, and can be implemented in various forms.
In the said embodiment, although the collection dish 4 was comprised with two division bodies which consisted of the 1st dish half body 4a and the 2nd dish half body 4b, the collection dish 4 is comprised by three or more division bodies. It may be.

  Moreover, when combining the 1st dish half body 4a and the 2nd dish half body 4b and forming the collection dish 4, you may have an engagement means to mutually engage. Next, FIG. 11 to be referred to is an exploded plan view of the collection dish for explaining the configuration of the modification of the collection dish.

As shown in FIG. 11, in the collection dish 4, the first dish half 4a and the second dish half 4b are engaged with each other by an engaging convex part 45b and an engaging concave part 45a. Means 45 is provided at the peripheral edge avoiding the carrier receiving ribs 42a and 42b.
The collection dish 40 having such an engagement means 45 is arranged such that the first dish half 4a and the second dish half 4b are moved into the housing 6 (see FIG. 7) or the nozzle head 55 of the air sampler 50 (see FIG. 8). ) Can be arranged more stably. Further, the collection dish 40 having the engaging means 45 is convenient to carry because the first dish half 4a and the second dish half 4b can be integrated.
The engaging means 45 is not limited to one provided integrally with the first dish half 4a and the second dish half 4b, and may be provided separately as a clip, for example.

In the above embodiment, when the microorganism counting device 10 is used to perform the microorganism counting analysis, the second dish half 4b holding the carrier for identification analysis 5b is removed from the housing 6 and then placed on the mounting portion 102. However, without removing the second dish half 4b holding the identification analysis carrier 5b, the identification analysis carrier 5b may also be subjected to counting analysis. At this time, the reagent R and the like are dispensed into the housing 6 through the through hole 41.
It goes without saying that both the counting analysis support 5a and the identification analysis support 5b may be subjected to identification analysis.

  In the above embodiment, the identification analysis is performed on the identification analysis carrier 5b after confirming the presence of the microorganism in the count analysis support 5a by performing the count analysis. Analysis can also be performed.

  In the above embodiment, it is assumed that the microorganisms collected by the detection object collecting tool 1 are counted by the microorganism counting device 10. However, the present invention is not incorporated into the microorganism counting device 10 and is manually performed. The reagent R may be dispensed into the housing and the microorganisms counted by the ATP method.

  In addition, the present invention may be applied to spore-forming bacteria such as Bacillus subtilis, and in this case, a nutrient cell conversion reagent such as an amino acid or a sugar can be included in the reagent described above.

  In the above embodiment, microorganisms are counted by the ATP method. However, the present invention is based on fluorescence generated by irradiating in vivo substances such as DNA, RNA, and NAD extracted from microorganisms with excitation light. The microorganisms may be counted.

  Further, when gram-negative bacilli are collected and counted by the detection object collector 1, the endotoxin contained in the cell membrane is used as an index, and based on the luminescence intensity when the endotoxin is reacted with limulus. The number of bacteria may be counted.

  Alternatively, microorganisms may be collected from the filter 7 and may be counted for culture.

  Moreover, in the said embodiment, although it has set as the structure which divides and arrange | positions the support | carrier 5 so that it can be divided | segmented into plurality by dividing | segmenting the collection dish 4, it will be in said embodiment if the support | carrier 5 can be divided and arranged in multiple. It is not limited, For example, the structure of following 2nd Embodiment may be sufficient.

(Second Embodiment)
Next, a detected object collecting tool according to a second embodiment of the present invention will be described.
In addition, since the microorganisms counting apparatus which mounts the to-be-detected object collection tool which concerns on this embodiment, and the counting principle of the microorganisms in the microorganisms counting apparatus are the same as that of 1st Embodiment, the detailed description is abbreviate | omitted.

<Detection object collector>
Next, FIG. 12 to be referred to is an exploded perspective view of the detection object collecting tool according to the second embodiment of the present invention, (a) is an exploded perspective view when looking down from obliquely above, and (b) is a perspective view. It is a disassembled perspective view at the time of looking up from diagonally downward. FIG. 13 is a cross-sectional view of the detection object collecting tool according to the second embodiment in a cross section corresponding to the VII-VII cross section of FIG. 5. FIG. 14 is a perspective view showing a state in which a carrier is divided in an object collecting tool according to a second embodiment of the present invention.
Note that in the second embodiment, the same components as those in the first embodiment are denoted by the same reference numerals, and detailed description thereof is omitted.
As shown in FIGS. 12 (a) and 12 (b), the detected object collecting tool 11 includes a collection dish 40 including a counting analysis support 5a and a lid 30 including an identification analysis support 5b. Except that the housing 6, the filter 7, and the filter fixing ring 8 are the same as those of the detected object collecting tool 1 according to the first embodiment (see FIGS. 6A and 6B). The lid 30 and the collection dish 40 will be mainly described.

Instead of the protrusion 33 (see FIGS. 6 (a) and 6 (b)) formed on the outer surface of the bottom portion of the lid body 3 in the first embodiment, the lid body 30 has an annular carrier receiving rib on its outer surface. 34 is erected. The outer diameter of the carrier receiving rib 34 is slightly smaller than the inner diameter of the through hole 44 of the collection dish 40 described below. Further, the height of the carrier receiving rib 34 is equal to the length of the through hole 44.
In the lid 30 shown in FIGS. 12A and 12B, reference numeral 31 denotes a second engagement claw that engages with the recess 53 of the air sampler 50 shown in FIG. 8, and reference numeral 32 denotes the first of the housing 6. It is the 3rd engaging claw inserted in 1L character slot 61a.

  As shown in FIGS. 12A and 12B, the collection dish 40 has a disk shape. A through-hole 44 that penetrates the collection dish 40 from the lower surface side to the upper surface side is formed in the central portion of the collection dish 40. The lower surface side of the collection dish 40 corresponds to “one surface side” in the claims, and the upper surface side of the collection dish 40 corresponds to “other surface side” in the claims.

As shown in FIG. 12A, the upper surface of the collection dish 40 is a flat surface so that it can come into contact with the outer surface of the bottom of the lid 30 described above.
In addition, on the lower surface of the collection dish 40, inner and outer double annular carrier receiving ribs 43 a and 43 b are erected around the through hole 44.

As described above, the carrier 5 in this embodiment includes the identification analysis carrier 5b accommodated in the carrier accommodation rib 34 of the lid 30 and the inner and outer double annular carrier accommodation ribs 43a and 43b of the collection dish 40. And a carrier for counting analysis 5a accommodated in between. Here, the carrier for identification analysis 5b corresponds to “another carrier” in the claims.
The identification analysis carrier 5 b is formed in a columnar shape in accordance with the space shape in the carrier receiving rib 34. The counting analysis carrier 5a is formed in an annular shape in accordance with the space shape between the carrier receiving ribs 43a and 43b.
In FIGS. 12A and 12B, reference numeral 7 is a filter including a hydrophilic filter 7a and a hydrophobic filter 7b, reference numeral 8 is a filter fixing ring, and reference numeral 63 is a shelf. Yes, reference numeral 64 a is a discharge opening of the funnel 64.

As shown in FIG. 13, the object collection tool 11 as described above has the collection dish 40 placed on the shelf 63 of the housing 6, and the housing 6 and the lid 30 are separated from each other. The collecting dish 4 is interposed, and the first L-shaped groove 61a and the third engaging claw 32 are connected to each other. At this time, the through hole 44 of the collection dish 40 is sealed with the carrier accommodating rib 34 of the lid 30 and the identification analysis carrier 5b accommodated therein.
That is, when the carrier receiving rib 34 of the lid 30 is fitted into the through-hole 44 of the collection dish 40, the identification analysis carrier 5 b accommodated in the carrier receiving rib 34 is placed on the lower surface side of the collection dish 40. It will face (one side).

And the to-be-detected object collector 11 shown in FIG. 13 is the same as the to-be-detected object collector 1 (refer FIG. 7) concerning the said 1st Embodiment, and the exit of the discharge opening 64a of the funnel part 64 is microorganisms. Is closed by a filter 7 (hydrophilic filter 7a and hydrophobic filter 7b). As a result, the internal space 66 becomes a space (closed space) separated from the external environment at least for microorganisms. Then, the carrier for counting analysis 5a held in the first dish half 4a and the carrier for identification analysis 5b held in the second dish half 4b are arranged in this closed space.
In FIG. 13, reference numeral 8 denotes a filter fixing ring.

<Usage of detection object collector>
Next, a method for collecting microorganisms with the detection object collecting tool 11 will be described.
When the microorganisms in the air are collected using the detection object collecting tool 11, the first dish placed on the lid 3 will be described with reference to FIG. 8 according to the first embodiment. Instead of the half 4a and the counting analysis carrier 5a, and the second dish half 4b and the identification analysis carrier 5b, the collection dish 40 assembled to the lid 30 in FIG. 13, and the counting analysis carrier 5a and An assembly composed of the carrier for identification analysis 5 b is placed on the pedestal 52 of the air sampler 50.
Then, in the same manner as in the first embodiment, microorganisms are collected on the count analysis carrier 5a and the identification analysis carrier 5b.

At this time, similarly to the case where the projection 33 of the lid 3 shown in FIG. 8 seals the through hole 41 (see FIG. 7) of the collection dish 4, the carrier receiving rib 34 and the identification of the lid 30 shown in FIG. Since the analysis carrier 5b seals the through hole 44 of the collection dish 40, the counting analysis carrier 5a and the identification analysis carrier 5b are flush with each other, and the turbulence of the received air flow is suppressed. . As a result, the counting analysis support 5a and the identification analysis support 5b can efficiently collect microorganisms.
After the above-described collection process is completed, the detection object collecting tool 11 that has returned to the state shown in FIG. 13 is transported by the user to the place where the microorganism counting device 10 is installed as it is (see FIG. 2). .
Next, the housing 6 is removed from the lid 30 by the user.
As shown in FIG. 14, the collection dish 40 holding the carrier for counting analysis 5a is removed from the lid 30, and then the housing 6 and the first plate are replaced with those shown in FIG. 3 according to the first embodiment. Similar to the one-dish half 4 a, it is arranged on the mounting portion 102 together with the housing 6. The count analysis carrier 5a is used for the count analysis of microorganisms as in the above embodiment.
On the other hand, as shown in FIG. 14, the second cover body 36 is attached to the carrier receiving rib 34 holding the identification analysis carrier 5b so as to cover the identification analysis carrier 5b.
The second cover body 36 has a bottomed cylindrical shape, and has an inner diameter that can be fitted to the carrier receiving rib 34. The carrier for identification analysis 5b is subjected to identification analysis in order to identify the type of microorganism when the presence of the microorganism is confirmed by the count analysis of the microorganism.
In addition, it can replace with this 2nd cover body 36, or can use together with this 2nd cover body 36, and can use the 1st cover body 35 (refer FIG. 9) in the said embodiment.

According to the detected object collector 11 and the method of using the same as described above, the same effects as those of the detected object collector 1 and the method of using the detected object collector 1 according to the first embodiment can be obtained, and as follows. It is also possible to achieve an advantageous effect.
According to the detected object collecting tool 11 and the method of using the same, the collecting dish 40 has the inside of the housing 6 and the air sampler 50 in a state where the carrier receiving rib 34 of the lid 30 is fitted in the through hole 44. It is arranged in the nozzle head 55. As a result, the collection dish 40 can be arranged more stably in the housing 6 and the nozzle head 55.
According to the detected object collecting tool 11 and the method of using the same, when the reagent R is brought into contact with the microorganism using the microorganism counting apparatus 10, the reagent is placed in the housing 6 through the through hole 44 of the collecting dish 40. Since R is dispensed, the communication between the inside of the housing 6 and the outside thereof is stopped at the size of the through hole 44. As a result, it is possible to prevent the inside of the housing 6 from being contaminated with a substance that causes disturbance of the count of microorganisms.

Although the second embodiment of the present invention has been described above, the present invention is not limited to the above-described embodiment, and can be implemented in various forms.
In the said embodiment, although the one collection dish 40 is provided, the collection dish 40 can be made into the collection dish 40 which can be divided | segmented into plurality similarly to the collection dish 4 in 1st Embodiment. .

DESCRIPTION OF SYMBOLS 1 Detected object collection tool 3 Cover body 4 Collection dish 4a 1st dish half 4b 2nd dish half 5 Carrier 5a Counting analysis carrier 5b Identification analysis carrier 6 Housing 7 Filter 7a Hydrophilic filter 7b Hydrophobic filter DESCRIPTION OF SYMBOLS 8 Filter fixing ring 11 Detected object collection tool 30 Cover body 33 Protrusion 34 Carrier accommodating rib 40 Collecting dish 41 Through hole 42a Carrier accommodating rib 43a Carrier accommodating rib 44 Through hole 45 Engaging means 45a Engaging recess 45b Engaging protrusion Part 64 funnel part 64a discharge opening 65 filter mounting part 65a filter housing part 65b ring support part 66 internal space

Claims (8)

The carrier that collects the object to be detected is divided and divided into a plurality of sections,
A collection dish for holding the carrier;
The detection object collector according to claim 1, wherein the carrier is disposed on one side of the collection dish. In the to-be-detected object collector of Claim 1,
The collection dish is configured by combining a plurality of divided bodies,
The detection object collecting tool, wherein the carrier is held in each of the divided bodies. In the to-be-detected object collector of Claim 2,
Further comprising a housing disposed relative to the collection dish to cover the carrier;
The collection dish has a through-hole connecting the one surface side and the other surface side,
The to-be-detected object collector characterized by the said through-hole of the said collection dish connecting the space formed between the said one surface side and the said housing, and the exterior. In the to-be-detected object collector of Claim 3,
The housing has a discharge opening for discharging the contents of the space to the outside of the housing, and a filter for separating the detection object is disposed outside the discharge opening. Collecting tool. In the to-be-detected object collector of Claim 1,
A collection dish for holding the carrier;
The collection dish has a through hole that connects the one side and the other side,
The collection dish holds the carrier on the one surface side,
In the through-hole of the collection dish, another carrier that is separable from the carrier is fitted so as to face the one surface side. In the to-be-detected object collector of Claim 5,
A housing disposed with respect to the collection dish so as to cover the carrier and the other carrier;
The through-hole of the collection dish that appears after removing the other carrier connects a space formed between the one surface side and the housing to the outside, and collects an object to be detected. Ingredients. In the to-be-detected object collector of Claim 6,
The housing has a discharge opening for discharging the contents of the space to the outside of the housing, and a filter for separating the detection object is disposed outside the discharge opening. Collecting tool. A method for using a detection object collecting tool in which a carrier for collecting a detection object is divided and divided into a plurality of sections.
After collecting the object to be detected with the carrier arranged on one side of the collection dish,
Dividing the carrier according to the compartments;
A part of the divided carrier is subjected to a first detection operation of the detection object, and the remainder of the divided carrier is subjected to a second detection operation of the detection object. How to use the detected object collector.

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