WO2019062436A1 - Instant inspection device - Google Patents
Instant inspection device Download PDFInfo
- Publication number
- WO2019062436A1 WO2019062436A1 PCT/CN2018/102899 CN2018102899W WO2019062436A1 WO 2019062436 A1 WO2019062436 A1 WO 2019062436A1 CN 2018102899 W CN2018102899 W CN 2018102899W WO 2019062436 A1 WO2019062436 A1 WO 2019062436A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- plunger
- syringe
- gas
- filled
- real
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/02—Burettes; Pipettes
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
Definitions
- the invention belongs to the field of medical detection, and in particular relates to a real-time inspection device.
- the reagent includes two separate components, enumerating: a detergent having a blood cell lysis function and an agglutinating agent for enhancing the agglutination effect, and enumerating: polyethylene glycol (PEG) and Salts, in addition, there are some reagents consisting of antibodies and preservatives. Usually, when the two components are mixed, the reagents are unstable and need to be mixed before use to achieve the best results.
- the on-site detection is difficult to apply for immunoturbidimetric reagents; the enumeration of immunoturbidimetric reagents for detecting children requires the collection of peripheral blood, and the reagent detection requires siphon blood collection tube and siphon blood collection tube injection.
- the entire inspection report time is about 40 minutes, especially It is difficult to popularize in the emergency department and basic hospital, the operation is cumbersome, and it is necessary to transfer samples to different departments, and the human factors are large.
- siphon sampling tube collection sample ⁇ sample transfer to the inspection department ⁇ insert the push rod Siphon sampling tube ⁇ Open the reagent cup cover and push the sample into the reagent cup ⁇ Adjust the pipette to 300uL ⁇ -Install the disposable pipette tip ⁇ Open the bottle cap and inject 300 uL reagent 1 into the reaction cup with pipette ⁇ Change Pipette tip ⁇ adjust the pipette to 100uL ⁇ install the disposable pipette tip ⁇ open the cap and pipette 100uL reagent 2 into the pipette ⁇ after mixing into the cuvette, the entire process takes about 40 minutes.
- the present invention provides a real-time testing device capable of realizing one-time quantitative filling of one or more component reagents, which can make testing more convenient and reagent loading accuracy. Improve, truly check out.
- a real-time testing device of the present invention comprises a syringe and a plunger, wherein the plunger is movably disposed in the syringe, and a liquid outlet of the syringe is provided with a blockage.
- a pre-filled cavity is formed between the plug and the plunger, the pre-filled cavity is pre-filled with liquid and gas, and the plunger is provided with a split at one end of the plug; the plunger is pushed, and the plunger is compressed
- the gas is pre-filled in the chamber, so that the displacement of the plunger drives the splitting material to break or split the plug, and continues to push the plunger, and the pre-filled liquid is injected into the reaction cup.
- the gas thickness in the pre-filled cavity is a
- the distance between the tip end of the pointed column and the blockage is b
- a and b satisfy a>b.
- the gas thickness in the pre-filled cavity is a
- the distance between the tip end of the pointed column and the blockage is b
- the gas in the pre-filled cavity is compressed by the plunger
- the thickness after the c is c, which satisfies ac>b.
- the plunger is connected to the prying or the plunger is integrated with the prying material.
- the cleavage is a pointed column structure, and a tip end of the pointed column is disposed at a distance from the clogging.
- the cross section of the pointed column is a cross shape, and the pointed column is gradually thickened from the plunger end to the tip end.
- a push rod is disposed on the opposite side of the splitting of the plunger, and the push rod is provided with a push handle.
- a single or a plurality of the syringes form an injection unit; wherein an injection unit composed of a plurality of the syringes includes at least a first syringe and a second syringe; the first syringe and the second injection
- the cartridges are juxtaposed or connected to each other in parallel; wherein each of the syringes is not connected to each other, and the push handles of the syringes are connected to each other integrally or independently of each other.
- a reaction cup is further included, and a liquid discharge end of the injection unit is disposed corresponding to the liquid inlet end of the reaction cup; and a sampler is further included, and the sampling end of the sampler protrudes into the reaction cup.
- reaction cup is detachably connected to the injection unit; the bottom of the cup of the reaction cup is electrically connected with a detection window, and the detection window is a transparent container having a cross-sectional area smaller than a cross-sectional area of the reaction cup.
- the inner wall of the syringe is provided with at least one ring-shaped positioning ring, and the tip of the pointed column has a spacing between the tip and the blockage when the plunger is at the positioning ring.
- the pre-filled cavity is filled with powdered solids and gas, or the pre-filled cavity is filled with a blocky solid and a gas.
- the invention has the advantages that the structure of the invention is simple, the quantitative filling of one or more component reagents can be realized at one time, the inspection can be more convenient, the precision of the reagent sample loading can be improved, and the real-time inspection can be realized;
- the reagent detection step is reduced to three steps, and the traditional detection time of more than 40 minutes is shortened to about 2 minutes. If the scheme can be effectively promoted, the operation efficiency in the medical detection field can be greatly improved.
- FIG. 1 is a schematic view of the overall structure of the present invention
- FIG. 2 is a schematic view of the structure of the two syringes
- FIG. 3 is a schematic view of the structure of the plunger, the push rod and the pointed column
- FIG. 4 is a schematic view of the structure of the reaction cup
- the present embodiment includes an injection unit and a reaction cup 7, the liquid discharge end of the injection unit is disposed corresponding to the liquid inlet end of the reaction cup 7, and the reagent in the injection unit can flow to the reaction cup. 7; further comprising a sampler 11 connected to the liquid discharge end of the injection unit, and the reaction cup 7 is detachably connected to the injection unit, in this embodiment: the injection unit The liquid outer ring is provided with a sealing ring groove 16, and the cup end 10 of the upper end of the reaction cup 7 is sleeved on the sealing ring groove 16, which is beneficial for disassembly and effectively prevents the reagent in the reaction cup 7 from splashing; the reaction cup 7 and In the assembled state of the injection unit, the sampling end 8 of the sampler 11 extends into the cuvette 7, facilitating the reaction of the collected sample in the reaction cup 7, and after the reaction cup 7 is removed, the sampler 11 follows the injection unit. The sampling and installation of the sampler 11 is facilitated.
- the cup bottom of the cuvette 7 is electrically connected to the detection window 9, and the detection window 9 is a transparent container having a cross-sectional area smaller than the cross-sectional area of the cuvette 7.
- the reaction cup is also a machine glass or a high transparent plastic.
- the transparent body, and the detection window 9 and the reaction cup 7 form a conjoined structure; the detection window 9 can intuitively judge the mixing degree of the reagent and the sample and preliminarily judge the reaction effect, for example, when the sample is mixed with the reagent 1 and the reagent 2
- the specific analyte undergoes a specific reaction, and the agglutination increases the turbidity of the solution.
- the optical instrument can change the scattering of the light after detecting the window 9. The change of the light scattering can be measured by the instrument, and the amount of light scattering is in the sample. The concentration of the analyte is proportional.
- the injection unit includes a single syringe or syringe set; the syringe set includes at least a first syringe 14 and a second syringe 13; the first syringe 14 and the second syringe 13 are juxtaposed;
- the plunger 3 is disposed in the syringe, wherein each of the syringes is not connected to each other; in the embodiment, the material of the plunger 3 is preferably a material such as silica gel, and the plunger 3 and the inner wall of the syringe are interspersed for improving the sealing performance.
- the outlet of the syringe is provided with a blockage 6, and the blockage 6 blocks the outlet.
- the blockage 6 can be increased or decreased according to the diameter of the outlet port.
- the material of the plug hole is not particularly limited, but must be blocked.
- the hole can be opened or smashed by the pointed column, and the outlet can be increased or decreased according to the need.
- the typical plug 6 is listed as a sealing plug of a plastic, glass, resin or the like, a sealing ball, or the like, or a heat seal.
- Each of the plungers 3 is provided with a push rod 2 on the opposite side of the splitting body, and the push rod 2 is provided with a push handle 1; the push handles 1 of each of the injection cylinders are connected to each other or are independent of each other, and a plurality of specific types In the case of a reagent, it is necessary to supply the reaction cup 7 in a sequential order, and the push handle 1 independent of each other can fulfill this requirement.
- the splitting is a structure of a pointed column 4, the tip end 5 of the pointed column 4 is spaced from the blockage 6; the cross section of the pointed column 4 is a cross, and the pointed column 4 is The end of the plunger 3 is gradually thickened to the tip end 5, and a cross-shaped section and a gradually thickened structure facilitate the flow of the reagent into the reaction cup.
- the pre-filled chamber 30 is filled with liquid and gas or filled with powder solids and gas at the same time or filled with bulk solids and gas; in this embodiment, the pre-filled chamber 30 is filled with reagents and gases at the same time;
- the gas thickness in the pre-filled cavity 30 is a
- the distance between the tip end 5 of the pointed post 4 and the plug 6 is b
- a and b satisfy a>b due to the material and
- the gas compression ratio cannot be increased indefinitely, so the thickness of the gas in the pre-filled cavity 30 after being compressed by the plunger 3 is c, and should also satisfy ac>b, which ensures the tip end 5 of the pointed column 4 The stroke can reach the blockage 6.
- the inner wall of the syringe is provided with at least one ring-shaped positioning ring 15 with a spacing between the tip end 5 of the pointed column 4 and the blockage 6 when the plunger 3 is at the positioning ring 15;
- the cross-section of the inner wall of the syringe is circular, elliptical or polygonal; the positioning ring 15 acts as a safety clasp for positioning and locking the initial position of the plunger 3 and the push rod 2.
- the sampler 11 is a quantitative capillary blood collection tube or a quantitative blood collection rod; the capillary end on the quantitative capillary blood collection tube is a sampling end 8 , and the fixed column end on the quantitative capillary blood collection tube is a connection end; sampling on the sampling rod The ring end is the sampling end 8 and the other end is the connecting end; wherein the sampling circle is a circular or elliptical sampling structure, and the sampling circle is notched or notched; the quantitative capillary collecting tube or the quantitative blood collecting rod is connected at the connecting end In the mounting holes 12 between the two outlet ports of the first syringe 14 and the second syringe 13.
- the method description of the device specifically includes the following steps: Step 1, the reaction cup 7 is detached from the injection unit, the sampler 11 collects the sample, and the reaction cup 7 is reinstalled; Step 2, simultaneously or stepwise pressing the first syringe 14 And the push rod 2 on the second syringe 13, the gas in the pre-filled chamber 30 in the first syringe 14 and the second syringe 13 is compressed until the two pointed columns 4 puncture the two outlets respectively.
- the plug 6, the first reagent in the first syringe 14 and the second reagent in the second syringe 13 are respectively ejected from the two outlets under the action of the compressed gas, and flow into the reaction cup 7; After mixing the reaction cup 7, the detection window 9 is observed and placed in the instrument for detection.
- the distance between the tip end 5 of the pointed column 4 and the blockage 6 may be increased or decreased according to the amount of liquid in the pre-filled cavity 30, or the pre-filled cavity 30 may be controlled.
- the reagent in the pre-filled chamber 30 can be applied to a part of the solid, the solid requirement is smaller than the inner diameter of the liquid outlet, the sharp shape 4 pushes the solid, the solid smashes or smashes the plug, and the solid comes out of the plug.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Clinical Laboratory Science (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Sampling And Sample Adjustment (AREA)
Abstract
Description
本发明属于医学检测领域,尤其涉及一种即时检验装置。The invention belongs to the field of medical detection, and in particular relates to a real-time inspection device.
目前免疫诊断试剂分析,列举免疫比浊分析法,试剂包括两个单独的组分,列举:具有血细胞裂解功能的去污剂以及增强凝集效应的凝集剂,列举:聚乙二醇(PEG)和盐,此外,还有一些由抗体和防腐剂组成的试剂,通常混合有两种组份后试剂不稳定,需要在使用前混合以达到最佳效果。受限于以上实验条件限制,免疫比浊试剂很难应用的现场即时检测(POCT);列举免疫比浊试剂法检测试剂儿童检测需要采集末梢血,试剂检测需要虹吸采血管、虹吸采血管推注杆、试剂1、试剂2、试剂杯、两种不同精度移液器、移液器吸头,并且需要临床科室采集完样本后送去检验科室检验,整个出检验报告时间在40分钟左右,特别是在急诊、基础医院很难普及,操作繁琐,并且需要转移样本到不同科室、操作人为影响因素大;传统典型试剂检测流程:虹吸采样管采集样本→样本转移到检验科室→将推注杆插入虹吸采样管→打开试剂杯盖将样本推入试剂杯→调节移液器到300uL→-安装一次性移液吸头→打开瓶盖后用移液器吸入300 uL试剂1加入反应杯中→更换移液器吸头→调节移液器到100uL→-安装一次性移液吸头→打开瓶盖后用移液器吸入100uL试剂2加入反应杯中→混匀后放入,全程需40分钟左右。At present, immunodiagnostic reagents are listed, and the immunoturbidimetric assay is listed. The reagent includes two separate components, enumerating: a detergent having a blood cell lysis function and an agglutinating agent for enhancing the agglutination effect, and enumerating: polyethylene glycol (PEG) and Salts, in addition, there are some reagents consisting of antibodies and preservatives. Usually, when the two components are mixed, the reagents are unstable and need to be mixed before use to achieve the best results. Limited by the above experimental conditions, the on-site detection (POCT) is difficult to apply for immunoturbidimetric reagents; the enumeration of immunoturbidimetric reagents for detecting children requires the collection of peripheral blood, and the reagent detection requires siphon blood collection tube and siphon blood collection tube injection. Rod, reagent 1, reagent 2, reagent cup, two different precision pipettes, pipette tips, and need to be sent to the laboratory for testing after the sample is collected by the clinical department. The entire inspection report time is about 40 minutes, especially It is difficult to popularize in the emergency department and basic hospital, the operation is cumbersome, and it is necessary to transfer samples to different departments, and the human factors are large. The traditional typical reagent detection process: siphon sampling tube collection sample → sample transfer to the inspection department → insert the push rod Siphon sampling tube→Open the reagent cup cover and push the sample into the reagent cup→Adjust the pipette to 300uL→-Install the disposable pipette tip→Open the bottle cap and inject 300 uL reagent 1 into the reaction cup with pipette~Change Pipette tip → adjust the pipette to 100uL → install the disposable pipette tip → open the cap and pipette 100uL reagent 2 into the pipette → after mixing into the cuvette, the entire process takes about 40 minutes.
发明目的:为了克服现有技术中存在的不足,本发明提供一种即时检验装置,能一次性实现一种或多种组分试剂的定量加注,可使检验更加方便、试剂加样量精度提高,真正做到即时检验。OBJECT OF THE INVENTION In order to overcome the deficiencies in the prior art, the present invention provides a real-time testing device capable of realizing one-time quantitative filling of one or more component reagents, which can make testing more convenient and reagent loading accuracy. Improve, truly check out.
技术方案:为实现上述目的,本发明的一种即时检验装置,包括注射筒和柱塞,所述柱塞活动设置于所述注射筒内,所述注射筒的出液口设置有堵塞物,所述堵塞物和所述柱塞之间形成预装腔,预装腔内预装液体及气体,所述柱塞靠近所述堵塞物的一端设置有捅开物;推动柱塞,柱塞压缩所述预装腔内气体,从而柱塞位移带动所述捅开物捅破或捅开所述堵塞物,继续推动柱塞,预装液体注入反应杯。Technical Solution: In order to achieve the above object, a real-time testing device of the present invention comprises a syringe and a plunger, wherein the plunger is movably disposed in the syringe, and a liquid outlet of the syringe is provided with a blockage. a pre-filled cavity is formed between the plug and the plunger, the pre-filled cavity is pre-filled with liquid and gas, and the plunger is provided with a split at one end of the plug; the plunger is pushed, and the plunger is compressed The gas is pre-filled in the chamber, so that the displacement of the plunger drives the splitting material to break or split the plug, and continues to push the plunger, and the pre-filled liquid is injected into the reaction cup.
进一步的,所述注射筒竖立状态下,所述预装腔中气体厚度为a,所述尖状柱的尖端与所述堵塞物的间距为b, a和b满足a>b。Further, in the erected state of the syringe, the gas thickness in the pre-filled cavity is a, the distance between the tip end of the pointed column and the blockage is b, a and b satisfy a>b.
进一步的,所述注射筒竖立状态下,所述预装腔中气体厚度为a,所述尖状柱的尖端与所述堵塞物的间距为b,所述预装腔中气体被柱塞压缩后的厚度为c,满足a-c>b。Further, in the erected state of the syringe, the gas thickness in the pre-filled cavity is a, the distance between the tip end of the pointed column and the blockage is b, and the gas in the pre-filled cavity is compressed by the plunger The thickness after the c is c, which satisfies ac>b.
进一步的,所述柱塞连接捅开物,或者柱塞与捅开物一体化。Further, the plunger is connected to the prying or the plunger is integrated with the prying material.
进一步的,所述捅开物为尖状柱结构,所述尖状柱的尖端与所述堵塞物间距设置。Further, the cleavage is a pointed column structure, and a tip end of the pointed column is disposed at a distance from the clogging.
进一步的,所述尖状柱的横切面为十字形,所述尖状柱从柱塞端到尖端逐渐变粗。Further, the cross section of the pointed column is a cross shape, and the pointed column is gradually thickened from the plunger end to the tip end.
进一步的,所述柱塞的捅开物对侧设置有推杆,所述推杆上设置有推柄。Further, a push rod is disposed on the opposite side of the splitting of the plunger, and the push rod is provided with a push handle.
进一步的,单个或多个所述注射筒形成注射单元;其中,由多个所述注射筒构成的注射单元至少包括第一注射筒和第二注射筒;所述第一注射筒和第二注射筒并列成一体或相互并列连接;其中各所述注射筒互不连通,各所述注射筒的推柄相互连为一体或相互独立。Further, a single or a plurality of the syringes form an injection unit; wherein an injection unit composed of a plurality of the syringes includes at least a first syringe and a second syringe; the first syringe and the second injection The cartridges are juxtaposed or connected to each other in parallel; wherein each of the syringes is not connected to each other, and the push handles of the syringes are connected to each other integrally or independently of each other.
进一步的,还包括反应杯,所述注射单元的出液端与所述反应杯的进液端对应设置;还包括采样器,所述采样器的采样端伸入所述反应杯中。Further, a reaction cup is further included, and a liquid discharge end of the injection unit is disposed corresponding to the liquid inlet end of the reaction cup; and a sampler is further included, and the sampling end of the sampler protrudes into the reaction cup.
进一步的,所述反应杯与所述注射单元可拆卸连接;所述反应杯的杯底导通设置有检测窗,所述检测窗为横截面积小于所述反应杯横截面积的透明容器。Further, the reaction cup is detachably connected to the injection unit; the bottom of the cup of the reaction cup is electrically connected with a detection window, and the detection window is a transparent container having a cross-sectional area smaller than a cross-sectional area of the reaction cup.
进一步的,所述注射筒的内壁至少设置有一圈凸起状定位环,所述柱塞在定位环处时,所述尖状柱的尖端与所述堵塞物之间具有间距。Further, the inner wall of the syringe is provided with at least one ring-shaped positioning ring, and the tip of the pointed column has a spacing between the tip and the blockage when the plunger is at the positioning ring.
进一步的,或所述预装腔内填充粉末固体和气体,或所述预装腔内填充有块状固体和气体。Further, the pre-filled cavity is filled with powdered solids and gas, or the pre-filled cavity is filled with a blocky solid and a gas.
有益效果:本发明的结构简单,能一次性实现一种或多种组分试剂的定量加注,可使检验更加方便、试剂加样量精度提高,真正做到即时检验;同时将传统复杂的试剂检测步骤精简成三个步骤,将传统的40多分钟的检测时间缩短到2分钟左右,该方案若能实现有效推广,能极大提高医学检测领域的运行效率。The invention has the advantages that the structure of the invention is simple, the quantitative filling of one or more component reagents can be realized at one time, the inspection can be more convenient, the precision of the reagent sample loading can be improved, and the real-time inspection can be realized; The reagent detection step is reduced to three steps, and the traditional detection time of more than 40 minutes is shortened to about 2 minutes. If the scheme can be effectively promoted, the operation efficiency in the medical detection field can be greatly improved.
附图1为本发明整体结构示意图;附图2为两注射筒结构示意图;附图3为柱塞、推杆和尖状柱结构示意图;附图4为反应杯结构示意图;附图5为单个注射筒结构示意图。1 is a schematic view of the overall structure of the present invention; FIG. 2 is a schematic view of the structure of the two syringes; FIG. 3 is a schematic view of the structure of the plunger, the push rod and the pointed column; FIG. 4 is a schematic view of the structure of the reaction cup; Schematic diagram of the syringe structure.
本实施例中,将发明创造用于医学样品检测领域,下面结合附图对本发明作更进一步的说明。In the present embodiment, the invention is applied to the field of medical sample detection, and the present invention will be further described below with reference to the accompanying drawings.
如附图1至4所示,本方案包括注射单元和反应杯7,所述注射单元的出液端与所述反应杯7的进液端对应设置,注射单元中的试剂可流至反应杯7中;还包括采样器11,所述采样器11连接设置在所述注射单元的出液端,同时所述反应杯7与所述注射单元可拆卸连接,本实施例中:注射单元的出液端外圈设置有密封环槽16,所述反应杯7上端的杯口10套于密封环槽16上,既有利于拆卸又有效防止了反应杯7中的试剂溅出;反应杯7与所述注射单元装配状态下,采样器11的采样端8伸入所述反应杯7中,便于采集的样本在反应杯7中的试剂反应,取下反应杯7后采样器11跟随注射单元,便于采样器11的采样和安装。As shown in FIGS. 1 to 4, the present embodiment includes an injection unit and a reaction cup 7, the liquid discharge end of the injection unit is disposed corresponding to the liquid inlet end of the reaction cup 7, and the reagent in the injection unit can flow to the reaction cup. 7; further comprising a sampler 11 connected to the liquid discharge end of the injection unit, and the reaction cup 7 is detachably connected to the injection unit, in this embodiment: the injection unit The liquid outer ring is provided with a sealing ring groove 16, and the cup end 10 of the upper end of the reaction cup 7 is sleeved on the sealing ring groove 16, which is beneficial for disassembly and effectively prevents the reagent in the reaction cup 7 from splashing; the reaction cup 7 and In the assembled state of the injection unit, the sampling end 8 of the sampler 11 extends into the cuvette 7, facilitating the reaction of the collected sample in the reaction cup 7, and after the reaction cup 7 is removed, the sampler 11 follows the injection unit. The sampling and installation of the sampler 11 is facilitated.
所述反应杯7的杯底导通检测窗9,所述检测窗9为横截面积小于所述反应杯7横截面积的透明容器,本实施例中反应杯也为机玻璃、高透明塑料等透明体,且检测窗9与所述反应杯7构成连体结构;检测窗9能直观的判断试剂和样品的混合均匀程度和初步判断反应效果,例如:当样本与试剂1和试剂2混合反应后特定的分析物发生特异反应、凝集使溶液的浊度增加,光学仪器可通过检测窗9后引起光的散射改变,光散射的改变可以通过仪器得到测量,同时,光散射量与样本中分析物的浓度成正比。The cup bottom of the cuvette 7 is electrically connected to the detection window 9, and the detection window 9 is a transparent container having a cross-sectional area smaller than the cross-sectional area of the cuvette 7. In this embodiment, the reaction cup is also a machine glass or a high transparent plastic. The transparent body, and the detection window 9 and the reaction cup 7 form a conjoined structure; the detection window 9 can intuitively judge the mixing degree of the reagent and the sample and preliminarily judge the reaction effect, for example, when the sample is mixed with the reagent 1 and the reagent 2 After the reaction, the specific analyte undergoes a specific reaction, and the agglutination increases the turbidity of the solution. The optical instrument can change the scattering of the light after detecting the window 9. The change of the light scattering can be measured by the instrument, and the amount of light scattering is in the sample. The concentration of the analyte is proportional.
所述注射单元包括单个注射筒或注射筒组;所述注射筒组至少包括第一注射筒14和第二注射筒13;所述第一注射筒14和第二注射筒13并列成一体;各所述注射筒内活动设置有柱塞3,其中各所述注射筒互不连通;本实施例中,柱塞3材料优选硅胶等材料,为提高密封性能,柱塞3与注射筒内壁过盈配合,所述注射筒的出液口处设置有堵塞物6,堵塞物6堵住出口,堵塞物6可根据出液口孔径增加或减少大小,堵孔物材料并不特别限定,但必须堵孔物可用尖状柱捅开或捅破,出口可根据需要增加或减少口径,本实施例中典型堵塞物6列举:塑料、玻璃、树脂等材料的密封塞、密封球等方式,或热封、胶粘合等方式封口的塑料薄膜、铝箔纸等材料;所述堵塞物6和所述柱塞3之间形成预装腔30,预装腔内30预装液体及气体,所述柱塞3靠近所述堵塞物6的一端设置有捅开物;推动柱塞3,柱塞3压缩所述预装腔30内气体,从而柱塞3位移带动所述捅开物捅破或捅开所述堵塞物6,继续推动柱塞3,预装液体注入反应杯;本实施例中所述柱塞3连接捅开物,或者柱塞3与捅开物一体化;本实施例中的的气体为空气、氮气或惰性气体等化学性质稳定的气体,保证了气体不与液体试剂反应。The injection unit includes a single syringe or syringe set; the syringe set includes at least a first syringe 14 and a second syringe 13; the first syringe 14 and the second syringe 13 are juxtaposed; The plunger 3 is disposed in the syringe, wherein each of the syringes is not connected to each other; in the embodiment, the material of the plunger 3 is preferably a material such as silica gel, and the plunger 3 and the inner wall of the syringe are interspersed for improving the sealing performance. Cooperating, the outlet of the syringe is provided with a blockage 6, and the blockage 6 blocks the outlet. The blockage 6 can be increased or decreased according to the diameter of the outlet port. The material of the plug hole is not particularly limited, but must be blocked. The hole can be opened or smashed by the pointed column, and the outlet can be increased or decreased according to the need. In the present embodiment, the typical plug 6 is listed as a sealing plug of a plastic, glass, resin or the like, a sealing ball, or the like, or a heat seal. a plastic film, aluminum foil or the like sealed in a manner such as a glue bond; a pre-filled cavity 30 is formed between the plug 6 and the plunger 3, and a liquid and a gas are pre-filled in the pre-filled cavity 30, the plunger 3 is provided near the end of the blockage 6 Pushing the plunger 3, the plunger 3 compresses the gas in the pre-filled cavity 30, so that the displacement of the plunger 3 drives the splitting material to break or split the plugged object 6, and continues to push the plunger 3 to pre-fill the liquid Injecting the reaction cup; in the embodiment, the plunger 3 is connected to the prying material, or the plunger 3 is integrated with the cleaving object; the gas in the embodiment is a chemically stable gas such as air, nitrogen or an inert gas. It is guaranteed that the gas does not react with the liquid reagent.
各所述柱塞3的捅开物对侧设置有推杆2,所述推杆2上设置有推柄1;各所述注射筒的推柄1相互连为一体或相互独立,特定多种试剂的情况下,需要有先后顺序的要求供给到反应杯7中,相互独立的推柄1能实现该要求。Each of the plungers 3 is provided with a push rod 2 on the opposite side of the splitting body, and the push rod 2 is provided with a push handle 1; the push handles 1 of each of the injection cylinders are connected to each other or are independent of each other, and a plurality of specific types In the case of a reagent, it is necessary to supply the reaction cup 7 in a sequential order, and the push handle 1 independent of each other can fulfill this requirement.
所述捅开物为尖状柱4结构,所述尖状柱4的尖端5与所述堵塞物6间距设置;所述尖状柱4的横切面为十字形,所述尖状柱4从柱塞3端到尖端5逐渐变粗,采用十字形截面和逐渐变粗结构有利于试剂流入反应杯。The splitting is a structure of a pointed column 4, the tip end 5 of the pointed column 4 is spaced from the blockage 6; the cross section of the pointed column 4 is a cross, and the pointed column 4 is The end of the plunger 3 is gradually thickened to the tip end 5, and a cross-shaped section and a gradually thickened structure facilitate the flow of the reagent into the reaction cup.
所述预装腔30内同时填充有液体和气体或同时填充粉末固体和气体或同时填充有块状固体和气体;本实施例中:所述预装腔30内同时填充有试剂和气体;所述注射筒竖立状态下,所述预装腔30中气体厚度为a,所述尖状柱4的尖端5与所述堵塞物6的间距为b,a和b满足a>b,由于材料和推力限制,气体压缩比不能无限增大,因此所述预装腔30中气体被柱塞3压缩后的厚度为c,还应满足a-c>b,该数学关系保证了尖状柱4的尖端5的行程能达到堵塞物6。The pre-filled chamber 30 is filled with liquid and gas or filled with powder solids and gas at the same time or filled with bulk solids and gas; in this embodiment, the pre-filled chamber 30 is filled with reagents and gases at the same time; In the erected state of the syringe, the gas thickness in the pre-filled cavity 30 is a, the distance between the tip end 5 of the pointed post 4 and the plug 6 is b, a and b satisfy a>b due to the material and The thrust limitation, the gas compression ratio cannot be increased indefinitely, so the thickness of the gas in the pre-filled cavity 30 after being compressed by the plunger 3 is c, and should also satisfy ac>b, which ensures the tip end 5 of the pointed column 4 The stroke can reach the blockage 6.
所述注射筒的内壁至少设置有一圈凸起状定位环15,所述柱塞3在定位环15处时,所述尖状柱4的尖端5与所述堵塞物6之间具有间距;所述注射筒的内壁横切面为圆形、椭圆形或多边形;定位环15作为安全卡环,用于定位及锁定柱塞3及推杆2的初始位置。The inner wall of the syringe is provided with at least one ring-shaped positioning ring 15 with a spacing between the tip end 5 of the pointed column 4 and the blockage 6 when the plunger 3 is at the positioning ring 15; The cross-section of the inner wall of the syringe is circular, elliptical or polygonal; the positioning ring 15 acts as a safety clasp for positioning and locking the initial position of the plunger 3 and the push rod 2.
所述采样器11为定量毛细采血管或定量采血棒;所述定量毛细采血管上的毛细管端为采样端8,定量毛细采血管上的固定柱端为连接端;所述采样棒上的采样圈端为采样端8,另一端为连接端;其中采样圈为圆形或椭圆形采样结构,且采样圈上开有缺口或无缺口;所述定量毛细采血管或定量采血棒的连接端安装于第一注射筒14和第二注射筒13的两出液口之间的安装孔12中。The sampler 11 is a quantitative capillary blood collection tube or a quantitative blood collection rod; the capillary end on the quantitative capillary blood collection tube is a sampling end 8 , and the fixed column end on the quantitative capillary blood collection tube is a connection end; sampling on the sampling rod The ring end is the sampling end 8 and the other end is the connecting end; wherein the sampling circle is a circular or elliptical sampling structure, and the sampling circle is notched or notched; the quantitative capillary collecting tube or the quantitative blood collecting rod is connected at the connecting end In the mounting holes 12 between the two outlet ports of the first syringe 14 and the second syringe 13.
该装置的方法说明,具体包括如下步骤:步骤1,将反应杯7从注射单元上拆下,采样器11采集样本后重新安装反应杯7;步骤2,同时或逐步按下第一注射筒14和第二注射筒13上的推杆2,第一注射筒14和第二注射筒13中的预装腔30内的气体被压缩,直至两尖状柱4分别戳破两出液口出的堵塞物6,第一注射筒14中的第一试剂和第二注射筒13中的第二试剂在压缩气体的作用下分别从两出液口喷出,并流至反应杯7中;步骤3,混匀反应杯7后观察检测窗9并放入仪器检测。The method description of the device specifically includes the following steps: Step 1, the reaction cup 7 is detached from the injection unit, the sampler 11 collects the sample, and the reaction cup 7 is reinstalled; Step 2, simultaneously or stepwise pressing the first syringe 14 And the push rod 2 on the second syringe 13, the gas in the pre-filled chamber 30 in the first syringe 14 and the second syringe 13 is compressed until the two pointed columns 4 puncture the two outlets respectively. The plug 6, the first reagent in the first syringe 14 and the second reagent in the second syringe 13 are respectively ejected from the two outlets under the action of the compressed gas, and flow into the reaction cup 7; After mixing the reaction cup 7, the detection window 9 is observed and placed in the instrument for detection.
补充说明:在多个连体的注射筒同时推注时,可根据预装腔30液体量、增加或减少尖状柱4的尖端5与堵塞物6的距离,或控制预装腔30中的气体量,从而根据需要达到加注液体出来的先后顺序;在同一预装腔30中,气体越多、液体越少,尖状柱4的尖端5可以离堵塞物越远;在特定情况下,预装腔30中的试剂可以适用于部分固体,固体要求小于出液口内径,尖状住4推动固体,固体捅破或捅开堵塞物,固体从堵孔物出来。Supplementary explanation: when a plurality of conjoined syringes are simultaneously bolused, the distance between the tip end 5 of the pointed column 4 and the blockage 6 may be increased or decreased according to the amount of liquid in the pre-filled cavity 30, or the pre-filled cavity 30 may be controlled. The amount of gas, so as to achieve the order of filling the liquid as needed; in the same pre-filled chamber 30, the more gas, the less the liquid, the farther the tip 5 of the pointed column 4 can be from the blockage; in certain cases, The reagent in the pre-filled chamber 30 can be applied to a part of the solid, the solid requirement is smaller than the inner diameter of the liquid outlet, the sharp shape 4 pushes the solid, the solid smashes or smashes the plug, and the solid comes out of the plug.
以上所述仅是本发明的优选实施方式,应当指出:对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。The above description is only a preferred embodiment of the present invention, and it should be noted that those skilled in the art can also make several improvements and retouchings without departing from the principles of the present invention. It should be considered as the scope of protection of the present invention.
Claims (12)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710918358.6A CN107576809B (en) | 2017-09-30 | 2017-09-30 | Instant inspection device |
| CN201710918358.6 | 2017-09-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2019062436A1 true WO2019062436A1 (en) | 2019-04-04 |
Family
ID=61040263
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/CN2018/102899 Ceased WO2019062436A1 (en) | 2017-09-30 | 2018-08-29 | Instant inspection device |
Country Status (2)
| Country | Link |
|---|---|
| CN (1) | CN107576809B (en) |
| WO (1) | WO2019062436A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107576809B (en) * | 2017-09-30 | 2024-07-23 | 江苏宝卫士生物科技有限公司 | Instant inspection device |
| CN109012778B (en) * | 2018-05-24 | 2021-03-16 | 顾裕宁 | Reagent prepackage type seals combination test tube for high school's chemistry |
| CN113549536A (en) * | 2021-07-13 | 2021-10-26 | 深圳赛桥生物创新技术有限公司 | Sterile cell sampling device and method based on totally-enclosed syringe |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009032645A1 (en) * | 2007-09-06 | 2009-03-12 | Siemens Healthcare Diagnostics, Inc. | Reagent cartridge |
| CN203132865U (en) * | 2012-12-25 | 2013-08-14 | 南京普朗医用设备有限公司 | Puncturing piston type sample feeding and sampling device |
| CN106111225A (en) * | 2016-08-16 | 2016-11-16 | 江苏康尚生物医疗科技有限公司 | A kind of multifunctional quantitatively pipettor |
| CN107576809A (en) * | 2017-09-30 | 2018-01-12 | 江苏宝卫士生物科技有限公司 | A kind of real-time test device |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101581729B (en) * | 2009-06-05 | 2012-06-27 | 何峰 | Liquid sample processing device |
| CN103760330B (en) * | 2013-12-31 | 2016-03-30 | 杭州迪图科技有限公司 | A kind ofly to collect and the device of analyte in test fluid sample |
| EP3025744A1 (en) * | 2014-11-28 | 2016-06-01 | Sulzer Mixpac AG | Apparatus and methods for storing and mixing separate substances |
| CN205080061U (en) * | 2015-10-13 | 2016-03-09 | 南京格耀生物科技有限公司 | Integration detects cell |
| CN206008744U (en) * | 2016-08-16 | 2017-03-15 | 江苏康尚生物医疗科技有限公司 | A kind of multifunctional quantitatively pipettor |
| CN207351745U (en) * | 2017-09-30 | 2018-05-11 | 江苏宝卫士生物科技有限公司 | A kind of prepackage type weight feed device |
-
2017
- 2017-09-30 CN CN201710918358.6A patent/CN107576809B/en active Active
-
2018
- 2018-08-29 WO PCT/CN2018/102899 patent/WO2019062436A1/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009032645A1 (en) * | 2007-09-06 | 2009-03-12 | Siemens Healthcare Diagnostics, Inc. | Reagent cartridge |
| CN203132865U (en) * | 2012-12-25 | 2013-08-14 | 南京普朗医用设备有限公司 | Puncturing piston type sample feeding and sampling device |
| CN106111225A (en) * | 2016-08-16 | 2016-11-16 | 江苏康尚生物医疗科技有限公司 | A kind of multifunctional quantitatively pipettor |
| CN107576809A (en) * | 2017-09-30 | 2018-01-12 | 江苏宝卫士生物科技有限公司 | A kind of real-time test device |
Also Published As
| Publication number | Publication date |
|---|---|
| CN107576809A (en) | 2018-01-12 |
| CN107576809B (en) | 2024-07-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1902484B (en) | Disposable fluid sample collection device | |
| CN112916064B (en) | A reagent pre-embedding and sample injection device and method, and a digital microfluidic chip including the same | |
| CN209624608U (en) | Microfluidic immune chip, piercing device and optical detection device | |
| CN107036847A (en) | A kind of applicator | |
| WO2019062436A1 (en) | Instant inspection device | |
| EP1788944A1 (en) | Method and apparatus for sampling and analysis of fluids | |
| CN104519976A (en) | Multi-part device for extracting plasma from blood | |
| US9186670B2 (en) | Functionalized microfluidic device and method | |
| WO2021027082A1 (en) | Sample collection and detection device and method | |
| EP2514528A1 (en) | Device and method for assessing the status of cells in a biological fluid | |
| WO2024212855A1 (en) | Totally-enclosed fully-integrated nucleic acid testing micro-fluidic chip | |
| CN107866196B (en) | Conjoined feeding device and method thereof | |
| CN101194154A (en) | Sample collection liquid container | |
| CN105214745B (en) | A kind of micro-fluidic chip | |
| CN204718871U (en) | A kind ofly store and mix lid and the device of solid-liquid | |
| CN215493304U (en) | Whole blood treatment and detection micro-fluidic chip | |
| CN118479154A (en) | Reagent storage assembly, reagent kit and sample detection method | |
| JP2008175608A (en) | Chemical reaction cartridge and method of use thereof | |
| WO2013127243A1 (en) | Prepackaged reagent cuvette structure | |
| CN106289933B (en) | Cover body and device for storing and mixing solid and liquid | |
| CN207351745U (en) | A kind of prepackage type weight feed device | |
| CN116099580A (en) | A microfluidic detection device | |
| WO2013045695A2 (en) | Method for delivering a sample of body fluid to an analysing system, a syringe designed for use therein and a kit comprising such a syringe | |
| CN110560184A (en) | Microfluidic chip, microfluidic reaction system and driving method | |
| CN105107449B (en) | A kind of combined type reaction cup |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18860406 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 18860406 Country of ref document: EP Kind code of ref document: A1 |