WO2012165685A1 - Sensor strip - Google Patents

Abstract

The present invention relates to a sensor strip device having a plurality of holes on a sensor strip and, according to the positions of the holes, indicates whether all three of the total cholesterol (TC), triglycerides (TG), and high-density lipoprotein (HDL) are detected, or TC and HDL are detected. The present invention provides a sensor strip device for measuring protein in the blood and comprises: an upper plate having a specimen inlet port; a pad section having a reaction pad for reacting to a specimen inserted into the specimen inlet port; and a lower plate having a display window that provides a location through which the reaction pad can be observed, wherein the lower plate includes a first hole, a second hole, and a third hole and allows the sensor strip device to detect any one of TC, TG, and HDL, detect TC, TG, and HDL, or detect TC and HDL, depending on combinations of the opening and closing of the first, second, and third holes.

Description

Sensor strip

The present invention relates to a sensor strip apparatus, and more particularly, to include a plurality of holes on the sensor strip, but to detect according to the position of the hole total cholesterol (TC), triglyceride (TG), high density lipoprotein (HDL) All three are related to a sensor strip device, which indicates either total cholesterol (TC) or high density lipoprotein (HDL).

The concentration of sugar in the serum is used as an indicator of diseases related to carbohydrate metabolism. When the measured value is outside the normal range, the onset of the disease is predicted. One method for this is colorimetry. The colorimetric method is a method of measuring the transmitted light or reflected light by comparing with the standard color by using the color tone of the sample material or the color reaction by the target component. That is, it is the analysis method which quantifies by comparing the color tone of a test liquid with the color tone of a standard liquid.

 In general, a measurement method using a test strip, that is, a sensor strip (biosensor strip), is used to test a specific characteristic value through a sample such as blood. For example, in the case of blood glucose measurement, the blood glucose is automatically inserted into the sensor strip inlet by inserting it into the inlet of the blood glucose meter, drawing a fingertip, and placing a small amount of blood at the fingertip onto the sensor strip inserted in the meter. The value is displayed on the screen of the glucose meter.

The sensor strip is used for quantitative or qualitative analysis of a sample taken from a human body, and a reagent for causing a chemical reaction with the sample is applied at a predetermined position.

The detection of blood through the sensor strip includes total cholesterol (TC), triglyceride (TG), high density lipoprotein (HDL), low density lipoprotein (LDL), and in particular, low density lipoprotein (LDL) is LDL = TC-HDL. -[0.2 × TG (triglyceride)]. Therefore, the detection of blood through the sensor strip is total cholesterol (TC), triglyceride (TG), high-density lipoprotein (HDL), etc. In order to detect and analyze them, specific reagents and specific structures according to the detection in the sensor strip are detected. Must be provided.

By the way, there are many types of sensor strips to detect total cholesterol (TC), triglyceride (TG), high density lipoprotein (HDL), etc., but there is one analysis device that reads and analyzes these sensor strips.

Therefore, in order to analyze these, identification information indicating whether the sensor strip which detects total cholesterol (TC), triglyceride (TG), high density lipoprotein (HDL), etc. is required.

The present invention is provided with a plurality of holes on the strip to detect the total cholesterol (TC), triglycerides (TG), high-density lipoprotein (HDL), all three of these, total cholesterol (TC) and high density It provides a sensor strip device indicating that any one of lipoprotein (HDL).

The problem to be solved of the present invention is to have a plurality of holes on the strip sensor, but to detect according to the position of the total cholesterol (TC), triglycerides (TG), high density lipoprotein (HDL), all three, It is to provide a sensor strip device indicating that either total cholesterol (TC) and high density lipoprotein (HDL).

Another problem to be solved of the present invention is that in the strip structure for measuring the multi-characteristics, the sample can reach the reaction pad uniformly and quickly with a small amount of sample and at the same time minimize the deviation of the measurement value To provide a means.

Another problem to be solved by the present invention is to provide a housing means that can minimize the deviation of the measured value and increase the production yield in mass production.

The present invention includes a blood plate including an upper plate having a sample inlet, a pad unit including a reaction pad reacting with a sample introduced from the sample inlet, and a lower plate having a display window penetrated at a position where the reaction pad can be identified. In the sensor strip device for measuring the protein in the inner, the lower plate is provided with a first hole, a second hole, a third hole, according to the combination of the opening and closing of each of the first hole, the second hole, the third hole Sensor strip device detects total cholesterol (TC), detects triglycerides (TG), detects high density lipoprotein (HDL), detects total cholesterol (TC) and triglyceride (TG) and high density lipoprotein (HDL), total cholesterol (TC) ) And high density lipoprotein (HDL) detection.

The display window is at least one of the first hole, the second hole, and the third hole.

In addition, the present invention includes a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a lower plate having a display window penetrated at a position where the reaction pad can be confirmed. In the sensor strip device for measuring the protein in the blood, wherein the lower plate has a second hole in the middle portion, the first hole in front of the second hole, each of the first hole, the second hole is opened And the sensor strip device is configured to detect any one of total cholesterol (TC), triglyceride (TG), and high density lipoprotein (HDL).

In addition, the present invention includes a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a lower plate having a display window penetrated at a position where the reaction pad can be confirmed. In the sensor strip device for measuring the protein in the blood, wherein the lower plate has a second hole in the middle portion, and the third hole behind the second hole, each of the second hole, the third hole is opened And the sensor strip device is configured to detect any one of total cholesterol (TC), triglyceride (TG), and high density lipoprotein (HDL).

In addition, the present invention includes a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a lower plate having a display window penetrated at a position where the reaction pad can be confirmed. In the sensor strip device for measuring the protein in the blood, wherein the lower plate has a first hole in the upper portion, a third hole in the lower portion, the combination of the opening and closing of each of the first hole, the third hole Accordingly, the sensor strip device is characterized in that it is made to detect any one of total cholesterol (TC), triglycerides (TG), high density lipoprotein (HDL).

In addition, the present invention includes a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a lower plate having a display window penetrated at a position where the reaction pad can be confirmed. In the sensor strip device for measuring protein in the blood, wherein the display window has a first hole, a second hole, a third hole, the sensor strip device is a total cholesterol (TC) as the second hole is opened or closed; ) And triglyceride (TG) and high density lipoprotein (HDL) detection, and detects any one of the total cholesterol (TC) and high density lipoprotein (HDL) detection.

When only the second hole is open, the sensor strip device is configured to detect only total cholesterol (TC).

As the first and second holes are opened, the sensor strip device is configured to detect either triglyceride (TG) or high density lipoprotein (HDL).

As the second and third holes are opened, the sensor strip device is configured to detect either triglyceride (TG) or high density lipoprotein (HDL).

As the first and third holes are opened, the sensor strip apparatus is configured to detect one or more of triglyceride (TG) and high density lipoprotein (HDL).

The first hole and the second hole. If all of the third holes are open, the sensor strip device is configured to detect both total cholesterol (TC), triglyceride (TG) and high density lipoprotein (HDL).

If the first and third holes are opened and the second hole is closed, the sensor strip device is configured to detect total cholesterol (TC) and high density lipoprotein (HDL).

The pad part includes a support having a display window penetrating up and down, and the reaction pad is attached on the display window of the support to react with the specimen.

The pad part may be attached on the reaction pad to filter the blood cells, the first and second hemolytic pads, and the sample pads attached to the first and second hemolytic pads to promote the spread of the sample in the transverse direction, and the first pad. And an adhesive film adhered to a support around the second anti-hemolysis pad to improve adhesion of the sample pad.

The bottom surface of the upper plate is formed with a flat compression surface protruding to apply a uniform pressure to the pad portion during assembly.

The upper plate has a fastening portion formed at a lower end thereof, and the lower plate has a second fastening portion fastened by a force fitting method corresponding to the fastening portion of the upper plate, and the pad portion has an upper through hole positioned at a first hole corresponding position. And a support having an intermediate hole positioned at a second hole corresponding position and a lower hole positioned at a third hole corresponding position, and attached to the support, attached to the upper hole, and reacting with a sample to form a triglyceride (TG). , A first reaction pad measuring one of high density lipoprotein (HDL) and total cholesterol (TC), attached to the support, attached to the intermediate through hole, and reacted with the sample to neutral fat (TG), high density lipoprotein (HDL), A second reaction pad for measuring the other of total cholesterol (TC), attached to the support, attached to the lower through-holes to react with the sample of triglycerides (TG), high-density lipoprotein (HDL), total cholesterol (TC) All It characterized in that made in a third reaction pad to measure one.

The pad unit may include: hemolysis prevention pads attached to the first reaction pad, the second reaction pad, and the third reaction pad to prevent hemolysis; The sample pad is adhered on the anti-hemolysis pads to promote the spread of the sample in the transverse direction.

A sample flow path having a narrow groove shape is formed in the upper plate along the longitudinal direction of the pressing surface.

The lower plate upper surface is formed with a strip seat concave in the shape of the pad portion so that the pad portion is seated during assembly, and the wings are extended on the left and right sides when the longitudinal direction of the lower plate is extended, and the lower plate has a longitudinal direction The handle is formed by extending one end of the mold.

The pad part is positioned between the upper plate and the lower plate forming the housing so that the color tone is changed according to the concentration of lipid (Lipid) or total cholesterol (TC) or triglyceride (TG) or high density lipoprotein (HDL) in the blood. Wherein, the pad portion, the support having at least one through hole; A reaction pad attached to the support and comprising an enzyme solution-immobilized nitrocellulose membrane; A hemolysis prevention pad layer mounted on the reaction pad and preventing hemolysis; And a sample pad mounted on the anti-hemolysis pad layer to allow blood samples to spread evenly within a rapid time to reach the anti-hemolysis pad layer evenly.

The support has three through holes, and the reaction pad is attached to one of the three through holes to measure total cholesterol (TC), the first reaction pad, the other one of the through holes attached to the high density lipoprotein (HDL) A second reaction pad for measuring a) and a third reaction pad for attaching to another one of the through holes of the dog to measure triglyceride.

The hemolysis prevention pad layer comprises two hemolysis prevention pads.

According to the present invention, a plurality of holes are provided on the strip sensor, and the detection of the total cholesterol (TC), triglyceride (TG), high density lipoprotein (HDL), all three, total cholesterol (TC) is to be detected according to the position of the hole. ) And a high density lipoprotein (HDL) to provide a sensor strip device, which has a simpler structure, the production yield is improved, it is easy to use.

According to the present invention, the strip device for measuring a single characteristic according to the present invention has a plastic housing having an upper and a lower plate type, and a nitrocellulose membrane, an antihemostatic pad, and a sample pad are laminated on the polypropylene plate support in order. Since it is placed in the plastic housing and the upper and lower plates are pinhole-bonded to each other, the production yield can be increased during mass production, and the amount of the upper and lower plates can be reduced to minimize the deviation of the measured value even though a small amount of blood is required.

In addition, the strip device for measuring the multi-characteristics of the present invention is improved production yield, the measurement value is minimized by the upper and lower plate detachable housing structure, evenly and quickly on each reaction pad with a small sample volume through the sample flow path structure The sample arrives. In other words, the criterion deviation is constant, uniform and rapid, so that the sample reaches the reaction pad, thereby making the measurement more accurate.

1 is an explanatory diagram for explaining a hole position identifier of a sensor strip according to an embodiment of the present invention.

2 is an exploded perspective view of a sensor strip according to a preferred embodiment of the present invention.

3 is a longitudinal sectional view showing a state of a pad portion of the sensor strip of FIG. 2.

4 is a bottom perspective view showing a state of an upper plate of the sensor strip of FIG. 2.

5 is a bottom perspective view showing a state of a pad portion of the sensor strip of FIG. 2.

6 is a bottom perspective view showing a state of the lower plate of the sensor strip of FIG. 2.

7 is a sensor strip according to another embodiment of the present invention, in which only a second hole and a third hole exist.

8 is a sensor strip according to another embodiment of the present invention, in which only a first hole and a second hole exist.

9 is an exploded perspective view of a sensor strip according to another preferred embodiment of the present invention.

10 is a longitudinal cross-sectional view showing a state of a pad portion of the sensor strip of FIG. 9.

FIG. 11 is a bottom perspective view illustrating the top plate of the sensor strip of FIG. 9.

12 is a bottom perspective view showing a state of a pad portion of the sensor strip of FIG. 9.

FIG. 13 is a bottom perspective view illustrating a bottom plate of the sensor strip of FIG. 9.

Hereinafter, embodiments of the present invention will be described with reference to the accompanying drawings. Unless otherwise defined or mentioned, terms indicating directions such as “up, down, left, and right” used in the present description are based on the states shown in the drawings. In addition, the same reference numerals throughout the embodiments indicate the same member.

The sensor strip according to the present invention includes a housing formed of the upper plate 100 and the lower plate 300, and a pad unit 200 provided between the upper plate 100 and the lower plate 300.

1 is an explanatory diagram for explaining a hole position identifier of a sensor strip according to an embodiment of the present invention.

The three holes, the first hole 315, the second hole 325, and the third hole 335, which are located in the lower plate 300, are combined with each other, so that total cholesterol (TC), triglyceride (TG), and high density lipoprotein (LPD) are combined. (HDL), all three of which indicate detection of either total cholesterol (TC) or high density lipoprotein (HDL).

In FIG. 1, when only the second hole 325 is present, total cholesterol (TC) is detected, and when only the first hole 315 and the second hole 325 are present (when open), high-density lipoprotein (HDL) is detected. When only the second hole 325 and the third hole 335 are present (opened), the triglyceride is detected. The first hole 315, the second hole 325, and the third hole are detected. When all holes 335 are present, total cholesterol (TC), triglycerides (TG), and high density lipoprotein (HDL) are detected, and only the first hole 315 and the third hole 335 are present (when opened). ) Is made to detect total cholesterol (TC) and high-density lipoprotein (HDL), but this is described for convenience of description, which is not intended to limit the present invention, in the present invention, three holes located in the lower plate 300, Note that any combination of the first hole 315, the second hole 325, and the third hole 335 can identify anything to be detected by the sensor strip.

Hereinafter, each configuration will be described in detail by dividing into a case of a sensor strip (Example 1) for measuring a single characteristic and a sensor strip (Example 2) for measuring a multi-characteristic.

<Example 1>

2 is an exploded perspective view of a sensor strip according to a preferred embodiment of the present invention, Figure 3 is a longitudinal sectional view showing a state of the pad portion of the sensor strip of Figure 2, Figure 4 is a view of the top plate of the sensor strip of Figure 2 5 is a bottom perspective view showing the state of the pad portion of the sensor strip of FIG. 2, and FIG. 6 is a bottom perspective view showing the bottom plate of the sensor strip of FIG.

The sensor strip of FIG. 2 includes an upper plate 100, a pad unit 200, and a lower plate 300.

The upper plate 100 will be described with reference to FIGS. 2 and 4.

The upper plate 100 is provided with a sample inlet 110 for injecting the sample, the fastening portion is formed on the bottom face downward.

The sample inlet 110 is formed as a hole located at the center of the upper plate 100. The blood sample is introduced through the sample inlet 110 to reach the sample pad 260 of the pad unit 200. In this case, the smaller the diameter of the sample inlet 110 is, the more the sample reaches and spreads at a predetermined portion of the sample pad 260, so that the deviation of each measured value is reduced.

Meanwhile, when the strip device is inserted into a separate measuring device (not shown), the guide rib 120 and the fixing groove 130 may be formed to improve the feeling of insertion and fixing force.

The guide rib 120 is configured to give a feeling of insertion when the strip device is inserted into the measuring device and to improve left and right fixing forces, and the fixing groove 130 corresponds to a fixing protrusion (not shown) formed in a separate measuring device (not shown). To increase the insertion force and improve the holding force when the strip device is inserted into the measuring device. On the contrary, fixing grooves may be formed in a separate measuring device (not shown).

The pressing plate 140 is formed at the bottom of the upper plate 100. The pressing plate 140 is formed in a plane protruding from the surroundings, and when the upper plate 100 is combined with the lower plate 300, the pressing plate 140 serves to improve the reproducibility of the specimen by applying a constant pressure to the pad unit 200.

Fastening protrusions 150 are formed on the bottom surface of the upper plate 100 in the present embodiment. The fastening protrusions 150 are respectively coupled to the fastening grooves 330 of the lower plate 300 to be described later to allow the upper plate 100 and the lower plate 300 to be assembled and compressed.

The pad unit 200 will be described with reference to FIGS. 2, 3, and 5.

The pad part 200 includes the support 270, the reaction pad 230, the hemolysis prevention pads 240 and 250, and the sample pad 260, but the reaction pad 230 is positioned on the support 270. Hemolysis prevention pads 240 and 250 are mounted thereon, and a specimen pad 260 is mounted on the hemolysis prevention pad.

The support 270 is a means for supporting the hemolysis prevention pads 240 and 250 and the specimen pad 260 and is formed of a plastic material. On the upper surface of the support 270, one side to which the anti-hemolytic pad can be attached is coated with adhesive and a release paper is attached. The strip display window 210 is formed to have a circular perforation so that there is no interference in the measurement portion. After the specimen reaches the reaction pad through the strip display window 210 to cause a reaction, the color of the reaction pad can be observed.

When the sample pad 260 drops the blood sample to the sample inlet 110, the blood spreads evenly within a fast time to allow to reach the next second hemolysis layer 250 evenly.

The adhesive film 220 is formed of a double-sided foam tape. When the adhesive film 220 is laminated on the support pad 270, the lamination of the test pad is not easy due to the thickness of the anti-hemolysis pads 240 and 250 and the reaction pad 230, which are first laminated. It is attached to both sides of each pad (230 to 250) to facilitate the lamination of the sample pad. At this time, the adhesive film 220 is best to use a double-sided tape of 0.4mm ~ 0.6mm thick. In the case of 0.4 mm or less with respect to the minimum thickness of each of the pads 230 to 250, the height correction effect is insufficient, and lamination is not easy. In the case of 0.6 mm or more, the height is overcorrected, and lamination is not easy.

The hemolysis prevention pads 240 and 250 are pads made of a material that can filter out blood cells in the blood, and are made of two layers, first and second, and completely filter out blood cells in the blood sample and fall down to the nitro cellulose layer. It has a function to prevent it, and when measuring HDL, LDL is pretreated with a filterable solution.

The reaction pad (nitro cellulose membrane layer; 230) is a reaction layer that reacts with Cholesterol or TG in the blood and is formed by dispensing an enzyme solution and a substrate mixed solution onto the nitro cellulose membrane layer and reacting with the blood. As the concentration of Cholesterol or TG increases, the layer becomes darker in color so that the concentration can be measured by a colorimeter (not shown).

The manufacturing process of the pad part 200 will be described below. The manufacturing process consists of three steps of preparing an enzyme solution-immobilized nitrocellulose membrane strip, a step of preparing an anti-hemolytic pad and a sample pad, and a step of manufacturing an analytical device.

In the enzyme solution-immobilized nitrocellulose membrane (reaction pad 230) strip manufacturing step, total Cholesterol or HDL or TG degrading enzyme is diluted with a buffer solution according to the measurement target, and the nitrocellulose membrane is uniformly soaked in the solution and evenly soaked at 40 ° C. It is fixed by drying for 30 minutes in a thermostat. In addition, the nitrocellulose film 230 is cut to a width of 5 mm, and then the release paper is removed from the support on which the adhesive is applied, and then attached on the strip display window 21.

In the hemolysis prevention pad and sample pad attachment strip manufacturing step, a double-sided tape in the form of a foam film was laminated on the outer edge of the strip on which the nitrocellulose membrane 230 was attached, and the hemolysis prevention primary and secondary pads cut to a width of 5 mm were laminated therebetween. After the adhesive film 220 is formed again using a double-sided tape, the sample pad 260 is attached thereto.

In the manufacturing step of the analytical device, the strip manufactured by the previous step is cut into a 5mm width with a multi-cutter, and then the compressed strip is covered with a housing cover seated inside the strip guide pin of the housing body and pressed to manufacture the analytical device.

The lower plate 300 will be described with reference to FIGS. 2 and 6.

The lower plate 300 is formed of a plastic material similar to the upper plate 100 and is coupled to the upper plate 100 to form a housing.

The second hole 325 is a through hole formed to overlap the above-described pad part display window (through hole) 210 and is a lower display window. A colorimetric measurement is performed by detecting a change of the reaction pad 230 through the second hole 325 and the pad display window 210.

The strip seating part 320 is formed to allow the pad part 200 to be seated with a small play according to the shape and size of the pad part 200.

The fastening groove 330 is coupled to the corresponding fastening protrusion 150 (see FIG. 4) in an interference fit manner and serves to maintain the housing structure by compressing the upper plate 100 and the lower plate 300 during assembly. On the other hand, the fastening groove 330 and the above-mentioned fastening protrusion 150 may be formed at positions opposite to each other. A pair of fastening grooves 330 and fastening protrusions 150 are defined as fastening portions.

The handle 350 is formed by elongating one end of the lower plate in the longitudinal direction to facilitate insertion of the strip device into the colorimetric measuring device. The handle 350 is preferably formed with an anti-slip rib 340 to prevent slipping when inserted and a reinforcement rib 360 to reduce stress or the like.

The wing 370 extends left and right with respect to the longitudinal direction of the lower plate 300 to form a width larger than the surroundings. The wing 370 serves to prevent interference by external light so that a more accurate colorimetric measurement can be made.

After seating the pad part 200 manufactured on the strip seating part 320 of the lower plate 300, the coupling protrusion 150 (see FIG. 4) and the coupling groove 330 of the upper plate 100 are combined to form a final strip device. Assembly is completed.

1 and 6 detect the total cholesterol (TC) when only the second hole 325 is present.

FIG. 7 is a sensor strip according to another embodiment of the present invention, and detects triglyceride (TG) when only the second hole 325 and the third hole 335 are present.

8 is a sensor strip according to another embodiment of the present invention, in which only the first hole 315 and the second hole 325 are present to detect high density lipoprotein (HDL).

 The location classification of the first hole 315, the second hole 325, and the third hole 335 may be classified by light, and in some cases, may be electrically detected. In the case of detecting by light, the intensity of light reflected from the first hole 315, the second hole 325, and the third hole 335 is set to a preset threshold (factory or background value, for example). It is determined whether or not the number is greater than '0'), and if it is exceeded (e.g., greater than 0), the hole is recognized as present. If not, it is recognized as not present (e.g., 0).

In the case of a sensor strip for measuring a single characteristic, that is, a sensor strip for detecting total cholesterol (TC), a sensor strip for detecting high density lipoprotein (HDL), and a sensor strip for detecting triglyceride (TG), the second hole ( 325 is a window for measuring a background measurement and a result value. That is, the second hole 325 detects the change of the reaction pad 230 through the pad display window 210 and performs colorimetric measurement. In some cases, the intensity of the reflected light of the second hole 325 is measured. Based on the reference, the intensity of the reflected light of the surrounding holes (first hole and third hole) may be compared to detect whether the surrounding holes (first hole and third hole) exist.

<Example 2>

Embodiment 2 relates to a case in which the sensor strip for measuring the multi-characteristics, that is, the sample inlet 110 is one, but there are three reaction pads 230a to 230c for measuring the characteristics as shown in FIG. 9.

FIG. 9 is an exploded perspective view of a sensor strip according to another exemplary embodiment of the present invention, FIG. 10 is a longitudinal cross-sectional view illustrating a pad portion of the sensor strip of FIG. 9, and FIG. 11 is a top view of the sensor strip of FIG. 9. 12 is a bottom perspective view showing the state of the pad portion of the sensor strip of FIG. 9, and FIG. 13 is a bottom perspective view showing the bottom plate of the sensor strip of FIG. 9.

9 and 11, the upper plate 10a will be described.

In the case of the upper plate 10, there is no significant difference compared to the first embodiment, but as illustrated in FIG. 11, the sample flow path 16 having a thin groove shape along the longitudinal direction of the pressing surface 120 may be formed. The sample flow path 160 allows the sample (blood) to rapidly spread in the longitudinal direction by using capillary phenomenon to move onto the reaction pads 220a to 220c provided separately.

The pad part 200a will be described with reference to FIGS. 9, 10, and 12.

As shown in FIG. 10, the pad part 200a has a difference in that one strip display window 210 is formed at each position of the reaction pads 220a to 220c.

Internally, as shown in FIG. 10, the reaction pads 220a and the hemolytic pads 240 and 250 are paired, respectively, and a total of three pairs are provided spatially separated along the length direction of the pad part 200a. . As described above, each reaction pad 220a to 220c is diluted with Total Cholesterol, HDL, and TG degrading enzyme separately as a buffer and precipitated nitrocellulose membrane in each solution. . One pad unit 200a is manufactured by using three reaction pads 220a to 220c manufactured one by one.

Each reaction pad 220a to 220c and the pair of hemolytic pads 240 and 250 are laminated on the strip display window 210 formed on the support 270a, respectively.

That is, the pad part 200a includes a support having three through-holes (display windows) penetrating up and down in the longitudinal direction, and is attached to one of the three through-holes (display windows) to react with a sample to produce high density lipoprotein (HDL). The first reaction pad 230a for measuring, the second reaction pad 230b for attaching to another one of the three holes (display window) and reacting with the sample to measure total cholesterol (Total Cholesterol), the three holes (display window) A third reaction pad (230c) attached to another one of the) and reacting with the sample to measure triglyceride, and attached to each of the first to third reaction pads to prevent hemolysis (blood cells). First and second anti-hemostatic pads, the sample pads adhering on the first and second anti-hemostatic pads to promote the spread of the sample in the transverse direction and the support around the first and second anti-hemostatic pads Part of the sample pad that is glued to It is provided with an adhesive film to improve the adhesion.

The lower plate 300a will be described with reference to FIGS. 9 and 13.

The lower plate 300a of the second embodiment is lower plate 300 (see FIG. 6) of the lower plate 300 (see FIG. 6) of the first embodiment, and the lower plate display window in which only the second hole 325 detects a result. In FIG. 13, which is the lower plate 300a of the second embodiment, all of the first hole 315, the second hole 325, and the third hole 335 are used as the lower plate display window for detecting a result. That is, the lower plate 300a of the second embodiment is formed such that a total of three lower plate display windows 31 overlap with the strip display window 210 formed on the support 27a of the pad unit 20 when the strip device is assembled.

9 and 13, when all of the first hole 315, the second hole 325, and the third hole 335 are present, total cholesterol (TC), triglyceride (TG), and high density lipoprotein (HDL) are detected. do.

14 is a sensor strip according to another embodiment of the present invention, in which only the first hole 315 and the third hole 335 are present to detect total cholesterol (TC) and high density lipoprotein (HDL).

 1, 2, 4, and 9, the sample inlet 110 is shown as a circle, but this is not intended to limit the present invention, and the sample inlet 110 may be a through hole of another form such as a square.

The measuring device for analyzing data from the sensor strip of the present invention can be configured as a device capable of measuring the lipid (Lipid) of photometry and blood glucose measurement of electrochemistry, among which the lipid measuring unit 3 It can consist of two optical channels. The value of the light reflected from the light emitting part (LED) of each optical channel reflected on the strip is read by the light receiving part, and the reflectance can be used to derive the lipid measurement result.

Although the preferred embodiments of the present invention have been described above, the technical spirit of the present invention is not limited to the above-described preferred embodiments, and various protein proteins in the blood without departing from the technical spirit of the present invention specified in the claims. This can be implemented with a sensor strip device.

The present invention is provided with a plurality of holes to be detected according to the location of the total cholesterol (TC), triglycerides (TG), high density lipoprotein (HDL), all three, total cholesterol (TC) and high density lipoprotein ( To a sensor strip device indicating any one of HDL). It is used for diabetic tests and the like, and has a simpler structure, so that the production yield is improved and it is convenient to use.

Claims (27)

1. Measurement of protein in blood including a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a bottom plate having a display window penetrated at a position where the reaction pad can be checked In the sensor strip device for

   The bottom plate is

    And a first hole, a second hole, and a third hole, wherein the sensor strip device detects total cholesterol and neutral fat according to a combination of opening and closing of each of the first hole, the second hole, and the third hole. (TG) detection, high density lipoprotein (HDL) detection, detection of total cholesterol (TC), triglyceride (TG) and high density lipoprotein (HDL), detection of total cholesterol (TC) and high density lipoprotein (HDL) Sensor strip device, characterized in that made to.
2. The method of claim 1,

   And the display window is at least one of a first hole, a second hole, and a third hole.
3. Measurement of protein in blood including a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a bottom plate having a display window penetrated at a position where the reaction pad can be checked In the sensor strip device for

   The bottom plate is

    It has a second hole in the middle portion,

   The first hole is provided in front of the second hole,

   According to the combination of opening and closing of each of the first and second holes, the sensor strip device is configured to detect any one of total cholesterol (TC), triglyceride (TG), and high density lipoprotein (HDL). Sensor strip device.
4. Measurement of protein in blood including a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a bottom plate having a display window penetrated at a position where the reaction pad can be checked In the sensor strip device for

   The bottom plate is

    It has a second hole in the middle portion,

    The third hole is provided at the rear of the second hole,

   According to the combination of opening and closing of each of the second and third holes, the sensor strip device is configured to detect any one of total cholesterol (TC), triglyceride (TG), and high density lipoprotein (HDL). Sensor strip device.
5. Measurement of protein in blood including a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a bottom plate having a display window penetrated at a position where the reaction pad can be checked In the sensor strip device for

   The bottom plate is

    The first hole is provided in the upper portion, the third hole is provided in the lower portion,

   According to a combination of opening and closing of each of the first and third holes, the sensor strip device is configured to detect any one of total cholesterol (TC), triglyceride (TG), and high density lipoprotein (HDL). Sensor strip device.
6. Measurement of protein in blood including a top plate having a sample inlet, a pad portion including a reaction pad reacting with a sample introduced from the sample inlet, and a bottom plate having a display window penetrated at a position where the reaction pad can be checked In the sensor strip device for

   The display window has a first hole, a second hole, a third hole,

   As the second hole opens or closes, the sensor strip device detects total cholesterol (TC), triglyceride (TG) and high density lipoprotein (HDL), and detects total cholesterol (TC) and high density lipoprotein (HDL). Sensor strip device, characterized in that configured to detect one.
7. The method according to claim 1 or 3 or 4,

   And only the second hole is open, wherein the sensor strip device is configured to detect only total cholesterol (TC).
8. The method of claim 3,

   And the sensor strip device detects any one of triglyceride (TG) and high density lipoprotein (HDL) as the first and second holes are opened.
9. The method of claim 4, wherein

   And the sensor strip device detects any one of triglyceride (TG) and high density lipoprotein (HDL) as the second and third holes are opened.
10. The method of claim 5,

    And the sensor strip device is configured to detect at least one of triglyceride (TG) and high density lipoprotein (HDL) as the first and third holes are opened.
11. The method of claim 6,

    The first hole and the second hole. If all of the third holes are open, the sensor strip apparatus is configured to detect both total cholesterol (TC), triglyceride (TG) and high density lipoprotein (HDL).
12. The method of claim 6,

    And the sensor strip device detects total cholesterol (TC) and high density lipoprotein (HDL) when the first and third holes are opened and the second hole is closed.
13. The method according to any one of claims 1 to 6,

    The upper plate is formed with a fastening portion downward at the bottom,

    The lower plate is a sensor strip device, characterized in that the second fastening portion is formed to be fastened in correspondence with the fastening portion of the upper plate is formed.
14. The method of claim 13,

    The pad part

    It is provided with a support having a display window penetrating up and down,

    The reaction pad is attached to the display window of the support, characterized in that the sensor strip device made to react with the sample.
15. The method of claim 14,

    The pad part

    First and second hemolytic pads attached to the reaction pad to filter out blood cells, sample pads attached to the first and second hemolytic pads to promote the spread of the sample in a transverse direction, and the first and second hemolytic pads; The sensor strip device, characterized in that further comprises an adhesive film adhered to the support around the anti-hemolysis pad to improve the adhesion of the sample pad.
16. The method of claim 15,

    Sensor strip device, characterized in that the bottom surface of the upper plate is formed with a flat pressing surface protruding to apply a uniform pressure to the pad portion during assembly.
17. The method of claim 6,

    The upper plate is formed with a fastening portion downward at the bottom,

    The lower plate has a second fastening portion which is fastened in an interference fit manner corresponding to the fastening portion of the upper plate,

    The pad part

    A support having an upper hole located at a first hole corresponding position, an intermediate hole located at a second hole corresponding position, and a lower hole located at a third hole corresponding position,

    A first reaction pad attached to the support and attached to the upper through hole to measure one of neutral fat (TG), high density lipoprotein (HDL), and total cholesterol (TC) by reacting with a sample;

    A second reaction pad attached to the support, attached to the intermediate through hole, and reacting with the sample to measure another of triglyceride (TG), high density lipoprotein (HDL), and total cholesterol (TC);

    It is attached to the support, it is attached to the lower through-holes and reacts with the sample, characterized in that it comprises a third reaction pad for measuring another one of neutral fat (TG), high density lipoprotein (HDL), total cholesterol (TC) Sensor strip device.
18. The method of claim 17,

    Hemolysis prevention pads attached to the first reaction pad, the second reaction pad, and the third reaction pad, respectively, to prevent hemolysis;

    A sample pad adhered to the anti-hemolysis pads to promote diffusion of the sample in a transverse direction;

    Sensor strip device further comprising.
19. The method of claim 18,

    Sensor strip device for measuring the protein in the blood is formed on the bottom surface of the upper plate is formed with a flat compression surface protruding to apply a uniform pressure to the pad portion during assembly.
20. The method of claim 19,

    And a sample flow passage having a narrow groove shape along the longitudinal direction of the pressing surface.
21. The method of claim 18,

    The lower strip upper surface is characterized in that the strip strip is formed in the pad portion concave so that the pad portion is seated during assembly.
22. The method of claim 15,

    Sensor strip device, characterized in that the left and right sides when the longitudinal reference of the lower plate is provided with an extension to extend the width of the wing.
23. The method of claim 18,

    Sensor strip device, characterized in that the handle is formed by extending the one end in the longitudinal direction.
24. The method according to any one of claims 1 to 6,

    The pad part is positioned between the upper plate and the lower plate forming the housing so that the color tone is changed according to the concentration of lipid (Lipid) or total cholesterol (TC) or triglyceride (TG) or high density lipoprotein (HDL) in the blood. Understand,

    The pad part

    A support having at least one through hole;

    A reaction pad attached to the support and comprising an enzyme solution-immobilized nitrocellulose membrane;

    A hemolysis prevention pad layer mounted on the reaction pad and preventing hemolysis;

    A sample pad mounted on the anti-hemolysis pad layer to allow blood samples to spread evenly within a quick time so that the sample can reach the anti-hemolysis pad layer evenly;

    Sensor strip device comprising a.
25. The method of claim 24,

    The support has three through holes,

    The reaction pad

    A first reaction pad attached to one of the three through holes to measure total cholesterol (TC),

    A second reaction pad attached to the other one of the through holes to measure high density lipoprotein (HDL),

    And a third reaction pad attached to another one of the through holes to measure triglyceride.
26. The method of claim 24

    Is provided with a pressing plate formed in a plane protruding from the bottom of the upper plate

    The pressing plate is a sensor strip device, characterized in that made to apply pressure to the pad portion when the upper plate and the lower plate is coupled.
27. The method of claim 24,

    The hemolysis prevention pad layer is characterized in that the sensor strip device comprising two anti-hemolysis pads.

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