CN111534430A - Ribonucleic acid detection panel and ribonucleic acid detection device - Google Patents
Ribonucleic acid detection panel and ribonucleic acid detection device Download PDFInfo
- Publication number
- CN111534430A CN111534430A CN202010350040.4A CN202010350040A CN111534430A CN 111534430 A CN111534430 A CN 111534430A CN 202010350040 A CN202010350040 A CN 202010350040A CN 111534430 A CN111534430 A CN 111534430A
- Authority
- CN
- China
- Prior art keywords
- sensing electrode
- layers
- layer
- disposed
- sensing
- 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.)
- Granted
Links
- 238000001514 detection method Methods 0.000 title claims abstract description 93
- 229920002477 rna polymer Polymers 0.000 title claims abstract description 66
- 239000000758 substrate Substances 0.000 claims abstract description 45
- 230000006698 induction Effects 0.000 claims abstract description 41
- 238000012545 processing Methods 0.000 claims description 23
- 230000002093 peripheral effect Effects 0.000 claims description 12
- 239000011521 glass Substances 0.000 claims description 9
- SKRWFPLZQAAQSU-UHFFFAOYSA-N stibanylidynetin;hydrate Chemical compound O.[Sn].[Sb] SKRWFPLZQAAQSU-UHFFFAOYSA-N 0.000 claims description 9
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 8
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 8
- 239000010931 gold Substances 0.000 claims description 6
- 239000007769 metal material Substances 0.000 claims description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 239000010949 copper Substances 0.000 claims description 5
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052737 gold Inorganic materials 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 238000007747 plating Methods 0.000 claims description 5
- -1 polyethylene terephthalate Polymers 0.000 claims description 5
- 239000002861 polymer material Substances 0.000 claims description 5
- 229910052709 silver Inorganic materials 0.000 claims description 5
- 239000004332 silver Substances 0.000 claims description 5
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 5
- 229910001887 tin oxide Inorganic materials 0.000 claims description 5
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 claims description 5
- 239000013615 primer Substances 0.000 description 41
- 241000700605 Viruses Species 0.000 description 20
- 230000008859 change Effects 0.000 description 15
- 108091070501 miRNA Proteins 0.000 description 13
- 239000002679 microRNA Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 210000003296 saliva Anatomy 0.000 description 10
- 241000711573 Coronaviridae Species 0.000 description 8
- 208000011200 Kawasaki disease Diseases 0.000 description 8
- 208000001725 mucocutaneous lymph node syndrome Diseases 0.000 description 8
- 230000008569 process Effects 0.000 description 6
- 239000000523 sample Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000003745 diagnosis Methods 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 238000003752 polymerase chain reaction Methods 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 206010009944 Colon cancer Diseases 0.000 description 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 2
- 230000004543 DNA replication Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 241001493065 dsRNA viruses Species 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000002372 labelling Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 108091086421 miR-223 stem-loop Proteins 0.000 description 2
- 108091023108 miR-30e stem-loop Proteins 0.000 description 2
- 108091027549 miR-30e-1 stem-loop Proteins 0.000 description 2
- 108091029213 miR-30e-2 stem-loop Proteins 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 208000025721 COVID-19 Diseases 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 108020004414 DNA Proteins 0.000 description 1
- 102000053602 DNA Human genes 0.000 description 1
- 208000020061 Hand, Foot and Mouth Disease Diseases 0.000 description 1
- 208000025713 Hand-foot-and-mouth disease Diseases 0.000 description 1
- 238000002123 RNA extraction Methods 0.000 description 1
- 239000013616 RNA primer Substances 0.000 description 1
- 239000013614 RNA sample Substances 0.000 description 1
- 108020004682 Single-Stranded DNA Proteins 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 238000001215 fluorescent labelling Methods 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 210000002751 lymph Anatomy 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 208000030194 mouth disease Diseases 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- WMHSAFDEIXKKMV-UHFFFAOYSA-N oxoantimony;oxotin Chemical compound [Sn]=O.[Sb]=O WMHSAFDEIXKKMV-UHFFFAOYSA-N 0.000 description 1
- 238000011897 real-time detection Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6816—Hybridisation assays characterised by the detection means
- C12Q1/6825—Nucleic acid detection involving sensors
Abstract
The invention provides a ribonucleic acid detection panel and a ribonucleic acid detection device, wherein the ribonucleic acid detection device comprises a control unit and a ribonucleic acid detection panel, the ribonucleic acid detection panel comprises a substrate, a plurality of induction electrode layers electrically connected with the control unit, at least one primer layer and a plurality of routing layers, the plurality of induction electrode layers are arranged on the first surface of the substrate, the at least one primer layer is arranged on the plurality of induction electrode layers and is insulated from each other, and the plurality of electrode routing layers are electrically connected with the plurality of induction electrodes and the control unit.
Description
Technical Field
The present invention relates to a panel and a device for detecting ribonucleic acid, and more particularly, to a panel and a device for detecting ribonucleic acid, which can shorten the detection time and reduce the cost.
Background
Since the disease condition of the user (such as kawasaki disease, colorectal cancer, hand-foot-mouth disease, novel coronavirus (COVID-19) or other RNA-bearing viruses) must be detected by the measurement platform of the hospital for marking (such as a Polymerase Chain Reaction (PCR) analyzer), then blood of the user is collected, miRNA virus is extracted by an RNA extraction instrument, miRNA is added in sequence, miRNA labeling reagent is added, and the miRNA labeling reagent is dropped onto a miRNA wafer for dyeing and scanning, so as to determine whether the user has a diagnosis according to the fluorescence brightness change and comparison data, professional instruments (such as the measurement platform and the RNA extractor) are required in the conventional method for detecting RNA (or miRNA) viruses, so that only specific professional medical staff can operate the professional instruments, thereby causing the problems of high detection difficulty and high cost. In addition, the conventional procedure for detecting virus by fluorescence labeling is complicated and complex, so that the detection time is long due to the fact that the detection time is at least 2 hours or more or two days or more.
Disclosure of Invention
An object of the present invention is to provide a ribonucleic acid detection panel that can achieve a reduction in detection time and cost.
Another object of the present invention is to provide a ribonucleic acid detection panel which is simple in detection operation and convenient in detection.
To achieve the above object, the present invention provides a ribonucleic acid detecting panel, which includes a substrate, a plurality of sensing electrode layers, at least one primer layer and a plurality of electrode routing layers, wherein the substrate has a first surface and a second surface opposite to the first surface, the plurality of sensing electrode layers are disposed on the first surface, the at least one primer layer is disposed on the plurality of sensing electrode layers and insulated from each other, the at least one primer layer is for reacting with a corresponding detecting body having ribonucleic acid, the plurality of electrode routing layers are disposed on the first surface, and the plurality of electrode routing layers are electrically connected to the plurality of sensing electrodes.
The first surface of the substrate is provided with an induction area and a peripheral area surrounding the induction area, the induction electrode layers are arranged on the first surface of the induction area, and the electrode routing layers are arranged on the first surface of the peripheral area.
The plurality of induction electrode layers are provided with a first induction electrode layer and a second induction electrode layer, the first induction electrode layer is arranged on the first surface in the induction area, the second induction electrode layer is arranged on the first induction electrode layer, and a first insulation layer is arranged between the first induction electrode layer and the second induction electrode layer.
The plurality of lead layers are arranged on the second induction electrode layer at intervals, and a second insulating layer is arranged between the plurality of lead layers and the second induction electrode layer.
The second insulating layer is provided with a plurality of grooves corresponding to the plurality of lead layers, the plurality of lead layers are accommodated in the plurality of grooves, and a micro-channel is defined between each lead layer and the inner wall corresponding to each groove.
The substrate is a glass substrate, a circuit board or a polyethylene terephthalate substrate.
At least one primer layer is formed on the plurality of sensing electrode layers by printing or plating.
The sensing electrode layers and the electrode routing layers are made of tin oxide (ITO), Indium Zinc Oxide (IZO) and Antimony Tin Oxide (ATO), and at least one lead layer is made of a high polymer material.
The induction electrode layers and the electrode routing layers are made of metal materials, and the metal materials are aluminum, gold, copper or silver materials.
The invention further provides a ribonucleic acid detection device, which comprises a control unit and a ribonucleic acid detection panel, wherein the ribonucleic acid detection panel comprises a substrate, a plurality of induction electrode layers, at least one primer layer and a plurality of electrode routing layers, the substrate is provided with a first surface and a second surface opposite to the first surface, the plurality of induction electrode layers are electrically connected with the control unit, the plurality of induction electrode layers are arranged on the first surface, the at least one primer layer is arranged on the plurality of induction electrode layers and is insulated from each other, the at least one primer layer is used for reacting with corresponding detection bodies with ribonucleic acid, the plurality of electrode routing layers are arranged on the first surface, and the plurality of electrode routing layers are electrically connected with the plurality of induction electrode layers and the control unit.
The control unit is electrically connected with the circuit board, the circuit board is provided with a display element, a processing unit, a wireless receiving and transmitting unit and a power supply unit, the processing unit is electrically connected with the control unit, the display element and the wireless receiving and transmitting unit, and the power supply unit is used for supplying power to the display element, the processing unit, the wireless receiving and transmitting unit and the ribonucleic acid detection panel.
The wireless transceiver unit comprises a Bluetooth unit, a Wi-Fi unit and an RF unit.
The display elements are a plurality of light emitting diodes or displays, and the control unit is a central processing unit, a microcontroller or a digital signal processor.
The control unit is arranged on the first surface of the substrate or the circuit board.
The first surface of the substrate is provided with an induction area and a peripheral area surrounding the induction area, the induction electrode layers are arranged on the first surface of the induction area, and the electrode routing layers are arranged on the first surface of the peripheral area.
The plurality of induction electrode layers are provided with a first induction electrode layer and a second induction electrode layer, the first induction electrode layer is arranged on the first surface in the induction area, the second induction electrode layer is arranged on the first induction electrode layer, and a first insulation layer is arranged between the first induction electrode layer and the second induction electrode layer.
The plurality of lead layers are arranged on the second induction electrode layer at intervals, and a second insulating layer is arranged between the plurality of lead layers and the second induction electrode layer.
The second insulating layer is provided with a plurality of grooves corresponding to the plurality of lead layers, the plurality of lead layers are accommodated in the plurality of grooves of the second insulating layer, and a micro-channel is defined between each lead layer and the inner wall corresponding to each groove.
The substrate is a glass substrate, a circuit board or a polyethylene terephthalate substrate, the plurality of sensing electrode layers and the plurality of electrode routing layers are made of metal materials, the metal materials are tin oxide (ITO), Indium Zinc Oxide (IZO) or antimony oxide tin oxide (ATO), aluminum, gold, copper or silver, and at least one lead layer is made of high polymer materials.
At least one primer layer is formed on the plurality of sensing electrode layers by printing or plating.
Therefore, through the design of the invention, the detection time can be shortened, the cost can be reduced, and the user can carry out self rapid detection, so that the detection operation is simple and the detection use is very convenient.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of the specification, illustrate embodiments of the invention and together with the description, serve to explain the principles of the invention. In the drawings, like reference numerals are used to indicate like elements. The drawings in the following description are directed to some, but not all embodiments of the invention. For a person skilled in the art, other figures can be derived from these figures without inventive effort.
FIG. 1 is a schematic exploded perspective view of a ribonucleic acid detection panel according to an embodiment of the present invention.
FIG. 2A schematically shows an assembled perspective view of a ribonucleic acid detection panel in an embodiment of the invention.
FIG. 2B is a schematic sectional view and a schematic partial enlarged view of a ribonucleic acid detection panel according to an embodiment of the present invention.
FIG. 2C is a schematic sectional view and a schematic partial enlarged view of an embodiment of a ribonucleic acid detection panel according to an embodiment of the present invention.
FIG. 3 is a schematic exploded perspective view of an apparatus for detecting ribonucleic acid according to another embodiment of the present invention.
FIG. 4A is a schematic perspective view of a ribonucleic acid detecting device according to another embodiment of the present invention.
Fig. 4B schematically illustrates a top view of fig. 4A in another embodiment of the present invention.
FIG. 5 is a perspective view schematically showing a second embodiment of the ribonucleic acid detecting device according to another embodiment of the present invention.
FIG. 6 is a perspective view schematically showing a third sample combination of ribonucleic acid detecting device according to another embodiment of the present invention.
Description of the reference numerals
Ribonucleic acid detection Panel 1
The first sensing electrode layer 113
Second sensing electrode layer 114
First insulating layer 117
Second insulating layer 118
Ribonucleic acid detection device 2
Processing unit 24
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below, and it is obvious that the described embodiments are some embodiments of the present invention, but not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention. It should be noted that the embodiments and features of the embodiments in the present application may be arbitrarily combined with each other without conflict.
The invention provides a ribonucleic acid detection panel and a ribonucleic acid detection device. FIG. 1 is a schematic exploded perspective view of a ribonucleic acid detection panel according to an embodiment of the present invention; FIG. 2A schematically shows an assembled perspective view of a ribonucleic acid detection panel according to an embodiment of the present invention; FIG. 2B is a schematic sectional view and a schematic partial enlarged view of a ribonucleic acid detection panel according to an embodiment of the present invention; FIG. 2C is a schematic sectional view and a schematic partial enlarged view of an embodiment of a ribonucleic acid detection panel according to an embodiment of the present invention. As shown in fig. 1, 2A and 2B, a Ribonucleic acid (RNA) detection panel 1 includes a substrate 11, a plurality of sensing electrode layers, at least one primer layer 115 and a plurality of electrode routing layers 116, where the substrate 11 is a glass substrate 11, a circuit board 22 (such as a flexible circuit board) or a polyethylene terephthalate (PET) substrate 11, and the substrate 11 in this embodiment is a glass substrate 11, but not limited thereto, the substrate 11 has a first surface 111 and a second surface 112 opposite to the first surface 111, the first surface 111 of the substrate 11 is provided with a sensing region 1111 and a peripheral region 1112 surrounding the sensing region 1111, the plurality of sensing electrode layers are disposed on the first surface 111 of the sensing region 1111, the plurality of electrode routing layers 116 are disposed on the first surface 111 of the peripheral region 1112, and the plurality of electrode routing layers 116 are electrically connected to the plurality of sensing electrode layers.
The plurality of sensing electrode layers are provided with a transparent or opaque first sensing electrode layer 113 and a transparent or opaque second sensing electrode layer 114, the first sensing electrode layer 113 is provided with a plurality of first sensing electrodes 1131 (such as X-axis sensing electrodes) arranged on the first surface 111 in the sensing region 1111, the second sensing electrode layer 114 is provided with a plurality of second sensing electrodes 1141 (such as Y-axis sensing electrodes) arranged on the first sensing electrode layer 113, and the plurality of first and second sensing electrodes 1131, 1141 are respectively represented as X-axis sensing electrodes and Y-axis sensing electrodes in this embodiment and are arranged in a staggered manner. The sensing electrode layers and the electrode routing layers 116 are made of metal, such as tin oxide (ITO), Indium Zinc Oxide (IZO), Antimony Tin Oxide (ATO), or a combination thereof, but not limited thereto, and in specific implementations, the metal may also be made of aluminum (Al), gold (Au), copper (cu), silver (Ag), or other metal (such as nickel (Ni), chromium (Cr), or an alloy thereof). In the embodiment, the form of the first and second sensing electrodes 1131 and 1141 is a diamond shape, but not limited thereto, and in an embodiment, the form of the first and second sensing electrodes 1131 and 1141 may be a strip, a bar, a wide strip, or a rectangle. In another embodiment, the first sensing electrodes 1131 are arranged on the first surface 111 in the sensing region 1111 in a matrix array (e.g., M × N array), the second sensing electrodes 1141 are arranged on the first sensing electrode layer 113 in a matrix array (e.g., M × N array), and the first and second sensing electrodes 1131, 1141 are insulated from each other.
In an alternative embodiment, the plurality of first and second sensing electrodes 1131, 1141 of the first and second sensing electrode layers 113, 114 are disposed on the first surface 111 of the substrate 11 in parallel and corresponding to each other, and the primer layer 115 is disposed on the first and second sensing electrode layers 113, 114 and is insulated from each other.
A first insulating layer 117 is disposed between the first and second sensing electrode layers 113, 114, the first insulating layer 117 is made of silicon dioxide (SiO)2). At least one primer layer 115 is formed on the plurality of sensing electrode layers by, for example, printing or plating, and the primer layer 115 and the plurality of sensing electrode layers are insulated from each other, the primer layer 115 is, in this embodiment, a plurality of primer layers 115 are disposed on the second sensing electrode layer 114 at intervals, the primer layer 115 is made of a polymer material for interacting with a corresponding sample (e.g., saliva of a user) with ribonucleic acid (or micro ribonucleic acid micro RNA), for example, when no RNA virus in the saliva of the user (i.e., the RNA sample) reacts with the primer layer 115 not matching the corresponding specificity and cannot be combined, no electrical change (e.g., no capacitance change or dielectric coefficient change) is formed as if fingers of the user do not touch the touch sensing region 1111, so that a fixed coupling capacitance exists between the first and second sensing electrodes 1131, 1141 of the first and second sensing electrode layers 113, 114, at this time, the electric field (electric lines of force) between the first and second sensing electrodes 1131, 1141 is fixed; when the saliva (i.e., the RNA detection body) of the user contains RNA virus and the primer layer 115 with corresponding specificity reacts with each other to generate a combination with an obvious electrical change (e.g., capacitance change or dielectric coefficient change) formed on the touch-sensitive area 1111 as if the user's finger touches, for example, the primer layer 115 and the second primer layer 115A capacitance is formed between the two sensing electrode layers 114, and at this time, an electric field (electric lines) originally fixedly distributed between the first and second sensing electrodes 1131, 1141 of the first and second sensing electrode layers 113, 114 changes (i.e., the electric field changes) because a portion of the electric lines are connected to the corresponding primer layer 115, thereby changing a capacitance value of the coupling capacitance between the first and second sensing electrodes 1131, 1141 (i.e., the capacitance value changes).
In addition, the primer layer 115 is a primer that reacts with a virus (e.g., kawasaki disease, colorectal cancer, hand-foot-and-mouth disease, new coronavirus (covi-19) or other RNA-bearing virus) with a corresponding specific specificity to generate a binding, for example, a primer with a specific specificity is designed in advance to detect a virus (e.g., new coronavirus (covi-19)), if the saliva (i.e., a test sample) of a user has RNA-bearing new coronavirus (covi-19) and the primer layer 115 with a corresponding new coronavirus to generate a binding, an electrical change is obvious, and the user is indicated to confirm (e.g., positive) that the new coronavirus (covi-19) (i.e., infectious virus) is obtained; if the saliva (i.e., the test sample) of the user does not contain viruses or other viruses (e.g., Kawasaki disease), the primer layer 115 corresponding to the detected novel coronavirus does not react with each other and cannot be combined with each other, and then the electrical change is not generated, it indicates that the user has not diagnosed (e.g., is negative) the novel coronavirus (i.e., has no virus infection). Wherein the primer is a small piece of single-stranded DNA or RNA, which serves as a starting point for DNA replication, and is artificially synthesized by DNA replication (RNA primer) and Polymerase Chain Reaction (PCR) in nature.
A second insulating layer 118 disposed between the plurality of seed layers 115 and the second sensing electrode layer 114, a third insulating layer 119 disposed between the first sensing electrode layer 113 and the substrate 11, and a material of the second and third insulating layers 118, 119 such as silicon dioxide (SiO)2) In an alternative embodiment, the third insulating layer 119 may be omitted, such that the first sensing electrode layer 113 is disposed on the first surface 111 of the substrate 11 (e.g., a glass substrate or a PET substrate).
The plurality of primer layers 115 are, for example, long strips, located in the sensing region 1111 and arranged at intervals in the X-axis direction (or the Y-axis direction) on the second insulating layer 118 corresponding to the crossing position of the plurality of first sensing electrodes 1131 and the plurality of second sensing electrodes 1141. In an embodiment, referring to fig. 2C, a plurality of grooves 1181 are disposed on the second insulating layer 118 at positions corresponding to the plurality of primer layers 115, the plurality of primer layers 115 are accommodated in the plurality of grooves 1181 of the second insulating layer 118, a micro channel 1182 is defined between each primer layer 115 and an inner wall corresponding to each groove 1181, and the micro channel 1182 is used for collecting a detection object (such as saliva), so as to increase a contact area between the detection object and the corresponding primer layer 115, thereby effectively improving detection accuracy and shortening detection time.
Therefore, through the design of the ribonucleic acid detection panel 1 of the present invention, the detection time can be shortened, the cost can be reduced, and the user can rapidly and instantly detect the physical condition of the user through the saliva of the user, thereby not only achieving the simple detection operation, but also being very convenient in detection use.
FIG. 3 is a schematic exploded perspective view of an apparatus for detecting ribonucleic acid according to another embodiment of the present invention; FIG. 4A is a schematic perspective view of a ribonucleic acid detecting device according to another embodiment of the present invention; FIG. 4B schematically illustrates a top view of FIG. 4A in another embodiment of the present invention; FIG. 5 is a schematic perspective view of a ribonucleic acid detecting device according to another embodiment of the present invention; FIG. 6 is a perspective view schematically showing a third sample assembly of the ribonucleic acid detecting device according to another embodiment of the present invention, with reference to FIG. 1. The present embodiment mainly applies the RNA detection panel 1 of the first embodiment to the RNA detection device 2, that is, the RNA detection device 2 of the present embodiment includes the control unit 21 and the RNA detection panel 1, and the structure, connection relationship and efficacy of the RNA detection panel 1 are the same as those of the RNA detection panel 1 of the first embodiment, and thus, the description thereof is omitted. The control unit 21 is a Central Processing Unit (CPU), a Microcontroller (MCU) or a Digital Signal Processor (DSP), and the control unit 21 is electrically connected to the plurality of electrode routing layers 116 and the plurality of sensing electrode layers, the control unit 21 determines whether the detecting body and the primer layer 115 have electrical variation according to a signal of the electrical variation transmitted by the plurality of sensing electrode layers (i.e., the plurality of first and second sensing electrodes 1131, 1141), and generates a detection result, where the detection result is a result of the electrical variation (e.g., the electrical variation) between the detecting body and the primer layer 115, or a result of the electrical variation (e.g., the electrical variation) between the detecting body and the primer layer 115.
The control unit 21 in the present embodiment is configured in three modes as follows: the first aspect is as shown in fig. 3, 4A, and 4B, the control unit 21 is disposed on the first surface 111 of the peripheral region 1112 of the substrate 11 (such as the glass substrate 11 or the PET substrate 11), and the control unit 21 is bonded to the first surface 111 of the substrate 11 by a chip-on-glass (COG) bonding method, the control unit 21 is electrically connected to the circuit board 22 (such as the flexible circuit board 22, FPC), and the circuit board 22 is integrated with the substrate 11 by a thermal compression bonding method, the circuit board 22 is provided with a display element 23, a processing unit 24, a wireless transceiver unit 25, and a power supply unit 26, the processing unit 24 is electrically connected to the control unit 21, the display element 23, and the wireless transceiver unit 25, the processing unit 24 is, such as a Central Processing Unit (CPU), a Digital Signal Processor (DSP) or a controller (MCU), for processing and executing signals, for example, the processing unit 24 performs processing according to an electrical change according to a detection result transmitted by the control unit 21, and generates the detection result information, which is displayed by the display device 23 (if it shows that the virus has been diagnosed positively), if the processing unit 24 processes the detection result transmitted by the control unit 21 without electrical change and generates the detection result information, the detection result information is displayed by the display device 23 (if it shows that the virus has been diagnosed negatively), so that the user can know whether the virus has been diagnosed or not from the display device 23.
The display device 23 is shown as a display for displaying the detection result information in the present embodiment, but not limited thereto, in other embodiments, the display device 23 can be a plurality of Light Emitting Diodes (LEDs), that is, the detection result is represented by a plurality of signals, for example, a bright red LED light represents positive diagnosis, and a bright blue LED light represents negative diagnosis. The power supply unit 26 is a battery in this embodiment, and the power supply unit 26 is used to provide power to the display element 23, the processing unit 24, the wireless transceiver 25 and the ribonucleic acid detection panel 1. In one embodiment, the power supply unit 26 may be a rechargeable battery, and the circuit board 22 is provided with a connection port (e.g., a Micro USB connection port) for charging the power supply unit 26.
The wireless transceiver unit 25 is a bluetooth unit (e.g., bluetooth transceiver) in this embodiment, and the bluetooth unit is used to wirelessly connect with an electronic device (e.g., smart phone, smart watch, computer, pen or tablet computer; not shown), so that the processing unit 24 wirelessly transmits the detection result information to the electronic device through the bluetooth unit for displaying. In particular implementations, the wireless transceiver unit 25 is a Wi-Fi unit or an RF (radio frequency) unit.
When a user wants to detect kawasaki disease (or Mucocutaneous lymph gland Syndrome) virus, the user can drip his own saliva (i.e. a detected body) onto the sensing region 1111, so that the miRNA with miRNA kawasaki disease virus in the saliva is selected from miR-30e-3P and the corresponding primer layer 115 for detecting kawasaki disease virus, and after the miRNA reacts with the primer layer to generate combination, the miRNA is obviously changed in electrical property (such as capacitance change), so that the control unit 21 can determine that the detected body and the primer layer 115 are changed in electrical property according to the signals of capacitance change transmitted by the first and second sensing electrodes 1131, 1141, and generates the detection result to be transmitted to the processing unit 24, so that the processing unit 24 processes the electrical change according to the detection result, and transmits the detection result information to the display device 23, so that the user can know the detection result information displayed by the display device 23 (see Table 1). If the miRNA in the saliva of the user is miR-223-3P (without miRNA kawasaki disease virus) and the primer layer 115 corresponding to detecting kawasaki disease virus is unable to react with each other, the processing unit 24 processes the detection result transmitted by the control unit 21 as the non-electrical change, and transmits the detection result information, so that the user can obtain the detection result information (as shown in table 1) displayed by the display element 23. Wherein, as shown in table 1, the graph of the detection results of the detection bodies and the corresponding primer layers is shown, the detection result value (e.g. 32.5) corresponding to the detection body miR-30e-3P in the graph is greater than the detection result value (e.g. 6.2) corresponding to the detection body miR-223-3P, the preset reference value of the detection result value in this embodiment is, for example, 15, that is, the detection result value is equal to or greater than 15, which indicates that the diagnosis is confirmed, and the larger the detection result value is, which indicates that the number of days with virus in the body of the user is longer, and the more serious the symptoms are, and if the detection result value is less than 15.
Table 1 table of detection results of detectors and corresponding primer layers according to another embodiment of the present invention
Therefore, the ribonucleic acid detection device 2 of the present invention is designed to detect diseases by electrical measurement, so that the detection time can be effectively shortened, such as 15 minutes, to detect diseases (such as disease virus) and reduce the cost, and any user can perform real-time detection at home, thereby achieving simple detection operation and convenient detection.
Finally, it should be noted that: in this document, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, an element defined by the phrase "comprising an …" does not exclude the presence of other identical elements in a process, method, article, or apparatus that comprises the element.
The above examples are only for illustrating the technical solutions of the present invention, and are not limited thereto. Although the present invention has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some technical features may be equivalently replaced; and such modifications or substitutions do not depart from the spirit and scope of the corresponding technical solutions of the embodiments of the present invention.
Claims (20)
1. A panel for detecting ribonucleic acid, comprising:
a substrate having a first surface and a second surface opposite the first surface;
a plurality of sensing electrode layers disposed on the first surface;
at least one primer layer, which is arranged on the plurality of sensing electrode layers and insulated from each other, and is used for reacting with a corresponding detection body with ribonucleic acid; and
and the electrode routing layers are arranged on the first surface and are electrically connected with the induction electrode layers.
2. The panel of claim 1, wherein the first surface of the substrate has a sensing area and a peripheral area surrounding the sensing area, the plurality of sensing electrode layers are disposed on the first surface of the sensing area, and the plurality of electrode traces are disposed on the first surface of the peripheral area.
3. The panel of claim 2, wherein the plurality of sensing electrode layers comprises a first sensing electrode layer and a second sensing electrode layer, the first sensing electrode layer is disposed on the first surface in the sensing region, the second sensing electrode layer is disposed on the first sensing electrode layer, and a first insulating layer is disposed between the first and second sensing electrode layers.
4. The panel of claim 3, wherein the plurality of primer layers are disposed on the second sensing electrode layer at intervals, and a second insulating layer is disposed between the plurality of primer layers and the second sensing electrode layer.
5. The panel of claim 4, wherein a plurality of grooves are formed in the second insulating layer at positions corresponding to the plurality of primer layers, the plurality of primer layers are accommodated in the plurality of grooves, and a micro-channel is defined between each primer layer and an inner wall of each groove.
6. The panel of claim 1, wherein the substrate is a glass substrate, a circuit board, or a polyethylene terephthalate substrate.
7. The panel of claim 1, wherein the at least one primer layer is formed on the plurality of sensing electrode layers by printing or plating.
8. The panel of claim 1, wherein the sensing electrode layers and the electrode routing layers are made of tin oxide (ITO), Indium Zinc Oxide (IZO), or Antimony Tin Oxide (ATO), and the at least one primer layer is made of a polymer material.
9. The panel of claim 1, wherein the sensing electrode layers and the electrode traces are made of metal, and the metal is aluminum, gold, copper or silver.
10. A ribonucleic acid detection device, comprising:
a control unit; and
a panel for ribonucleic acid detection, comprising:
a substrate having a first surface and a second surface opposite the first surface;
a plurality of sensing electrode layers electrically connected to the control unit, the plurality of sensing electrode layers being disposed on the first surface;
at least one primer layer, which is arranged on the plurality of sensing electrode layers and insulated from each other, and is used for reacting with a corresponding detection body with ribonucleic acid; and
and the electrode routing layers are arranged on the first surface and are electrically connected with the sensing electrode layers and the control unit.
11. The apparatus according to claim 10, wherein the control unit is electrically connected to a circuit board, the circuit board is provided with a display device, a processing unit, a wireless transceiver unit and a power supply unit, the processing unit is electrically connected to the control unit, the display device and the wireless transceiver unit, and the power supply unit is used to provide power to the display device, the processing unit, the wireless transceiver unit and the ribonucleic acid detection panel.
12. The apparatus according to claim 11, wherein the wireless transceiver is a Bluetooth unit, a Wi-Fi unit, and an RF unit.
13. The apparatus according to claim 11, wherein the display device is a plurality of light emitting diodes or a display, and the control unit is a central processing unit, a microcontroller or a digital signal processor.
14. The apparatus according to claim 11, wherein the control unit is disposed on the first surface of the substrate or on the circuit board.
15. The apparatus according to claim 10, wherein the first surface of the substrate has a sensing area and a peripheral area surrounding the sensing area, the plurality of sensing electrode layers are disposed on the first surface of the sensing area, and the plurality of electrode routing layers are disposed on the first surface of the peripheral area.
16. The apparatus according to claim 15, wherein the plurality of sensing electrode layers comprises a first sensing electrode layer and a second sensing electrode layer, the first sensing electrode layer is disposed on the first surface in the sensing region, the second sensing electrode layer is disposed on the first sensing electrode layer, and a first insulating layer is disposed between the first and second sensing electrode layers.
17. The apparatus according to claim 16, wherein the primer layers are disposed on the second sensing electrode layer at intervals, and a second insulating layer is disposed between the primer layers and the second sensing electrode layer.
18. The apparatus according to claim 17, wherein the second insulating layer has a plurality of grooves corresponding to the plurality of primer layers, the primer layers are received in the grooves of the second insulating layer, and a micro-channel is defined between each primer layer and an inner wall of each groove.
19. The apparatus of claim 10, wherein the substrate is a glass substrate, a circuit board or a polyethylene terephthalate substrate, the sensing electrode layers and the electrode routing layers are made of a metal material, the metal material Is Tin Oxide (ITO), Indium Zinc Oxide (IZO) or Antimony Tin Oxide (ATO), aluminum, gold, copper or silver, and the at least one primer layer is made of a polymer material.
20. The apparatus according to claim 10, wherein the at least one primer layer is formed on the plurality of sensing electrode layers by printing or plating.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010350040.4A CN111534430B (en) | 2020-04-28 | 2020-04-28 | Ribonucleic acid detection panel and ribonucleic acid detection device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010350040.4A CN111534430B (en) | 2020-04-28 | 2020-04-28 | Ribonucleic acid detection panel and ribonucleic acid detection device |
Publications (2)
Publication Number | Publication Date |
---|---|
CN111534430A true CN111534430A (en) | 2020-08-14 |
CN111534430B CN111534430B (en) | 2023-12-29 |
Family
ID=71979036
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010350040.4A Active CN111534430B (en) | 2020-04-28 | 2020-04-28 | Ribonucleic acid detection panel and ribonucleic acid detection device |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111534430B (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101592627A (en) * | 2009-03-19 | 2009-12-02 | 苏州纳米技术与纳米仿生研究所 | The making integrated approach of multichannel high-sensitive biosensor |
US20100072976A1 (en) * | 2008-09-23 | 2010-03-25 | National Chiao Tung University | Sensing element, manufacturing method thereof, and biological detection system employing such sensing element |
US20110308313A1 (en) * | 2010-06-17 | 2011-12-22 | Geneasys Pty Ltd | Humidity sensor |
TWM462368U (en) * | 2013-02-04 | 2013-09-21 | Wen Wang | Electrochemical biosensor without hematocrit correction |
TW202141033A (en) * | 2020-04-20 | 2021-11-01 | 關鍵禾芯科技股份有限公司 | Ribonucleic acid test panel and ribonucleic acid test device |
-
2020
- 2020-04-28 CN CN202010350040.4A patent/CN111534430B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100072976A1 (en) * | 2008-09-23 | 2010-03-25 | National Chiao Tung University | Sensing element, manufacturing method thereof, and biological detection system employing such sensing element |
CN101592627A (en) * | 2009-03-19 | 2009-12-02 | 苏州纳米技术与纳米仿生研究所 | The making integrated approach of multichannel high-sensitive biosensor |
US20110308313A1 (en) * | 2010-06-17 | 2011-12-22 | Geneasys Pty Ltd | Humidity sensor |
TWM462368U (en) * | 2013-02-04 | 2013-09-21 | Wen Wang | Electrochemical biosensor without hematocrit correction |
TW202141033A (en) * | 2020-04-20 | 2021-11-01 | 關鍵禾芯科技股份有限公司 | Ribonucleic acid test panel and ribonucleic acid test device |
Also Published As
Publication number | Publication date |
---|---|
CN111534430B (en) | 2023-12-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10983648B2 (en) | Touch input device | |
EP3089008B1 (en) | Touch input device | |
CN105630226B (en) | Touch window | |
US20090277695A1 (en) | Method of Forming Touch Sensing Circuit Pattern | |
EP2911043B1 (en) | Touch window and touch device | |
RU2008128215A (en) | MOBILE TERMINAL | |
US20060050062A1 (en) | Input device | |
TWI749529B (en) | Ribonucleic acid test panel and ribonucleic acid test device | |
EP3037934B1 (en) | Switch device | |
TW201918843A (en) | Touch panel and wearable device | |
US11556202B2 (en) | Force sensing touch panel | |
JP2015018538A (en) | Input signal identification method for touch panel | |
US11281306B2 (en) | Input device with key input and touch input, and operating method thereof | |
CN109791462A (en) | Reversed keyboard components | |
CN102667694B (en) | Input device, display device, and portable terminal | |
CN111534430A (en) | Ribonucleic acid detection panel and ribonucleic acid detection device | |
US20100182276A1 (en) | Touch panel and method of detecting press operation position thereon | |
JP2021185824A (en) | Ribonucleic acid detection panel and ribonucleic acid detection device | |
US20210354127A1 (en) | Ribonucleic acid test panel and ribonucleic acid test device | |
US9274658B2 (en) | Method for detecting biomolecules using a capacitive touch screen | |
CN107565945A (en) | Input unit and its operation method with key-press input and touching input | |
KR101748173B1 (en) | Touch detecting apparatus | |
KR101030730B1 (en) | Touch input apparatus and method | |
KR100956973B1 (en) | Multi touch panel in resistive type | |
US20110032208A1 (en) | Complex resistance type coordinate input device |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
TA01 | Transfer of patent application right | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20230718 Address after: 1st to 2nd floors, Building 4, No. 1628 Lizheng Road, Lingang New Area, China (Shanghai) Pilot Free Trade Zone, Pudong New Area, Shanghai Applicant after: Gangxiu Technology (Shanghai) Co.,Ltd. Address before: Floor 7-2, No. 145, Zhengjiu Road, Zhubei, Hsinchu County Applicant before: KEYCORE TECHNOLOGY Corp. |
|
GR01 | Patent grant | ||
GR01 | Patent grant |