TW202215031A - Nucleic acid detection disc and nucleic acid detection device - Google Patents
Nucleic acid detection disc and nucleic acid detection device Download PDFInfo
- Publication number
- TW202215031A TW202215031A TW110122809A TW110122809A TW202215031A TW 202215031 A TW202215031 A TW 202215031A TW 110122809 A TW110122809 A TW 110122809A TW 110122809 A TW110122809 A TW 110122809A TW 202215031 A TW202215031 A TW 202215031A
- Authority
- TW
- Taiwan
- Prior art keywords
- nucleic acid
- cover plate
- detection
- channel
- observation
- Prior art date
Links
Images
Landscapes
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
Abstract
Description
本發明涉及核酸檢測技術領域,尤其涉及一種核酸檢測盒及核酸檢測設備。The present invention relates to the technical field of nucleic acid detection, in particular to a nucleic acid detection box and nucleic acid detection equipment.
目前針對分子診斷、形態學、免疫學等的檢測大多是在專業實驗室中進行,傳統的檢測過程一般包括以下步驟:先在大中型檢測設備執行核酸擴增;之後將擴增的核酸人工轉移至電泳檢測設備進行電泳檢測;最後再將電泳檢測結果人工轉移至專用螢光分析儀上進行結果分析。整個檢測過程所需設備複雜、體積大,檢測效率低,靈活性差,成本高,操作複雜,對操作人員的專業水準要求較高,需要由熟練的技術人員來操作,不能實現即時定量檢測,且不能實現家庭可攜式檢測。At present, most of the detections for molecular diagnosis, morphology, immunology, etc. are carried out in professional laboratories. The traditional detection process generally includes the following steps: first perform nucleic acid amplification in large and medium-sized detection equipment; then manually transfer the amplified nucleic acid To electrophoresis detection equipment for electrophoresis detection; finally, the electrophoresis detection results are manually transferred to a special fluorescence analyzer for result analysis. The equipment required for the entire detection process is complex, bulky, low in detection efficiency, poor in flexibility, high in cost, complex in operation, and requires a high level of professionalism for operators. Home portable testing is not possible.
有鑑於此,為克服上述缺陷的至少之一,有必要提供一種核酸檢測盒。In view of this, in order to overcome at least one of the above-mentioned defects, it is necessary to provide a nucleic acid detection kit.
另,本申請還提供了一種採用上述核酸檢測盒進行核酸檢測的核酸檢測設備。In addition, the present application also provides a nucleic acid detection device for nucleic acid detection using the above nucleic acid detection box.
本發明提供了一種核酸檢測盒,該核酸檢測盒包括檢測芯片和鐳射發射裝置。所述檢測芯片包括第一蓋板、間隔層及第二蓋板,所述間隔層相對的兩表面分別與所述第一蓋板和所述第二蓋板鄰接,所述第一蓋板、所述間隔層以及所述第二蓋板圍設形成通道,所述通道用於承載檢測液以便所述檢測液可在所述通道內進行核酸擴增反應從而得到產物液珠,所述第一蓋板設有觀察窗;所述鐳射發射裝置設置於所述通道的外側,所述鐳射發射裝置用於朝向所述通道內發射鐳射;所述鐳射用以照射所述產物液珠以使所述產物液珠發出螢光信號,所述觀察窗用於觀察所述螢光信號。The present invention provides a nucleic acid detection box, which comprises a detection chip and a laser emission device. The detection chip includes a first cover plate, a spacer layer and a second cover plate, two opposite surfaces of the spacer layer are respectively adjacent to the first cover plate and the second cover plate, the first cover plate, The spacer layer and the second cover plate are surrounded to form a channel, and the channel is used to carry a detection solution so that the detection solution can perform a nucleic acid amplification reaction in the channel to obtain product beads, and the first The cover plate is provided with an observation window; the laser emitting device is arranged on the outside of the channel, and the laser emitting device is used for emitting laser toward the channel; the laser is used to irradiate the product liquid beads to make the The product beads emit a fluorescent signal, and the viewing window is used to observe the fluorescent signal.
本申請實施方式中,所述檢測芯片還包括設置於所述第二蓋板靠近所述第一蓋板一側的驅動迴路、設置於所述第一蓋板靠近所述第二蓋板一側的導電層、設置於所述驅動迴路靠近所述第一蓋板一側的第一介電層以及設置於所述導電層靠近所述第二蓋板一側的第二介電層,所述驅動迴路和所述導電層均與電源電性連接,所述第一介電層與所述第二介電層之間形成所述通道。In the embodiment of the present application, the detection chip further includes a drive circuit disposed on the side of the second cover plate close to the first cover plate, and disposed on the side of the first cover plate close to the second cover plate The conductive layer, the first dielectric layer disposed on the side of the driving circuit close to the first cover plate, and the second dielectric layer disposed on the side of the conductive layer close to the second cover plate, the The driving circuit and the conductive layer are both electrically connected to a power source, and the channel is formed between the first dielectric layer and the second dielectric layer.
本申請實施方式中,所述驅動迴路包括加樣區、核酸擴增區以及觀察區,所述觀察窗對應所述觀察區設置。In the embodiment of the present application, the driving circuit includes a sample application area, a nucleic acid amplification area, and an observation area, and the observation window is set corresponding to the observation area.
本申請實施方式中,所述核酸擴增區的數量為兩個,所述觀察區位於兩個所述核酸擴增區之間。In the embodiment of the present application, the number of the nucleic acid amplification regions is two, and the observation region is located between the two nucleic acid amplification regions.
本申請實施方式中,所述驅動迴路還包括試劑存儲區,所述試劑存儲區內設置有探針或螢光試劑。In the embodiment of the present application, the driving circuit further includes a reagent storage area, and the reagent storage area is provided with a probe or a fluorescent reagent.
本申請實施方式中,所述觀察區位於所述核酸擴增區遠離所述加樣區的一側。In the embodiment of the present application, the observation area is located on the side of the nucleic acid amplification area away from the sample application area.
本申請實施方式中,所述觀察區包括三個觀察位點,三個所述觀察位點上分別設置不同的螢光試劑。In the embodiment of the present application, the observation area includes three observation sites, and different fluorescent reagents are respectively set on the three observation sites.
本申請實施方式中,所述檢測芯片還包括設置於所述第一蓋板和/或所述第二蓋板遠離所述通道一側的加熱元件。In the embodiment of the present application, the detection chip further includes a heating element disposed on the side of the first cover plate and/or the second cover plate away from the channel.
本申請實施方式中,所述核酸檢測盒還包括一盒體,所述檢測芯片和所述鐳射發射裝置均設於所述盒體內,所述盒體對應所述觀察窗設有一開口。In the embodiment of the present application, the nucleic acid detection box further includes a box body, the detection chip and the laser emitting device are both disposed in the box body, and the box body is provided with an opening corresponding to the observation window.
本發明還提供一種核酸檢測設備,該核酸檢測設備包括如上所述的核酸檢測盒以及圖像採集裝置。所述圖像採集裝置設置於所述觀察窗遠離所述通道的一側,所述圖像採集裝置用於經由所述觀察窗採集所述螢光信號。The present invention also provides a nucleic acid detection device, which includes the nucleic acid detection box and the image acquisition device as described above. The image acquisition device is disposed on a side of the observation window away from the channel, and the image acquisition device is used for acquiring the fluorescent signal through the observation window.
相較於習知技術,本發明提供的核酸檢測設備可以實現在PCR過程中進行即時螢光檢測,根據螢光強度大小可以對PCR擴增後的DNA進行定量,可以實現即時定量檢測核酸的量;核酸檢測設備整體結構簡單,檢測操作簡便,操作過程對專業要求低,檢測效率高,極大降低了檢測成本;同時,檢測過程靈活性強,無需在固定的實驗室中進行,檢測設備便攜,可以實現社區檢測或家庭檢測。Compared with the prior art, the nucleic acid detection device provided by the present invention can realize real-time fluorescent detection during the PCR process, and can quantify the DNA amplified by PCR according to the fluorescence intensity, and can realize the real-time quantitative detection of the amount of nucleic acid. The overall structure of the nucleic acid detection equipment is simple, the detection operation is simple, the operation process has low professional requirements, and the detection efficiency is high, which greatly reduces the detection cost; at the same time, the detection process is flexible and does not need to be carried out in a fixed laboratory, and the detection equipment is portable. Community testing or home testing can be achieved.
下面將結合本發明實施例中的附圖,對本發明實施例中的技術方案進行清楚、完整地描述,顯然,所描述的實施例僅僅是本發明一部分實施例,而不是全部的實施例。The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only a part of the embodiments of the present invention, but not all of the embodiments.
需要說明的是,當元件被稱為“固定於”另一個元件,它可以直接在另一個元件上或者也可以存在居中的元件。當一個元件被認為是“連接”另一個元件,它可以是直接連接到另一個元件或者可能同時存在居中元件。當一個元件被認為是“設置於”另一個元件,它可以是直接設置在另一個元件上或者可能同時存在居中元件。本文所使用的術語“垂直的”、“水準的”、“左”、“右”以及類似的表述只是為了說明的目的。It should be noted that when an element is referred to as being "fixed to" another element, it can be directly on the other element or intervening elements may also be present. When an element is referred to as being "connected" to another element, it can be directly connected to the other element or intervening elements may also be present. When an element is referred to as being "disposed on" another element, it can be directly disposed on the other element or intervening elements may also be present. The terms "vertical," "horizontal," "left," "right," and similar expressions are used herein for illustrative purposes only.
以下所描述的系統實施方式僅僅是示意性的,所述模組或電路的劃分,僅僅為一種邏輯功能劃分,實際實現時可以有另外的劃分方式。此外,顯然“包括”一詞不排除其他單元或步驟,單數不排除複數。系統請求項中陳述的多個單元或裝置也可以由同一個單元或裝置藉由軟體或者硬體來實現。第一,第二等詞語用來表示名稱,而並不表示任何特定的順序。The system implementations described below are only illustrative, and the division of the modules or circuits is only a logical function division, and other division methods may be used in actual implementation. Furthermore, it is clear that the word "comprising" does not exclude other units or steps and the singular does not exclude the plural. Multiple units or means stated in the system claim may also be implemented by the same unit or means through software or hardware. The terms first, second, etc. are used to denote names and do not denote any particular order.
除非另有定義,本文所使用的所有的技術和科學術語與屬於本發明的技術領域的技術人員通常理解的含義相同。本文中在本發明的說明書中所使用的術語只是為了描述具體的實施例的目的,不是旨在於限制本發明。本文所使用的術語“及/或”包括一個或多個相關的所列項目的任意的和所有的組合。Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The terms used herein in the description of the present invention are for the purpose of describing specific embodiments only, and are not intended to limit the present invention. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items.
請參閱圖1至圖4,為本發明實施例提供的一種核酸檢測盒100,該核酸檢測盒100包括一盒體1、檢測芯片2以及鐳射發射裝置3。該檢測芯片2設置於該盒體1內,該檢測芯片2包括第一蓋板21、間隔層22及第二蓋板23,該間隔層22相對的兩表面分別與該第一蓋板21和該第二蓋板23接觸,該第一蓋板21、該間隔層22以及該第二蓋板23圍設形成通道5,該通道5用於承載檢測液6以便該檢測液6可在該通道5內進行核酸擴增反應從而得到產物液珠8。該第一蓋板21設有觀察窗29;該鐳射發射裝置3設置於該通道5的外側,該鐳射發射裝置3用於朝向該通道5內發射鐳射7。該鐳射7用以照射該產物液珠8,以使所述產物液珠8發出螢光信號9,最終經由所述觀察窗29可以獲取所述螢光信號9。Please refer to FIGS. 1 to 4 , which are a nucleic
請參閱圖1至圖4,該盒體1包括第一殼體11、第二殼體12、設置於該第二殼體12的加樣口13以及設置於該第一殼體11上的開口14。該第一殼體11與該第二殼體12共同圍設形成一容納腔(圖未示),該檢測芯片2和該鐳射發射裝置3均容置於該容納腔內。該加樣口13對應該檢測芯片2設置,用於向該檢測芯片2內加入含有核酸樣本的檢測液6。該開口14對應該觀察窗29設置,後續圖像採集裝置能夠經由該開口14和該觀察窗29採集該檢測芯片2中產物液珠8發射出的螢光信號9。Please refer to FIG. 1 to FIG. 4 , the
請參閱圖3,本實施方式中,該第一殼體11和該第二殼體12藉由卡合的方式連接,另外,該第一殼體11和該第二殼體12卡合後還可以在四周藉由螺絲進行緊固,增加該第一殼體11與該第二殼體12的連接牢固性。Please refer to FIG. 3 , in this embodiment, the
請參閱圖1,本實施方式中,該盒體1的側壁還設置有一安裝口15,該安裝口15用於安裝一連接器4,其中該連接器4與檢測芯片2和鐳射發射裝置3電性連接,藉由該連接器4實現檢測芯片2與鐳射發射裝置3與外界電源電性連接。該連接器4整體位於該容納腔內並由該安裝口15露出該盒體1,從而方便該連接器4與外界的電源電性連接。Please refer to FIG. 1 , in this embodiment, the side wall of the
本實施方式中,該盒體1為塑膠材質。In this embodiment, the
請參閱圖2與圖3,該檢測芯片2還包括設置於該第二蓋板23靠近該第一蓋板21一側的驅動迴路24、設置於該驅動迴路24靠近該第一蓋板21一側的第一介電層26、設置於該第一蓋板21靠近該第二蓋板23一側的導電層25以及設置於該導電層25靠近該第二蓋板23一側的第二介電層27,該驅動迴路24和該導電層25均與該連接器4電性連接,藉由為該驅動迴路24和該導電層25通電或斷電可以實現該檢測液6在該通道5內按照規定的路徑移動。Please refer to FIG. 2 and FIG. 3 , the detection chip 2 further includes a
本實施方式中,請參閱圖3,結合參閱圖2,該驅動迴路24包括多個呈陣列排布的驅動電極241以及與所述驅動電極241電性連接的控制電極242,該控制電極242與該連接器4電性連接。具體地,該驅動迴路24為薄膜電晶體(Thin Film Transistor, TFT)驅動迴路,又由於檢測液6具有導電性,結合介電潤濕原理(Electrowetting-On-Dielectric, EWOD),能夠實現檢測液6在通道5內按預定路徑進行移動。利用TFT原理,能夠選擇性開啟或關閉某個驅動電極241與導電層25之間的電路,從而改變該驅動電極241與導電層25之間的電壓來改變該檢測液6與第一介電層26和第二介電層27之間的潤濕特性,進而控制該檢測液6在通道5內按預定的路徑移動。如圖6所示,檢測液6在電極I、電極H和電極G上移動,當檢測液6在電極H上時,對電極G和導電層25之間施加電壓,給予電極G電壓Vd,同時斷開電極H和導電層25之間的電壓,此時檢測液6與第一介電層26和第二介電層27之間的潤濕特性發生改變,以使電極H與檢測液6之間的液-固接觸角變大,電極G與檢測液6之間的液-固接觸角變小,從而促使檢測液6從電極H往電極G移動。In this embodiment, please refer to FIG. 3 and FIG. 2 in combination, the
本實施方式中,該第一介電層26和該第二介電層27均為絕緣疏水層,具體可以是聚四氟乙烯塗層,一方面可以起到絕緣疏水的作用,另一方面還能夠使檢測液6在規定路徑內移動的更順暢,避免移動過程中液珠破裂。In the present embodiment, the first
本實施方式中,結合參閱圖3,該驅動迴路24可以採用金屬刻蝕的方法或電鍍的方法形成於該第二蓋板23的表面。In this embodiment, referring to FIG. 3 , the driving
本實施方式中,該控制電極242集成在該第二蓋板23的同一邊緣,藉由將該第二蓋板23設置該控制電極242的一邊插入該連接器4內實現該檢測芯片2與該連接器4的電性連接。In this embodiment, the
請參閱圖3與圖4,本實施方式中,該驅動迴路24根據不同的用途可以分為多個區域,分別是加樣區A,多個核酸擴增區C以及觀察區D,該觀察窗29對應該觀察區D設置。該檢測芯片2上的該加樣區A與盒體1上的加樣口13連通,藉由從該加樣口13向該加樣區A加入包含核酸樣本的檢測液6。核酸擴增區C用於實現核酸樣本的擴增反應得到核酸擴增產物,核酸擴增產物與螢光試劑結合得到產物液珠8,觀察區D用於觀察產物液珠8在鐳射7照射下的螢光信號9。Please refer to FIG. 3 and FIG. 4. In this embodiment, the driving
檢測液6在該核酸擴增區C進行核酸擴增反應,該核酸擴增區C包括可以包括多個區域,具體區域的數量可以根據實際的檢測需求而定。該觀察區D內的產物液珠8發射的螢光信號9可經由該觀察窗29被圖像採集裝置採集。即時螢光定量PCR技術的原理是:螢光試劑(螢光染料或DNA探針)被設計成需要跟特定的DNA結合後才會有螢光特性,因此,當DNA藉由PCR擴增後數量增多,被活化螢光物質就越多,與螢光試劑結合的DNA數量增多,則螢光強度越強,因此,只需要檢測螢光的強度便可以對擴增的特定DNA進行定量。The
請參閱圖5,另一實施方式中,該驅動迴路24還可以包括試劑存儲區B、該試劑存儲區B用於存儲螢光試劑(例如螢光染料或螢光探針)。該檢測液6至少包含核酸樣本和引物,並不包含螢光試劑,而螢光試劑(例如螢光染料或DNA探針)被提前塗覆在試劑存儲區B內,加入檢測液6後再與螢光試劑結合。此方式可以在核酸擴增前與螢光試劑混合,也可以在核酸擴增後與螢光試劑混合,具體根據實際情況選擇。Referring to FIG. 5 , in another embodiment, the driving
請參閱圖6,又一實施方式中,螢光試劑設置於觀察區D內,觀察區D設置於核酸擴增區C遠離加樣區A的一側,本實施方式中,核酸擴增結束後,核酸擴增產物將與觀察區D內的螢光試劑結合。Please refer to FIG. 6, in another embodiment, the fluorescent reagent is arranged in the observation area D, and the observation area D is arranged on the side of the nucleic acid amplification area C away from the sample application area A. In this embodiment, after the nucleic acid amplification is completed , the nucleic acid amplification product will bind to the fluorescent reagent in the observation area D.
請參閱圖3、圖5與圖6,該檢測芯片2還包括設置於該第一蓋板21和/或該第二蓋板23遠離該通道5一側的加熱元件28,該加熱元件28對應該核酸擴增區C設置,用於為檢測液6加熱。Please refer to FIG. 3 , FIG. 5 and FIG. 6 , the detection chip 2 further includes a
本實施方式中,該加熱元件28對應該核酸擴增區C設置有兩個加熱區域,具體加熱溫度範圍分別為90℃-105℃和40℃-75℃。In this embodiment, the
本實施方式中,在組裝好該檢測芯片2後會在通道5內注入矽油,檢測液6會在矽油內按規定路徑移動。In this embodiment, after the detection chip 2 is assembled, silicone oil is injected into the
請參閱圖2,本實施方式中,該第一蓋板21和該第二蓋板23均為玻璃板,該間隔層22為雙面膠框,藉由雙面膠框黏貼在第一蓋板21和第二蓋板23的邊緣,從而共同組成一密封的通道5。其中,可以根據實際需求藉由設計不同厚度的間隔層22來調整該通道5的容量。Please refer to FIG. 2 , in this embodiment, the
本實施方式中,該核酸檢測盒100大致為一立方體結構。In this embodiment, the nucleic
本實施方式中,該核酸檢測盒100是一次性使用品,每個檢測樣本使用一個核酸檢測盒100,因此,核酸檢測盒100無需清洗流程。In this embodiment, the nucleic
本發明可以根據不同的需求設計核酸擴增區C、試劑存儲區B和觀察區D的數量和具體位置。在實際檢測過程中,具體可以包括以下三種不同的實施方式。The present invention can design the number and specific positions of the nucleic acid amplification area C, the reagent storage area B and the observation area D according to different requirements. In the actual detection process, the following three different implementations may be specifically included.
一實施方式中,請參閱圖2至圖4,該核酸擴增區C的數量為兩個,該觀察區D的數量為一個,該觀察區D位於兩個核酸擴增區C之間,本實施方式中不需要設置試劑存儲區B。In one embodiment, please refer to FIG. 2 to FIG. 4 , the number of the nucleic acid amplification areas C is two, the number of the observation area D is one, and the observation area D is located between the two nucleic acid amplification areas C. In the embodiment, the reagent storage area B does not need to be provided.
具體實現即時螢光定量PCR的過程為:向加樣區A加入檢測液6,此時可以將同時包含核酸樣本、引物、螢光試劑(例如螢光染料或DNA探針)的檢測液6由加樣口13注入加樣區A內;包含核酸樣本和螢光試劑的檢測液6在驅動電極241的驅動下按照規定路徑在兩個核酸擴增區C之間往復移動進行擴增反應直接得到產物液珠8,在擴增過程中,產物液珠8會經過觀察區D,此時,產物液珠8在鐳射7的照射下會發出螢光信號9,便可以藉由圖像採集裝置經由觀察窗29採集觀察區D處結合螢光試劑的產物液珠8發出的螢光信號9,完成即時螢光定量PCR的過程。本實施方式中,隨著PCR擴增反應的進行,螢光強度不斷增大,當螢光強度達到最大值後不再增大,而是趨於穩定,此時,PCR擴增反應結束,因此,可以根據螢光強度的變化來準確判斷擴增反應的結束時間。The specific process of realizing real-time fluorescent quantitative PCR is as follows: adding
本實施方式中,鐳射發射裝置3從通道5的側面發射鐳射7,鐳射7在通道5內傳遞,具體地,鐳射7的光譜為200nm~480nm,螢光試劑發出的螢光的光譜為500nm~700nm。當鐳射7與產物液珠8交會,產物液珠8內的螢光試劑發出螢光信號9,圖像採集裝置經過開口14和觀察窗29偵測並採集螢光信號9,形成螢光圖像再藉由主機顯示器進行顯示。In this embodiment, the
另一實施方式中,請參閱圖2、圖4與圖5,該核酸擴增區C的數量為兩個,該觀察區D的數量為一個,該觀察區D位於兩個核酸擴增區C之間,同時該驅動迴路24還包括一個試劑存儲區B。In another embodiment, please refer to FIG. 2, FIG. 4 and FIG. 5, the number of the nucleic acid amplification area C is two, the number of the observation area D is one, and the observation area D is located in two nucleic acid amplification areas C. Meanwhile, the
具體實現即時螢光定量PCR的過程是:向加樣區A加入未包含螢光試劑的檢測液6,該檢測液6至少包含核酸樣本和引物,而螢光試劑(例如螢光染料或DNA探針)被提前塗覆在試劑存儲區B內;檢測液6在驅動電極241的驅動下由加樣區A移動至試劑存儲區B與螢光試劑混合,混合了應該試劑的檢測液6再按照規定路徑在兩個核酸擴增區C之間往復移動進行擴增得到產物液珠8,在擴增過程中,產物液珠8會經過觀察區D,此時,產物液珠8在鐳射7的照射下會發出螢光信號9,便可以藉由圖像採集裝置經由觀察窗29採集觀察區D處的產物液珠8發出的螢光信號9,完成即時螢光定量PCR的過程。本實施方式中,隨著PCR擴增反應的進行,螢光強度不斷增大,當螢光強度達到最大值後不再增大,而是趨於穩定,此時,PCR擴增反應結束,因此,可以根據螢光強度的變化來準確判斷擴增反應的結束時間。The specific process of realizing real-time fluorescence quantitative PCR is: adding a
又一實施方式中,請參閱圖2與圖6,該核酸擴增區C的數量為兩個,觀察區D的數量為一個,未設置試劑存儲區B,其中觀察區D位於兩個核酸擴增區C遠離加樣區A的一側,且該觀察區D包含三個觀察位點(D1, D2, D3),三個觀察位點(D1, D2, D3)上分別設置不同的螢光試劑,具體設置有基因檢測需要的不同DNA探針。In yet another embodiment, please refer to FIG. 2 and FIG. 6 , the number of nucleic acid amplification areas C is two, the number of observation areas D is one, and the reagent storage area B is not provided, wherein the observation area D is located in two nucleic acid amplification areas. The side of the extension area C away from the sample addition area A, and the observation area D includes three observation sites (D1, D2, D3), and different fluorescent lights are set on the three observation sites (D1, D2, D3) respectively. The reagents are specifically provided with different DNA probes required for gene detection.
本實施方式中,觀察位元點D1和觀察位點D3上分別設置兩種病毒基因探針(具體為RdRp基因探針、N基因探針),觀察位點D2上設置人組織內參基因探針(Beta_actin基因探針)。In this embodiment, two kinds of viral gene probes (specifically, RdRp gene probes and N gene probes) are set on the observation site D1 and the observation site D3 respectively, and the human tissue internal reference gene probe is set on the observation site D2 (Beta_actin gene probe).
具體實現即時螢光定量PCR的過程是:向加樣區A加入不包含螢光試劑的檢測液6,該檢測液6至少包含核酸樣本和引物,而螢光試劑(具體為基因探針)被提前設置觀察區D的不同觀察位點上,本實施方式是檢測液6先在兩個核酸擴增區C之間往復移動進行核酸擴增反應得到核酸擴增產物,核酸擴增產物再移動至觀察區D與三個不同觀察位點(D1, D2, D3)上的不同探針結合形成產物液珠8進行顯色,再藉由鐳射發射裝置3發射鐳射7,當鐳射7與產物液珠8交會,產物液珠8內與相應DNA結合的DNA探針發出螢光信號9,圖像採集裝置經由開口14和觀察窗29偵測並採集觀察區D上三個觀察位點(D1, D2, D3)發出的螢光信號9,形成螢光圖像,最後藉由主機進行顯示。The specific process of realizing real-time fluorescence quantitative PCR is as follows: adding a
為了驗證螢光試劑在核酸擴增前後添加對螢光檢測的影響,圖7採用三種不同的檢測液分別進行螢光檢測。圖7中第一樣本為DNA先加G108-G染料,再進行PCR擴增;第二樣本為DNA先進行PCR擴增,再加G108-G染料;第三樣本為DNA不進行PCR擴增,但有添加G108-G染料。In order to verify the effect of adding fluorescent reagents before and after nucleic acid amplification on fluorescent detection, three different detection solutions were used for fluorescent detection respectively in FIG. 7 . In Figure 7, the first sample is DNA with G108-G dye added first, and then PCR amplification is performed; the second sample is DNA, which is PCR amplified first, and then G108-G dye is added; the third sample is DNA without PCR amplification , but with the addition of G108-G dye.
對以上三個樣本分別進行螢光檢測,得到如圖8的檢測結果。從圖8可以看出,第一樣本和第二樣本的螢光強度類似,第三樣本基本沒有螢光反應。第一樣本和第二樣本的對比說明在PCR擴增之前或之後添加螢光試劑均可,對檢測結果無影響。第一樣本和第二樣本與第三樣本對比可知,螢光試劑需要與特定DNA結合後才具有螢光特性,也就是不經過PCR擴增的DNA即便添加了螢光試劑,也不會有螢光反應。藉由以上三樣本螢光檢測結果的對比可知,採用本申請的上述核酸檢測盒100進行即時螢光定量PCR能夠實現即時檢測和精確定量,檢測結果準確,檢測速度快,且操作方便。Fluorescence detection was performed on the above three samples respectively, and the detection results as shown in Figure 8 were obtained. It can be seen from FIG. 8 that the fluorescence intensities of the first sample and the second sample are similar, and the third sample basically has no fluorescence reaction. The comparison between the first sample and the second sample shows that the fluorescent reagent can be added before or after PCR amplification, which has no effect on the detection result. Comparing the first sample and the second sample with the third sample, it can be seen that the fluorescent reagent needs to be combined with a specific DNA to have fluorescent properties, that is, the DNA that has not been amplified by PCR will not have fluorescent reagents even if the fluorescent reagent is added. Fluorescent response. It can be seen from the comparison of the fluorescence detection results of the above three samples that the real-time fluorescence quantitative PCR using the nucleic
相較於習知技術,本發明的核酸檢測盒100藉由結合檢測芯片和鐳射發射裝置能夠實現即時螢光定量核酸擴增檢測;檢測液在檢測芯片內完成核酸擴增反應後可以直接進入螢光檢測,無需將核酸擴增產物進行電泳檢測便可以即時得到核酸擴增產物的螢光圖像;降低了對操作人員的要求,降低了檢測成本,極大提升了檢測效率。而且核酸檢測盒的尺寸較小,適用於可攜式核酸檢測設備。Compared with the prior art, the nucleic
請參閱圖9,結合參閱圖2,本發明還提供了一種核酸檢測設備200,該核酸檢測設備200包括主機201、如上所述的核酸檢測盒100以及圖像採集裝置202,該主機201上設置有一檢測盒安裝槽(圖未示),該核酸檢測盒100安裝在該檢測盒安裝槽內。該圖像採集裝置202設置於所述觀察窗29遠離所述通道5的一側,該圖像採集裝置202用於藉由該觀察窗29採集所述螢光信號9,並將螢光信號9轉化為螢光圖像,並將螢光圖像傳輸至主機201進行處理,主機201將處理後的螢光圖像藉由顯示幕(圖未示)進行顯示,根據該螢光圖像可以得出核酸檢測結果。還可以將檢測結果上傳到用戶端,供相關人員查閱。Please refer to FIG. 9 , in conjunction with FIG. 2 , the present invention also provides a nucleic
相較於習知技術,本發明提供的核酸檢測設備藉由主機、核酸檢測盒以及圖像採集裝置的配合可以實現在PCR過程中進行螢光檢測,得到即時螢光圖像,根據螢光強度大小可以對PCR擴增後的DNA進行定量,可以實現即時定量檢測核酸的量;核酸檢測設備整體結構簡單,檢測操作簡便,操作過程對專業要求低,檢測效率高,極大降低了檢測成本;同時,檢測過程靈活性強,無需在固定的實驗室中進行,檢測設備便攜,可以實現社區檢測或家庭檢測。Compared with the prior art, the nucleic acid detection equipment provided by the present invention can realize fluorescence detection during the PCR process through the cooperation of the host, the nucleic acid detection box and the image acquisition device, and obtain a real-time fluorescence image, according to the fluorescence intensity. The size can quantify the DNA after PCR amplification, and can realize the real-time quantitative detection of the amount of nucleic acid; the overall structure of the nucleic acid detection equipment is simple, the detection operation is simple, the operation process requires low professional requirements, and the detection efficiency is high, which greatly reduces the detection cost; , The testing process is flexible, and does not need to be carried out in a fixed laboratory. The testing equipment is portable, and community testing or home testing can be realized.
100:核酸檢測盒 1:盒體 11:第一殼體 12:第二殼體 13:加樣口 14:開口 15:安裝口 2:檢測芯片 21:第一蓋板 22:間隔層 23:第二蓋板 24:驅動迴路 241:驅動電極 242:控制電極 25:導電層 26:第一介電層 27:第二介電層 28:加熱組件 29:觀察窗 3:鐳射發射裝置 4:連接器 5:通道 6:檢測液 7:鐳射 8:產物液珠 9:螢光信號 A:加樣區 B:試劑存儲區 C:核酸擴增區 D:觀察區 D1,D2,D3:觀察位點 200:核酸檢測設備 201:主機 202:圖像採集裝置 100: Nucleic acid detection kit 1: Box body 11: The first shell 12: Second shell 13: Injection port 14: Opening 15: Mounting port 2: Detection chip 21: The first cover 22: Spacer layer 23: Second cover 24: Drive circuit 241: Drive Electrode 242: Control Electrode 25: Conductive layer 26: The first dielectric layer 27: Second Dielectric Layer 28: Heating components 29: Observation window 3: Laser launcher 4: Connector 5: Channel 6: Detection solution 7: Laser 8: Product beads 9: Fluorescent signal A: Sample adding area B: Reagent storage area C: nucleic acid amplification region D: observation area D1, D2, D3: observation sites 200: Nucleic acid detection equipment 201: Host 202: Image acquisition device
圖1為本發明一實施方式提供的核酸檢測盒的結構示意圖。FIG. 1 is a schematic structural diagram of a nucleic acid detection cassette provided by an embodiment of the present invention.
圖2為本發明一實施方式提供的核酸檢測盒的剖面圖。FIG. 2 is a cross-sectional view of a nucleic acid detection cartridge according to an embodiment of the present invention.
圖3為本發明一實施方式提供的檢測芯片的俯視圖。FIG. 3 is a top view of a detection chip according to an embodiment of the present invention.
圖4為本發明一實施方式提供的檢測芯片內產物液珠發出螢光信號的示意圖。4 is a schematic diagram of a fluorescent signal emitted by a product droplet in a detection chip provided by an embodiment of the present invention.
圖5為本發明另一實施方式提供的檢測芯片的俯視圖。FIG. 5 is a top view of a detection chip provided by another embodiment of the present invention.
圖6為本發明又一實施方式提供的檢測芯片的俯視圖。FIG. 6 is a top view of a detection chip according to another embodiment of the present invention.
圖7為採用本發明提供的核酸檢測盒進行三種樣本的螢光檢測的檢測液圖片。FIG. 7 is a picture of the detection solution for fluorescent detection of three kinds of samples using the nucleic acid detection box provided by the present invention.
圖8為採用本發明提供的核酸檢測盒進行三種樣本的螢光檢測的螢光圖像。FIG. 8 is a fluorescent image of fluorescent detection of three kinds of samples using the nucleic acid detection cartridge provided by the present invention.
圖9為本發明一實施方式提供的核酸檢測設備的結構示意圖。FIG. 9 is a schematic structural diagram of a nucleic acid detection device according to an embodiment of the present invention.
100:核酸檢測盒 100: Nucleic acid detection kit
1:盒體 1: Box body
11:第一殼體 11: The first shell
12:第二殼體 12: Second shell
13:加樣口 13: Injection port
14:開口 14: Opening
15:安裝口 15: Mounting port
2:檢測芯片 2: Detection chip
29:觀察窗 29: Observation window
3:鐳射發射裝置 3: Laser launcher
4:連接器 4: Connector
Claims (10)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202063085368P | 2020-09-30 | 2020-09-30 | |
US63/085,368 | 2020-09-30 | ||
US202163140466P | 2021-01-22 | 2021-01-22 | |
US63/140,466 | 2021-01-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
TW202215031A true TW202215031A (en) | 2022-04-16 |
TWI781660B TWI781660B (en) | 2022-10-21 |
Family
ID=81044394
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW110122809A TWI781660B (en) | 2020-09-30 | 2021-06-22 | Nucleic acid detection disc and nucleic acid detection device |
Country Status (2)
Country | Link |
---|---|
CN (1) | CN114317223A (en) |
TW (1) | TWI781660B (en) |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7727723B2 (en) * | 2006-04-18 | 2010-06-01 | Advanced Liquid Logic, Inc. | Droplet-based pyrosequencing |
ATE542921T1 (en) * | 2006-04-18 | 2012-02-15 | Advanced Liquid Logic Inc | DROPLET-BASED PYROSEQUENCING |
JP4489088B2 (en) * | 2007-03-23 | 2010-06-23 | 株式会社東芝 | Nucleic acid detection device |
US20110312709A1 (en) * | 2010-06-17 | 2011-12-22 | Geneasys Pty Ltd | Loc device for detecting target nucleic acid sequences using electrochemiluminescent probes and calibration probes with detection photosensors and calibration photosensors |
EP3458597B1 (en) * | 2016-05-18 | 2022-09-07 | Roche Diagnostics GmbH | Quantitative real time pcr amplification using an electrowetting-based device |
CA3038535A1 (en) * | 2016-10-01 | 2018-04-05 | Berkeley Lights, Inc. | Dna barcode compositions and methods of in situ identification in a microfluidic device |
CN106979940A (en) * | 2017-04-17 | 2017-07-25 | 浙江大学 | A kind of device and method for carrying out nucleic acid amplification detection |
JP6921638B2 (en) * | 2017-06-16 | 2021-08-18 | 株式会社東芝 | Nucleic acid detection and quantification method, chip, assay kit, nucleic acid detection and quantification device and program |
RU2769999C2 (en) * | 2017-12-28 | 2022-04-14 | Адор Диагностикс С.Р.Л | Electrophoretic chip and method for fast detection of the presence of target nucleic acid molecules |
TWI685656B (en) * | 2018-04-26 | 2020-02-21 | 財團法人國家實驗研究院 | A photoelectrical device for concentration detection, method for concentration detection thereof and method for testing effectiveness drug on bacteria |
CN110452803A (en) * | 2019-08-27 | 2019-11-15 | 东南大学 | A kind of nucleic acid rapid amplifying detection method and device |
CN110791423A (en) * | 2019-11-15 | 2020-02-14 | 上海速创诊断产品有限公司 | Nucleic acid detection device, method and system |
-
2021
- 2021-06-22 CN CN202110693498.4A patent/CN114317223A/en active Pending
- 2021-06-22 TW TW110122809A patent/TWI781660B/en active
Also Published As
Publication number | Publication date |
---|---|
CN114317223A (en) | 2022-04-12 |
TWI781660B (en) | 2022-10-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN113567525A (en) | Systems and methods for capillary electrophoresis, isoelectric point and molecular weight analysis | |
US9128046B2 (en) | Slide holder assembly for comet assay | |
CN110295109B (en) | Digital PCR detection method based on microfluidic droplet printing system and application thereof | |
Zhang et al. | Advances in integrated digital microfluidic platforms for point-of-care diagnosis: A review | |
TW202219267A (en) | Nucleic acid detection disc and nucleic acid detection device | |
CN113324985B (en) | Centrifugal micro-fluidic detection device and centrifugal micro-fluidic detection system | |
US20220099576A1 (en) | Nucleic acid detection kit and nucleic acid detection device | |
TWI781660B (en) | Nucleic acid detection disc and nucleic acid detection device | |
CN109868215A (en) | A kind of detection system, detection method and device, computer readable storage medium | |
CN111812091B (en) | Chip gel electrophoresis and online UV-VIS imaging detection device thereof | |
CN115772466A (en) | Molecular detection all-in-one machine equipment | |
US20220097055A1 (en) | Nucleic acid detection kit and nucleic acid detection device | |
CN112284865A (en) | Slide pretreatment system | |
TW202215032A (en) | Nucleic acid detection disc and nucleic acid detection device | |
US20220099620A1 (en) | Nucleic acid detection kit and nucleic acid detection device | |
WO2023133377A1 (en) | Electrochemical cell devices and methods of manufacturing | |
US20220057362A1 (en) | Auxiliary Electrodes and Methods for Using and Manufacturing the Same | |
US20220099621A1 (en) | Nucleic acid detection kit and nucleic acid detection device | |
CN209745989U (en) | Qualitative/quantitative biochip detection device | |
US11499918B2 (en) | Cell detection method and cell detection device | |
CN220099014U (en) | Real-time fluorescence detector of CRISPR nucleic acid biosensor | |
JP7110474B2 (en) | Electrophoresis device capable of independently electrophoresing multiple samples | |
US20220099622A1 (en) | Nucleic acid detection kit and nucleic acid detection device | |
CN116478814A (en) | In situ hybridization device and target detection method | |
Zheng et al. | Sensors & Diagnostics |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
GD4A | Issue of patent certificate for granted invention patent |