Sample collection device for newborn inherited metabolic disease gene diagnosis
By installing blood sample protection components and protection component limit structures on the blood sample collection card, the problem of blood sample collection card being easily contaminated during transmission, transportation and storage is solved, ensuring the accuracy of the detection results and improving the convenience of the device.
Patent Information
- Application Number
- CN202510057780.1
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-01-14
- Publication Date
- 2025-05-09
- Estimated Expiration
- Not applicable · inactive patent
AI Technical Summary
During the genetic diagnosis of neonatal genetic metabolic diseases, blood spots on blood sample collection cards are prone to contact with foreign objects during transmission, transportation and storage, resulting in contamination, which in turn affects the accuracy of the detection results.
A sample collection device including a blood sample protection component is designed. The blood sample protection component consists of connecting cardboard, covering cardboard and protective film, and is fixed by the limit structure of the protection component to ensure that the blood sample is not contaminated during the collection, delivery and storage process.
It effectively avoids contact between blood spots on the blood sample collection card and external objects, reduces the risk of contamination, thus ensuring the accuracy of the detection results, and conveniently fixing and removing blood sample protection components, improving the convenience of use of the device.
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Figure CN119949823A_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of blood sample collection, and in particular to a sample collection device for gene diagnosis of neonatal genetic metabolic diseases. Background Art
[0002] Genetic diagnosis of neonatal inherited metabolic diseases is an advanced medical method that aims to accurately determine whether a newborn has inherited metabolic diseases through genetic testing technology. Genes are the carriers of genetic information of life and support the basic structure and function of life. The occurrence of inherited metabolic diseases is often closely related to gene mutations. Through genetic diagnosis, potential inherited metabolic disease risks can be discovered early before the newborn has typical symptoms, providing valuable time for subsequent intervention and treatment;
[0003] The published patent application number is: CN202123260486.7, which discloses a sample collection device for genetic diagnosis, including a sampling tube, wherein the bottom end of the sampling tube is threadedly connected to a sealing cap, the inner bottom end of the sampling tube is fixedly connected to a fixing ring, and the inner wall of the fixing ring is fixedly connected to a dust-proof brush, the upper inner part of the sampling tube is threadedly connected to an external threaded ring, and the top of the external threaded ring is fixedly connected to a limiting disk, the internal parts of the external threaded ring and the limiting disk are movably connected with a movable push tube, and the bottom end of the movable push tube is penetrated and connected with a protective sleeve, so that the sampling cotton can better sample the oral mucosa through the cooperation of the cotton swab stick and the sampling cotton, and the position of the sampling cotton can be protected by the protective sleeve, and the sampling cotton can be better moved to the interior of the sampling tube with the cooperation of the dust-proof brush, so that the oral mucosa on the sampling cotton is not easily contaminated, thereby increasing the accuracy of oral mucosa detection.
[0004] In the genetic diagnosis of neonatal inherited metabolic diseases, it is necessary to collect blood samples from the newborn. Usually, medical staff will collect a few drops of blood from the heel of the newborn and drop them on a blood sample collection card to form a blood spot as a sample for testing. However, during the delivery, transportation and storage of the blood sample collection card, the blood spot on the blood sample collection card is easily in contact with foreign objects, so the blood spot is easily contaminated, which in turn affects the accuracy of the test results. Summary of the invention
[0005] The main purpose of the present invention is to provide a sample collection device for genetic diagnosis of neonatal genetic metabolic diseases, which can effectively solve the problems in the background technology.
[0006] To achieve the above object, the technical solution adopted by the present invention is:
[0007] A sample collection device for genetic diagnosis of inherited metabolic diseases in newborns comprises a blood sample collection card, on which a blood sample protection component is installed, the blood sample protection component consists of a connecting cardboard, a covering cardboard and a protective film, the covering cardboard has two pieces and is fixedly installed at both ends of the connecting cardboard, the protective film has two pieces and is fixedly installed at one end of the two connecting cardboards, and a protective component limiting structure is slidably installed on the blood sample collection cardboard.
[0008] Preferably, the protection component limiting structure is composed of a connecting base rod, a limiting connecting plate and a limiting baffle, wherein the limiting connecting plates are respectively fixedly mounted on both ends of the connecting base rod, and the limiting baffles are respectively fixedly mounted on one end of the two limiting connecting plates.
[0009] Preferably, the blood sample collection card is provided with an information filling area and a blood collection area.
[0010] Preferably, an installation through groove is provided on the blood sample collection card between the information filling area and the blood collection area, and an installation guide groove is provided at the edge of the blood sample collection card near the blood collection area, and both the installation through groove and the installation guide groove penetrate the blood sample collection card.
[0011] Preferably, the connecting cardboard on the blood sample protection component passes through the installation groove opened on the blood sample collection card, the two covering cardboards are respectively located on both sides of the blood sample collection card, and the protective film is close to the blood collection area on the blood sample collection card.
[0012] Preferably, the connecting base rod on the limiting structure of the protection component is slidably installed in a mounting guide groove provided on the blood sample collection card.
[0013] Preferably, the two limiting connecting plates on the limiting structure of the protection component are respectively located on two sides of the blood sample collection card.
[0014] Compared with the prior art, the present invention has the following beneficial effects:
[0015] 1. By setting a blood sample protection component on the blood sample collection card, the blood sample protection component can protect the blood sample collected on the blood sample collection card, thereby preventing the blood spot on the blood sample collection card from contacting with foreign objects during the delivery, transportation and storage of the blood sample collection card, thereby preventing the blood spot from being contaminated, and ultimately ensuring the accuracy of the test results;
[0016] 2. By setting a protection component limiting structure, the blood sample protection component can be conveniently fixed, and the blood sample protection component can also be conveniently released, thereby making the blood sample collection card easier to use. BRIEF DESCRIPTION OF THE DRAWINGS
[0017] Figure 1This is a schematic diagram of the structure of the blood sample protection component of the present invention when the blood sampling area is shielded and protected;
[0018] Figure 2 This is a schematic diagram of the structure of the blood sample protection component of the present invention when it is unfolded;
[0019] Figure 3 This is a schematic diagram of the structure of the blood sample protection component after being disassembled;
[0020] Figure 4 It is a schematic diagram of the structure of the protective component limiting structure after being disassembled.
[0021] In the figure: 1. blood sample collection card; 2. blood sample protection component; 3. protection component limiting structure; 4. information filling area; 5. blood collection area; 6. installation groove; 7. connecting cardboard; 8. covering cardboard; 9. protective film; 10. connecting base rod; 11. limiting connecting plate; 12. limiting baffle; 13. installing guide groove. DETAILED DESCRIPTION
[0022] In order to make the technical means, creative features, objectives and effects achieved by the present invention easy to understand, the present invention is further explained below in conjunction with specific implementation methods.
[0023] See also Figure 1 , Figure 2 , Figure 3 , Figure 4 As shown, a sample collection device for genetic diagnosis of inherited metabolic diseases in newborns comprises a blood sample collection card 1, on which a blood sample protection component 2 is installed, the blood sample protection component 2 is composed of a connecting cardboard 7, a covering cardboard 8 and a protective film 9, there are two covering cardboards 8 and they are fixedly installed at both ends of the connecting cardboards 7, there are two protective films 9 and they are fixedly installed at one end of the two connecting cardboards 7, a protection component limiting structure 3 is slidably installed on the blood sample collection card 1, the protection component limiting structure 3 is composed of a connecting base rod 10, a limiting connecting plate 11 and a limiting baffle 12, the limiting connecting plate 11 is fixedly installed at both ends of the connecting base rod 10, the limiting baffle 12 2 are respectively fixedly mounted at one end of the two limiting connecting plates 11. When genetic diagnosis of genetic metabolic diseases is performed on newborns, the blood sample collection card 1 can be used to collect blood from the newborns. The method is to first use a needle to puncture the heel of the newborn, and then collect the blood on the blood sample collection card 1, and then use the blood sample protection component 2 to protect the collected blood sample. At this time, the connecting paperboard 7 on the blood sample protection component 2 can be bent so that the two protective films 9 on the two covering paperboards 8 are respectively attached to the two sides of the blood sample collection card 1, and then the protection component limiting structure 3 is slid on the blood sample collection card 1, so that the blood sample protection component 2 can be fixed using the protection component limiting structure 3.
[0024] Specifically, the blood sample collection card 1 is provided with an information filling area 4 and a blood collection area 5, an installation groove 6 is opened on the blood sample collection card 1 and between the information filling area 4 and the blood collection area 5, and an installation guide groove 13 is opened at the edge of the blood sample collection card 1 and near the blood collection area 5. The installation groove 6 and the installation guide groove 13 both penetrate the blood sample collection card 1. When using the blood sample collection card 1 to collect blood samples, the blood sample can be dropped into the blood collection area 5 on the blood sample collection card 1, so that the blood is immersed in the blood collection area 5.
[0025] Finally, by setting a blood sample protection component 2 on the blood sample collection card 1, the blood sample protection component 2 can protect the blood sample collected on the blood sample collection card 1, thereby preventing the blood spot on the blood sample collection card 1 from contacting with foreign objects during the transfer, transportation and storage of the blood sample collection card 1, thereby preventing the blood spot from being contaminated, and ultimately ensuring the accuracy of the test result. By setting a protection component limiting structure 3, the blood sample protection component 2 can be conveniently fixed, and the blood sample protection component 2 can also be conveniently released, thereby making the blood sample collection card 1 easier to use.
[0026] Furthermore, the connecting cardboard 7 on the blood sample protection component 2 passes through the installation groove 6 opened on the blood sample collection card 1, and the two covering cardboards 8 are respectively located on both sides of the blood sample collection card 1, and the protective film 9 is close to the blood collection area 5 on the blood sample collection card 1. When the blood sample protection component 2 is used to protect the blood sample, the connecting cardboard 7 can be bent, so that the two protective films 9 are respectively attached to the two sides of the blood collection area 5. Conversely, when the blood collection area 5 needs to be used, the connecting cardboard 7 can be bent in the opposite direction, so that the protective film 9 is out of contact with the blood sample collection card 1, thereby exposing the blood collection area 5.
[0027] Furthermore, the connecting base rod 10 on the protection component limiting structure 3 is slidably installed in the installation guide groove 13 opened on the blood sample collection card 1, and the two limiting connecting plates 11 on the protection component limiting structure 3 are respectively located on both sides of the blood sample collection card 1. When the protection component limiting structure 3 is used to fix the blood sample protection component 2, the protection component limiting structure 3 can be pulled, so that the two limiting baffles 12 are finally blocked on the outside of the two covering cardboards 8 respectively, and the blood sample protection component 2 is fixed at this time. Conversely, when the fixation of the blood sample protection component 2 needs to be released, the protection component limiting structure 3 can be pushed in the opposite direction, so that the two limiting baffles 12 are finally moved away from the outside of the two covering cardboards 8 respectively, and the fixation of the blood sample protection component 2 is released at this time; when the protection component limiting structure 3 moves on the blood sample collection card 1, the connecting cardboard 7 will slide in the installation guide groove 13.
[0028] The above description is only a preferred embodiment of the present invention and is not intended to limit the present invention. Although the present invention has been described in detail with reference to the aforementioned embodiments, it is still possible for a person skilled in the art to modify the technical solutions described in the aforementioned embodiments or to replace some of the technical features therein by equivalents. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention shall be included in the protection scope of the present invention. The protection scope of the present invention is defined by the attached claims and their equivalents.
Claims
1. A sample collection device for genetic diagnosis of inherited metabolic diseases in newborns, comprising a blood sample collection card (1), characterized in that: The blood sample collection card (1) is provided with a blood sample protection component (2), the blood sample protection component (2) is composed of a connecting cardboard (7), a covering cardboard (8) and a protective film (9), the covering cardboard (8) having two pieces and being fixedly mounted on the two ends of the connecting cardboard (7), the protective film (9) having two pieces and being fixedly mounted on one end of the two connecting cardboards (7), and the blood sample collection card (1) having a protection component limiting structure (3) being slidably mounted.
2. A sample collection device for genetic diagnosis of neonatal inherited metabolic diseases according to claim 1, characterized in that: The protection component limiting structure (3) is composed of a connecting base rod (10), a limiting connecting plate (11) and a limiting baffle (12); the limiting connecting plates (11) are respectively fixedly mounted on both ends of the connecting base rod (10); and the limiting baffle (12) is respectively fixedly mounted on one end of the two limiting connecting plates (11).
3. A sample collection device for genetic diagnosis of neonatal inherited metabolic diseases according to claim 1, characterized in that: The blood sample collection card (1) is provided with an information filling area (4) and a blood collection area (5).
4. A sample collection device for genetic diagnosis of neonatal inherited metabolic diseases according to claim 2, characterized in that: An installation through groove (6) is provided on the blood sample collection card (1) between the information filling area (4) and the blood sampling area (5), and an installation guide groove (13) is provided at the edge of the blood sample collection card (1) and at a position close to the blood sampling area (5). Both the installation through groove (6) and the installation guide groove (13) penetrate the blood sample collection card (1).
5. The sample collection device for genetic diagnosis of neonatal inherited metabolic diseases according to claim 3, characterized in that: The connecting paperboard (7) on the blood sample protection component (2) passes through the installation slot (6) provided on the blood sample collection card (1), and the two covering paperboards (8) are respectively located on both sides of the blood sample collection card (1).
6. The sample collection device for genetic diagnosis of neonatal inherited metabolic diseases according to claim 3, characterized in that: The protective film (9) is close to one side of the blood sampling area (5) on the blood sample collection card (1).
7. A sample collection device for genetic diagnosis of neonatal inherited metabolic diseases according to claim 4, characterized in that: The connecting base rod (10) on the protection component limiting structure (3) is slidably mounted in a mounting guide rail groove (13) provided on the blood sample collection card (1).
8. The sample collection device for genetic diagnosis of neonatal inherited metabolic diseases according to claim 5, characterized in that: The two limiting connecting plates (11) on the limiting structure (3) of the protection component are respectively located on two sides of the blood sample collection card (1).
Citation Information
Patent Citations
Sample collection device for gene diagnosis
CN217090769U