Enzyme-linked immunosorbent assay device and method used for on-site diagnosis
An enzyme-linked immunosorbent adsorption and detection device technology, which is applied in the field of immunoassays, can solve the problems of not being able to give quantitative results and limited application occasions, and achieve the effects of shortening the detection time, convenient storage and transportation, and convenient operation
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Embodiment 1
[0027] Such as figure 1 and 2 As shown, an enzyme-linked immunosorbent assay device for on-site diagnosis includes a bottom plate 2, a cover plate 1 and a sealing layer 3. The bottom plate 2 is connected to the cover plate through a connecting piece 4, and the two can be relatively closed or opened. The base plate 2 is provided with a plurality of first reaction holes 6 along its transverse direction, and a scale line 5 is provided along the longitudinal direction of the base plate; the cover plate 1 is provided with a plurality of second reaction holes 8, and when the cover plate and the base plate are bonded together, the first reaction holes 6 overlaps with the second reaction hole 8, the second reaction hole 8 communicates with the indicator hole 9 through the gas channel 10, and the indicator hole 9 communicates with the liquid outlet 7 through the reading channel 11; the gas channel 10 is shorter than the reading channel 11 The sealing layer 3 is located between the bas...
Embodiment 2
[0030] Taking the detection of carcinoembryonic antigen (CEA) as an example to illustrate the specific manufacturing method of the device:
[0031] 1. Structural production: first use the drawing software such as AUTOCAD to design the structure of the cover plate and the bottom plate, and then read the designed file through the control software of the laser cutting machine, and cut out two rectangular PMMA plates of equal size (size 76mm×25mm×1mm), one is used as a cover plate, and one is used as a bottom plate, and then the structures on the two substrates are etched by laser to form figure 2 The structure shown (the diameter of the first and second reaction holes is 5mm, and the depth is 0.5mm; the width and length of the gas channel are respectively 1mm and 10mm; the width and length of the reading channel are respectively 1mm and 50mm; the liquid outlet The diameter is 5mm); then the double-sided tape is cut into a rectangle with the same size as the cover plate and the s...
example 3
[0044] The processing and operation method for another example of carcinoembryonic antigen (CEA) detection is given below, and the device is processed based on photolithography technology, specifically:
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