Chip device for jointly detecting typical tumor markers for physical examination and screening for women

Abstract

The invention relates to a chip device for jointly detecting typical tumor markers for physical examination and screening for women, and belongs to the field of analysis and tests. Substrates of micro-fluidic chips which are used for jointly detecting eight typical tumor markers and are applicable to women are made of PDMS, namely polydimethylsiloxane, and have merits in the aspects of prices and processes, but difficult shortcomings can be caused. The chip device aims to overcome the difficult shortcomings. The scheme mainly includes that a substrate is made of selected PDMS with original ecological surfaces, a hinge type fixture attached with miniature ultrasonic transducers is manually fastened and positioned at a location adjacent to a sample liquid flow end point of a micro-fluidic chip, and ultrasonic reducers are arranged at a sample injection end of the micro-fluidic chip, so that the ultrasonic intensity can be quickly progressively reduced in short distances, interfacial tension difference can be formed at two ends of the micro-fluidic chip, and sample liquid flow can be promoted to flow towards the direction of the end point along originally hydrophobic capillary channels. The chip device has the advantage that micro-pumps can be completely omitted.

Description

technical field [0001] The invention relates to a chip device for combined detection of typical tumor markers aimed at female physical examination and screening, and belongs to the field of analysis and testing. Background technique [0002] Tumor markers (tumor markers, TM) refer to a class of substances produced by tumor cells themselves or produced by the body's response to tumor cells during the occurrence and proliferation of tumors, reflecting the existence and growth of tumors, including Proteins, hormones, enzymes (isoenzymes) and oncogene products, etc. Testing the tumor markers in the patient's blood or body fluids can detect tumors early in the tumor screening, observe the curative effect of tumor treatment and judge the prognosis of patients. Currently, the tumor markers commonly used clinically are: (1) alpha-fetoprotein (AFP) is a marker for primary liver cancer, testicular cancer, ovarian cancer and other tumors; (2) carcinoembryonic antigen (CEA) is a marker...

AI Technical Summary

Problems solved by technology

[0008] But it's not that simple

[0009] First, this polydimethylsiloxane material, the material referred to by the acronym PDMS, is itself a strongly hydrophobic material. Microchannels are built on this material. If the microchannels are not targeted The modification operation of the surface of the channel, then, after the overall assembly is completed, that is, after the cover is covered, because the inner surface of the micro channel in the structure occupies most of the inner surface of the liquid flow channel, then the PDMS micro channel The strong hydrophobic characteristic of the inner surface of the channel is the decisive factor, which will make it very difficult for the polar liquid flow similar to the aqueous solution to pass through, and its flow resistance is so large that even ordinary micropumps are difficult to push. Of course, If the cover sheet also chooses to use the PDMS material, then the problem is basically the same, with little difference; therefore, in the prior art, it is necessary to modify and modify the inner surface of the microchannel on the PDMS material; then , is this modification operation for the inner surface of the PDMS microchannel very troublesome? That's not the problem. What constitutes a serious technical problem is another problem: the PDMS polymer molecules in the bulk phase of the PDMS material substrate have the characteristics of automatic diffusion and migration to the surface. The characteristics of polymer molecules diffusing and migrating to the surface automatically will make the modified state of the inner surface of the microchannel modified by the surface modification unable to maintain for a long enough time, and the microgroove after surface modification The maintenance time of the inner surface state of the channel is roughly only enough to complete the time required for the internal test experiment in the laboratory; in other words, the inner surface of the PDMS microchannel after surface modification or surface modification is formed after modification The surface state of the surface does not last long, but quickly tends to or changes back to the surface state before the surface modification, and returns to the original strongly hydrophobic surface state in a relatively short period of time. Then, just imagine, Can such microfluidic chips be produced in large quantities, stored in large quantities, and widely promoted? The answer is obvious, that is, impossible

This problem has also existed for many years, and so far, it has not been properly solved

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