CN109187937B

CN109187937B - Capillary type cancer cell culture detection growth device

Info

Publication number: CN109187937B
Application number: CN201810983898.7A
Authority: CN
Inventors: 王媛媛
Original assignee: First Affiliated Hospital of Henan University of Science and Technology
Current assignee: First Affiliated Hospital of Henan University of Science and Technology
Priority date: 2018-08-20
Filing date: 2018-08-20
Publication date: 2020-03-13
Anticipated expiration: 2038-08-20
Also published as: CN109187937A

Abstract

Capillary type cancer cell culture detection growth device, which belongs to the technical field of medical detection and comprises a lighting part (1), a sample placing part (2), a result part (3), a part spacing plate (12), a main bracket (41), a secondary bracket (42), a moving wheel (20), a main power line plug (10) and a main power line (11), wherein the capillary type cancer cell culture detection growth device utilizes the characteristic that cancer cells do not adhere to the wall, once cancer tissue blocks are cut off and put into a culture solution, the speed of the dispersion of the cancer cells is far higher than that of the cells in the normal somatic tissue block, then the sample bowl is used for expanding and displaying the cell dispersion speed, and by means of the control panel, the light sensitive plate, the light sensitive result processor and the printer, the results are analyzed and processed, so that the aims of knowing whether the pathological tissue block is a cancer cell tissue block or not and determining whether the patient has cancer or not can be achieved in a short time. The device is simple to manufacture, high in operability, low in cost and obvious in effect.

Description

Capillary type cancer cell culture detection growth device

Technical Field

The invention relates to a capillary type cancer cell culture detection growth device, and belongs to the technical field of medical detection.

Background

Currently, indicators such as meclizin are generally used to detect whether a person has cancer during cancer detection? However, this method is only an aid, and a positive answer cannot be given to whether the person to be tested is cancerous or not. Therefore, in a hospital, when a person has related symptoms and needs to be diagnosed, a pathological examination is performed on the person, a tissue sample of the patient is obtained, and then, the sample cells are cultured, and after several days, it is known whether the patient has cancer? Since the patient is already symptomatic, if the patient is truly suffering from cancer, a period of several days is sufficient to allow the cancer cells to spread throughout the body, greatly delaying the optimal treatment period. Therefore, the capillary type cancer cell culture detection and growth device is necessary to find out whether a pathological tissue block is a cancer cell tissue block in a short time and determine whether a patient has cancer or not.

Disclosure of Invention

In order to overcome the problem that how to finish the confirmation of cancer cells in a short time after obtaining pathological tissue blocks, the invention provides a capillary type cancer cell culture detection growth device, which utilizes the characteristic that cancer cells do not adhere to the wall, and once a cancer tissue block is cut down and put into a culture solution, the dispersion speed of the cancer cells is far higher than that of cells in a normal somatic tissue block, then, a sample pot is utilized to expand and display the dispersion speed of the cells, and the result is rapidly analyzed and processed by a control panel, a photosensitive plate, a photosensitive result processor and a printer, so that whether the pathological tissue block is the cancer cell tissue block or not can be known in a short time, and whether a diagnostician has cancer or not can be confirmed.

The technical scheme adopted by the invention for solving the technical problems is as follows:

the capillary type cancer cell culture detection growth device comprises an illumination part 1, a sample placing part 2, a result part 3, a part spacing plate 12, a main bracket 41, a secondary bracket 42, a moving wheel 20, a main power line plug 10 and a main power line 11, and is characterized in that: the sample placing part 2 is cuboid, the length of the cuboid is 10-20 cm, the width of the cuboid is 30-50 cm, the height of the cuboid is 40-60 cm, the outer wall of the sample placing part 2 is a stainless steel or aluminum alloy metal plate, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the sample placing part 2 is fixed on the upper surfaces of the main bracket 41 and the auxiliary bracket 42; the sample placing part 2 comprises a power line 16, a sample bowl 17 and a sample inlet 5; the sample bowl 17 is arranged in the center of the bottom wall of the sample placing part 2 and consists of a sample bowl dish 32, a sample bowl dish wall 33, a sample bowl dish cavity 34, a tube fixing cylinder 35, a sample block 36, a cell culture liquid surface 37, a cell culture liquid 38, a capillary cell sucking tube 39 and a capillary cell sucking tube cavity 40; the sample bowl 32 is a container for containing cell culture solution 38, a fixed tube-fixing barrel 35, a capillary cell-sucking tube 39 and a sample block 36, is made of stainless steel or aluminum alloy, is bowl-shaped, has a round bowl opening, the diameter of the round bowl is 5-10 cm, the depth of the sample bowl 32 is 1-5 cm, the walls around the sample bowl 32 are sample bowl walls 33, and the sample bowl walls 33 are made of stainless steel or aluminum alloy; the space surrounded by the sample bowl dish wall 33 is a sample bowl dish cavity 34, and the outer surface of the bottom of the sample bowl dish wall 33 is welded with the inner surface of the central bottom wall of the sample placing part 2; the solid tube barrels 35 are 8 cylinders for fixing the capillary cell-absorbing tubes 39 and are arranged on the sample pot vessel wall 33 behind the sample pot vessel 32, after the capillary cell-absorbing tubes 39 are inserted into the solid tube barrels 35, all the solid tube barrels 35 are abutted together, the space is reserved above the sample pot vessel wall 33 in front of the sample pot vessel 32, light 4 irradiates the capillary cell-absorbing tubes 39 exposed above the solid tube barrels 35, the cross section of each solid tube barrel 35 is circular, the inner diameter of each circular ring is 1-2 mm, the outer diameter of each circular ring is 2-5 mm, the length of each solid tube barrel 35 is 1-2 cm, the solid tube barrels 35 are made of stainless steel or aluminum alloy materials and are vertically fixed on the inner surface of the sample pot vessel wall 33 at the upper opening edge of the sample pot vessel 32 through welding; the sample block 36 is a pathological tissue block after operation, the activity of cells in the cell culture solution 38 can be maintained, the sample block 36 is cuboid, and the side length of the cuboid is 0.1-5 mm; the cell culture solution 38 is used for maintaining normal survival and growth proliferation of cells to be detected in the sample block 36, and the cell culture solution 38 adopts RPMI1640 or DMEM cell culture medium commonly used in laboratories; the cell culture liquid surface 37 is the upper surface of the liquid of the cell culture liquid 38 after the cell culture liquid 38 is added to the cuvette chamber 34; the capillary cell-sucking tube 39 is a thin tube with the inner diameter equal to or less than 1 mm, the length is 5-15 cm, the upper end is directly opened in a cavity in the sample placing part 2, the lower end is immersed in the cell culture solution 38 below the cell culture solution surface 37, after the capillary cell-sucking tube 39 is placed in the solid tube barrel 35, a gap is obliquely arranged between the lower end of the capillary cell-sucking tube 39 and the inner surface of the bottom wall of the sample pot 32 for the cell culture solution 38 to enter the capillary cell-sucking tube cavity 40 from the sample pot cavity 34, the capillary cell-sucking tube 39 is made of transparent glass, and the tube cavity of the capillary cell-sucking tube 39 is the capillary cell-sucking tube cavity 40.

The illumination part 1 is cuboid, the length of the cuboid is 10-20 cm, the width of the cuboid is 30-50 cm, the height of the cuboid is 40-60 cm, the outer wall of the illumination part 1 is a stainless steel or aluminum alloy metal plate, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the illumination part 1 is fixed on the upper surfaces of the main bracket 41 and the auxiliary bracket 42; the central part of the upper edge of the front wall of the illumination part 1 is connected with a general power line 11, and the illumination part 1 comprises a light-emitting lamp holder 7, a light intensity control holder 13, a light-emitting bulb 14 and a light-gathering lamp shade 15; the luminous lamp holder 7 is a component which fixedly installs the luminous bulb 14 at the center of the rear wall of the lighting part 1 by screw connection, has the same structure and function as the known lamp holder with a screw inside, and comprises an inner layer structure and an outer layer structure, wherein the inner layer structure is a cylindrical metal sheet, the lower end of the cylindrical metal sheet is connected with a strand of a power cord, and the cylindrical wall can be meshed with the metal sheet at the tail part of the luminous bulb 14 and screwed and pasted together after the luminous bulb 14 is screwed; the outer layer of the light-emitting lamp holder 7 is made of plastic or ceramic, the bottom end of the outer layer of the light-emitting lamp holder 7 is of an upper and lower double-layer structure, a metal sheet is arranged inside the upper layer at the bottom end of the outer layer of the light-emitting lamp holder 7, the outside of the metal sheet is connected with a power line, and the inside of the metal sheet is connected with a welding sample metal at the bottom of the light-emitting bulb 14 after the light-emitting bulb 14 is screwed into the light; a power line and a screw are arranged in the lower layer at the bottom end of the outer layer of the light-emitting lamp holder 7, two strands of the power line are separated, each single strand is connected with one part, one single strand is connected with a metal sheet in the upper layer at the bottom end of the outer layer of the light-emitting lamp holder 7, and the other single strand is connected with the lower end of a cylindrical metal sheet in the inner layer of the light-emitting lamp holder 7; the light-emitting bulb 14 is a component which can convert electric energy into light energy when being electrified, the structure and the function are the same as those of a well-known spherical high-pressure mercury lamp, the light-emitting bulb 14 is fixedly arranged on a light-emitting lamp holder 7 in the center of the rear wall of the lighting part 1 through spiral connection, and the positive and negative poles of the light-emitting bulb 14 and a metal structure corresponding to the light-emitting lamp holder 7 form a conductive path; the light intensity control seat 13 is fixed in the center of the lighting part 1, is in a cuboid shape, has the length of 9-18 cm, the width of 25-40 cm and the height of 30-50 cm, and comprises a voltage stabilizer, a ballast and a cooling fan; the spotlight cover 15 is a component which gathers the light 4 generated by the light bulb 14 as a point light source and directs the light to be emitted backwards, and is in a horn shape, the cylinder of the thin end of the horn is arranged around the light-emitting lamp holder 7, the diameter of the cylinder is 3-5 cm and is larger than the outer diameter of the light-emitting lamp holder 7, and the distance between the cylinder and the light-emitting lamp holder 7 is 0.3-0.5 cm; from the rear end position of the light-emitting lamp holder 7, the diameter of the trumpet shape of the spotlight shade 15 is gradually increased, the maximum diameter is 5-10 cm, the rear edge of the spotlight shade 15 is fixed in the center of the front wall of the sample placing part 2 through welding, the wall of the spotlight shade 15 is of a double-layer structure, the outer layer is an aluminum alloy layer, the thickness of the aluminum alloy layer is 0.5-1 mm, the inner layer is a mirror glass layer capable of reflecting light, and the thickness of the mirror glass layer is 0.3-0.8 mm.

The result part 3 is a component for sensing the intensity of the light 4 after passing through the capillary suction tube 39 and displaying the result on the display screen 27 of the control panel 6 or printing the result by the printer 26, the result part 3 is cuboid, the length of the cuboid is 10-20 cm, the width is 30-50 cm, the height is 40-60 cm, the outer wall of the result part 3 is a metal plate made of stainless steel or aluminum alloy, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the result part 3 is fixed on the upper surfaces of the main bracket 41 and the auxiliary bracket 42; the result section 3 includes a control board 6, a photosensitive web 18, a photosensitive result processor 29, and a printer 26; the structure and function of the control panel 6 are the same as those of the known water heater, the control panel controls the on-off and result display of various electric components in the capillary type cancer cell culture detecting and growing device, a chip is arranged in the control panel 6, the chip is connected with the control keyboard 19 and the display screen 27, the intensity of the light 4 which is sensed by the light sensing plate 18 and penetrates through the capillary cell sucking tube 39 can be displayed on the display screen 27 after being processed by the light sensing result processor 29, and an operator determines whether the printing is needed; the light-sensitive plate 18 is in the shape of a circular plate, the diameter of the circular plate is 6-12 cm, the light-sensitive plate is arranged in the center of a part partition plate 12 between the sample placing part 2 and the result part 3, the light 4 irradiated from the light-gathering lamp shade 15 can be completely irradiated on the light-sensitive plate 18, and the light-sensitive plate is mainly made of a semiconductor material with high light sensitivity, can convert the light into electric charges, and has the same structure and function as a well-known photoreceptor CCD; the sensitization result processor 29 has the same structure and function as the analog-digital converter of the known CCD, a chip is arranged in the sensitization result processor 29, the charges converted by the sensitization plate 18 are converted into digital signals through the chip, the digital signals are stored by a flash memory or a built-in hard disk card in the sensitization result processor 29 after being compressed, data are transmitted to a computer in the sensitization result processor 29, the digital signals analyzed and processed by the computer are displayed on a display screen 27 or printed out through a printer 26 by means of processing of the computer, the sensitization result processor 29 is cuboid, the length of the cuboid is 5-10 cm, the width of the cuboid is 10-20 cm, the height of the cuboid is 20-30 cm, the front wall of the cuboid is closely attached to the rear surface of the partial partition plate 12 and is connected with the partial partition plate 12 through welding, and the bottom wall of the cuboid is closely attached to the upper part of the front part; the printer 26 has the same structure and function as a known printer, and can print the result after receiving the signal command of the control panel 6, wherein the printer 26 comprises a paper placing box 23, a paper placing box cover 24, a paper placing box handle 25 and a paper outlet 28; the paper placing box 23 is a structure for placing printing paper, and is in a cuboid shape, the length of the cuboid is 8-16 cm, the width of the cuboid is 10-30 cm, and the height of the cuboid is 5-10 cm; the paper placing box cover 24 is the rear wall of the paper placing box 23 and is arranged at the lower part of the rear wall of the result part 3 through a hinge and a spring, 1 paper placing box handle 25 is arranged at the center of the outer surface of the paper placing box cover 24, the structure and the function of the paper placing box handle 25 are the same as those of a known handle, the paper placing box handle is arranged at the center of the upper surface of the paper placing box cover 24, two ends of the paper placing box handle are fixed on the paper placing box cover 24 through a bolt structure, the center of the paper placing box cover 24 bulges outwards and is separated from the paper placing box cover 24, the distance between the paper placing box handle 25 and the upper surface of the paper placing box cover 24 is gradually increased from two ends to the middle, the maximum distance can reach 5 cm, after the paper placing box cover 24 is pulled, the paper placing box cover 24 moves outwards and downwards, the paper placing box 23 is opened, after printing paper is placed; the paper outlet 28 is an opening through which printed paper is discharged from the printer 26, is provided at an upper portion of a rear wall of the paper output unit 3, and has a rectangular shape with a length of 10 to 30 cm and a width of 2 to 4 cm.

The sample inlet 5 of the sample placing part 2 is an opening which is positioned above the sample bowl 32 on the top wall of the sample placing part 2 and is convenient for placing the sample block 36 into the sample bowl 32, and the sample inlet 5 comprises a connecting hinge 8, a cover lifting handle 9, a sample inlet cover 30 and a sample inlet hole 31; the connecting hinges 8 have the same structure and function as the known hinges, and are 2 in number and are all arranged between the sample inlet cover 30 and the sample inlet hole 31, so that the sample inlet cover 30 can be conveniently lifted or lowered; the sample inlet cover 30 is a cuboid shaped plate which covers the sample inlet hole 31 and is made of stainless steel or aluminum alloy, the length of the cuboid is 12-22 cm, the width of the cuboid is 12-22 cm, and the thickness of the cuboid is 0.3-0.5 mm; the injection port hole 31 is square, and the side length of the square is 10-20 cm; the structure and the function of the lifting cover handle 9 are the same as those of a known handle, the lifting cover handle is arranged in the center of the upper surface of the sample inlet cover 30, two ends of the lifting cover handle are fixed on the sample inlet cover 30 through a bolt structure, the center of the lifting cover handle is upwards bulged and is separated from the sample inlet cover 30, the distance between the lifting cover handle 9 and the upper surface of the sample inlet cover 30 is gradually increased from two ends to the middle, and the maximum distance can reach 5 cm.

The main bracket 41 and the secondary bracket 42 are welded together to form a bracket at the bottom of the whole capillary cancer cell culture detection and growth device, wherein the main bracket 41 is a bracket at the four peripheries of the bottom of the capillary cancer cell culture detection and growth device and comprises 4 brackets which are made of manganese steel I-shaped steel, the cross sections of an upper steel body and a lower steel body of the I-shaped steel are rectangles, the length of each rectangle is 2-5 cm, the width of each rectangle is 0.5-1 cm, the cross section of a central steel body of the I-shaped steel is a rectangle, the length of each rectangle is 2-4 cm, and the width of each rectangle is 0.3-1.5 cm; the auxiliary bracket 42 is a bracket in the middle of the bottom of the capillary cancer cell culture detection growth device, and the number of the auxiliary bracket is 5, wherein 2 brackets are arranged in the length direction of the capillary cancer cell culture detection growth device, 3 brackets are arranged in the width direction of the capillary cancer cell culture detection growth device, the brackets are made of manganese steel I-shaped steel, the cross sections of an upper steel body and a lower steel body of the I-shaped steel are rectangles, the length of each rectangle is 1-3 cm, the width of each rectangle is 0.4-0.8 cm, the cross section of a central steel body of the I-shaped steel is a rectangle, the length of each rectangle is 2.2-4.4 cm, and the width of each rectangle is 0.3-1.5.

The moving wheels 20 are wheels for the capillary type cancer cell culture detection and growth device to be moved conveniently, the structure and the function of the wheels are 4 wheels which are the same as those of the known wheels, 1 wheel is respectively arranged at four corners of a main bracket 41 at the bottom of the capillary type cancer cell culture detection and growth device, and each moving wheel 20 comprises a moving wheel body 21 and a moving wheel frame 22; the movable wheel frame 22 is a connecting frame for fixing the movable wheel body 21 on the main frame 41, the upper part is welded with the main frame 41, and the lower part is fixed at two ends of the central rotating shaft of the movable wheel body 21; the structure and function of the movable wheel body 21 are the same as those of a known wheel body, and the movable wheel body is made of cast iron and is in a round cake shape, wherein the diameter of the round cake is 10-30 cm, and the thickness of the round cake is 1-3 cm.

The capillary type cancer cell culture detection growth device has the beneficial effects that the capillary type cancer cell culture detection growth device utilizes the characteristic that cancer cells do not adhere to the wall, once a cancer tissue block is cut down and placed in a culture solution, the dispersion speed of the cancer cells is far higher than that of cells in a normal somatic tissue block, then, the dispersion speed of the cells is expanded and displayed by utilizing the sample bowl, and the result is rapidly analyzed and processed by virtue of the control panel, the light-sensitive plate, the light-sensitive result processor and the printer, so that the aims of knowing whether a pathological tissue block is the cancer cell tissue block in a short time and determining whether a diagnostician has the cancer are achieved. The capillary type cancer cell culture and detection growth device is simple to manufacture, strong in operability, low in cost and obvious in effect.

Drawings

The invention is further described below with reference to the accompanying drawings.

FIG. 1 is a schematic diagram of the overall structure of the capillary cancer cell culture growth detection device of the present invention.

FIG. 2 is a schematic diagram of the overall structure of a sample bowl of the capillary cancer cell culture growth detection device.

In the figure, 1, an illuminating part, 2, a sample placing part, 3, a result part, 4, light, 5, a sample inlet, 6, a control board, 7, a luminous lamp holder, 8, a connecting hinge, 9, a lifting cover handle, 10, a general power line plug, 11, a general power line, 12, a part partition board, 13, a light intensity control seat, 14, a luminous bulb, 15, a condenser lamp cover, 16, a power line, 17, a sample pot, 18, a photosensitive plate, 19, a control keyboard, 20, a moving wheel, 21, a moving wheel body, 22, a moving wheel frame, 23, a paper placing box, 24, a paper placing box cover, 25, a paper placing box handle, 26, a printer, 27, a display screen, 28, a paper outlet, 29, a photosensitive result processor, 30, a sample inlet cover, 31, a sample inlet hole, 32, a sample pot, 33, a sample pot wall, 34, a sample pot cavity, 35, a solid tube, 36, a sample block, 37, a cell culture solution, 39. a capillary cell tube, 40. a capillary cell lumen, 41. a main stent, 42. a secondary stent.

Detailed Description

The first embodiment is as follows:

as shown in the figure, the capillary type cancer cell culture detecting and growing device of the invention comprises an illumination part 1, a sample placing part 2, a result part 3, a part partition plate 12, a main bracket 41, a secondary bracket 42, a moving wheel 20, a main power line plug 10 and a main power line 11. The lighting part 1 is a component for generating light 4, the light 4 is generated from the light-emitting bulb 14, and is gathered by the light-gathering lampshade 15 and is shot to the capillary cell-absorbing tube 39 of the sample bowl 17 in parallel, whether the liquid absorbed in the capillary cell-absorbing tube cavity 40 contains cells or not can cause the capillary cell-absorbing tube 39 to have light transmittance with different degrees, after the light 4 penetrates through the capillary cell-absorbing tube 39, light intensity stimulation with different sizes can be formed on the light-sensing plate 18 for receiving the light 4, after the processing of the light-sensing result processor 29, the result can be reflected on the display screen 27, and an operator can print the result by using the printer 26 according to the needs for recording and keeping or delivering to a patient; the illumination part 1 is cuboid, the length of the cuboid is 10-20 cm, the width of the cuboid is 30-50 cm, the height of the cuboid is 40-60 cm, the outer wall of the illumination part 1 is a stainless steel or aluminum alloy metal plate, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the illumination part 1 is fixed on the upper surfaces of the main bracket 41 and the auxiliary bracket 42; the main bracket 41 and the secondary bracket 42 are welded together to form a bracket at the bottom of the whole capillary cancer cell culture detection and growth device, wherein the main bracket 41 is a bracket at the four peripheries of the bottom of the capillary cancer cell culture detection and growth device, 4 brackets are totally made of manganese steel I-shaped steel, the cross sections of an upper steel body and a lower steel body of the I-shaped steel are rectangles, the length of each rectangle is 2-5 cm, the width of each rectangle is 0.5-1 cm, the cross section of a central steel body of the I-shaped steel is a rectangle, the length of each rectangle is 2-4 cm, and the width of each rectangle is 0.3-1.5 cm; the secondary bracket 42 is a bracket in the middle of the bottom of the capillary cancer cell culture detection growth device, and 5 brackets are shown in figure 1, wherein 2 brackets are arranged in the length direction of the capillary cancer cell culture detection growth device, 3 brackets are arranged in the width direction of the capillary cancer cell culture detection growth device and are made of manganese steel I-shaped steel, the cross sections of an upper steel body and a lower steel body of the I-shaped steel are rectangles, the length of each rectangle is 1-3 cm, the width of each rectangle is 0.4-0.8 cm, the cross section of a central steel body of the I-shaped steel is a rectangle, the length of each rectangle is 2.2-4.4 cm, and the width of each rectangle is 0.3-1.5 cm; the center of the upper edge of the front wall of the lighting part 1 is connected with a total power line 11, the total power line 11 is a known double-strand copper core power line, the cross section of each strand of copper core is circular, and the diameter of the circle is 3-5 mm; one end of the main power line 11 is connected with a main power line plug 10, the other end of the main power line 11 is connected with the control panel 6, and then electric energy is transmitted to a component needing power through a power line 16; the general power line plug 10 is a known two-phase power line plug, is provided with two protruding metal sheets and can be just inserted into a jack on a known power socket, so that external electric energy is introduced into the capillary type cancer cell culture detection and growth device; the back wall of the illumination part 1 and the front wall of the sample placing part 2 share one metal plate, the illumination part 1 and the sample placing part 2 are separated by the plate, the plate is also called a part separating plate 12, the back wall of the sample placing part 2 and the front wall of the result part 3 also share one metal plate, the sample placing part 2 and the result part 3 are separated by the plate, the plate is also called a part separating plate 12, the part separating plate 12 is a stainless steel or aluminum alloy metal plate, and the thickness of the metal plate is 3-5 mm; the lighting unit 1 includes a light emitting lamp socket 7, a light intensity control socket 13, a light emitting bulb 14, and a condenser lamp cover 15. The luminous lamp holder 7 is a component which fixedly installs the luminous bulb 14 at the center of the back wall of the lighting part 1 by screw connection, the structure and the function are the same as the known lamp holder with a screw inside, the lamp holder comprises an inner layer structure and an outer layer structure, the inner layer structure is a cylindrical metal sheet, the lower end of the cylindrical metal sheet is connected with a strand of a power cord, the cylindrical wall can be meshed with the metal sheet at the tail part of the luminous bulb 14 and screwed and pasted together after the luminous bulb 14 is screwed on, so that the welding-like metal at the glass base part of the luminous bulb 14 can be connected with the cylindrical metal sheet; the outer layer of the light-emitting lamp holder 7 is made of plastic or ceramic, the bottom end of the outer layer of the light-emitting lamp holder 7 is of an upper and lower double-layer structure, a metal sheet is arranged inside the upper layer at the bottom end of the outer layer of the light-emitting lamp holder 7, the outside of the metal sheet is connected with a power line, and the inside of the metal sheet is connected with a welding sample metal at the bottom of the light-emitting bulb 14 after the light-emitting bulb 14 is screwed into the light; the inside power cord and the screw of being provided with of lower floor of 7 outer layers bottoms of luminous lamp stand, the power cord double-strand is separated, and every single strand is connected a part respectively, and the sheetmetal of 7 outer layers bottoms upper strata inside of luminous lamp stand is connected to a single strand, and the lower extreme of 7 inner layer cylindric sheetmetals of luminous lamp stand is connected to another single strand to form a conducting path with the conductive metal in the luminous lamp stand 7 and the conductive metal of luminous bulb 14, after accepting the electric energy through the power cord, make luminous bulb 14 luminous. The light-emitting bulb 14 is a component which can convert electric energy into light energy when being electrified, the structure and the function are the same as those of a well-known spherical high-pressure mercury lamp, the light-emitting bulb 14 is an electric light source with high efficiency and long service life, and comprises a fluorescent bulb shell and a discharge tube, the discharge tube is thin and short, is only the size of a finger of a person, is internally provided with high-pressure mercury vapor, the outside of the discharge tube is provided with the cotton spherical fluorescent bulb shell, the discharge tube generates strong visible light and ultraviolet light after being electrified, and the ultraviolet light irradiates on the fluorescent bulb shell to emit a large amount of visible light. When the light-emitting bulb 14 works, current passes through the high-pressure mercury vapor to be ionized and excited, collision among electrons, atoms and ions in the discharge tube is formed, light is emitted, a resonance line with the wavelength of 253.7nm is absorbed during discharge, and the intensity of a visible line is increased. The light bulb 14 is fixedly arranged on the light base 7 at the center of the rear wall of the lighting part 1 through screw connection, and the positive and negative poles of the light bulb 14 and the corresponding metal structure of the light base 7 form a conductive path. The light intensity control base 13 is a component for fixing the light emitting lamp base 7 and ensuring the normal work of the light emitting bulb 14, is fixed in the center of the lighting part 1, is in a cuboid shape, has the length of 9-18 cm, the width of 25-40 cm and the height of 30-50 cm, and comprises a voltage stabilizer, a ballast and a cooling fan. The structure and function of the voltage stabilizer are the same as those of the known voltage stabilizer, the structure and function of the voltage stabilizer are cuboid, the length of the cuboid is 3-6 cm, the width is 8-10 cm, the height is 10-15 cm, the voltage stabilizer is equipment for stabilizing output voltage, and the voltage stabilizer comprises a voltage regulating circuit, a control circuit, a servo motor and the like, when input voltage or load changes, the control circuit samples, compares and amplifies the input voltage or the load, then drives the servo motor to rotate, so that the position of a carbon brush of the voltage regulator is changed, and the stability of the output voltage is kept by automatically adjusting the turn ratio of a coil. The ballast has the same structure and function as the well-known ballast, is in a cuboid shape, the length of the cuboid is 4-6 cm, the width is 9-12 cm, the height is 10-15 cm, the ballast is equipment for playing a current limiting role and generating instant high voltage for a light-emitting bulb 14, and is manufactured by winding enameled wires on an iron core made of silicon steel, so that the coil with the iron core, when the power is switched on/off instantly, high voltage is generated by self-induction and is applied to two ends of the filament of the light-emitting bulb 14, the action is performed alternately, when the starter is closed, the filament of the light-emitting bulb 14 is conducted to generate heat through the current-limiting of the ballast, when the starter is opened, the ballast generates high voltage by self-induction and is added on the filament of the light-emitting bulb 14, the filament emits electrons, and the electrons bombard the high-voltage mercury vapor to ionize and excite the high-voltage mercury vapor to form collision among electrons, atoms and ions in the discharge tube so as to emit light. The structure and function of the cooling fan are the same as those of the well-known electric fan, the cooling fan is cylindrical, one end of the cooling fan is opened towards the luminous bulb 14, and the other end of the cooling fan is opened on the front wall of the light intensity control seat 13 and the front wall of the lighting part 1, so that heat generated by the luminous bulb 14 is quickly dissipated. The spotlight cover 15 is a component which gathers the light 4 generated by the light bulb 14 as a point light source and directs the light to be emitted backwards, and is in a horn shape, the cylinder of the thin end of the horn is arranged around the light-emitting lamp holder 7, the diameter of the cylinder is 3-5 cm and is larger than the outer diameter of the light-emitting lamp holder 7, and the distance between the cylinder and the light-emitting lamp holder 7 is 0.3-0.5 cm; from the rear end position of the light-emitting lamp holder 7, the diameter of the trumpet shape of the light-gathering lamp shade 15 is gradually increased, the maximum diameter is 5-10 cm, namely the rear edge of the light-gathering lamp shade 15 is arranged at an opening in the center of the front wall of the sample placing part 2, the rear edge of the light-gathering lamp shade 15 is fixed in the center of the front wall of the sample placing part 2 through welding, the wall of the light-gathering lamp shade 15 is of a double-layer structure, the outer layer is an aluminum alloy layer, the thickness of the aluminum alloy layer is 0.5-1 mm, the inner layer is a mirror glass layer capable of reflecting light, and the thickness of the. The sample placing part 2 is a part for placing a sample pot 17 in the middle of a capillary type cancer cell culture detection growth device, which can enable free cancer cells in a sample block 36 placed in the sample pot 17 from a sample inlet 5 to move upwards in a capillary cell sucking tube cavity 40 along the wall of a capillary cell sucking tube 39, the sample placing part 2 is in a cuboid shape, the length of the cuboid is 10-20 cm, the width of the cuboid is 30-50 cm, the height of the cuboid is 40-60 cm, the outer wall of the sample placing part 2 is a stainless steel or aluminum alloy metal plate, the thickness of the metal plate is 3-5 mm, and the metal plate at the bottom wall of the sample placing part 2 is fixed on the upper surfaces of a main bracket 41 and a secondary bracket 42; the front and rear walls of the sample placement section 2 are also called a section spacer 12 because they are common to the result section 3 and the illumination section 1; the sample placing part 2 comprises a power line 16, a sample bowl 17 and a sample inlet 5. The power cord 16 is a known double-strand copper core power cord, the cross section of each strand of copper core is circular, and the diameter of the circle is 2-4 mm; the power supply line 16 is provided at the center of the inner surface of the bottom wall of the sample-placing portion 2. The sample bowl 17 is a member provided in the center of the bottom wall of the sample placement section 2 and adapted to hold the sample block 36 and to move the cancer cells in the sample block 36 upward in the capillary pipette cavity 40 along the wall of the capillary pipette 39, and the sample bowl 17 is composed of a sample bowl dish 32, a sample bowl dish wall 33, a sample bowl dish cavity 34, a tube fixing cylinder 35, a sample block 36, a cell culture liquid surface 37, a cell culture liquid 38, a capillary pipette 39, and a capillary pipette cavity 40. The sample bowl 32 is a container for containing cell culture solution 38, a fixed tube-fixing barrel 35, a capillary cell-sucking tube 39 and a sample block 36, is made of stainless steel or aluminum alloy, is bowl-shaped, has a round bowl opening, the diameter of the round bowl is 5-10 cm, the depth of the sample bowl 32 is 1-5 cm, the walls around the sample bowl 32 are sample bowl walls 33, and the sample bowl walls 33 are made of stainless steel or aluminum alloy; the space surrounded by the sample bowl dish wall 33 is a sample bowl dish cavity 34, and the outer surface of the bottom of the sample bowl dish wall 33 is welded with the inner surface of the central bottom wall of the sample placing part 2. The solid tube barrels 35 are 8 cylinders for fixing the capillary cell-sucking tubes 39, and are arranged on the sample pot vessel wall 33 at the rear of the sample pot vessel 32, when the capillary cell-sucking tubes 39 are inserted into the solid tube barrels 35, all the solid tube barrels 35 are abutted together, the space is reserved above the sample pot vessel wall 33 at the front of the sample pot vessel 32, the light 4 irradiates the capillary cell-sucking tubes 39 exposed above the solid tube barrels 35, the light transmission conditions of the light 4 passing through the capillary cell-sucking tubes 39 are different due to different cell densities of different pathological tissue blocks, the cross section of each solid tube barrel 35 is circular, the inner diameter of the circular ring is 1-2 mm, the outer diameter of the circular ring is 2-5 mm, the length of each solid tube barrel 35 is 1-2 cm, the solid tube barrels 35 are made of stainless steel or aluminum alloy, the solid tube barrels are vertically fixed on the inner surface of the sample pot vessel wall 33 at the upper opening of the sample pot vessel 32 through welding, after the capillary cell-sucking tubes 39 are inserted into the solid tube barrels 35, the capillary pipette 39 can be ensured to be vertically erected in the cell culture solution 38 in the sample bowl chamber 34. The sample 36 is a pathological tissue mass after operation, the activity of cells in the cell culture solution 38 can be maintained, and the sample 36 is cuboid, and the side length of the cuboid is 0.1-5 mm. The cell culture solution 38 is used for maintaining normal survival and growth and proliferation of cells to be detected in the sample block 36, the cell culture solution 38 adopts RPMI1640 or DMEM cell culture medium commonly used in laboratories, and the dosage of the cell culture solution 38 is determined according to actual needs, and the cell culture solution surface 37 is 1-5 mm higher than the lower end of the capillary suction cell tube 39. The cell culture liquid surface 37 is the upper surface of the liquid of the cell culture liquid 38 after the cell culture liquid 38 is added to the cuvette chamber 34. The capillary cell-sucking tube 39 is a thin tube with an inner diameter equal to or less than 1 mm, the length is 5-15 cm, the upper end of the capillary cell-sucking tube is directly opened in a cavity in the sample-placing part 2, the lower end of the capillary cell-sucking tube 39 is immersed in the cell culture solution 38 below the cell culture solution surface 37, after the capillary cell-sucking tube 39 is placed in the solid tube barrel 35, a gap is obliquely arranged between the lower end of the capillary cell-sucking tube 39 and the inner surface of the bottom wall of the sample pot 32, the cell culture solution 38 enters the capillary cell-sucking tube cavity 40 from the sample pot cavity 34, the capillary cell-sucking tube 39 is made of transparent glass, the cavity of the capillary cell-sucking tube 39 is the capillary cell-sucking tube cavity 40, and the cell culture solution 38 can be sucked into. The sample inlet 5 is an opening which is positioned above the sample bowl 32 on the top wall of the sample placing part 2 and is convenient for placing the sample block 36 into the sample bowl 32, and the sample inlet 5 comprises a connecting hinge 8, a lifting cover handle 9, a sample inlet cover 30 and a sample inlet hole 31. The connecting hinges 8 have the same structure and function as the known hinges, and are 2 in number and are all arranged between the sample inlet cover 30 and the sample inlet hole 31, so that the sample inlet cover 30 can be conveniently lifted or lowered. The sample inlet cover 30 is a rectangular plate covering the sample inlet hole 31, and is made of stainless steel or aluminum alloy, the length of the rectangular plate is 12-22 cm, the width of the rectangular plate is 12-22 cm, and the thickness of the rectangular plate is 0.3-0.5 mm. The injection port hole 31 is square, and the side length of the square is 10-20 cm. The structure and the function of the lifting cover handle 9 are the same as those of a known handle, the lifting cover handle is arranged in the center of the upper surface of the sample inlet cover 30, two ends of the lifting cover handle are fixed on the sample inlet cover 30 through a bolt structure, the center of the lifting cover handle is upwards bulged and is separated from the sample inlet cover 30, the distance between the lifting cover handle 9 and the upper surface of the sample inlet cover 30 is gradually increased from two ends to the middle, and the maximum distance can reach 5 cm. The result part 3 is a part for sensing the intensity of the light 4 after passing through the capillary pipette 39 and displaying the result on the display screen 27 of the control panel 6 or printing the result by the printer 26, the result part 3 is cuboid, the length of the cuboid is 10-20 cm, the width is 30-50 cm, the height is 40-60 cm, the outer wall of the result part 3 is a metal plate made of stainless steel or aluminum alloy, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the result part 3 is fixed on the upper surfaces of the main bracket 41 and the auxiliary bracket 42; the results section 3 includes a control board 6, a photosensitive web 18, a photosensitive results processor 29, and a printer 26. The structure and function of the control board 6 are the same as those of the known water heater, the control board controls the on-off and result display of various electric parts in the capillary type cancer cell culture detecting and growing device, a chip is arranged in the control board 6, the chip is connected with the control keyboard 19 and the display screen 27, the intensity of the light 4 which is sensed by the light sensing plate 18 and penetrates through the capillary suction tube 39 can be displayed on the display screen 27 after being processed by the light sensing result processor 29, and an operator determines whether the printing is needed. The light-sensing plate 18 is in the shape of a circular plate with a diameter of 6-12 cm, is arranged in the center of the partition plate 12 between the sample-placing part 2 and the result part 3, and the light 4 irradiated from the light-gathering lamp shade 15 can be totally irradiated on the light-sensing plate 18, is mainly made of a high-sensitivity semiconductor material, can convert the light into electric charges, and has a structure and a function similar to those of a known photoreceptor CCD. The sensitization result processor 29 is similar to the analog-digital converter of the known CCD in structure and function, and is internally provided with a chip, the charges converted by the sensitization plate 18 are converted into digital signals by the chip, the digital signals are stored by a flash memory or a built-in hard disk card in the sensitization result processor 29 after being compressed, data are transmitted to a computer in the sensitization result processor 29, the digital signals analyzed and processed by the computer are displayed on a display screen 27 or printed by a printer 26 by means of processing of the computer, the sensitization result processor 29 is in a cuboid shape, the length of the cuboid is 5-10 cm, the width of the cuboid is 10-20 cm, the height of the cuboid is 20-30 cm, the front wall is closely attached to the rear surface of the partial partition plate 12 and is connected with the partial partition plate 12 by welding, and the bottom wall is closely attached to the upper part of the front part of the paper placing box 23. The printer 26 is configured and functions as a known printer, and prints out a result after receiving a signal command from the control board 6, and the printer 26 includes a paper cassette 23, a paper cassette cover 24, a paper cassette handle 25, and a paper outlet 28. The paper placing box 23 is a structure for placing printing paper, and is in a cuboid shape, the length of the cuboid is 8-16 cm, the width of the cuboid is 10-30 cm, and the height of the cuboid is 5-10 cm. The paper placing box cover 24 is the rear wall of the paper placing box 23 and is arranged at the lower part of the rear wall of the result part 3 through a hinge and a spring, 1 paper placing box handle 25 is arranged at the center of the outer surface of the paper placing box cover 24, the structure and the function of the paper placing box handle 25 are the same as those of a known handle, the paper placing box handle is arranged at the center of the upper surface of the paper placing box cover 24, two ends of the paper placing box handle are fixed on the paper placing box cover 24 through a bolt structure, the center of the paper placing box cover 24 bulges outwards and is separated from the paper placing box cover 24, the distance between the paper placing box handle 25 and the upper surface of the paper placing box cover 24 is gradually increased from two ends to the middle, the maximum distance can reach 5 centimeters, after the paper placing box cover 24 is pulled, the paper placing box cover 24 moves outwards and downwards, the paper placing box 23 is opened, after printing paper is placed. The paper outlet 28 is an opening through which printed paper is discharged from the printer 26, is provided at an upper portion of a rear wall of the paper output unit 3, and has a rectangular shape with a length of 10 to 30 cm and a width of 2 to 4 cm. The moving wheels 20 are wheels for the capillary type cancer cell culture detecting and growing device to be moved conveniently, the structure and the function of the wheels are 4 wheels which are the same as those of the known wheels, 1 wheel is respectively arranged at four corners of a main bracket 41 at the bottom of the capillary type cancer cell culture detecting and growing device, and each moving wheel 20 comprises a moving wheel body 21 and a moving wheel frame 22. The movable wheel frame 22 is a connecting frame for fixing the movable wheel body 21 on the main frame 41, the upper portion is welded with the main frame 41, and the lower portion is fixed at two ends of the central rotating shaft of the movable wheel body 21, so as to ensure that the movable wheel body 21 can rotate around the central rotating shaft. The structure and function of the movable wheel body 21 are the same as those of a known wheel body, the movable wheel body is made of cast iron and is in a round cake shape, the diameter of the round cake is 10-30 cm, the thickness of the round cake is 1-3 cm, and the round cake can rotate around a central rotating shaft.

The foregoing shows and describes the general principles and broad features of the present invention and advantages thereof. It will be understood by those skilled in the art that the present invention is not limited to the embodiments described above, which are merely illustrative of the principles of the invention, but that various changes and modifications may be made without departing from the spirit and scope of the invention, which is defined by the appended claims and their equivalents.

Claims

1. Capillary cancer cell culture detects growth device comprises illumination portion (1), the portion of putting a kind (2), result portion (3), portion space board (12), main support (41), from support (42), removal wheel (20), total power cord plug (10) and total power cord (11), its characterized in that: the sample placing part (2) is cuboid, the length of the cuboid is 10-20 cm, the width of the cuboid is 30-50 cm, the height of the cuboid is 40-60 cm, the outer wall of the sample placing part (2) is a stainless steel or aluminum alloy metal plate, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the sample placing part (2) is fixed on the upper surfaces of the main bracket (41) and the auxiliary bracket (42); the sample placing part (2) comprises a power line (16), a sample bowl (17) and a sample inlet (5); the sample bowl (17) is arranged in the center of the bottom wall of the sample placing part (2) and consists of a sample bowl dish (32), a sample bowl dish wall (33), a sample bowl dish cavity (34), a tube fixing tube (35), a sample block (36), a cell culture liquid level (37), a cell culture liquid (38), a capillary cell sucking tube (39) and a capillary cell sucking tube cavity (40); the sample bowl dish (32) is a container for containing cell culture solution (38), a fixed tube fixing barrel (35) and placing a capillary cell sucking tube (39) and a sample block (36), is made of stainless steel or aluminum alloy and is bowl-shaped, the bowl opening is circular, the diameter of the circle is 5-10 cm, the depth of the sample bowl dish (32) is 1-5 cm, the walls around the sample bowl dish (32) are sample bowl dish walls (33), and the sample bowl dish walls (33) are made of stainless steel or aluminum alloy; the space surrounded by the sample bowl dish wall (33) is a sample bowl dish cavity (34), and the outer surface of the bottom of the sample bowl dish wall (33) is welded with the inner surface of the central bottom wall of the sample placing part (2); the cell fixing tubes (35) are 8 cylinders for fixing the capillary cell-sucking tubes (39), and are arranged on the cell-sucking wall (33) behind the cell-sucking vessel (32), after the capillary cell-sucking tubes (39) are inserted into the cell fixing tubes (35), all the cell fixing tubes (35) are abutted together, the upper part of the cell-sucking wall (33) in front of the cell-sucking vessel (32) is empty, light (4) irradiates the capillary cell-sucking tubes (39) exposed above the cell fixing tubes (35), the cross section of each cell fixing tube (35) is circular, the inner diameter of the circular ring is 1-2 mm, the outer diameter of the circular ring is 2-5 mm, the length of each cell fixing tube (35) is 1-2 cm, the cell fixing tubes (35) are made of stainless steel or aluminum alloy, and are vertically fixed on the inner surface of the cell-sucking wall (33) at the upper opening edge of the cell-sucking vessel (32) through welding; the sample block (36) is a pathological tissue block after operation, the activity of cells in the cell culture solution (38) can be maintained, the sample block (36) is cuboid, and the side length of the cuboid is 0.1-5 mm; the cell culture solution (38) is used for maintaining normal survival and growth and proliferation of cells to be detected in the sample block (36), and the cell culture solution (38) adopts RPMI1640 or DMEM cell culture medium which is commonly used in laboratories; the cell culture liquid level (37) is the upper surface of the cell culture liquid (38) after the cell culture liquid (38) is added to the sample bowl dish cavity (34); the capillary cell-sucking tube (39) is a thin tube with the inner diameter equal to or less than 1 millimeter, the length is 5-15 centimeters, the upper end of the capillary cell-sucking tube is directly opened in a cavity in the sample placing part (2), the lower end of the capillary cell-sucking tube is immersed in cell culture solution (38) below a cell culture solution surface (37), after the capillary cell-sucking tube (39) is placed in the solid tube barrel (35), a gap is obliquely formed between the lower end of the capillary cell-sucking tube (39) and the inner surface of the bottom wall of the sample pot (32) for allowing the cell culture solution (38) to enter the capillary cell-sucking tube cavity (40) from the sample pot cavity (34), the capillary cell-sucking tube (39) is made of transparent glass, and the tube cavity of the capillary cell-sucking tube (39) is the capillary cell.

2. The capillary cancer cell culture growth device of claim 1, wherein: the illumination part (1) is cuboid, the length of the cuboid is 10-20 cm, the width of the cuboid is 30-50 cm, the height of the cuboid is 40-60 cm, the outer wall of the illumination part (1) is a stainless steel or aluminum alloy metal plate, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the illumination part (1) is fixed on the upper surfaces of the main bracket (41) and the auxiliary bracket (42); the center of the upper edge of the front wall of the illumination part (1) is connected with a main power line (11), and the illumination part (1) comprises a light-emitting lamp holder (7), a light intensity control holder (13), a light-emitting bulb (14) and a light-gathering lamp cover (15); the luminous lamp holder (7) is a component which fixedly installs the luminous bulb (14) at the center of the rear wall of the lighting part (1) through screw connection, the structure and the function are the same as those of the known lamp holder with a screw inside, the lamp holder comprises an inner layer structure and an outer layer structure, the inner layer structure is a cylindrical metal sheet, the lower end of the cylindrical metal sheet is connected with one strand of a power cord, and the cylindrical wall can be meshed with the metal sheet at the tail part of the luminous bulb (14) to be screwed and pasted together after the luminous bulb (14) is screwed; the outer layer of the light-emitting lamp holder (7) is made of plastic or ceramic, the bottom end of the outer layer of the light-emitting lamp holder (7) is of an upper and lower double-layer structure, a metal sheet is arranged inside the upper layer at the bottom end of the outer layer of the light-emitting lamp holder (7), the outside of the metal sheet is connected with a power line, and the inside of the metal sheet is connected with welding-like metal at the bottom of the light-emitting bulb (14) after the light-emitting bulb (14) is screwed into the light-emitting lamp; a power line and a screw are arranged in the lower layer of the bottom end of the outer layer of the light-emitting lamp holder (7), two strands of the power line are separated, each single strand is connected with one part, one single strand is connected with a metal sheet in the upper layer of the bottom end of the outer layer of the light-emitting lamp holder (7), and the other single strand is connected with the lower end of a cylindrical metal sheet in the inner layer of the light-emitting lamp holder (7); the light-emitting bulb (14) is a component which can convert electric energy into light energy when being electrified, the structure and the function of the light-emitting bulb are the same as those of a well-known spherical high-pressure mercury lamp, the light-emitting bulb (14) is fixedly arranged on a light-emitting lamp holder (7) in the center of the rear wall of the lighting part (1) through spiral connection, and the positive and negative poles of the light-emitting bulb (14) and a metal structure corresponding to the light-emitting lamp holder (7) form a conductive path; the light intensity control seat (13) is fixed at the center of the lighting part (1) and is cuboid, the length of the cuboid is 9-18 cm, the width of the cuboid is 25-40 cm, the height of the cuboid is 30-50 cm, and the light intensity control seat comprises a voltage stabilizer, a ballast and a cooling fan; the spotlight lampshade (15) is a component which gathers and directs the light (4) generated by the light-emitting bulb (14) as a point light source to be emitted backwards, and is in a horn shape, a cylinder at the thin end of the horn is arranged around the light-emitting lamp holder (7), the diameter of the cylinder is 3-5 cm and is larger than the outer diameter of the light-emitting lamp holder (7), and the distance between the cylinder and the light-emitting lamp holder is 0.3-0.5 cm; starting from the rear end position of the light-emitting lamp holder (7), the diameter of the trumpet shape of the light-gathering lamp shade (15) is gradually increased, the maximum diameter is 5-10 cm, the rear edge of the light-gathering lamp shade (15) is fixed in the center of the front wall of the sample placing part (2) through welding, the wall of the light-gathering lamp shade (15) is of a double-layer structure, the outer layer is an aluminum alloy layer, the thickness of the aluminum alloy layer is 0.5-1 mm, the inner layer is a mirror glass layer capable of reflecting light, and the thickness of the mirror glass layer is 0.3-0.8 mm.

3. The capillary cancer cell culture growth device of claim 1, wherein: the result part (3) is a component for sensing the intensity of the light (4) after penetrating through the capillary pipette (39) and displaying the result on a display screen (27) of the control panel (6) or printing the result by a printer (26), the result part (3) is cuboid, the length of the cuboid is 10-20 cm, the width of the cuboid is 30-50 cm, the height of the cuboid is 40-60 cm, the outer wall of the result part (3) is a metal plate made of stainless steel or aluminum alloy, the thickness of the metal plate is 3-5 mm, and the metal plate on the bottom wall of the result part (3) is fixed on the upper surfaces of the main bracket (41) and the auxiliary bracket (42); the result part (3) comprises a control board (6), a photosensitive plate (18), a photosensitive result processor (29) and a printer (26); the structure and function of the control panel (6) are the same as those of the known water heater, the control panel controls the on-off and result display of various electric components in the capillary cancer cell culture detection and growth device, a chip is arranged in the control panel (6), the chip is connected with a control keyboard (19) and a display screen (27), the intensity of light (4) which is sensed by a light sensing plate (18) and penetrates through a capillary cell (39) can be displayed on the display screen (27) after being processed by a light sensing result processor (29), and an operator determines whether printing is needed; the light sensing plate (18) is in a circular plate shape, the diameter of the circular plate is 6-12 cm, the light sensing plate is arranged in the center of a part partition plate (12) between the sample placing part (2) and the result part (3), light rays (4) irradiated from a light-gathering lamp shade (15) can be completely irradiated on the light sensing plate (18), and the light sensing plate is mainly made of a semiconductor material with high light sensitivity and can convert the light rays into charges, and the structure and the function of the light sensing plate are similar to those of a known light sensor CCD; the structure and function of the photosensitive result processor (29) are the same as those of an analog-to-digital converter of a known CCD, a chip is arranged in the photosensitive result processor, the charges converted by the photosensitive plate (18) are converted into digital signals by a chip, the digital signals are stored by a flash memory or a built-in hard disk card inside a photosensitive result processor (29) after being compressed, and the data is transmitted to a computer in a photosensitive result processor (29), the digital signal analyzed and processed by the computer is displayed on a display screen (27) or printed out by a printer (26) by the processing means of the computer, the photosensitive result processor (29) is cuboid, the length of the cuboid is 5-10 cm, the width of the cuboid is 10-20 cm, the height of the cuboid is 20-30 cm, the front wall of the cuboid is clung to the rear surface of the partition board (12), and is connected with the part spacing plate (12) by welding, and the bottom wall is clung to the upper part of the front part of the paper placing box (23); the printer (26) has the same structure and function as the known printer, and can print the result after receiving the signal instruction of the control panel (6), wherein the printer (26) comprises a paper placing box (23), a paper placing box cover (24), a paper placing box handle (25) and a paper outlet (28); the paper placing box (23) is a structure for placing printing paper and is in a cuboid shape, the length of the cuboid is 8-16 cm, the width of the cuboid is 10-30 cm, and the height of the cuboid is 5-10 cm; the paper box cover (24) is the rear wall of the paper box (23) and is arranged at the lower part of the rear wall of the result part (3) through a hinge and a spring, the center of the outer surface of the paper box cover (24) is provided with 1 paper box handle (25), the structure and the function of the paper box handle (25) are the same as those of a known handle, the paper box handle is arranged at the center of the upper surface of the paper box cover (24), two ends of the paper box handle are fixed on the paper box cover (24) through a bolt structure, the center bulges outwards, is separated from the paper box cover (24), the distance between the paper box handle (25) and the upper surface of the paper box cover (24) is gradually increased from two ends to the middle, the maximum distance can reach 5 cm, after the paper box cover (24) is pulled, the paper placing box cover (24) moves outwards and downwards to open the paper placing box (23), after the printing paper is placed in the paper placing box (23), hands are loosened, the paper placing box cover (24) is restored to the original position under the action of the spring, and the printing paper is fixed in the paper placing box (23); the paper outlet (28) is an opening for printed paper to come out of the printer (26), is arranged at the upper part of the rear wall of the paper outlet (3), is rectangular, and has the length of 10-30 cm and the width of 2-4 cm.

4. The capillary cancer cell culture growth device of claim 1, wherein: the sample inlet (5) of the sample placing part (2) is an opening which is positioned above a sample bowl dish (32) on the top wall of the sample placing part (2) and is convenient for placing a sample block (36) into the sample bowl dish (32), and the sample inlet (5) comprises a connecting hinge (8), a lifting cover handle (9), a sample inlet cover (30) and a sample inlet hole (31); the structure and the function of the connecting hinges (8) are the same as those of the known hinges, and the connecting hinges are 2 and are all arranged between the sample inlet cover (30) and the sample inlet hole (31), so that the sample inlet cover (30) can be conveniently lifted or descended; the sample inlet cover (30) is a cuboid-shaped plate which covers the sample inlet hole (31) and is made of stainless steel or aluminum alloy, the length of the cuboid is 12-22 cm, the width of the cuboid is 12-22 cm, and the thickness of the cuboid is 0.3-0.5 mm; the injection port hole (31) is square, and the side length of the square is 10-20 cm; the structure and the function of the lifting cover handle (9) are the same as those of a known handle, the lifting cover handle is arranged in the center of the upper surface of the sample inlet cover (30), two ends of the lifting cover handle are fixed on the sample inlet cover (30) through a bolt structure, the center of the lifting cover handle is upwards bulged and is separated from the sample inlet cover (30), the distance between the lifting cover handle (9) and the upper surface of the sample inlet cover (30) is gradually increased from two ends to the middle, and the maximum distance can reach 5 cm.

5. The capillary cancer cell culture growth device of claim 1, wherein: the main bracket (41) and the secondary bracket (42) are welded together to form a bracket at the bottom of the whole capillary cancer cell culture detection and growth device, wherein the main bracket (41) is a bracket at the four peripheries of the bottom of the capillary cancer cell culture detection and growth device, 4 brackets are totally made of manganese steel I-shaped steel, the cross sections of an upper steel body and a lower steel body of the I-shaped steel are rectangles, the length of each rectangle is 2-5 cm, the width of each rectangle is 0.5-1 cm, the cross section of a central steel body of the I-shaped steel is a rectangle, the length of each rectangle is 2-4 cm, and the width of each rectangle is 0.3-1.5 cm; the auxiliary bracket (42) is a bracket in the middle of the bottom of the capillary cancer cell culture detection growth device, and the number of the auxiliary bracket is 5, wherein 2 brackets are arranged in the length direction of the capillary cancer cell culture detection growth device, 3 brackets are arranged in the width direction of the capillary cancer cell culture detection growth device and are made of manganese steel I-shaped steel, the cross sections of an upper steel body and a lower steel body of the I-shaped steel are rectangles, the length of each rectangle is 1-3 cm, the width of each rectangle is 0.4-0.8 cm, the cross section of a central steel body of the I-shaped steel is a rectangle, the length of each rectangle is 2.2-4.4 cm, and the width of each rectangle is 0.3-1.5 cm.

6. The capillary cancer cell culture growth device of claim 1, wherein: the moving wheels (20) are wheels for the capillary type cancer cell culture detection and growth device to be moved conveniently, the structure and the function of the wheels are 4 wheels which are the same as those of the known wheels, 1 wheel is respectively arranged at four corners of a main bracket (41) at the bottom of the capillary type cancer cell culture detection and growth device, and each moving wheel (20) comprises a moving wheel body (21) and a moving wheel carrier (22); the movable wheel carrier (22) is a connecting support for fixing the movable wheel body (21) on the main support (41), the upper part of the movable wheel carrier is welded with the main support (41), and the lower part of the movable wheel carrier is fixed at two ends of a central rotating shaft of the movable wheel body (21); the structure and the function of the movable wheel body (21) are the same as those of a known wheel body, the movable wheel body is made of cast iron and is in a round cake shape, the diameter of the round cake is 10-30 cm, and the thickness of the round cake is 1-3 cm.