CN116530500A - Preservation device of nail emulsion surgical operation biopsy sample - Google Patents
Preservation device of nail emulsion surgical operation biopsy sample Download PDFInfo
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- CN116530500A CN116530500A CN202310754645.3A CN202310754645A CN116530500A CN 116530500 A CN116530500 A CN 116530500A CN 202310754645 A CN202310754645 A CN 202310754645A CN 116530500 A CN116530500 A CN 116530500A
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- sealing end
- shell
- storage tube
- nail
- wall
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- 238000004321 preservation Methods 0.000 title claims abstract description 36
- 238000001574 biopsy Methods 0.000 title claims abstract description 33
- 239000000839 emulsion Substances 0.000 title claims abstract description 32
- 238000007789 sealing Methods 0.000 claims abstract description 130
- 239000012528 membrane Substances 0.000 claims abstract description 70
- 238000000926 separation method Methods 0.000 claims abstract description 48
- 230000002779 inactivation Effects 0.000 claims abstract description 29
- 239000007788 liquid Substances 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
- 239000012188 paraffin wax Substances 0.000 claims description 45
- 239000007938 effervescent tablet Substances 0.000 claims description 27
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 24
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 10
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 5
- 239000001569 carbon dioxide Substances 0.000 claims description 5
- 229920001973 fluoroelastomer Polymers 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 229920001971 elastomer Polymers 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- -1 polytetrafluoroethylene Polymers 0.000 claims description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 3
- 239000001993 wax Substances 0.000 claims description 3
- 238000002955 isolation Methods 0.000 claims description 2
- 239000008267 milk Substances 0.000 claims 1
- 230000001575 pathological effect Effects 0.000 abstract description 26
- 230000000694 effects Effects 0.000 abstract description 10
- 239000000243 solution Substances 0.000 description 23
- 239000002775 capsule Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 3
- 230000000712 assembly Effects 0.000 description 2
- 238000000429 assembly Methods 0.000 description 2
- 230000003139 buffering effect Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000003113 dilution method Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N1/00—Preservation of bodies of humans or animals, or parts thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N1/00—Preservation of bodies of humans or animals, or parts thereof
- A01N1/02—Preservation of living parts
- A01N1/0236—Mechanical aspects
- A01N1/0263—Non-refrigerated containers specially adapted for transporting or storing living parts whilst preserving, e.g. cool boxes, blood bags or "straws" for cryopreservation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W90/00—Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
- Y02W90/10—Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Hematology (AREA)
- Mechanical Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The application discloses a preservation device for a nail emulsion surgical biopsy sample, which relates to the technical field of sample preservation devices and comprises a main body, a shell I and a separation membrane; the main body comprises a rear sealing end, a front sealing end and a storage tube fixed between the rear sealing end and the front sealing end; the first shell is fixed between the rear sealing end and the front sealing end; the storage tube is positioned in the first shell; the separation membrane is fixed between the rear sealing end and the front sealing end; the space surrounded by the outer wall of the storage tube, the inner wall of the separation film, the rear sealing end and the front sealing end is an inactivation cavity; the space surrounded by the inner wall of the shell, the outer wall of the separation film, the rear sealing end and the front sealing end is an air cavity; the inactivation cavity is filled with corrosive liquid; the internal air pressure of the air cavity is in a positive pressure state; after the storage tube is damaged, the corrosive liquid loaded in the inactivation cavity can enter the storage tube to inactivate the pathological sample, so that the technical effect of harmless treatment efficiency of the pathological sample is improved.
Description
Technical Field
The invention relates to the technical field of sample preservation devices, in particular to a preservation device for a nail emulsion surgical biopsy sample.
Background
The nail emulsion surgical biopsy sample refers to a sample of pathological tissue taken from a focus position of a patient, is usually used for further detection after making a slice, or is stored by a special preservation device for later scientific research, wherein a container for storing the pathological sample is usually good in sealing performance; the transmission of pathogens in pathological samples exists in various forms, wherein most infectious pathogens can be transmitted through air or tissue fluid of the pathological samples, so that the storage device of the pathological samples needs to maintain good sealing performance, and medical accidents caused by leakage and diffusion of the pathological sample tissues are prevented.
For example, the chinese patent publication No. CN112674073B discloses an anti-pollution pathological sample storage device with a protective interlayer, wherein a pathological sample is placed in a storage tube, and when the storage tube is impacted by external force or foreign matter, the storage tube is not easy to be damaged due to the fact that the elastic ball is used for buffering and redirecting the external force and the foreign matter impact to a certain extent; even if the storage tube is damaged due to external force, the pathological sample can be contacted with corrosive liquid loaded in the storage cavity after being leaked, so that harmless treatment is carried out on the pathological sample, and medical accidents are not easy to cause.
However, in the use process of the device, after the storage tube is damaged, the leaked part of the pathological sample can be contacted with corrosive liquid loaded in the storage cavity, the corrosive liquid can not enter the storage tube to inactivate the pathological sample, and the efficiency of harmless treatment on the pathological sample is low.
Disclosure of Invention
According to the preservation device for the nail emulsion surgical biopsy sample, the technical problem that the efficiency of harmless treatment on the pathological sample is low because corrosive liquid can not enter the storage tube to inactivate the pathological sample is solved, the technical effect that the corrosive liquid loaded in the inactivation cavity can enter the storage tube to inactivate the pathological sample after the storage tube is damaged is solved, and the efficiency of harmless treatment on the pathological sample is improved.
The embodiment of the application provides a preservation device of a nail emulsion surgical biopsy sample, which comprises a main body, a first shell and a separation membrane;
the main body comprises a rear sealing end, a front sealing end and a storage tube fixed between the rear sealing end and the front sealing end;
the first shell is integrally in a circular tube shape, and the first shell is fixed between the rear sealing end and the front sealing end;
the storage tube is positioned in the first shell;
the whole shape of the separation membrane is a circular tube shape, and the separation membrane is fixed between the rear sealing end and the front sealing end;
the inner diameter of the separation membrane is larger than the outer diameter of the storage tube, and the inner diameter of the first shell is larger than the outer diameter of the separation membrane;
the space surrounded by the outer wall of the storage tube, the inner wall of the separation film, the rear sealing end and the front sealing end is an inactivation cavity;
the space surrounded by the first inner wall of the shell, the outer wall of the separation film, the rear sealing end and the front sealing end is an air cavity;
the inactivation cavity is filled with corrosive liquid;
the internal air pressure of the air cavity is in a positive pressure state.
Further, the storage tube is a hollow cylinder with one end open;
the rear sealing end and the front sealing end are circular plates with the same diameter, the opening end of the storage tube is fixedly connected with the front sealing end, and one end of the storage tube far away from the front sealing end is fixedly connected with the rear sealing end;
a circular opening is formed in the middle of the front sealing end, a circular sealing cover is connected in the opening through threads, and the size of the sealing cover is the same as that of the opening of the storage tube;
the diameter of the rear sealing end is not smaller than the outer diameter of the first shell.
Further, the corrosive liquid in the inactivation cavity is concentrated sulfuric acid solution;
the separation membrane is made of fluororubber, and the first shell is made of polytetrafluoroethylene;
the storage tube, the rear sealing end, the front sealing end and the sealing cover are all made of glass.
Further, the central axes of the front sealing end, the rear sealing end, the storage tube, the first shell and the separation membrane are positioned on the same straight line;
the length of the first shell is the same as the length of the storage tube, and the length of the separation membrane is the same as the length of the storage tube.
Further, the device also comprises a second shell;
the second shell is integrally in a circular tube shape, the length of the second shell is the same as that of the storage tube, and the second shell is fixed between the rear sealing end and the front sealing end;
the inner diameter of the second shell is larger than the outer diameter of the first shell, and the central shafts of the first shell and the second shell are positioned on the same straight line;
the space enclosed by the outer wall of the first shell, the inner wall of the second shell, the rear sealing end and the front sealing end is a water cavity, and the water cavity is filled with water.
Further, the size of the space capacity of the water cavity is larger than that of the inactivation cavity;
the second shell is made of acrylic materials.
Further, a plurality of paraffin components are uniformly fixed on the outer side wall of the shell, and the whole paraffin component is a cylinder and is positioned in the water cavity;
the paraffin component comprises a limiting net, wrapped paraffin and built-in effervescent tablets;
the whole limiting net is a hollow cylinder with an opening at the bottom end, and the opening at the bottom end of the limiting net is fixed on the outer wall of the shell;
the limiting net is internally provided with wrapped paraffin, the wrapped paraffin is internally provided with built-in effervescent tablets in a wax sealing mode, and the limiting net is used for limiting the built-in effervescent tablets.
Further, a plurality of warning components are arranged on the outer side wall of the shell;
the warning component comprises a pressure limiting valve and an outer bag body;
the pressure limiting valves and the outer bag bodies are the same in number and correspond to each other one by one;
the pressure limiting valve is embedded on the two side walls of the shell, and an outer bag body is fixed at an opening of one end of the pressure limiting valve, which is far away from the first shell;
the water cavity is communicated with the inner part of the outer bag body through a pressure limiting valve, and the outer bag body is a hollow hemisphere when not subjected to external force.
Further, the built-in effervescent tablet is a carbon dioxide effervescent tablet;
the pressure limiting valve is used for setting a pressure limiting value which is larger than the pressure value in the water cavity;
the outer bag body is made of rubber.
Further, the device also comprises a tubular membrane;
the paraffin components and the warning components are the same in number and correspond to each other one by one;
the tubular membranes and the paraffin components are the same in number and correspond to each other one by one;
the tubular film is integrally in a circular tube shape and is fixed between the first outer wall and the second inner wall of the shell;
the paraffin component is positioned in the corresponding tubular membrane, and one end of the tubular membrane, which is far away from the first shell, is sleeved outside the pressure limiting valve in the corresponding warning component, so that the tubular membrane plays an isolating role;
the inside of the tubular membrane is filled with water.
One or more technical solutions provided in the embodiments of the present application at least have the following technical effects or advantages:
by providing a preservation device for a nail emulsion surgical biopsy sample comprising a housing and a separation membrane; the device main body comprises a rear sealing end, a front sealing end and a storage tube fixed between the rear sealing end and the front sealing end; the first shell is integrally in a circular tube shape, and the first shell is fixed between the rear sealing end and the front sealing end; the storage tube is positioned in the first shell; the whole shape of the separation membrane is a circular tube shape, and the separation membrane is fixed between the rear sealing end and the front sealing end; the inner diameter of the separation membrane is larger than the outer diameter of the storage tube, and the inner diameter of the first shell is larger than the outer diameter of the separation membrane; the space surrounded by the outer wall of the storage tube, the inner wall of the separation film, the rear sealing end and the front sealing end is an inactivation cavity; the space surrounded by the inner wall of the shell, the outer wall of the separation film, the rear sealing end and the front sealing end is an air cavity; the inactivation cavity is filled with corrosive liquid; the inside atmospheric pressure of air cavity is in the malleation state, effectively solved among the prior art deposit the pipe impaired back, the part that pathological sample leaked just can with the corrosive liquid contact of loading in the storage cavity afterwards, corrosive liquid can not get into and deposit the pipe and carry out the inactivation to pathological sample and handle, the lower technical problem of efficiency to pathological sample do harmless treatment, and then realized to deposit the pipe impaired back, the corrosive liquid that the inactivation intracavity loaded can get into and deposit the pipe and carry out the inactivation to pathological sample, improved the technological effect to pathological sample do harmless treatment's efficiency.
Drawings
FIG. 1 is a schematic view showing the structure of a preservation device of a nail emulsion surgical biopsy sample of the present invention;
FIG. 2 is a schematic view showing the appearance of a preservation device for a nail emulsion surgical biopsy sample according to the present invention;
FIG. 3 is a schematic view of the housing of the preservation device of the nail emulsion surgical biopsy sample of the present invention in two positions;
FIG. 4 is a schematic view of the location of the paraffin components of the preservation device of the nail emulsion surgical biopsy sample of the present invention;
FIG. 5 is a schematic view of the paraffin assembly of the preservation device of the nail emulsion surgical biopsy sample of the present invention;
FIG. 6 is a schematic illustration of the position of a warning assembly of the preservation device of a nail emulsion surgical biopsy sample of the present invention;
FIG. 7 is a schematic view of the warning assembly of the preservation device of the nail emulsion surgical biopsy sample of the present invention;
FIG. 8 is a schematic view showing an inflated state of an outer balloon of the preservation device of the nail emulsion surgical biopsy sample of the present invention;
FIG. 9 is a schematic view of the tubular membrane position of the preservation device of the nail emulsion surgical biopsy sample of the present invention;
fig. 10 is a schematic view of a tubular membrane of the built-in effervescent tablet of the preservation device of the nail emulsion surgical biopsy sample of the present invention after encountering water.
In the figure:
a main body 100, a storage tube 110, a rear sealing end 120, a front sealing end 130, a sealing cover 131;
the device comprises a first shell 200, a paraffin component 210, a limiting net 211, a wrapping paraffin 212 and a built-in effervescent tablet 213;
a separation membrane 300, an inactivation chamber 310, an air chamber 320;
the device comprises a second shell 400, a water cavity 410, a warning component 420, a pressure limiting valve 421 and an outer bag 422;
tubular membrane 500.
Detailed Description
In order that the invention may be readily understood, a more complete description of the invention will be rendered by reference to the appended drawings; the preferred embodiments of the present invention are illustrated in the drawings, however, the present invention may be embodied in many different forms and is not limited to the embodiments described herein; rather, these embodiments are provided so that this disclosure will be thorough and complete.
It should be noted that the terms "vertical", "horizontal", "upper", "lower", "left", "right", and the like are used herein for illustrative purposes only and do not represent the only embodiment.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs; the terminology used herein in the description of the invention is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention; the term "and/or" as used herein includes any and all combinations of one or more of the associated listed items.
Referring to fig. 1, a schematic structural diagram of a preservation device for a nail emulsion surgical biopsy sample according to the present invention is shown; the preservation device of the nail emulsion surgical biopsy sample comprises a main body 100, a first shell 200 and a separation membrane 300; the main body 100 includes a rear sealing end 120, a front sealing end 130, and a storage tube 110 fixed between the rear sealing end 120 and the front sealing end 130; the first shell 200 is integrally circular and tubular, and the first shell 200 is fixed between the rear sealing end 120 and the front sealing end 130; the storage tube 110 is positioned inside the first shell 200; the overall shape of the separation membrane 300 is a circular tube shape, and the separation membrane 300 is fixed between the rear sealing end 120 and the front sealing end 130; the inner diameter of the separation membrane 300 is larger than the outer diameter of the storage tube 110, and the inner diameter of the first housing 200 is larger than the outer diameter of the separation membrane 300; the space surrounded by the outer wall of the storage tube 110, the inner wall of the separation membrane 300, the rear sealing end 120 and the front sealing end 130 is an inactivation cavity 310; the space surrounded by the inner wall of the first shell 200, the outer wall of the separation membrane 300, the rear sealing end 120 and the front sealing end 130 is an air cavity 320; the inactivation chamber 310 is filled with a corrosive liquid; the internal air pressure of the air chamber 320 is in a positive pressure state; after the storage tube 110 is damaged, the corrosive liquid loaded in the inactivation cavity 310 can enter the storage tube 110 to inactivate the pathological sample, so that the technical effect of harmless treatment efficiency of the pathological sample is improved.
Example 1
As shown in fig. 1 and 2, the preservation device of the nail emulsion surgical biopsy sample of the present application includes a main body 100, a first housing 200, and a separation film 300; the main body 100 includes a storage tube 110, a rear sealing end 120, and a front sealing end 130; the storage tube 110 is a hollow cylinder with one end open; the rear sealing end 120 and the front sealing end 130 are circular plates with the same diameter, the opening end of the storage tube 110 is fixedly connected with the front sealing end 130, and the end of the storage tube 110 away from the front sealing end 130 is fixedly connected with the rear sealing end 120; a circular opening is formed in the middle of the front sealing end 130, a circular sealing cover 131 is connected in the opening through threads, and the size of the sealing cover 131 is the same as that of the opening of the storage tube 110; the first housing 200 is in a circular tube shape, the length of the first housing 200 is the same as the length of the storage tube 110, and the first housing 200 is fixed between the rear sealing end 120 and the front sealing end 130; the storage tube 110 is positioned inside the first shell 200; the overall shape of the separation membrane 300 is a circular tube, the length of the separation membrane 300 is the same as the length of the storage tube 110, and the separation membrane 300 is fixed between the rear sealing end 120 and the front sealing end 130; the inner diameter of the separation membrane 300 is larger than the outer diameter of the storage tube 110, and the inner diameter of the first shell 200 is larger than the outer diameter of the separation membrane 300; the diameter of the rear sealing end 120 is not smaller than the outer diameter of the first shell 200; the space surrounded by the outer wall of the storage tube 110, the inner wall of the separation membrane 300, the rear sealing end 120 and the front sealing end 130 is an inactivation cavity 310; the space enclosed by the inner wall of the first shell 200, the outer wall of the separation membrane 300, the rear sealing end 120 and the front sealing end 130 is an air cavity 320; the inactivation chamber 310 is filled with a corrosive liquid.
Preferably, the corrosive liquid in the inactivation chamber 310 is a concentrated sulfuric acid solution; the internal air pressure of the air chamber 320 is in a positive pressure state.
Preferably, the separating film 300 is made of fluororubber, and the first housing 200 is made of polytetrafluoroethylene; the storage tube 110, the rear sealing end 120, the front sealing end 130 and the sealing cover 131 are all made of glass.
Preferably, the central axes of the front sealing end 130, the rear sealing end 120, the storage tube 110, the first housing 200 and the separation membrane 300 are positioned on the same straight line.
Further, as shown in fig. 3, the preservation device of the nail emulsion surgical biopsy sample of the present application further comprises a second housing 400; the second housing 400 is integrally in a circular tube shape, the length of the second housing 400 is the same as that of the storage tube 110, and the second housing 400 is fixed between the rear sealing end 120 and the front sealing end 130; the inner diameter of the second shell 400 is larger than the outer diameter of the first shell 200, and the central axes of the first shell 200 and the second shell 400 are positioned on the same straight line; the space enclosed by the outer wall of the first shell 200, the inner wall of the second shell 400, the rear sealing end 120 and the front sealing end 130 is a water cavity 410, and the water cavity 410 is filled with water; the volume of the water chamber 410 is greater than the volume of the inactivation chamber 310.
Preferably, the second housing 400 is made of acrylic material.
The technical scheme in the embodiment of the application at least has the following technical effects or advantages:
the outer shell I200 is responsible for bearing pressure, and the air cavity 320 in the shell I200 is used for damping vibration, so that the whole device cannot deform too much when being pressed; the air cavity 320 extrudes the concentrated sulfuric acid solution in the inactivation cavity 310 to a certain extent, so that the hydraulic pressure of the concentrated sulfuric acid solution is high, and when the storage tube 110 is damaged, the concentrated sulfuric acid solution is extruded into the storage tube 110 under the positive pressure effect, so that the inactivation efficiency is high; a water cavity 410 is arranged between the second shell 400 and the first shell 200, when the concentrated sulfuric acid solution seeps out of the first shell 200 or broken fragments of the damaged storage tube 110 puncture the first shell 200, a small amount of the concentrated sulfuric acid solution contacts with water, the concentrated sulfuric acid solution is diluted, and the reaction in the dilution process is not too severe; the two layers of hard shells of the second shell 400 and the first shell 200 have better protection effect, and the water in the middle water cavity 410 can serve as a buffer medium to play a certain role in buffering.
Example two
When the concentrated sulfuric acid solution in the inactivation chamber 310 in the above embodiment seeps out of the first housing 200 or the damaged storage tube 110 breaks the first housing 200, the sample in the storage tube 110 is already inactivated, but it cannot be distinguished from the appearance of the device whether the sample in a certain preservation device is inactivated; the embodiment of the application is optimized to a certain extent on the basis of the embodiment.
As shown in fig. 4 and 5, a plurality of paraffin assemblies 210 are uniformly fixed on the outer side wall of the first housing 200, and the paraffin assemblies 210 are integrally cylindrical and are positioned in the water cavity 410; the paraffin assembly 210 comprises a limiting net 211, a wrapping paraffin 212 and a built-in effervescent tablet 213; the whole limiting net 211 is a hollow cylinder with an opening at the bottom end, and the opening at the bottom end of the limiting net 211 is fixed on the outer wall of the first shell 200; the limiting net 211 is internally provided with a wrapping paraffin 212, the wrapping paraffin 212 is internally provided with a built-in effervescent tablet 213 in a wax seal, the built-in effervescent tablet 213 is a carbon dioxide effervescent tablet, and the limiting net 211 is used for limiting the built-in effervescent tablet 213.
As shown in fig. 6 and 7, a plurality of warning components 420 are disposed on the outer side wall of the second housing 400; the warning assembly 420 includes a pressure limiting valve 421 and an outer bladder 422; the pressure limiting valves 421 and the outer bag bodies 422 are the same in number and correspond to each other one by one; the pressure limiting valve 421 is embedded on the side wall of the second casing 400, and an outer bag 422 is fixed at an opening of one end of the pressure limiting valve 421 away from the first casing 200; the water cavity 410 is communicated with the inside of the outer bag body 422 through a pressure limiting valve 421, and the outer bag body 422 is a hollow hemisphere when not subjected to external force; the pressure limiting valve 421 sets a pressure limiting value greater than the pressure value inside the water chamber 410.
Preferably, the outer bladder 422 is made of rubber.
As shown in fig. 5, 7 and 8, when the concentrated sulfuric acid solution seeps out of the first housing 200, a small amount of the concentrated sulfuric acid solution contacts with water, a large amount of heat is released during dilution of the concentrated sulfuric acid solution, after the wrapped paraffin 212 beside the seeped portion of the concentrated sulfuric acid solution is melted at a high temperature, the built-in effervescent tablet 213 sealed inside the wrapped paraffin 212 contacts with water and releases carbon dioxide gas, the internal pressure of the water cavity 410 becomes large, when the internal pressure of the water cavity 410 exceeds the set value of the pressure limiting valve 421, the pressure limiting valve 421 is opened, so that carbon dioxide or water in the water cavity 410 enters into the outer capsule 422, and the outer capsule 422 expands in a direction away from the second housing 400, thereby playing a role of warning.
The technical scheme in the embodiment of the application at least has the following technical effects or advantages:
by adding the wrapping paraffin 212 wrapping the built-in effervescent tablet 213, when the concentrated sulfuric acid solution seeps out, the wrapping paraffin 212 contacts with water and releases a large amount of heat, so that the built-in effervescent tablet 213 contacts with water to generate a large amount of gas after the wrapping paraffin 212 is dissolved, and the outer capsule 422 plays a role in marking and alarming after being pressed and expanded; the process of generating gas after the built-in effervescent tablet 213 contacts with water plays a certain stirring role on the water, so that the concentrated sulfuric acid solution is diluted more fully and rapidly; the built-in effervescent tablet 213 releases gas, so that the internal pressure of the device is increased, and if the storage tube 110 is damaged, the concentrated sulfuric acid solution can be better extruded into the storage tube 110; the plurality of outer bladders 422 can play a role in shock absorption and protection after being inflated.
Example III
When the concentrated sulfuric acid solution in the inactivation chamber 310 in the above embodiment seeps out of the first housing 200 or the damaged storage tube 110 breaks through the first housing 200, it is difficult for a worker to identify the leakage position of the concentrated sulfuric acid solution by the appearance of the device; the embodiment of the application is optimized to a certain extent on the basis of the embodiment.
As shown in fig. 9, the preservation device of the nail emulsion surgical biopsy sample of the present application further includes a tubular membrane 500; the number of the paraffin components 210 is the same as that of the warning components 420, and the paraffin components and the warning components are in one-to-one correspondence; the number of the tubular membranes 500 is the same as that of the paraffin components 210 and the tubular membranes are in one-to-one correspondence with the paraffin components; the tubular membrane 500 is integrally in a circular tube shape, and the tubular membrane 500 is fixed between the outer wall of the first shell 200 and the inner wall of the second shell 400; the paraffin components 210 are positioned in the corresponding tubular membranes 500, and one end of the tubular membrane 500 far away from the first shell 200 is sleeved outside the pressure limiting valve 421 in the corresponding warning component 420, so that the tubular membrane 500 plays a role in isolation; the inside of the tubular membrane 500 is filled with water.
Preferably, the tubular membrane 500 is made of fluororubber.
As shown in fig. 10, after the wrapped paraffin 212 in the paraffin assembly 210 is melted, the built-in effervescent tablet 213 releases gas when meeting water, and the outer capsule 422 in the warning assembly 420 is correspondingly expanded under pressure, so that the exudation position of the concentrated sulfuric acid solution can be marked; the built-in effervescent tablet 213 reacts with water, so that the outer capsule 422 expands and vibrates, and can play a certain role in stirring water, thereby being beneficial to the dilution process of the exuded concentrated sulfuric acid solution.
The technical scheme in the embodiment of the application at least has the following technical effects or advantages:
the paraffin components 210 are in one-to-one correspondence with the warning components 420 and are communicated through the tubular membrane 500, so that the paraffin components 210 are separated from water outside the tubular membrane 500, the built-in effervescent tablets 213 cannot contact with the water outside the tubular membrane 500, and the phenomenon that concentrated sulfuric acid solution exudes more seriously due to too severe reaction of the built-in effervescent tablets 213 in water is prevented; after the wrapped paraffin 212 in the paraffin assembly 210 is melted, the outer bag 422 in the corresponding warning assembly 420 is inflated, so that the approximate position of exudation of the concentrated sulfuric acid solution can be displayed; the built-in effervescent tablet 213 reacts with water to vibrate the outer capsule 422, thereby playing a certain role in stirring water and accelerating dilution of exuded concentrated sulfuric acid.
The above description is only of the preferred embodiments of the present invention and is not intended to limit the present invention, but various modifications and variations can be made to the present invention by those skilled in the art. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention should be included in the protection scope of the present invention.
Claims (10)
1. A preservation device for a nail emulsion surgical biopsy sample, characterized by comprising a main body (100), a first shell (200) and a separation membrane (300);
the main body (100) includes a rear sealing end (120), a front sealing end (130), and a storage tube (110) fixed between the rear sealing end (120) and the front sealing end (130);
the first shell (200) is integrally in a circular tube shape, and the first shell (200) is fixed between the rear sealing end (120) and the front sealing end (130);
the storage tube (110) is positioned inside the first shell (200);
the whole shape of the separation membrane (300) is a circular tube shape, and the separation membrane (300) is fixed between the rear sealing end (120) and the front sealing end (130);
the inner diameter of the separation membrane (300) is larger than the outer diameter of the storage tube (110), and the inner diameter of the first shell (200) is larger than the outer diameter of the separation membrane (300);
the space surrounded by the outer wall of the storage tube (110), the inner wall of the separation membrane (300), the rear sealing end (120) and the front sealing end (130) is an inactivation cavity (310);
the space surrounded by the inner wall of the first shell (200), the outer wall of the separation membrane (300), the rear sealing end (120) and the front sealing end (130) is an air cavity (320);
the inactivation chamber (310) is filled with a corrosive liquid;
the internal air pressure of the air chamber (320) is in a positive pressure state.
2. Preservation apparatus for nail-emulsion surgical biopsy samples according to claim 1, characterized in that the storage tube (110) is a hollow cylinder open at one end;
the rear sealing end (120) and the front sealing end (130) are circular plates with the same diameter, the opening end of the storage tube (110) is fixedly connected with the front sealing end (130), and one end of the storage tube (110) far away from the front sealing end (130) is fixedly connected with the rear sealing end (120);
a circular opening is formed in the middle of the front sealing end (130), a circular sealing cover (131) is connected in an opening internal thread manner, and the size of the sealing cover (131) is the same as that of the opening of the storage tube (110);
the diameter of the rear sealing end (120) is not smaller than the outer diameter of the first shell (200).
3. Preservation apparatus of a nail emulsion surgical biopsy sample according to claim 2, characterized in that the corrosive liquid in the inactivation chamber (310) is a concentrated sulfuric acid solution;
the separation membrane (300) is made of fluororubber, and the first shell (200) is made of polytetrafluoroethylene;
the storage tube (110), the rear sealing end (120), the front sealing end (130) and the sealing cover (131) are all made of glass.
4. A preservation apparatus of a nail emulsion surgical biopsy sample according to claim 3, wherein the central axes of the front sealing end (130), the rear sealing end (120), the storage tube (110), the first housing (200) and the separation membrane (300) are positioned on the same straight line;
the first shell (200) has the same length as the storage tube (110), and the separation membrane (300) has the same length as the storage tube (110).
5. Preservation device for a nail emulsion surgical biopsy sample according to claim 4, further comprising a second housing (400);
the second shell (400) is integrally in a circular tube shape, the length of the second shell (400) is the same as that of the storage tube (110), and the second shell (400) is fixed between the rear sealing end (120) and the front sealing end (130);
the inner diameter of the second shell (400) is larger than the outer diameter of the first shell (200), and the central axes of the first shell (200) and the second shell (400) are positioned on the same straight line;
the space enclosed by the outer wall of the first shell (200), the inner wall of the second shell (400), the rear sealing end (120) and the front sealing end (130) is a water cavity (410), and the water cavity (410) is filled with water.
6. Preservation apparatus of a nail emulsion surgical biopsy sample according to claim 5, characterized in that the spatial capacity of the water chamber (410) is greater than the spatial capacity of the inactivation chamber (310);
the second shell (400) is made of acrylic materials.
7. The preservation device of nail emulsion surgical biopsy samples according to claim 6, characterized in that a plurality of paraffin components (210) are uniformly fixed on the outer side wall of the first shell (200), and the paraffin components (210) are integrally cylindrical and are positioned in the water cavity (410);
the paraffin component (210) comprises a limiting net (211), wrapping paraffin (212) and a built-in effervescent tablet (213);
the whole limiting net (211) is a hollow cylinder with an opening at the bottom end, and the opening at the bottom end of the limiting net (211) is fixed on the outer wall of the first shell (200);
the limiting net (211) is internally provided with wrapping paraffin (212), the wrapping paraffin (212) is internally provided with a built-in effervescent tablet (213) in a wax seal mode, and the limiting net (211) is used for limiting the built-in effervescent tablet (213).
8. The preservation device of nail emulsion surgical biopsy samples according to claim 7, characterized in that a plurality of warning components (420) are arranged on the outer side wall of the second shell (400);
the warning component (420) comprises a pressure limiting valve (421) and an outer bag body (422);
the pressure limiting valves (421) and the outer bag bodies (422) are the same in number and correspond to each other one by one;
the pressure limiting valve (421) is embedded on the side wall of the second shell (400), and an outer bag body (422) is fixed at the opening of one end of the pressure limiting valve (421) far away from the first shell (200);
the water cavity (410) is communicated with the inside of the outer bag body (422) through a pressure limiting valve (421), and the outer bag body (422) is a hollow hemisphere when not subjected to external force.
9. Preservation device for a nail-milk surgical biopsy sample according to claim 8, characterized in that the built-in effervescent tablet (213) is a carbon dioxide effervescent tablet;
the pressure limiting value set by the pressure limiting valve (421) is larger than the pressure value in the water cavity (410);
the outer bag body (422) is made of rubber.
10. Preservation device for a nail emulsion surgical biopsy sample according to claim 9, characterized in that it further comprises a tubular membrane (500);
the paraffin components (210) and the warning components (420) are the same in number and in one-to-one correspondence;
the number of the tubular membranes (500) is the same as that of the paraffin components (210) and the tubular membranes are in one-to-one correspondence with the paraffin components;
the tubular film (500) is integrally in a circular tube shape, and the tubular film (500) is fixed between the outer wall of the first shell (200) and the inner wall of the second shell (400);
the paraffin component (210) is positioned in the corresponding tubular membrane (500), one end of the tubular membrane (500) far away from the first shell (200) is sleeved outside the pressure limiting valve (421) in the corresponding warning component (420), and the tubular membrane (500) plays a role in isolation;
the inside of the tubular membrane (500) is filled with water.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202310754645.3A CN116530500B (en) | 2023-06-26 | 2023-06-26 | Preservation device of nail emulsion surgical operation biopsy sample |
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| Application Number | Priority Date | Filing Date | Title |
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| CN202310754645.3A CN116530500B (en) | 2023-06-26 | 2023-06-26 | Preservation device of nail emulsion surgical operation biopsy sample |
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| CN116530500B CN116530500B (en) | 2023-09-29 |
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| CN116530500B (en) | 2023-09-29 |
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