WO2019050251A1 - Device for reducing size of biological tissue - Google Patents

Device for reducing size of biological tissue Download PDF

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Publication number
WO2019050251A1
WO2019050251A1 PCT/KR2018/010278 KR2018010278W WO2019050251A1 WO 2019050251 A1 WO2019050251 A1 WO 2019050251A1 KR 2018010278 W KR2018010278 W KR 2018010278W WO 2019050251 A1 WO2019050251 A1 WO 2019050251A1
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WO
WIPO (PCT)
Prior art keywords
hole
plate
rims
protrusions
group
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PCT/KR2018/010278
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French (fr)
Korean (ko)
Inventor
이준석
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이준석
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Priority claimed from KR1020180101991A external-priority patent/KR102051223B1/en
Application filed by 이준석 filed Critical 이준석
Priority to US16/635,621 priority Critical patent/US11987786B2/en
Priority to JP2020531411A priority patent/JP6898686B2/en
Priority to CN201880052037.5A priority patent/CN111032107B/en
Priority to EP18854041.3A priority patent/EP3679961A4/en
Publication of WO2019050251A1 publication Critical patent/WO2019050251A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/02Blood transfusion apparatus

Definitions

  • embodiments are directed to a biomedical tissue fining apparatus.
  • Fat tissue which is a type of living tissue, is obtained from a subject such as a person or an animal by suction or incision. Since the fat tissue thus obtained is large in size and contains a large amount of fibrous material, it is difficult to implant it into a subject using a fine needle. Accordingly, devices for reducing the size of living tissue, such as large-sized fat tissue, have been developed.
  • U.S. Patent No. 6,139,757 discloses a method of separating cells from blood using a variable porosity filter.
  • An object according to an embodiment is to provide a device for reducing the size of a living tissue in a scratch or tearing manner.
  • An object according to an embodiment is to provide an apparatus for gradually reducing the size of a living tissue.
  • a biomedical tissue refinement apparatus includes a plate; And a through hole penetrating the front and rear of the plate and defined by a plurality of rims of the plate, wherein the plurality of rims each include a protrusion protruding toward a central portion of the through hole, While passing through the hole, the biotissue can be scratched and torn by the protrusion, which can be reduced in size.
  • the projecting portion is narrowed toward the central portion of the through hole and can form a peak.
  • the plurality of rims may include linear portions formed on both sides with respect to the protruding portion.
  • the protrusion can be formed at the center of the rim.
  • the first group of protrusions and the second group of protrusions can be formed in a plurality of rims in various ways.
  • the protrusions of the first group appear continuously along the rims of some of the plurality of rims
  • the protrusions of the second group may appear consecutively along the remaining rims of the plurality of rims.
  • the first group of protrusions and the second group of protrusions may alternate in different directions along the plurality of rims.
  • each of the protrusions of the first group and the extension of each of the protrusions of the second group may not be in contact with each other nor may they be parallel to each other. In other words, the extension of the first direction and the extension of the second direction may be in a twisted position.
  • the biomedical tissue fining device comprises: an extension extending from each of the plurality of rims toward a central portion of the through hole; And a distal end portion formed at an end of the extended portion and configured to scratch and tear the living tissue.
  • the living tissue microfabrication apparatus may further include an additional extension formed on the opposite side of the extended portion with respect to the proximal end portion and extending toward the central portion of the through hole.
  • the projecting direction of the projecting portion may not be parallel to the moving direction of the living tissue passing through the through hole.
  • the apparatus includes a first plate, a first through-hole passing through the front and rear of the first plate and defined by a plurality of first rims of the first plate, A first projection including a first projection projecting toward a center of the first screen; And a second through hole penetrating the front and rear sides of the second plate and defined by a plurality of second rims of the second plate and a second through hole penetrating the front and rear sides of the second plate and defined by a plurality of second rims of the second plate, Wherein the first through hole and the second through hole overlap each other, and the size of the first through hole is larger than the size of the second through hole .
  • the projecting direction of the first projecting portion and the second projecting portion may be the same or intersect with each other without being parallel to the moving direction of the living tissue sequentially passing through the first through hole and the second through hole.
  • the biomedical tissue refining apparatus can reduce the size of a living tissue by a scratch or a tear method.
  • the biomedical tissue refinement apparatus can gradually reduce the size of a living tissue.
  • FIG. 1 is a perspective view schematically showing a biomedical tissue refinement apparatus according to an embodiment of the present invention.
  • FIG. 2 is an exploded side view schematically showing an apparatus for biomedical tissue refinement according to an embodiment.
  • FIG 3 is a cross-sectional view schematically showing a part of a biomedical tissue refinement apparatus according to an embodiment.
  • FIG. 4 is a plan view schematically illustrating a screen according to an embodiment.
  • FIG. 5 is an enlarged view of an exemplary embodiment of the portion A of FIG. 4; FIG.
  • FIG. 6 is an enlarged view of another exemplary embodiment of FIG. 4A.
  • FIG. 7 is a side view schematically illustrating a screen according to one embodiment.
  • FIG. 8 is an enlarged view of an exemplary embodiment of FIG. 7B.
  • FIG. 9 is an enlarged cross-sectional view of one exemplary embodiment of a screen and a portion thereof in accordance with one embodiment.
  • FIG. 10 is an enlarged cross-sectional view of another exemplary embodiment of a screen and a portion thereof in accordance with an embodiment.
  • FIG. 11 is a plan view schematically illustrating an example of a plurality of stacked screens according to an embodiment.
  • FIG. 12 is a sectional view taken along line 12-12 in Fig.
  • FIG. 13 is a plan view schematically illustrating another example of a plurality of stacked screens according to an embodiment.
  • FIG. 14 is a sectional view taken along line 14-14 of Fig.
  • first, second, A, B, (a), and (b) may be used. These terms are intended to distinguish the constituent elements from other constituent elements, and the terms do not limit the nature, order or order of the constituent elements.
  • FIG. 1 is a perspective view schematically showing a biomedical tissue refinement apparatus according to an embodiment
  • FIG. 2 is an exploded side view schematically showing a biomedical tissue refinement apparatus according to an embodiment
  • FIG. 3 is a cross- Figure 2 is a cross-sectional view schematically showing a part of the device.
  • the biomedical tissue refinement apparatus 1 is configured to maximize contact with a living tissue and to miniaturize a living tissue to obtain a biomolecule of a desired size.
  • the biological tissue may include adipose tissue.
  • the living tissue can be obtained from a subject such as a human being, an animal, or the like, in a manner such as suction or incision.
  • the biomedical tissue refinement apparatus 1 may include a screen 10, a sealing member 12, a front cover 14, and a rear cover 16.
  • the screen 10 is configured to reduce the size of the living tissue.
  • the screen 10 may have a disk shape. While the lumpy living tissue passes through the screen 10, the screen 10 may be configured to scratch or tear the lumpy living tissue.
  • the sealing member 12 is configured to surround the outside of the screen 10.
  • the sealing member 12 may form a seal between the screen 10 and the front cover 14 and the rear cover 16.
  • the sealing member 12 may have an annular shape.
  • the sealing member 12 may be formed of a rubber material.
  • the front cover 14 and the rear cover 16 are configured to receive the screen 10 and the sealing member 12, respectively.
  • the front cover 14 and the rear cover 16 can be coupled to each other.
  • the front cover 14 and the rear cover 16 may be rotationally coupled.
  • the front cover 14 and the rear cover 16 may each have an inlet port and an outlet port through which the living tissue flows and a passage connecting the inlet port and the outlet port is formed between the front cover 14 and the rear cover 16 .
  • the biotissue or mass thereof can enter the interior of the front cover 14 through the inlet and pass out of the interior of the rear cover 16 through the outlet after passing through the screen 10 along the passageway.
  • FIG. 4 is a plan view schematically illustrating a screen according to an embodiment.
  • the screen 10 may include a plate 110 and at least one through hole 120.
  • the plate 110 may have a disc shape.
  • the plate 110 may be circular.
  • the plate 110 may be formed of a material suitable for preventing contamination of living tissue.
  • the through hole 120 is configured to maximize the contact with the living tissue and make the living tissue finer.
  • the through holes 120 pass through the front and rear of the plate 110 and are defined by a plurality of rims of the plate 110.
  • the plurality of rims of the plate 110 defining the through holes 120 may have irregular dimensions.
  • the plate 110 may be entirely plate molded so that the position of the through hole 120 is changed in the plate 110 or the shape of the through hole 120 is not deformed by an external force.
  • FIG. 5 is an enlarged view of an exemplary embodiment of the portion A of FIG. 4; FIG.
  • a plurality of rims 111 defining the through holes 120 may define the through holes 120 so that the through holes 120 have a substantially rectangular shape.
  • the plurality of rims 111 may each include a protrusion 112.
  • the protrusion 112 is configured to protrude toward the center of the through hole 120. As the biotissue passes through the through hole 120, the protrusion 112 is configured to scratch or tear the biotissue. On the other hand, fibers larger than the through-holes 120 may not pass through the through-holes 120.
  • the protruding direction of the protruding portion 112 may not be parallel to the moving direction of the living tissue passing through the through hole 120.
  • the projecting direction of the protrusion 112 may be parallel to the tangential direction of the plate 110, or may be a set angle with respect to the tangential direction of the plate 110.
  • the angle formed by the protrusion 112 with respect to the plate 110 may be set to an acute angle, an obtuse angle, or a reflex angle.
  • the projecting portion 112 is narrowed toward the central portion of the through hole 120 and can form a tip 1121.
  • the protrusion 112 may have the shape of a triangle.
  • the plurality of rims 111 may include linear portions 114 and 116 formed on both sides with respect to the protruding portion 112.
  • the protrusion 112 may be located at the center of the rim 111 thereof.
  • the linear portions 114, 116 may be the same length so that the protrusions 112 are at the center of the rim 111.
  • the protrusions 112 of one of the rims 111 and the protrusions of the opposite rims may face each other toward the center of the through hole 120.
  • the lengths of the linear portions 114 and 116 may be set differently. The length of the linear portions 114, 116 can be adjusted in consideration of the size of the protrusion 112.
  • the irregular shape of the through hole 120 defined by the plurality of rims 111 as described above and the sharp cross section of the plurality of rims 111 cause a pressure applied to the living tissue passing through the through hole 120 And the lumpy biotissue may be scratched or torn.
  • FIG. 6 is an enlarged view of another exemplary embodiment of FIG. 4A.
  • a plurality of rims 111 'defining the through holes 120 may be defined by defining the through holes 120 so that the through holes 120 have polygons having substantially four or more corners. can do.
  • the plurality of rims 111 ' may include a protrusion 112' configured to protrude toward the center of the through hole 120.
  • the protrusion 112 ' is narrowed toward the central portion of the through hole 120 and can form a tip 1121.
  • the plurality of rims 111 ' are formed such that the linear portions formed on both sides with respect to the protruding portion 112' are not present, or even if they are present, the length is relatively large compared to the size of the protruding portion 112 ' It can be short.
  • the plurality of protrusions 112 ' may be adjacent to each other along the plurality of rims 111'.
  • FIG. 7 is a side view schematically illustrating a screen according to an embodiment
  • FIG. 8 is an enlarged view of an exemplary embodiment of FIG. 7B.
  • a screen 20 may include a plate 210 and a through hole 220.
  • the protrusions 212a and 212b of the plurality of rims 211a and 211b of the plate 210 may establish a set angle with respect to the tangential direction of the plate 210.
  • the moving direction of the lumen-like living tissue BM passing through the through hole 220 at the front and rear of the screen 20 may not be parallel to the protruding direction of the protrusions 212a and 212b.
  • the protrusions 212a and 212b may be configured to refine the living tissue BM by scratching or tearing the living tissue BM rather than slicing the living tissue BM.
  • the plurality of rims 211a and 211b may include protrusions 212a and 212b having at least one directionality with respect to the tangential direction of the plate 210.
  • the plurality of protrusions 212a and 212b may be divided into a plurality of groups according to their protruding directions.
  • the plurality of protrusions 212a, 212b may be angled relative to the plate 210 to define a first group of protrusions protruding in a first direction with respect to the plate 210, And a second group of protrusions protruding in a second direction with respect to the plate 210.
  • first direction and the second direction may be different from each other.
  • the fact that the first direction and the second direction are different from each other means that they are not parallel to each other.
  • the protrusion 212a in the first direction protrudes to the left of the plate 210 with reference to Fig. 8
  • the protrusion 212b in the second direction protrudes to the right of the plate 210 with reference to Fig. can do.
  • first group of protrusions 212a and the second group of protrusions 212b may be adjacent to each other. In a preferred example, the first group of protrusions 212a and the second group of protrusions 212b may alternate with each other.
  • the plurality of protrusions 212a of the first group and the plurality of protrusions 212b of the second group are grouped and may be adjacent within each group.
  • the first group of protrusions 212a may be continuously formed on the rims of some of the plurality of rims 211a and 211b
  • the second group of protrusions 212b may be continuously formed on the remaining rims have.
  • the arrangements of the first group of protrusions 212a and the second group of protrusions 212b may be various.
  • the extension of the first group of protrusions 212a and the extension of the second group of protrusions 212b may or may not be parallel to each other. In other words, the extension of the first group of protrusions 212a and the extension of the second group of protrusions 212b may be at a skew position in the three-dimensional space.
  • the vertex at which the rim 211a including the first group of protrusions 212a and the rim 211b including the second group of protrusions 212b meet as the origin The first direction being the direction in which the protrusions 212a protrude is defined as the x axis, the second direction in which the second group of protrusions 212b protrude is defined as the y axis, the outward in the first direction and the second direction is defined as the z axis
  • the vector from the rim 212a including the first group of protrusions 212a to the tip of the protrusion 212a is (1, 0, -1), and the second group of protrusions 212b
  • the vector from the containing edge 212b to the tip of the protrusion 212b may be (-1, 0, 1).
  • FIG. 9 is an enlarged cross-sectional view of one exemplary embodiment of a screen and a portion thereof in accordance with one embodiment.
  • a screen 30 may include a plate 310 and a through hole 320.
  • a plurality of rims 311 of the plate 310 defining the through holes 320 may be formed with a sharp cross section over the entire plurality of rims 311.
  • the screen 30 is formed at the distal end of the extending portion 314 and the extending portion 314 extending from each of the plurality of rims 311 toward the central portion of the through hole 320, (Not shown).
  • the extension 314 may have any suitable shape.
  • the extension 314 may be formed obliquely with respect to the plane of the plate 310.
  • the extension 314 may have an outwardly curved shape with respect to the plate 310.
  • FIG. 10 is an enlarged cross-sectional view of another exemplary embodiment of a screen and a portion thereof in accordance with an embodiment.
  • a screen 40 may include a plate 410 and a through hole 420.
  • a plurality of extensions 414 and 415 may be formed on both sides of the rim 411 defining the through hole 420 with respect to the tip 416.
  • the plurality of extensions 414, 415 may be formed in a plurality of rims 411 at an angle to the plate 410 at respective set angles.
  • the inclination angles of the plurality of extensions 414, 415 relative to the plate 410 may be substantially the same.
  • the plurality of extensions 414, 415 may have an outwardly curved shape with respect to the plate 310.
  • the curved directions of the plurality of extending portions 414 and 415 may be different from each other.
  • the radius of curvature of the plurality of extensions 414, 415 may be substantially the same so that the tip 416 is centered between the plurality of extensions 414, 415.
  • FIG. 11 is a plan view schematically showing an example of a plurality of stacked screens according to an embodiment
  • FIG. 12 is a sectional view taken along line 12-12 in FIG.
  • the biomedical tissue refinement apparatus 5 is configured such that a plurality of screens 50a, 50b, and 50c are sequentially laminated.
  • the plurality of screens 50a, 50b and 50c may include through holes 520a, 520b and 520c defined by plates 510a, 510b and 510c and a plurality of rims 511a, 511b and 511c, respectively. have.
  • the plurality of screens 50a, 50b and 50c may include projections 512a, 512b and 512c projecting toward the respective through holes 520a, 520b and 520c.
  • one extended portion and a leading end portion may be formed on the plurality of frames 511a, 511b, and 511c.
  • FIG. 13 is a plan view schematically showing another example of a plurality of stacked screens according to an embodiment
  • FIG. 14 is a sectional view taken along line 14-14 of FIG.
  • the biomedical tissue refinement apparatus 6 may include a plurality of screens 60a, 60b, and 60c.
  • the plurality of screens 60a, 60b and 60c are respectively provided with through holes 620a, 620b and 620c defined by the plates 610a, 610b and 610c, a plurality of rims 611a, 611b and 611c and protrusions 612a , 612b, 612c.
  • a plurality of extensions may be formed on both sides of the plurality of rims 611a, 611b, and 611c on the basis of one prong.
  • the through-holes 620a, 620b, and 620c of the plurality of screens 60a, 60b, and 60c that are stacked in order are arranged in a direction Respectively.

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  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Surgical Instruments (AREA)

Abstract

A device for reducing the size of biological tissue according to an embodiment comprises: a plate; and a thru-hole which penetrates the front and the rear of the plate and is defined by a plurality of edges of the plate, wherein each of the plurality of edges comprises a protruding part protruding toward a center part of the thru-hole, and biological tissue may be reduced in size by being scratched and torn by the protruding parts while passing through the thru-hole.

Description

생체조직 미세화 장치A biomedical tissue fining device
이하, 실시예들은 생체조직 미세화 장치에 관한 것이다.Hereinafter, embodiments are directed to a biomedical tissue fining apparatus.
생체조직의 일 종류인 지방조직은 사람, 동물 등의 대상체로부터 흡인 또는 절개(incision) 등의 방식으로 획득된다. 이렇게 획득된 지방조직은 그 크기가 크고 많은 양의 섬유질을 포함하고 있으므로, 미세한 바늘을 이용하여 대상체에 이식하기 어려움이 있다. 이에, 크기가 큰 지방조직과 같은 생체조직의 크기를 감소시키는 장치가 개발되고 있다. 예를 들어, 미국 등록특허공보 제6,139,757호는 가변적인 다공성을 가지는 필터를 사용하여 혈액으로부터 세포를 분리하는 방법을 개시하고 있다.Fat tissue, which is a type of living tissue, is obtained from a subject such as a person or an animal by suction or incision. Since the fat tissue thus obtained is large in size and contains a large amount of fibrous material, it is difficult to implant it into a subject using a fine needle. Accordingly, devices for reducing the size of living tissue, such as large-sized fat tissue, have been developed. For example, U.S. Patent No. 6,139,757 discloses a method of separating cells from blood using a variable porosity filter.
일 실시예에 따른 목적은 긁음(scratch) 또는 찢음(tear) 방식으로 생체조직의 크기를 감소시키는 장치를 제공하는 것이다.An object according to an embodiment is to provide a device for reducing the size of a living tissue in a scratch or tearing manner.
일 실시예에 따른 목적은 생체조직의 크기를 점진적으로 감소시키는 장치를 제공하는 것이다.An object according to an embodiment is to provide an apparatus for gradually reducing the size of a living tissue.
일 실시예에 따른 생체조직 미세화 장치는 플레이트; 및 상기 플레이트의 전후방을 관통하며 상기 플레이트의 복수 개의 테두리들에 의해 규정된 관통 구멍을 포함하고, 상기 복수 개의 테두리들은 상기 관통 구멍의 중심부를 향해 돌출하는 돌출부를 각각 포함하고, 생체조직이 상기 관통 구멍을 통과하는 동안, 생체조직은 상기 돌출부에 의해 긁히고 찢어져 그 크기가 감소할 수 있다.According to one embodiment, a biomedical tissue refinement apparatus includes a plate; And a through hole penetrating the front and rear of the plate and defined by a plurality of rims of the plate, wherein the plurality of rims each include a protrusion protruding toward a central portion of the through hole, While passing through the hole, the biotissue can be scratched and torn by the protrusion, which can be reduced in size.
상기 돌출부는 상기 관통 구멍의 중심부를 향해 폭이 좁아지며 첨단을 형성할 수 있다.The projecting portion is narrowed toward the central portion of the through hole and can form a peak.
상기 복수 개의 테두리들은 돌출부를 기준으로 양 측에 형성되는 선형부들을 각각 포함할 수 있다. 다시 말하면, 돌출부는 그 테두리의 중심부에 형성될 수 있다.The plurality of rims may include linear portions formed on both sides with respect to the protruding portion. In other words, the protrusion can be formed at the center of the rim.
상기 플레이트에 대해 각도를 이루며 상기 플레이트를 기준으로 제1방향으로 돌출하는 제1그룹의 돌출부들; 및 상기 플레이트에 대해 각도를 이루며 상기 플레이트를 기준으로 상기 제1방향과 다른 제2방향으로 돌출하는 제2그룹의 돌출부들을 포함할 수 있다. 다시 말하면, 제1그룹의 돌출부들 및 제2그룹의 돌출부들은 다양한 방식으로 복수 개의 테두리들에 형성될 수 있다. 비제한적인 예에서, 제1그룹의 돌출부들은 복수 개의 테두리들 중 일부의 테두리들을 따라 연속하여 나타나고, 제2그룹의 돌출부들은 복수 개의 테두리들 중 나머지 테두리들을 따라 연속하여 나타날 수 있다.A first group of protrusions angled with respect to the plate and projecting in a first direction with respect to the plate; And a second group of protrusions projecting in a second direction different from the first direction at an angle relative to the plate and with respect to the plate. In other words, the first group of protrusions and the second group of protrusions can be formed in a plurality of rims in various ways. In a non-limiting example, the protrusions of the first group appear continuously along the rims of some of the plurality of rims, and the protrusions of the second group may appear consecutively along the remaining rims of the plurality of rims.
상기 제1그룹의 돌출부들 및 상기 제2그룹의 돌출부들은 상기 복수 개의 테두리들을 따라 서로 다른 방향으로 교번할 수 있다.The first group of protrusions and the second group of protrusions may alternate in different directions along the plurality of rims.
상기 제1그룹의 돌출부들의 각각의 연장선 및 제2그룹의 돌출부들의 각각의 연장선은 서로 만나지도 않고 서로 평행하지도 않을 수 있다. 다시 말하면, 상기 제1방향의 연장선 및 제2방향의 연장선은 꼬인 위치에 있을 수 있다.The extension of each of the protrusions of the first group and the extension of each of the protrusions of the second group may not be in contact with each other nor may they be parallel to each other. In other words, the extension of the first direction and the extension of the second direction may be in a twisted position.
상기 생체조직 미세화 장치는 상기 복수 개의 테두리들의 각각으로부터 상기 관통 구멍의 중심부를 향해 연장하는 연장부; 및 상기 연장부의 말단에 형성되며 생체조직을 긁고 찢도록 구성된 첨단부를 더 포함할 수 있다.Wherein the biomedical tissue fining device comprises: an extension extending from each of the plurality of rims toward a central portion of the through hole; And a distal end portion formed at an end of the extended portion and configured to scratch and tear the living tissue.
상기 생체조직 미세화 장치는 상기 첨단부를 기준으로 상기 연장부의 반대편에 형성되고 상기 관통 구멍의 중심부를 향해 연장하는 추가적인 연장부를 더 포함할 수 있다.The living tissue microfabrication apparatus may further include an additional extension formed on the opposite side of the extended portion with respect to the proximal end portion and extending toward the central portion of the through hole.
상기 돌출부의 돌출 방향은 상기 관통 구멍을 통과하는 생체조직의 이동 방향에 대해 평행하지 않을 수 있다.The projecting direction of the projecting portion may not be parallel to the moving direction of the living tissue passing through the through hole.
일 실시예에 따른 생체조직 미세화 장치는 제1플레이트와, 상기 제1플레이트의 전후방을 관통하여 상기 제1플레이트의 복수 개의 제1테두리들에 의해 규정된 제1관통 구멍과, 상기 제1관통 구멍의 중심부를 향해 돌출하는 제1돌출부를 포함하는 제1스크린; 및 상기 제1플레이트에 적층(laminate)되는 제2플레이트와, 상기 제2플레이트의 전후방을 관통하며 상기 제2플레이트의 복수 개의 제2테두리들에 의해 규정된 제2관통 구멍과, 상기 제2관통 구멍의 중심부를 향해 돌출하는 제2돌출부를 포함하는 제2스크린을 포함하고, 상기 제1관통 구멍과 상기 제2관통 구멍은 중첩되고, 상기 제1관통 구멍의 크기가 상기 제2관통 구멍의 크기보다 클 수 있다.The apparatus includes a first plate, a first through-hole passing through the front and rear of the first plate and defined by a plurality of first rims of the first plate, A first projection including a first projection projecting toward a center of the first screen; And a second through hole penetrating the front and rear sides of the second plate and defined by a plurality of second rims of the second plate and a second through hole penetrating the front and rear sides of the second plate and defined by a plurality of second rims of the second plate, Wherein the first through hole and the second through hole overlap each other, and the size of the first through hole is larger than the size of the second through hole .
상기 제1돌출부 및 상기 제2돌출부의 돌출 방향은 상기 제1관통 구멍과 상기 제2관통 구멍을 순차적으로 통과하는 생체조직의 이동 방향에 대해 평행하지 않고 서로 같거나 교차할 수 있다.The projecting direction of the first projecting portion and the second projecting portion may be the same or intersect with each other without being parallel to the moving direction of the living tissue sequentially passing through the first through hole and the second through hole.
일 실시예에 따른 생체조직 미세화 장치는 긁음(scratch) 또는 찢음(tear) 방식으로 생체조직의 크기를 감소시킬 수 있다.The biomedical tissue refining apparatus according to one embodiment can reduce the size of a living tissue by a scratch or a tear method.
일 실시예에 따른 생체조직 미세화 장치는 생체조직의 크기를 점진적으로 감소시킬 수 있다.The biomedical tissue refinement apparatus according to an embodiment can gradually reduce the size of a living tissue.
일 실시예에 따른 생체조직 미세화 장치의 효과는 이상에서 언급된 것들에 한정되지 않으며, 언급되지 아니한 다른 효과들은 아래의 기재로부터 통상의 기술자에게 명확하게 이해될 수 있을 것이다.The effects of the biomedical tissue refining apparatus according to one embodiment are not limited to those mentioned above, and other effects not mentioned can be clearly understood by those skilled in the art from the following description.
도 1은 일 실시예에 따른 생체조직 미세화 장치를 개략적으로 나타낸 사시도이다.FIG. 1 is a perspective view schematically showing a biomedical tissue refinement apparatus according to an embodiment of the present invention.
도 2는 일 실시예에 따른 생체조직 미세화 장치를 개략적으로 나타낸 분해 측면도이다.2 is an exploded side view schematically showing an apparatus for biomedical tissue refinement according to an embodiment.
도 3은 일 실시예에 따른 생체조직 미세화 장치의 일부를 개략적으로 나타낸 횡단면도이다.3 is a cross-sectional view schematically showing a part of a biomedical tissue refinement apparatus according to an embodiment.
도 4는 일 실시예에 따른 스크린을 개략적으로 나타낸 평면도이다.4 is a plan view schematically illustrating a screen according to an embodiment.
도 5는 도 4의 A부분의 일 예시적 형태를 확대한 확대도이다.FIG. 5 is an enlarged view of an exemplary embodiment of the portion A of FIG. 4; FIG.
도 6은 도 4의 A부분의 또 다른 예시적 형태를 확대한 확대도이다.FIG. 6 is an enlarged view of another exemplary embodiment of FIG. 4A.
도 7은 일 실시예에 따른 스크린을 개략적으로 나타낸 측면도이다.7 is a side view schematically illustrating a screen according to one embodiment.
도 8은 도 7의 B부분의 일 예시적 형태를 확대한 확대도이다.FIG. 8 is an enlarged view of an exemplary embodiment of FIG. 7B.
도 9는 일 실시예에 따른 스크린 및 그 일부의 일 예시적 형태의 단면을 확대한 도면이다.9 is an enlarged cross-sectional view of one exemplary embodiment of a screen and a portion thereof in accordance with one embodiment.
도 10은 일 실시예에 따른 스크린 및 그 일부의 또 다른 예시적 형태의 단면을 확대한 도면이다.10 is an enlarged cross-sectional view of another exemplary embodiment of a screen and a portion thereof in accordance with an embodiment.
도 11은 일 실시예에 따른 적층된 복수 개의 스크린들의 일 예를 개략적으로 나타낸 평면도이다.11 is a plan view schematically illustrating an example of a plurality of stacked screens according to an embodiment.
도 12는 도 11의 12-12에서 바라본 단면도이다.12 is a sectional view taken along line 12-12 in Fig.
도 13은 일 실시예에 따른 적층된 복수 개의 스크린들의 또 다른 예를 개략적으로 나타낸 평면도이다.13 is a plan view schematically illustrating another example of a plurality of stacked screens according to an embodiment.
도 14는 도 13의 14-14에서 바라본 단면도이다.14 is a sectional view taken along line 14-14 of Fig.
이하, 실시예들을 예시적인 도면을 통해 상세하게 설명한다. 각 도면의 구성요소들에 참조부호를 부가함에 있어서, 동일한 구성요소들에 대해서는 비록 다른 도면상에 표시되더라도 가능한 한 동일한 부호를 가지도록 하고 있음에 유의해야 한다. 또한, 실시예를 설명함에 있어, 관련된 공지 구성 또는 기능에 대한 구체적인 설명이 실시예에 대한 이해를 방해한다고 판단되는 경우에는 그 상세한 설명은 생략한다.Hereinafter, embodiments will be described in detail with reference to exemplary drawings. It should be noted that, in adding reference numerals to the constituent elements of the drawings, the same constituent elements are denoted by the same reference numerals even though they are shown in different drawings. In the following description of the embodiments, detailed description of known functions and configurations incorporated herein will be omitted when it may make the best of an understanding clear.
또한, 실시예의 구성 요소를 설명하는 데 있어서, 제 1, 제 2, A, B, (a), (b) 등의 용어를 사용할 수 있다. 이러한 용어는 그 구성 요소를 다른 구성 요소와 구별하기 위한 것일 뿐, 그 용어에 의해 해당 구성 요소의 본질이나 차례 또는 순서 등이 한정되지 않는다. 어떤 구성 요소가 다른 구성요소에 "연결", "결합" 또는 "접속"된다고 기재된 경우, 그 구성 요소는 그 다른 구성요소에 직접적으로 연결되거나 접속될 수 있지만, 각 구성 요소 사이에 또 다른 구성 요소가 "연결", "결합" 또는 "접속"될 수도 있다고 이해되어야 할 것이다.In describing the components of the embodiment, terms such as first, second, A, B, (a), and (b) may be used. These terms are intended to distinguish the constituent elements from other constituent elements, and the terms do not limit the nature, order or order of the constituent elements. When a component is described as being "connected", "coupled", or "connected" to another component, the component may be directly connected or connected to the other component, Quot; may be " connected, " " coupled, " or " connected. &Quot;
어느 하나의 실시예에 포함된 구성요소와, 공통적인 기능을 포함하는 구성요소는, 다른 실시예에서 동일한 명칭을 사용하여 설명하기로 한다. 반대되는 기재가 없는 이상, 어느 하나의 실시예에 기재한 설명은 다른 실시예에도 적용될 수 있으며, 중복되는 범위에서 구체적인 설명은 생략하기로 한다.The components included in any one embodiment and the components including common functions will be described using the same names in other embodiments. Unless otherwise stated, the description of any one embodiment may be applied to other embodiments, and a detailed description thereof will be omitted in the overlapping scope.
도 1은 일 실시예에 따른 생체조직 미세화 장치를 개략적으로 나타낸 사시도이고, 도 2는 일 실시예에 따른 생체조직 미세화 장치를 개략적으로 나타낸 분해 측면도이고, 도 3은 일 실시예에 따른 생체조직 미세화 장치의 일부를 개략적으로 나타낸 횡단면도이다.FIG. 1 is a perspective view schematically showing a biomedical tissue refinement apparatus according to an embodiment, FIG. 2 is an exploded side view schematically showing a biomedical tissue refinement apparatus according to an embodiment, FIG. 3 is a cross- Figure 2 is a cross-sectional view schematically showing a part of the device.
도 1 및 도 2를 참조하면, 일 실시예에 따른 생체조직 미세화 장치(1)는 원하는 크기의 생체조직을 획득하기 위해 생체조직과의 접촉을 최대화하고 생체조직을 미세화하도록 구성된다. 예를 들어, 생체조직은 지방조직을 포함할 수 있다. 생체조직은 사람, 동물 등 생물체와 같은 대상체로부터 흡인 또는 절개와 같은 방식으로 획득될 수 있다.Referring to FIGS. 1 and 2, the biomedical tissue refinement apparatus 1 according to one embodiment is configured to maximize contact with a living tissue and to miniaturize a living tissue to obtain a biomolecule of a desired size. For example, the biological tissue may include adipose tissue. The living tissue can be obtained from a subject such as a human being, an animal, or the like, in a manner such as suction or incision.
생체조직 미세화 장치(1)는 스크린(10), 밀봉 부재(12), 전방 커버(14) 및 후방 커버(16)를 포함할 수 있다.The biomedical tissue refinement apparatus 1 may include a screen 10, a sealing member 12, a front cover 14, and a rear cover 16.
스크린(10)은 생체조직의 크기를 감소시키도록 구성된다. 예를 들어, 스크린(10)은 디스크 형상을 구비할 수 있다. 덩어리 형태의 생체조직이 스크린(10)을 통과하는 동안, 스크린(10)은 덩어리 형태의 생체조직을 긁거나 찢도록 구성될 수 있다.The screen 10 is configured to reduce the size of the living tissue. For example, the screen 10 may have a disk shape. While the lumpy living tissue passes through the screen 10, the screen 10 may be configured to scratch or tear the lumpy living tissue.
밀봉 부재(12)는 스크린(10)의 외부를 감싸도록 구성된다. 밀봉 부재(12)는 스크린(10)과 전방 커버(14) 및 후방 커버(16) 사이의 밀봉을 형성할 수 있다. 밀봉 부재(12)는 고리 형상을 구비할 수 있다. 예를 들어, 밀봉 부재(12)는 고무 재질로 형성될 수 있다.The sealing member 12 is configured to surround the outside of the screen 10. The sealing member 12 may form a seal between the screen 10 and the front cover 14 and the rear cover 16. [ The sealing member 12 may have an annular shape. For example, the sealing member 12 may be formed of a rubber material.
전방 커버(14) 및 후방 커버(16)는 각각 스크린(10) 및 밀봉 부재(12)를 수용하도록 구성된다. 전방 커버(14) 및 후방 커버(16)는 서로 결합될 수 있다. 예를 들어, 전방 커버(14) 및 후방 커버(16)는 회전 결합될 수 있다.The front cover 14 and the rear cover 16 are configured to receive the screen 10 and the sealing member 12, respectively. The front cover 14 and the rear cover 16 can be coupled to each other. For example, the front cover 14 and the rear cover 16 may be rotationally coupled.
전방 커버(14) 및 후방 커버(16)는 각각 생체조직이 유동하는 유입구 및 유출구를 구비할 수 있으며, 유입구와 유출구를 연결하는 통로가 전방 커버(14) 및 후방 커버(16) 사이에 형성될 수 있다. 생체조직 또는 이의 덩어리는 유입구를 통해 전방 커버(14)의 내부로 진입하고, 통로를 따라 스크린(10)을 통과한 후, 후방 커버(16)의 내부로부터 유출구를 통해 외부로 빠져나갈 수 있다.The front cover 14 and the rear cover 16 may each have an inlet port and an outlet port through which the living tissue flows and a passage connecting the inlet port and the outlet port is formed between the front cover 14 and the rear cover 16 . The biotissue or mass thereof can enter the interior of the front cover 14 through the inlet and pass out of the interior of the rear cover 16 through the outlet after passing through the screen 10 along the passageway.
도 4는 일 실시예에 따른 스크린을 개략적으로 나타낸 평면도이다.4 is a plan view schematically illustrating a screen according to an embodiment.
도 4를 참조하면, 스크린(10)은 플레이트(110) 및 적어도 하나 이상의 관통 구멍(120)을 포함할 수 있다.Referring to FIG. 4, the screen 10 may include a plate 110 and at least one through hole 120.
플레이트(110)는 디스크 형상을 구비할 수 있다. 예를 들어, 플레이트(110)는 원형일 수 있다. 플레이트(110)는 생체조직의 오염을 방지하기에 적합한 물질로 형성될 수 있다.The plate 110 may have a disc shape. For example, the plate 110 may be circular. The plate 110 may be formed of a material suitable for preventing contamination of living tissue.
관통 구멍(120)은 생체조직과의 접촉을 최대화하고 생체조직을 미세화하도록 구성된다. 관통 구멍(120)은 플레이트(110)의 전후방을 관통하며 플레이트(110)의 복수 개의 테두리들에 의해 규정된다. 관통 구멍(120)을 규정하는 플레이트(110)의 복수 개의 테두리들은 불규칙적인 치수를 가질 수 있다.The through hole 120 is configured to maximize the contact with the living tissue and make the living tissue finer. The through holes 120 pass through the front and rear of the plate 110 and are defined by a plurality of rims of the plate 110. The plurality of rims of the plate 110 defining the through holes 120 may have irregular dimensions.
플레이트(110)는 플레이트(110)에 관통 구멍(120)이 형성된 위치가 바뀌거나 관통 구멍(120)의 형상이 외력에 의해 변형되지 않도록 전체적으로 플레이트 몰딩(plate molding)될 수 있다.The plate 110 may be entirely plate molded so that the position of the through hole 120 is changed in the plate 110 or the shape of the through hole 120 is not deformed by an external force.
도 5는 도 4의 A부분의 일 예시적 형태를 확대한 확대도이다.FIG. 5 is an enlarged view of an exemplary embodiment of the portion A of FIG. 4; FIG.
도 5를 참조하면, 관통 구멍(120)을 규정하는 복수 개의 테두리(111)들은 관통 구멍(120)이 실질적으로 사각형을 가지도록 관통 구멍(120)을 규정할 수 있다.Referring to FIG. 5, a plurality of rims 111 defining the through holes 120 may define the through holes 120 so that the through holes 120 have a substantially rectangular shape.
복수 개의 테두리(111)들은 각각 돌출부(112)를 포함할 수 있다. 돌출부(112)는 관통 구멍(120)의 중심부를 향해 돌출하도록 구성된다. 생체조직이 관통 구멍(120)을 통과할 때, 돌출부(112)는 생체조직을 긁거나 찢도록 구성된다. 한편, 생체조직을 이루는 성분 중 관통 구멍(120)보다 큰 섬유질(fiber)은 관통 구멍(120)을 통과하지 못할 수 있다.The plurality of rims 111 may each include a protrusion 112. The protrusion 112 is configured to protrude toward the center of the through hole 120. As the biotissue passes through the through hole 120, the protrusion 112 is configured to scratch or tear the biotissue. On the other hand, fibers larger than the through-holes 120 may not pass through the through-holes 120.
돌출부(112)의 돌출 방향은 관통 구멍(120)을 통과하는 생체조직의 이동 방향에 대해 평행하지 않을 수 있다. 일 예에서, 돌출부(112)의 돌출 방향은 플레이트(110)의 접선 방향과 평행하거나, 플레이트(110)의 접선 방향에 대해 설정 각도를 이룰 수 있다. 여기서, 돌출부(112)가 플레이트(110)에 대해 이루는 각도는 예각(acute angle), 둔각(obtuse angle) 또는 우각(reflex angle)으로 설정될 수 있다.The protruding direction of the protruding portion 112 may not be parallel to the moving direction of the living tissue passing through the through hole 120. In one example, the projecting direction of the protrusion 112 may be parallel to the tangential direction of the plate 110, or may be a set angle with respect to the tangential direction of the plate 110. Here, the angle formed by the protrusion 112 with respect to the plate 110 may be set to an acute angle, an obtuse angle, or a reflex angle.
돌출부(112)는 관통 구멍(120)의 중심부를 향해 그 폭이 좁아지며 첨단(1121)을 형성할 수 있다. 예를 들어, 돌출부(112)는 삼각형의 형태를 구비할 수 있다.The projecting portion 112 is narrowed toward the central portion of the through hole 120 and can form a tip 1121. For example, the protrusion 112 may have the shape of a triangle.
복수 개의 테두리(111)들은 돌출부(112)를 기준으로 양 측에 형성되는 선형부들(114, 116)을 포함할 수 있다. 다시 말하면, 돌출부(112)는 그 테두리(111)의 중심부에 위치할 수 있다. 일 예에서, 선형부들(114, 116)은 돌출부(112)가 테두리(111)의 중심에 있도록 그 길이가 동일할 수 있다. 이 경우, 어느 하나의 테두리(111)의 돌출부(112)와 이와 마주보는 테두리의 돌출부는 관통 구멍(120)의 중심부를 향해 서로 마주볼 수 있다. 도시되지 않은 예에서, 선형부들(114, 116)의 길이는 서로 다르게 설정될 수도 있다. 선형부들(114, 116)의 길이는 돌출부(112)의 크기를 고려하여 조절될 수 있다.The plurality of rims 111 may include linear portions 114 and 116 formed on both sides with respect to the protruding portion 112. In other words, the protrusion 112 may be located at the center of the rim 111 thereof. In one example, the linear portions 114, 116 may be the same length so that the protrusions 112 are at the center of the rim 111. In this case, the protrusions 112 of one of the rims 111 and the protrusions of the opposite rims may face each other toward the center of the through hole 120. In the example not shown, the lengths of the linear portions 114 and 116 may be set differently. The length of the linear portions 114, 116 can be adjusted in consideration of the size of the protrusion 112.
이상과 같은 복수 개의 테두리(111)들에 의해 규정된 관통 구멍(120)의 불규칙적인 형상, 복수 개의 테두리(111)들의 날카로운 단면 등에 의해, 관통 구멍(120)을 통과하는 생체조직에 압력이 가해지며 덩어리 형태의 생체조직이 긁히거나 찢어질 수 있다.The irregular shape of the through hole 120 defined by the plurality of rims 111 as described above and the sharp cross section of the plurality of rims 111 cause a pressure applied to the living tissue passing through the through hole 120 And the lumpy biotissue may be scratched or torn.
도 6은 도 4의 A부분의 또 다른 예시적 형태를 확대한 확대도이다.FIG. 6 is an enlarged view of another exemplary embodiment of FIG. 4A.
도 6을 참조하면, 관통 구멍(120)을 규정하는 복수 개의 테두리(111')들은 관통 구멍(120)이 실질적으로 4개 이상의 코너(corner)들을 가지는 다각형을 가지도록 관통 구멍(120)을 규정할 수 있다. 복수 개의 테두리(111')들은 관통 구멍(120)의 중심부를 향해 돌출하도록 구성된 돌출부(112')를 포함할 수 있다. 돌출부(112')는 관통 구멍(120)의 중심부를 향해 그 폭이 좁아지며 첨단(1121)을 형성할 수 있다.Referring to FIG. 6, a plurality of rims 111 'defining the through holes 120 may be defined by defining the through holes 120 so that the through holes 120 have polygons having substantially four or more corners. can do. The plurality of rims 111 'may include a protrusion 112' configured to protrude toward the center of the through hole 120. The protrusion 112 'is narrowed toward the central portion of the through hole 120 and can form a tip 1121.
이 실시예에서, 복수 개의 테두리(111')들은 돌출부(112')를 기준으로 양 측에 형성되는 선형부들이 존재하지 않거나, 존재하더라도 그 길이가 돌출부(112')의 크기에 비해 상대적으로 매우 짧을 수 있다. 다시 말하면, 복수 개의 돌출부(112')들은 복수 개의 테두리(111')들을 따라 서로 인접하게 이어질 수 있다.In this embodiment, the plurality of rims 111 'are formed such that the linear portions formed on both sides with respect to the protruding portion 112' are not present, or even if they are present, the length is relatively large compared to the size of the protruding portion 112 ' It can be short. In other words, the plurality of protrusions 112 'may be adjacent to each other along the plurality of rims 111'.
도 7은 일 실시예에 따른 스크린을 개략적으로 나타낸 측면도이고, 도 8은 도 7의 B부분의 일 예시적 형태를 확대한 확대도이다.FIG. 7 is a side view schematically illustrating a screen according to an embodiment, and FIG. 8 is an enlarged view of an exemplary embodiment of FIG. 7B.
도 7 및 도 8을 참조하면, 일 실시예에 따른 스크린(20)은 플레이트(210) 및 관통 구멍(220)을 포함할 수 있다. 이 실시예에서, 플레이트(210)의 복수 개의 테두리들(211a, 211b)의 돌출부들(212a, 212b)은 플레이트(210)의 접선 방향에 대해 설정 각도를 이룰 수 있다. 이에 따라, 스크린(20)의 전후방으로 관통 구멍(220)을 통과하는 덩어리 형태의 생체조직(BM)의 이동 방향은 돌출부들(212a, 212b)의 돌출 방향에 대해 평행하지 않을 수 있다. 다시 말하면, 돌출부들(212a, 212b)은 생체조직(BM)을 슬라이스(slice)하기 보다는 긁음(scratch) 또는 찢음(tear) 방식으로 생체조직(BM)을 미세화하도록 구성될 수 있다.7 and 8, a screen 20 according to an embodiment may include a plate 210 and a through hole 220. [ The protrusions 212a and 212b of the plurality of rims 211a and 211b of the plate 210 may establish a set angle with respect to the tangential direction of the plate 210. In this embodiment, The moving direction of the lumen-like living tissue BM passing through the through hole 220 at the front and rear of the screen 20 may not be parallel to the protruding direction of the protrusions 212a and 212b. In other words, the protrusions 212a and 212b may be configured to refine the living tissue BM by scratching or tearing the living tissue BM rather than slicing the living tissue BM.
복수 개의 테두리들(211a, 211b)은 플레이트(210)의 접선 방향에 대해 적어도 하나 이상의 방향성을 가지는 돌출부(212a, 212b)를 포함할 수 있다. 다시 말하면, 복수 개의 돌출부(212a, 212b)들은 그 돌출 방향에 따라 복수 개의 그룹들로 나뉠 수 있다. 예를 들어, 복수 개의 돌출부(212a, 212b)들은 플레이트(210)에 대해 각도를 이루며 플레이트(210)를 기준으로 제1방향으로 돌출하는 제1그룹의 돌출부들 및 플레이트(210)에 대해 각도를 이루며 플레이트(210)를 기준으로 제2방향으로 돌출하는 제2그룹의 돌출부들로 나뉠 수 있다.The plurality of rims 211a and 211b may include protrusions 212a and 212b having at least one directionality with respect to the tangential direction of the plate 210. [ In other words, the plurality of protrusions 212a and 212b may be divided into a plurality of groups according to their protruding directions. For example, the plurality of protrusions 212a, 212b may be angled relative to the plate 210 to define a first group of protrusions protruding in a first direction with respect to the plate 210, And a second group of protrusions protruding in a second direction with respect to the plate 210.
여기서, 제1방향과 제2방향은 서로 다를 수 있다. 제1방향과 제2방향이 서로 다르다는 것은 서로 평행하지 않다는 것을 의미한다. 예를 들어, 제1방향의 돌출부(212a)는 도 8을 기준으로 플레이트(210)의 좌측으로 돌출하고, 제2방향의 돌출부(212b)는 도 8을 기준으로 플레이트(210)의 우측으로 돌출할 수 있다.Here, the first direction and the second direction may be different from each other. The fact that the first direction and the second direction are different from each other means that they are not parallel to each other. For example, the protrusion 212a in the first direction protrudes to the left of the plate 210 with reference to Fig. 8, and the protrusion 212b in the second direction protrudes to the right of the plate 210 with reference to Fig. can do.
일 예에서, 제1그룹의 돌출부(212a) 및 제2그룹의 돌출부(212b)는 서로 인접할 수 있다. 바람직한 예에서, 제1그룹의 돌출부(212a) 및 제2그룹의 돌출부(212b)는 서로 교번할 수 있다.In one example, the first group of protrusions 212a and the second group of protrusions 212b may be adjacent to each other. In a preferred example, the first group of protrusions 212a and the second group of protrusions 212b may alternate with each other.
도시되지 않은 예에서, 제1그룹의 복수 개의 돌출부(212a)들 및 제2그룹의 복수 개의 돌출부(212b)들은 무리를 이루며 각 그룹 내에서 인접할 수 있다. 이 경우, 제1그룹의 돌출부(212a)들은 복수 개의 테두리들(211a, 211b) 중 일부의 테두리들에 연속적으로 형성되고, 제2그룹의 돌출부(212b)들은 나머지 테두리들에 연속적으로 형성될 수 있다.In the example not shown, the plurality of protrusions 212a of the first group and the plurality of protrusions 212b of the second group are grouped and may be adjacent within each group. In this case, the first group of protrusions 212a may be continuously formed on the rims of some of the plurality of rims 211a and 211b, and the second group of protrusions 212b may be continuously formed on the remaining rims have.
이상과 같이, 제1그룹의 돌출부(212a) 및 제2그룹의 돌출부(212b)의 배치 방식은 다양할 수 있다.As described above, the arrangements of the first group of protrusions 212a and the second group of protrusions 212b may be various.
일 실시예에서, 제1그룹의 돌출부(212a)의 연장선 및 제2그룹의 돌출부(212b)의 연장선은 서로 만나지도 않고 서로 평행하지도 않을 수 있다. 다시 말하면, 제1그룹의 돌출부(212a)의 연장선 및 제2그룹의 돌출부(212b)의 연장선은 3차원 공간 상에서 서로 꼬인 위치(skew position)에 있을 수 있다. 예를 들어, 제1그룹의 돌출부(212a)를 포함하는 테두리(211a)와 제2그룹의 돌출부(212b)를 포함하는 테두리(211b)가 만나는 꼭지점(vertex)을 원점으로 하고, 제1그룹의 돌출부(212a)가 돌출하는 방향인 제1방향을 x축으로, 제2그룹의 돌출부(212b)가 돌출하는 방향인 제2방향을 y축으로, 제1방향과 제2방향의 외적을 z축으로 설정하면, 제1그룹의 돌출부(212a)를 포함하는 테두리(212a)로부터 그 돌출부(212a)의 첨단까지의 벡터는 (1, 0, -1)이고, 제2그룹의 돌출부(212b)를 포함하는 테두리(212b)로부터 그 돌출부(212b)의 첨단까지의 벡터는 (-1, 0, 1)일 수 있다.In one embodiment, the extension of the first group of protrusions 212a and the extension of the second group of protrusions 212b may or may not be parallel to each other. In other words, the extension of the first group of protrusions 212a and the extension of the second group of protrusions 212b may be at a skew position in the three-dimensional space. For example, the vertex at which the rim 211a including the first group of protrusions 212a and the rim 211b including the second group of protrusions 212b meet as the origin, The first direction being the direction in which the protrusions 212a protrude is defined as the x axis, the second direction in which the second group of protrusions 212b protrude is defined as the y axis, the outward in the first direction and the second direction is defined as the z axis The vector from the rim 212a including the first group of protrusions 212a to the tip of the protrusion 212a is (1, 0, -1), and the second group of protrusions 212b The vector from the containing edge 212b to the tip of the protrusion 212b may be (-1, 0, 1).
도 9는 일 실시예에 따른 스크린 및 그 일부의 일 예시적 형태의 단면을 확대한 도면이다.9 is an enlarged cross-sectional view of one exemplary embodiment of a screen and a portion thereof in accordance with one embodiment.
도 9를 참조하면, 일 실시예에 따른 스크린(30)은 플레이트(310) 및 관통 구멍(320)을 포함할 수 있다. 이 실시예에서, 관통 구멍(320)을 규정하는 플레이트(310)의 복수 개의 테두리(311)들에는 복수 개의 테두리(311)들의 전체에 걸쳐 날카로운 단면이 형성될 수 있다. 예를 들어, 스크린(30)은 복수 개의 테두리(311)들의 각각으로부터 관통 구멍(320)의 중심부를 향해 연장하는 연장부(314) 및 연장부(314)의 말단에 형성되며 생체조직을 긁고 찢도록 구성된 첨단부(316)를 포함할 수 있다.Referring to FIG. 9, a screen 30 according to one embodiment may include a plate 310 and a through hole 320. In this embodiment, a plurality of rims 311 of the plate 310 defining the through holes 320 may be formed with a sharp cross section over the entire plurality of rims 311. For example, the screen 30 is formed at the distal end of the extending portion 314 and the extending portion 314 extending from each of the plurality of rims 311 toward the central portion of the through hole 320, (Not shown).
연장부(314)는 임의의 적합한 형상을 구비할 수 있다. 일 예에서, 연장부(314)는 플레이트(310)의 평면을 기준으로 경사지게 형성될 수 있다. 또 다른 예에서, 연장부(314)는 플레이트(310)를 기준으로 외측으로 만곡된 형태를 가질 수 있다.The extension 314 may have any suitable shape. In one example, the extension 314 may be formed obliquely with respect to the plane of the plate 310. In another example, the extension 314 may have an outwardly curved shape with respect to the plate 310.
도 10은 일 실시예에 따른 스크린 및 그 일부의 또 다른 예시적 형태의 단면을 확대한 도면이다.10 is an enlarged cross-sectional view of another exemplary embodiment of a screen and a portion thereof in accordance with an embodiment.
도 10을 참조하면, 일 실시예에 따른 스크린(40)은 플레이트(410) 및 관통 구멍(420)을 포함할 수 있다. 이 실시예에서, 관통 구멍(420)을 규정하는 복수 개의 테두리(411)들에는 첨단부(416)를 기준으로 양 측에 복수 개의 연장부들(414, 415)이 형성될 수 있다. 일 예에서, 복수 개의 연장부들(414, 415)은 플레이트(410)에 대해 각각의 설정 각도로 경사지게 복수 개의 테두리(411)들에 형성될 수 있다. 바람직한 예에서, 플레이트(410)에 대한 복수 개의 연장부들(414, 415)의 경사 각도는 실질적으로 동일할 수 있다.Referring to FIG. 10, a screen 40 according to one embodiment may include a plate 410 and a through hole 420. In this embodiment, a plurality of extensions 414 and 415 may be formed on both sides of the rim 411 defining the through hole 420 with respect to the tip 416. [ In one example, the plurality of extensions 414, 415 may be formed in a plurality of rims 411 at an angle to the plate 410 at respective set angles. In a preferred example, the inclination angles of the plurality of extensions 414, 415 relative to the plate 410 may be substantially the same.
추가적인 실시예에서, 복수 개의 연장부들(414, 415)들은 플레이트(310)를 기준으로 외측으로 만곡된 형태를 가질 수 있다. 이 경우, 복수 개의 연장부들(414, 415)들의 만곡 방향은 서로 다를 수 있다. 일 예에서, 첨단부(416)가 복수 개의 연장부들(414, 415)들 사이의 중심에 위치하도록 복수 개의 연장부들(414, 415)들의 곡률 반경은 실질적으로 동일할 수 있다.In a further embodiment, the plurality of extensions 414, 415 may have an outwardly curved shape with respect to the plate 310. In this case, the curved directions of the plurality of extending portions 414 and 415 may be different from each other. In one example, the radius of curvature of the plurality of extensions 414, 415 may be substantially the same so that the tip 416 is centered between the plurality of extensions 414, 415.
도 11은 일 실시예에 따른 적층된 복수 개의 스크린들의 일 예를 개략적으로 나타낸 평면도이고, 도 12는 도 11의 12-12에서 바라본 단면도이다.FIG. 11 is a plan view schematically showing an example of a plurality of stacked screens according to an embodiment, and FIG. 12 is a sectional view taken along line 12-12 in FIG.
도 11 및 도 12를 참조하면, 일 실시예에 따른 생체조직 미세화 장치(5)는 복수 개의 스크린들(50a, 50b, 50c)이 차례로 적층(laminate)되도록 구성된다. 복수 개의 스크린들(50a, 50b, 50c)은 각각 플레이트(510a, 510b, 510c) 및 복수 개의 테두리들(511a, 511b, 511c)에 의해 규정되는 관통 구멍(520a, 520b, 520c)을 포함할 수 있다. 복수 개의 스크린들(50a, 50b, 50c)은 각각의 관통 구멍(520a, 520b, 520c)을 향해 돌출하는 돌출부(512a, 512b, 512c)를 포함할 수 있다. 앞서, 도 9를 참조하여 설명한 바와 같이, 복수 개의 테두리들(511a, 511b, 511c)에는 하나의 연장부와 첨단부가 형성될 수 있다.Referring to FIGS. 11 and 12, the biomedical tissue refinement apparatus 5 according to an embodiment is configured such that a plurality of screens 50a, 50b, and 50c are sequentially laminated. The plurality of screens 50a, 50b and 50c may include through holes 520a, 520b and 520c defined by plates 510a, 510b and 510c and a plurality of rims 511a, 511b and 511c, respectively. have. The plurality of screens 50a, 50b and 50c may include projections 512a, 512b and 512c projecting toward the respective through holes 520a, 520b and 520c. As described above with reference to FIG. 9, one extended portion and a leading end portion may be formed on the plurality of frames 511a, 511b, and 511c.
이 실시예에서, 차례로 적층되는 복수 개의 스크린들(50a, 50b, 50c)의 각각의 관통 구멍(520a, 520b, 520c)은 (도 12를 기준으로 위로부터 아래로) 그 크기가 감소하는 방향으로 서로 중첩될 수 있다. 이에 따라, 복수 개의 스크린들(50a, 50b, 50c)을 통과하는 생체조직은 복수 개의 테두리들(511a, 511b, 511c)에 형성된 날카로운 단면 및/또는 그 돌출부(512a, 512b, 512c)의 형상에 의해 압력을 받으며 점진적으로 미세화 될 수 있다.In this embodiment, the through- holes 520a, 520b, and 520c of the plurality of screens 50a, 50b, and 50c that are stacked one after another in the direction of decreasing the size (from top to bottom with reference to FIG. 12) They can overlap each other. Accordingly, the living tissue passing through the plurality of screens 50a, 50b, and 50c may have a sharp cross section formed on the plurality of rims 511a, 511b, and 511c and / or a shape of the protrusions 512a, 512b, and 512c And can be gradually refined.
도 13은 일 실시예에 따른 적층된 복수 개의 스크린들의 또 다른 예를 개략적으로 나타낸 평면도이고, 도 14는 도 13의 14-14에서 바라본 단면도이다.FIG. 13 is a plan view schematically showing another example of a plurality of stacked screens according to an embodiment, and FIG. 14 is a sectional view taken along line 14-14 of FIG.
도 13 및 도 14를 참조하면, 일 실시예에 따른 생체조직 미세화 장치(6)는 복수 개의 스크린들(60a, 60b, 60c)을 포함할 수 있다. 복수 개의 스크린들(60a, 60b, 60c)은 각각 플레이트(610a, 610b, 610c), 복수 개의 테두리들(611a, 611b, 611c)에 의해 규정되는 관통 구멍(620a, 620b, 620c) 및 돌출부(612a, 612b, 612c)를 포함할 수 있다. 앞서, 도 10을 참조하여 설명한 바와 같이, 복수 개의 테두리들(611a, 611b, 611c)에는 하나의 첨단부를 기준으로 양 측에 복수 개의 연장부들이 형성될 수 있다.Referring to FIGS. 13 and 14, the biomedical tissue refinement apparatus 6 according to an embodiment may include a plurality of screens 60a, 60b, and 60c. The plurality of screens 60a, 60b and 60c are respectively provided with through holes 620a, 620b and 620c defined by the plates 610a, 610b and 610c, a plurality of rims 611a, 611b and 611c and protrusions 612a , 612b, 612c. As described above with reference to FIG. 10, a plurality of extensions may be formed on both sides of the plurality of rims 611a, 611b, and 611c on the basis of one prong.
이 실시예에서도 마찬가지로, 차례로 적층되는 복수 개의 스크린들(60a, 60b, 60c)의 각각의 관통 구멍(620a, 620b, 620c)은 (도 14를 기준으로 위로부터 아래로) 그 크기가 감소하는 방향으로 서로 중첩될 수 있다.Similarly, in this embodiment, the through- holes 620a, 620b, and 620c of the plurality of screens 60a, 60b, and 60c that are stacked in order are arranged in a direction Respectively.
이상과 같이 실시예들이 비록 한정된 실시예와 도면에 의해 설명되었으나, 해당 기술분야에서 통상의 지식을 가진 자라면 상기의 기재로부터 다양한 수정 및 변형이 가능하다. 예를 들어, 설명된 기술들이 설명된 방법과 다른 순서로 수행되거나, 및/또는 설명된 시스템, 구조, 장치, 회로 등의 구성요소들이 설명된 방법과 다른 형태로 결합 또는 조합되거나, 다른 구성요소 또는 균등물에 의하여 대치되거나 치환되더라도 적절한 결과가 달성될 수 있다.While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. For example, it is to be understood that the techniques described may be performed in a different order than the described methods, and / or that components of the described systems, structures, devices, circuits, Lt; / RTI > or equivalents, even if it is replaced or replaced.

Claims (11)

  1. 플레이트; 및plate; And
    상기 플레이트의 전후방을 관통하며 상기 플레이트의 복수 개의 테두리(edge)들에 의해 규정된 관통 구멍;A through hole passing through the front and rear of the plate and defined by a plurality of edges of the plate;
    을 포함하고,/ RTI >
    상기 복수 개의 테두리들은 상기 관통 구멍의 중심부를 향해 돌출하는 돌출부를 각각 포함하고,The plurality of rims each include a protrusion protruding toward the central portion of the through hole,
    생체조직이 상기 관통 구멍을 통과하는 동안, 생체조직은 상기 돌출부에 의해 긁히고 찢어져 그 크기가 감소하는 생체조직 미세화 장치.Wherein the biotissue is scratched and torn by the protruding portion while the biotissue passes through the through hole, and the size of the biotissue is reduced.
  2. 제1항에 있어서,The method according to claim 1,
    상기 돌출부는 상기 관통 구멍의 중심부를 향해 폭이 좁아지며 첨단을 형성하는 생체조직 미세화 장치.Wherein the projecting portion is narrowed toward the central portion of the through hole and forms a tip.
  3. 제1항에 있어서,The method according to claim 1,
    상기 복수 개의 테두리들은 돌출부를 기준으로 양 측에 형성되는 선형부들을 각각 포함하는 생체조직 미세화 장치.Wherein the plurality of rims each include linear portions formed on both sides with respect to the protruding portion.
  4. 제1항에 있어서,The method according to claim 1,
    상기 플레이트에 대해 각도를 이루며 상기 플레이트를 기준으로 제1방향으로 돌출하는 제1그룹의 돌출부들; 및A first group of protrusions angled with respect to the plate and projecting in a first direction with respect to the plate; And
    상기 플레이트에 대해 각도를 이루며 상기 플레이트를 기준으로 상기 제1방향과 다른 제2방향으로 돌출하는 제2그룹의 돌출부들;A second group of protrusions angled with respect to the plate and projecting in a second direction different from the first direction with respect to the plate;
    을 포함하는 생체조직 미세화 장치.And a biochemical microfabrication apparatus.
  5. 제4항에 있어서,5. The method of claim 4,
    상기 제1그룹의 돌출부들 및 상기 제2그룹의 돌출부들은 상기 복수 개의 테두리들을 따라 서로 다른 방향으로 교번하는 생체조직 미세화 장치.Wherein the protrusions of the first group and the protrusions of the second group alternate in different directions along the plurality of rims.
  6. 제4항에 있어서,5. The method of claim 4,
    상기 제1그룹의 돌출부들의 각각의 연장선 및 상기 제2그룹의 돌출부들의 각각의 연장선은 서로 만나지도 않고 서로 평행하지도 않은 생체조직 미세화 장치.Wherein an extension of each of the protrusions of the first group and an extension of each of the protrusions of the second group do not meet with each other and are not parallel to each other.
  7. 제1항에 있어서,The method according to claim 1,
    상기 복수 개의 테두리들의 각각으로부터 상기 관통 구멍의 중심부를 향해 연장하는 연장부; 및An extension extending from each of the plurality of rims toward a central portion of the through hole; And
    상기 연장부의 말단에 형성되며 생체조직을 긁고 찢도록 구성된 첨단부;A tip portion formed at an end of the extended portion and configured to scratch and tear the living tissue;
    를 더 포함하는 생체조직 미세화 장치.Further comprising a biochemical microfabricator.
  8. 제7항에 있어서,8. The method of claim 7,
    상기 첨단부를 기준으로 상기 연장부의 반대편에 형성되고 상기 관통 구멍의 중심부를 향해 연장하는 추가적인 연장부를 더 포함하는 생체조직 미세화 장치.Further comprising an additional extension formed on the opposite side of the proximal portion relative to the proximal portion and extending toward the center of the through-hole.
  9. 제1항에 있어서,The method according to claim 1,
    상기 돌출부의 돌출 방향은 상기 관통 구멍을 통과하는 생체조직의 이동 방향에 대해 평행하지 않은 생체조직 미세화 장치.And the projecting direction of the projecting portion is not parallel to the moving direction of the living tissue passing through the through hole.
  10. 제1플레이트와, 상기 제1플레이트의 전후방을 관통하여 상기 제1플레이트의 복수 개의 제1테두리들에 의해 규정된 제1관통 구멍과, 상기 제1관통 구멍의 중심부를 향해 돌출하는 제1돌출부를 포함하는 제1스크린; 및A first through hole penetrating the front and rear sides of the first plate and defined by a plurality of first rims of the first plate and a first protrusion protruding toward the center of the first through hole, A first screen comprising; And
    상기 제1플레이트에 적층되는 제2플레이트와, 상기 제2플레이트의 전후방을 관통하며 상기 제2플레이트의 복수 개의 제2테두리들에 의해 규정된 제2관통 구멍과, 상기 제2관통 구멍의 중심부를 향해 돌출하는 제2돌출부를 포함하는 제2스크린;A second through hole penetrating the front and rear sides of the second plate and defined by a plurality of second rims of the second plate and a second through hole defined by a plurality of second rims of the second plate, A second projection including a second projection projecting toward the second projection;
    을 포함하고,/ RTI >
    상기 제1관통 구멍과 상기 제2관통 구멍은 중첩되고, 상기 제1관통 구멍의 크기가 상기 제2관통 구멍의 크기보다 큰 생체조직 미세화 장치.Wherein the first through hole overlaps with the second through hole and the size of the first through hole is larger than the size of the second through hole.
  11. 제10항에 있어서,11. The method of claim 10,
    상기 제1돌출부 및 상기 제2돌출부의 돌출 방향은 상기 제1관통 구멍과 상기 제2관통 구멍을 순차적으로 통과하는 생체조직의 이동 방향에 대해 평행하지 않고 서로 같거나 교차하는 생체조직 미세화 장치.Wherein the projecting directions of the first projecting portion and the second projecting portion are the same or intersect with each other without being parallel to the moving direction of the living tissue sequentially passing through the first through hole and the second through hole.
PCT/KR2018/010278 2017-09-05 2018-09-04 Device for reducing size of biological tissue WO2019050251A1 (en)

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US16/635,621 US11987786B2 (en) 2017-09-05 2018-09-04 Device for reducing size of biological tissue
JP2020531411A JP6898686B2 (en) 2017-09-05 2018-09-04 Biological tissue miniaturization device
CN201880052037.5A CN111032107B (en) 2017-09-05 2018-09-04 Device for reducing the size of biological tissue
EP18854041.3A EP3679961A4 (en) 2017-09-05 2018-09-04 Device for reducing size of biological tissue

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112867571A (en) * 2019-04-09 2021-05-28 李晙硕 Screen device, system for reducing size of biological tissue including the same, method for reducing size of biological tissue using the same, and method for separating target substance from biological tissue associated therewith

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6139757A (en) 1996-03-28 2000-10-31 Terumo Kabushiki Kaisha Method of separating cells from blood using a filter having a changeable porosity
JP2006187616A (en) * 2004-12-29 2006-07-20 Depuy Mitek Inc Cutting/grinding system and method
KR100748487B1 (en) * 2006-05-16 2007-08-10 장동 Tissue volume reduction by raidiofrequencny energy
KR20090020680A (en) * 2006-06-08 2009-02-26 키폰 에스에이알엘 Tissue debulking device and method of using the same
US20110264115A1 (en) * 2008-09-24 2011-10-27 The General Hospital Corporation Method and apparatus for grafting of skin tissue
JP6082816B2 (en) * 2013-09-02 2017-02-15 株式会社ラステック Medical perforated plate and medical perforated plate manufacturing method

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6139757A (en) 1996-03-28 2000-10-31 Terumo Kabushiki Kaisha Method of separating cells from blood using a filter having a changeable porosity
JP2006187616A (en) * 2004-12-29 2006-07-20 Depuy Mitek Inc Cutting/grinding system and method
KR100748487B1 (en) * 2006-05-16 2007-08-10 장동 Tissue volume reduction by raidiofrequencny energy
KR20090020680A (en) * 2006-06-08 2009-02-26 키폰 에스에이알엘 Tissue debulking device and method of using the same
US20110264115A1 (en) * 2008-09-24 2011-10-27 The General Hospital Corporation Method and apparatus for grafting of skin tissue
JP6082816B2 (en) * 2013-09-02 2017-02-15 株式会社ラステック Medical perforated plate and medical perforated plate manufacturing method

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP3679961A4 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112867571A (en) * 2019-04-09 2021-05-28 李晙硕 Screen device, system for reducing size of biological tissue including the same, method for reducing size of biological tissue using the same, and method for separating target substance from biological tissue associated therewith
JP2022508637A (en) * 2019-04-09 2022-01-19 ジュンソク イ、 Screen exchange device, biological tissue miniaturization system including this, biological tissue miniaturization method using this, and method for separating target substance from biological tissue related thereto.
JP7201830B2 (en) 2019-04-09 2023-01-10 ジュンソク イ、 Screen exchange device, biological tissue micronization system including the same, biological tissue micronization method using the same, and related method for separating target material from biological tissue
CN112867571B (en) * 2019-04-09 2023-04-28 李晙硕 Screen exchange device, system and method for reducing the size of biological tissue

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