KR101358341B1 - Lifting unit for removing wrinkle - Google Patents

Abstract

The invention relates to a wrinkle remover lifting unit according to the invention, the lifting unit is for removing wrinkles, the skin tissue is coupled to the corresponding predetermined skin tissue lifting (lifting) in order to being used as the absorbent chamber ; Upper end to both sides protrude obliquely from top to bottom direction to be fixed to the skin tissue for the first projection and second projection each having an anchor (anchor) has a structure, wherein the absorbent for fixing one end of the thread or the fixing screw hole holes are formed, the water absorbent material having the same base body and the chamber ; The open distal end is closed and rear end is inserted into the hollow chamber of the absorbent, and wherein one side of the tip during insertion of the fixed body wherein the base body has a first protrusion protrudes from inside to outside to be fixed to a first fixing hole is formed, wherein the tip end side to the other of said fixed body is inserted into said hollow base body to the outside, or inserted into a leaving for causing the cannula and a second fixing hole is formed ; A hollow cannula inserted into the base body to the outside of the skin leaving the tissue to secure the end, the cannula is inserted into the hollow to the exterior of the fixture for the extrusion provided with a separate needle.

Description

Lifting unit for removing wrinkle

The present invention relates to a lifting unit for wrinkle removal, and more particularly, to a lifting unit for wrinkle removal that can perform wrinkle removal more simply and easily.

Cosmetic surgery is a collective term for surgery, which is performed mainly for the partial injuries of the human body, correction of deformities, or cosmetic surgery. However, in recent years, surgery for cosmetic surgery has become a mainstay.

Plastic surgery is performed for various purposes, but it is also performed when the skin of a specific area is drooping or fat is accumulated and the body shape is changed unsatisfactorily or when wrinkles are formed on a specific area to restore the area tightly. .

In the surgical method for removing wrinkles, an incision method using a method of removing a drooped tissue after a large skin incision is largely performed, and it is not necessary to make an incision. Lifting is roughly classified as a non-incision method of removing wrinkles.

In the case of the former, since the skin is excessively incised, it is not only difficult to operate, but also takes a considerable time to cure after surgery.

Therefore, the latter surgical technique has been widely used in recent years. The latter procedure does not cut the skin, but instead uses a specially treated thread, an absorbent thread with a diameter of about 0.5 mm made of synthetic fibers such as silicone or polypropylene. It is a surgical method that removes wrinkles and revitalizes the skin by pulling up the aged skin and aged soft tissue (SMAS) in the skin.

By using a needle through simple local anesthesia, it is possible to minimize the occurrence of scars, which is the biggest disadvantage of the operation with a scalpel, not only reduce irritation or damage of the surgical site, but also less bleeding or swelling due to the surgery. In addition, it gives a natural tension after surgery to make the skin look elastic and youthful.

Absorbent yarns used in such surgical methods are typically present in a variety of threads that are slowly absorbed and melted by the human body for 6 to 8 months.

The surgical method using the absorbent thread had problems such as an increase in the skin tissue of the part where the absorbent thread was fixed or slipping in the skin tissue after the operation.

In order to improve such a problem, recently, a surgical method of removing wrinkles using absorbent yarns having barbs (cobs) formed on an outer surface thereof has been used. The absorbent yarn having the barb has the property of not being slipped by the barb, so it does not loosen well after sealing.

However, even when using the absorbent yarn with the barb formed there is a problem that the lifting effect is lowered because it is not completely fixed and does not remain firmly in the skin tissue due to the slip occurs.

Republic of Korea Patent Publication No. 10-0939581 (2010.01.22.)

Accordingly, an object of the present invention is to provide a lifting unit for removing wrinkles that can overcome the above-mentioned conventional problems.

Another object of the present invention to provide a lifting unit for removing wrinkles that can be operated to be firmly fixed to the skin tissue.

Still another object of the present invention is to provide a lifting unit for removing wrinkles, which can perform a simple or rapid wrinkle removal operation or procedure.

According to an embodiment of the present invention for achieving some of the technical problems described above, the lifting unit for wrinkle removal according to the present invention, the absorbent yarn is used to be coupled to a predetermined skin tissue and used to lift the skin tissue; ; Anchors (anchor) structure each having a first projection and a second projection for protruding obliquely from the top to the lower side on both sides of the upper end to be fixed to the skin tissue, the fixing groove or fixing for fixing one end of the absorbent seal A fixed body having a hole and having the same material as the absorbent yarn; The front end is closed and the rear end is open and has a hollow into which the absorbent thread is inserted. On one side of the front end, a first protrusion of the fixing body protrudes from the inside to the outside and is fixed when the fixing body is inserted. A cannula, and a cannula having a second fixing hole formed at another side of the tip to allow the fixture to be inserted into the hollow or to disengage the inserted fixture; In order to detach the fixture inserted into the hollow of the cannula to be fixed to the skin tissue, a separator is inserted into the hollow of the cannula and pushes the fixture outward.

The fixing groove may be formed from the center of the upper end portion of the fixing body to an adjacent portion of the lower end, and the fixing hole may be formed at the lower end of the fixing body.

The lifting unit has a ring forming member to form a hook-shaped ring in the bone tissue to fix the other end of the absorbent thread fixed to the skin tissue to the bone tissue of an adjacent human body. Further provided, the ring forming member may have a hollow cylindrical shape and a blade formed to protrude in the form of a sawtooth at the end.

The second fixing hole is formed so that one side is extended to the front end side of the cannula than the first fixing hole has a larger size than the first fixing hole, the other side of the second fixing hole is the second projection of the fixing body May have a structure in which the protrusion protrudes from the inside to the outside.

One side of the cannula may be further provided with a third fixing hole spaced apart from or adjacent to the first fixing hole or the second fixing hole to extend to the rear end in the longitudinal direction of the cannula.

According to the present invention, one end of the absorbent thread is supported and fixed by a fixture, and the other end is supported and fixed by a ring formed in bone tissue or the like, so that both ends of the absorbent thread can be fixed and the fixed state can be maintained for a long time, lifting The effect can be stable and effective. It can also be performed simply and quickly wrinkle removal surgery or procedures.

1 is a perspective view of a lifting unit for removing wrinkles according to an embodiment of the present invention,
Figure 2 is a perspective view of the fixture of Figure 1,
3 is an enlarged view of a part of the cannula of FIG.
4 is a partial cross-sectional view of the cannula of FIG. 1,
5 is a partial cross-sectional view of a state in which the fixture is inserted into the cannula of FIG. 1,
6 is a view showing a ring formed using the ring forming member and the ring forming member.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings without intending to intend to provide a thorough understanding of the present invention to a person having ordinary skill in the art to which the present invention belongs.

Figure 1 is a perspective view of the lifting unit 100 for removing wrinkles according to an embodiment of the present invention, Figure 2 is a perspective view of the fixture of Figure 1, Figure 3 is a partially enlarged view of the cannula of Figure 1, Figure 4 is a partial cross-sectional view of the cannula of FIG. 1, FIG. 5 is a partial cross-sectional view of a state in which a fixture is inserted into the cannula of FIG. 1.

As shown in Figures 1 to 5, the lifting unit 100 for removing wrinkles according to an embodiment of the present invention is an absorbent seal 110, the fixture 120, the cannula 130, the separation needle 140 It is provided. In addition, the ring forming member 150 may be further provided.

The absorbent thread 110 generally refers to a thread used for surgery or a procedure in a hospital, and refers to a thread that can be melted or absorbed from skin tissue in a human body.

Absorbent thread used for lifting is used for general thread lifting and absorbs barb (cob) -free absorbent thread (PDO), and attaches the barb to the outer surface so that the barb acts as a support throughout the dermal and soft tissue layers of the skin. It may include absorbent yarns, and other spiral yarns may act as a rubber band to pull as well as a strong elasticity and may include a whirlwind absorbent yarn that naturally pulls the muscle in the desired direction. In addition, surgical catgut, plain surgical catgut (Atype catgut), chromic catgut, dexon suture (polyglylic acid), vicryl sutue (polyglatin 910), PDS suture, monocryl suture, maxon suture and the like.

The absorbent yarn is bound to a given skin tissue and will be used to lift the skin tissue.

The fixture 120 has an anchor structure or an arrowhead shape, as shown in (a) and (b) of FIG. 2. The fixing body 120 has a first protrusion 122a and a second protrusion 122b for protruding obliquely from top to bottom on both side surfaces of the upper end to be fixed to the skin tissue. The first protrusion 122a and the second protrusion 122b have a structure that gradually widens from the upper side to the lower side, and an end portion thereof is sharply formed so as to be fixed to the skin tissue. The end of the protrusion 122b is lodged in the skin tissue to be fixed.

The fixing body 120 is fixed to the first protrusion 122a and the second protrusion 122b by the skin tissue when a force (tension) is applied in the skin tissue downward direction. This is to maintain.

The fixing body 120 is provided with a fixing groove 124 or a fixing hole 126 for fixing one end of the absorbent seal, the fixing groove 124 is shown in Figure 2 (a), It may have a structure that is formed from the center of the upper end portion of the fixing body 120 to the lower end portion, the fixing hole 126 is shown in the lower portion of the fixing body 120, as shown in FIG. Can be formed. In addition, fixing grooves or fixing holes for fixing one end of the absorbent seal may be formed in various structures.

The fixture 120 is formed of the same material as the absorbent yarn 110, so that it is melted or absorbed in the human body together with the absorbent yarn 110.

The cannula 130 has a structure in which the front end is closed and the rear end is open to have a hollow into which the absorbent seal 110 is inserted.

As shown in FIGS. 3 and 4, the cannula 130 has a first fixing hole 132a and a second fixing hole 132b formed at the tip portion thereof.

The first fixing hole 132a is formed at one side of the front end of the cannula 130, and when the fixing body 120 is inserted, the first protrusion 122a of the fixing body 120 moves from inside to outside. It is intended to protrude and be fixed. The second fixing hole 132b is formed at the other side of the tip, and is provided to allow the fixing body 120 to be inserted into the hollow of the cannula 130 or to detach the inserted fixing body 120 to the outside. Can be.

To this end, the second fixing hole 132a is formed such that one side (front end direction) is further extended to the front end side of the cannula 130 than the first fixing hole 132a and thus more than the first fixing hole 132a. It will have a large size. In addition, the other side of the second fixing hole 132b (the rear end side of the cannula) has a structure in which the second protrusion 122b of the fixing body 120 protrudes from the inside to the outside.

That is, the other side of the second fixing hole 132b (the rear end side of the cannula) is formed at a position symmetrical with the other side of the first fixing hole 132a (the rear end side of the cannula), and the second fixing hole ( One side of the 132b (the direction of the front end of the cannula) may have a structure formed in a position extending toward the front end than one side of the first fixing hole (132a).

The first fixing hole 132a may have an elliptical structure extending from the front end side to the rear end side along the longitudinal direction of the cannula 130, and the second fixing hole 132b may have a longitudinal direction of the cannula 130. Along the front end side is formed long to the rear end side, it may have an elliptical structure extending longer toward the front end than the first fixing hole (132a).

In addition, the cannula 130 is fixed at one side (the side in which the first fixing hole 132a or the second fixing hole 132b is formed) in the first fixing hole 132a or the second fixing hole 132b. A third fixing hole 132c may be further provided to be spaced apart or adjacent to extend to the rear end in the longitudinal direction of the cannula 130.

The third fixing hole (132c), the absorbent seal 110, one end of which is connected to the fixing body 120 is inserted into the hollow of the cannula 130, the separation needle 140 to the When the insert 120 is inserted into the hollow of the cannula 130 to separate and detach the fixture 120, the absorbent seal 110 in the hollow is inserted into the third fixing hole by insertion of the separating needle 140. It is to be moved through the 132c, to prevent damage of the absorbent seal 110 by the separator needle 140, and to facilitate insertion of the separator needle 140 into the hollow of the cannula (130). .

Since the cannula 130 is inserted into the human body, the thickness of the cannula 130 should be as thin as possible. Therefore, the inside of the cannula 130 may have a size enough to allow the separation needle 140 to be inserted therein. When the absorbent seal 110 is damaged, the third fixing hole 132c may be provided in order to prevent the damage and to facilitate the insertion of the separator needle 140.

The cannula 130 may be divided into a handle portion and a human injection portion. The human body injection portion should be formed thinner than the handle portion, and the interior of the human body injection portion and the handle portion has a hollow structure.

The separation needle 140 is inserted into the hollow of the cannula 130 to be fixed to the skin tissue by leaving the fixture 120 inserted into the hollow of the cannula 130 to the outside, the fixture 120 ) To push the outside into the skin tissue.

The separation needle 140 has a length corresponding to the length of the cannula 130, it should have a size for insertion into the hollow of the cannula (130). In addition, the separating needle 140 may have a tip portion thinner or thinner than a rear end portion to push the fixing body 120 to the outside.

6 (a) is a perspective view of the ring forming member 150, Figure 6 (b) shows a state in which the absorbent seal 110 is fixed to the ring formed by the ring forming member 150.

As shown in (a) of FIG. 6, the ring forming member 150 has one end fixed to the fixing body 120 so that the other end of the absorbent seal 110 fixed to the skin tissue is adjacent to the bone of the human body. In order to fix the tissue to the hook-shaped ring 162 in the bone tissue.

The ring forming member 150 may have a structure in which a blade protruding in a sawtooth shape at the end in a hollow cylindrical shape.

As shown in (b) of FIG. 6, when the end portion of the ring forming member 150 is in contact with the bone tissue or a specific portion 160 of the human body in an oblique direction, the ring forming member 150 is applied. A part of the end of the) is dug into the contact portion and the remaining portion is exposed to the outside, a hook-shaped ring 162 is formed in the contact portion is inserted into the hollow of the ring forming member 150.

Then, when the ring forming member 150 is removed, the ring 162 is maintained, and the other end portion of the absorbent seal 110 may be fixedly coupled to the ring 162.

Hereinafter, a method of removing wrinkles using the lifting unit 100 according to the present invention will be described with reference to FIGS. 1 to 6.

First, in the state where the absorbent yarn 110 is inserted from the rear end of the cannula 130 in the tip direction and one end of the absorbent yarn 110 comes out through the second fixing hole 132b, the absorbent yarn One end of the 110 is fixed to the fixing groove 124 or the fixing hole 126 of the fixing body 120.

Thereafter, the fixing body 120 having one end of the absorbent seal 110 fixed thereto is inserted into the hollow portion of the front end of the cannula 130 through the second fixing hole 132b. At this time, as shown in FIG. 5, the first protrusion 122a of the fixing body 120 protrudes and is fixed to the first fixing hole 132a and the second of the second fixing body 120. The protrusion 122b is mounted to be fixed to the other side of the second fixing hole 132b. In order to maintain the mounting state of the fixture 120, the absorbent seal 110 may be maintained in a tight tension state.

Next, the cannula 130 to which the fixture 120 is mounted and the absorbent seal 110 is inserted can be positioned at a desired position (for example, between the subcutaneous layer and the dermis layer) with skin or tissue. Break through the tissue or skin and push it to a specific location on the skin or tissue. That is, the tip portion of the cannula 130 to reach a specific position of the skin or tissue.

In this state, the separation needle 140 is pushed into the hollow of the cannula 130 in the front end direction from the rear end of the cannula 130 so that the fixing body 120 passes through the second fixing hole 132b. Allow them to leave your organization. When the fixture 120 is separated into the skin or tissue, the fixture 120 may be supported by the first protrusion 122a and the second protrusion 122b to be fixed at the corresponding position.

Next, when the cannula 130 is removed from the skin or tissue, the fixture 120 and the absorbent seal 110 remain in the skin or tissue. In this state, by pulling the absorbent yarn 110 as desired, the wrinkles are removed, and the ring forming member 150 is used in an adjacent portion to fix the other end of the absorbent yarn 110 (b) of FIG. As shown in the figure, the ring 162 is formed and the other end of the absorbent seal 110 is coupled to the ring 162 to be fixed.

As described above, according to the present invention, one end of the absorbent thread is supported and fixed by the fixing body 120, and the other end is supported and fixed by the ring 162, so that both ends of the absorbent thread are fixed and The fixed state can be maintained for a long time, so that the lifting effect can be stably and effectively maintained.

The foregoing description of the embodiments is merely illustrative of the present invention with reference to the drawings for a more thorough understanding of the present invention, and thus should not be construed as limiting the present invention. It will be apparent to those skilled in the art that various changes and modifications may be made without departing from the basic principles of the present invention.

110: absorbent thread 120: fixed body
130: cannula 140: separation needle
150; Ring forming member

Claims (5)

In the lifting unit for wrinkle removal:
An absorbent thread used to bind to the predetermined skin tissue and to be used for lifting the skin tissue;
Anchors (anchor) structure each having a first projection and a second projection for protruding obliquely from the top to the lower side on both sides of the upper end to be fixed to the skin tissue, the fixing groove or fixing for fixing one end of the absorbent seal A fixed body having a hole and having the same material as the absorbent yarn;
The front end is closed and the rear end is open and has a hollow into which the absorbent thread is inserted. On one side of the front end, a first protrusion of the fixing body protrudes from the inside to the outside and is fixed when the fixing body is inserted. A cannula, and a cannula having a second fixing hole formed at another side of the tip to allow the fixture to be inserted into the hollow or to disengage the inserted fixture;
And a separating needle inserted into the hollow of the cannula to push the fixture to the outside in order to detach the fixture inserted into the hollow of the cannula to fix the skin tissue to the outside. The method according to claim 1,
The fixing groove is formed from the center of the upper end portion of the fixing body to the lower portion adjacent to the lifting unit, characterized in that the fixing hole is formed in the lower end of the fixing body. The method according to claim 1, The lifting unit,
One end is fixed to the fixing body is further provided with a ring forming member for forming a hook-shaped ring in the bone tissue to fix the other end of the absorbent thread fixed to the skin tissue adjacent to the human bone tissue, The ring forming member is a hollow cylindrical lifting unit characterized in that it has a structure in which the blade protruding in the form of a sawtooth at the end. The method according to claim 1,
The second fixing hole is formed so that one side is extended to the front end side of the cannula than the first fixing hole has a larger size than the first fixing hole, the other side of the second fixing hole is the second projection of the fixing body Lifting unit characterized in that the structure is fixed to protrude from the inside to the outside The method according to claim 1,
Lifting unit, characterized in that one side of the cannula is further provided with a third fixing hole which is spaced apart from or adjacent to the first fixing hole or the second fixing hole extending to the rear end in the longitudinal direction of the cannula.

Images