CN217847324U - Bionic bracket for promoting diabetic tendon injury repair - Google Patents

Abstract

The utility model discloses a promote prosthetic bionical support of diabetic tendon damage, it includes, base, guide arm one, guide arm two, guide arm three, guide arm four, annotate the liquid subassembly, guide arm one, guide arm two, guide arm three, four vertical pegs graft on the base of guide arm, notes liquid subassembly set up on guide arm three, guide arm four, connecting rod one on be connected with connecting rod two, rotate between the tip of connecting rod two and the wall portion of connecting rod one and be connected, notes liquid subassembly including annotating liquid pipe, flowing back soft board communicate in the bottom of annotating the liquid pipe, seted up the outage on the flowing back soft board, the patient foot is placed on the base, rotates connecting rod two after that, adjusts the angle of annotating the liquid pipe to make the stiff board of flowing back patient's instep attached in the affected part of the fluid flow of exosome through annotating in liquid pipe to the stiff board of flowing back, arrange to patient's instep affected part through the outage of flowing back soft board after that is favorable to the restoration of patient's instep tendon damage.

Description

Bionic bracket for promoting diabetic tendon injury repair

Technical Field

The utility model relates to a tendon injury repair technique field, concretely relates to promote prosthetic bionical support of diabetic tendon injury.

Background

The tendon is a dense connective tissue in the shape of a cord or a membrane at both ends of the muscle belly, which is convenient for muscle attachment and fixation. The muscle tendon is attached to two or more different bones, the traction of the muscle tendon can make the muscle contract to drive the different bones to move, each skeletal muscle is divided into two parts of muscle abdomen and muscle tendon, the muscle abdomen is made of muscle fiber, is red and soft and has contraction capacity, the muscle tendon is made of dense connective tissue, is white and hard and has no contraction capacity. The tendons attach skeletal muscles to bone. The long muscle tendon is usually in the form of round cord, while the broad muscle tendon is in the form of membrane, called aponeurosis.

When the tendon of the diabetic patient is damaged, the tendon of the foot surface of the diabetic patient is exposed, so that the tendon repair is inconvenient to the foot surface, the foot of the diabetic patient is easy to move, and the exosome is not convenient to inject into the affected part.

SUMMERY OF THE UTILITY MODEL

In order to solve the defects of the prior art, the utility model aims at providing a bionic bracket for promoting the repair of diabetic tendon injury.

In order to achieve the technical purpose, the utility model adopts the following technical scheme.

A biomimetic scaffold for facilitating diabetic tendon injury repair, comprising:

base, guide arm one, guide arm two, guide arm three, guide arm four, annotate the liquid subassembly, guide arm one, guide arm two, guide arm three, guide arm four vertical pegs graft on the base, annotate the liquid subassembly and set up on guide arm three, guide arm four, guide arm three, all overlap and be equipped with adapter sleeve three on the guide arm four, be connected with connecting rod one between two adapter sleeve three, adapter sleeve three accessible fastener is fixed in guide arm three, guide arm four, connecting rod one on be connected with connecting rod two, rotate between the tip of connecting rod two and the wall portion of connecting rod one and be connected, annotate the liquid subassembly including annotating liquid pipe, flowing back soft board, annotate the liquid pipe and set up in the tip of connecting rod two, annotate the wall portion of liquid pipe and the tip of connecting rod two is articulated, the flowing back soft board communicate in the bottom of annotating the liquid pipe, seted up the outage on the flowing back soft board.

As a further improvement, guide arm three, guide arm four go up the cover and are equipped with adapter sleeve four, two adapter sleeves are connected with connecting rod three between four, four accessible fasteners of adapter sleeve are fixed in guide arm three, guide arm four on, the below of connecting rod three be provided with the clamp plate, the clamp plate passes through the sliding sleeve cover and locates connecting rod three on.

As a further improvement, guide arm one, guide arm two on be provided with and be used for carrying out spacing stop gear to the patient ankle, stop gear includes adapter sleeve one, limiting plate one, adapter sleeve two, limiting plate two, adapter sleeve one, two do not overlap and locate guide arm one, guide arm two on, limiting plate one connect on adapter sleeve one, limiting plate two connect on adapter sleeve two, adapter sleeve one, adapter sleeve two accessible fasteners are fixed in guide arm one, guide arm two on.

As the utility model discloses a further improvement, limiting plate one, two relative arrangements of limiting plate, limiting plate one, limiting plate two are the arc, can enclose to close to patient's ankle after limiting plate one, the cooperation of limiting plate two.

As a further improvement of the utility model, the end parts of the first limiting plate and the second limiting plate are provided with fixing holes.

Compared with the prior art, the utility model, the progress and the advantage of obtaining lie in the utility model discloses in the use:

1. the angle of annotating the liquid pipe is adjusted in the adjustment to can make the attached affected part in patient's instep of flowing back soft board, be favorable to carrying out the exosome to patient's instep and annotate the liquid.

2. When the base was arranged in to patient's foot, the clamp plate can contact with patient's instep to carry on spacingly to patient's foot, limiting plate one, two are the arcs, can enclose to close patient's ankle after limiting plate one, the cooperation of limiting plate two, guarantee the smooth injection of the exosome.

Drawings

In order to more clearly illustrate the technical solution of the embodiments of the present invention, the drawings required to be used in the embodiments of the present invention will be briefly described below. It is obvious that the drawings described below are only some embodiments of the invention, and that for a person skilled in the art, other drawings can be obtained from these drawings without inventive effort.

Fig. 1 is a schematic view of the overall structure of the present invention.

Fig. 2 is a schematic view of the limiting mechanism of the present invention.

Fig. 3 is the installation schematic diagram of the liquid injection assembly of the present invention.

Fig. 4 is a schematic view of the structure of the liquid discharge soft board of the present invention.

The indications in the figures are:

1. a base; 2. a first guide rod; 3. a second guide rod; 4. a third guide rod; 5. a guide rod IV; 6. a limiting mechanism; 7. a liquid injection assembly; 8. a first connecting sleeve; 9. a first limiting plate; 10. a second connecting sleeve; 11. a second limiting plate; 12. connecting sleeves III; 13. a first connecting rod; 14. a second connecting rod; 15. a liquid injection pipe; 16. a liquid discharge soft board; 17. a third connecting rod; 18. connecting sleeves IV; 19. and (7) pressing a plate.

Detailed Description

The technical solution of the present invention is further explained by the following embodiments with reference to the accompanying drawings.

Wherein the showings are for the purpose of illustration only and are shown by way of illustration only and not in actual form, and are not to be construed as limiting the present patent; for a better understanding of the embodiments of the present invention, some parts of the drawings may be omitted, enlarged or reduced, and do not represent the size of an actual product; it will be understood by those skilled in the art that certain well-known structures in the drawings and descriptions thereof may be omitted.

The same or similar reference numbers in the drawings of the embodiments of the present invention correspond to the same or similar components; in the description of the present invention, it should be understood that if the terms "upper", "lower", "left", "right", "inner", "outer", etc. are used to indicate the orientation or positional relationship based on the orientation or positional relationship shown in the drawings, it is only for convenience of description and simplification of description, but it is not indicated or implied that the device or element referred to must have a specific orientation, be constructed in a specific orientation, and be operated, and therefore, the terms describing the positional relationship in the drawings are used only for illustrative purposes and are not to be construed as limiting the present patent, and the specific meaning of the terms will be understood by those skilled in the art according to the specific circumstances.

In the description of the present invention, unless otherwise explicitly specified or limited, the term "connected" or the like, if appearing to indicate a connection relationship between the components, is to be understood broadly, for example, as being either a fixed connection, a detachable connection, or an integral part; can be mechanically or electrically connected; they may be directly connected or indirectly connected through intervening media, or may be connected through one or more other components or may be in an interactive relationship with one another. The specific meaning of the above terms in the present invention can be understood in specific cases to those skilled in the art.

As shown in fig. 1-4, a biomimetic scaffold for promoting diabetic tendon injury repair, comprising:

the liquid injection device comprises a base 1, a first guide rod 2, a second guide rod 3, a third guide rod 4, a fourth guide rod 5 and a liquid injection assembly 7, wherein the first guide rod 2, the second guide rod 3, the third guide rod 4 and the fourth guide rod 5 are vertically inserted on the base 1, the liquid injection assembly 7 is arranged on the third guide rod 4 and the fourth guide rod 5, connecting sleeves three 12 are respectively sleeved on the third guide rod 4 and the fourth guide rod 5, a first connecting rod 13 is connected between the two connecting sleeves three 12, the connecting sleeves three 12 can be fixed on the third guide rod 4 and the fourth guide rod 5 through fasteners, the first connecting rod 13 is connected with a second connecting rod 14, the end part of the second connecting rod 14 is rotatably connected with the wall part of the first connecting rod 13, annotate liquid subassembly 7 including annotating liquid pipe 15, flowing back soft board 16, annotate liquid pipe 15 and set up in the tip of two 14 connecting rods, the wall portion of annotating liquid pipe 15 is articulated with the tip of two 14 connecting rods, flowing back soft board 16 communicate in the bottom of annotating liquid pipe 15, the outage has been seted up on the flowing back soft board 16, the patient foot is placed on base 1, rotate two 14 connecting rods after that, adjust the angle of annotating liquid pipe 15, thereby make 16 attached affected parts in patient instep of flowing back soft board, the exosome flows to in the flowing back soft board 16 through annotating liquid pipe 15 after that, the outage through 16 soft boards of flowing back is arranged to patient instep affected part after that, thereby be favorable to the restoration of patient instep tendon damage.

More specifically, three 4 guide arms, four 5 guide arms on the cover be equipped with four 18 connecting sleeves, be connected with three 17 connecting rods between two four 18 connecting sleeves, four 18 connecting sleeves accessible fasteners are fixed in on three 4 guide arms, the four 5 guide arms of guide arm, three 17 connecting rods's below be provided with clamp plate 19, on clamp plate 19 locates three 17 connecting rods through the sliding sleeve cover, when the base 1 was arranged in to the patient foot, clamp plate 19 can with the contact of patient's instep to it is spacing to patient's foot.

As shown in fig. 2, the first guide arm 2, the second guide arm 3 on be provided with and be used for carrying out spacing stop gear 6 to the patient's ankle, stop gear 6 includes first adapter sleeve 8, first limiting plate 9, second adapter sleeve 10, second limiting plate 11, first adapter sleeve 8, second adapter sleeve 10 overlap respectively and locate on first guide arm 2, the second guide arm 3, first limiting plate 9 connect on first adapter sleeve 8, second limiting plate 11 connects on second adapter sleeve 10, first adapter sleeve 8, second adapter sleeve 10 accessible fastener are fixed in on first guide arm 2, the second guide arm 3.

More specifically, limiting plate one 9, two 11 mutual dispositions of limiting plate, limiting plate one 9, two 11 are the arcwall, can enclose to close the patient ankle after the cooperation of limiting plate one 9, two 11 limiting plates.

More specifically, the end portions of the first limiting plate 9 and the second limiting plate 11 are provided with fixing holes, and the first limiting plate 9 and the second limiting plate 11 can be fixed through pin bodies.

The working principle is as follows:

the utility model discloses in the use, the patient foot is placed on base 1, rotate connecting rod two 14 after that, the angle of liquid pipe 15 is annotated in the adjustment, thereby make the attached affected part in patient's instep of flowing back soft board 16, the exosome flows to flowing back soft board 16 in through annotating liquid pipe 15 after that, arrange to patient's instep affected part through the outage of flowing back soft board 16 after that, thereby be favorable to the restoration of patient's instep tendon damage, when the patient foot was arranged in on base 1, clamp plate 19 can contact with patient's instep, thereby carry on spacingly to the patient foot, limiting plate one 9, limiting plate two 11 is the arc, limiting plate one 9, can enclose to close to the patient's ankle after the cooperation of limiting plate two 11.

It should be understood that the above-described embodiments are merely illustrative of the preferred embodiments of the present invention and the technical principles thereof. It will be understood by those skilled in the art that various modifications, equivalents, changes, and the like can be made to the present invention. However, these modifications are within the scope of the present invention as long as they do not depart from the spirit of the present invention. In addition, certain terms used in the specification and claims of the present application are not limiting, but are used merely for convenience of description.

Claims (8)

1. The utility model provides a promote bionical support of diabetic tendon injury restoration which characterized in that, it includes:

base, guide arm one, guide arm two, guide arm three, guide arm four, annotate the liquid subassembly, guide arm one, guide arm two, guide arm three, guide arm four vertical pegs graft on the base, the liquid subassembly of annotating set up in guide arm three, guide arm four on all overlap and be equipped with adapter sleeve three, be connected with connecting rod one between two adapter sleeves three, adapter sleeve three accessible fastener is fixed in guide arm three, guide arm four on, connecting rod one on be connected with connecting rod two, rotate between the tip of connecting rod two and the wall portion of connecting rod one and be connected.

2. The bionic scaffold for promoting repair of diabetic tendon injury as claimed in claim 1, wherein the liquid injection assembly comprises a liquid injection pipe and a liquid discharge soft plate, the liquid injection pipe is disposed at the end of the second connecting rod, the wall of the liquid injection pipe is hinged to the end of the second connecting rod, the liquid discharge soft plate is communicated with the bottom of the liquid injection pipe, and a liquid discharge hole is formed in the liquid discharge soft plate.

3. The bionic scaffold for promoting diabetic tendon injury repair as claimed in claim 1, wherein a connecting sleeve four is sleeved on the guide rod three and the guide rod four, a connecting rod three is connected between the two connecting sleeves four, the connecting sleeve four can be fixed on the guide rod three and the guide rod four by fasteners, and a pressing plate is arranged below the connecting rod three.

4. The biomimetic scaffold for promoting diabetic tendon injury repair according to claim 3, wherein the pressure plate is sleeved on the third connecting rod through a sliding sleeve.

5. The bionic scaffold for promoting diabetic tendon injury repair as claimed in claim 4, wherein a limiting mechanism for limiting the ankle of the patient is disposed on the first guide rod and the second guide rod, the limiting mechanism includes a first connecting sleeve, a first limiting plate, a second connecting sleeve and a second limiting plate, the first connecting sleeve and the second connecting sleeve are respectively sleeved on the first guide rod and the second guide rod, the first limiting plate is connected to the first connecting sleeve, the second limiting plate is connected to the second connecting sleeve, and the first connecting sleeve and the second connecting sleeve can be fixed to the first guide rod and the second guide rod through fasteners.

6. The biomimetic scaffold for promoting repair of diabetic tendon injury according to claim 5, wherein the first limiting plate and the second limiting plate are oppositely arranged and are arc-shaped plates.

7. The bionic scaffold for promoting repair of diabetic tendon injury as claimed in claim 6, wherein the first and second limiting plates cooperate to enclose the ankle of the patient.

8. The bionic scaffold for promoting diabetic tendon injury repair of claim 7, wherein fixing holes are formed at the end parts of the first limiting plate and the second limiting plate.

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