WO2012118305A2

WO2012118305A2 - Method for manufacturing allogeneic soft-tissue transplant having autologous stem cell transplanted therein

Info

Publication number: WO2012118305A2
Application number: PCT/KR2012/001443
Authority: WO
Inventors: 심영복; 이광일; 장주웅; 이정수
Original assignee: 주식회사 코리아본뱅크
Priority date: 2011-02-28
Filing date: 2012-02-24
Publication date: 2012-09-07
Also published as: WO2012118305A3

Abstract

The present invention relates to a method for manufacturing an allogeneic soft-tissue transplant having an autologous stem cell injected therein on the basis of an allogeneic soft tissue base derived from an allogeneic organism, and the present invention enables the manufacturing of an allogeneic soft tissue transplant for efficiently replacing a damaged soft tissue of a human body.

Description

How to prepare an allogeneic soft tissue transplant with autologous stem cells

The present invention relates to a method for producing an allogeneic soft tissue implant implanted into a human body using a soft tissue derived from an allogeneic organism as a support.

At present, interest in health around the world is increasing day by day. In particular, steady exercise is recognized as an essential condition for maintaining a healthy life. However, while proper exercise helps maintain good health, excessive exercise can rather harm health. As a representative example, when an abnormality occurs in the musculoskeletal system due to excessive exercise, the patient may not even be able to behave, and it is often difficult to cure without receiving physical therapy for a long time. In particular, if the cruciate ligament is damaged in the knee area, physical therapy alone cannot recover the damage, but the situation is being treated by transplanting the patient's own tissue. However, the transplantation of the autologous tissue also requires continuous rehabilitation treatment, and unlike the original inherent ligaments, the transplanted autologous tissues are markedly inferior in physical properties and cannot be viewed as a practical treatment. Therefore, there is a need for allogeneic soft tissue implants that can maintain their physical properties, significantly reduce immune rejection, and replace them as closely as possible with their own soft tissues in order to treat damaged ligaments, ie, damaged soft tissues. to be.

The present invention is to produce an allogeneic soft tissue implant in which autologous stem cells are injected, based on the allogeneic soft tissue support derived from allogeneic organisms to efficiently replace damaged soft tissues of the human body.

The present invention includes the steps of obtaining an allogeneic soft tissue support obtained from a human or animal body; Washing and sterilizing the obtained soft tissue support; Treating the washed and sterilized homologous soft tissue support with an enzyme solution to remove immune rejection cells; Forming one or more pores on the allogeneic soft tissue support from which the immune rejection cells have been removed; Injecting autologous stem cells of a user into the formed pores; And culturing allogeneic soft tissue scaffolds into which the autologous stem cells have been injected.

According to one embodiment of the invention, the allogeneic soft tissue support may be ligaments or bone fragment connecting ligaments.

According to an embodiment of the present invention, the washing and sterilizing step may include treating hydrogen peroxide on the obtained homogeneous soft tissue support and applying ultrasonic waves.

According to one embodiment of the invention, the treated hydrogen peroxide has a concentration selected from the concentration range of 0.1 to 5.0 percent (%), the applied ultrasound may have an output selected from the range of 120 to 400 watts (W). have.

According to one embodiment of the invention, the washing and sterilizing step may include the step of treating the radiation protective material to the obtained homogeneous soft tissue support, and irradiating the radiation.

According to one embodiment of the invention, the radiation protection material to be treated is cobalt 60 (Co ⁶⁰ ), and the radiation to be irradiated may be gamma rays selected from the range of 12 to 50 kilograms (kGy).

According to one embodiment of the invention, the step of removing the immune rejection cells may be treating an enzyme solution comprising trypsin, collagenase and protease.

According to one embodiment of the invention, the step of removing the immune rejection cells may further comprise the step of washing by washing with physiological saline after treating the enzyme solution to the washed and sterile homologous soft tissue support. .

According to one embodiment of the present invention, the step of removing the immune rejection cells is treated with an enzyme solution to the washed and sterilized homologous soft tissue scaffold, followed by washing with physiological saline, followed by osmotic treatment with distilled water. It may further comprise a step.

According to one embodiment of the invention, in the step of forming the one or more pores, the pore may have a size selected from the range of 1 to 1000 micrometers (μm).

According to one embodiment of the invention, the step of injecting the autologous stem cells may further comprise the step of injecting the autologous stem cell supporting promoter prior to or simultaneously with the injection of the autologous stem cells.

According to one embodiment of the invention, culturing the allogeneic soft tissue support may further comprise providing a physical stimulus to the allogeneic soft tissue support.

According to one embodiment of the invention, the physical stimulus may be provided to the allogeneic soft tissue support at a frequency of up to once per second.

According to one embodiment of the present invention, the provision of the physical stimulus provides a tensile stimulus at both ends of the allogeneic soft tissue support, or provides a twist in both transverse directions of the allogeneic soft tissue support based on the longitudinal axis of the allogeneic soft tissue support. Alternatively, or at the same time to provide a tensile stimulus at both ends of the allogeneic soft tissue support, and to provide a twist in both transverse directions of the allogeneic soft tissue support based on the longitudinal axis of the allogeneic soft tissue support.

According to one embodiment of the present invention, providing tensile stimulation at both ends of the allogeneic soft tissue support extends both ends of the allogeneic soft tissue support in the longitudinal direction, and one end is 10% of the total length of the allogeneic soft tissue support. At the same time as extending in the following range may be to extend the other end in the range of less than 10% of the total length of the allogeneic soft tissue support.

According to one embodiment of the present invention, providing a twist in both transverse directions of the allogeneic soft tissue support rotates both ends of the allogeneic soft tissue support, while at the same time rotating one end in a range of 45 degrees or less in a clockwise direction. It may be to rotate the end in a range of 45 degrees or less counterclockwise.

According to one embodiment of the present invention, the culturing step may be carried out in a range of 7 days or less.

According to the method for producing allogeneic soft tissue implants of the present invention, allogeneic soft tissue implants capable of efficiently replacing damaged soft tissues of the human body can be prepared by injecting and culturing autologous stem cells into allogeneic soft tissue supports derived from allogeneic organisms.

Figure 1 illustrates the individual steps for implementing a method for producing allogeneic soft tissue implants according to one embodiment of the present invention.

Figure 2 shows the individual steps for implementing the support cleaning and sterilization step included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention.

Figure 3 shows the individual steps for implementing the step of removing the immune rejection response cells included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention.

Figure 4 illustrates a method for implementing a pore forming step included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention.

Figure 5 shows the individual steps for implementing the autologous stem cell injection step included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention.

Figure 6 shows the step of providing a physical stimulus in the culture of allogeneic soft tissue support included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention.

Figure 7 shows the tensile strength measurement results before and after the clearant process treatment of allogeneic tibial tendon according to an embodiment of the present invention.

Figure 8 shows the results of the measurement of tensile strength following irradiation after the normal irradiation and clearant process treatment of the tibia tendon of humans and pigs according to an embodiment of the present invention.

Figure 9 shows a scanning electron microscope (SEM) photograph of the surface and cross-section of the allogeneic soft tissue support before and after the step of removing the immune rejection cells included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention.

Figure 10 shows a hematoxylin & eosin staining picture of the cross section of the allogeneic soft tissue support before and after the step of removing the immune rejection cells included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention.

Figure 11 shows the results of measuring the DNA residual amount of pig tibia tendon before and after decellularization according to an embodiment of the present invention.

12 shows stem cells carrying collagen gel (0.5%) and (B) stem cells carrying collagen gel (1.0) according to the concentration of stem cells 1x10 ⁵ , 2x10 ⁵ and 5x10 ⁵ cells / cm ² according to an embodiment of the present invention. %) Results of measurement of cell proliferation rates on the first, third and seventh days of culture are shown.

FIG. 13 shows the results of real time PCR analysis of stem cell-supported gel-grafted tibial tendon before and after physical stimulation in a bioincubator according to one embodiment of the present invention.

Figure 14 shows the results of GAG content analysis of the stem cell-supported gel transplant group subjected to physical stimulation in the incubator according to an embodiment of the present invention.

Figure 15 shows the results of collagen content analysis of the stem cell-supported gel transplant group subjected to physical stimulation in the incubator according to an embodiment of the present invention.

Hereinafter, with reference to the accompanying drawings will be described in detail an embodiment of the present invention. The following description is merely a means for easily understanding the embodiments of the present invention, and is not intended to limit the protection scope of the present invention.

1 illustrates the individual steps for implementing a method for producing a homologous soft tissue scaffold in accordance with one embodiment of the present invention.

Method for producing allogeneic soft tissue implant according to an embodiment of the present invention comprises the steps of obtaining (100) an allogeneic soft tissue support obtained from a human or animal body; Washing and sterilizing the obtained allogeneic soft tissue support (200); Treating the washed and sterilized allogeneic soft tissue support with an enzyme solution to remove immune rejection cells (300); Forming one or more pores in the allogeneic soft tissue support from which the immune rejection cells have been removed (400); Injecting an autologous stem cell of the user into the formed pore (500); And culturing the allogeneic soft tissue support infused with the autologous stem cells (600).

According to FIG. 1, the method for preparing allogeneic soft tissue implants according to an embodiment of the present invention includes a step 100 of obtaining an allogeneic soft tissue support obtained from a human or animal body. The soft tissue generally refers to tissues that connect, support, or surround organs or other structures of the body as tissues in the body, not bone, and include, for example, ligaments, tendons, Achilles tendons, tibiaris tendons, and the like. There is this. The soft tissue is mainly distributed in the site supporting or maintaining the weight of the body, and serves to support and maintain repetitive movement, for example bending, twisting, rotation, and the like. Since the soft tissue is highly related to the movement of the body, if an abnormality occurs in the soft tissue or a corresponding body portion thereof, the soft tissue may cause a fatal disease in the exercise system. On the other hand, the same kind refers to a relationship that can be recognized as the same individual or medically homogeneous. Accordingly, the soft tissue homograft according to the present invention refers to an implant including soft tissue that can be mutually transplanted between the same individual or between medically recognized homologous individuals. The allogeneic soft tissue support refers to a support that is directly removed from its body or is a structure of the body obtained separately from a medically recognized homogenous individual and replaced in the treatment site. In addition, the allogeneic soft tissue support may be legally collected from a donated body. The allogeneic soft tissue support may be a structure itself separated from the body, but may be combined with other body structures for proper implantation. For example, the allogeneic soft tissue support may be the ligament itself, but may also be a structure associated with one or more bone fragments, such as a bone fragment-ligament complex structure or a bone fragment-ligament-bone fragment complex structure. In addition, the allogeneic soft tissue support may be implemented in various sizes and / or shapes according to the body portion to be implanted.

According to FIG. 1, the method for preparing allogeneic soft tissue implants according to an embodiment of the present invention includes a step 200 of washing and sterilizing the obtained allogeneic soft tissue support. In order for the allogeneic soft tissue implant to be transplanted to the other body without side effects such as complications, harmful bacteria and the like as well as foreign substances contained in the allogeneic soft tissue support obtained from the human body or the body of the animal should be completely removed. The washing and sterilizing step 200 according to the present invention may be implemented in various physical or chemical methods, respectively, but it is preferable to simultaneously apply the chemical method as well as the physical method. The washing and sterilizing step 200 may be implemented in various methods for physically and / or chemically washing and sterilizing the obtained homogenous soft tissue support. Details thereof will be described below with reference to FIG. 2.

According to Figure 1, the method for producing allogeneic soft tissue implant according to an embodiment of the present invention as a third step, the step of removing the immune rejection cells by treating the washed and sterilized homogenous soft tissue support with an enzyme solution (300) It includes. Removing the immune rejection cells is implemented by treating an enzyme solution. The enzyme solution is used to remove intrinsic cells present in the human or animal body prior to transplantation from which the allogeneic soft tissue support has been obtained. Intrinsic cells present in the body of a human or animal prior to the transplant may act as antigens to the immune system of another human or animal body. In this case, various immune reactions are induced in the transplanted body, and unexpected side effects may occur due to muscle pain or atrophy in the course of the immune response. Therefore, there is a need to suppress the immune rejection reaction by treating various enzymes capable of removing the intrinsic cells included in the allogeneic soft tissue implant. Removing the immune rejection cells by treating the enzyme solution may be implemented in various ways, but the detailed description will be described below with reference to FIG. 3.

According to FIG. 1, the method for preparing allogeneic soft tissue implants according to an embodiment of the present invention includes a step 400 as a fourth step, forming one or more pores on the allogeneic soft tissue support from which the immune rejection-reactive cells have been removed. . The pore is a portion on which autologous stem cells to be described below are carried. The pore is formed by applying a microneedle to the allogeneic soft tissue support. According to FIG. 4, the surface of the homogeneous soft tissue support 10 from which the immune rejection cells have been removed by the third step is stimulated by the microneedle 420 (eg, M100SWBL model, Korea). Is formed. The size (diameter) of the pore 410 may be selected from the range of about 1 to about 1000 micrometers (μm), it is preferably formed of a size (diameter) of about 10 micrometers (μm). The number of the pores 410 is not particularly limited, but it is preferable that as many pores as possible be formed in the surface area of the allogeneic soft tissue support 10. After the pore 410 is formed, a substance for appropriately anchoring the autologous stem cells may be further introduced before or after the autologous stem cells to be described below are introduced. The additionally introduced material may include growth factors and the like.

According to FIG. 1, the method for preparing allogeneic soft tissue implants according to an embodiment of the present invention includes a step 500 of injecting autologous stem cells of a user into the formed pores. The autologous stem cells refer to stem cells present in the body to be transplanted. The stem cell is generally defined as a cell having the possibility of being differentiated into various kinds of cells constituting the body, such as nerves, blood, cartilage, etc., if necessary to remain undifferentiated into specific cells. The stem cells are currently used in a variety of regenerative medicine fields, and are sequentially replacing or supplementing classical drug treatments or surgical treatments. In particular, adult stem cells are cells that constitute specific tissues in the body, and they provide a minimum amount of cells that exist in the body in small amounts and maintain a normal state when the body is externally affected. Do this. In particular, the adult stem cells have an advantage of being capable of autologous transplantation because the immune rejection response is insignificant or nonexistent in the field of transplantation for organ regeneration. The autologous stem cells according to the present invention may use various stem cells of the body to be transplanted, but it is preferable to use autologous stem cells obtained from bone marrow of the body to be transplanted. The autologous stem cells are injected into the pores formed in the fourth step and incubated under appropriate conditions with the allogeneic soft tissue support in the culturing step to be described below to be an allogeneic soft tissue implant.

According to FIG. 1, a method for preparing allogeneic soft tissue implants according to an embodiment of the present invention includes a step (600) of culturing allogeneic soft tissue support into which autologous stem cells are injected. The culturing step 600 is implemented under appropriate conditions so that the allogeneic soft tissue scaffold into which the autologous stem cells are injected can be an allogeneic soft tissue implant with optimal transplant conditions. In this case, the appropriate conditions may be considered appropriate temperature, proper pressure, suitable period. Meanwhile, the culturing step 600 may further include providing a physical stimulus to the allogeneic soft tissue support. The physical stimulus providing step will be described in detail later with reference to FIG. 6.

Figure 2 shows the individual steps for implementing the scaffold cleaning and sterilization step included in the method for producing a homogeneous soft tissue scaffold according to an embodiment of the present invention.

According to FIG. 2, the washing and sterilizing the obtained allogeneic soft tissue support 200 may include treating hydrogen peroxide with the obtained allogeneic soft tissue support and applying ultrasonic wave 210. Treating the allogeneic soft tissue support with a radioprotectant and irradiating the radiation 220.

By treating the obtained peroxide soft tissue support with hydrogen peroxide and applying ultrasonic waves (200), not only the chemical washing sterilization effect but also the physical washing sterilization effect on the allogeneic soft tissue support can be obtained. On the other hand, the hydrogen peroxide treatment and ultrasonic application step 200 may contribute to the strengthening of physical properties, such as tensile strength (tensile strength) of the homogeneous soft tissue support in a particular region. For example, ligaments obtained from the human body are treated with hydrogen peroxide in the concentration range of about 0.1 to about 5.0 percent (%) and ultrasonic waves in the power range of about 120 to about 400 watts (W) result in increased tensile strength of the ligaments. Appeared. Thus, in the step 200 of treating hydrogen peroxide and applying ultrasonic waves to the obtained homogeneous soft tissue scaffold, the treated hydrogen peroxide has a concentration selected from a concentration range of 0.1 to 5.0 percent (%) and the applied ultrasonic waves are 120 It is preferred to have an output selected from the range of from 400 watts (W), in particular the hydrogen peroxide treated has a concentration range of 0.5% percent (%) and more preferably the applied ultrasound has a 120 watt (W) output. . In addition, the sterilization effect may be maximized by treating the obtained allogeneic soft tissue support with a radiation protective material and irradiating the radiation 220. Typically, the homogeneous soft tissue scaffold may be sterilized by irradiation with radiation, but by using the radiation protective material, adverse effects may be minimized by radiation. The radiation protective material to be treated may vary, but is preferably cobalt 60 (Co ⁶⁰ ), the radiation to be irradiated may be selected within a variety of ranges, preferably selected from the range of 12 to 50 klogy (kGy) It is a gamma ray. Meanwhile, in the step 200 of washing and sterilizing the obtained homogenous soft tissue support, treating the obtained homogenous soft tissue support with hydrogen peroxide, applying ultrasonic wave 210 and treating the radiation protective material, and radiation Examining step 220 may be applied individually as well as applied separately. In this case, in the step of washing and sterilizing the obtained homologous soft tissue support (200), the hydrogen homogenate is treated to the obtained homologous soft tissue support, and after applying the ultrasound (210), thereafter, the radiation protective material is treated. It is preferable to apply the step 220 of irradiating radiation.

Figure 3 shows the individual steps for implementing the step of removing the immune rejection cells included in the method for producing a homologous soft tissue scaffold according to an embodiment of the present invention.

According to FIG. 3, the step of removing the immune rejection cells 300 includes treating the enzyme solution 310 and / or washing with water saline 320. The enzyme solution may include various enzymes for removing immune rejection cells, but preferably includes trypsin, collagenase and protease. For example, the enzyme solution may contain about 0.25% trypsin (0.02% EDTA, invitrogen Corp., USA), about 3 mg collagenase A (0.15 U / mg, Sigma aldrich, USA) and about 15 mg protease (4.8 U / mg, Sigma aldrich, USA), and the enzyme solution may be stirred onto the homogenous soft tissue support with a solution of about 40 ml at about 37 ° C. and about 120 rpm for about 4 hours (using a shaking incubator, Yen Biotech, South Korea). On the other hand, the washing step of washing with brine 320 is for washing to remove the remaining enzyme solution. Therefore, the step of removing the immune rejection cells (300) further comprises the step of washing (320) an enzyme solution to the washed and sterilized homologous soft tissue scaffold and additionally washing (320) with physiological saline. can do. In addition, the step (300) of removing the immune rejection cells is treated with an enzyme solution in the washed and sterilized homogenous soft tissue support (310), washed with physiological saline (320), followed by osmotic treatment with distilled water ( 330) may further comprise the step of washing. However, since the physiological saline is to be used for washing, the content, salinity, etc. of the components of the physiological saline are not particularly limited. For example, the physiological saline may be treated with the solution of about 40 ml at about 4 ° C. and about 120 rpm on the allogeneic soft tissue scaffold, and may be treated continuously for about 12 hours after three repeated treatments of about 1 minute. . In this case, after washing with physiological saline, osmotic treatment with distilled water may be performed, and for example, ultrasonication may be performed at an output of about 240 watts (W) for about 5 minutes (using ultra sonicator). , Biofree, South Korea). Figure 9a is a scanning electron microscope (SEM) photograph of the surface and cross-section of the allogeneic soft tissue support before removing the immune rejection cells included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention, Figure 9b is SEM (scanning electron microscope) photograph of the surface and cross-section of the allogeneic soft tissue support after the step of removing the immune rejection cells included in the method for producing an allogeneic soft tissue implant according to an embodiment of the present invention. In addition, Figure 10a is a hematoxylin & eosin stained photo of the cross-section of the allogeneic soft tissue support before the step of removing the immune rejection cells included in the method for producing allogeneic soft tissue implants according to an embodiment of the present invention, Figure 10b is It is a hematoxylin & eosin staining picture of the cross section of the allogeneic soft tissue support after the step of removing the immune rejection cells included in the method for producing a homogenous soft tissue implant according to an embodiment. 9B and 10B, it can be seen that the cells of the allogeneic soft tissue graft were removed by removing the immune rejection-responsive cells.

Figure 5 shows the individual steps for implementing the autologous stem cell injection step included in the method for producing allogeneic soft tissue support according to an embodiment of the present invention.

According to FIG. 5, injecting autologous stem cells of the user into the formed pores 500 further includes injecting autologous stem cell support promoting material 510 before or simultaneously with the injection of autologous stem cells 520. It may include. The autologous stem cell supporting promoter is concentrated and lyophilized to a high concentration of a liquid containing water-soluble proteins such as collagen, gelatin, BMP2, BMP4, BMP7, PDGF, TGF-beta at high concentration, and then rehydrated to give a constant viscosity. As a material reconstituted with a chewy liquid, autologous stem cells injected into the pore can be induced to properly settle in the allogeneic soft tissue support. The autologous stem cell supporting promoter is purely manufactured from bones of the human body without the addition of external substances, and therefore, there is no immune rejection response to the body to be transplanted, and is bioactive. Therefore, the additional injection of the autologous stem cell support promoting material, the autologous stem cells show significant bone induction ability and bone conduction ability in the allogeneic soft tissue support, and easily adapts to the body by maintaining viscosity by collagen components.

Figure 6 shows the step of providing a physical stimulus in the culture of allogeneic soft tissue support included in the method for producing allogeneic soft tissue support according to an embodiment of the present invention.

According to FIG. 6, culturing the allogeneic soft tissue support into which the autologous stem cells are injected (600) further includes providing a physical stimulus to the allogeneic soft tissue support (610). As already explained, the soft tissues present in the body are distributed to areas that support or maintain the weight of the body and serve to support and maintain repetitive movements such as bending, twisting, and rotation. Enemies are stimulated. By providing the physical stimulus, by applying the various external stimuli to the allogeneic soft tissue implant to be implanted, the alloplastic soft tissue graft can be efficiently differentiated within the implanted body and easily integrated into the implanted body's native tissue. Make sure Thus, the physical stimulus may be variously implemented to be similar to the stimulus applied to the soft tissue present in the body, but preferably in relation to the motor stimulus, it may be a torsional and / or tensile stimulus. According to an embodiment of the present invention, the provision of the physical stimulus 610 provides a tensile stimulus 611 at both ends of the allogeneic soft tissue support, or the amount of the allogeneic soft tissue support based on the longitudinal axis of the allogeneic soft tissue support. Torsion 612 in the transverse direction, or to both ends of the allogeneic soft tissue support, while providing a tensile stimulus 611 at the same time as the torsion in both transverse directions of the allogeneic soft tissue support relative to the longitudinal axis of the allogeneic soft tissue support. ) May be provided. Specifically, providing tensile stimulus 611 at both ends of the allogeneic soft tissue support extends both ends of the allogeneic soft tissue support in the longitudinal direction, but one end is in the range of 10% or less of the total length of the allogeneic soft tissue support. At the same time as extending the other end in the range of less than 10% of the total length of the allogeneic soft tissue support, providing a twist 612 in both transverse directions of the allogeneic soft tissue support both ends of the allogeneic soft tissue support While rotating, one end may be rotated to a range of 45 degrees or less in the clockwise direction and the other end may be rotated to a range of 45 degrees or less in a counterclockwise direction. In addition, the physical stimulus including the tensile stimulus 611 and / or the torsional stimulus 612 may be provided at various frequencies, but is preferably provided at a frequency of less than once per second. Meanwhile, the culturing step 600 including the physical stimulus providing step 610 may be performed for various periods, but may be preferably performed within a range of about 7 days or less. In accordance with the step of providing the physical stimulation, the ligament tissue of the pig was obtained and tested to determine whether the allogeneic soft tissue support can have a strength similar to that of the normal tissue of the human body. About 10% tensile stimulation (pulling both ends to about 5%) and about 90 degrees torsional stimulation (rotating one end about 45 degrees clockwise, the other end about 45 degrees counterclockwise) ) Was given once per second for 1 day, 4 days and 7 days to determine the respective intensity. As a result, the maximum load value (Newton (N)) was about 354.9 Newtons (N) for the control group that provided no stimulation, about 380.8 Newtons (N) for the experimental group that provided stimulation for 1 day. It was measured about 418.6 Newtons (N) for the experimental group that provided stimulation for one day and about 818.1 Newtons (N) for the experimental group that provided stimulation for 7 days. The results showed that porcine ligament tissues that were continuously provided with tensile and torsional stimuli could reach values close to the strengths similar to normal tissues of the human body.

Specifically, the results of real time PCR analysis of collagen type I, type III and tenascin-c genes of stem cell-supported gel-graft tibia tendon, which were physically stimulated for 1, 3, and 7 days in the incubator. The collagen type I gene was increased three times to 0.11 ± 0.01 and 0.34 ± 0.02 in the 1st and 7th day. The collagen III gene increased by 2.2-fold in the 1st and 7th days to 0.31 ± 0.01 and 0.67 ± 0.03. Tenascin-C increased 1.9 fold to 0.42 ± 0.01 and 0.79 ± 0.02 for Day 1 and Day 7. The increase of tenascin-C, a representative marker of ligament tissue, was confirmed. Through this, the physically stimulated human bone marrow-derived mesenchymal stem cells were differentiated into ligament tissue.

Specifically, the analysis of the content of GAG secreted in the culture medium of the stem cell-supported gel transplant group (5x10 ⁵ cell / cm ² ) inoculated on the surface of the pig tibia tendon in the incubator and the group without physical stimulation Proceeded. After culturing the cultures for 1, 3, 7 days, the absorbance was measured at 656 nm using a GAG assay kit. The linear regression of the standard chondroitin-4-sulfate curve yielded 99.9%. The group with physical stimulation showed higher GAG content than the group without physical stimulation, and the group without physical stimulation showed 14.187 ± 0.080 μg / μl on day 1, 25.542 ± 0.599 μg / μl on day 3, and 36.346 ± 0.843 μg on day 7 / Μl, physical stimulation was 14.986 ± 0.765 μg / μl on day 1, 33.298 ± 0.936 μg / μl on day 3, and 44.791 ± 0.087 μg / μl on day 7. As a result, the stem cell supported gel transplantation group cultured with physical stimulation for 7 days was increased by about 23% compared to the group without stimulation.

Specifically, the content of collagen secreted in the culture medium of the stem cell supporting gel transplanted group (5x10 ⁵ cell / cm ² ) inoculated on the surface of swine tibial tendon in the incubator and the group without physical stimulation Proceeded. After culturing the cultures for 1, 3, 7 days, the absorbance was measured at 550 nm using a collagen assay kit. The linear regression value of the standard collagen curve was 99.9%. The group with physical stimulation showed higher collagen content than the group without physical stimulation, and the group without physical stimulation showed 0.769 ± 0.012 μg / μl on day 1, 0.949 ± 0.052 μg / μl on day 3, and 1.382 ± 0.028 μg on day 7 / Μl, physical stimulation was 0.811 ± 0.106 μg / μl on day 1, 1.218 ± 0.072 μg / μl on day 3, 1.803 ± 0.065 μg / μl on day 7. As a result, the stem cell supported gel transplantation group cultured with physical stimulation for 7 days was increased by about 30% compared to the group without stimulation.

Hereinafter, one or more embodiments will be described in more detail with reference to Examples. However, these examples are provided to illustrate one or more embodiments illustratively and the scope of the present invention is not limited to these examples.

실험예 1: 동종 연조직 지지체의 멸균Experimental Example 1: Sterilization of allogeneic soft tissue scaffold

In order to obtain a soft tissue support, pig patella and tibia were obtained. The obtained soft tissue support was sterilized using Clearant Process® (US2005 / 6,908,591B2), which was subjected to chemical agents to the tissue and then subjected to high dose gamma-ray sterilization. The specific method is as follows.

A radiation protection solution was prepared by mixing 16.2% propylene glycol, 22.1% DMSO, 2.7% mannitol and 3.8% tetrahalose and 60.0% purified water. The homogenous gun to be sterilized was placed in a sterile pouch, a solution prepared in proportion to the weight of the tissue, and then subjected to thermal bonding packaging. After chemical treatment in accordance with the Clearant Process® process, the tissue moisture is removed with a sterile towel (20-30% moisture residue), and the lyophilized tissue is freeze-dried and the cryopreserved tissue is packaged. Frozen storage. The total time required for drug treatment of tissues was 25 hours, followed by an additional 24 hours for tissues for lyophilized storage. In addition, sterilization was performed in gamma rays (0, 25, 50 KGy). After treatment with clearant, the bones of the irradiated bones were found to have an increased tensile strength compared to the case of normal irradiation.

실험예 2: 동종 연조직 지지체의 면역거부반응 억제Experimental Example 2 Inhibition of Immune Rejection of Allogeneic Soft Tissue Scaffold

<실험예 2-1> 면역거부반응 억제를 위한 연조직 지지체의 탈세포화Experimental Example 2-1 Decellularization of Soft Tissue Scaffold for Inhibition of Immune Rejection

Decellularization was performed to remove tissue antigens for cellular components from the washed and sterilized soft tissue scaffolds. The decellularization process was performed using enzyme solution treatment, water treatment and osmotic treatment, and the specific method is as follows.

For treatment of the enzyme solution, the frozen pork tendon tendon (12 cm long, 1 cm wide) was taken out of a -70 ° C. deep freezer, and then placed in sterile distilled water and thawed at 37 ° C. in a water bath (DongA, KOREA) for 30 minutes. Enzyme cocktail solution after thawing [500 ml of 0.25% trypsin (T4049, SIGMA, USA), 37.5 ml of collagenase A (C0130, SIGMA, USA), protease (P4630, SIGMA, USA) 187.5] 500 Ten tibial tendons were placed in a 1,000 ml beaker containing ㎖, and stirred for 4 hours at 120 rpm and 37 ° C in a shaker incubator (NB-205V, N-BIOTEK, KOREA).

After 4 hours for flushing, the enzyme cocktail solution was removed and 500 ml of saline was added. Thereafter, the mixture was washed by stirring in a shaker incubator at 120 rpm and 4 ° C. for 1 hour. This process was repeated three times, and the last washing process was carried out for 12 hours.

After 12 hours for osmotic treatment, saline was removed and 500 ml of sterile distilled water was added. Then, it treated for 5 minutes on 240w conditions using the ultrasonic apparatus. Sterile distilled water was removed, and 500 ml of physiological saline was added and treated for 5 minutes under 240w conditions using an ultrasonic apparatus.

<실험예 2-2> 탈세포화된 지지체의 주사전자현미경 촬영Experimental Example 2-2 Scanning Electron Micrograph of Decellularized Support

The appearance of tissue before and after decellularization of porcine tibia tendon was confirmed by scanning electron microscopy (5kV, JSM-6380, Jeol Inc., JAPAN). The specific method is as follows. The washed and sterilized pork tibia tendon obtained above was washed with 1 M phosphate buffer (70011, GIBCO, USA, pH 7.4). Then, 2.5% glutaraldehyde (glutaraldehyde) (340855, SIGMA, USA) was added to fix the solution, and then fixed at 4 ° C. for 24 hours. After washing with sterile PBS, the concentration of alcohol was increased to 50, 70, 80, 90, and 100% for 1 hour and then dehydrated. The dehydrated tissue was placed in a humidity controller (Dry keeper, Sanplatec, JAPAN) and dried at room temperature. The dried tissue was fixed to the specimen holder using double-sided tape, and then coated with 200 μm thick platinum using a plasma sputter. Subsequently, the appearance morphology of the tissue was observed 30 and 300 times using a low magnification scanning electron microscope.

<실험예 2-3> 탈세포화된 지지체의 조직학적 염색Experimental Example 2-3 Histological Staining of Decellularized Supports

Cell nuclei and cytoplasm distributed in tissues were stained with hematoxylin and eosin to determine the distribution patterns and appearance of cells present in the tibia tendon before and after decellularization. The specific experimental method is as follows.

Tissue staining pretreatment was performed as follows. Tissue process (STP 120, Thermo scientific, USA) equipment was used under the following program conditions.

Table 1

Reagent Container No.	Reagent	Soaking time (Immersion Time) in hours: minutes	Stirring ate
Reagent Container No.	Reagent	Soaking time (Immersion Time) in hours: minutes	rpm.	The program value (Programed value)
One	Formalin	12:00	60	One
2	Formalin	12:00	60	One
3	Alcohol 70%	01:30	60	One
4	Alcohol 80%	01:30	60	One
5	Alcohol 95%	01:30	60	One
6	Alcohol 100%	01:00	60	One
7	Alcohol 100%	01:00	60	One
8	Alcohol 100%	01:00	60	One
9	Xylene	01:30	60	One
10	Xylene	01:30	60	One
11	Paraffin	02:00	60	One
12	Paraffin	02:00	60	One

In order to fabricate tissue block specimens, the tissues infiltrated with paraffin solution were placed on a hot base of a tissue embedding system (Histocentre 3, Thermo, USA), and paraffin was first applied. The tissue was put in slightly swollen state. After that, paraffin was filled up. After placing the paraffin block on a cold plate of the tissue embedding system and hardening for 10 minutes, the mold base was removed and stored at room temperature.

In order to fabricate the tissue slides, a tissue slicer (Finess met, Thermo, USA) and a microtome blade were used to trim to 10 μm and tissue sections were made to 4 μm thick. Float in a container containing tap water, and then floated with a slide in a preheated water bath, the tissue sections were attached to each slide and dried at 60 ℃.

Thereafter, H & E staining was performed. Specific dyeing methods are as follows.

In order to perform the deparaffinization process, the tissue slide was soaked three times for 10 minutes in a glass stain jar containing xylene. To perform the water procedure, the tissue slides were soaked for 5 minutes in the first glass staining vessel containing 99.9% alcohol. Tissue slides were transferred to a second glass staining vessel containing 99.9% alcohol for 5 minutes. Tissue slides were transferred to a second glass staining container containing 95% alcohol for 3 minutes. Tissue slides were transferred to a second glass staining vessel containing 80% alcohol for 3 minutes. Tissue slides were transferred to a second glass staining vessel containing 70% alcohol for 3 minutes. Transfer to running tap water for 1 minute.

To carry out the nuclear staining process, the solution was transferred to Harris hematoxylin for 10 minutes and then soaked in running tap water for 3 minutes.

To perform the decolorization process, tapping three times in a glass staining vessel containing 1% alcoholic HCl (alcoholic HCl), and then immersed in running tap water for 3 minutes. For the neutralization process, it was transferred to a glass dyeing vessel containing 1% ammonia water for 1 minute and soaked in flowing tap water for 3 minutes. To carry out the cytostaining procedure, it was transferred to Eosin for 1 minute. Thereafter, tapping was performed three times in a glass staining container containing 70% alcohol to dehydrate. The tissue slides were then soaked for 15 minutes in a glass stained container containing clean xylene. Then, a forceps was used to drop a drop of mount solution onto the tissue slide contained in xylene, cover the cover glass, and photograph the microscope.

<실험예 2-4> 탈세포화된 지지체의 DNA 잔류량 측정Experimental Example 2-4 DNA Residual Measurement of Decellularized Supports

Porcine tibial tendon was frozen at −20 ° C. for 24 hours before and after decellularization and water was removed using a lyophilizer. Thereafter, residual DNA was examined to confirm the amount of residual cells.

DNA quantification was measured using the DNEasy kit (69506-250, Qiagen, USA). The specific method is as follows. Before and after decellularization, 25 mg of lyophilized tissue was placed in a 1.5 ml microcentrifuge tube, followed by addition of 180 µl of ATL buffer. 20 μl of Proteinase K was added to the tube, and after stirring, the mixture was allowed to stand at 55 ° C. in a heating block until the tissue was completely decomposed (the stirring was performed every 2 hours). After confirming the decomposition, the mixture was mixed using a vortex mixer for 15 seconds. 200 μl of AL buffer was added to the tube, mixed using a vortex mixer, and allowed to stand for 10 minutes at 70 ° C. in a thermal block. 200 μl of 99.9% alcohol was added to the tube and mixed using a vortex mixer. The mixed samples were placed in a DNeasy spin column coupled to a 2 ml collection tube and centrifuged (8,000 rpm) for 1 minute to remove the filtrate from the collection tube. 500 µl of AW1 buffer was added to a DNeasy spin column coupled to a 2 ml collection tube, followed by centrifugation (8,000 rpm) for 1 minute to remove the filtrate from the collection tube. 500 μl of AW2 buffer was added to a DNeasy spin column coupled to a 2 ml collection tube and centrifuged (17,000 rpm) for 3 minutes to allow the DNeasy membrane to dry completely. The liquid in contact with the DNeasy spin column was confirmed, and when contacted, centrifugation (17,000 rpm) was further performed for 1 minute. To the new 1.5 ml microcentrifuge tube was combined DNeasy spin column dried DNeasy membrane, and 200 μl of AE buffer was added and allowed to stand at room temperature for 1 minute. Then, centrifugation (8,000 rpm) was performed for 1 minute, and the liquid eluted in the 1.5 ml micro centrifuge tube was used. The eluted solution was measured using a DNA quantification program of Nanodrop (nanodrop 2000, thermo, USA). As a result, it was confirmed that the residual amount of DNA was significantly low in the tibiar dog that performed the decellularization step as follows.

TABLE 2

Sample	DNA Retention (ng / mg)
Tibial tendon without decellularization	269.9 ± 10.9
Tibial tendon undergoing decellularization	62.7 ± 8.5

실험예 3: 자가 줄기 세포 담지 촉진 물질을 이용한 줄기 세포의 주입Experimental Example 3 Injection of Stem Cells Using an Autologous Stem Cell Support Promoting Material

<실험예 3-1>: 세포 담지 촉진 물질의 제조Experimental Example 3-1: Production of Cell Support Promoter

In order to inject autologous stem cells into tibia dogs with autologous stem cells, cell supporting promoters were prepared in the following manner.

Collagen gel extracted from pig skin by treatment with pepsin in a sterile process system was purchased from Bioland Co., Ltd., and as a result of checking the test report, more than 99% of collagen was in type I form.

Reconstitution buffer for gelling collagen solution 2.2% NaHCO in 0.05 N NaOH aqueous solution₃(90421-C, SAFC Bioscience, USA) and 200 mM HEPES (H4034, SIGMA, USA) were dissolved and the total volume was adjusted to 100 ml. Filter sterilization using a 0.2 ㎛ syringe filter (16534, Satorius stedim, USA), and refrigerated 4 ℃ until use. PBS solution Filter sterilization using a 0.2 ㎛ syringe filter, and refrigerated at 4 ℃ until use.

The final collagen solution was prepared by mixing an acid-soluble collagen gel solution: PBS (10 × concentrated solution): reconstitution buffer solution 8: 1: 1. When mixed, it was placed in a styrofoam box containing ice to prevent rapid gelation of the neutral collagen gel.

<실험예 3-2>: 세포 담지 촉진 물질에서 자가 줄기 세포의 증식률 확인Experimental Example 3-2 Confirmation of Proliferation Rate of Autologous Stem Cells from Cell Support Promoter

Human bone marrow-derived mesenchymal stem cells collected after centrifugation were divided into 1x10 ⁵ , 2x10 ^5, and 5x10 ⁵ cell / cm ² groups, respectively, and slowly mixed with the neutral collagen gel prepared above to prevent bubbles from being generated. 150 μl of the cell-supported collagen gel was dispensed into 48 well culture plate dishes and allowed to stand for 1 hour in an incubator (NB-203XLSP, N-Biotek, KOREA) at 37 ° C. and 5% CO ₂ . Confirmation of gelation after 1 hour (translucent), a-MEM (12571, GIBCO, USA) 200 with 10% FBS (16000, GIBCO, USA), 1% penicillin-streptomycin (15140, GIBCO, USA) 200 Μl aliquots were added. Thereafter, incubation was performed at 37 ° C. in a 5% CO ₂ incubator.

Cell viability of

day

1, 3, and 7 of collagen gel culture based on collagen gel concentration (0.5, 1.0%) and human bone marrow-derived mesenchymal stem cell numbers (1x10 ⁵ , 2x10 ⁵ and 5x10 ⁵ cell / cm ² ) It was. The detailed measuring method is as follows. Vials (5 ml) contained in the EZ Cytox assay kit (Cat. No EZ3000, DAIL LAB, KOREA) were removed and transferred into a clean bench. 3 ml of a-MEM containing 10% FBS and 1% penicillin-streptomycin was added to a 15 ml cornical tube using a pipette and mixed with 300 µl of EZ Cytox reagent. . The medium used for culturing the stem cell loaded collagen gel was removed by vacuum suction method, and 200 μl of each medium mixed with EZ Cytox reagent was added to each well of a 48 well culture plate dish. Incubation was performed at 37 ° C. in a 5% CO ₂ incubator for 1 hour. Absorbance was measured at 450 nm wavelength using an ELISA reader (1420, PerkinElmer, USA) (see FIG. 12).

<실험예 3-3>: 자가 줄기 세포가 담지된 중성 콜라겐의 제조의 줄기 세포에 주입Experimental Example 3-3: Injection into Stem Cells Producing Neutral Collagen Supported with Autologous Stem Cells

It was formed by applying a microfine needle (M100SWBL model, Korea) to the decellularized tibial tendon in order to inject autologous stem cells. The pore diameter was about 10 micrometers (μm). The stem cell loaded collagen gel prepared in Experimental Example 3-2 was injected into the tibial tendon in which the pores were formed.

실험예 4: 물리적 자극을 이용한 연조직 지지체 배양 Experimental Example 4: Soft tissue support culture using physical stimulation

<실험예 4-1>: 물리적 자극을 동반한 연조직 지지체 배양 Experimental Example 4-1: Soft Tissue Scaffold Culture with Physical Stimulation

The physical strength propensity of stem cell-supported gel grafts inoculated into tibial tendon was compared and analyzed according to physical stimulation conditions and time settings in the incubator. In other words, to determine the effect on the strength of the implant was carried out in the following way. Specimens were prepared in a size of 12 × 1 cm ² (horizontal × vertical) and then mounted in the chamber. In the experimental group, 10% (2 mm each end) tension stimulation, 90 ° (torsion stimulation 45 ° in the clockwise and counterclockwise directions, respectively) and frequency of 1 Hz on the computer program. The experiment was conducted by giving a physical stimulus in the incubator for 1, 3, and 7 days under conditions (Table 3), and the control group was incubated for 7 days without physical stimulation in the incubator chamber.

TABLE 3

group		Physical stimulus conditions						Payback period	N number
		Tension (10%)		Torsion (90˚)		Frequency
		Top	bottom	Top	bottom	Top	bottom
Control	-	-	-	-	-	-	-	7 days	3
Experimental group	One	2 mm	2 mm	45˚	45˚	1 hz	1 hz	1 day	3
	2	2 mm	2 mm	45˚	45˚	1 hz	1 hz	4 days	3
	3	2 mm	2 mm	45˚	45˚	1 hz	1 hz	7 days	3

<실험예 4-2>: 물리적 자극을 준 줄기세포 담지겔 이식군의 실시간 PCR 분석Experimental Example 4-2 Real-Time PCR Analysis of Stem Cell Carrying Gel Transplant Group with Physical Stimulation

MRNA was analyzed to analyze the expression of genes according to the differentiation of cells in the transplanted group. RNA was extracted using the RNeasy mini kit (74136, Qiagen, USA). Into the collected tissue 30 mg 600 μl of RLT Plus buffer was homogenized. The supernatant was carefully removed by centrifugation and pipetting at maximum RPM for 3 minutes. The gDNA removal spin column was placed in a 2 ml collection tube and homogenized to add dissolved tissue. The column was removed by centrifugation at 10,000 x g for 30 seconds, leaving the filtered solution. 600 μl of 70% ethanol was placed in a collection tube and pipetted to mix. Raise the RNeasy spin column in a new 2 ml collection tube and add 1,000 μl of mixture. The lid was closed and centrifuged at 10,000 xg for 15 seconds and the filtrate was removed. 700 μl of RW1 buffer was placed on an RNeasy spin column, centrifuged at 10,000 × g for 15 seconds, and the filtrate was removed. 500 μl of RPE buffer was added to an RNeasy spin column, centrifuged at 10,000 × g for 15 seconds, and the filtrate was removed. 500 μl of RPE buffer was added to an RNeasy spin column, centrifuged at 10,000 × g for 2 minutes, and the filtrate was removed. The RNeasy spin column was placed in a new 1.5 mL collection tube, 50 μl of RNase-free water was added to the spin column membrane, and centrifuged at 10,000 × g for 1 minute to obtain RNA extract.

was used ^{SuperScript ® VILO cDNA Synthesis Kit (11754-050} , Invitrogen, USA) to make the cDNA synthesis, it was performed in the following way. 4 μl of 5 × VILO Reaction Mix, 2 μl of 10x SuperScript Enzyme Mix, 2.5 μl of RNA were added, and DEPC-treated water was added to adjust the final volume to 20 μl. The mixed reagents were incubated at 25 ° C. for 10 minutes, incubated at 42 ° C. for 60 minutes, and reacted at 85 ° C. for 5 minutes and terminated. Store at -20 ° C freezer until use.

Then, it was used as the ^{SYBR ® Premix Ex Taq (RR420Q,} TaKaRa, JAPAN) for the Real time PCR analysis was performed in the following way. 12.5 μl of SYBR ^® Premix Ex Taq (1x), 0.5 μl of 0.2 uM PCR Forward Primer, 0.5 μl of 0.2 uM PCR Reverse Primer, 2.0 μl of cDNA synthesis sample and 9.5 μl of DW water were mixed to adjust the total volume to 25 μl. Using a real time PCR instrument (TP800, TaKaRa, JAPAN) 1 step was carried out for 30 seconds at 1 cylce, 95 ℃, 2 step was carried out 40 cycles for 5 seconds at 95 ℃, 30 seconds at 60 ℃. The primers used collagen type I, type III and tenascin-c (Table 4).

Table 4

Genes	Forward primer sequences	Reverse primer sequences
Collagen i	5'-CAGGGTGTTCCTGGAGACCT-3 '(SEQ ID NO: 1)	3'-AGGAGAGCCATCAGCACCTT-5 '(SEQ ID NO: 2)
Collagen iii	5'-GAAAATGGAAAACCTGGGGA-3 '(SEQ ID NO: 3)	3'-CACCCTTTGGACCAGGACTT-5 '(SEQ ID NO: 4)
Tenascin-c	5'-TACAGCCTGGCAGACCTGAG-3 '(SEQ ID NO: 5)	3'-ATTGCTTGGGAGCAGTCCTT-5 '(SEQ ID NO: 6)
GAPDH	5'-AAGGGTCATCATCTCTGCCC-3 '(SEQ ID NO: 7)	3'-GTGATGGCATGGACTGTGGT-5 '(SEQ ID NO: 8)

<실험예 4-2>: 물리적 자극을 준 줄기세포 담지겔 이식군의 GAG 분석Experimental Example 4-2: GAG Analysis of the Stem Cell Carrying Gel Transplant Group with Physical Stimulation

The contents of GAG secreted from the medium of the stem cell-supported gel transplanted group (5x10 ⁵ cell / cm ² ) inoculated on the surface of swine tibial tendon in the incubator and the group without physical stimulation were analyzed. . After culturing the culture medium for 1, 3, 7 days, GAG (Glycosaminoglycan) content analysis was performed using a GAG assay kit. The detailed method is as follows. Sulfated Glycosaminoglycan (0-5 ㎍) was used as a standard reagent in a microcentrifuge tube, and the final volume was adjusted to 100 100 with purified water. The medium of the stem cell supporting gel transplant group cultured for 1, 3 and 7 days was placed in a microcentrifuge tube, and the final volume was adjusted to 100 μl. 1.0 ml of glycosaminoglycan Dye Reagent was added to all the prepared tubes, followed by mixing for 30 minutes using a vortex mixer. It was then centrifuged at 10,000 xg for 10 minutes. After centrifugation, the supernatant was removed and the tube was flipped over to remove the solution at the bottom or wall of the tube, and absorbent paper was used. 1 ml of Blyscan Dissociation Reagent was added to the glycosaminoglycan-dye complex pellet, and the dye bound to glycosaminoglycan was dissolved using a vortex mixer for 10 minutes. Absorbance was measured at a wavelength of 656 nm using a UV spectrometer. Final concentration of GAG was quantified using a standard curve of chondroitin-4-sulfate (see FIG. 14).

<실험예 4-2>: 물리적 자극을 준 줄기세포 담지겔 이식군의 콜라겐 분석Experimental Example 4-2: Collagen Analysis of Stem Cell Carrying Gel Transplant Group with Physical Stimulation

The contents of collagen secreted in the culture medium of the stem cell-supported gel transplanted group (5x10 ⁵ cell / cm ² ) inoculated on the surface of swine tibial tendon in the incubator were not physically stimulated. . After culturing the culture medium for 1, 3, 7 days, the collagen content was analyzed using the collagen assay kit. The detailed method is as follows. Collagen solution (0-50 μg) was used as a standard reagent in a microcentrifuge tube, and the final volume was adjusted to 100 μl with purified water. The medium of the stem cell supporting gel transplant group cultured for 1, 3 and 7 days was placed in a microcentrifuge tube, and the final volume was adjusted to 100 μl. 1 ml of Sircol dye reagent was added to all the prepared tubes, followed by mixing for 30 minutes using a vortex mixer. It was then centrifuged at 10,000 xg for 10 minutes. After centrifugation, the supernatant was removed and the tube was flipped over to remove the solution at the bottom or wall of the tube and absorbent paper was used. Alkali reagent was added to the collagen-dye complex pellet, and the dyes bound with the collagen were dissolved using a vortex mixer for 10 minutes. Absorbance was measured at a wavelength of 550 nm using a UV spectrometer. The final concentration of collagen was quantified using the standard curve of collagen (see FIG. 15).

SEQ ID NO: 1 cagggtgttc ctggagacct

SEQ ID NO: aggagagcca tcagcacctt

SEQ ID NO: gaaaatggaa aacctgggga

SEQ ID NO: caccctttgg accaggactt

SEQ ID NO: tacagcctgg cagacctgag

SEQ ID NO 6: attgcttggg agcagtcctt

SEQ ID NO: aagggtcatc atctctgccc

SEQ ID NO: gtgatggcat ggactgtggt

Claims

Obtaining an allogeneic soft tissue support obtained from the body of a human or animal;

Washing and sterilizing the obtained soft tissue support;

Treating the washed and sterilized homologous soft tissue support with an enzyme solution to remove immune rejection cells;

Forming one or more pores on the allogeneic soft tissue support from which the immune rejection cells have been removed;

Injecting autologous stem cells of a user into the formed pores; And

Culturing allogeneic soft tissue scaffolds into which the autologous stem cells are injected;

A method for producing an allogeneic soft tissue implant comprising autologous stem cells.
The method of claim 1, wherein the allogeneic soft tissue scaffold is ligament or bone fragment connecting ligament.
The method of claim 1, wherein the washing and sterilizing step comprises treating hydrogen peroxide with the obtained allogeneic soft tissue support and applying ultrasonic waves.
The method of claim 3, wherein the hydrogen peroxide to be treated has a concentration selected from the concentration range of 0.1 to 5.0 percent (%), the ultrasonic waves applied has an output selected from the range of 120 to 400 watts (W). Methods of Making Allogeneic Soft Tissue Implants.
The method of claim 1, wherein the washing and sterilizing comprises treating the obtained allogeneic soft tissue support with a radiation protective material and irradiating the same.
The method of claim 5, wherein the radiation protective material to be treated is cobalt 60 (Co 60 ), and the radiation to be irradiated is gamma rays selected from the range of 12 to 50 kilograms (kGy).
The method of claim 1, wherein removing the immune rejection cells comprises treating an enzyme solution comprising trypsin, collagenase and protease.
The method of claim 1, wherein the removing the immune rejection cells further comprises the step of washing by washing with physiological saline after treating the enzyme solution to the washed and sterile allogeneic soft tissue support. Methods of making soft tissue implants.
The method of claim 1, wherein removing the immune rejection cells further comprises washing the sterilized homologous soft tissue scaffold with an enzyme solution followed by washing with physiological saline, followed by an osmotic treatment with distilled water. Allogeneic soft tissue implant manufacturing method comprising a.
The method of claim 1, wherein in forming the one or more pores, the pores have a size selected from the range of 1 to 1000 micrometers (μm).
The method of claim 1, wherein the injecting the autologous stem cells further comprises injecting autologous stem cell support promoting substances prior to or simultaneously with the autologous stem cell injection.
The method of claim 1, wherein culturing the allogeneic soft tissue support further comprises providing a physical stimulus to the allogeneic soft tissue support.
12. The method of claim 11, wherein the physical stimulus is provided to the allogeneic soft tissue support at a frequency of up to once per second.
The method of claim 11, wherein providing the physical stimulus provides tensile stimulation at both ends of the allogeneic soft tissue support, provides twist in both transverse directions of the allogeneic soft tissue support about the longitudinal axis of the allogeneic soft tissue support, or A method for producing an allogeneic soft tissue implant, characterized in that it provides tensile stimulation at both ends of the allogeneic soft tissue support and at the same time provides a twist in both transverse directions of the allogeneic soft tissue support based on the longitudinal axis of the allogeneic soft tissue support.
15. The method of claim 13, wherein providing tensile stimulation to both ends of the allogeneic soft tissue support extends both ends of the allogeneic soft tissue support in the longitudinal direction, with one end being less than 10% of the total length of the allogeneic soft tissue support. At the same time as extending the other end of the allogeneic soft tissue implant manufacturing method, characterized in that extending to less than 10% of the total length of the soft tissue support.
The method of claim 13, wherein providing twist in both transverse directions of the allogeneic soft tissue support rotates both ends of the allogeneic soft tissue support, while rotating one end to a range of 45 degrees or less in the clockwise direction and at the same time the other end. Method for producing a homologous soft tissue implant, characterized in that it rotates in the clockwise 45 degrees or less range.
The method of claim 1, wherein the culturing step is performed in a range of 7 days or less.