Patent Application
20180008750
The present invention relates to an artificial biomembrane using a silk matrix and a method of manufacturing the same and, more particularly, to an artificial biomembrane using a silk matrix, which is biocompatible and may exhibit high cell culture capacity, and a method of manufacturing the same.
Also, the present invention relates to an artificial biomembrane using a silk matrix, which has superior tensile strength and elongation, which are required of biomembranes, and to a method of manufacturing the same.
Among a variety of materials for use in medical applications, animal-derived collagen has high biocompatibility and tissue compatibility. Further, it exhibits hemostatic functions, and is completely degraded and absorbed in vivo.
Collagen is obtained through extraction and purification from connective tissues of a variety of organs, such as the skin, bones, cartilage, tendons, and internal organs of animals, using an acid solubilization process, an alkali solubilization process, a pH-neutral solubilization process, or an enzyme solubilization process.
Typically available extracted collagen for medical applications is degraded on the molecular scale to the level of monomers to oligomers, and is preserved in a powder or liquid phase.
Extracted collagen is very rapidly converted into a sol when coming into contact with water, body fluids or blood, because the collagen molecule is degraded to the monomer to oligomer level.
Hence, such collagen is used in a manner in which it is applied on the surface of a synthetic polymer material, such as nylon or silicone, to realize a predetermined hardness so as to be biocompatible when molded as a medical material. Furthermore, an extracted collagen molded product is being utilized through chemical crosslinking using a crosslinking agent, or physical crosslinking using radiation, e-beams, UV light, heat, etc., in order to retain the shape thereof for a predetermined period of time when applied in vivo.
When collagen is used in combination with such a synthetic polymer material, the synthetic polymer material may be left behind as a foreign material in vivo, making it easy to cause disorders such as granulomatosis, inflammation, etc. Thus, such a material cannot be applied to all cells or organs.
Even when the collagen material is crosslinked, the properties of the collagen, especially its tensile strength, may not be readily increased, thus making it impossible to use collagen as a medical material that is required for a suture process.
Moreover, the use of the crosslinking agent such as glutaraldehyde or epoxy is problematic because the crosslinking agent is toxic in vivo and because the inherent biochemical properties of collagen, especially the effect of promoting cell proliferation, may be lost.
Collagen cannot be imparted with satisfactory properties through physical crosslinking, and moreover, it is difficult to crosslink collagen so as to control the absorption rate in vivo.
In the case where the brain or various organs undergo a surgical operation due to diverse diseases or trauma and then the surgical wounds are closed, the incised dura mater, pericardium, pleura, peritoneum or serous membrane should be sutured again and closed. Due to such a suture, a shrunken portion may be formed, or the membrane may be partially excised, and thus the surgical wounds cannot be completely closed, and a defect may be created in the membrane.
When such a defect is allowed to remain, organs such as the brain, heart, lungs, and intestines may escape through the defect in the membrane, undesirably causing serious disorder or exposing the organs to the surrounding water or air, owing to which the surgical wounds do not heal.
Hence, a medical replacement membrane usable as a preservative for such a defect may be exemplified by lyophilized human dura mater collected from a dead body, a porous expanded polytetrafluoroethylene (EPTFE) film, polypropylene mesh, a Teflon sheet, a Dacron sheet, etc.
However, the use of human dura mater may entail a concern about epileptic seizures after surgery due to the adhesion of preserved human dura mater and brain parenchyma tissue. In particular, EPTFE is not degraded in vivo but may remain as a foreign material, thereby readily leading to infection. Furthermore, when it contacts the bio-tissue, tissue cells may generate apodyopsis. In this way, the existing membranes are known to cause many postoperative complications.
Accordingly, various materials for biomembranes, which possess biochemical properties, have properties suitable for suture treatment, and are able to retain their shapes for a predetermined period of time after application in vivo, are being developed.
Related techniques include Korean Patent Application Publication No. 10-2002-0036225 (Laid-open date: May 16, 2002, Title: Biomembrane for the protection and treatment of skin disease) and Korean Patent No. 10-1280722 (Registration Date: Jun. 25, 2013, Title: Thin film multilocular structure made of collagen, member for tissue regeneration containing the same, and method for producing the same).
Accordingly, an object of the present invention is to provide an artificial biomembrane using a silk matrix and a method of manufacturing the same, wherein the manufacturing process is relatively simple, and thus the manufacturing cost may be reduced compared to when manufacturing typical artificial biomembranes, and the artificial biomembrane may exhibit high cell culture capacity and biocompatibility.
Another object of the present invention is to provide an artificial biomembrane using a silk matrix and a method of manufacturing the same, wherein the artificial biomembrane has superior tensile strength and elongation, which are required of biomembranes.
The technical problem according to the present invention is not limited to the above objects, and other objects that are not described herein will be obviously understood by those having ordinary skill in the art from the following description.
In order to accomplish the above objects, the present invention provides an artificial biomembrane using a silk matrix, which is configured such that a silk matrix having a cross-section with a first thickness, produced from silkworms, is subjected to planar division into two or more silk matrix pieces having a predetermined shape with the first thickness.
In addition, the present invention provides an artificial biomembrane using a silk matrix, which is configured such that a silk matrix having a cross-section with a first thickness, produced from silkworms, is subjected to thickness division into two or more silk matrix portions having a second thickness, which is less than the first thickness.
In addition, the present invention provides an artificial biomembrane using a silk matrix, which is configured such that a silk matrix having a cross-section with a first thickness, produced from silkworms, is subjected to planar division into two or more silk matrix pieces having a predetermined shape with the first thickness, and each of the silk matrix pieces having the first thickness is subjected to thickness division into silk matrix pieces having a second thickness, which is less than the first thickness.
According to the present invention, the artificial biomembrane has superior tensile strength and elongation, which are required of biomembranes, and can also manifest high cell culture capacity and biocompatibility. Furthermore, the manufacturing process thereof is simple, thereby reducing the manufacturing cost compared to when producing typical artificial biomembranes.
Unless otherwise stated, the meanings of the terms, descriptions, etc., disclosed in the present specification may be those that are typically used in the art to which the present invention belongs. Hereinafter, a detailed description will be given of the present invention.
A biomembrane refers to a membrane that constitutes a cell membrane or an organelle. That is, it functions as a boundary with the outside to prevent nucleic acids, proteins, and other biomaterials from being discharged to the outside, and is responsible for creating an independent environment to sustain life activity. Furthermore, a biomembrane is provided around the cells to protect the cells from the external environment, and plays a role as the passage for the transport of materials between the cytoplasm and the external environment.
The biomembrane has to have properties suitable for a suture process, and has to retain its shape for a predetermined period of time even after application in vivo. Also, the biomembrane is composed of a material that prevents adhesion to surgical wounds, entails no concern about infection, does not cause tissue degeneration, and promotes regeneration activity.
An artificial biomembrane is generally utilized as an artificial medical replacement membrane for use in an artificial neural tube, an artificial spinal cord, an artificial esophagus, artificial organs, artificial blood vessels, artificial valves, replaceable dura mater, artificial drum skins, etc.
However, the artificial biomembrane, which is currently available, is pretreated through physical crosslinking, etc. in order to ensure the above properties, but is problematic because it may become toxic in vivo upon long-term application, or it may remain as a foreign material in vivo. Furthermore, such an artificial biomembrane is made of expensive material because pretreatment and chemical treatment processes are performed in order to ensure the above properties, and thus the use thereof is difficult.
Therefore, in the present invention, the artificial biomembrane using a silk matrix is manufactured, the use of which is relatively simple, thus considerably reducing the production cost thereof compared to when manufacturing typical artificial biomembranes. Moreover, such an artificial biomembrane may exhibit superior cell culture capacity, biocompatibility, high tensile strength, and high elongation. Below is a detailed description thereof, made with reference to various examples.
As illustrated in
1. First Step: Preparation of silk matrix pieces having first thickness
A silk matrix having a cross-section with a first thickness, produced from silkworms, is subjected to planar division into two or more pieces having an appropriate shape, thus obtaining silk matrix pieces having the first thickness.
When silkworms become mature silkworms to protect themselves, they begin to transform into pupae by spinning cocoons. When a silkworm transforms into a pupa, it spins a cocoon to make a pupal casing having a round and elongated shape. The casing is oval-shaped, and shows various colors depending on the kind of silkworm, and both ends thereof are slightly pointed and are thick. However, in the course of building cocoons by the silkworms, when a sheet on which the silkworms are placed is moved so as to disturb the formation of normal cocoons by the silkworms, silkworms do not make cocoons. The silkworms are artificially induced to spin cocoons on the sheet by moving the sheet on which the silkworms are placed, whereby the cocoons are spun in the form of a planar sheet, yielding a silk matrix.
Based on the above features, as illustrated in
As illustrated in
In the case where the sheet on which silkworms are placed is moved to form a silk matrix, the movement thereof may be carried out variously. The sheet may be moved in a manner of being rotated, repeatedly tilted upward and downward and/or leftward and rightward, or vibrated. Alternatively, the sheet may be moved through a combination of rotation and repeated tilting upward and downward and/or leftward and rightward. The number or rate of movement or tilting processes may be appropriately set in order to ensure that the silk matrix has the desired shape.
The shape of the sheet on which silkworms are placed is not limited. A circular shape or a rectangular shape may be applied. Alternatively, any shape may be applied so long as silkworms do not spin cocoons normally in response to the movement of the sheet.
In another modification, the method of manufacturing an artificial biomembrane using a silk matrix of Example 2 according to the present invention, as illustrated in
1. First Step: Preparation of Silk Matrix Portions Having Second Thickness
A silk matrix having a cross-section with a first thickness, produced from silkworms, is subjected to thickness division into two or more portions having a second thickness, which is less than the first thickness.
The silk matrix 10 having the first thickness is produced from silkworms in such a manner that silkworms spin cocoons while being forced to move on the sheet, as in the description of
The first thickness of the silk matrix 10 may vary depending on the number of silkworms used to prepare the silk matrix and the period of time that the silkworms require to spin cocoons.
As shown in
The silk matrix portions 30 having the second thickness may be used unchanged as the artificial biomembrane. Alternatively, portions of the silk matrix portions 30 having the second thickness may be utilized by adjusting the size thereof so as to be suitable for some end use. Further, packing or sterile treatment and chemical treatment may be additionally performed, as necessary.
In a further modification, the method of manufacturing an artificial biomembrane using a silk matrix of Example 3 according to the present invention, as illustrated in
1. First Step: Preparation of Silk Matrix Pieces Having First Thickness
A silk matrix having a cross-section with a first thickness, produced from silkworms, is subjected to planar division into two or more pieces having an appropriate shape, thus forming silk matrix pieces 20 having the first thickness.
In this case, the silk matrix pieces 20 having the first thickness are formed in the same manner as in the first step of the description of
When the first thickness of the silk matrix pieces 20 thus formed is suitable for use in an artificial biomembrane, such silk matrix pieces may be used without change. In the case where these silk matrix pieces are thick and difficult to use, they should be additionally subjected to the following second step so as to have a thickness suitable for artificial biomembranes. The second step is described below.
2. Second Step: Preparation of Silk Matrix Pieces (Artificial Biomembrane) Having Second Thickness
Silk matrix pieces 40 having a second thickness, suitable for use as an artificial biomembrane, are prepared.
The silk matrix pieces 20 having the first thickness, obtained in the first step, are configured as illustrated in
The first thickness of the silk matrix pieces 20 may vary depending on the number of silkworms used to prepare the silk matrix and the period of time that the silkworms require to spin cocoons.
When the silk matrix pieces 20 having the first thickness are suitable for use in an artificial biomembrane, they may be used without change. As illustrated in
The silk matrix pieces 40 having a second thickness may be used unchanged as an artificial biomembrane for any purpose. Further, packing or sterile treatment and chemical treatment may be additionally performed, as necessary.
A better understanding of the present invention may be obtained through the following examples and test examples, which are set forth to illustrate, but are not to be construed to limit the scope of the present invention.
As illustrated in
The above tilting process was performed for one day, equilibrium was maintained for two days, and the above tilting process was performed again, whereby a silk matrix was produced from the silkworms in about three days. The silk matrix had a thickness of about 0.01 mm.
As shown in
As illustrated in
The above tilting process was performed for one day, equilibrium was maintained for two days, and the above tilting process was performed again, whereby a silk matrix was produced from the silkworms in about three days. The silk matrix had a thickness of about 0.7 mm.
As shown in
As illustrated in
The above tilting process was performed for one day, equilibrium was maintained for two days, and the above tilting process was performed again, whereby a silk matrix was produced from the silkworms in about three days. The silk matrix had a thickness of about 0.7 mm.
The silk matrix was then cut using scissors so as to undergo planar division in a rectangular shape, thus forming silk matrix pieces 20.
As illustrated in
An artificial biomembrane 4 (silk matrix B) according to the present invention was manufactured in the same manner as in Example 3, with the exception that silk matrix pieces 40 having a thickness of 0.2 mm were formed.
An artificial biomembrane 5 (silk matrix C) according to the present invention was manufactured in the same manner as in Example 3, with the exception that silk matrix pieces 40 having a thickness of 0.4 mm were formed.
1. Test Method
The morphology of the silk matrix was observed using SEM, as illustrated in
2. Test Results
As illustrated in
1. Test Method
In order to measure the mechanical properties of the artificial biomembrane using the silk matrix according to the present invention depending on the thickness thereof, tensile testing was performed using a universal testing machine (DAEYEONG, Korea). To this end, a dry sample and a wet sample resulting from immersion in saline for 1 hr were measured to determine the mechanical properties thereof. As a control, a commercially available collagen membrane was used. Analytical samples were manufactured to a size of 20×2.5 (width×length) mm, and the manufactured membrane was stretched at a gauge length of 20 mm and a rate of 10 mm/min. The results are shown in Table 1 below.
2. Test Results
As is apparent from Table 1, the artificial biomembrane using the silk matrix according to the present invention exhibited variable tensile strength and elongation depending on the thickness thereof. The tensile strength and elongation were increased with an increase in the thickness of the membrane, and were also superior in a wet state, rather than a dry state. However, the tensile strength of the collagen membrane useful as a commercially available artificial biomembrane was decreased by a factor of 1/16 in a wet state. Therefore, the artificial biomembrane using the silk matrix, according to the present invention, maintained its properties for a long period of time compared to the collagen membrane in a wet state.
1. Test Method
In order to evaluate the cell culture capacity of the artificial biomembrane, mouse-derived fibroblasts L929 were cultured on the artificial biomembrane under conditions of 37° C. and 5% CO2. The medium for cell culture was a DMEM medium (Dulbecco's Modified Eagles Medium-high glucose, WelGENE, Korea), containing 10% (v/v) FBS (fetal bovine serum, GIBCO), 100 U streptomycin, and 100 μg/ml penicillin (GIBCO). The cell culture capacity of the artificial biomembrane was measured in terms of relative activity using an MTT method.
The results are shown in
2. Test Results
As illustrated in
That is, the artificial biomembrane according to the present invention can be confirmed to be suitable for use as a biomembrane requiring cell growth capacity.
Although the preferred examples and test examples of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims. The scope of the present invention is shown not in the above description but in the claims, and all differences within the range equivalent thereto will be understood to be incorporated in the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2015-0146629 | Oct 2015 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2016/005779 | 6/1/2016 | WO | 00 |
