CN113430159B - Bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold - Google Patents

Bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold Download PDF

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CN113430159B
CN113430159B CN202110547777.XA CN202110547777A CN113430159B CN 113430159 B CN113430159 B CN 113430159B CN 202110547777 A CN202110547777 A CN 202110547777A CN 113430159 B CN113430159 B CN 113430159B
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polyester
bioactive substance
mesh sheet
collagen
sheet layer
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CN113430159A (en
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高毅
李阳
张贵锋
彭青
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Guangdong Qianhui Biotechnology Co ltd
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Guangdong Qianhui Biotechnology Co ltd
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/0062—General methods for three-dimensional culture
    • C—CHEMISTRY; METALLURGY
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    • C12N2513/00—3D culture
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2533/00—Supports or coatings for cell culture, characterised by material
    • C12N2533/30—Synthetic polymers
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2533/00—Supports or coatings for cell culture, characterised by material
    • C12N2533/50—Proteins
    • C12N2533/54—Collagen; Gelatin
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2533/00—Supports or coatings for cell culture, characterised by material
    • C12N2533/70—Polysaccharides
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N2533/00—Supports or coatings for cell culture, characterised by material
    • C12N2533/90—Substrates of biological origin, e.g. extracellular matrix, decellularised tissue

Abstract

The application provides a bionical extracellular matrix bioactive substance coating polyester netted lamellar support, it is in including netted lamellar and the cover of surface carboxylation the bioactive substance coating on the netted lamellar surface of polyester, netted lamellar adopts the polyester material to make, the bioactive substance coating passes through netted lamellar forms through coupling many times, the bioactive substance coating still is equipped with the seal coat outward. This application combines together through possessing certain mechanical properties, the advantage of plasticity with the good biocompatibility of natural macromolecular material with synthetic polyester macromolecular material for the support of this application not only has certain mechanical strength and good biocompatibility, provides bionical cultivation environment for cell culture.

Description

Bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold
Technical Field
The application relates to the technical field of tissue engineering, in particular to a bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold.
Background
The physiological activities such as cell proliferation, differentiation, metabolism and the like are seriously influenced by the regulation and control of a microenvironment, and the bioreactor is a biological reaction device for producing cells in a large scale or harvesting cell culture products. Wherein, the anchorage dependent cells are mainly added with a bracket material in a reactor to provide a cell growth surface, and the high-density culture of the cells is realized through the high specific surface area of the material.
At present, commonly used scaffold materials in bioreactors mainly comprise microcarriers Cytodex, Cytopore microcarriers, fibrous scaffolds and the like. The microcarrier Cytodex as a cell surface adhesion matrix is a spherical two-dimensional cell culture material, and cells naturally settle on the surface of the microcarrier under the action of gravity, and the shape of the cells is changed from spherical to flat. In this mode of culture, the cells undergo dedifferentiation, which gradually deprives the cultured cells of many physiological characteristics of the tissues from which they are derived. Although scale-up of cells can be achieved, the activity and function of cells are difficult to maintain effectively. Meanwhile, the liquid shearing force of the reactor in the mode of the cell coating material can damage the survival rate and the function of the cells. The Cytopore microcarrier is a porous microcarrier, and cells grow in the pores of the material, so that three-dimensional culture can be realized, and the damage of shearing force to the cells can be reduced. The culture mode of the reactor based on the Cytopore microcarrier is a stirring type, and although the porous structure can reduce the damage of the shearing force to the cells to a certain extent, the influence of the shearing force to the cells cannot be fundamentally eliminated. Fibrous scaffolds such as Fibra Disk carriers have certain mechanical strength and good mechanical properties, and can realize an in-vitro three-dimensional culture structure of cells, but the biocompatibility of a pure high polymer material is still certain defects compared with that of a natural extracellular matrix component.
Disclosure of Invention
The purpose of the application is to provide a bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold which has certain mechanical strength and good biocompatibility, is beneficial to cell adhesion, promotes cell differentiation and proliferation, maintains cell functions and can realize high cell yield.
In order to achieve the above object, the present application provides the following technical solutions:
the utility model provides a net lamellar support of bionical extracellular matrix bioactive substance cladding polyester, is in including the netted lamellar of surface carboxylation and cover the bioactive substance cladding on the netted lamellar surface of polyester, netted lamellar adopts the polyester material to make, the bioactive substance cladding passes through netted lamellar is through coupling many times and forms, still be equipped with the seal coat outside the bioactive substance cladding.
Further setting: the polyester material is one or a combination of a plurality of polycaprolactone, carbonic acid polyester, ethylene terephthalate, polybutylene terephthalate, local terephthalic acid trimethylene terephthalate, poly-1, 4-cyclohexanedimethylene terephthalate fiber and poly-2, 6-naphthalenedicarboxylic acid ethylene diester.
Further setting: the net-shaped sheet layer is formed by spun-bonding the polyester material, and the diameter of single net-shaped fiber of the net-shaped sheet layer is 25-35 mu m.
Further setting: the thickness of the reticular lamellar layer is 100-500 mu m, and the porosity of the reticular lamellar layer is 45-85%.
Further setting: the bioactive substance coating is formed by coupling the following solutions in sequence: collagen solution, mixed solution containing collagen and glycosaminoglycan, and acellular matrix solution.
Further setting: the collagen is one or more of type I, type II and type III collagen.
Further setting: the sealing layer is formed by at least one of lysine, arginine or glycine
Compared with the prior art, the scheme of the application has the following advantages:
in the bionic extracellular matrix bioactive substance coating polyester reticular lamellar support, the advantages of certain mechanical property and plasticity of the synthetic polyester polymer material are combined with the good biocompatibility of the natural polymer material, so that the support not only has certain mechanical strength and good biocompatibility, and provides a bionic culture environment for cell culture, and promotes the adhesion, growth and proliferation and functional activity maintenance of cells in a reactor, but also has higher porosity and specific surface area after coating, is beneficial to meeting the requirements of high quality, high density and long-term function maintenance of the cells during production by transferring energy, and can become an ideal loading material for cells of a perfusion (filling) bed/support reactor.
Additional aspects and advantages of the present application will be set forth in part in the description which follows and, in part, will be obvious from the description, or may be learned by practice of the present application.
Drawings
The foregoing and/or additional aspects and advantages of the present application will become apparent and readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings of which:
the foregoing and/or additional aspects and advantages of the present application will become apparent and readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings of which:
FIG. 1 is a process flow diagram of a method of making a bioactive material-coated polyester mesh-sheet stent of the present application;
FIG. 2 is the XPS analysis of a polyethylene terephthalate mesh sheet scaffold material without a bioactive coating;
FIG. 3 is the XPS analysis of a collagen-coated polyethylene terephthalate mesh sheet scaffold material;
FIG. 4 is an FTIR spectrum of a mesh sheet scaffold material before and after coating with a bioactive substance;
FIG. 5 shows a structure for measuring the specific surface area of a scaffold material of a mesh sheet before and after coating with a bioactive substance;
FIG. 6 shows the measurement results of the porosity of the scaffolds with mesh sheets before and after coating with bioactive substances;
FIG. 7 is an image of C3A hepatocytes cultured with the coated mesh sheet scaffold material, as observed by scanning electron microscopy on day 7;
FIG. 8 is an image of the mesenchymal stem cells cultured with the coated mesh-sheet scaffold material, observed under a scanning electron microscope at day 7;
FIG. 9 is an ELISA image of the difference in functional activity expression of C3A hepatocytes after incubation with the mesh-sheet scaffold material before and after coating.
Detailed Description
Reference will now be made in detail to embodiments of the present application, examples of which are illustrated in the accompanying drawings, wherein like or similar reference numerals refer to the same or similar elements or elements having the same or similar function throughout. The embodiments described below with reference to the drawings are exemplary only for the purpose of explaining the present application and are not to be construed as limiting the present application.
The application relates to a bionic extracellular matrix bioactive substance coating polyester reticular lamellar support, which constructs a simulated cell in-vivo growth microenvironment through bionic extracellular matrix components, has good structural stability and mechanical properties, is suitable for large-scale three-dimensional culture of adherent cells in vitro, and can realize large-scale culture of cells and promote the maintenance of cell bioactivity and functions.
The bionic extracellular matrix bioactive substance coating polyester reticular lamellar stent (hereinafter referred to as a coating polyester reticular lamellar stent) comprises a reticular lamellar layer and a bioactive substance coating layer which covers the surface of the reticular lamellar layer, wherein the reticular lamellar layer is made of a polyester material, the surface of the reticular lamellar layer can be coupled for many times after carboxylation to form a bioactive substance coating layer, and a sealing layer is also arranged outside the bioactive substance coating layer.
Specifically, the polyester material for forming the mesh-shaped sheet layer comprises one or a plurality of compositions of polycaprolactone, carbonic acid polyester, ethylene terephthalate, polybutylene terephthalate, trimethylene terephthalate, poly-1, 4-cyclohexanedimethylene terephthalate fiber and poly-2, 6-naphthalenedicarboxylate, the polyester material is made into the mesh-shaped sheet layer by means of spun bonding, reinforcement and the like, the thickness of the mesh-shaped sheet layer is 100-500 mu m, the diameter of a single mesh-shaped fiber of the mesh-shaped sheet layer is 25-35 mu m, the porosity is 45-85%, so that the mesh-shaped sheet layer has good flexibility and plasticity, the taking and the shaping are convenient, the mesh-shaped sheet layer can be designed into any size, the stacking area of the material in a reactor can be increased by folding the mesh-shaped sheet layer into a certain angle, so as to facilitate the subsequent coating treatment, increase the growth area of the cells in a limited space and realize the high-density culture of the cells.
The net-shaped sheet layer is required to be subjected to carboxylation treatment and activation crosslinking treatment before being coated, and particularly, the cleaned net-shaped sheet layer can be soaked in a strong alkaline solution to break ester groups of a polyester material to expose carboxyl groups, then the carboxylated net-shaped sheet layer is soaked in an MES solution (0.1mol MES +0.5mol sodium chloride, pH is 4.7-6.0) to be activated, EDC and NHS are added into the MES solution in proportion to be further activated and crosslinked, the final concentration of EDC is 2-5 mmol/ml, the proportion of EDC and NHS can be 1: 2-1: 9, the carboxyl groups of the net-shaped sheet layer can be adjusted to be in an active state through the activation and crosslinking steps, and the strength of subsequent linkage of the carboxyl groups is enhanced at the same time, so that the covalent linkage of the bionic extracellular matrix bioactive substance and the polyester synthetic high polymer material is realized through the activation and crosslinking of the net-shaped sheet layer, a bioactive material coating is then formed on the mesh sheet.
The bioactive substance coating layer is formed by sequentially coupling a collagen solution, a mixed solution containing collagen and hyaluronic acid and a acellular matrix solution, wherein the pH of the collagen solution is 7.2-7.5, the concentration of the collagen solution is 3-12 mg/ml, the collagen in the collagen solution is one or a mixture of more than one of type I, type II and type III collagen, for example, the type I collagen and the type III collagen are mixed, and the ratio of the type I collagen to the type III collagen is 3: 1-1: 3; the mixed solution contains the collagen with the concentration of 3-12 mg/ml and hyaluronic acid with the concentration of 10mg/ml, and the pH value of the mixed solution is 7.2-7.5; the acellular matrix solution is prepared from livers, kidneys, hearts or umbilical cords of animal sources, and is prepared by cutting animal organ tissues into small pieces, stirring the small pieces for 1 to 4 hours by using a solution containing 0.01 to 0.04 percent of pancreatin and 0.03 to 0.07 percent of EDTA (ethylene diamine tetraacetic acid), soaking the small pieces in 2 to 5 percent of Triton X-100 and stirring the soaked pieces for 1 to 4 hours, then soaking the pieces in 3 to 6 percent of sodium deoxycholate solution for 1 to 4 hours to obtain an acellular matrix scaffold, freeze-drying and grinding the acellular matrix scaffold into powder, digesting the powder with pepsin hydrochloride for 48 to 96 hours, and then preparing the acellular matrix solution into 3 to 12 mg/ml. The reticular lamina is coupled and coated for three times, and collagen in the collagen solution, the mixed solution and the acellular matrix solution is coupled with carboxyl on the surface of the reticular lamina to form a net structure containing three different active substances, so that the polyester reticular lamina can obtain higher porosity and specific surface area, and can meet the requirements of high quality, high density and long-term function maintenance of cells during production, and the coated polyester reticular lamina stent has good biocompatibility, is favorable for cell adhesion, promotes cell differentiation and proliferation, and maintains cell functions.
In addition, the mesh-shaped sheet layer needs to be subjected to carboxylation treatment before being coated, specifically, the cleaned mesh-shaped sheet layer can be soaked into MES solution (0.1mol MES +0.5mol sodium chloride, pH is 4.7-6.0) for activation, EDC and NHS are added into the MES solution in proportion for further activation and crosslinking, the final concentration of EDC is 2-5 mmol/ml, and the proportion of EDC and NHS can be 1: 2-1: 9.
After the coating, the reticular sheet layer can form a sealing layer on the surface of the reticular sheet layer by adding at least one of lysine, arginine or glycine with the concentration of 20mmol/ml, and the sealing layer occupies the position of a group which can be chemically reacted by the coating by utilizing amino acid molecules such as lysine, arginine and glycine, so that the activity of the coating is passivated, the consumption of the coating is avoided, and the service life of the coating is prolonged.
The bionic extracellular matrix bioactive substance coating polyester mesh sheet layer bracket simulates the physiological environment in a cell body to construct a three-dimensional culture system by coating the bionic extracellular matrix on the mesh sheet layer, so that the constructed physiological environment is close to the actual physiological environment of the cell body, the mesh sheet layer is coupled for three times, namely, the mesh sheet layer is covalently connected with three different active substances through carboxyl, specifically comprises proteins such as I type, II type, III type collagen, fibronectin and the like, glycosaminoglycan such as hyaluronic acid, heparan sulfate and the like and various cell growth factors, so as to form a coating of the bionic extracellular matrix bioactive substance outside the mesh sheet layer, can support and connect tissue structures, regulate the occurrence of tissues and the physiological activities of cells, and can influence the morphology, proliferation, functions, and the physiological activities of the cells, Survival, differentiation, migration and other life phenomena. The cells are cultivated in the net rack structure of the bionic extracellular matrix bioactive substance constructed in the application, and the coating is used as a growth support of the cells, so that the cells can be differentiated to generate a certain three-dimensional specific structure, and the in-vivo state is simulated to the maximum extent. Meanwhile, the net-shaped sheet layer can provide support for a coating of a bionic extracellular matrix bioactive substance constructed outside the net-shaped sheet layer, so that the bionic extracellular matrix bioactive substance coating polyester net-shaped sheet layer support has good structural stability and mechanical property, has good mechanical property, and can realize in-vitro three-dimensional culture of cells.
In conclusion, the bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold combines the advantages of certain mechanical property and plasticity of a synthetic polyester high polymer material with good biocompatibility of a natural high polymer material, so that the scaffold not only has certain mechanical strength and good biocompatibility, provides a bionic culture environment for cell culture, promotes adhesion, growth and proliferation of cells in a reactor and functional activity maintenance, has higher porosity and specific surface area after coating, is beneficial to meeting the requirements of high quality, high density and long-term function maintenance of the cells during production by a mass transfer agent, and can become an ideal loading material for cells of a perfusion (filling) bed/scaffold reactor.
The application also relates to a preparation method of the polyester reticular lamellar scaffold with the bioactive substance coating, in particular to a preparation method of the polyester reticular lamellar scaffold with the bionic extracellular matrix bioactive substance coating, please refer to fig. 1, and the preparation method specifically comprises the following steps:
(1) the polyester material is consolidated into a mesh sheet by spunbonding.
Preferably, the polyester material in this embodiment comprises one or more of polycaprolactone, carbonic acid polyester, ethylene terephthalate, polybutylene terephthalate, trimethylene terephthalate, poly-1, 4-cyclohexanedimethylene terephthalate, and poly-2, 6-naphthalenedicarboxylate, and is made into a mesh sheet by a spun-bonded, reinforced process. The thickness of the reticular lamina layer manufactured by the embodiment is 100-500 mu m, the porosity is 45-85%, the diameter of a single reticular fiber is 25-35 mu m, and the reticular lamina layer has certain softness and plasticity, so that the reticular lamina layer is convenient to take, shape and stack in a reactor in subsequent processing. The reactor can be used for designing the formed reticular sheet layer into any shape, and can be folded into a certain angle to increase the stacking area of the reticular sheet layer in the reactor.
(2) The mesh sheet is washed and dried.
And respectively cleaning the mesh sheet layer by using ethanol, acetone and ultrapure water for 8-15 min to remove organic impurities and water-soluble impurities on the surface of the mesh sheet layer, and drying at 40-80 ℃ overnight.
(3) And (3) carrying out carboxylation treatment on the washed and dried reticular lamina layer by using a strong alkaline solution.
And soaking the cleaned and dried net-shaped sheet layer in a strong alkaline solution for 20-50 min to break ester groups of the polyester net-shaped sheet layer to expose carboxyl groups.
Preferably, the solute of the strongly alkaline solution in this embodiment is at least one of sodium hydroxide, potassium hydroxide and lithium hydroxide, and the strongly alkaline solution contains solute% to 20% by mass volume percentage.
(4) Activating and crosslinking the network sheet layer.
Firstly, the reticular lamina after the carboxylation treatment is soaked in 2- (N-morpholino) ethanesulfonic acid (abbreviated as MES) solution for primary activation, and the activation time is 30 min-4 h. Preferably, the MES solution of the embodiment comprises 0.1 mol/L2- (N-morpholino) ethanesulfonic acid and 0.5mol/L sodium chloride, and the pH of the MES solution is adjusted to 4.6-6.0.
Subsequently, 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (abbreviated as EDC, which is water-soluble carbodiimide) and N-hydroxysuccinimide (abbreviated as NHS), which are commonly used as a carboxyl group activating reagent and a phosphate group activating agent, crosslinking of proteins and nucleic acids, are proportionally added to the MES solution, and the coupling efficiency is effectively promoted by combining EDC and NHS. Preferably, the final concentration of EDC in MES is 2-5 mmol/ml, and the ratio of EDC and NHS is 1: 2-1: 9, so that the reticular lamina is activated and cross-linked for a second time, and the reaction time is 15 min-3 h, so as to activate the carboxyl of the reticular lamina to an optimal state for coupling with a bionic extracellular matrix.
In addition, in the process of the secondary activation and crosslinking, the activation and crosslinking reaction can be stopped by adding 2-mercaptoethanol into the MES solution so as to carry out the next step.
(5) The mesh sheet is coupled a plurality of times to form a bioactive material coating on the mesh sheet.
In this example, the bioactive substance coating is formed on the mesh sheet by three times of coupling to the mesh sheet, specifically in three stages:
firstly, preparing a collagen solution, wherein the collagen solution contains collagen with the concentration of 3-12 mg/ml, and the collagen is one or a mixture of more than one of type I, type II and type III collagen, for example, the ratio of the type I collagen to the type III collagen is 3: 1-1: 1, and simultaneously, the pH value of the collagen solution is adjusted to 7.2-7.5. And putting the activated reticular lamina into the collagen solution to perform primary coupling with the collagen for 30 min-4 h, namely, covalently connecting the collagen with carboxyl through amino so as to couple the collagen to the reticular lamina.
Subsequently, the network sheet layer is subjected to a secondary coupling treatment. Specifically, a mixed solution containing collagen with a concentration of 3-12 mg/ml and 10-80 mg/ml of glycosaminoglycan is prepared, hyaluronic acid is preferably used as glycosaminoglycan in the embodiment, the collagen is the same as the collagen in the primary coupling stage, and the pH value of the mixed solution is adjusted to 7.2-7.5. And putting the mesh sheet layer subjected to the primary coupling into the mixed solution to perform secondary coupling with the collagen and the glycosaminoglycan, wherein the coupling time is 30 min-4 h, and then the collagen and the glycosaminoglycan are coupled onto the mesh sheet layer.
And finally, carrying out three times of coupling treatment on the reticular lamina. Specifically, a decellularized matrix solution required for the third coupling is prepared, the decellularized matrix solution is a solution which removes cell components from tissues or organs by adopting physical, chemical, enzymatic hydrolysis and other methods, the structure and the components of extracellular matrix are reserved, the extracellular matrix is a compound secreted by cells of the tissues and organs to the outside, is a compound of structural protein and functional protein, and comprises type I collagen, type III collagen, fibronectin, glycosaminoglycan, various cell growth factors and the like, and the decellularized matrix gel coating can be formed on the reticular lamina by the third coupling of the decellularized tissue solution.
Preferably, the decellularized tissue solution is prepared by taking organ tissues of animal origin as tissue materials, such as liver, kidney, heart or umbilical cord, and the like, cutting the organ tissues of animal origin into small pieces, stirring the small pieces with a solution containing 0.01 to 0.04 percent of pancreatin and 0.03 to 0.07 percent of Ethylene Diamine Tetraacetic Acid (EDTA) for 1 to 4 hours, soaking and stirring the small pieces with a 2 to 5 percent of polyethylene glycol octyl phenyl ether solution (TritonX-100) for 1 to 4 hours, then soaking the small pieces in a 3 to 6 percent of sodium deoxycholate solution for 1 to 4 hours, freeze-drying and grinding the soaked small pieces into powder, digesting the powder with pepsin hydrochloride for 48 to 96 hours, and preparing the decellularized matrix solution of 3 to 12 mg/ml. And (3) putting the secondarily coupled reticular lamina into the acellular matrix solution to be coupled with collagen of the reticular lamina, wherein the coupling time is 30 min-4 h.
Through the coupling of the different solutions in the three stages described above, coatings of three different materials can be formed on the mesh sheet, each coating having a different active substance and a different function.
(6) And sealing the coated reticular lamina to obtain the bioactive substance coated polyester reticular lamina stent.
And sealing the coated reticular lamina layer by adding at least one of lysine, arginine or glycine of 20-50 mmol/ml to protect the coating of the reticular lamina layer, and obtaining the bionic extracellular matrix bioactive substance coated polyester reticular lamina support after sealing.
And finally, performing electron beam radiation sterilization treatment on the obtained bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold at 10-20 kGy, and then preserving at 4 ℃.
The preparation method of the bioactive substance coating polyester reticular lamellar stent is characterized in that a polyester material is spun-bonded and processed to form a reticular lamellar layer, the reticular lamellar layer is carboxylated, activated, crosslinked, coupled and sealed to form a coating, the covalent connection between a bionic extracellular matrix and a synthetic high-molecular polyester material is realized by adjusting parameters, no special equipment such as a plasma surface treatment machine is needed, toxic chemical substances are not introduced at the same time, and the safety quality of biological product production is ensured.
In addition, the polyester mesh sheet scaffold coated with the bionic extracellular matrix bioactive substance for cell culture of the present application was subjected to relevant tests and used for animal cell culture experiments, and the polyester mesh sheet of the present application is exemplified by a polyethylene terephthalate mesh sheet, and the results show that:
the polyethylene terephthalate reticular lamellar scaffold material coated with the bionic extracellular matrix bioactive substance is subjected to X-ray photoelectron spectroscopy (XPS) analysis and Fourier infrared (FTIR) analysis, and the results shown in figures 1-5 are respectively obtained. Wherein, fig. 2 is the result of XPS analysis of the pet mesh sheet stent material without the bioactive substance coating, and the material is mainly composed of C element and O element. FIG. 3 shows the XPS analysis of a polyethylene terephthalate mesh sheet scaffold coated with collagen type I and collagen type III at a ratio of 3:1, with the presence of N in the major components of the scaffold, indicating that covalent attachment of the bioactive agent to the scaffold has been achieved. FIG. 4 is an FTIR spectrum of the material of the reticulated lamellar scaffold before and after coating with the bioactive substance, curve A representing no coating and curve B representing a significant difference after coating, curve B at 1550cm-1、1665cm-1And 3330cm-1Characteristic absorption peaks (Amid II, Amid I and Amid A) of collagen appear nearby, further suggesting that covalent attachment of the bioactive substance to the material has been achieved. FIGS. 5 and 6 are the results of measuring the specific surface area and porosity of the mesh-layered scaffold material before and after coating with the bioactive substance, respectively, wherein A is uncoated and B represents coated, and it can be seen that the specific surface area and porosity of the mesh-layered scaffold material after coating are significantly improved.
And filling the materials before and after the coating of the bioactive substances into a circulating perfusion type cell culture system and a bioreactor (ZL201510738480.6) thereof which are constructed in advance for large-scale culture of the hepatic cells and the mesenchymal stem cells, wherein images observed under a scanning electron microscope when the coated reticular lamellar scaffold material is used for culturing the C3A hepatic cells and the mesenchymal stem cells on day 7 are respectively shown in figures 7 and 8, so that a large amount of cells can grow and are tightly attached to the materials, the cells are tightly connected with one another, and part of the cells show the symptom of similar tissue cluster growth. Further evaluating the difference of functional activity expression of the C3A hepatocytes after being cultured by the mesh-sheet scaffold material before and after collagen coating, collecting culture medium supernatants on days 1, 3 and 5 respectively, and performing ELISA detection, wherein the results are shown in FIG. 9, wherein A is uncoated, and B represents coated, and the results show that the albumin secretion amount of the mesh-sheet scaffold material after coating is significantly higher than that of the mesh-sheet scaffold material after coating, and the mesh-sheet scaffold material after coating is favorable for promoting cell differentiation and functional expression.
The foregoing is only a partial embodiment of the present application, and it should be noted that, for those skilled in the art, several modifications and decorations can be made without departing from the principle of the present application, and these modifications and decorations should also be regarded as the protection scope of the present application.

Claims (3)

1. A bionic extracellular matrix bioactive substance coating polyester reticular lamellar scaffold is characterized in that: the biological active substance coating layer covered on the surface of the polyester mesh sheet layer is formed by spinning a polyester material, the diameter of single mesh fiber of the mesh sheet layer is 25-35 mu m, the thickness of the mesh sheet layer is 100-500 mu m, the porosity of the mesh sheet layer is 45-85%, the biological active substance coating layer covered on the surface of the polyester mesh sheet layer is formed by coupling the mesh sheet layer subjected to activation crosslinking treatment for multiple times through a collagen solution, a mixed solution containing collagen and glycosaminoglycan and a acellular matrix solution in sequence, the collagen is one or a mixture of more than one of collagen I, collagen II and collagen III, and the mesh sheet layer subjected to activation crosslinking treatment is formed by performing primary activation on the mesh sheet layer subjected to surface carboxylation through a 2- (N-morpholino) ethanesulfonic acid solution and adding 1- The (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride and the N-hydroxysuccinimide are subjected to secondary activation, and a sealing layer is also arranged outside the bioactive substance coating.
2. The biomimetic extracellular matrix bioactive substance coated polyester mesh sheet scaffold according to claim 1, wherein: the polyester material is one or a combination of a plurality of polycaprolactone, carbonic acid polyester, ethylene terephthalate, polybutylene terephthalate, polytrimethylene terephthalate, poly-1, 4-cyclohexanedimethylene terephthalate fiber and poly-2, 6-naphthalenedicarboxylic acid ethylene diester.
3. The biomimetic extracellular matrix bioactive substance coated polyester mesh sheet scaffold according to claim 1, wherein: the blocking layer is formed of at least one of lysine, arginine, or glycine.
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