NERVE CONDUIT LOADED WITH ADIPOSE-DERIVED STEM CELLS AND PREPARATION METHOD THEREOF

Abstract

A nerve conduit loaded with adipose-derived stem cells and a preparation method thereof are provided. The preparation method includes: S1, adding polycaprolactone and polyvinylpyrrolidone into a binary organic solvent, performing ultrasonic treatment, and then adding reduced graphene oxide nanoparticles to obtain a spinning solution; S2, electrospinning with the spinning solution and then washing for several times to obtain a semi-finished conduit product; and S3, injecting a cell mixture into the semi-finished conduit product to obtain the nerve conduit. A fiber surface of the nerve conduit has groove structures, and thus a specific surface area and cell adhesion sites are increased, and adhesion and proliferation of cells are facilitated. By loading the adipose-derived stem cells, neurotrophic phenotypic effect of peripheral nerve scaffold is improved, and can effectively avoid immunological rejection of transplantation, promote orientational growth of axons into the nerve conduit and promote myelination effect of Schwann cells.

Claims

1. A preparation method of a nerve conduit loaded with adipose-derived stem cells, comprising: S1, adding polycaprolactone and polyvinylpyrrolidone into a binary organic solvent, performing ultrasonic treatment, and then adding reduced graphene oxide nanoparticles to obtain a spinning solution; S2, electrospinning with the spinning solution obtained in the S1, and then washing for several times to obtain a semi-finished conduit product; and S3, injecting a cell mixture into the semi-finished conduit product obtained in the S2 to obtain the nerve conduit. wherein the binary organic solvent is organic solvents of dichloromethane and dimethylformamide, and a volume ratio of the dichloromethane to the dimethylformamide is (2~4): 1; wherein in the S2, the electrospinning comprises: the spinning solution is added into a syringe, a receiving bar has a receiving distance of 10 centimeters (cm) ~ 20 cm and a rotational speed of 5 revolutions per minute (rpm) ~15 rpm, a voltage of 10 kilovolts (kV) ~ 20 kV is applied, a speed of a propelling pump is 2 milliliters per hour (mL/h) ~ 3 mL/h, and a negative voltage applied between two ends of an insulating bar is -2 kV ~ -1 kV; wherein in the S2, a detergent for the washing comprises alcohol and/or water; wherein a surface of the nerve conduit loaded with adipose-derived stem cells has groove structures.

2. The preparation method according to claim 1, wherein in the S1, time of the performing ultrasonic treatment is 20 ~ 40 minutes.

3. The preparation method according to claim 1, wherein in the S3, a density of adipose-derived mesenchymal stem cells in the cell mixture is 10.sup.6/mL ~ 10.sup.8/mL.

4. The preparation method according to claim 1, wherein in the S3, an injection ratio of the cell mixture to the semi-finished conduit product is 100 microliters per centimeter (.Math.L/cm) ~ 200 .Math.L/cm.

5. A nerve conduit loaded with adipose-derived stem cells prepared by the preparation method according to claim 1.

6. The nerve conduit loaded with adipose-derived stem cells according to claim 5, wherein a length of the nerve conduit is 1 cm ~ 2 cm, an inner diameter of the nerve conduit is 2 millimeters (mm) ~ 4 mm, and a wall thickness of the nerve conduit is 0.4 mm ~ 0.45 mm.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0029] FIG. 1A illustrates a schematic structural diagram of generating grooves on a surface of a nerve conduit.

[0030] FIG. 1B illustrates a schematic diagram of a cell-fiber scaffold interface.

[0031] FIG. 2 illustrates a schematic diagram of reduced graphene oxide nanoparticles on surfaces of electrospun fibers.

[0032] FIG. 3 illustrates a scanning electron microscope (SEM) image of inner and outer layers of a nerve conduit.

[0033] FIG. 4 illustrates a photogram of a nerve conduit.

[0034] FIG. 5 illustrates a diagram of showing survival of adipose-derived stem cells after being in vitro cultured on a scaffold for 3 days.

[0035] FIG. 6A illustrates a situation of a scaffold loaded with cells when taken out after being implanted in vivo for 18 weeks.

[0036] FIG. 6B illustrates a situation of nerve regeneration in the scaffold after being implanted in vivo for 18 weeks.

[0037] FIG. 7 illustrates a schematic structural view of an electrospinning device.

DETAILED DESCRIPTION OF EMBODIMENTS

[0038] Technical solutions in embodiments of the invention will be clearly and completely described below in conjunction with the accompanying drawings of the embodiments of the invention. Apparently, the embodiments as described are only some of embodiments of the invention, rather than all of embodiments of the invention. Based on the embodiments as described of the invention, all other embodiments obtained by those skilled in the art without creative work are within the scope of protection of the invention.

[0039] It should be noted that the embodiments as described of the invention and features in the embodiments can be combined with each other on the prerequisite of without conflict.

[0040] The invention will be further described with reference to the accompanying drawings and specific embodiments, but not as a limitation of the invention.

Embodiment 1

[0041] This embodiment provides a preparation method of a nerve conduit, including steps as follows.

[0042] S1, adding 1 gram (g) of polycaprolactone and 0.8 g of polyvinylpyrrolidone into 10 milliliters (mL) of dichloromethane/dimethylformamide organic solvent (a volume ratio of dichloromethane to dimethylformamide is 3:1), performing ultrasonic treatment for 30 minutes, and then adding 2% (w/w, i.e., weight to weight ratio) of reduced graphene oxide nanoparticles to obtain a spinning solution.

[0043] S2, adding the spinning solution obtained in the S1 into a syringe, electrospinning under conditions that a receiving distance of a receiving bar is 15 cm (i.e., a distance from the receiving bar to the syringe is 15 cm), a rotational speed of the receiving bar is 10 revolutions per minute (rpm), a voltage of 15 kilovolts (kV) is applied (for generation of an electric field), a speed of a propelling pump (for driving the syringe) is 2.5 milliliter per hour (mL/h), and a negative voltage applied between two ends of an insulating bar is -1.5 kV, and then washing with alcohol and water for three times to remove the polyvinylpyrrolidone and thereby obtain groove structures on a fiber surface, thereby obtaining a semi-finished conduit product. Moreover, FIG. 7 illustrates an electrospinning device including the syringe, the receiving bar, the propelling pump and the insulating bar, and a basic structure thereof is well-known to those skilled in the art and thus will not be described in detail herein. In addition, the voltage of 15 kV is generally applied on a needle of the syringe.

[0044] S3, injecting a cell mixture into an inner wall of the semi-finished conduit product obtained in the S2 according to a ratio of 133 microliters per centimeter (.Math.L/cm), and curing at a constant temperature of 37° C. (°C) to obtain the nerve conduit. In the cell mixture, a density of adipose-derived mesenchymal stem cells is 10.sup.7/mL, and the cell mixture further includes Corning Matrigel®.

Embodiment 2

[0045] This embodiment provides another preparation method of a nerve conduit, including steps as follows.

[0046] S1, adding 1 g of polycaprolactone and 0.4 g of polyvinylpyrrolidone into 10 mL of dichloromethane/dimethylformamide organic solvent (a volume ratio of dichloromethane to dimethylformamide is 3:1), performing ultrasonic treatment for 20 minutes, and then adding 1% (w/w) of reduced graphene oxide nanoparticles to obtain a spinning solution.

[0047] S2, adding the spinning solution obtained in the S1 into a syringe, electrospinning under conditions that a receiving distance of a receiving bar is 15 cm, a rotational speed of the receiving bar is 10 rpm, a voltage of 15 kV is applied, a speed of a propelling pump is 2.5 mL/h, and a negative voltage applied between two ends of an insulating bar is -1.5 kV, and then washing with alcohol and water for three times to remove the polyvinylpyrrolidone and thereby obtain groove structures on a fiber surface, thereby obtaining a semi-finished conduit product.

[0048] S3, injecting a cell mixture into an inner wall of the semi-finished conduit product obtained in the S2 according to a ratio of 105 .Math.L/cm, and curing by ultraviolet light illumination for 5 minutes to obtain the nerve conduit. In the cell mixture, a density of adipose-derived mesenchymal stem cells is 10.sup.7/mL, and the cell mixture further includes 1% (wt%) of GrowDex® hydrogel.

Embodiment 3

[0049] This embodiment provides still another preparation method of a nerve conduit, including steps as follows.

[0050] S1, adding 1.2 g of polycaprolactone and 0.8 g of polyvinylpyrrolidone into 10 mL of dichloromethane/dimethylformamide organic solvent (a volume ratio of dichloromethane to dimethylformamide is 3:1), performing ultrasonic treatment for 40 minutes, and then adding 2.5% (w/w) of reduced graphene oxide nanoparticles to obtain a spinning solution.

[0051] S2, adding the spinning solution obtained in the S1 into a syringe, electrospinning under conditions that a receiving distance of a receiving bar is 15 cm, a rotational speed of the receiving bar is 10 rpm, a voltage of 15 kV is applied, a speed of a propelling pump is 2.5 mL/h, and a negative voltage applied between two ends of an insulating bar is -1.5 kV, and then washing with alcohol and water for three times to remove the polyvinylpyrrolidone and obtain groove structures on a fiber surface, thereby obtaining a semi-finished conduit product.

[0052] S3, injecting a cell mixture into an inner wall of the semi-finished conduit product obtained in the S2 according to a ratio of 133 .Math.L/cm to obtain the nerve conduit. In the cell mixture, a density of adipose-derived mesenchymal stem cells is 10.sup.7/mL, and the cell mixture further includes fibrinogen-thrombin.

Testing Embodiment

[0053] The appearance of the nerve conduit obtained in the embodiment 1 was visually observed, and a length, a wall thickness and an inner diameter were measured. As shown in FIG. 4, a result was that the length of the nerve conduit was 1.5 cm, the wall thickness of the nerve conduit was 0.4 mm, and the inner diameter of the nerve conduit was 3 mm.

[0054] The nerve conduit was observed under a scanning electron microscope, and the result is shown in FIGS. 2-3.

[0055] The nerve conduit was implanted into a nerve defect site in an animal body, and after 18 weeks, it was taken out and cut open for observation. The results are shown in FIGS. 6A and 6B, and nerve growth can be observable in the conduit.

[0056] In summary, the illustrated embodiments of the invention improve the neurotrophic phenotype effect of peripheral nerve scaffold by loading adipose-derived stem cells, and meanwhile, the adipose-derived stem cells can effectively avoid an immunological rejection of transplantation, can promote an orientational growth of axons into the nerve conduit and can promote a myelinization effect of Schwann cells. Moreover, a fiber surface of the nerve conduit loaded with adipose-derived stem cells according to the illustrated embodiments of the invention has groove structures, so that a specific surface area and cell adhesion sites are increased, and thus adhesion and proliferation of cells are facilitated; and meanwhile, a peripheral nerve microenvironment can promote adipose orientational differentiation of derived mesenchymal stem cells in neurogenic direction, and promote the stem cells to secrete more neurotrophic factors (GDNF, NGF and the like), thereby improving the migration and growth of supporting cells (Schwann cells and vascular endothelial cells), and accelerating the repair and regeneration of nerve defects. In addition, the nerve conduit loaded with adipose-derived stem cells according to the illustrated embodiments of the invention is added with the reduced graphene oxide nanoparticles, which can respond to bioelectric signals in the peripheral nerve microenvironment, promote the neurogenic differentiation of the adipose-derived stem cells, construct cell bioelectric signal intelligent response and cell information feedback, and accelerate the repair and regeneration of nerves.

[0057] The above description is only preferred embodiments of the invention, and is not intended to limit implementations and scope of protection of the invention. For those skilled in the art, it should be appreciated that all equivalent substitutions and obvious changes made based on contents of the specification and the accompanying drawings of the invention should be included in the scope of protection of the invention.