Method for Preparing an Induced Osteogenesis Formulation

Abstract

The application is related to a method for preparing an induced osteogenesis formulation, the method comprises the following steps: (1) a human dental matrix is decalcified; (2) then an exogenous active protein BMP, i.e. bone morphogenetic protein is added to the decalcified dental matrix, resulting in the induced osteogenesis formulation

Claims

1. A method for preparing an induced osteogenesis formulation, the method comprises the following steps: (1) a human dental matrix is decalcified; (2) then an exogenous active protein BMP, i.e. bone morphogenetic protein is added to the decalcified dental matrix, resulting in the induced osteogenesis formulation.

2. The method according to claim 1, wherein after the dental matrix is decalcified in step (1), a dental matrix granule or lyophilized powder is obtained.

3. The method according to claim 2, wherein in step (2), the method of adding the exogenous active protein BMP to the decalcified dental matrix is as follows: the exogenous BMP and the dental matrix granule or lyophilized powder are respectively dissolved in a phosphate buffer of PH=7.2, then mixed together, put in an agitator for uniform and slow agitation, the agitation rate is 20-120 Rotation Per Minute, meanwhile being in a water bath kettle with a varying temperature.

4. The method according to claim 3, wherein a temperature sequence in the water bath kettle is as follows: 26° C., 8 hours; 30° C., 6 hours; 28° C., 8 hours; 28° C., 12 hours; then the temperature is kept at a constant temperature of 30° C. and the agitation is continued.

5. The method according to claim 4, wherein during agitation the protein concentration of BMP in the mixed solution is detected every 3 hours, and the agitation is stopped until the concentration decreases below 20% to 25% of the initial BMP concentration.

6. A method for preparing induced osteogenesis formulation, the method comprises the following steps: (1) two parts of dental matrix is decalcified; (2) then bone morphogenetic protein was extracted from the two parts of decalcified dental matrix; (3) finally the extracted bone morphogenetic protein is mixed with one part of the decalcified dental matrix, resulting in the induced osteogenesis formulation.

7. The method according to claim 6, wherein the method for extracting bone morphogenetic protein is as follows: the decalcified dental matrix powder is suspended in a phosphate buffer of PH=7.2; the phosphate buffer is heated in a water bath kettle for 280 hours, the temperature is 35-40° C., during heating treatment the solution is continually agitated; then centrifuged, and the supernatant is separated from the precipitate, a target protein is purified and concentrated from the supernatant by a conventional molecular sieve, finally obtaining a BMP protein active extract.

8. The method according to claim 7, wherein a molecular weight of the extracted active BMP protein is 20 to 50 kda.

9. The method according to claim 8, wherein the extracted BMP small molecule protein is mixed with one part of the dental matrix granule or lyophilized powder after decalcification and protein extraction, and the BMP small molecule is bound with the granule or lyophilized powder.

10. The method according to claim 9, wherein said method for binding is as follows: firstly one part of the two parts of the dental matrix powder after decalcification and protein extraction is suspended in a phosphate buffer of PH=7.0, then the BMP protein extracted from the two parts of dental matrix is dissolved in the phosphate buffer, then mixed together, and put in an agitator for uniform and slow agitation, the agitation rate is 20 to 120 Rotation Per Minute, meanwhile agitated at room temperature or 25 to 30° C. for 12 to 56 hours, during agitation the concentration of the BMP protein in the mixed solution is detected every 3 hours, until the concentration decreases below 10% to 15% of initial BMP concentration and the agitation is stopped, then centrifuged, the supernatant is removed, the remaining powder is filtered, then dried at low temperature.

11. A method for preparing an induced osteogenesis formulation, the method comprises the following steps: (1) an exogenous bone matrix is decalcified; (2) then protein is removed from the decalcified bone matrix; (3) an exogenous bone morphogenetic protein is mixed with the bone matrix treated in step (2), the induced osteogenesis formulation is formed by the exogenous protein and the bone matrix.

12. The method according to claim 11, wherein said bone is a human bone, and the steps for decalcifying the human bone is as follows: (1) collected human bone is put in a container with clean water, and stored at a temperature below 5° C.; (2) the raw material bone is immersed and disinfected with 1.2% sodium hypochlorite, the time is 30 to 55 minutes, and the temperature is 35 to 40° C.; (3) useless parts on the bone are removed; (4) the bone tissue is pulverized into granule or lyophilized powder by a mechanical method, the average particle diameter is 0.10 to 0.25 mm; (5) the bone tissue pulverized into the granule or lyophilized powder is immersed and disinfected with 1.2% sodium hypochlorite, the immersion and disinfection time is 10 to 45 minutes, the temperature is 35 to 40° C.; (6), the bone tissue granule or lyophilized powder is put in a 0.65 to 0.72 N hydrochloric acid solution, immersed at 38° C. for 16 to 20 hours to complete decalcification; and (7), dried at low temperature, to obtain a decalcified bone matrix powder or particle.

13. The method according to claim 12, wherein the method for extracting protein from the bone matrix after decalcifying treatment is as follows: a. firstly hydrogen peroxide is removed from the decalcified bone, and washed with a sterile water for many times until no hydrogen peroxide is present; to obtain a bone matrix powder; then 1000 g of the decalcified bone powder is suspended in 2 L phosphate buffer of PH=7.2; b. the temperature within an enzymolysis kettle is adjusted to 48 to 50° C., 0.35 g pancreatin is added when the pH value is adjusted to 8.5; the reaction time of the enzymes are all 12 to 56 hours, and the protein is degraded; after completion of the treatment, centrifuged, and the supernatant is separated from the precipitate, the supernatant is removed, the precipitate is retained, and dried, to obtain a decalcified and deproteinated bone powder particle.

14. The method according to claim 13, wherein the exogenous BMP is dissolved in a phosphate buffer of PH=7.2, then mixed with a phosphate buffer including the decalcified and deproteinated bone powder, and put in a agitator for uniform and slow agitation, the agitation rate is 20 to 120 Rotation Per Minute, meanwhile being in water bath kettle with a varying temperature.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0024] FIG. 1 is a diagram of comparison results of effects on osteoblast proliferation of Example 1 to 3 with a control CK.

[0025] FIG. 2 is a diagram of comparison results of effects on osteoblast proliferation of Example 1, 4, 5 with the control CK.

[0026] FIG. 3 is a diagram of results of a comparative experiment of effects on MC-3T3 cell ALP activity of Example 1 to 3 with the control CK.

[0027] FIG. 4 is a diagram of results of a comparative experiment of effect on MC-3T3 cell ALP activity of Example 1, 4 and 5 with the control CK.

BENEFICIAL EFFECT

[0028] The formulations for promoting bone tissue growth or repair provided by the present invention has a equivalent effect to the conventional human dental matrix, some of them are better than the existing human dental matrix, thereby providing some alternative products, and reducing product cost, and meeting the growing market demand.

DETAILED DESCRIPTION OF THE EMBODIMENTS

Example 1: Decalcification Treatment of Human Dental Matrix and Addition of Exogenous BMP Protein

[0029] 1. The step for decalcifying human dental matrix is as follows:

[0030] (1) Collected human teeth were placed into a container with clean water, stored at a temperature below 5° C.;

[0031] (2) Raw material teeth were immersed and disinfected with 1.2% sodium hypochlorite, the time was 55 minute, and the temperature was 30° C. (or other temperatures, e.g., 35, 30, 38, 40° C.);

[0032] (3) Useless parts on the teeth were removed;

[0033] (4) The tooth tissue was pulverized into granule or lyophilized powder by a mechanical method, the average particle diameter was 0.25 mm (e.g., 0.2, 0.5, 0.6, 0.7, 0.8, 1.0, 1.2 mm);

[0034] (5) The tooth tissue pulverized into granule or lyophilized powder was immersed and disinfected with 1.2% sodium hypochlorite, the immersion and disinfection time was 45 minutes, the temperature was 35 to 40° C.;

[0035] (6) The tooth tissue granule or lyophilized powder was put in a 0.65 (or 0.67, 0.68, 0.67, 0.72) N hydrochloric acid solution, and immersed at 38° C. for 16 hours to complete the decalcification;

[0036] (7) Dried at low temperature, and immersed in a 3% hydrogen peroxide at 35° C. for 30 minutes. Through detection, the dental matrix granule or lyophilized powder decalcified by this method was fine and uniform, the morphology was consistent, being in a shape of round bar, the length was about 100 to 200 nm, and the diameter was about 50 to 100 nm.

[0037] 2. Addition of exogenous BMP protein.

[0038] a. To 1000 g of the tooth matrix decalcified in step (7) an exogenous BMP protein was added, the method for adding the exogenous protein is as follows:

[0039] b. Firstly the hydrogen peroxide was removed from the dental matrix decalcified in step (7), and washed with sterile water for many times until no hydrogen peroxide was present, to obtain 100 g of human dental matrix powder;

[0040] c. Then the decalcified dental matrix powder was suspended in 1 L phosphate buffer of PH=7.2;

[0041] d. An exogenous BMP-2 (1.0 g, purchased from Shanghai Wheat Warehouse Biological Technology Co., Ltd) was dissolved in the phosphate buffer PH=7.2 of same volume, then the two buffer solutions were mixed together, and placed onto an agitator for uniform and slow agitation, the agitation rate was 30 to 80 Rotation Per Minute, meanwhile being in a water bath kettle with a varying temperature, the temperature sequence was as follows: 26° C., 8 hours; 30° C., 6 hours; 28° C., 8 hours; 28° C., 12 hours; then kept at a constant temperature of 30° C. and the agitation was continued, the protein concentration of BMP-2 in the mixed solution was detected every 3 hours, until the concentration decreased below 20% to 25% of the initial BMP-2 concentration and agitation was stopped, then centrifuged, the supernatant was removed, the remaining powder was filtered, then dried at low temperature to obtain a lyophilized powder of human dental matrix. Through detection, the dental matrix granule or lyophilized powder decalcified by this method was fine and uniform, the morphology was consistent, being in a shape of round bar, the length was about 100 to 220 nm, and the diameter was about 40 to 110 nm.

Example 2: Decalcification Treatment of Human Dental Matrix and Addition of Exogenous BMP Protein

[0042] The difference with Example 1 is that the exogenous protein is BMP-7, and the other conditions are all same.

Example 3: Decalcification Treatment of Human Dental Matrix and Addition of Exogenous BMP Protein

[0043] The difference with Example 1 is the mixed buffer solution was in a water bath kettle of constant temperature, the temperature was 15, 20, 35, 38° C., the time was 34 hours or more, the protein concentration of BMP-2 in the mixed solution was detected every 3 hours, the agitation was stopped until the concentration decreased below 20% to 25% of the initial BMP-2 concentration, then centrifuged, the supernatant was removed, the remaining powder was filtered, then dried at low temperature obtain the human dental matrix, put in 70% ethanol solution at 5° C. and stored for use. Through detection, the dental matrix granule or lyophilized powder decalcified by this method was fine and uniform, the morphology was consistent, being in a shape of round bar, the length was about 100 to 220 nm, and the diameter was about 40 to 110 nm.

Example 4: Decalcification and Deproteinization (BMP) Treatment of Two Parts of Human Dental Matrix, Mixing of Extracted BMP Protein with One Part of Decalcified and Deproteinized Human Dental Matrix Powder

[0044] 1. The step for decalcifying human dental matrix is as follows:

[0045] (1) Collected human teeth were put in a container with clean water, stored at a temperature below 5° C.;

[0046] (2) Raw material teeth were immersed and disinfected with 1.2% sodium hypochlorite, the time was 55 minutes, and the temperature was 30° C. (or other temperatures, e.g., 35, 30, 38, 40° C.);

[0047] (3) Useless parts of the teeth were removed;

[0048] (4) The tooth tissue was pulverized into granule or lyophilized powder by mechanical method, the average particle diameter was 0.25 mm (e.g., 0.2, 0.5, 0.6, 0.7, 0.8, 1.0, 1.2 mm);

[0049] (5) Then the tooth tissue pulverized into granule or lyophilized powder was immersed and disinfected with 1.0% sodium hypochlorite, the immersion and disinfection time was 45 minutes, and the temperature was 35 to 40° C.;

[0050] (6) The tooth tissue granule or lyophilized powder was put in a 0.65 (or 0.67, 0.68, 0.67, 0.72) N hydrochloric acid solution, and immersed at 38° C. for 20 hours to complete the decalcification;

[0051] (7) Dried at low temperature, then immersed in 3% hydrogen peroxide at 35° C. for 30 minutes.

[0052] 2. Extraction treatment of BMP protein.

[0053] A protein extraction treatment was conducted to 1000 g powder of the dental matrix decalcified in step (7), the method for extracting BMP protein is as follows:

[0054] a. Firstly hydrogen peroxide was removed from the dental matrix decalcified in step (7), and washed with sterile water for many times until no hydrogen peroxide was present, to obtain 1000 g of human dental matrix powder;

[0055] b. Then 1000 g of the decalcified dental matrix powder was suspended in 5 L phosphate buffer of PH=7.2;

[0056] c. The phosphate buffer of step (b) was heated in the water bath kettle for 280 hours, the temperature was 40° C., during the heat treatment the buffer was continually agitated; then centrifuged, the supernatant was separated from the precipitate, the target protein was isolated from the supernatant by a molecular sieve then purified and concentrated, finally a active extract of BMP protein was obtained, through detection, its molecular weight was 20 to 50 kda. The precipitated powder was filtered, dried, recovered, to obtain 980 g deproteinated dental matrix powder.

[0057] d. The decalcified and deproteinated dental matrix powder was mixed with the extracted BMP protein, the step of the treatment is as follows:

[0058] Firstly, the dental matrix powder after decalcification and BMP protein extraction was suspend in a phosphate buffer of PH=7.0 (100 g/L, preparing 5 L solution, totally 500 g), then the BMP protein extracted from 1000 g human dental matrix (step c) was dissolved in a phosphate buffer, then the two buffer solutions were mixed together, and placed onto the agitator for uniform and slow agitation, the agitation rate was 30 to 80 Rotation Per Minute, meanwhile agitated at room temperature or 25 to 30° C. for 12 to 24 hours, during agitation the protein concentration of BMP in the mixed solution was detected every 3 hours, the agitation was stopped until the concentration decreased below 10% to 15% of the initial BMP concentration, then centrifuged, the supernatant was remove, the remaining powder was filtered, then dried at low temperature to obtain a matrix, put in a 70% ethanol solution at 5° C. and stored for use.

[0059] Through detection, the dental matrix granule or lyophilized powder decalcified by this method was fine and uniform, the morphology was consistent, being in a shape of round bar, the length was about 80 to 180 nm, and the diameter was about 30 to 70 nm.

Example 5: Decalcification and Deproteination Treatment of Exogenous Human Bone and Addition of Exogenous BMP Protein

[0060] 1. The step for decalcifying human bone is as follows:

[0061] (1) Collected human bone was put in a container with clean water, and stored at temperature below 5° C.;

[0062] (2) The raw material bone was immersed and disinfected with a 2.0% sodium hypochlorite, the time was 55 minutes, and the temperature was 37° C. (or other temperature, e.g., 35, 30, 38, 40° C.);

[0063] (3) Useless parts on the bone were removed;

[0064] (4) The bone tissue was pulverized into granule by mechanical method, the average particle diameter was 0.25 mm (e.g., 0.2, 0.5, 0.6, 0.7, 0.8, 1.0, 1.2 mm, or other particle diameters, e.g., 50 to 100, 120 to 200 nm);

[0065] (5) The pulverized granule was immersed and disinfected with a 1.5% sodium hypochlorite, the immersion and disinfection time was 45 minutes, and the temperature was 35 to 40° C.;

[0066] (6) The bone tissue granule was put in a 0.65 (or 0.67, 0.68, 0.67, 0.72) N hydrochloric acid solution, and immersed at 38° C. for 16 hours to complete the decalcification;

[0067] (7) Dried at low temperature to obtain a lyophilized powder or particle, and immersed in 3% hydrogen peroxide at 35° C. for 30 minutes.

[0068] Through detection, the bone granule or lyophilized powder decalcified by this method was fine and uniform, the morphology was consistent, being in a shape of round bar, the length was about 120 to 240 nm, and the diameter was about 60 to 120 nm.

[0069] 2. Degradation treatment of BMP protein.

[0070] The protein extraction treatment method of 1000 g powder of the bone matrix decalcified in step (7) is as follows:

[0071] a. Firstly hydrogen peroxide was removed from the bone matrix decalcified in step (7), washed with sterile water for many times until no hydrogen peroxide was present, to obtain 1000 g of bone matrix powder; then 1000 g decalcified bone powder was suspended in a 2 L phosphate buffer of PH=7.2;

[0072] b. In order to make the enzymolysis reaction reach an ideal degree in conjunction with production input cost, pancreatin was chosen in the experiment, the temperature in the enzymolysis kettle was adjusted to 48 to 50° C., 0.35 g pancreatin was added when the pH value was adjusted to 8.5; the reaction time of the enzyme were all 12 to 56 hours, and a protein degradation treatment was conducted; after completion of the treatment, centrifuged, the supernatant was separated from the precipitate, the supernatant was removed, the precipitate was retained and dried, to obtain 900 g of decalcified and deproteinated bone powder.

[0073] c. Then, 1000 g decalcified and deproteinated bone powder was suspended in a 5 L phosphate buffer of PH=7.2;

[0074] d. An exogenous BMP-2 (1.0 g, purchased from Shanghai Wheat Warehouse Biological Technology Co., Ltd) was dissolved in a phosphate buffer of same volume and PH=7.2, then the two buffer solutions were mixed together, and placed onto the agitator for uniform and slow agitation, the agitation rate was 30 to 80 Rotation Per Minute, meanwhile being in a water bath kettle with a varying temperature, the temperature sequence was as follows: 26° C., 8 hours; 30° C., 6 hours; 28° C., 8 hours; 28° C., 12 hours; then kept at a constant temperature of 30° C. and the agitation was continued, the protein concentration of BMP-2 in the mixed solution was detected every 3 hours, agitation was stopped until the concentration decreased below 5% to 6% of the initial BMP-2 concentration, then centrifuged, the supernatant was removed, the remaining powder was filtered, then dried at low temperature to obtain bone matrix, put in a 70% ethanol solution at 5° C. and stored for use.

[0075] Through detection, the bone matrix granule or lyophilized powder decalcified by this method was fine and uniform, the morphology was consistent, being in a shape of round bar, the length was about 122 to 240 nm, and the diameter was about 60 to 110 nm.

Example 6: Effect Verification of Bone Induced Osteogenesis Formulation

[0076] 1. Materials and Methods

[0077] 1.1. Experiment Equipments

[0078] Enzyme label plate (24-wells, 96-wells), microplate reader (Model 550), electric centrifuge (80-2 Type), cell incubator (Heraeus BB6220 Type), two-way magnetic heating agitator (Jiangsu Jintan Medical Instrument Factory), pH meter (Shanghai Precision Scientific Instrument Co., Ltd.), constant temperature water bath kettle (Jiangsu Jintan Medical Instrument Factory), medical clean bench (Suzhou Purification Equipment Factory).

[0079] 1.2. Experiment Materials

[0080] A parallel-controlled (CK) treatment experiment was carried out for the materials derived from Example 1 to 5 of the present invention and a commercial dental matrix from Shenzhen GMCB Biological Products Development Co., Ltd., standard fetal bovine serum (Hangzhou Sijiqing Biological Engineering Materials Co., Ltd.), DMEM medium (Sigma), 0.25% trypsin (Sigma), Tritonx-100 (Shanghai Sangon Biotech), ALP standard kit (Shanghai Sangon Biotech).

[0081] 2. Experiment Methods

[0082] 2.1. Cultivation of MC-3T3 Osteoblast:

[0083] MC-3T3 osteoblast was recovered in a conventional medium containing 10% fetal bovine serum, cultured at a condition of 50 ml/L CO.sub.2, saturated humidity, 37° C., the medium was changed after 24 hours, after growth to 80%, digested with a 2.5/L trypsin, passaged, and experiments were carried out to the cells of the 3rd to 4th generations.

[0084] 2.2. Study on Proliferation of MC to 3T3 Osteoblast.

[0085] Before experiment, 0.1 gram of the matrix powder of Example 1 to 5 of the present invention and the commercial dental matrix powder from Shenzhen GMCB Biological Products Development Co., Ltd. were weighed and added into the 24-well plate, each sample was added into three wells on average, ultraviolet was irradiated for 30 minutes for sterilization. The cells in logarithmic phase were digested to make a cell suspension, the concentration was adjusted, such that the inoculum density was 1×10.sup.4/ml, and added into the 24-well plate, 1 ml per well, cultured under a condition of 50 ml/L CO.sub.2, saturated humidity, 37° C. for 2, 4, 6 days, four wells in each culture plate were successively selected, and 160 μl (microliter) of MTT solution was added, the culture was continued for 4 hours, the culture medium was discarded, 1.2 ml DMSO was added, oscillated for 10 minutes, 200 μl (microliter) was put into the 96-well plate, each example was put into three wells on average, an absorbance value was detected at wavelength of 490 nm by ELISA reader, the cell density was estimated using MTT method cell counting standard curve. The above experiment results were analyzed by one-way ANOVA of SPSS statistic software.

[0086] The results are as follows:

[0087] The MTT assay results of different treatments are seen in FIGS. 1 to 2. With the culture time, the cell number in each group is increased. The cell proliferation number in the material inoculated group of Example 1, 3, 4, 5 of the present invention is significantly higher than the control group CK. By statistical analysis, there are statistical differences between the materials in Example 1, 3, 4, 5 and the control CK (P<0.05) (FIG. 1 and FIG. 2). This further demonstrate that the osteogenesis matrix of the present invention obtain has higher activity than the commercial matrix of the prior art, having a great application prospect.

[0088] 2.3. ALP Activity Assay of MC-3T3 Cell.

[0089] The method for cell seeding is same as above, after culture for 2, 4, 6 days, the culture medium was discarded, washed with PBS (0.01 mol/L) 3 times, 800 μl (microliter) of 2 ml/L Triton X was added, placed in a refrigerator at 4° C. over night, then 300 μl ALP substrate was added, kept at 37° C. for 40 minutes, the reaction was stopped by 0.1 mol/L KOH, 200 μl (microliter) was transferred into the 96-well plate, each sample was in three well on average, absorbance A was detected by ELISA reader at 410 nm, i.e., the absorbance A represents activity of cell alkaline phosphatase. In order to eliminate the effect of difference in proliferation rates on the alkaline phosphatase activity, the following correction was carried out: average alkaline phosphatase activity of osteoblast=detected absorbance A value/osteoblast proliferation rate at the same time. The results of the above experiment were analyzed by one-way ANOVA of SPSS statistic software.

[0090] The results are as follows:

[0091] Referring to FIGS. 3 and 4. As can be seen from FIG. 3, the activities of the dental matrix obtained in Example 1 and 3 of the present invention are significantly higher than activity of the dental matrix of the prior art. In addition, this also confirms that BMP-2 protein is the main active protein, it plays an important role in bone repair or growth. With the culture time, alkaline phosphatase activities of the cells in each group are all increased, the alkaline phosphatase activities of Example 1 and 3 are higher than those of the control group. By statistical analysis, there are statistical differences (P<0.05) between Example 1 and the control CK, Example 3, 4 and 5 and the control CK, having a significant difference. This further demonstrates that the osteogenesis matrix obtained by the present invention has a higher activity than the commercial matrix of the prior art.

[0092] In addition, our additional experiments prove that (the method used is adding exogenous protein as shown in Example 1 and adding exogenous protein as shown in Example 5), among all the exogenous BMP proteins, for example, the exogenous BMP protein is one or more of BMP-2, BMP-1, BMP-3, BMP-4, BMP-5, BMP-6 or BMP-7, when one exogenous protein was used alone, the effect of the exogenous proteins BMP-2, BMP-3 and BMP-7 were better than other proteins.

[0093] In addition, we conducted a parallel-controlled (CK) treatment experiment on the matrix particle or dry powder obtain by Example 1, 3, 4, 5 with the commercial dental matrix from Shenzhen GMCB Biological Products Development Co. Ltd., and investigated the repair effect on senile fracture, secondary fracture as well as remoral head necrosis in phase 3 and 4. As a result, it is found that, compared to the existing commercially available dental matrix material (osteogenesis particle or formulation), efficacies of the matrix particle or dry powder in obtain in Example 1, 3, 4, 5 of the present invention are markedly better than current commercial dental matrix material, especially the efficacy of the dental matrix obtained in Example 1, 3, 4 is the best, particularly Example 1 and 4. This may be because that the existing dental matrix material directly undergoes the decalcification treatment, the active protein contained in it is relatively less, and during acidic decalcifying treatment, a great denaturated damage may be caused to the active BMP protein, thus the effect is not ideal, furthermore the decalcification treatment has a large arbitrary, there is large inter-batch differences in the performance of the products. The present invention can significantly improve the efficacy by a simple treatment; in addition, from January 2014 to January 2016, the dental matrix were stored at normal temperature and an activity assay was conducted, the results indicate that after storage at normal temperature for about 2 years, despite the activity was slightly reduced (reduction of about 5 to 10%) (detailed experiment procedure and detailed data are omitted), they maintained high activity after 2 years of storage, its activity is almost 2 to 4 fold of the activity of the current commercial products. This provides a new approach for large-scale standardized commercial production of the induced osteogenesis product with a more marked effect.