Preparation and osteogenic effect study of small intestinal submucosa sponge

  • Mei WANG ,
  • Bo-wen LI ,
  • Si-wen WANG ,
  • Yu-hua LIU
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  • 1. Department of Prosthodontics, Peking University School and Hospital of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Laboratory for Digital and Material Technology of Stomatology & Beijing Key Laboratory of Digital Stomatology, Beijing 100081, China
    2. Department of Prosthodontics, Tongji University School and Hospital of Stomatology, Shanghai 200072, China

Received date: 2018-10-09

  Online published: 2020-10-15

Abstract

Objective: To prepare and evaluate the basic properties in vitro of a novel small intestinal submucosa (SIS) sponge, and to describe the bone formation ability of the SIS sponge in vivo. Methods: The SIS sponge was prepared by freeze-drying method. To evaluate the physicochemical properties of the sponge, electron microscope observation, porosity test, water absorption ability and mechanical property were conducted in vitro. The cytotoxicity of the SIS sponge was performed by cell counting kit-8 method. In vivo experiments, eighteen extraction sockets of premolar of three Beagle dogs were randomly divided into three groups: SIS sponge group (SIS sponge), positive control group (Bio-Oss granules and Bio-Gide membrane) and control group(no treatment). The animals were sacrificed 4 weeks and 12 weeks after operation, and micro computed tomography (Micro-CT) was applied to measure the bone volume fraction (BV/TV) and bone mineralized density (BMD). The data were analyzed with one-way ANOVA. Results: The average pore diameter of the SIS sponge was (194.90±30.39) μm, the porosity was 92.31%±0.24%, the water absorption rate was 771.50%±40.90%, and the compressive elastic modulus was (2.20±0.19) kPa. There was no significant difference in cell proliferation ability between SIS sponge and control group (P>0.05). Micro-CT quantitative results showed that BV/TV of SIS sponge group (52.81%±3.21%) and positive control group (58.30%±9.36%) were significantly higher than that of control group (38.65%±4.80%) 4 weeks after operation (P <0.05). The BMD of SIS sponge group [(887.09±61.02) mg/cm3], positive control group [(952.05±132.78) mg/cm3] and control group [(879.29±74.27) mg/cm3] showed no statistical difference 4 weeks after operation (P>0.05). The BV/TV of positive control group (60.57%± 6.56%) was significantly higher than that of SIS sponge group (47.89%±3.59%) and control group (42.99%±2.54%) 12 weeks after operation (P < 0.05). BMD of SIS sponge group [(1047±89.95) mg/cm3] and positive control group [(1101.37±98.85) mg/cm3] were significantly higher than that of control group [(890.36±79.79) mg/cm3] 12 weeks after operation (P <0.05). Conclusion: The SIS sponge has satisfying physicochemical properties and biocompatibility. The SIS sponge significantly increased bone volume fraction in the early stage of bone formation (4 weeks) and bone mineralized density in the late stage of bone formation (12 weeks).

Cite this article

Mei WANG , Bo-wen LI , Si-wen WANG , Yu-hua LIU . Preparation and osteogenic effect study of small intestinal submucosa sponge[J]. Journal of Peking University(Health Sciences), 2020 , 52(5) : 952 -958 . DOI: 10.19723/j.issn.1671-167X.2020.05.027

References

[1] Avilaortiz G, Elangovan S, Kramer KWO, et al. Effect of alveolar ridge preservation after tooth extraction: A systematic review and meta-analysis[J]. J Dent Res, 2014,93(10):950-958.
[2] López M, Fanny, Gómez M, et al. Implants failures related to endodontic treatment. An observational retrospective study[J]. Clin Oral Implant Res, 2015,26(9):992-995.
[3] Horváth A, Mardas N, Mezzomo LA, et al. Alveolar ridge preservation. A systematic review[J]. Clin Oral Investig, 2013,17(2):341-363.
[4] Bose S, Roy M, Bandyopadhyay A. Recent advances in bone tissue engineering scaffolds[J]. Trends Biotechnol, 2012,30(10):546-554.
[5] 蒋欣泉. 骨缺损修复生物材料与骨再生[J]. 中华口腔医学杂志, 2017,52(10):600-604.
[6] Andrée B, B?r A, Haverich A, et al. Small intestinal submucosa segments as matrix for tissue engineering: review[J]. Tissue Eng Part B, 2013,19(4):279-291.
[7] Nezhad ZM, Poncelet A, Kerchove LD, et al. Small intestinal submucosa extracellular matrix (CorMatrix?) in cardiovascular surgery: A systematic review [J]. Interact Cardiovasc Thorac Surg, 2016,22(6):839-850.
[8] Li M, Zhang C, Mao Y, et al. A cell-engineered small intestinal submucosa-based bone mimetic construct for bone regeneration[J]. Tissue Eng Part A, 2018,24(13):1099-1111.
[9] 房艳, 倪伟民, 单伟, 等. 海绵状的小肠粘膜下层促进成骨样细胞增殖分化[J]. 中国生物工程杂志, 2013,33(6):18-23.
[10] Kim KS, Lee J Y, Kang YM, et al. Small intestine submucosa sponge for in vivo support of tissue-engineered bone formation in the presence of rat bone marrow stem cells[J]. Biomaterials, 2010,31(6):1104-1113.
[11] Lin X, Chen J, Qiu P, et al. Biphasic hierarchical extracellular matrix scaffold for osteochondral defect regeneration[J]. Osteoarthritis Cartilage, 2018,26(3):433-444.
[12] Cunniffe GM, Díazpayno PJ, Ramey JS, et al. Growth plate extracellular matrix-derived scaffolds for large bone defect healing[J]. Eur Cells Mater, 2017,33(1):130-142.
[13] Wang W, Zhang X, Chao NN, et al. Preparation and charac-terization of proangiogenic gel derived from small intestinal submucosa[J]. Acta Biomaterialia, 2016,29(1):135-148.
[14] Lin X, Robinson M, Petrie T, et al. Small intestinal submucosa-derived extracellular matrix bioscaffold significantly enhances angiogenic factor secretion from human mesenchymal stromal cells[J]. Stem Cell Res Ther, 2015,6(1):164-176.
[15] Kim MS, Hong KD, Shin HW, et al. Preparation of porcine small intestinal submucosa sponge and their application as a wound dressing in full-thickness skin defect of rat[J]. Int J Biol Macromol, 2005,36(1/2):54-60.
[16] Li M, Zhang C, Cheng M, et al. Small intestinal submucosa: A potential osteoconductive and osteoinductive biomaterial for bone tissue engineering[J]. Mater Sci Eng C Biomim Supramol Syst, 2017,75(6):149-156.
[17] Dimitriou R, Mataliotakis GI, Calori GM, et al. The role of barrier membranes for guided bone regeneration and restoration of large bone defects: current experimental and clinical evidence[J]. BMC Med, 2012,10(1):81-105.
[18] Rouwkema J, Rivron NC, Blitterswijk CAV. Vascularization in tissue engineering[J]. Trends Biotechnol, 2008,26(8):434-441.
[19] Bola?os MAC, Buttigieg J, Triana JCB. Development and characterization of a novel porous small intestine submucosa-hydroxyapatite scaffold for bone regeneration[J]. Mater Sci Eng C Biomim Supramol Syst, 2017,72(3):519-525.
[20] 孙慧哲, 田伟, 曾亮, 等. 猪小肠黏膜下基质海绵的制备[J]. 中国组织工程研究, 2016,20(21):3110-3116.
[21] Sarkar AD, Singhvi N, Shetty JN, et al. The local effect of alendronate with intra-alveolar collagen sponges on post extraction alveolar ridge resorption: A clinical trial[J]. J Oral Maxillofac Surg, 2015,14(2):344-356.
[22] Gilbert TW, Stewartakers AM, Simmonsbyrd A, et al. Degradation and remodeling of small intestinal submucosa in canine achilles tendon repair[J]. J Bone Joint Surg Am, 2007,89(3):621-630.
[23] Wu W, Li B, Liu Y, et al. Effect of multilaminate small intestinal submucosa as a barrier membrane on bone formation in a rabbit mandible defect model[J]. Biomed Res Int, 2018(2):1-11.
[24] Kim JJ, Schwarz F, Song HY, et al. Ridge preservation of extraction sockets with chronic pathology using Bio-Oss Collagen with or without collagen membrane: An experimental study in dogs[J]. Clin Oral Implant Res, 2017(28):727-733.
[25] Wang F, Li Q, Wang Z. A comparative study of the effect of Bio-Oss? in combination with concentrated growth factors or bone marrow-derived mesenchymal stem cells in canine sinus grafting [J]. J Oral Pathol Med, 2017,46(7):528-536.
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