Modification of β-TCP/PLGA scaffold and its effect on bone regeneration in vivo

Liulan Lin , Haitao Gao

Journal of Wuhan University of Technology Materials Science Edition ›› 2016, Vol. 31 ›› Issue (2) : 454 -460.

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Journal of Wuhan University of Technology Materials Science Edition ›› 2016, Vol. 31 ›› Issue (2) : 454 -460. DOI: 10.1007/s11595-016-1391-y
Organic Materials

Modification of β-TCP/PLGA scaffold and its effect on bone regeneration in vivo

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Abstract

In order to look for the best proportion of β-tricalcium phosphate(β-TCP) and poly(lactide-co-glycolide) (PLGA) we fabricated porous composites β-TCP/PLGA scaffold using freeze-drying method. Morphological characterization using scanning electron microscopy showed that the interconnected pore distribution was even and there was no significant difference with the increase of PLGA content. Moreover, the porosity, compressive strength and degradation in vitro were characterized. The fabricated scaffolds with increased PLGA in the composites β-TCP/PLGA scaffolds will get stronger mechanical property and better appearance, furthermore, get suitable environment for cells. According to the evaluation indexes for the tissue engineering scaffold, the group of scaffold (β-TCP/PLGA=6:4) was selected to evaluate the induced cell adhesion and proliferative ability of the scaffolds. Then as transplant embed into the bone critical defect sites on rats femur. The repairing processes of bone defect sites were characterized by X-ray analysis within 12 weeks. X-ray analysis showed that the bone defect sites all displayed the formation of callus obviously, In summary, our data suggest that the scaffold (β-TCP/PLGA=6:4) has a promising clinical future in regeneration of bone critical defects.

Keywords

modification / scaffold / freeze-drying / transplant / regeneration

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Liulan Lin, Haitao Gao. Modification of β-TCP/PLGA scaffold and its effect on bone regeneration in vivo. Journal of Wuhan University of Technology Materials Science Edition, 2016, 31(2): 454-460 DOI:10.1007/s11595-016-1391-y

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References

[1]

Thomson R, Yaszemski M, Mikos AG. Lanza R, Langer R, Chick W. Polymer Scaffold Processing[C]. Principles of Tissue Engineering, 1997 Texas: RG LandesCo. 263-272.

[2]

Agrwal CM, Athansiou KA, Heckman JD, Biodegradable P-P. Polymers for Tissue Engineering in Orthopaedics[J]. Mater. Sci. Forum, 1997, 250: 115-228.

[3]

Alexandra M G, Maria J, Andrea C S, et al. Multifunctional Polymer Scaffolds with Adjustable Pore Size and Chemoattractant Gradients for Studying Cell Matrix Invasion[J]. Biomaterials, 2014, 35: 611-619.

[4]

Barry I R, Shepherd RF, Hanson JN, et al. Directwrite Assembly of 3D Hydrogel Scaffolds for Guided Cell Growth[J]. Adv. Mater., 2009, 21: 2407-2410.

[5]

Lad SP, Bagley JH, Ugiliweneza B, et al. BMP and Cancer Risk: Results of a Large, Propensity Matched Study[J]. Neurosurgery, 2012, 71(2): S90-91.

[6]

Li H, Yan YG, Wei J, et al. Bone Substitute Biomedical Material of Multi-(amino acid) Copolymer:in Vitro Degradation and Biocompatibility[J]. J. Mater. Sci. Mater. Med., 2011, 22(11): 2555-2563.

[7]

Sen MK, Miclau T. Autologous Iliac Crest Bone Graft: Should it Still be the Gold Standard for Treating Nonunions[J]?. Injury, 2007, 38(S1): S75-80.

[8]

Mikos AG, Herring SW, Ochareon P, et al. Engineering Complex Tissues[J]. Tissue Eng., 2006, 12: 3307-3339.

[9]

Hao W, Hu Y Y, Wei YY, et al. Collagen I Gel can Facilitate Homogenous Bone Formation of Adipose-derived Stem Cells in PLGA-beta-TCP Scaffold[J]. Cells Tissues Organs, 2009 89-102.

[10]

Kneser U, Schaefer DJ, Polykandriotis E, et al. Tissue Engineering of Bone:the Reconstructive Surgeon’s Point of View[J]. J. Cell Mol. Med., 2006, 10(1): 7-19.

[11]

Yu D, Li Q, Mu X, et al. Bone Regeneration of Critical Calvarial Defect in Goat Model by PLGA/TCP/rhBMP-2 Scaffolds Prepared by Lowtemperature Rapid Prototyping Technology Int[J]. J. OralMaxillofac. Surg., 2008, 37: 929-934.

[12]

Wu LB, Ding JD. In vitro Degradation of Three-dimensional Porous Poly(D,Llactide-co-glycolide) Scaffolds for Tissue Engineering[J]. Biomaterials, 2004, 25: 5821-5830.

[13]

Yang F, Cui WJ, Xiong Z, et al. Poly (L,L-lactide-co-glycolide)/tricalcium Phosphate Composite Scaffold and its Various Changes during Degradation in vitro[J]. Polym. Degrad. Stab., 2006, 91: 3065-3073.

[14]

Bucholz RW. Nonallograft Osteoconductive Bone Graft Substitutes[J]. Clin. Ortho. p Rela. t Res., 2002, 395: 44-52.

[15]

Loher S, Reboul V, Brunner TJ, et al. Loaded with TGF-b1 Induces Differentiation of Mesenchymal Stem Cells in Vivo for Enhancing Cartilage Repair[J]. J. Biomed. Mater. Res., 2006, 77A: 785-794.

[16]

Ekrol I, Hajducka C, Court-Brown C, et al. A Comparison of rhBMP-7(OP-1) and Autogenous Graft for Metaphyseal Defects after Osteotomy of the Distal Radius[J]. Injury, 2008, 39: S73-82.

[17]

Shao H, Shao J, Bian H, Zhao Q, et al. OIC-A006-loaded True Bone Ceramic Heals Rabbit Critical-sized Segmental Radial Defect[J]. Die Pharmazie, 2012, 67(3): 247-252.

[18]

Cai M, Liu X, Shao J, et al. OIC-A006 Promotes Osteogenesis in vitro and in vivo[J]. Pharmazie, 2008, 63(10): 751-756.

[19]

Perets A, Baruch Y, Weisbuch F, et al. Enhancing the Vascularization of Three-dimensional Porous Alginate Scaffolds by Incorporating Controlled Release Basic Fibroblast Growth Factor Microspheres[J]. J. Biomed. Mater. Res., 2003, 65A: 489-497.

[20]

Zheng C. The Design of Degradational Protein-Organisms Microspheres[D], 2006 Hangzhou: Zhejiang University.

[21]

Ungaro F, Biondi M, d’Angelo I, et al. Microsphere-integrated Collagen Scaffolds for Tissue Engineering: Effect of Microsphere Formulation and Scaffold Properties on Protein Release Kinetics[J]. J. Control Release, 2006, 113: 128-136.

[22]

Hitzman CJ, Elmquist WF, Wattenberg LW, et al. Development of a Respirable, Sustained Release Microcarrier for 5-fluorouracil I: In Vitro Assessment of Liposomes, Microspheres, and Lipid Coated Nanoparticles[J]. J. Pharm. Sci., 2006, 95: 1114-1126.

[23]

Hong Y, Gao CY, Xie Y, et al. Collagen-coated Polylactide Microspheres as Chondrocyte Microcarriers[J]. Biomaterials, 2005, 26: 6305-6313.

[24]

Ara M, Watanabe M, Imai Y. Controlled Drug Release from a Novel Injectable Biodegradable Microsphere/scaffold Composite Based on Poly(propylene fumarate)[J]. J. Biomed Mater Res., 2006, 77A: 103-111.

[25]

Jaklenec A, Wan E, Murray ME, et al. Novel Scaffolds Fabricated Fromprotein-loaded Microspheres for Tissue Engineering[J]. Biomaterials, 2008, 29(2): 185-192.

[26]

Juergen S, Khaled E, Florence S, et al. How Autocatalysis Accelerates Drug Release from PLGA-Based Microparticles: A Quantitative Treatment[J]. Biomacromolecules, 2005, 6: 2312-2319.

[27]

Yanfang Y, Yunhui Z, Gongwen T, et al. In Vitro Degradation of Porous Poly(L-lactide-co-glycolide)/ß-tricalcium Phosphate (PLGA/ß-TCP) Scaffolds under Dynamic and Static Conditions[J]. Polymer Degradation and Stability, 2008, 93: 1838-1845.

[28]

Liulan L, Zhikun W, Liping Z, et al. The Influence of Prefreezing Temperature on Pore Structure in Freeze-dried ß-TCP Scaffolds[J]. J. Engineering in Medicine, 2012, 227(1): 50-57.

[29]

Freed LE, Vunjak-Novakovic G, Langer R. Cultivation of Cell-polymer Cartilage Implants in Bioreactors[J]. J. Cell Biochem., 1993, 5: 257-264.

[30]

Yanoso-Scholl L, Jacobson JA, Braica G, et al. Evaluation of Dense Polylactic Acid/betatricalcium Phosphate Scaffolds for Bone Tissue Engineering[J]. J. Biomed. Mater. Res. A, 2010, 95: 717-726.

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