The correlation between the internal structure and vascularization of controllable porous bioceramic materials in vivo: A quantitative study

Tissue Engineering - Part A

Volumn 16, Issue 12, 2010, Pages 3791-3803

  Bai, Feng ^a   Wang, Zhen ^a   Lu, Jianxi ^b   Liu, Jian ^a   Chen, Gongyi ^a   Lv, Rong ^a   Wang, Jun ^a   Lin, Kaili ^b   Zhang, Jinkang ^a   Huang, Xin ^a  

^a FOURTH MILITARY MEDICAL UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF CERAMICS   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MATERIALS; BLOOD; BLOOD VESSELS; NUCLEAR MEDICINE; PORE SIZE; SCAFFOLDS; SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY; TOMOGRAPHY; TRANSMISSION CONTROL PROTOCOL;

BIOCERAMIC MATERIALS; BIOCERAMIC SCAFFOLDS; CASTING TECHNIQUES; DISK-TYPE; IN-VIVO; INTERNAL STRUCTURE; MACROPORE SIZE; MACROPORES; MACROPOROUS; OPTIMAL CONDITIONS; POROUS BIOCERAMIC; POROUS STRUCTURES; QUANTITATIVE STUDY; RABBIT MODELS; REVASCULARIZATION; TRI-CALCIUM PHOSPHATES; UPPER LIMITS; VASCULARIZATION;

BIOMATERIALS;

ORYCTOLAGUS CUNICULUS;

BETA-TRICALCIUM PHOSPHATE; BIOMATERIAL; CALCIUM PHOSPHATE; TISSUE SCAFFOLD;

ANIMAL; ARTICLE; CHEMISTRY; METHODOLOGY; POROSITY; RABBIT; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; TISSUE ENGINEERING;

ANIMALS; BIOCOMPATIBLE MATERIALS; CALCIUM PHOSPHATES; POROSITY; RABBITS; TISSUE ENGINEERING; TISSUE SCAFFOLDS; TOMOGRAPHY, EMISSION-COMPUTED, SINGLE-PHOTON;

EID: 78650041547     PISSN: 19373341     EISSN: 1937335X     Source Type: Journal    
DOI: 10.1089/ten.tea.2010.0148     Document Type: Article

References (41)

1. Langer, R., and Vacanti, J.P. Tissue engineering. Science 260, 920, 1993.
2. Rouwkema, J., Rivron, N.C., and Van Blitterswijk, C.A. Vascularization in tissue engineering. Trends Biotechnol 26, 434, 2008.
3. Elcin, A.E., and Elcin, Y.M. Localized angiogenesis induced by human vascular endothelial growth factor-activated PLGA sponge. Tissue Eng 12, 959, 2006.
4. Smith, M.K., Peters, M.C., Richardson, T.P., Garbern, J.C., and Mooney, D.J. Locally enhanced angiogenesis promotes transplanted cell survival. Tissue Eng 10, 63, 2004.
5. Koch, S., Yao, C., Grieb, G., Prevel, P., Noah, E.M., and Steffens, G.C.M. Enhancing angiogenesis in collagen matrices by covalent incorporation of VEGF. J Mater Sci Mater Med 17, 735, 2006.
6. Neil, D., Stephan, D., Deon, B., Christian, S., Michael, B., Andreas, H.Z., and Peter, Z. The dosage dependence of VEGF stimulation on scaffold neovascularisation. Bioma-terials 29, 3531, 2008.
7. Warnke, P.H., Springer, I.N., Wiltfang, J., Acil, Y., Eufinger, H., and Wehmoller, M. Growth and transplantation of a custom vascularised bone graft in a man. Lancet 364, 766, 2004.
8. Warnke, P.H., Wiltfang, J., Springer, I., Acil, Y., Bolte, H., and Kosmahl, M. Man as living bioreactor: fate of an exog-enously prepared customized tissue engineered mandible. Biomaterials 27, 3163, 2006.
9. Levenberg, S., Rouwkema, J., Macdonald, M., Garfein, E.S., Kohane, D.S., and Darland, D.C. Engineering vascularized skeletal muscle tissue. Nat Biotechnol 23, 879, 2005.
10. Laschke, M.W., Strohe, A., Scheuer, C., Eglin, D., Verrier, S., Alini, M.T., Pohlemann, T., and Menger, M.D. In vivo bio-compatibility and vascularization of biodegradable porous polyurethane scaffolds for tissue engineering. Acta Biomater 5, 1991, 2009.
11. Schwartz, Z., Braun, G., and Kohavi, D. Effects of hy-droxyapatite implants on primary mineralization during rat tibial healing: biochemical and morphometric analysis. J Biomed Mater Res 27, 1029, 1993.
12. Druecke, D., Langer, S., Lamme, E., Pieper, J., Ugarkovic, M., and Steinau, H.U. Neovascularization of poly (ether ester) block-copolymer scaffolds in vivo: long-term investigations using intravital fluorescent microscopy. J Biomed Mater Res 68, 10, 2004.
13. Maddalena, M., Silvia, S., Roberta, M., Laura, D., Francesco, B., Ranieri, C., and Rodolfo, Q. Role of scaffold internal structure on in vivo bone formation in macroporous calcium phosphate bioceramics. Biomaterials 27, 3230, 2006.
14. Tsuruga, E., Takita, H., Itoh, H., Wakisaka, Y., and Kuboki, Y. Pore size of porous hydroxyapatite as the cell-substratum controls BMP-induced osteogenesis. J Biochem 121, 317, 1997.
15. Lu, J.X., Flautre, B., Anselme, K., Hardouin, P., Gallur, A., Descamps, M., et al. Role of interconnections in porous bio-ceramics on bone recolonization in vitro and in vivo. J Mater Sci Mater Med 10, 111, 1999.
16. Kuboki, Y., Jin, Q., Kikuchi, M., Mamood, J., and Takita, H. Geometry of artificial ECM: sizes of pores controlling phe-notype expression in BMP-induced osteogenesis and chon-drogenesis. Connect Tissue Res 43, 529, 2002.
17. Kuboki, Y., Jin, Q., and Takita, H. Geometry of carriers controlling phenotypic expression in BMP-induced osteo-genesis and chondrogenesis. J Bone Joint Surg Am 83, 105, 2001.
18. Vassilis, K., and David, K. Porosity of 3D biomaterial scaffolds and osteogenesis. Biomaterials 26, 5474, 2005.
19. Moore, M.J., Jabbari, E., Ritman, E.L., Lu, L.C., Currier, B.L., and Windebank, A.J. Quantitative analysis of inter-connectivity of porous biodegradable scaffolds with micro-computed tomography. J Biomed Mater Res Part A 71, 258, 2004.
20. Park, S.N., Park, J.C., Kim, H.O., Song, M.J., and Suh, H. Characterization of porous collagen/hyaluronic acid scaffold modified by 1-ethyl-3-(3-dimethylaminopropyl) carbo-diimide cross-linking. Biomaterials 23, 1205, 2002.
21. Lin, A.S., Barrows, T.H., Cartmell, S.H., and Guldberg, R.E. Microarchitectural and mechanical characterization of oriented porous polymer scaffolds. Biomaterials 24, 481, 2003.
22. Henno, S., Lambotte, J.C., Glez, D., Guigand, M., Lancien, G., and Cathelineau, G. Characterisation and quantification of angiogenesis in b-tricalcium phosphate implants by im-munohistochemistry and transmission electron microscopy. Biomaterials 24, 3173, 2003.
23. Xueming, W., Guoxian, P., Dan, J., Kuanhai, W., and Shan, J. Monitoring the vascularization of tissue engineered bone in rhesus. Chin J Clin Rehabil 37, 87, 2006.
24. Civelek, A.C., Pacheco, E.M., Natara-jan, T.K., Wagner, H.N., and Iliff, N.T. Quantitative measurement of vascular-ization and vascular ingrowth rate of hydroxyapatite ocular implant by Tc-99mMDP bone imaging. Clin Nucl Med 20, 779, 1995.
25. Songfeng, X., Yunyu, H., Kaili, L., Zhen, W., Lin, W., Jiang C., Feng, B., and Siyu, N. In vivo study of porous calcium silicate bioceramic in extra-osseous sites. J Inorg Mater 23, 611, 2008.
26. Ozawa, M., Tanaka, K., Morikawa, S., Chazono, M., and Fujii, K. Clinical study of the pure b-tricalcium phosphate-reports of 167 cases. J East Jpn Orthop Traumatol 12, 409, 2000.
27. Chazono, M., Tanaka, T., Komaki, H., and Fujii, K. Bone formation and bioresorption after implantation of in-jectable b-tricalcium phosphate granules-hyaluronate complex in rabbit bone defects. J Biomed Mater Res 70A, 542, 2004.
28. Kondo, N., Ogose, A., Tokunaga, K., Ito, T., Arai, K., and Kudo, N. Bone formation and resorption of highly purified b-tricalcium phosphate in the rat femoral condyle. Bioma-terials 26, 5600, 2005.
29. Ogose, A., Kondo, N., Umezu, H., Hotta, T., Kawashima, H., and Tokunaga, K. Histological assessment in grafts of highly purified beta-tricalcium phosphate (OSferions) in human bones. Biomaterials 27, 1542, 2006.
30. Lu, J., Descamps, M., Dejou, J., Koubi, G., Hardouin, P., and Lemaltre, J. The biodegradation mechanism of calcium phosphate biomaterials in bone. J Biomed Mater Res Appl Biomater 63, 408, 2002.
31. Bohner, M. Calcium orthophosphates in medicine: from ceramics to calcium phosphate cements. Injury 31, 37, 2000.
32. Min, L., Benjamin, M., and James, C.Y. Effect of scaffold architecture and pore size on smooth muscle cell growth. J Biomed Mater Res A 87, 1010, 2009.
33. Oliveira, J.F., Aguiar, P.F., Rossi, A.M., and Soares, G.A. Effect process parameters on the characteristics of porous calcium phosphate ceramics for bone tissue scaffolds. Artif Organs 27, 406, 2003.
34. Gauthier, O., Bouler, J.M., Aguado, E., Pilet, P., and Daculsi, G. Macroporous biphasic calcium phosphate ceramics: influence of macropore diameter and macro-porosity percentage on bone ingrowth. Biomaterials 19, 133, 1998.
35. Takatoshi, O., Koji, I., Ikuho, Y., Hideyuki, M., Giichiro, K., and Yoshinori, G. The effect of the microstructure of b-tri-calcium phosphate on the metabolism of subsequently formed bone tissue. Biomaterials 28, 2612, 2007.
36. Mankani, M.H., Kuznetsov, S.A., Fowler, B., Kingman, A., and Robey, P.G. In vivo bone formation by human bone marrow stromal cells: effect of carrier particle size and shape. Biotechnol Bioeng 72, 96, 2001.
37. Monika, R., Alexander, W., John, W.C., Joost, T.D., and Peter, F. The effect of geometry on three-dimensional tissue growth. J R Soc Interface 5, 1173, 2008.
38. Henry, H.A., Krishna, B., Peter, N., and Abhay, P. Structural variants of biodegradable polyesterurethane in vivo evokea cellular and angiogenic response that is dictated by architecture. Acta Biomater 5, 29, 2009.
39. Hollister, S.J. Porous scaffold design for tissue engineering. Nat Mater 4, 518, 2005.
40. Wilson, C.E., de Bruijn, J.D., van Blitterswijk, C.A., Verbout, A.J., and Dhert, W.J. Design and fabrication of standardized hydroxyapatite scaffolds with a defined macro-architecture by rapid prototyping for bone-tissue- engineering research. J Biomed Mater Res 68A, 123, 2004.
41. Riebal, G.D., Boden, S.D., and Whitesides, T.E. The effect of nicotine on incorporation of cancellous bone graft in an animal model. Spine 20, 2198, 1995.