Zinc-containing apatite layers on external fixation rods promoting cell activity

Acta Biomaterialia

Volumn 6, Issue 3, 2010, Pages 962-968

  Wang, Xiupeng ^a   Ito, Atsuo ^a   Sogo, Yu ^a   Li, Xia ^a   Oyane, Ayako ^a  

^a NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

Author keywords

External fixation; Fibroblast; Osteoblast; Tissue regeneration; Zinc

Indexed keywords

APATITE; CALCIUM PHOSPHATE; CELL CULTURE; CHLORINE COMPOUNDS; FIBROBLASTS; TISSUE; TITANIUM; ZINC CHLORIDE;

APATITE LAYERS; CELL ACTIVITY; EXTERNAL FIXATION; FIBROBLAST; IN-VITRO;

TISSUE REGENERATION;

ALKALINE PHOSPHATASE; APATITE; BIOMATERIAL; CALCIUM; CALCIUM PHOSPHATE; PHOSPHORUS; TITANIUM DIOXIDE; ZINC CHLORIDE;

ANIMAL CELL; ARTICLE; CELL ACTIVITY; CELL DENSITY; CELL DIFFERENTIATION; CELL PROLIFERATION; CELL STRAIN 3T3; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DNA CONTENT; ENZYME ACTIVITY; EXTERNAL FIXATOR; FIBROBLAST; IN VITRO STUDY; INFECTION RATE; MATERIAL COATING; NONHUMAN; OSTEOBLAST; PRECIPITATION; PRIORITY JOURNAL; PROTEIN CONTENT;

EID: 75149194698     PISSN: 17427061     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.actbio.2009.08.038     Document Type: Article

References (29)

1. Bosetti M., Masse A., Tobin E., and Cannas M. Silver coated materials for external fixation devices: in vitro biocompatibility and genotoxicity. Biomaterials 23 3 (2002) 887-892
2. Mutsuzaki H., Ito A., Sakane M., Sogo Y., Oyane A., and Ochiai N. Fibroblast growth factor-2-apatite composite layers on titanium screw to reduce pin tract infection rate. J Biomed Mater Res B Appl Biomater 86B 2 (2008) 365-374
3. Wang X., Ito A., Sogo Y., Li X., Tsurushima H., and Oyane A. Ascorbate-apatite composite and ascorbate-FGF-2-apatite composite layers formed on external fixation rods and their effects on cell activity in vitro. Acta Biomater 5 (2009) 2647-2656
4. Wang X., Ito A., Sogo Y., Li X., and Oyane A. Silicate-apatite composite layers on external fixation rods and in vitro evaluation using fibroblast and osteoblast. J Biomed Mater Res A (2009) 10.1002/jbm.a.3243
5. Prasad A.S. Zinc: an overview. Nutrition 11 Suppl. 1 (1995) 93-99
6. Andrews M., and Gallagher-Allred C. Role of zinc in wound healing. Adv Wound Care 12 (1999) 137-138
7. Yamaguchi M., Oishi H., and Suketa Y. Zinc stimulation of bone protein synthesis in tissue culture. Activation of aminoacyl-tRNA synthetase. Biochem Pharmacol 37 21 (1988) 4075-4080
8. El-Kattan A, Michniak B. Percutaneous permeation of zinc from non-woven fabrics impregnated with zinc sulfate monohydrate formulations using epiderm™. In: Presented at the 6th World Biomaterials Congress in Kumuela, Hawaii, May 15-20, 2000.
9. Lansdown A., Mirastschijski U., Stubbs N., Scanlon E., and Agren M. Zinc in wound healing: theoretical, experimental, and clinical aspects. Wound Repair Regen 15 (2007) 2-16
10. Seto K., Yoneta T., Suda H., and Tamaki H. Effect of polaprezinc (N-(3-aminopropionyl)-l-histidinato zinc), a novel antiulcer agent containing zinc, on cellular proliferation: role of insulin-like growth factor I. Biochem Pharmacol 58 2 (1999) 245-250
11. Yamaguchi M., Oishi H., and Suketa Y. Stimulatory effect of zinc on bone formation in tissue culture. Biochem Pharmacol 36 22 (1987) 4007-4012
12. Moonga B.S., and Dempster D.W. Zinc is a potent inhibitor of osteoclastic bone resorption in vitro. J Bone Miner Res 10 3 (1995) 453-457
13. Ito A., Ojima K., Naito H., Ichinose N., and Tateishi T. Preparation, solubility, and cytocompatibility of zinc-releasing calcium phosphate ceramics. J Biomed Mater Res 50 2 (2000) 178-183
14. Li X., Sogo Y., Ito A., Mutsuzaki H., Ochiai N., Kobayashi T., et al. The optimum zinc content in set calcium phosphate cement for promoting bone formation in vivo. Mater Sci Eng C 29 (2009) 969-975
15. Yokoyama Y., Oyane A., and Ito A. Preparation of a bonelike apatite-polymer fiber composite using a simple biomimetic process. J Biomed Mater Res B Appl Biomater 86B 2 (2008) 341-352
16. Kageyama Y., Yokohama Y., Suzuki K., Harada Y., and Kokubo T. Response of soft tissue against hydroxyapatite coated on polymers. Bioceramics 7 (1994) 165-170
17. Beck Jr. G.R., Sullivan E.C., Moran E., and Zerler B. Relationship between alkaline phosphatase levels, osteopontin expression, and mineralization in differentiating MC3T3-E1 osteoblasts. J Cell Biochem 68 2 (1998) 269-280
18. Aubin J.E., Liu F., Malaval L., and Gupta A.K. Osteoblast and chondroblast differentiation. Bone 17 Suppl. 2 (1995) 77S-83S
19. Malaval L., Liu F., Roche P., and Aubin J.E. Kinetics of osteoprogenitor proliferation and osteoblast differentiation in vitro. J Cell Biochem 74 4 (1999) 616-627
20. Otsuka M., Marunaka S., Matsuda Y., Ito A., Layrolle P., Naito H., et al. Calcium level-responsive in-vitro zinc release from zinc containing tricalcium phosphate (ZnTCP). J Biomed Mater Res 52 4 (2000) 819-824
21. Fujii E., Ohkubo M., Tsuru K., Hayakawa S., Osaka A., Kawabata K., et al. Selective protein adsorption property and characterization of nano-crystalline zinc-containing hydroxyapatite. Acta Biomater 2 1 (2006) 69-74
22. Sogo Y., Sakurai T., Onuma K., and Ito A. The most appropriate (Ca + Zn)/P molar ratio to minimize the zinc content of ZnTCP/HAP ceramic used in the promotion of bone formation. J Biomed Mater Res 62 3 (2002) 457-463
23. Watanabe S., Wang X.E., Hirose M., Kivilioto T., Osada T., Miwa H., et al. Insulin-like growth factor I plays a role in gastric wound healing: evidence using a zinc derivative, polaprezinc, and an in vitro rabbit wound repair model. Aliment Pharmacol Ther 12 11 (1998) 1131-1138
24. Tarnow P., Agren M., Steenfos H., and Jansson J.O. Topical zinc oxide treatment increases endogenous gene expression of insulin-like growth factor-1 in granulation tissue from porcine wounds. Scand J Plast Reconstr Surg Hand Surg 28 4 (1994) 255-259
25. van Eickels M., Vetter H., and Grohe C. Angiotensin-converting enzyme (ACE) inhibition attenuates insulin-like growth factor-I (IGF-I) induced cardiac fibroblast proliferation. Br J Pharmacol 131 8 (2000) 1592-1596
26. Gillery P., Leperre A., Maquart F.X., and Borel J.P. Insulin-like growth factor-I (Igf-I) stimulates protein-synthesis and collagen gene-expression in monolayer and lattice cultures of fibroblasts. J Cell Physiol 152 2 (1992) 389-396
27. Yateman M.E., Claffey D.C., Hughes S.C.C., Frost V.J., Wass J.A.H., and Holly J.M.P. Cytokines modulate the sensitivity of human fibroblasts to stimulation with insulin-like growth factor-I (Igf-I) by altering endogenous Igf-binding protein-production. J Endocrinol 137 1 (1993) 151-159
28. Delves H.T. Assessment of trace element status. Clin Endocrinol Metab 14 3 (1985) 725-760
29. Ito A., Kawamura H., Otsuka M., Ikeuchi M., Ohgushi H., Ishikawa K., et al. Zinc-releasing calcium phosphate for stimulating bone formation. Mater Sci Eng C 22 1 (2002) 21-25