Cell-induced response by tetracyclines on human bone marrow colonized hydroxyapatite and Bonelike®

被引:46
作者
Gomes, P. S. [1 ]
Santos, J. D. [2 ,3 ]
Fernandes, M. H. [1 ]
机构
[1] Univ Porto FMDUP, Fac Med Dent, Lab Farmacol & Biocompatibilidade Celular, P-4200392 Oporto, Portugal
[2] Univ Porto, Seccao Mat, DEMM, Fac Engn, P-4200465 Oporto, Portugal
[3] Inst Engn Biomed INEB, Lab Biomat, P-4150180 Oporto, Portugal
关键词
Tetracyclines; osteoblasts; hydroxyapatite; bonelike;
D O I
10.1016/j.actbio.2007.12.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Semi-synthetic tetracyclines are commonly used antibiotics that also seem to play an important role in the modulation of the immuno-inflammatory imbalance, verified in several bone diseases. The association of a therapeutic agent (that prevents bacterial infection and induces tissue formation) to a biomaterial aiming to repair/regenerate bone defects could contribute to a more predictable clinical outcome. The present study intends to evaluate the proliferation and functional activity of osteoblast-induced human bone marrow cells, cultured on the surface of hydroxyapatite (HA) and Bonelike (R), in the presence of therapeutic concentrations of doxycycline and minocycline. First passage bone marrow cells were cultured for 35 days on the surface of HA and Bonelike (R) discs, in the absence or presence of 1 mu g ml(-1) doxycycline and minocycline. Cultures performed in standard tissue culture plates were used as control. Doxycycline or minocycline induced cell proliferation and increased the extent of matrix mineralization in osteoblastic cell cultures established in the three substrates. Also, an improved biological behavior was verified in seeded Bonelike (R) compared with HA. The results suggest that the local delivery of tetracyclines might associate the antimicrobial activity in implant-related bone infection with an eventual induction of osteoblastic proliferation and maintenance of the characteristic biological activity of these cells. (c) 2008 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:630 / 637
页数:8
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