4.3 Article

Bactericidal property and biocompatibility of gentamicin-loaded mesoporous carbonated hydroxyapatite microspheres

出版社

ELSEVIER
DOI: 10.1016/j.msec.2013.04.021

关键词

Carbonated hydroxyapatite; Mesopore; Drug delivery system; Bactericidal property; Biocompatibility

资金

  1. Fund for Key Disciplines of Shanghai Municipal Education Commission [J50206]
  2. Natural Science Foundation of China [51002095, 30973038]
  3. Program of Shanghai Normal University [DZL124, DCL201303]
  4. Science and Technology Commission of Shanghai Municipality [12JC1405600]
  5. Innovation Foundation of Shanghai Education Committee [11YZ86]
  6. Special Research Fund for Cultivating Outstanding Young Teachers in Shanghai Universities [ssd10008]
  7. National Postdoctor Science Foundation of China [20100470734, 201104293]
  8. K.C. Wong Education Foundation of Hong Kong

向作者/读者索取更多资源

Implant-associated infection is a serious problem in orthopaedic surgery. One of the most effective ways is to introduce a controlled antibiotics delivery system into the bone filling materials, achieving sustained release of antibiotics in the local sites of bone defects. In the present work, mesoporous carbonated hydroxyapatite microspheres (MCHMs) loaded with gentamicin have been fabricated according to the following stages: (i) the preparation of the MCHMs by hydrothermal method using calcium carbonate microspheres as sacrificial templates, and (ii) loading gentamicin into the MCHMs. The MCHMs exhibit the 3D hierarchical nanostructures constructed by nanoplates as building blocks with mesopores and macropores, which make them have the higher drug loading efficiency of 70-75% than the conventional hydroxyapatite particles (HAPs) of 20-25%. The gentamicin-loaded MCHMs display the sustained drug release property, and the controlled release of gentamicin can minimize significantly bacterial adhesion and prevent biofilm formation against S. epidermidis. The biocompatibility tests by using human bone marrow stromal cells (hBMSCs) as cell models indicate that the gentamicin-loaded MCHMs have as excellent biocompatibility as the HAPs, and the dose of the released gentamicin from the MCHMs has no toxic effects on the hBMSCs. Hence, the gentamicin-loaded MCHMs can be served as a simple, non-toxic and controlled drug delivery system to treat bone infections. (C) 2013 Elsevier B.V. All rights reserved.

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