Literature DB >> 30678975

In vivo efficiency of antimicrobial inorganic bone grafts in osteomyelitis treatments.

G Mestres1, M A Fernandez-Yague2, D Pastorino2, E B Montufar3, C Canal2, M C Manzanares-Céspedes4, M P Ginebra5.   

Abstract

The purpose of the present work was to evaluate in vivo different antimicrobial therapies to eradicate osteomyelitis created in the femoral head of New Zealand rabbits. Five phosphate-based cements were evaluated: calcium phosphate cements (CPC) and calcium phosphate foams (CPF), both in their pristine form and loaded with doxycycline hyclate, and an intrinsic antimicrobial magnesium phosphate cement (MPC; not loaded with an antibiotic). The cements were implanted in a bone previously infected with Staphylococcus aureus to discern the effects of the type of antibiotic administration (systemic vs. local), porosity (microporosity, i.e. <5 μm vs. macroporosity, i.e. >5 μm) and type of antimicrobial mechanism (release of antibiotic vs. intrinsic antimicrobial activity) on the improvement of the health state of the infected animals. A new method was developed, with a more comprehensive composite score that integrates 5 parameters of bone infection, 4 parameters of bone structural integrity and 4 parameters of bone regeneration. This method was used to evaluate the health state of the infected animals, both before and after osteomyelitis treatment. The results showed that the composite score allows to discern statistically significant differences between treatments that individual evaluations were not able to identify. Despite none of the therapies completely eradicated the infection, it was observed that macroporous materials (CPF and CPFd, the latter loaded with doxycycline hyclate) and intrinsic antimicrobial MPC allowed a better containment of the osteomyelitis. This study provides novel insights to understand the effect of different antimicrobial therapies in vivo, and a promising comprehensive methodology to evaluate the health state of the animals was developed. We expect that the implementation of such methodology could improve the criteria to select a proper antimicrobial therapy.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Calcium phosphate cements; Calcium phosphate foams; Drug delivery; In vivo; Magnesium phosphate cements; Osteomyelitis

Mesh:

Substances:

Year:  2018        PMID: 30678975     DOI: 10.1016/j.msec.2018.11.064

Source DB:  PubMed          Journal:  Mater Sci Eng C Mater Biol Appl        ISSN: 0928-4931            Impact factor:   7.328


  5 in total

1.  Elution properties of a resorbable magnesium phosphate cement.

Authors:  Brandon L Roller; Aaron M Stoker; James L Cook
Journal:  J Clin Orthop Trauma       Date:  2020-06-17

Review 2.  Therapeutics and delivery vehicles for local treatment of osteomyelitis.

Authors:  Leah H Cobb; Emily M McCabe; Lauren B Priddy
Journal:  J Orthop Res       Date:  2020-04-21       Impact factor: 3.494

Review 3.  Innovations in osteomyelitis research: A review of animal models.

Authors:  Kylie M Roux; Leah H Cobb; Marc A Seitz; Lauren B Priddy
Journal:  Animal Model Exp Med       Date:  2021-01-13

4.  Bone regeneration capacity of newly developed spherical magnesium phosphate cement granules.

Authors:  Andreas Fuchs; Dorothea Kreczy; Theresa Brückner; Uwe Gbureck; Philipp Stahlhut; Melanie Bengel; Andreas Hoess; Berthold Nies; Julia Bator; Uwe Klammert; Christian Linz; Andrea Ewald
Journal:  Clin Oral Investig       Date:  2021-10-23       Impact factor: 3.606

5.  Characterization and Biomechanical Study of a Novel Magnesium Potassium Phosphate Cement.

Authors:  Zhenchuan Han; Bo Wang; Bowen Ren; Yihao Liu; Nan Zhang; Zheng Wang; Jianheng Liu; Keya Mao
Journal:  Life (Basel)       Date:  2022-07-05
  5 in total

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