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Nanocomposite orthopaedic bone cement combining long-acting dual antimicrobial drugs.
Yang, Lirong; Yergeshov, Abdulla A; Al-Thaher, Yazan; Avdokushina, Svetlana; Statsenko, Evgeny; Abdullin, Timur I; Prokopovich, Polina.
Afiliação
  • Yang L; School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, UK.
  • Yergeshov AA; Institute of Fundamental Medicine and Biology, Kazan (Volga Region) Federal University, 18 Kremlyovskaya St., 420008 Kazan, Russia.
  • Al-Thaher Y; School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, UK.
  • Avdokushina S; Institute of Fundamental Medicine and Biology, Kazan (Volga Region) Federal University, 18 Kremlyovskaya St., 420008 Kazan, Russia.
  • Statsenko E; Institute of Geology and Petroleum Technologies, 4/5 Kremlyovskaya St., 420111 Kazan, Russia.
  • Abdullin TI; Institute of Fundamental Medicine and Biology, Kazan (Volga Region) Federal University, 18 Kremlyovskaya St., 420008 Kazan, Russia.
  • Prokopovich P; School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, UK. Electronic address: prokopovichp@cf.ac.uk.
Biomater Adv ; 153: 213538, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37390562
Antibiotic loaded bone cements are widely used in total joint replacement (TJR); despite many limitations such as a burst release which leads to antibiotic concentration below inhibitory levels and possibly contributing to the selection of antibiotic resistant strains. In order to address such limitations and to simultaneously address antibiotic resistance and short-term antimicrobial activity, we developed a nanocomposite bone cement capable of providing a controlled release of antimicrobial agents from bone cement to act as prophylaxis or treatment against prosthetic joint infections (PJIs). Gentamicin and chlorhexidine were loaded in combination on silica nanoparticles surface using layer-by-layer coating technique (LbL) combining hydrolysable and non-hydrolysable polymers. The drug release from the nanocomposite continued for >50 days at concentrations higher than the commercial formulation containing the same amount of antimicrobial drugs, where burst release for few days were observed. Moreover, the nanocomposite bone cement showed superior antimicrobial inhibition without adversely affecting the mechanical properties or the ability of osteoblasts to grow. In vivo experiments with an infected bone lesion model along with mass-spectrometric analysis also provided further evidence of efficacy and safety of the implanted nanocomposite material as well as its prolonged drug eluting profile. The developed nanocomposite bone cement has the potential to reduce PJIs and enable treatment of resistant established infections; moreover, the newly developed LbL based nano-delivery system may also have wider applications in reducing the threat posed by antimicrobial resistance.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cimentos Ósseos / Nanocompostos / Nanopartículas Limite: Animals / Humans Idioma: En Revista: Biomater Adv Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cimentos Ósseos / Nanocompostos / Nanopartículas Limite: Animals / Humans Idioma: En Revista: Biomater Adv Ano de publicação: 2023 Tipo de documento: Article