| Literature DB >> 29702474 |
Maria-Viorica Ciocilteu1, Andreea Gabriela Mocanu1, Adriana Mocanu1, Catalin Ducu2, Oana Elena Nicolaescu1, Valentin Costel Manda1, Adina Turcu-Stiolica1, Claudiu Nicolicescu3, Razvan Melinte4, Maria Balasoiu4, Octavian Croitoru1, Johny Neamtu1.
Abstract
The main objective of this study was to synthesize hydroxyapatite-ciprofloxacin composites using a chemical precipitation method and to evaluate the properties and in vitro release profile of the drug from the hydroxyapatite-ciprofloxacin composites. Composite characterization was achieved by FT-IR, XRD and DLS. Ciprofloxacin determination was accomplished by HPLC, resulting in good incorporation efficiency of the drug (18.13 %). The in vitro release study (Higuchi model C = K t1/2 and Ritger-Peppas model, C = K t0.6) showed a diffusion-controlled mechanism. The antibacterial activity showed that the bacterial growth inhibition zones were approximately equal for the synthesis composites and for the mechanical mixture on the Staphylococcus aureus germ. The use of hydroxyapatite, which is a biocompatible, bioactive and osteoconductive material, with ciprofloxacin, which has good antibacterial activity in this composite, makes it suitable for the development of bone grafts. Furthermore, the synthesis process allows a slow local release of the drug.Entities:
Keywords: antibacterial activity; hydroxiapatite-ciprofloxacin composites; in vitro release profile; wet precipitation synthesis
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Year: 2018 PMID: 29702474 DOI: 10.2478/acph-2018-0011
Source DB: PubMed Journal: Acta Pharm ISSN: 1330-0075 Impact factor: 2.230