Szczegóły publikacji
Opis bibliograficzny
Injectable gellan gum-based nanoparticles-loaded system for the local delivery of vancomycin in osteomyelitis treatment / Urszula POSADOWSKA, Monika Brzychczy-Włoch, Elżbieta PAMUŁA // Journal of Materials Science: Materials in Medicine ; ISSN 0957-4530. — 2016 — vol. 27 iss. 1, s. [1–9]. — Bibliogr. s. [8–9], Abstr. — Publikacja dostępna online od: 2015-11-30. — Od 2015 r. zmiana formatowania czasopisma (brak ciągłej paginacji)
Autorzy (3)
- AGHCibor Urszula
- Brzychczy-Włoch Monika
- AGHPamuła Elżbieta
Dane bibliometryczne
| ID BaDAP | 95231 |
|---|---|
| Data dodania do BaDAP | 2016-01-13 |
| Tekst źródłowy | URL |
| DOI | 10.1007/s10856-015-5604-2 |
| Rok publikacji | 2016 |
| Typ publikacji | artykuł w czasopiśmie |
| Otwarty dostęp |  |
| Creative Commons | |
| Czasopismo/seria | Journal of Materials Science-Materials in Medicine |
Abstract
Infection spreading in the skeletal system leading to osteomyelitis can be prevented by the prolonged administration of antibiotics in high doses. However systemic antibiotherapy, besides its inconvenience and often low efficacy, provokes numerous side effects. Thus, we formulated a new injectable nanoparticle-loaded system for the local delivery of vancomycin (Vanc) applied in a minimally-invasive way. Vanc was encapsulated in poly(Llactide-co-glycolide) nanoparticles (NPs) by double-emulsification. The size (258 ± 11 nm), polydispersity index (0.240 ± 0.003) and surface potential (-25.9 ± 0.2 mV) of NPs were determined by dynamic light scattering and capillary electrophoresis measurements. They have a spherical morphology and a smooth topography as observed using atomic force microscopy. Vanc loading and encapsulation efficiencies were 8.8 ± 0.1 and 55.2 ± 0.5 %, respectively, based on fluorescence spectroscopy assays. In order to ensure injectability, NPs were suspended in gellan gum and cross-linked with Ca2?; also a portion of dissolved antibiotic was added to the system. The resulting system was found to be injectable (extrusion force 11.3 ± 1.1 N), reassembled its structure after breaking as shown by rheology tests and ensured required burst release followed by sustained Vanc delivery. The system was cytocompatible with osteoblast-like MG-63 cells (no significant impact on cells’ viability was detected). Growth of Staphylococcus spp. reference strains and also those isolated from osteomyelitic joints was inhibited in contact with the injectable system. As a result we obtained a biocompatible system displaying ease of application (low extrusion force), self-healing ability after disruption, adjustable drug release and antimicrobial properties.
