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dc.creatorAndrade, Ângela L.-
dc.creatorMilitani, Isabela A.-
dc.creatorAlmeida, Katia J. de-
dc.creatorBelchior, Jadson C.-
dc.creatorReis, Sérgio C. dos-
dc.creatorSilva, Rosangela M. F. Costa e-
dc.creatorDomingues, Rosana Z.-
dc.date.accessioned2019-05-07T17:33:39Z-
dc.date.available2019-05-07T17:33:39Z-
dc.date.issued2018-04-
dc.identifier.citationANDRADE, Â. L. et al. Theoretical and experimental studies of the controlled release of tetracycline incorporated into bioactive glasses. AAPS PharmSciTech, [S.l.], v. 19, n. 3, p. 1287–1296, Apr. 2018.pt_BR
dc.identifier.urihttps://link.springer.com/article/10.1208/s12249-017-0931-xpt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/34090-
dc.description.abstractSeveral authors have studied the release profile of drugs incorporated in different devices. However, to the best of our knowledge, although many studies have been done on the release of tetracycline, in these release devices, no study has investigated if the released compound is actually the tetracycline, or, instead, a degraded product. This approach is exploited here. In this work, we analyse the influence of two drying methods on the tetracycline delivery behaviour of synthesised glasses using the sol-gel process. We compare the drying methods results using both theoretical models and practical essays, and analyse the chemical characteristic of the released product in order to verify if it remains tetracycline. Samples were freeze-dried or dried in an oven at 37°C and characterised by several methods such as Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TG), differential thermogravimetric analysis (DTG), differential thermal analyses (DTA) and gas adsorption analysis (BET). The released concentration of tetracycline hydrochloride was studied as a function of time, and it was measured by ultraviolet spectrophotometry in the tetracycline wavelength. The drug delivery profiles were reasonably consistent with a diffusion model analysis. In addition, we observed higher release rates for the freeze-dried compared to those dried in an oven at 37°C. This higher release can be attributed to larger pore size for the freeze-dried sample systems with tetracycline, which promoted more water penetration, improving the drug diffusion. The analysis of the solution obtained in the release tests using high-performance liquid chromatography- mass spectrometry (HPLC-MS) confirmed that tetracycline was being released.pt_BR
dc.languageen_USpt_BR
dc.publisherSpringerpt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceAAPS PharmSciTechpt_BR
dc.subjectRelease drugpt_BR
dc.subjectDryingpt_BR
dc.subjectDiffusion modelpt_BR
dc.subjectGlasspt_BR
dc.subjectTetracyclinept_BR
dc.titleTheoretical and experimental studies of the controlled release of tetracycline incorporated into bioactive glassespt_BR
dc.typeArtigopt_BR
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