| Literature DB >> 23916887 |
Marios Spanakis1, Nikolaos Bouropoulos2, Dimitrios Theodoropoulos3, Lamprini Sygellou4, Sinead Ewart5, Anastasia Maria Moschovi4, Angeliki Siokou4, Ioannis Niopas1, Kyriakos Kachrimanis3, Vladimiros Nikolakis6, Paul A Cox5, Ioannis S Vizirianakis1, Dimitrios G Fatouros7.
Abstract
Zeolite particles with different pore diameter and particle size were loaded with the model anticancer drug 5-fluorouracil. The loaded zeolites were characterized by means of SEM, XRD, DSC, XPS, N2 physisorption and FT-IR. Higher loading of 5-FU was observed for NaX-FAU than BEA. Release studies were carried out in HCl 0.1N. Release of 5-FU from NaX-FAU showed exponential-type behaviour with the drug fully released within 10 min. In the case of BEA, the kinetics of 5-FU shows a multi-step profile with prolonged release over time. Molecular dynamics simulations showed that diffusion of the drug molecule through the BEA framework is lower than for NaX-FAU due to increased van der Waals interaction between the drug and the framework. The effect of zeolitic particles on the viability of Caco-2 monolayers showed that the NaX-FAU particles cause a reduction of cell viability in a more pronounced way compared with the BEA particles. FROM THE CLINICAL EDITOR: This article describes zeolite-based nanoparticles in generating time-controlled release of 5-FU from zeolite preparations for anti-cancer therapy.Entities:
Keywords: Controlled release; Cytocompatibility; Molecular modeling; Zeolites
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Year: 2013 PMID: 23916887 DOI: 10.1016/j.nano.2013.06.016
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307