| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 600865 | Colloids and Surfaces B: Biointerfaces | 2012 | 8 Pages |
A novel pH-sensitive drug delivery system based on functionalized silica nanotubes was developed for the incorporation of non-steroidal anti-inflammatory drugs (NSAIDs), aimed at a tailored drug release in acidic conditions characteristic of inflamed tissues. Silica nanotubes (SNTs) were synthesized by a nanoporous alumina template assisted sol–gel method. Inner surfaces were physically and chemically modified to improve both the functionalization and subsequent incorporation of the drug. Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and transmission electron microscopy (TEM) were used to characterize the designed nanocarriers and their functionalization. To achieve the highest degree of functionalization, three types of aminosilanes were tested and calcination conditions were optimized. APTES was shown to be the most effective aminosilane regarding the functionalization of the SNTs’ inner surface and an adequate calcination temperature (220 °C) was found to attain mechanical stability without compromising functionalization efficiency. Finally, the incorporation of naproxen into the nanotubes was accessed by fluorescence measurements and drug release studies were performed, revealing that the electrostatic linkage ensures effective release of the drug in the acidic pH typical of inflamed cells, while maintaining the SNT-drug conjugates stable at the typical bloodstream pH.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► pH-sensitive drug delivery system for the incorporation of non-steroidal anti-inflammatory drugs (NSAIDs). ► Electrostatic linkage ensures effective release of the drug in the acidic pH typical of inflamed cells. ► The SNT-drug conjugates are stable at the typical bloodstream pH.
