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A new type of mesoporous silica nanoparticle (MSN) was synthesized in fluoride media via sol–gel technique using TritonX 100 and Tween-20. The surface area and pore volume of the MSN particles were modified by varying the concentration of Tween-20. The prepared MSN nanoparticles with large surface area and pore volume (T-2, T-3) were selected to accommodate the model drug duloxetine hydrochloride (DX) for evaluation of their drug-loading and release abilities. Calcined and DX loaded nanoparticles were characterized by Brunauer–Emmett–Teller technique (BET), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric (TG) analysis and UV-diffuse reflectance (UV-DRS). In vitro release studies proved that the particle displays an initial burst release followed by sustained release for up to 140h. From the studies it is evident that the synthesized particle may be useful as a carrier for sustained release of active pharmaceutical ingredients (APIs).
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