Colloids and Interface Science Communications · 2014 · 38 citations · 22 references
PharmacyPharmaceuticsPharmacologyDrug DeliveryNanoparticle Drug DeliveryOral Drug DeliveryControlled Release MechanismsDrug EncapsulationDrug LoadingNanocarriers For TherapeuticsNanoparticle CharacterizationOral NanocarriersAmorphous State CharacterizationCarbon DioxideConcentrationMesoporous MaterialsMicroporous MaterialsNonpolar SolventsPorous SilicaSilica-based Adsorbents
A model molecule, ibuprofen, was loaded in the pores of mesoporous silica by adsorption from nonpolar solvents (liquid carbon dioxide and cyclohexane) and from a polar solvent (methanol). It was sufficient with a very low concentration of ibuprofen in the nonpolar solvents to achieve maximum loading of ibuprofen in the mesoporous particles. When using liquid carbon dioxide, the pores of the mesoporous silica particles were filled completely with ibuprofen at a lower ibuprofen concentration than similar experiments performed with cyclohexane. When methanol was used, the maximum amount of loaded ibuprofen was never achieved. Furthermore, x-ray scattering showed that all ibuprofen loaded into the mesoporous particles were in an amorphous state. Ibuprofen was released from the mesoporous particles to water within a couple of minutes, regardless of solvent used for loading. It was found that the release of ibuprofen from mesoporous silica was much faster than that of crystalline ibuprofen.
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Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism
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