Abstract
Mesoporous silica- and carbon-based materials, including bioactive glasses, have proven potential as components of medical devices and as drug carriers. From an application perspective, knowledge about the shelf-life stability of these materials under various conditions is vital. Here, mesoporous bioactive glasses (MBGs) synthesized by aerosol-assisted spray-drying and by a batch sol–gel method, mesoporous silicas of SBA-15 type, and mesoporous carbons CMK-1 and CMK-3 have been stored under varying conditions, e.g. at different temperature and relative humidity (RH), and in different storage vessels. The results show that the silica-based materials stored in Eppendorfs are sensitive to humidity. Spray dried MBGs decompose within 1 month at a RH >5%, whilst sol–gel MBGs are more stable up to a RH >60%. Changing the storage vessel to sealed glass flasks increases the MBGs lifetime significantly, with no degradation during 2 months of storage at a RH = 75%. SBA-15 stored in Eppendorfs are more stable compared to MBGs, and addition of F- ions added during the synthesis affects the material degradation rate. Mesoporous carbons are stable under all conditions for all time points. This systematic study clearly demonstrates the importance of storage conditions for mesoporous materials which is crucial knowledge for commercialization of these materials.
Highlights
Mesoporous silica- and carbon-based materials have during the last 25 years gained significant interest as drug delivery systems
The aim of this study is to investigate the possible structural alteration of mesoporous silica- and carbon-based materials such as Mesoporous bioactive glasses (MBGs) with therapeutic ions, mesoporous silicas of SBA-15 type, and mesoporous carbons of CMK-1 and CMK-3 types upon storage
All MBGs retain their spherical morphology during storage, accelerated storage conditions (40 °C and 75 % relative humidity) for 6 months clearly have the largest effect on their pore characteristics
Summary
Mesoporous silica- and carbon-based materials have during the last 25 years gained significant interest as drug delivery systems. Due to their large specific surface area, pore size of 2–15 nm, and controllable composition, these materials can be tailored to be loaded with both hydrophilic and hydrophobic drugs enabling a targeted delivery. Mesoporous silica and carbon particles have attracted interest as drug delivery systems [14,15]. Monodispersed mesoporous silica particles of SBA-15 type have shown potential in both drug delivery and enzyme immobilization [16,17], and can be synthesized with various morphologies and porosities [18].
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