“…Consequently, extensive research activities have concentrated on the development of carrier materials and delivery theories [1,2,3,4,5,6] that incorporate a controllable release process, high loading efficiency, low toxicity, and excellent biodegradability. Till now, mesoporous inorganic solids, such as zeolites [7,8] and silica [9,10] (pure or functionalized by a postsynthetic modification), biocompatible dendritic macromolecules or polymers [11], and lipids [12] and metal clusters [13,14], have been taken as possible candidates for drug storage. However, these materials suffer from several limitations [7], namely, low drug-loading capacities (<5 wt %), rapid drug release, and toxicity.…”