100402-13-9Relevant academic research and scientific papers
Drug encapsulation and release by mesoporous silica nanoparticles: The effect of surface functional groups
Tan, Si Yu,Ang, Chung Yen,Li, Peizhou,Yap, Qi Ming,Zhao, Yanli
, p. 11276 - 11282 (2014)
Mesoporous silica nanoparticles (MSNPs) have been widely used as drug carriers for stimuli-responsive drug delivery. Herein, a catalysis screening technique was adopted for analyzing the effects of chain length, terminal group, and density of disulfide-appended functional ligands on the surface of MSNPs on drug-loading capacity and glutathione-triggered drug-release kinetics. The ligand with an intermediate length (5 carbon atoms) and a bulky terminal group (cyclohexyl) that complexes with theβ-cyclodextrin ring showed the highest drug loading capacity as well as good release kinetics. In addition, decreasing the surface coverage of the functional ligands led to an enhancement in drug release. In vitro drug-delivery experiments on a melanoma cell line (B16-F10) by using the functionalized MSNPs further supported the conclusion. The results obtained may serve as a general guide for developing more effective MSNP systems for drug delivery. Maximizing drug release from drug carriers is important to achieve better therapeutic efficiency. Using glutathione (GSH)-triggered drug-release systems as a case study, the effect of the nature of surface functional groups on mesoporous silica nanoparticles on drug-loading and drug-release capabilities was investigated.
