作者: Si Yu Tan , Chung Yen Ang , Zhong Luo , Peizhou Li , Kim Truc Nguyen
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摘要: Glutamate receptor antagonists have been known to play a crucial role in the treatment of many neuronal diseases. Recently, these also shown therapeutic effects cancer. In this study, an ionotropic glutamate (iGlu) antagonist, 4-hydroxyphenylacetyl spermine (L1), was used concurrently with common anticancer drug, doxorubicin (Dox), for simultaneous cancer therapy. Mesoporous silica nanoparticles (MSNPs) were employed as delivery vehicle both L1 and Dox by conjugating iGlu antagonist on surface encapsulating within mesopores. then trapped mesopores functionalizing redox-cleavable capping group MSNP surface, it could be released upon exposure reductive glutathione. vitro studies B16F10 NIH3T3 cell lines revealed that exhibited well targeting effects. addition, use proved synergistic The present work demonstrated feasibility employing system deliver neuroprotective drug efficient treatment.