| Literature DB >> 26618618 |
Shun Yang1, Dongyun Chen1, Najun Li1, Qingfeng Xu1, Hua Li1, Frank Gu2, Jianping Xie3, Jianmei Lu1.
Abstract
Efficient drug loading and selectivity in drug delivery are two key features of a good drug-carrier design. Here we report on such a drug carrier formed by using hollow mesoporous silica nanoparticles (HMS NPs) as the core and specifically designed multifunctional amphiphilic agents as the encapsulating shell. These nanocarriers combine the advantages of the HMS NP core (favorable physical and structural properties) and the versatility of an organic-based shell (e.g., specificity in chemical properties and modifiability). Moreover, both the properties of the core and the shell can be independently varied. The varied core and shell could then be integrated into a single device (drug carrier) to provide efficient and specific drug delivery. In vitro and in vivo data suggests that these drug nanocarriers are biocompatible and are able to deliver hydrophobic drugs selectively to target tumor cells. After the break of the pH-labile linkages in the shell, the drug payload can be released and the tumor cells are killed.Entities:
Keywords: biocompatible materials; core-shell materials; drug delivery; hollow spheres; mesoporous materials
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Year: 2015 PMID: 26618618 DOI: 10.1002/smll.201503121
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281