共 94 条
Azobenzene Polyesters Used as Gate-Like Scaffolds in Nanoscopic Hybrid Systems
被引:18
作者:
Bernardos, Andrea
[1
,2
]
Mondragon, Laura
[1
]
Javakhishvili, Irakli
[3
]
Mas, Nuria
[1
]
de la Torre, Cristina
[1
]
Martinez-Manez, Ramon
[1
]
Sancenon, Felix
[1
]
Barat, Jose M.
[2
]
Hvilsted, Soren
[3
]
Orzaez, Mar
[4
,5
]
Perez-Paya, Enrique
[4
,5
]
Amoros, Pedro
[6
]
机构:
[1] Univ Politecn Valencia, Dept Quim, Univ Valencia, Unidad Mixta,Ctr Reconocimiento Mol & Desarrollo, Valencia 46022, Spain
[2] Univ Politecn Valencia, Dept Tecnol Alimentos, Valencia 46022, Spain
[3] Tech Univ Denmark, Dept Chem & Biochem Engn, Danish Polymer Ctr, DK-2800 Lyngby, Denmark
[4] Ctr Invest Principe Felipe, Lab Peptidos & Prot, Valencia 46012, Spain
[5] IBV CSIC, Valencia 46010, Spain
[6] Univ Valencia, Inst Ciencia Mat ICMUV, Valencia 46071, Spain
关键词:
azo compounds;
drug delivery;
enzymes;
mesoporous materials;
polyesters;
MESOPOROUS SILICA NANOPARTICLES;
RESPONSIVE CONTROLLED-RELEASE;
DRUG-DELIVERY;
GUEST MOLECULES;
SUPRAMOLECULAR CHEMISTRY;
PH-DRIVEN;
POLYMERS;
STORAGE;
FUNCTIONALIZATION;
TRANSPORT;
D O I:
10.1002/chem.201200787
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The synthesis and characterisation of new capped silica mesoporous nanoparticles for on-command delivery applications is reported. Functional capped hybrid systems consist of MCM-41 nanoparticles functionalised on the external surface with polyesters bearing azobenzene derivatives and rhodamine B inside the mesopores. Two solid materials, Rh-PAzo8-S and Rh-PAzo6-S, containing two closely related polymers, PAzo8 and PAzo6, in the pore outlets have been prepared. Materials Rh-PAzo8-S and Rh-PAzo6-S showed an almost zero release in water due to steric hindrance imposed by the presence of anchored bulky polyesters, whereas a large delivery of the cargo was observed in the presence of an esterase enzyme due to the progressive hydrolysis of polyester chains. Moreover, nanoparticles Rh-PAzo8-S and Rh-PAzo6-S were used to study the controlled release of the dye in intracellular media. Nanoparticles were not toxic for HeLa cells and endocytosis-mediated cell internalisation was confirmed by confocal microscopy. Furthermore, the possible use of capped materials as a drug-delivery system was demonstrated by the preparation of a new mesoporous silica nanoparticle functionalised with PAzo6 and loaded with the cytotoxic drug camptothecin (CPT-PAzo6-S). Following cell internalisation and lysosome resident enzyme-dependent gate opening, CPT-PAzo6-S induced CPT-dependent cell death in HeLa cells.
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页码:13068 / 13078
页数:11
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