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.
引用
收藏
页码:13068 / 13078
页数:11
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