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Enzyme-responsive multifunctional surfaces for controlled uptake/release of (bio)molecules
被引:4
|作者:
Mortato, Mariangela
[1
,2
]
Argentiere, Simona
[3
]
De Gregorio, Gian Luca
[4
]
Gigli, Giuseppe
[1
,2
,4
]
Blasi, Laura
[2
]
机构:
[1] Univ Salento, Super Sch ISUFI, I-73100 Lecce, Italy
[2] NNL Lecce, CNR Inst Nanosci, I-73100 Lecce, Italy
[3] Fdn Filarete, I-20139 Milan, Italy
[4] Fdn Ist Italiano Tecnol, Ctr Biomol Nanotechnol, I-73010 Arnesano Lecce, Italy
关键词:
Enzyme-responsive surfaces;
Drug/biomolecules delivery;
Tissue engineering;
Streptavidin-biotin interaction;
Biotinylated depolymerized chitosan;
Cathepsin D;
BIORESPONSIVE HYDROGELS;
BREAST-CANCER;
CATHEPSIN-D;
DELIVERY-SYSTEM;
CHITOSAN;
DEPOLYMERIZATION;
DOXORUBICIN;
PEROXIDE;
DESIGN;
NANOPARTICLES;
D O I:
10.1016/j.colsurfb.2014.08.034
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
The current trend in the development of biomaterials is towards bioactive and biodegradable systems. In particular, enzyme-responsive structures are useful tools to realize biodegradable surfaces for the controlled delivery of biomolecules/drugs through a triggered surface erosion process. Up to now, enzyme-responsive structures have been designed by covalent linkage between synthetic polymers and biodegradable functionalities that are responsive to chemical and biological cues (i.e. proteases or pH) [1-4]. Here, we present a novel approach to achieve enzyme-responsive surface-attached networks by exploiting the non-covalent interaction between streptavidin and biotin. The functional component of this three-dimensional (3D) structure is a layer of biotinylated peptides that are degraded by the action of specific proteases. The system was stable under typical physiological conditions; however, it was efficiently degraded upon enzyme exposure. Further, the controlled release of biomolecules and drugs - previously entrapped into the surface-attached network - was demonstrated to occur as a consequence of the enzymatic cleavage. This versatile approach does not require complex chemical procedures. Interestingly, it can be easily adapted to different enzyme-peptide partners and therefore is very attractive for tissue replacement, drug delivery and biosensing. (C) 2014 Elsevier B.V. All rights reserved.
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页码:89 / 95
页数:7
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