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.
引用
收藏
页码:89 / 95
页数:7
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