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
相关论文
共 50 条
  • [1] Enzyme-responsive liposomes for controlled drug release
    Wei, Yan
    Lv, Jiajing
    Zhu, Shiyu
    Wang, Sicheng
    Su, Jiacan
    Xu, Can
    DRUG DISCOVERY TODAY, 2024, 29 (07)
  • [2] Enzyme-responsive polymer hydrogel particles for controlled release
    Thornton, Paul D.
    Mart, Robert J.
    Ulijn, Rein V.
    ADVANCED MATERIALS, 2007, 19 (09) : 1252 - +
  • [3] Secreted Enzyme-Responsive System for Controlled Antifungal Agent Release
    Bernardos, Andrea
    Bozik, Matej
    Montero, Ana
    Perez-Esteve, Edgar
    Garcia-Casado, Esther
    Lhotka, Miloslav
    Frankova, Adela
    Marcos, Maria Dolores
    Barat, Jose Manuel
    Martinez-Manez, Ramon
    Kloucek, Pavel
    NANOMATERIALS, 2021, 11 (05)
  • [4] Construction of multifunctional porous silica nanocarriers for pH/enzyme-responsive drug release
    Qiu, Li
    Zhang, Weirui
    Wang, Shuyun
    Zhang, Xu
    Zhao, Yanbao
    Cao, Liuqin
    Sun, Lei
    MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2017, 81 : 485 - 491
  • [5] Enzyme-responsive multifunctional nanocarriers for combinational chemotherapy
    Pan, Jie
    Liu, Weijiao
    Li, Juheng
    Wan, Dong
    JOURNAL OF CONTROLLED RELEASE, 2017, 259 : E62 - E63
  • [6] An Enzyme-Responsive Controlled Release System of Mesoporous Silica Coated with Konjac Oligosaccharide
    Guo, Wei
    Yang, Chunyu
    Cui, Liru
    Lin, Huiming
    Qu, Fengyu
    LANGMUIR, 2014, 30 (01) : 243 - 249
  • [7] An enzyme-responsive controlled release system based on a dual-functional peptide
    Li, X.
    Burger, S.
    O'Connor, A. J.
    Ong, L.
    Karas, J. A.
    Gras, S. L.
    CHEMICAL COMMUNICATIONS, 2016, 52 (29) : 5112 - 5115
  • [8] Controlling protein retention on enzyme-responsive surfaces
    Rawsterne, Rachel E.
    Gough, Julie E.
    Rutten, Frank J. M.
    Pham, Nhan T.
    Poon, Wilson C. K.
    Flitsch, Sabine L.
    Maltman, Beatrice
    Alexander, Morgan R.
    Ulijn, Rein V.
    SURFACE AND INTERFACE ANALYSIS, 2006, 38 (11) : 1505 - 1511
  • [9] Enzyme-responsive surface erosion of poly(ethylene carbonate) for controlled drug release
    Chu, Dafeng
    Curdy, Catherine
    Riebesehl, Bernd
    Zhang, Yi
    Beck-Broichsitter, Moritz
    Kissel, Thomas
    EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2013, 85 (03) : 1232 - 1237
  • [10] Enzyme-responsive polysaccharide supramolecular nanoassembly for enhanced DNA encapsulation and controlled release
    Yuhui Zhang
    Lijuan Wang
    Jie Wang
    Siqintana Xin
    Xianliang Sheng
    Chinese Chemical Letters, 2021, 32 (06) : 1902 - 1906