Bacteria-responsive multilayer coatings comprising polycationic nanospheres for bacteria biofilm prevention on urinary catheters

被引:75
作者
Francesko, Antonio [1 ]
Fernandes, Margarida M. [1 ]
Ivanova, Kristina [1 ]
Amorim, Sara [2 ,3 ]
Reis, Rui L. [2 ,3 ]
Pashkuleva, Iva [2 ,3 ]
Mendoza, Ernest [4 ]
Pfeifer, Annett [5 ]
Heinze, Thomas [5 ]
Tzanov, Tzanko [1 ]
机构
[1] Univ Politecn Cataluna, Dept Chem Engn, Grp Biotecnol Mol & Ind, Rambla St Nebridi 22, Terrassa 08222, Spain
[2] Univ Minho, Headquarters European Inst Excellence Tissue Engn, Res Grp Biomat Biodegradables & Biomimet 3Bs, Avepk, P-4805017 Barco, Guimaraes, Portugal
[3] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[4] Univ Politecn Cataluna, Ctr Recerca & Nanoengn, Grp Nanomat Aplicats, Terrassa 08222, Spain
[5] Univ Jena, Inst Organ Chem & Macromol Chem, Ctr Excellence Polysaccharide Res, D-07745 Jena, Germany
关键词
Polycation; Nanospheres; Layer-by-layer fabrication; Antibacterial surfaces; Biofilm inhibition; PSEUDOMONAS-AERUGINOSA; TRIGGERED RELEASE; DRUG-RELEASE; DEPOLYMERIZATION; NANOCAPSULES; ADHESION; SURFACE; FILMS;
D O I
10.1016/j.actbio.2016.01.020
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This work reports on the development of infection-preventive coatings on silicone urinary catheters that contain in their structure and release on demand antibacterial polycationic nanospheres. Polycationic aminocellulose conjugate was first sonochemically processed into nanospheres to improve its antibacterial potential compared to the bulk conjugate in solution (AC(sol)). Afterward the processed aminocellulose nanospheres (AC(NSs)) were combined with the hyaluronic acid (HA) polyanion to build a layer-by-layer construct on silicone surfaces. Although the coating deposition was more effective when HA was coupled with ACsol than with AC(NSs), the AC(NSs)-based coatings were thicker and displayed smoother surfaces due to the embedment of intact nanospheres. The antibacterial effect of AC(NSs) multilayers was 40% higher compared to AC(sol) coatings. This fact was further translated into more effective prevention of Pseudomonas aeruginosa biofilm formation. The coatings were stable in the absence of bacteria, whereas their disassembling occurred gradually during incubation with P. aeruginosa, and thus eradicate the biofilm upon release of antibacterial agents. Only 5 bilayers of HA/AC(NSs) were sufficient to prevent the biofilm formation, in contrast to the 10 bilayers of AC(Sol) required to achieve the same effect. The antibiofilm efficiency of (HA/AC(NSs))(10) multilayer construct built on a Foley catheter was additionally validated under dynamic conditions using a model of the catheterized bladder in which the biofilm was grown during seven days. Statement of Significance Antibacterial layer-by-layer coatings were fabricated on silicone that efficiently prevents Pseudomonas aeruginosa biofilm formation during time beyond the useful lifetime of the currently employed urinary catheters in medical practice. The coatings are composed of intact, highly antibacterial polycationic-nanospheres processed from aminated cellulose and bacteria-degrading glycosaminoglycan hyaluronic acid. The importance of incorporating nanoscale structures within bacteria-responsive surface coatings to impart durable antibacterial and self-defensive properties to the medical indwelling devices is highlighted. (C) 2016 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:203 / 212
页数:10
相关论文
共 44 条
[1]   Rhamnolipid-induced removal of lipopolysaccharide from Pseudomonas aeruginosa:: Effect on cell surface properties and interaction with hydrophobic substrates [J].
Al-Tahhan, RA ;
Sandrin, TR ;
Bodour, AA ;
Maier, RM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (08) :3262-3268
[2]   Interactions between Exogenous FGF-2 and Sulfonic Groups: in Situ Characterization and Impact on the Morphology of Human Adipose-Derived Stem Cells [J].
Amorim, Sara ;
Pires, Ricardo A. ;
da Costa, Diana Soares ;
Reis, Rui L. ;
Pashkuleva, Iva .
LANGMUIR, 2013, 29 (25) :7983-7992
[3]   Controlled drug release from porous polyelectrolyte multilayers [J].
Berg, MC ;
Zhai, L ;
Cohen, RE ;
Rubner, MF .
BIOMACROMOLECULES, 2006, 7 (01) :357-364
[4]  
BONDE GJ, 1957, ACTA PHARMACOL TOX, V13, P194
[5]   Interactions between biocide cationic agents and bacterial biofilms [J].
Campanac, C ;
Pineau, L ;
Payard, A ;
Baziard-Mouysset, G ;
Roques, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (05) :1469-1474
[6]   Enzyme multilayers on colloid particles:: Assembly, stability, and enzymatic activity [J].
Caruso, F ;
Schüler, C .
LANGMUIR, 2000, 16 (24) :9595-9603
[7]   Polysaccharide-based polyelectrolyte multilayers [J].
Crouzier, Thomas ;
Boudou, Thomas ;
Picart, Catherine .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2010, 15 (06) :417-426
[8]   Surface microstructure and antibacterial property of an active-screen plasma alloyed austenitic stainless steel surface with Cu and N [J].
Dong, Y. ;
Li, X. ;
Bell, T. ;
Sammons, R. ;
Dong, H. .
BIOMEDICAL MATERIALS, 2010, 5 (05)
[9]   Biofilms and device-associated infections [J].
Donlan, RM .
EMERGING INFECTIOUS DISEASES, 2001, 7 (02) :277-281
[10]   Oxidative depolymerization of polysaccharides by reactive oxygen/nitrogen species [J].
Duan, Jinyou ;
Kasper, Dennis L. .
GLYCOBIOLOGY, 2011, 21 (04) :401-409