Proteomic analysis of silica hybrid sol-gel coatings: a potential tool for predicting the biocompatibility of implants in vivo

被引:39
作者
Romero-Gavilan, F. [1 ]
Sanchez-Perez, A. M. [2 ]
Araujo-Gomes, N. [1 ,2 ]
Azkargorta, M. [4 ]
Iloro, I. [4 ]
Elortza, F. [4 ]
Gurruchaga, M. [3 ]
Goni, I. [3 ]
Suay, J. [1 ]
机构
[1] Univ Jaume 1, Dept Ind Syst & Design, Castellon de La Plana, Spain
[2] Univ Jaume 1, Dept Med, Castellon de La Plana, Spain
[3] Univ Basque Country, Fac Ciencias Quim, San Sebastian, Spain
[4] ProteoRed ISCII, CIBERehd, CIC BioGUNE, Prote Platform, Derio, Spain
关键词
Haemocompatibility; osteoimmunology; fibrous capsule; bone regeneration; dental implants; C-reactive protein; COMPLEMENT ACTIVATION; INNATE IMMUNE; BONE; BIOMATERIALS; TITANIUM; INFLAMMATION; PROTEINS; DEGRADATION; ADSORPTION; FRAGMENTS;
D O I
10.1080/08927014.2017.1356289
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The interactions of implanted biomaterials with the host organism determine the success or failure of an implantation. Normally, their biocompatibility is assessed using in vitro tests. Unfortunately, in vitro and in vivo results are not always concordant; new, effective methods of biomaterial characterisation are urgently needed to predict the in vivo outcome. As the first layer of proteins adsorbed onto the biomaterial surfaces might condition the host response, mass spectrometry analysis was performed to characterise these proteins. Four distinct hybrid sol-gel biomaterials were tested. The in vitro results were similar for all the materials examined here. However, in vivo, the materials behaved differently. Six of the 171 adsorbed proteins were significantly more abundant on the materials with weak biocompatibility; these proteins are associated with the complement pathway. Thus, protein analysis might be a suitable tool to predict the in vivo outcomes of implantations using newly formulated biomaterials.
引用
收藏
页码:676 / 689
页数:14
相关论文
共 54 条
[1]   Foreign body reaction to biomaterials [J].
Anderson, James M. ;
Rodriguez, Analiz ;
Chang, David T. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :86-100
[2]   Future challenges in the in vitro and in vivo evaluation of biomaterial biocompatibility [J].
Anderson, James M. .
REGENERATIVE BIOMATERIALS, 2016, 3 (02) :73-77
[3]   Binding of C3 fragments on top of adsorbed plasma proteins during complement activation on a model biomaterial surface [J].
Andersson, J ;
Ekdahl, KN ;
Lambris, JD ;
Nilsson, B .
BIOMATERIALS, 2005, 26 (13) :1477-1485
[4]   High-throughput proteomic characterization of plasma rich in growth factors (PRGF-Endoret)-derived fibrin clot interactome [J].
Anitua, Eduardo ;
Prado, Roberto ;
Azkargorta, Mikel ;
Rodriguez-Suarez, Eva ;
Iloro, Ibon ;
Casado-Vela, Juan ;
Elortza, Felix ;
Orive, Gorka .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2015, 9 (11) :E1-E12
[5]   Blood plasma contact activation on silicon, titanium and aluminium [J].
Arvidsson, Sara ;
Askendal, Agneta ;
Tengvall, Pentti .
BIOMATERIALS, 2007, 28 (07) :1346-1354
[6]   Tissue engineering tools for modulation of the immune response [J].
Boehler, Ryan M. ;
Graham, John G. ;
Shea, Lonnie D. .
BIOTECHNIQUES, 2011, 51 (04) :239-+
[7]   The pentraxins PTX3 and SAP in innate immunity, regulation of inflammation and tissue remodelling [J].
Bottazzi, Barbara ;
Inforzato, Antonio ;
Messa, Massimo ;
Barbagallo, Marialuisa ;
Magrini, Elena ;
Garlanda, Cecilia ;
Mantovani, Alberto .
JOURNAL OF HEPATOLOGY, 2016, 64 (06) :1416-1427
[8]  
BRASH JL, 1984, THROMB HAEMOSTASIS, V51, P326
[9]   Osteoimmunomodulation for the development of advanced bone biomaterials [J].
Chen, Zetao ;
Klein, Travis ;
Murray, Rachael Z. ;
Crawford, Ross ;
Chang, Jiang ;
Wu, Chengtie ;
Xiao, Yin .
MATERIALS TODAY, 2016, 19 (06) :304-321
[10]  
Chiriac Aurica P., 2011, Recent Patents on Materials Science, V4, P224, DOI 10.4028/www.scientific.net/MSF.688.224