Anti-sessile bacterial and cytocompatibility properties of CHX-loaded nanohydroxyapatite

被引:17
作者
Barros, J. [1 ,2 ,3 ,4 ]
Grenho, L. [1 ,2 ,3 ]
Fernandes, M. H. [5 ]
Manuel, C. M. [4 ,6 ]
Melo, L. F. [4 ]
Nunes, O. C. [4 ]
Monteiro, F. J. [1 ,2 ,3 ]
Ferraz, M. P. [7 ]
机构
[1] Univ Porto, I3S, P-4100 Oporto, Portugal
[2] INEB Inst Engn Biomed, Oporto, Portugal
[3] Univ Porto, Dept Engn Met & Mat, FEUP Fac Engn, P-4100 Oporto, Portugal
[4] Univ Porto, Dept Chem Engn, LEPABE Lab Proc Engn Environm Biotechnol & Energy, P-4100 Oporto, Portugal
[5] Univ Porto, Fac Med Dent, P-4100 Oporto, Portugal
[6] Univ Lusofona Porto, Oporto, Portugal
[7] Univ Fernando Pessoa, CEBIMED Ctr Estudos Biomed, Oporto, Portugal
关键词
Nanohydroxyapatite; Chlorhexidine digluconate; Anti-sessile; Cytocompatibility; BIOFILM FORMATION; CIPROFLOXACIN IMPLANTS; ANTIMICROBIAL PEPTIDES; DELIVERY-SYSTEM; COATED TITANIUM; BASIC DYE; CHLORHEXIDINE; ADSORPTION; HYDROXYAPATITE; ANTIBACTERIAL;
D O I
10.1016/j.colsurfb.2015.04.034
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Nanohydroxyapatite possesses exceptional biocompatibility and bioactivity regarding bone cells and tissues, justifying its use as a coating material or as a bone substitute. Unfortunately, this feature may also encourage bacterial adhesion and biofilm formation. Surface functionalization with antimicrobials is a promising strategy to reduce the likelihood of bacterial infestation and colonization on medical devices. Chlorhexidine digluconate is a common and effective antimicrobial agent used for a wide range of medical applications. The purpose of this work was the development of a nanoHA biomaterial loaded with CHX to prevent surface bacterial accumulation and, simultaneously, with good cytocompatibility, for application in the medical field. CHX (5-1500 mg/L) was loaded onto nanoHA discs and the materials were evaluated for CHX adsorption and release profile, physic-chemical features, antibacterial activity against Escherichia coli, Staphylococcus aureus and Staphylococcus epidermidis, and cytocompatibility toward L929 fibroblasts. Results showed that the adsorption of CHX on nanoHA surface occurred by electrostatic interactions between the cationic group of CHX and the phosphate group of nanoHA. The release of CHX from CHX-loaded nanoHA showed a fast initial rate followed by a slower kinetics release, due to constraints caused by dilution and diffusion-limiting processes. NanoHA.50 to nanoHA.1500 showed strong anti-sessile activity, inhibiting bacterial adhesion and the biofilm formation. CHX-nanoHA caused a dose- and time-dependent inhibitory effect on the proliferation of fibroblasts for nanoHA.100 to nanoHA.1500. Cellular behavior on nanoHA.5 and nanoHA.50 was similar to control. Therefore, CHX-loaded nanoHA surfaces appear as a promising alternative to prevention of devices-related infections. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:305 / 314
页数:10
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