Functionalisation of Ti6Al4V components fabricated using selective laser melting with a bioactive compound

被引:52
|
作者
Vaithilingam, Jayasheelan [1 ]
Kilsby, Samuel [2 ]
Goodridge, Ruth D. [1 ]
Christie, Steven D. R. [2 ]
Edmondson, Steve [3 ]
Hague, Richard J. M. [1 ]
机构
[1] Univ Nottingham, Addit Mfg & Printing Res Grp 3D, Sch Engn, Nottingham NG7 2RD, England
[2] Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England
[3] Univ Manchester, Sch Mat, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
Selective laser melting (SLM); Self-assembled monolayers (SAMs); Additive manufacturing; Functionalisation; X-ray photoelectron spectroscopy (XPS); SELF-ASSEMBLED MONOLAYERS; COBALT-CHROMIUM ALLOY; 316L STAINLESS-STEEL; XPS CHARACTERIZATION; SURFACE; STENTS; FILMS; ADSORPTION; TI-6AL-4V; STABILITY;
D O I
10.1016/j.msec.2014.10.015
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Surface modification of an implant with a biomolecule is used to improve its biocompatibility and to reduce postimplant complications. In this study, a novel approach has been used to functionalise phosphonic acid monolayers with a drug. Ti6Al4V components fabricated using selective laser melting (SLM) were functionalised with Paracetamol (a pharmaceutically relevant biomolecule) using phosphonic acid based self-assembled monolayers (SAMs). The attachment, stability of the monolayers on the SLM fabricated surface and functionalisation of SAMs with Paracetamol were studied using X-ray photoelectron spectroscopy (XPS) and surface wettability measurements. The obtained results confirmed that SAMs were stable on the Ti6Al4V surface for over four weeks and then began to desorb from the surface. The reaction used to functionalise the phosphonic add monolayers with Paracetamol was noted to be successful. Thus, the proposed method has the potential to immobilise drugs/proteins to SAM coated surfaces and improve their biocompatibility and reduce post-implant complications. Crown Copyright (C) 2014 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 61
页数:10
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