Gold nanoparticles on titanium and interaction with prototype protein
Identifieur interne : 005268 ( Main/Exploration ); précédent : 005267; suivant : 005269Gold nanoparticles on titanium and interaction with prototype protein
Auteurs : J. Daniel Padmos [Canada] ; Paul Duchesne ; Michael Dunbar [Canada] ; Peng Zhang [Canada]Source :
- Journal of Biomedical Materials Research Part A [ 1549-3296 ] ; 2010-10.
Descripteurs français
English descriptors
- KwdEn :
- Active amount, Active lysozyme, Active protein, Activity assay results, Activity assays, Adsorption, Anova test, Aqueous haucl4 solution, Article figure, Assay, Aunp, Aunp coverage, Aunp diameters, Aunp surface chemistry, Aunps, Bare aunp, Bare aunps, Beaker, Biological molecules, Biomed mater, Biomedical, Biomedical materials research, Biosci bioeng, Chem, Clin implant dent relat, Control discs, Cooh, Dalhousie university, Depletion method, Deposition, Different groups, Disc, Electroless, Electroless deposition, Enzymatic activity, Equal variances, Etching, Gold nanoparticles, Gold surfaces, Haucl4, Higher amounts, Implant, Implant materials, Implant surfaces, Lysozyme, Lysozyme adsorption, Lysozyme coverage, Lysozyme solution, Metal ions, Metallic gold, Micrococcus lysodeikticus, Nanoparticles, Nanostructured surfaces, Normality tests, Nova scotia, Orthopedic applications, Orthopedic implants, Oxide, Oxide layer, Phys chem, Plain aunps, Protein adsorption, Protein amounts, Protein solution, Prototype protein, Qualitative etching, Scanning electron microscopy, Second focus, Standard deviation, Standard solution, Surface area, Surface chemistry, Tio2, Titanium, Titanium implants, Titanium surfaces, Variance, Various deposition methods, Weak interactions, Wiley periodicals.
- Teeft :
- Active amount, Active lysozyme, Active protein, Activity assay results, Activity assays, Adsorption, Anova test, Aqueous haucl4 solution, Article figure, Assay, Aunp, Aunp coverage, Aunp diameters, Aunp surface chemistry, Aunps, Bare aunp, Bare aunps, Beaker, Biological molecules, Biomed mater, Biomedical, Biomedical materials research, Biosci bioeng, Chem, Clin implant dent relat, Control discs, Cooh, Dalhousie university, Depletion method, Deposition, Different groups, Disc, Electroless, Electroless deposition, Enzymatic activity, Equal variances, Etching, Gold nanoparticles, Gold surfaces, Haucl4, Higher amounts, Implant, Implant materials, Implant surfaces, Lysozyme, Lysozyme adsorption, Lysozyme coverage, Lysozyme solution, Metal ions, Metallic gold, Micrococcus lysodeikticus, Nanoparticles, Nanostructured surfaces, Normality tests, Nova scotia, Orthopedic applications, Orthopedic implants, Oxide, Oxide layer, Phys chem, Plain aunps, Protein adsorption, Protein amounts, Protein solution, Prototype protein, Qualitative etching, Scanning electron microscopy, Second focus, Standard deviation, Standard solution, Surface area, Surface chemistry, Tio2, Titanium, Titanium implants, Titanium surfaces, Variance, Various deposition methods, Weak interactions, Wiley periodicals.
Abstract
Modifying titanium (Ti) implant surfaces with functional proteins can strengthen the interface between prosthesis and bone. A prototype system was developed using gold nanoparticles (AuNPs) to immobilize proteins onto Ti. An electroless (galvanic displacement) deposition method was first used to form AuNPs of controlled size and coverage on commercial Ti foil (giving Ti‐AuNPs). Parameters were then modified to create two groups of discs (n = 26) with different average AuNP diameters. Scanning electron microscopy and X‐ray photoelectron spectroscopy were used to characterize the morphology and surface structure of Ti‐AuNPs. To study the interaction of Ti‐AuNPs with proteins, Ti discs (n = 8) modified with plain AuNPs and discs (n = 8) modified with thiol (HSRCOOH)‐functionalized AuNPs were treated with lysozyme solution. The amount and activity of the lysozyme on the discs were examined with Micro‐BCA and enzymatic assays. Lysozyme was immobilized onto the discs, and the assays showed that the discs with thiol‐functionalized AuNPs, discs with bare AuNPs, and Ti controls had average lysozyme adsorptions of 23 × 104, 2.3 × 104, and 5.7 × 104 μg/m2, respectively. The activity assays showed that 21.5, 18.4, and 12.5% of the adsorbed lysozyme was active on the discs with thiol‐functionalized AuNPs, discs with bare AuNPs, and Ti controls, respectively. This technique holds promise for binding functional biomolecules to surgical implants, hence possibly creating implant surfaces that react to their local environment. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2010.
Url:
DOI: 10.1002/jbm.a.32826
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Modifying titanium (Ti) implant surfaces with functional proteins can strengthen the interface between prosthesis and bone. A prototype system was developed using gold nanoparticles (AuNPs) to immobilize proteins onto Ti. An electroless (galvanic displacement) deposition method was first used to form AuNPs of controlled size and coverage on commercial Ti foil (giving Ti‐AuNPs). Parameters were then modified to create two groups of discs (n = 26) with different average AuNP diameters. Scanning electron microscopy and X‐ray photoelectron spectroscopy were used to characterize the morphology and surface structure of Ti‐AuNPs. To study the interaction of Ti‐AuNPs with proteins, Ti discs (n = 8) modified with plain AuNPs and discs (n = 8) modified with thiol (HSRCOOH)‐functionalized AuNPs were treated with lysozyme solution. The amount and activity of the lysozyme on the discs were examined with Micro‐BCA and enzymatic assays. Lysozyme was immobilized onto the discs, and the assays showed that the discs with thiol‐functionalized AuNPs, discs with bare AuNPs, and Ti controls had average lysozyme adsorptions of 23 × 104, 2.3 × 104, and 5.7 × 104 μg/m2, respectively. The activity assays showed that 21.5, 18.4, and 12.5% of the adsorbed lysozyme was active on the discs with thiol‐functionalized AuNPs, discs with bare AuNPs, and Ti controls, respectively. This technique holds promise for binding functional biomolecules to surgical implants, hence possibly creating implant surfaces that react to their local environment. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2010.</div>
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