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Bimetallic silver-platinum nanoparticles with combined osteo-promotive and antimicrobial activity.

Identifieur interne : 000282 ( Main/Corpus ); précédent : 000281; suivant : 000283

Bimetallic silver-platinum nanoparticles with combined osteo-promotive and antimicrobial activity.

Auteurs : Marina Breisch ; Viktoria Grasmik ; Kateryna Loza ; Kevin Pappert ; Alexander Rostek ; Nadine Ziegler ; Alfred Ludwig ; Marc Heggen ; Matthias Epple ; Jörg C. Tiller ; Thomas A. Schildhauer ; Manfred Köller ; Christina Sengstock

Source :

RBID : pubmed:30959494

English descriptors

Abstract

Bimetallic alloyed silver-platinum nanoparticles (AgPt NP) with different metal composition from Ag10Pt90 to Ag90Pt10 in steps of 20 mol% were synthesized. The biological effects of AgPt NP, including cellular uptake, cell viability, osteogenic differentiation and osteoclastogenesis as well as the antimicrobial activity towards Staphylococcus aureus and Escherichia coli were analyzed in comparison to pure Ag NP and pure Pt NP. The uptake of NP into human mesenchymal stem cells was confirmed by cross-sectional focused-ion beam preparation and observation by scanning and transmission electron microscopy in combination with energy-dispersive x-ray analysis. Lower cytotoxicity and antimicrobial activity were observed for AgPt NP compared to pure Ag NP. Thus, an enhanced Ag ion release due to a possible sacrificial anode effect was not achieved. Nevertheless, a Ag content of at least 50 mol% was sufficient to induce bactericidal effects against both Staphylococcus aureus and Escherichia coli. In addition, a Pt-related (≥50 mol% Pt) osteo-promotive activity on human mesenchymal stem cells was observed by enhanced cell calcification and alkaline phosphatase activity. In contrast, the osteoclastogenesis of rat primary precursor osteoclasts was inhibited. In summary, these results demonstrate a combinatory osteo-promotive and antimicrobial activity of bimetallic Ag50Pt50 NP.

DOI: 10.1088/1361-6528/ab172b
PubMed: 30959494

Links to Exploration step

pubmed:30959494

Le document en format XML

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<name sortKey="Breisch, Marina" sort="Breisch, Marina" uniqKey="Breisch M" first="Marina" last="Breisch">Marina Breisch</name>
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<name sortKey="Loza, Kateryna" sort="Loza, Kateryna" uniqKey="Loza K" first="Kateryna" last="Loza">Kateryna Loza</name>
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<name sortKey="Pappert, Kevin" sort="Pappert, Kevin" uniqKey="Pappert K" first="Kevin" last="Pappert">Kevin Pappert</name>
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<name sortKey="Rostek, Alexander" sort="Rostek, Alexander" uniqKey="Rostek A" first="Alexander" last="Rostek">Alexander Rostek</name>
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<name sortKey="Epple, Matthias" sort="Epple, Matthias" uniqKey="Epple M" first="Matthias" last="Epple">Matthias Epple</name>
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<name sortKey="Loza, Kateryna" sort="Loza, Kateryna" uniqKey="Loza K" first="Kateryna" last="Loza">Kateryna Loza</name>
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<name sortKey="Ziegler, Nadine" sort="Ziegler, Nadine" uniqKey="Ziegler N" first="Nadine" last="Ziegler">Nadine Ziegler</name>
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<name sortKey="Epple, Matthias" sort="Epple, Matthias" uniqKey="Epple M" first="Matthias" last="Epple">Matthias Epple</name>
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<term>Anti-Bacterial Agents (chemistry)</term>
<term>Anti-Bacterial Agents (pharmacology)</term>
<term>Cell Differentiation (drug effects)</term>
<term>Cell Line (MeSH)</term>
<term>Escherichia coli (drug effects)</term>
<term>Escherichia coli Infections (drug therapy)</term>
<term>Humans (MeSH)</term>
<term>Mesenchymal Stem Cells (cytology)</term>
<term>Mesenchymal Stem Cells (drug effects)</term>
<term>Metal Nanoparticles (chemistry)</term>
<term>Osteogenesis (drug effects)</term>
<term>Platinum (chemistry)</term>
<term>Platinum (pharmacology)</term>
<term>Silver (chemistry)</term>
<term>Silver (pharmacology)</term>
<term>Staphylococcal Infections (drug therapy)</term>
<term>Staphylococcus aureus (drug effects)</term>
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<term>Anti-Bacterial Agents</term>
<term>Platinum</term>
<term>Silver</term>
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<term>Anti-Bacterial Agents</term>
<term>Platinum</term>
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<term>Cell Differentiation</term>
<term>Escherichia coli</term>
<term>Mesenchymal Stem Cells</term>
<term>Osteogenesis</term>
<term>Staphylococcus aureus</term>
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<term>Escherichia coli Infections</term>
<term>Staphylococcal Infections</term>
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<div type="abstract" xml:lang="en">Bimetallic alloyed silver-platinum nanoparticles (AgPt NP) with different metal composition from Ag
<sub>10</sub>
Pt
<sub>90</sub>
to Ag
<sub>90</sub>
Pt
<sub>10</sub>
in steps of 20 mol% were synthesized. The biological effects of AgPt NP, including cellular uptake, cell viability, osteogenic differentiation and osteoclastogenesis as well as the antimicrobial activity towards Staphylococcus aureus and Escherichia coli were analyzed in comparison to pure Ag NP and pure Pt NP. The uptake of NP into human mesenchymal stem cells was confirmed by cross-sectional focused-ion beam preparation and observation by scanning and transmission electron microscopy in combination with energy-dispersive x-ray analysis. Lower cytotoxicity and antimicrobial activity were observed for AgPt NP compared to pure Ag NP. Thus, an enhanced Ag ion release due to a possible sacrificial anode effect was not achieved. Nevertheless, a Ag content of at least 50 mol% was sufficient to induce bactericidal effects against both Staphylococcus aureus and Escherichia coli. In addition, a Pt-related (≥50 mol% Pt) osteo-promotive activity on human mesenchymal stem cells was observed by enhanced cell calcification and alkaline phosphatase activity. In contrast, the osteoclastogenesis of rat primary precursor osteoclasts was inhibited. In summary, these results demonstrate a combinatory osteo-promotive and antimicrobial activity of bimetallic Ag
<sub>50</sub>
Pt
<sub>50</sub>
NP.</div>
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<ArticleTitle>Bimetallic silver-platinum nanoparticles with combined osteo-promotive and antimicrobial activity.</ArticleTitle>
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<Abstract>
<AbstractText>Bimetallic alloyed silver-platinum nanoparticles (AgPt NP) with different metal composition from Ag
<sub>10</sub>
Pt
<sub>90</sub>
to Ag
<sub>90</sub>
Pt
<sub>10</sub>
in steps of 20 mol% were synthesized. The biological effects of AgPt NP, including cellular uptake, cell viability, osteogenic differentiation and osteoclastogenesis as well as the antimicrobial activity towards Staphylococcus aureus and Escherichia coli were analyzed in comparison to pure Ag NP and pure Pt NP. The uptake of NP into human mesenchymal stem cells was confirmed by cross-sectional focused-ion beam preparation and observation by scanning and transmission electron microscopy in combination with energy-dispersive x-ray analysis. Lower cytotoxicity and antimicrobial activity were observed for AgPt NP compared to pure Ag NP. Thus, an enhanced Ag ion release due to a possible sacrificial anode effect was not achieved. Nevertheless, a Ag content of at least 50 mol% was sufficient to induce bactericidal effects against both Staphylococcus aureus and Escherichia coli. In addition, a Pt-related (≥50 mol% Pt) osteo-promotive activity on human mesenchymal stem cells was observed by enhanced cell calcification and alkaline phosphatase activity. In contrast, the osteoclastogenesis of rat primary precursor osteoclasts was inhibited. In summary, these results demonstrate a combinatory osteo-promotive and antimicrobial activity of bimetallic Ag
<sub>50</sub>
Pt
<sub>50</sub>
NP.</AbstractText>
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<Language>eng</Language>
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