Effect of S53P4 bone substitute on staphylococcal adhesion and biofilm formation on other implant materials in normal and hypoxic conditions
To study the effect of bioactive glass bone substitute granules (S53P4) on bacterial adhesion and biofilm formation on other simultaneously used implant materials and the role of the hypoxic conditions to the adhesion. Bacterial and biofilm formation were studied on materials used both in middle ear...
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Veröffentlicht in: | Journal of materials science. Materials in medicine 2015-09, Vol.26 (9), p.239-10, Article 239 |
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creator | Pérez-Tanoira, R. García-Pedrazuela, M. Hyyrynen, T. Soininen, A. Aarnisalo, A. Nieminen, Mikko T. Tiainen, V.-M. Konttinen, Y. T. Kinnari, T. J. |
description | To study the effect of bioactive glass bone substitute granules (S53P4) on bacterial adhesion and biofilm formation on other simultaneously used implant materials and the role of the hypoxic conditions to the adhesion. Bacterial and biofilm formation were studied on materials used both in middle ear prostheses and in fracture fixtures (titanium, polytetrafluoroethylene, polydimethylsiloxane and bioactive glass plates) in the presence or absence of S53P4 granules. The experiments were done either in normal atmosphere or in hypoxia simulating atmospheric conditions of middle ear, mastoid cavity and sinuses. We used two collection strains of
Staphylococcus aureus
and
Staphylococcus epidermidis
. In the presence of bioglass and hypoxic conditions the adhesion of the planktonic bacterial cells was decreased for most of the materials. The biofilm formation was decreased for
S. epidermidis
on titanium and polydimethylsiloxane in both atmospheric conditions and on bioglass plates in normoxia. For
S. aureus
the biofilm formation was decreased on bioglass plates and polytetrafluoroethylene in normoxia. Hypoxia produces a decrease in the biofilm formation only for
S. aureus
on polytetrafluoroethylene and for
S. epidermidis
on bioglass plates. However, in none of the cases bioactive glass increased the bacterial or biofilm adhesion. The presence of bioglass in normoxic and hypoxic conditions prevents the bacterial and biofilm adhesion on surfaces of several typical prosthesis materials in vitro. This may lead to diminishing postoperative infections, however, further in vivo studies are needed. |
doi_str_mv | 10.1007/s10856-015-5569-1 |
format | Article |
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Staphylococcus aureus
and
Staphylococcus epidermidis
. In the presence of bioglass and hypoxic conditions the adhesion of the planktonic bacterial cells was decreased for most of the materials. The biofilm formation was decreased for
S. epidermidis
on titanium and polydimethylsiloxane in both atmospheric conditions and on bioglass plates in normoxia. For
S. aureus
the biofilm formation was decreased on bioglass plates and polytetrafluoroethylene in normoxia. Hypoxia produces a decrease in the biofilm formation only for
S. aureus
on polytetrafluoroethylene and for
S. epidermidis
on bioglass plates. However, in none of the cases bioactive glass increased the bacterial or biofilm adhesion. The presence of bioglass in normoxic and hypoxic conditions prevents the bacterial and biofilm adhesion on surfaces of several typical prosthesis materials in vitro. This may lead to diminishing postoperative infections, however, further in vivo studies are needed.</description><identifier>ISSN: 0957-4530</identifier><identifier>EISSN: 1573-4838</identifier><identifier>DOI: 10.1007/s10856-015-5569-1</identifier><identifier>PMID: 26403279</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adhesion ; Bacteria ; Bacterial Adhesion - drug effects ; Biocompatibility ; Biocompatibility Studies ; Biofilms ; Bioglass ; Biomaterials ; Biomedical Engineering and Bioengineering ; Biomedical materials ; Bone Substitutes - pharmacology ; Ceramics ; Chemistry and Materials Science ; Colony Count, Microbial ; Composites ; Formations ; Glass ; Hydrogen-Ion Concentration ; Materials Science ; Natural Materials ; Oxygen - metabolism ; Plates ; Polymer Sciences ; Prostheses and Implants ; Regenerative Medicine/Tissue Engineering ; Staphylococcus aureus ; Staphylococcus aureus - drug effects ; Staphylococcus aureus - physiology ; Staphylococcus epidermidis ; Staphylococcus epidermidis - drug effects ; Staphylococcus epidermidis - physiology ; Surfaces and Interfaces ; Surgical implants ; Thin Films</subject><ispartof>Journal of materials science. Materials in medicine, 2015-09, Vol.26 (9), p.239-10, Article 239</ispartof><rights>Springer Science+Business Media New York 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-4a0b76f7d3a381863e4197bb493fe8c0502a6020c5c986137347c5c86493f9673</citedby><cites>FETCH-LOGICAL-c541t-4a0b76f7d3a381863e4197bb493fe8c0502a6020c5c986137347c5c86493f9673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10856-015-5569-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10856-015-5569-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26403279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pérez-Tanoira, R.</creatorcontrib><creatorcontrib>García-Pedrazuela, M.</creatorcontrib><creatorcontrib>Hyyrynen, T.</creatorcontrib><creatorcontrib>Soininen, A.</creatorcontrib><creatorcontrib>Aarnisalo, A.</creatorcontrib><creatorcontrib>Nieminen, Mikko T.</creatorcontrib><creatorcontrib>Tiainen, V.-M.</creatorcontrib><creatorcontrib>Konttinen, Y. T.</creatorcontrib><creatorcontrib>Kinnari, T. J.</creatorcontrib><title>Effect of S53P4 bone substitute on staphylococcal adhesion and biofilm formation on other implant materials in normal and hypoxic conditions</title><title>Journal of materials science. Materials in medicine</title><addtitle>J Mater Sci: Mater Med</addtitle><addtitle>J Mater Sci Mater Med</addtitle><description>To study the effect of bioactive glass bone substitute granules (S53P4) on bacterial adhesion and biofilm formation on other simultaneously used implant materials and the role of the hypoxic conditions to the adhesion. Bacterial and biofilm formation were studied on materials used both in middle ear prostheses and in fracture fixtures (titanium, polytetrafluoroethylene, polydimethylsiloxane and bioactive glass plates) in the presence or absence of S53P4 granules. The experiments were done either in normal atmosphere or in hypoxia simulating atmospheric conditions of middle ear, mastoid cavity and sinuses. We used two collection strains of
Staphylococcus aureus
and
Staphylococcus epidermidis
. In the presence of bioglass and hypoxic conditions the adhesion of the planktonic bacterial cells was decreased for most of the materials. The biofilm formation was decreased for
S. epidermidis
on titanium and polydimethylsiloxane in both atmospheric conditions and on bioglass plates in normoxia. For
S. aureus
the biofilm formation was decreased on bioglass plates and polytetrafluoroethylene in normoxia. Hypoxia produces a decrease in the biofilm formation only for
S. aureus
on polytetrafluoroethylene and for
S. epidermidis
on bioglass plates. However, in none of the cases bioactive glass increased the bacterial or biofilm adhesion. The presence of bioglass in normoxic and hypoxic conditions prevents the bacterial and biofilm adhesion on surfaces of several typical prosthesis materials in vitro. This may lead to diminishing postoperative infections, however, further in vivo studies are needed.</description><subject>Adhesion</subject><subject>Bacteria</subject><subject>Bacterial Adhesion - drug effects</subject><subject>Biocompatibility</subject><subject>Biocompatibility Studies</subject><subject>Biofilms</subject><subject>Bioglass</subject><subject>Biomaterials</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedical materials</subject><subject>Bone Substitutes - pharmacology</subject><subject>Ceramics</subject><subject>Chemistry and Materials Science</subject><subject>Colony Count, Microbial</subject><subject>Composites</subject><subject>Formations</subject><subject>Glass</subject><subject>Hydrogen-Ion Concentration</subject><subject>Materials Science</subject><subject>Natural Materials</subject><subject>Oxygen - metabolism</subject><subject>Plates</subject><subject>Polymer Sciences</subject><subject>Prostheses and Implants</subject><subject>Regenerative Medicine/Tissue Engineering</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Staphylococcus aureus - physiology</subject><subject>Staphylococcus epidermidis</subject><subject>Staphylococcus epidermidis - drug effects</subject><subject>Staphylococcus epidermidis - physiology</subject><subject>Surfaces and Interfaces</subject><subject>Surgical implants</subject><subject>Thin Films</subject><issn>0957-4530</issn><issn>1573-4838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkt1qFTEUhYMo9lh9AG8k4I03Y3cmv3MppVqhYMH2OmQyiSdlZjImGfC8gw9tpqeKCKIkkM3Ot1YSshB6SeAtAZBnmYDiogHCG85F15BHaEe4pA1TVD1GO-i4bBincIKe5XwHAKzj_Ck6aQUD2spuh75feO9swdHjz5xeM9zH2eG89rmEshaH44xzMcv-MEYbrTUjNsPe5VD7Zh5wH6IP44R9TJMpW3ebZe8SDtMymrng2ncpmDHjMON548Z76f6wxG_BYhvnIWzS_Bw98ZVzLx7WU3T7_uLm_LK5-vTh4_m7q8ZyRkrDDPRSeDlQQxVRgjpGOtn3rKPeKQscWiOgBcttpwShkjJZayU2oBOSnqI3R98lxa-ry0VPIVs31uu6uGZNFNTBKWX_RqUC3jKq1H-g1Vcq2ZKKvv4DvYtrmuubN6pjgnIJlSJHyqaYc3JeLylMJh00Ab0FQB8DoGsA9BYAvTm_enBe-8kNvxQ_f7wC7RHIdWv-4tJvR__V9Qfp37pj</recordid><startdate>20150901</startdate><enddate>20150901</enddate><creator>Pérez-Tanoira, R.</creator><creator>García-Pedrazuela, M.</creator><creator>Hyyrynen, T.</creator><creator>Soininen, A.</creator><creator>Aarnisalo, A.</creator><creator>Nieminen, Mikko T.</creator><creator>Tiainen, V.-M.</creator><creator>Konttinen, Y. 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Materials in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pérez-Tanoira, R.</au><au>García-Pedrazuela, M.</au><au>Hyyrynen, T.</au><au>Soininen, A.</au><au>Aarnisalo, A.</au><au>Nieminen, Mikko T.</au><au>Tiainen, V.-M.</au><au>Konttinen, Y. T.</au><au>Kinnari, T. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of S53P4 bone substitute on staphylococcal adhesion and biofilm formation on other implant materials in normal and hypoxic conditions</atitle><jtitle>Journal of materials science. Materials in medicine</jtitle><stitle>J Mater Sci: Mater Med</stitle><addtitle>J Mater Sci Mater Med</addtitle><date>2015-09-01</date><risdate>2015</risdate><volume>26</volume><issue>9</issue><spage>239</spage><epage>10</epage><pages>239-10</pages><artnum>239</artnum><issn>0957-4530</issn><eissn>1573-4838</eissn><abstract>To study the effect of bioactive glass bone substitute granules (S53P4) on bacterial adhesion and biofilm formation on other simultaneously used implant materials and the role of the hypoxic conditions to the adhesion. Bacterial and biofilm formation were studied on materials used both in middle ear prostheses and in fracture fixtures (titanium, polytetrafluoroethylene, polydimethylsiloxane and bioactive glass plates) in the presence or absence of S53P4 granules. The experiments were done either in normal atmosphere or in hypoxia simulating atmospheric conditions of middle ear, mastoid cavity and sinuses. We used two collection strains of
Staphylococcus aureus
and
Staphylococcus epidermidis
. In the presence of bioglass and hypoxic conditions the adhesion of the planktonic bacterial cells was decreased for most of the materials. The biofilm formation was decreased for
S. epidermidis
on titanium and polydimethylsiloxane in both atmospheric conditions and on bioglass plates in normoxia. For
S. aureus
the biofilm formation was decreased on bioglass plates and polytetrafluoroethylene in normoxia. Hypoxia produces a decrease in the biofilm formation only for
S. aureus
on polytetrafluoroethylene and for
S. epidermidis
on bioglass plates. However, in none of the cases bioactive glass increased the bacterial or biofilm adhesion. The presence of bioglass in normoxic and hypoxic conditions prevents the bacterial and biofilm adhesion on surfaces of several typical prosthesis materials in vitro. This may lead to diminishing postoperative infections, however, further in vivo studies are needed.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>26403279</pmid><doi>10.1007/s10856-015-5569-1</doi><tpages>10</tpages></addata></record> |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Adhesion Bacteria Bacterial Adhesion - drug effects Biocompatibility Biocompatibility Studies Biofilms Bioglass Biomaterials Biomedical Engineering and Bioengineering Biomedical materials Bone Substitutes - pharmacology Ceramics Chemistry and Materials Science Colony Count, Microbial Composites Formations Glass Hydrogen-Ion Concentration Materials Science Natural Materials Oxygen - metabolism Plates Polymer Sciences Prostheses and Implants Regenerative Medicine/Tissue Engineering Staphylococcus aureus Staphylococcus aureus - drug effects Staphylococcus aureus - physiology Staphylococcus epidermidis Staphylococcus epidermidis - drug effects Staphylococcus epidermidis - physiology Surfaces and Interfaces Surgical implants Thin Films |
title | Effect of S53P4 bone substitute on staphylococcal adhesion and biofilm formation on other implant materials in normal and hypoxic conditions |
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