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Microbiological evaluation of peracetic acid for disinfection of acrylic resins
Purpose: The aim of this study was to assess the efficacy of peracetic acid (PAA) for the disinfection of dental acrylic resins experimentally contaminated with Candida albicans, Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa. Methods: Fifteen materials were used for each type of...
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Published in: | Revista odonto ciência 2011, Vol.26 (3), p.238-241 |
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creator | Stopiglia, Cheila Denise Ottonelli Carissimi, Mariana Scroferneker, Maria Lúcia Fortes, Carmen Beatriz Borges |
description | Purpose: The aim of this study was to assess the efficacy of peracetic acid (PAA) for the disinfection of dental acrylic resins experimentally contaminated with Candida albicans, Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa. Methods: Fifteen materials were used for each type of resin (thermosetting, self-curing and microwave-curing). Each material was placed in a test tube containing culture medium with a suspension of each microorganism and then incubated. The materials were rinsed and transferred to other tubes containing 50 mL of water for 5 min, 0.2% peracetic acid for 5 min or glutaraldehyde for 30 min. The materials were placed in the culture agar and incubated. Microbial growth was determined by colony counting after plating. Results: Candida albicans growth was inhibited by peracetic acid and glutaraldehyde treatments. The number of colonies on resins treated with saline was greater than 105 CFU/mL. In resins infected with E. coli, S. aureus and P. aeruginosa the colony growth was not inhibited by saline and peracetic acid, but it was totally inhibited by glutaraldehyde. Conclusion: Surface disinfection using peracetic acid effectively inhibited C. albicans growth on all acrylic resins. |
doi_str_mv | 10.1590/S1980-65232011000300008 |
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Methods: Fifteen materials were used for each type of resin (thermosetting, self-curing and microwave-curing). Each material was placed in a test tube containing culture medium with a suspension of each microorganism and then incubated. The materials were rinsed and transferred to other tubes containing 50 mL of water for 5 min, 0.2% peracetic acid for 5 min or glutaraldehyde for 30 min. The materials were placed in the culture agar and incubated. Microbial growth was determined by colony counting after plating. Results: Candida albicans growth was inhibited by peracetic acid and glutaraldehyde treatments. The number of colonies on resins treated with saline was greater than 105 CFU/mL. In resins infected with E. coli, S. aureus and P. aeruginosa the colony growth was not inhibited by saline and peracetic acid, but it was totally inhibited by glutaraldehyde. Conclusion: Surface disinfection using peracetic acid effectively inhibited C. albicans growth on all acrylic resins.</description><identifier>ISSN: 1980-6523</identifier><identifier>ISSN: 0102-9460</identifier><identifier>EISSN: 1980-6523</identifier><identifier>DOI: 10.1590/S1980-65232011000300008</identifier><language>eng ; por</language><publisher>Porto Alegre: EDIPUCRS</publisher><subject>Acids ; Candida albicans ; Colonies ; Dental hygiene ; Dental restorative materials ; DENTISTRY, ORAL SURGERY & MEDICINE ; Disinfection ; Escherichia coli ; Glutaraldehyde ; Oxidation ; Peracetic acid ; Pseudomonas aeruginosa ; Resins ; Staphylococcus aureus</subject><ispartof>Revista odonto ciência, 2011, Vol.26 (3), p.238-241</ispartof><rights>Copyright EDIPUCRS 2011</rights><rights>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2188-5f58d3bae002a760011be075c1869ee298b83d486bb3abd6224ce650d5d5ecbf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2162765489?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,24150,25753,27924,27925,37012,44590</link.rule.ids></links><search><creatorcontrib>Stopiglia, Cheila Denise Ottonelli</creatorcontrib><creatorcontrib>Carissimi, Mariana</creatorcontrib><creatorcontrib>Scroferneker, Maria Lúcia</creatorcontrib><creatorcontrib>Fortes, Carmen Beatriz Borges</creatorcontrib><title>Microbiological evaluation of peracetic acid for disinfection of acrylic resins</title><title>Revista odonto ciência</title><addtitle>Rev. odonto ciênc</addtitle><description>Purpose: The aim of this study was to assess the efficacy of peracetic acid (PAA) for the disinfection of dental acrylic resins experimentally contaminated with Candida albicans, Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa. Methods: Fifteen materials were used for each type of resin (thermosetting, self-curing and microwave-curing). Each material was placed in a test tube containing culture medium with a suspension of each microorganism and then incubated. The materials were rinsed and transferred to other tubes containing 50 mL of water for 5 min, 0.2% peracetic acid for 5 min or glutaraldehyde for 30 min. The materials were placed in the culture agar and incubated. Microbial growth was determined by colony counting after plating. Results: Candida albicans growth was inhibited by peracetic acid and glutaraldehyde treatments. The number of colonies on resins treated with saline was greater than 105 CFU/mL. In resins infected with E. coli, S. aureus and P. aeruginosa the colony growth was not inhibited by saline and peracetic acid, but it was totally inhibited by glutaraldehyde. Conclusion: Surface disinfection using peracetic acid effectively inhibited C. albicans growth on all acrylic resins.</description><subject>Acids</subject><subject>Candida albicans</subject><subject>Colonies</subject><subject>Dental hygiene</subject><subject>Dental restorative materials</subject><subject>DENTISTRY, ORAL SURGERY & MEDICINE</subject><subject>Disinfection</subject><subject>Escherichia coli</subject><subject>Glutaraldehyde</subject><subject>Oxidation</subject><subject>Peracetic acid</subject><subject>Pseudomonas aeruginosa</subject><subject>Resins</subject><subject>Staphylococcus aureus</subject><issn>1980-6523</issn><issn>0102-9460</issn><issn>1980-6523</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp1kNtKAzEQhoMoWKvP4ILXWydJk81eSvEElV6o10sOE0lZm5pshb690XoC8WKYYeb_Z4aPkFMKEypaOL-nrYJaCsYZUAoAvASoPTL6Huz_qg_JUc5LANFyoUZkcRdsiibEPj4Fq_sKX3W_0UOIqyr6ao1JWxyCrbQNrvIxVS7ksPJovyTapm1fBAlLPx-TA6_7jCefeUwery4fZjf1fHF9O7uY15ZRpWrhhXLcaARgupFQPjcIjbBUyRaRtcoo7qZKGsO1cZKxqUUpwAkn0BrPx2Sy25ttwD52y7hJq3Kw-8DR_cFRDGc7wzrFlw3m4cfCqGSNFFPVFlWzUxUoOSf03TqFZ522HYXuHfe_-98AAs9wNQ</recordid><startdate>201101</startdate><enddate>201101</enddate><creator>Stopiglia, Cheila Denise Ottonelli</creator><creator>Carissimi, Mariana</creator><creator>Scroferneker, Maria Lúcia</creator><creator>Fortes, Carmen Beatriz Borges</creator><general>EDIPUCRS</general><general>Pontifícia Universidade Católica do Rio Grande do Sul</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>CLZPN</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PADUT</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>GPN</scope></search><sort><creationdate>201101</creationdate><title>Microbiological evaluation of peracetic acid for disinfection of acrylic resins</title><author>Stopiglia, Cheila Denise Ottonelli ; 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Methods: Fifteen materials were used for each type of resin (thermosetting, self-curing and microwave-curing). Each material was placed in a test tube containing culture medium with a suspension of each microorganism and then incubated. The materials were rinsed and transferred to other tubes containing 50 mL of water for 5 min, 0.2% peracetic acid for 5 min or glutaraldehyde for 30 min. The materials were placed in the culture agar and incubated. Microbial growth was determined by colony counting after plating. Results: Candida albicans growth was inhibited by peracetic acid and glutaraldehyde treatments. The number of colonies on resins treated with saline was greater than 105 CFU/mL. In resins infected with E. coli, S. aureus and P. aeruginosa the colony growth was not inhibited by saline and peracetic acid, but it was totally inhibited by glutaraldehyde. 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subjects | Acids Candida albicans Colonies Dental hygiene Dental restorative materials DENTISTRY, ORAL SURGERY & MEDICINE Disinfection Escherichia coli Glutaraldehyde Oxidation Peracetic acid Pseudomonas aeruginosa Resins Staphylococcus aureus |
title | Microbiological evaluation of peracetic acid for disinfection of acrylic resins |
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