Antimicrobial Peptide P60.4Ac-Containing Creams and Gel for Eradication of Methicillin-Resistant Staphylococcus aureus from Cultured Skin and Airway Epithelial Surfaces
We previously found the LL-37-derived peptide P60.4Ac to be effective against methicillin-resistant Staphylococcus aureus (MRSA) on human epidermal models (EMs). The goal of this study was to identify the preferred carrier for this peptide for topical application on skin and mucosal surfaces. We pre...
Gespeichert in:
Veröffentlicht in: | Antimicrobial agents and chemotherapy 2016-07, Vol.60 (7), p.4063-4072 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4072 |
---|---|
container_issue | 7 |
container_start_page | 4063 |
container_title | Antimicrobial agents and chemotherapy |
container_volume | 60 |
creator | Haisma, Elisabeth M Göblyös, Anikó Ravensbergen, Bep Adriaans, Alwin E Cordfunke, Robert A Schrumpf, Jasmijn Limpens, Ronald W A L Schimmel, Kirsten J M den Hartigh, Jan Hiemstra, Pieter S Drijfhout, Jan Wouter El Ghalbzouri, Abdoelwaheb Nibbering, Peter H |
description | We previously found the LL-37-derived peptide P60.4Ac to be effective against methicillin-resistant Staphylococcus aureus (MRSA) on human epidermal models (EMs). The goal of this study was to identify the preferred carrier for this peptide for topical application on skin and mucosal surfaces. We prepared P60.4Ac in three formulations, i.e., a water-in-oil cream with lanolin (Softisan 649), an oil-in-water cream with polyethylene glycol hexadecyl ether (Cetomacrogol), and a hydroxypropyl methylcellulose (hypromellose) 4000 gel. We tested the antimicrobial efficacy of the peptide in these formulations against mupirocin-resistant and -sensitive MRSA strains on EMs and bronchial epithelial models (BEMs). The cytotoxic effects of formulated P60.4Ac on these models were determined using histology and WST-1 and lactate dehydrogenase assays. Moreover, we assessed the stability of the peptide in these formulations with storage for up to 3 months. Killing of MRSA by P60.4Ac in the two creams was less effective than that by P60.4Ac in the hypromellose gel. In agreement with those findings, P60.4Ac in the hypromellose gel was highly effective in eradicating the two MRSA strains from EMs. We found that even 0.1% (wt/wt) P60.4Ac in the hypromellose gel killed >99% of the viable planktonic bacteria and >85% of the biofilm-associated bacteria on EMs. Hypromellose gels containing 0.1% and 0.5% (wt/wt) P60.4Ac effectively reduced the numbers of viable MRSA cells from BEMs by >90%. No cytotoxic effects of P60.4Ac in the hypromellose gel with up to 2% (wt/wt) P60.4Ac on keratinocytes in EMs and in the hypromellose gel with up to 0.5% (wt/wt) P60.4Ac on epithelial cells in BEMs were observed. High-performance liquid chromatography analysis showed that P60.4Ac was stable in the Softisan cream and the hypromellose gel but not in the Cetomacrogol cream. We conclude that P60.4Ac formulated in hypromellose gel is both stable and highly effective in eradicating MRSA from colonized EMs and BEMs. |
doi_str_mv | 10.1128/AAC.03001-15 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4914645</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1808679271</sourcerecordid><originalsourceid>FETCH-LOGICAL-a451t-64d75fc5be626412dda78b92242880bf035950094e71aab30466ba9e7405d0463</originalsourceid><addsrcrecordid>eNp1kUFv1DAQhS0Eokvhxhn5CBJZ7MR2kgtSFC0FqYiKhbM1cZyui2MvtgPaf8TPxNstFRw4jZ7m-ZvxPISeU7KmtGzedF2_JhUhtKD8AVpR0jaF4K14iFaECFGwhrAz9CTGG5I1b8ljdFbWlLKyblboV-eSmY0KfjBg8ZXeJzNqfCXImnWq6L1LYJxx17gPGuaIwY34Qls8-YA3AUajIBnvsJ_wR512RhlrjSs-62hiApfwNsF-d7BeeaWW_H4JOpcp-Bn3i01Zjnj7zbhbcmfCTzjgzd6knbbHjbZLmEDp-BQ9msBG_eyunqOv7zZf-vfF5aeLD313WQDjNBWCjTWfFB-0KAWj5ThC3QxtWbKyacgwkYq3nJCW6ZoCDBVhQgzQ6poRPmZRnaO3J-5-GWY9Ku1SACv3wcwQDtKDkf92nNnJa_9DspYywXgGvLwDBP990THJ2USlrQWn_RIlbUgj6jZHkK2vT9Z8_hiDnu7HUCKP4cocrrwNV9Ij-dXJDnEu5Y1fgsuX-J_3xd_fuAf_Sb76DehEroE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1808679271</pqid></control><display><type>article</type><title>Antimicrobial Peptide P60.4Ac-Containing Creams and Gel for Eradication of Methicillin-Resistant Staphylococcus aureus from Cultured Skin and Airway Epithelial Surfaces</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Haisma, Elisabeth M ; Göblyös, Anikó ; Ravensbergen, Bep ; Adriaans, Alwin E ; Cordfunke, Robert A ; Schrumpf, Jasmijn ; Limpens, Ronald W A L ; Schimmel, Kirsten J M ; den Hartigh, Jan ; Hiemstra, Pieter S ; Drijfhout, Jan Wouter ; El Ghalbzouri, Abdoelwaheb ; Nibbering, Peter H</creator><creatorcontrib>Haisma, Elisabeth M ; Göblyös, Anikó ; Ravensbergen, Bep ; Adriaans, Alwin E ; Cordfunke, Robert A ; Schrumpf, Jasmijn ; Limpens, Ronald W A L ; Schimmel, Kirsten J M ; den Hartigh, Jan ; Hiemstra, Pieter S ; Drijfhout, Jan Wouter ; El Ghalbzouri, Abdoelwaheb ; Nibbering, Peter H</creatorcontrib><description>We previously found the LL-37-derived peptide P60.4Ac to be effective against methicillin-resistant Staphylococcus aureus (MRSA) on human epidermal models (EMs). The goal of this study was to identify the preferred carrier for this peptide for topical application on skin and mucosal surfaces. We prepared P60.4Ac in three formulations, i.e., a water-in-oil cream with lanolin (Softisan 649), an oil-in-water cream with polyethylene glycol hexadecyl ether (Cetomacrogol), and a hydroxypropyl methylcellulose (hypromellose) 4000 gel. We tested the antimicrobial efficacy of the peptide in these formulations against mupirocin-resistant and -sensitive MRSA strains on EMs and bronchial epithelial models (BEMs). The cytotoxic effects of formulated P60.4Ac on these models were determined using histology and WST-1 and lactate dehydrogenase assays. Moreover, we assessed the stability of the peptide in these formulations with storage for up to 3 months. Killing of MRSA by P60.4Ac in the two creams was less effective than that by P60.4Ac in the hypromellose gel. In agreement with those findings, P60.4Ac in the hypromellose gel was highly effective in eradicating the two MRSA strains from EMs. We found that even 0.1% (wt/wt) P60.4Ac in the hypromellose gel killed >99% of the viable planktonic bacteria and >85% of the biofilm-associated bacteria on EMs. Hypromellose gels containing 0.1% and 0.5% (wt/wt) P60.4Ac effectively reduced the numbers of viable MRSA cells from BEMs by >90%. No cytotoxic effects of P60.4Ac in the hypromellose gel with up to 2% (wt/wt) P60.4Ac on keratinocytes in EMs and in the hypromellose gel with up to 0.5% (wt/wt) P60.4Ac on epithelial cells in BEMs were observed. High-performance liquid chromatography analysis showed that P60.4Ac was stable in the Softisan cream and the hypromellose gel but not in the Cetomacrogol cream. We conclude that P60.4Ac formulated in hypromellose gel is both stable and highly effective in eradicating MRSA from colonized EMs and BEMs.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AAC.03001-15</identifier><identifier>PMID: 27114278</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Anti-Bacterial Agents ; Anti-Bacterial Agents - pharmacology ; Anti-Infective Agents - pharmacology ; Bronchi - cytology ; Cells, Cultured ; Cryoelectron Microscopy ; Epithelium ; Epithelium - microbiology ; Experimental Therapeutics ; Humans ; In Vitro Techniques ; Methicillin-Resistant Staphylococcus aureus ; Methicillin-Resistant Staphylococcus aureus - drug effects ; Methicillin-Resistant Staphylococcus aureus - pathogenicity ; Mupirocin - pharmacology ; Peptides ; Peptides - pharmacology ; Skin ; Skin - microbiology ; Staphylococcus aureus</subject><ispartof>Antimicrobial agents and chemotherapy, 2016-07, Vol.60 (7), p.4063-4072</ispartof><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved. 2016 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a451t-64d75fc5be626412dda78b92242880bf035950094e71aab30466ba9e7405d0463</citedby><cites>FETCH-LOGICAL-a451t-64d75fc5be626412dda78b92242880bf035950094e71aab30466ba9e7405d0463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914645/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914645/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27114278$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haisma, Elisabeth M</creatorcontrib><creatorcontrib>Göblyös, Anikó</creatorcontrib><creatorcontrib>Ravensbergen, Bep</creatorcontrib><creatorcontrib>Adriaans, Alwin E</creatorcontrib><creatorcontrib>Cordfunke, Robert A</creatorcontrib><creatorcontrib>Schrumpf, Jasmijn</creatorcontrib><creatorcontrib>Limpens, Ronald W A L</creatorcontrib><creatorcontrib>Schimmel, Kirsten J M</creatorcontrib><creatorcontrib>den Hartigh, Jan</creatorcontrib><creatorcontrib>Hiemstra, Pieter S</creatorcontrib><creatorcontrib>Drijfhout, Jan Wouter</creatorcontrib><creatorcontrib>El Ghalbzouri, Abdoelwaheb</creatorcontrib><creatorcontrib>Nibbering, Peter H</creatorcontrib><title>Antimicrobial Peptide P60.4Ac-Containing Creams and Gel for Eradication of Methicillin-Resistant Staphylococcus aureus from Cultured Skin and Airway Epithelial Surfaces</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>We previously found the LL-37-derived peptide P60.4Ac to be effective against methicillin-resistant Staphylococcus aureus (MRSA) on human epidermal models (EMs). The goal of this study was to identify the preferred carrier for this peptide for topical application on skin and mucosal surfaces. We prepared P60.4Ac in three formulations, i.e., a water-in-oil cream with lanolin (Softisan 649), an oil-in-water cream with polyethylene glycol hexadecyl ether (Cetomacrogol), and a hydroxypropyl methylcellulose (hypromellose) 4000 gel. We tested the antimicrobial efficacy of the peptide in these formulations against mupirocin-resistant and -sensitive MRSA strains on EMs and bronchial epithelial models (BEMs). The cytotoxic effects of formulated P60.4Ac on these models were determined using histology and WST-1 and lactate dehydrogenase assays. Moreover, we assessed the stability of the peptide in these formulations with storage for up to 3 months. Killing of MRSA by P60.4Ac in the two creams was less effective than that by P60.4Ac in the hypromellose gel. In agreement with those findings, P60.4Ac in the hypromellose gel was highly effective in eradicating the two MRSA strains from EMs. We found that even 0.1% (wt/wt) P60.4Ac in the hypromellose gel killed >99% of the viable planktonic bacteria and >85% of the biofilm-associated bacteria on EMs. Hypromellose gels containing 0.1% and 0.5% (wt/wt) P60.4Ac effectively reduced the numbers of viable MRSA cells from BEMs by >90%. No cytotoxic effects of P60.4Ac in the hypromellose gel with up to 2% (wt/wt) P60.4Ac on keratinocytes in EMs and in the hypromellose gel with up to 0.5% (wt/wt) P60.4Ac on epithelial cells in BEMs were observed. High-performance liquid chromatography analysis showed that P60.4Ac was stable in the Softisan cream and the hypromellose gel but not in the Cetomacrogol cream. We conclude that P60.4Ac formulated in hypromellose gel is both stable and highly effective in eradicating MRSA from colonized EMs and BEMs.</description><subject>Anti-Bacterial Agents</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Bronchi - cytology</subject><subject>Cells, Cultured</subject><subject>Cryoelectron Microscopy</subject><subject>Epithelium</subject><subject>Epithelium - microbiology</subject><subject>Experimental Therapeutics</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Methicillin-Resistant Staphylococcus aureus</subject><subject>Methicillin-Resistant Staphylococcus aureus - drug effects</subject><subject>Methicillin-Resistant Staphylococcus aureus - pathogenicity</subject><subject>Mupirocin - pharmacology</subject><subject>Peptides</subject><subject>Peptides - pharmacology</subject><subject>Skin</subject><subject>Skin - microbiology</subject><subject>Staphylococcus aureus</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFv1DAQhS0Eokvhxhn5CBJZ7MR2kgtSFC0FqYiKhbM1cZyui2MvtgPaf8TPxNstFRw4jZ7m-ZvxPISeU7KmtGzedF2_JhUhtKD8AVpR0jaF4K14iFaECFGwhrAz9CTGG5I1b8ljdFbWlLKyblboV-eSmY0KfjBg8ZXeJzNqfCXImnWq6L1LYJxx17gPGuaIwY34Qls8-YA3AUajIBnvsJ_wR512RhlrjSs-62hiApfwNsF-d7BeeaWW_H4JOpcp-Bn3i01Zjnj7zbhbcmfCTzjgzd6knbbHjbZLmEDp-BQ9msBG_eyunqOv7zZf-vfF5aeLD313WQDjNBWCjTWfFB-0KAWj5ThC3QxtWbKyacgwkYq3nJCW6ZoCDBVhQgzQ6poRPmZRnaO3J-5-GWY9Ku1SACv3wcwQDtKDkf92nNnJa_9DspYywXgGvLwDBP990THJ2USlrQWn_RIlbUgj6jZHkK2vT9Z8_hiDnu7HUCKP4cocrrwNV9Ij-dXJDnEu5Y1fgsuX-J_3xd_fuAf_Sb76DehEroE</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Haisma, Elisabeth M</creator><creator>Göblyös, Anikó</creator><creator>Ravensbergen, Bep</creator><creator>Adriaans, Alwin E</creator><creator>Cordfunke, Robert A</creator><creator>Schrumpf, Jasmijn</creator><creator>Limpens, Ronald W A L</creator><creator>Schimmel, Kirsten J M</creator><creator>den Hartigh, Jan</creator><creator>Hiemstra, Pieter S</creator><creator>Drijfhout, Jan Wouter</creator><creator>El Ghalbzouri, Abdoelwaheb</creator><creator>Nibbering, Peter H</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20160701</creationdate><title>Antimicrobial Peptide P60.4Ac-Containing Creams and Gel for Eradication of Methicillin-Resistant Staphylococcus aureus from Cultured Skin and Airway Epithelial Surfaces</title><author>Haisma, Elisabeth M ; Göblyös, Anikó ; Ravensbergen, Bep ; Adriaans, Alwin E ; Cordfunke, Robert A ; Schrumpf, Jasmijn ; Limpens, Ronald W A L ; Schimmel, Kirsten J M ; den Hartigh, Jan ; Hiemstra, Pieter S ; Drijfhout, Jan Wouter ; El Ghalbzouri, Abdoelwaheb ; Nibbering, Peter H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a451t-64d75fc5be626412dda78b92242880bf035950094e71aab30466ba9e7405d0463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Anti-Bacterial Agents</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Bronchi - cytology</topic><topic>Cells, Cultured</topic><topic>Cryoelectron Microscopy</topic><topic>Epithelium</topic><topic>Epithelium - microbiology</topic><topic>Experimental Therapeutics</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Methicillin-Resistant Staphylococcus aureus</topic><topic>Methicillin-Resistant Staphylococcus aureus - drug effects</topic><topic>Methicillin-Resistant Staphylococcus aureus - pathogenicity</topic><topic>Mupirocin - pharmacology</topic><topic>Peptides</topic><topic>Peptides - pharmacology</topic><topic>Skin</topic><topic>Skin - microbiology</topic><topic>Staphylococcus aureus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haisma, Elisabeth M</creatorcontrib><creatorcontrib>Göblyös, Anikó</creatorcontrib><creatorcontrib>Ravensbergen, Bep</creatorcontrib><creatorcontrib>Adriaans, Alwin E</creatorcontrib><creatorcontrib>Cordfunke, Robert A</creatorcontrib><creatorcontrib>Schrumpf, Jasmijn</creatorcontrib><creatorcontrib>Limpens, Ronald W A L</creatorcontrib><creatorcontrib>Schimmel, Kirsten J M</creatorcontrib><creatorcontrib>den Hartigh, Jan</creatorcontrib><creatorcontrib>Hiemstra, Pieter S</creatorcontrib><creatorcontrib>Drijfhout, Jan Wouter</creatorcontrib><creatorcontrib>El Ghalbzouri, Abdoelwaheb</creatorcontrib><creatorcontrib>Nibbering, Peter H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial agents and chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haisma, Elisabeth M</au><au>Göblyös, Anikó</au><au>Ravensbergen, Bep</au><au>Adriaans, Alwin E</au><au>Cordfunke, Robert A</au><au>Schrumpf, Jasmijn</au><au>Limpens, Ronald W A L</au><au>Schimmel, Kirsten J M</au><au>den Hartigh, Jan</au><au>Hiemstra, Pieter S</au><au>Drijfhout, Jan Wouter</au><au>El Ghalbzouri, Abdoelwaheb</au><au>Nibbering, Peter H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimicrobial Peptide P60.4Ac-Containing Creams and Gel for Eradication of Methicillin-Resistant Staphylococcus aureus from Cultured Skin and Airway Epithelial Surfaces</atitle><jtitle>Antimicrobial agents and chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>60</volume><issue>7</issue><spage>4063</spage><epage>4072</epage><pages>4063-4072</pages><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>We previously found the LL-37-derived peptide P60.4Ac to be effective against methicillin-resistant Staphylococcus aureus (MRSA) on human epidermal models (EMs). The goal of this study was to identify the preferred carrier for this peptide for topical application on skin and mucosal surfaces. We prepared P60.4Ac in three formulations, i.e., a water-in-oil cream with lanolin (Softisan 649), an oil-in-water cream with polyethylene glycol hexadecyl ether (Cetomacrogol), and a hydroxypropyl methylcellulose (hypromellose) 4000 gel. We tested the antimicrobial efficacy of the peptide in these formulations against mupirocin-resistant and -sensitive MRSA strains on EMs and bronchial epithelial models (BEMs). The cytotoxic effects of formulated P60.4Ac on these models were determined using histology and WST-1 and lactate dehydrogenase assays. Moreover, we assessed the stability of the peptide in these formulations with storage for up to 3 months. Killing of MRSA by P60.4Ac in the two creams was less effective than that by P60.4Ac in the hypromellose gel. In agreement with those findings, P60.4Ac in the hypromellose gel was highly effective in eradicating the two MRSA strains from EMs. We found that even 0.1% (wt/wt) P60.4Ac in the hypromellose gel killed >99% of the viable planktonic bacteria and >85% of the biofilm-associated bacteria on EMs. Hypromellose gels containing 0.1% and 0.5% (wt/wt) P60.4Ac effectively reduced the numbers of viable MRSA cells from BEMs by >90%. No cytotoxic effects of P60.4Ac in the hypromellose gel with up to 2% (wt/wt) P60.4Ac on keratinocytes in EMs and in the hypromellose gel with up to 0.5% (wt/wt) P60.4Ac on epithelial cells in BEMs were observed. High-performance liquid chromatography analysis showed that P60.4Ac was stable in the Softisan cream and the hypromellose gel but not in the Cetomacrogol cream. We conclude that P60.4Ac formulated in hypromellose gel is both stable and highly effective in eradicating MRSA from colonized EMs and BEMs.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>27114278</pmid><doi>10.1128/AAC.03001-15</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0066-4804 |
ispartof | Antimicrobial agents and chemotherapy, 2016-07, Vol.60 (7), p.4063-4072 |
issn | 0066-4804 1098-6596 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4914645 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Anti-Bacterial Agents Anti-Bacterial Agents - pharmacology Anti-Infective Agents - pharmacology Bronchi - cytology Cells, Cultured Cryoelectron Microscopy Epithelium Epithelium - microbiology Experimental Therapeutics Humans In Vitro Techniques Methicillin-Resistant Staphylococcus aureus Methicillin-Resistant Staphylococcus aureus - drug effects Methicillin-Resistant Staphylococcus aureus - pathogenicity Mupirocin - pharmacology Peptides Peptides - pharmacology Skin Skin - microbiology Staphylococcus aureus |
title | Antimicrobial Peptide P60.4Ac-Containing Creams and Gel for Eradication of Methicillin-Resistant Staphylococcus aureus from Cultured Skin and Airway Epithelial Surfaces |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T01%3A13%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antimicrobial%20Peptide%20P60.4Ac-Containing%20Creams%20and%20Gel%20for%20Eradication%20of%20Methicillin-Resistant%20Staphylococcus%20aureus%20from%20Cultured%20Skin%20and%20Airway%20Epithelial%20Surfaces&rft.jtitle=Antimicrobial%20agents%20and%20chemotherapy&rft.au=Haisma,%20Elisabeth%20M&rft.date=2016-07-01&rft.volume=60&rft.issue=7&rft.spage=4063&rft.epage=4072&rft.pages=4063-4072&rft.issn=0066-4804&rft.eissn=1098-6596&rft_id=info:doi/10.1128/AAC.03001-15&rft_dat=%3Cproquest_pubme%3E1808679271%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1808679271&rft_id=info:pmid/27114278&rfr_iscdi=true |