Elucidation of Antimicrobial Activity of Non-Covalently Dispersed Carbon Nanotubes
Microorganisms have begun to develop resistance because of inappropriate and extensive use of antibiotics in the hospital setting. Therefore, it seems to be necessary to find a way to tackle these pathogens by developing new and effective antimicrobial agents. Carbon nanotubes (CNTs) have attracted...
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description | Microorganisms have begun to develop resistance because of inappropriate and extensive use of antibiotics in the hospital setting. Therefore, it seems to be necessary to find a way to tackle these pathogens by developing new and effective antimicrobial agents. Carbon nanotubes (CNTs) have attracted growing attention because of their remarkable mechanical strength, electrical properties, and chemical and thermal stability for their potential applications in the field of biomedical as therapeutic and diagnostic nanotools. However, the impact of carbon nanotubes on microbial growth has not been fully investigated. The primary purpose of this research study is to investigate the antimicrobial activity of CNTs, particularly double-walled and multi-walled nanotubes on representative pathogenic strains such as Gram-positive bacteria
, Gram-negative bacteria
,
, and fungal strain
. The dispersion ability of CNT types (double-walled and multi-walled) treated with a surfactant such as sodium dodecyl-benzenesulfonate (SDBS) and their impact on the microbial growth inhibition were also examined. A stock concentration 0.2 mg/mL of both double-walled and multi-walled CNTs was prepared homogenized by dispersing in surfactant solution by using probe sonication. UV-vis absorbance, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) were used for the characterization of CNTs dispersed in the surfactant solution to study the interaction between molecules of surfactant and CNTs. Later, scanning electron microscopy (SEM) was used to investigate how CNTs interact with the microbial cells. The antimicrobial activity was determined by analyzing optical density growth curves and viable cell count. This study revealed that microbial growth inhibited by non-covalently dispersed CNTs was both depend on the concentration and treatment time. In conclusion, the binding of surfactant molecules to the surface of CNTs increases its ability to disperse in aqueous solution. Non-covalent method of CNTs dispersion preserved their structure and increased microbial growth inhibition as a result. Multi-walled CNTs exhibited higher antimicrobial activity compared to double-walled CNTs against selected pathogens. |
doi_str_mv | 10.3390/ma13071676 |
format | Article |
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, Gram-negative bacteria
,
, and fungal strain
. The dispersion ability of CNT types (double-walled and multi-walled) treated with a surfactant such as sodium dodecyl-benzenesulfonate (SDBS) and their impact on the microbial growth inhibition were also examined. A stock concentration 0.2 mg/mL of both double-walled and multi-walled CNTs was prepared homogenized by dispersing in surfactant solution by using probe sonication. UV-vis absorbance, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) were used for the characterization of CNTs dispersed in the surfactant solution to study the interaction between molecules of surfactant and CNTs. Later, scanning electron microscopy (SEM) was used to investigate how CNTs interact with the microbial cells. The antimicrobial activity was determined by analyzing optical density growth curves and viable cell count. This study revealed that microbial growth inhibited by non-covalently dispersed CNTs was both depend on the concentration and treatment time. In conclusion, the binding of surfactant molecules to the surface of CNTs increases its ability to disperse in aqueous solution. Non-covalent method of CNTs dispersion preserved their structure and increased microbial growth inhibition as a result. Multi-walled CNTs exhibited higher antimicrobial activity compared to double-walled CNTs against selected pathogens.</description><identifier>ISSN: 1996-1944</identifier><identifier>EISSN: 1996-1944</identifier><identifier>DOI: 10.3390/ma13071676</identifier><identifier>PMID: 32260216</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antibiotics ; Antiinfectives and antibacterials ; Antimicrobial agents ; Aqueous solutions ; Bacteria ; Biocompatibility ; Carbon ; Carbon nanotubes ; Covalence ; Diagnostic systems ; Dispersion ; Electrical properties ; Electron microscopy ; Fourier transforms ; Gram-positive bacteria ; Klebsiella ; Membrane filters ; Microorganisms ; Nanomaterials ; Optical density ; Pathogens ; Pseudomonas aeruginosa ; Surfactants ; Thermal stability ; Transmission electron microscopy</subject><ispartof>Materials, 2020-04, Vol.13 (7), p.1676</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-98311ad348ee1c753dc5af433694d1efddbd50e0d53987b37c6843d90787caaf3</citedby><cites>FETCH-LOGICAL-c406t-98311ad348ee1c753dc5af433694d1efddbd50e0d53987b37c6843d90787caaf3</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/PMC7178397/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178397/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32260216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saleemi, Mansab Ali</creatorcontrib><creatorcontrib>Fouladi, Mohammad Hosseini</creatorcontrib><creatorcontrib>Yong, Phelim Voon Chen</creatorcontrib><creatorcontrib>Wong, Eng Hwa</creatorcontrib><title>Elucidation of Antimicrobial Activity of Non-Covalently Dispersed Carbon Nanotubes</title><title>Materials</title><addtitle>Materials (Basel)</addtitle><description>Microorganisms have begun to develop resistance because of inappropriate and extensive use of antibiotics in the hospital setting. Therefore, it seems to be necessary to find a way to tackle these pathogens by developing new and effective antimicrobial agents. Carbon nanotubes (CNTs) have attracted growing attention because of their remarkable mechanical strength, electrical properties, and chemical and thermal stability for their potential applications in the field of biomedical as therapeutic and diagnostic nanotools. However, the impact of carbon nanotubes on microbial growth has not been fully investigated. The primary purpose of this research study is to investigate the antimicrobial activity of CNTs, particularly double-walled and multi-walled nanotubes on representative pathogenic strains such as Gram-positive bacteria
, Gram-negative bacteria
,
, and fungal strain
. The dispersion ability of CNT types (double-walled and multi-walled) treated with a surfactant such as sodium dodecyl-benzenesulfonate (SDBS) and their impact on the microbial growth inhibition were also examined. A stock concentration 0.2 mg/mL of both double-walled and multi-walled CNTs was prepared homogenized by dispersing in surfactant solution by using probe sonication. UV-vis absorbance, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) were used for the characterization of CNTs dispersed in the surfactant solution to study the interaction between molecules of surfactant and CNTs. Later, scanning electron microscopy (SEM) was used to investigate how CNTs interact with the microbial cells. The antimicrobial activity was determined by analyzing optical density growth curves and viable cell count. This study revealed that microbial growth inhibited by non-covalently dispersed CNTs was both depend on the concentration and treatment time. In conclusion, the binding of surfactant molecules to the surface of CNTs increases its ability to disperse in aqueous solution. Non-covalent method of CNTs dispersion preserved their structure and increased microbial growth inhibition as a result. Multi-walled CNTs exhibited higher antimicrobial activity compared to double-walled CNTs against selected pathogens.</description><subject>Antibiotics</subject><subject>Antiinfectives and antibacterials</subject><subject>Antimicrobial agents</subject><subject>Aqueous solutions</subject><subject>Bacteria</subject><subject>Biocompatibility</subject><subject>Carbon</subject><subject>Carbon nanotubes</subject><subject>Covalence</subject><subject>Diagnostic systems</subject><subject>Dispersion</subject><subject>Electrical properties</subject><subject>Electron microscopy</subject><subject>Fourier transforms</subject><subject>Gram-positive bacteria</subject><subject>Klebsiella</subject><subject>Membrane filters</subject><subject>Microorganisms</subject><subject>Nanomaterials</subject><subject>Optical density</subject><subject>Pathogens</subject><subject>Pseudomonas aeruginosa</subject><subject>Surfactants</subject><subject>Thermal stability</subject><subject>Transmission electron microscopy</subject><issn>1996-1944</issn><issn>1996-1944</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkVtLxDAQhYMouqgv_gAp-CJCNem0SfMiLOt6gWUF0eeQJqlmaZs1aRf23xvvq3mZwHxzODMHoSOCzwE4vmglAcwIZXQLjQjnNCU8z7c3_nvoMIQFjg-AlBnfRXuQZRRnhI7Qw7QZlNWyt65LXJ2Mu962VnlXWdkkY9Xble3X752569KJW8nGdH2zTq5sWBofjE4m0ldxeC471w-VCQdop5ZNMIdfdR89XU8fJ7fp7P7mbjKepSrHtE95CYRIDXlpDFGsAK0KWecAlOeamFrrShfYYF0AL1kFTNEyB80xK5mSsoZ9dPmpuxyq1mgVfXnZiKW3rfRr4aQVfzudfRHPbiUYYSVwFgVOvwS8ex1M6EVrgzJNIzvjhiAyKBktONAioif_0IUbfBfX-6AKHJfhkTr7pOL9QvCm_jFDsHhPS_ymFeHjTfs_6Hc28AaXlJAL</recordid><startdate>20200403</startdate><enddate>20200403</enddate><creator>Saleemi, Mansab Ali</creator><creator>Fouladi, Mohammad Hosseini</creator><creator>Yong, Phelim Voon Chen</creator><creator>Wong, Eng Hwa</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200403</creationdate><title>Elucidation of Antimicrobial Activity of Non-Covalently Dispersed Carbon Nanotubes</title><author>Saleemi, Mansab Ali ; Fouladi, Mohammad Hosseini ; Yong, Phelim Voon Chen ; Wong, Eng Hwa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-98311ad348ee1c753dc5af433694d1efddbd50e0d53987b37c6843d90787caaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antibiotics</topic><topic>Antiinfectives and antibacterials</topic><topic>Antimicrobial agents</topic><topic>Aqueous solutions</topic><topic>Bacteria</topic><topic>Biocompatibility</topic><topic>Carbon</topic><topic>Carbon nanotubes</topic><topic>Covalence</topic><topic>Diagnostic systems</topic><topic>Dispersion</topic><topic>Electrical properties</topic><topic>Electron microscopy</topic><topic>Fourier transforms</topic><topic>Gram-positive bacteria</topic><topic>Klebsiella</topic><topic>Membrane filters</topic><topic>Microorganisms</topic><topic>Nanomaterials</topic><topic>Optical density</topic><topic>Pathogens</topic><topic>Pseudomonas aeruginosa</topic><topic>Surfactants</topic><topic>Thermal stability</topic><topic>Transmission electron microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saleemi, Mansab Ali</creatorcontrib><creatorcontrib>Fouladi, Mohammad Hosseini</creatorcontrib><creatorcontrib>Yong, Phelim Voon Chen</creatorcontrib><creatorcontrib>Wong, Eng Hwa</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saleemi, Mansab Ali</au><au>Fouladi, Mohammad Hosseini</au><au>Yong, Phelim Voon Chen</au><au>Wong, Eng Hwa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elucidation of Antimicrobial Activity of Non-Covalently Dispersed Carbon Nanotubes</atitle><jtitle>Materials</jtitle><addtitle>Materials (Basel)</addtitle><date>2020-04-03</date><risdate>2020</risdate><volume>13</volume><issue>7</issue><spage>1676</spage><pages>1676-</pages><issn>1996-1944</issn><eissn>1996-1944</eissn><abstract>Microorganisms have begun to develop resistance because of inappropriate and extensive use of antibiotics in the hospital setting. Therefore, it seems to be necessary to find a way to tackle these pathogens by developing new and effective antimicrobial agents. Carbon nanotubes (CNTs) have attracted growing attention because of their remarkable mechanical strength, electrical properties, and chemical and thermal stability for their potential applications in the field of biomedical as therapeutic and diagnostic nanotools. However, the impact of carbon nanotubes on microbial growth has not been fully investigated. The primary purpose of this research study is to investigate the antimicrobial activity of CNTs, particularly double-walled and multi-walled nanotubes on representative pathogenic strains such as Gram-positive bacteria
, Gram-negative bacteria
,
, and fungal strain
. The dispersion ability of CNT types (double-walled and multi-walled) treated with a surfactant such as sodium dodecyl-benzenesulfonate (SDBS) and their impact on the microbial growth inhibition were also examined. A stock concentration 0.2 mg/mL of both double-walled and multi-walled CNTs was prepared homogenized by dispersing in surfactant solution by using probe sonication. UV-vis absorbance, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) were used for the characterization of CNTs dispersed in the surfactant solution to study the interaction between molecules of surfactant and CNTs. Later, scanning electron microscopy (SEM) was used to investigate how CNTs interact with the microbial cells. The antimicrobial activity was determined by analyzing optical density growth curves and viable cell count. This study revealed that microbial growth inhibited by non-covalently dispersed CNTs was both depend on the concentration and treatment time. In conclusion, the binding of surfactant molecules to the surface of CNTs increases its ability to disperse in aqueous solution. Non-covalent method of CNTs dispersion preserved their structure and increased microbial growth inhibition as a result. Multi-walled CNTs exhibited higher antimicrobial activity compared to double-walled CNTs against selected pathogens.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>32260216</pmid><doi>10.3390/ma13071676</doi><oa>free_for_read</oa></addata></record> |
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subjects | Antibiotics Antiinfectives and antibacterials Antimicrobial agents Aqueous solutions Bacteria Biocompatibility Carbon Carbon nanotubes Covalence Diagnostic systems Dispersion Electrical properties Electron microscopy Fourier transforms Gram-positive bacteria Klebsiella Membrane filters Microorganisms Nanomaterials Optical density Pathogens Pseudomonas aeruginosa Surfactants Thermal stability Transmission electron microscopy |
title | Elucidation of Antimicrobial Activity of Non-Covalently Dispersed Carbon Nanotubes |
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