High Bactericidal Self-Assembled Nano-Monolayer of Silver Sulfadiazine on Hydroxylated Material Surfaces.
Identifieur interne : 000238 ( Main/Corpus ); précédent : 000237; suivant : 000239High Bactericidal Self-Assembled Nano-Monolayer of Silver Sulfadiazine on Hydroxylated Material Surfaces.
Auteurs : Angelo Taglietti ; Giacomo Dacarro ; Daniele Barbieri ; Lucia Cucca ; Pietro Grisoli ; Maddalena Patrini ; Carla Renata Arciola ; Piersandro PallaviciniSource :
- Materials (Basel, Switzerland) [ 1996-1944 ] ; 2019.
Abstract
Anti-infective surfaces are a modern strategy to address the issue of infection related to the clinical use of materials for implants and medical devices. Nanocoatings, with their high surface/mass ratio, lend themselves to being mono-layered on the material surfaces to release antibacterial molecules and prevent bacterial adhesion. Here, a "layer-by-layer" (LbL) approach to achieve a self-assembled monolayer (SAM) with high microbicidal effect on hydroxylated surfaces is presented, exploiting the reaction between a monolayer of thiolic functions on glass/quartz surfaces and a newly synthesized derivative of the well-known antibacterial compound silver sulfadiazine. Using several different techniques, it is demonstrated that a nano-monolayer of silver sulfadiazine is formed on the surfaces. The surface-functionalized materials showed efficient bactericidal effect against both Gram-positive and Gram-negative bacteria. Interestingly, bactericidal self-assembled nano-monolayers of silver sulfadiazine could be achieved on a large variety of materials by simply pre-depositing glass-like SiO2 films on their surfaces.
DOI: 10.3390/ma12172761
PubMed: 31466275
PubMed Central: PMC6748069
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Volta", Università di Pavia, via Bassi 6, 27100 Pavia, Italy.</nlm:affiliation></affiliation></author><author><name sortKey="Arciola, Carla Renata" sort="Arciola, Carla Renata" uniqKey="Arciola C" first="Carla Renata" last="Arciola">Carla Renata Arciola</name><affiliation><nlm:affiliation>Laboratorio di Patologia delle Infezioni Associate all'Impianto, IRCCS Istituto Ortopedico Rizzoli, via di Barbiano 1/10, 40136 Bologna, Italy. carlarenata.arciola@ior.it.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, via San Giacomo 14, 40126 Bologna, Italy. carlarenata.arciola@ior.it.</nlm:affiliation></affiliation></author><author><name sortKey="Pallavicini, Piersandro" sort="Pallavicini, Piersandro" uniqKey="Pallavicini P" first="Piersandro" last="Pallavicini">Piersandro Pallavicini</name><affiliation><nlm:affiliation>Dipartimento di Chimica, Sezione di Chimica Generale, Università di Pavia, viale Taramelli 12, 27100 Pavia, Italy.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Materials (Basel, Switzerland)</title><idno type="ISSN">1996-1944</idno><imprint><date when="2019" type="published">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Anti-infective surfaces are a modern strategy to address the issue of infection related to the clinical use of materials for implants and medical devices. Nanocoatings, with their high surface/mass ratio, lend themselves to being mono-layered on the material surfaces to release antibacterial molecules and prevent bacterial adhesion. Here, a "layer-by-layer" (LbL) approach to achieve a self-assembled monolayer (SAM) with high microbicidal effect on hydroxylated surfaces is presented, exploiting the reaction between a monolayer of thiolic functions on glass/quartz surfaces and a newly synthesized derivative of the well-known antibacterial compound silver sulfadiazine. Using several different techniques, it is demonstrated that a nano-monolayer of silver sulfadiazine is formed on the surfaces. The surface-functionalized materials showed efficient bactericidal effect against both Gram-positive and Gram-negative bacteria. Interestingly, bactericidal self-assembled nano-monolayers of silver sulfadiazine could be achieved on a large variety of materials by simply pre-depositing glass-like SiO<sub>2</sub> films on their surfaces.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">31466275</PMID><DateRevised><Year>2020</Year><Month>10</Month><Day>01</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Print">1996-1944</ISSN><JournalIssue CitedMedium="Print"><Volume>12</Volume><Issue>17</Issue><PubDate><Year>2019</Year><Month>Aug</Month><Day>28</Day></PubDate></JournalIssue><Title>Materials (Basel, Switzerland)</Title><ISOAbbreviation>Materials (Basel)</ISOAbbreviation></Journal><ArticleTitle>High Bactericidal Self-Assembled Nano-Monolayer of Silver Sulfadiazine on Hydroxylated Material Surfaces.</ArticleTitle><ELocationID EIdType="pii" ValidYN="Y">E2761</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.3390/ma12172761</ELocationID><Abstract><AbstractText>Anti-infective surfaces are a modern strategy to address the issue of infection related to the clinical use of materials for implants and medical devices. Nanocoatings, with their high surface/mass ratio, lend themselves to being mono-layered on the material surfaces to release antibacterial molecules and prevent bacterial adhesion. Here, a "layer-by-layer" (LbL) approach to achieve a self-assembled monolayer (SAM) with high microbicidal effect on hydroxylated surfaces is presented, exploiting the reaction between a monolayer of thiolic functions on glass/quartz surfaces and a newly synthesized derivative of the well-known antibacterial compound silver sulfadiazine. Using several different techniques, it is demonstrated that a nano-monolayer of silver sulfadiazine is formed on the surfaces. The surface-functionalized materials showed efficient bactericidal effect against both Gram-positive and Gram-negative bacteria. Interestingly, bactericidal self-assembled nano-monolayers of silver sulfadiazine could be achieved on a large variety of materials by simply pre-depositing glass-like SiO<sub>2</sub> films on their surfaces.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Taglietti</LastName><ForeName>Angelo</ForeName><Initials>A</Initials><Identifier Source="ORCID">0000-0003-0141-9201</Identifier><AffiliationInfo><Affiliation>Dipartimento di Chimica, Sezione di Chimica Generale, Università di Pavia, viale Taramelli 12, 27100 Pavia, Italy. angelo.taglietti@unipv.it.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Dacarro</LastName><ForeName>Giacomo</ForeName><Initials>G</Initials><Identifier Source="ORCID">0000-0002-8928-4972</Identifier><AffiliationInfo><Affiliation>Dipartimento di Chimica, Sezione di Chimica Generale, Università di Pavia, viale Taramelli 12, 27100 Pavia, Italy. giacomo.dacarro@unipv.it.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Barbieri</LastName><ForeName>Daniele</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Dipartimento di Chimica, Sezione di Chimica Generale, Università di Pavia, viale Taramelli 12, 27100 Pavia, Italy.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cucca</LastName><ForeName>Lucia</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Dipartimento di Chimica, Sezione di Chimica Generale, Università di Pavia, viale Taramelli 12, 27100 Pavia, Italy.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Grisoli</LastName><ForeName>Pietro</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Dipartimento di Scienze del Farmaco, Università di Pavia, viale Taramelli 10, 27100 Pavia, Italy.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Patrini</LastName><ForeName>Maddalena</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Dipartimento di Fisica, "A. Volta", Università di Pavia, via Bassi 6, 27100 Pavia, Italy.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Arciola</LastName><ForeName>Carla Renata</ForeName><Initials>CR</Initials><Identifier Source="ORCID">0000-0003-0382-0066</Identifier><AffiliationInfo><Affiliation>Laboratorio di Patologia delle Infezioni Associate all'Impianto, IRCCS Istituto Ortopedico Rizzoli, via di Barbiano 1/10, 40136 Bologna, Italy. carlarenata.arciola@ior.it.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, via San Giacomo 14, 40126 Bologna, Italy. carlarenata.arciola@ior.it.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Pallavicini</LastName><ForeName>Piersandro</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Dipartimento di Chimica, Sezione di Chimica Generale, Università di Pavia, viale Taramelli 12, 27100 Pavia, Italy.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2019</Year><Month>08</Month><Day>28</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Materials (Basel)</MedlineTA><NlmUniqueID>101555929</NlmUniqueID><ISSNLinking>1996-1944</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">anti-infective materials</Keyword><Keyword MajorTopicYN="N">antimicrobial</Keyword><Keyword MajorTopicYN="N">nanocoatings</Keyword><Keyword MajorTopicYN="N">self-assembled monolayer</Keyword><Keyword MajorTopicYN="N">sulfadiazine</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2019</Year><Month>07</Month><Day>14</Day></PubMedPubDate><PubMedPubDate 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