Tin-containing fluoride solutions as anti-erosive agents in enamel: an in vitro tin-uptake, tissue-loss, and scanning electron micrograph study.
Identifieur interne : 000356 ( Main/Exploration ); précédent : 000355; suivant : 000357Tin-containing fluoride solutions as anti-erosive agents in enamel: an in vitro tin-uptake, tissue-loss, and scanning electron micrograph study.
Auteurs : Nadine Schlueter [Allemagne] ; Martin Hardt ; Adrian Lussi ; Frank Engelmann ; Joachim Klimek ; Carolina GanssSource :
- European journal of oral sciences [ 1600-0722 ] ; 2009.
Descripteurs français
- KwdFr :
- Cariostatiques (administration et posologie), Cariostatiques (usage thérapeutique), Composés de l'étain (usage thérapeutique), Diamines (usage thérapeutique), Déminéralisation dentaire (anatomopathologie), Déminéralisation dentaire (prévention et contrôle), Déminéralisation dentaire (étiologie), Fluorure de sodium (usage thérapeutique), Fluorures (usage thérapeutique), Fluorures d'étain (administration et posologie), Fluorures d'étain (usage thérapeutique), Humains (MeSH), Microanalyse par sonde électronique (MeSH), Microscopie électronique à balayage (MeSH), Reminéralisation des dents (MeSH), Solubilité de l'émail dentaire (effets des médicaments et des substances chimiques), Émail dentaire (effets des médicaments et des substances chimiques), Émail dentaire (métabolisme), Émail dentaire (ultrastructure), Érosion dentaire (anatomopathologie), Érosion dentaire (prévention et contrôle), Étain (pharmacocinétique).
- MESH :
- administration et posologie : Cariostatiques, Fluorures d'étain.
- anatomopathologie : Déminéralisation dentaire, Érosion dentaire.
- effets des médicaments et des substances chimiques : Solubilité de l'émail dentaire, Émail dentaire.
- métabolisme : Émail dentaire.
- pharmacocinétique : Étain.
- prévention et contrôle : Déminéralisation dentaire, Érosion dentaire.
- usage thérapeutique : Cariostatiques, Composés de l'étain, Diamines, Fluorure de sodium, Fluorures, Fluorures d'étain, Émail dentaire.
- étiologie : Déminéralisation dentaire.
- Humains, Microanalyse par sonde électronique, Microscopie électronique à balayage, Reminéralisation des dents.
English descriptors
- KwdEn :
- Cariostatic Agents (administration & dosage), Cariostatic Agents (therapeutic use), Dental Enamel (drug effects), Dental Enamel (metabolism), Dental Enamel (ultrastructure), Dental Enamel Solubility (drug effects), Diamines (therapeutic use), Electron Probe Microanalysis (MeSH), Fluorides (therapeutic use), Humans (MeSH), Microscopy, Electron, Scanning (MeSH), Sodium Fluoride (therapeutic use), Tin (pharmacokinetics), Tin Compounds (therapeutic use), Tin Fluorides (administration & dosage), Tin Fluorides (therapeutic use), Tooth Demineralization (etiology), Tooth Demineralization (pathology), Tooth Demineralization (prevention & control), Tooth Erosion (pathology), Tooth Erosion (prevention & control), Tooth Remineralization (MeSH).
- MESH :
- chemical , administration & dosage : Cariostatic Agents, Tin Fluorides.
- chemical , pharmacokinetics : Tin.
- chemical , therapeutic use : Cariostatic Agents, Diamines, Fluorides, Sodium Fluoride, Tin Compounds, Tin Fluorides.
- drug effects : Dental Enamel, Dental Enamel Solubility.
- etiology : Tooth Demineralization.
- metabolism : Dental Enamel.
- pathology : Tooth Demineralization, Tooth Erosion.
- prevention & control : Tooth Demineralization, Tooth Erosion.
- ultrastructure : Dental Enamel.
- Electron Probe Microanalysis, Humans, Microscopy, Electron, Scanning, Tooth Remineralization.
Abstract
Tin-containing fluoride solutions can reduce erosive tissue loss, but the effects of the reaction between tin and enamel are still not clear. During a 10-d period, enamel specimens were cyclically demineralized (0.05 M citric acid, pH 2.3, 6 x 5 min d(-1)) and remineralized (between the demineralization cycles and overnight). In the negative-control group, no further treatment was performed. Three groups were treated (2 x 2 min d(-1)) with tin-containing fluoride solutions (400, 1,400 or 2,100 ppm Sn2+, all 1,500 ppm F-, pH 4.5). Three additional groups were treated with test solutions twice daily, but without demineralization. Tissue loss was determined profilometrically. Energy-dispersive X-ray spectroscopy was used to measure the tin content on and within three layers (10 mum each) beneath the surface. In addition, scanning electron microscopy was conducted. All test preparations significantly reduced tissue loss. Deposition of tin on surfaces was higher without erosion than with erosion, but no incorporation of tin into enamel was found without demineralization. Under erosive conditions, both highly concentrated solutions led to the incorporation of tin up to a depth of 20 mum; the less-concentrated solution led to small amounts of tin in the outer 10 mum. The efficacy of tin-containing solutions seems to depend mainly on the incorporation of tin into enamel.
DOI: 10.1111/j.1600-0722.2009.00647.x
PubMed: 19627355
Affiliations:
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Giessen</wicri:regionArea><wicri:noRegion>Giessen</wicri:noRegion><wicri:noRegion>Giessen</wicri:noRegion><wicri:noRegion>Giessen</wicri:noRegion></affiliation></author><author><name sortKey="Hardt, Martin" sort="Hardt, Martin" uniqKey="Hardt M" first="Martin" last="Hardt">Martin Hardt</name></author><author><name sortKey="Lussi, Adrian" sort="Lussi, Adrian" uniqKey="Lussi A" first="Adrian" last="Lussi">Adrian Lussi</name></author><author><name sortKey="Engelmann, Frank" sort="Engelmann, Frank" uniqKey="Engelmann F" first="Frank" last="Engelmann">Frank Engelmann</name></author><author><name sortKey="Klimek, Joachim" sort="Klimek, Joachim" uniqKey="Klimek J" first="Joachim" last="Klimek">Joachim Klimek</name></author><author><name sortKey="Ganss, Carolina" sort="Ganss, Carolina" uniqKey="Ganss C" first="Carolina" last="Ganss">Carolina Ganss</name></author></analytic><series><title level="j">European journal of oral sciences</title><idno type="eISSN">1600-0722</idno><imprint><date 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(effets des médicaments et des substances chimiques)</term><term>Émail dentaire (effets des médicaments et des substances chimiques)</term><term>Émail dentaire (métabolisme)</term><term>Émail dentaire (ultrastructure)</term><term>Érosion dentaire (anatomopathologie)</term><term>Érosion dentaire (prévention et contrôle)</term><term>Étain (pharmacocinétique)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en"><term>Cariostatic Agents</term><term>Tin Fluorides</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacokinetics" xml:lang="en"><term>Tin</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Cariostatic Agents</term><term>Diamines</term><term>Fluorides</term><term>Sodium Fluoride</term><term>Tin Compounds</term><term>Tin Fluorides</term></keywords><keywords scheme="MESH" qualifier="administration et posologie" 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Scanning</term><term>Tooth Remineralization</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Humains</term><term>Microanalyse par sonde électronique</term><term>Microscopie électronique à balayage</term><term>Reminéralisation des dents</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Tin-containing fluoride solutions can reduce erosive tissue loss, but the effects of the reaction between tin and enamel are still not clear. During a 10-d period, enamel specimens were cyclically demineralized (0.05 M citric acid, pH 2.3, 6 x 5 min d(-1)) and remineralized (between the demineralization cycles and overnight). In the negative-control group, no further treatment was performed. Three groups were treated (2 x 2 min d(-1)) with tin-containing fluoride solutions (400, 1,400 or 2,100 ppm Sn2+, all 1,500 ppm F-, pH 4.5). Three additional groups were treated with test solutions twice daily, but without demineralization. Tissue loss was determined profilometrically. Energy-dispersive X-ray spectroscopy was used to measure the tin content on and within three layers (10 mum each) beneath the surface. In addition, scanning electron microscopy was conducted. All test preparations significantly reduced tissue loss. Deposition of tin on surfaces was higher without erosion than with erosion, but no incorporation of tin into enamel was found without demineralization. Under erosive conditions, both highly concentrated solutions led to the incorporation of tin up to a depth of 20 mum; the less-concentrated solution led to small amounts of tin in the outer 10 mum. The efficacy of tin-containing solutions seems to depend mainly on the incorporation of tin into enamel.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19627355</PMID><DateCompleted><Year>2009</Year><Month>11</Month><Day>02</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1600-0722</ISSN><JournalIssue CitedMedium="Internet"><Volume>117</Volume><Issue>4</Issue><PubDate><Year>2009</Year><Month>Aug</Month></PubDate></JournalIssue><Title>European journal of oral sciences</Title><ISOAbbreviation>Eur J Oral Sci</ISOAbbreviation></Journal><ArticleTitle>Tin-containing fluoride solutions as anti-erosive agents in enamel: an in vitro tin-uptake, tissue-loss, and scanning electron micrograph study.</ArticleTitle><Pagination><MedlinePgn>427-34</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1600-0722.2009.00647.x</ELocationID><Abstract><AbstractText>Tin-containing fluoride solutions can reduce erosive tissue loss, but the effects of the reaction between tin and enamel are still not clear. During a 10-d period, enamel specimens were cyclically demineralized (0.05 M citric acid, pH 2.3, 6 x 5 min d(-1)) and remineralized (between the demineralization cycles and overnight). In the negative-control group, no further treatment was performed. Three groups were treated (2 x 2 min d(-1)) with tin-containing fluoride solutions (400, 1,400 or 2,100 ppm Sn2+, all 1,500 ppm F-, pH 4.5). Three additional groups were treated with test solutions twice daily, but without demineralization. Tissue loss was determined profilometrically. Energy-dispersive X-ray spectroscopy was used to measure the tin content on and within three layers (10 mum each) beneath the surface. In addition, scanning electron microscopy was conducted. All test preparations significantly reduced tissue loss. Deposition of tin on surfaces was higher without erosion than with erosion, but no incorporation of tin into enamel was found without demineralization. Under erosive conditions, both highly concentrated solutions led to the incorporation of tin up to a depth of 20 mum; the less-concentrated solution led to small amounts of tin in the outer 10 mum. The efficacy of tin-containing solutions seems to depend mainly on the incorporation of tin into enamel.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Schlueter</LastName><ForeName>Nadine</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>Department of Conservative and Preventive Dentistry, Dental Clinic, Justus Liebig University Giessen, Giessen, Germany. nadine.schlueter@dentist.med.unigiessen.de</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hardt</LastName><ForeName>Martin</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Lussi</LastName><ForeName>Adrian</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Engelmann</LastName><ForeName>Frank</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Klimek</LastName><ForeName>Joachim</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Ganss</LastName><ForeName>Carolina</ForeName><Initials>C</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016449">Randomized Controlled Trial</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Eur J Oral Sci</MedlineTA><NlmUniqueID>9504563</NlmUniqueID><ISSNLinking>0909-8836</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D002327">Cariostatic Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D003959">Diamines</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D017971">Tin Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D014002">Tin Fluorides</NameOfSubstance></Chemical><Chemical><RegistryNumber>1BQV3749L5</RegistryNumber><NameOfSubstance UI="C023599">stannous chloride</NameOfSubstance></Chemical><Chemical><RegistryNumber>7440-31-5</RegistryNumber><NameOfSubstance UI="D014001">Tin</NameOfSubstance></Chemical><Chemical><RegistryNumber>8NY9L8837D</RegistryNumber><NameOfSubstance UI="C495399">Olaflur</NameOfSubstance></Chemical><Chemical><RegistryNumber>8ZYQ1474W7</RegistryNumber><NameOfSubstance UI="D012969">Sodium Fluoride</NameOfSubstance></Chemical><Chemical><RegistryNumber>Q80VPU408O</RegistryNumber><NameOfSubstance UI="D005459">Fluorides</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D002327" MajorTopicYN="N">Cariostatic Agents</DescriptorName><QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName><QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003743" MajorTopicYN="N">Dental Enamel</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003747" MajorTopicYN="N">Dental Enamel Solubility</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003959" MajorTopicYN="N">Diamines</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004577" MajorTopicYN="N">Electron Probe Microanalysis</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005459" MajorTopicYN="N">Fluorides</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008855" MajorTopicYN="N">Microscopy, Electron, Scanning</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012969" MajorTopicYN="N">Sodium Fluoride</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014001" MajorTopicYN="N">Tin</DescriptorName><QualifierName UI="Q000493" MajorTopicYN="Y">pharmacokinetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017971" MajorTopicYN="N">Tin Compounds</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014002" MajorTopicYN="N">Tin Fluorides</DescriptorName><QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName><QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017001" MajorTopicYN="N">Tooth Demineralization</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000517" MajorTopicYN="N">prevention & control</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014077" MajorTopicYN="N">Tooth Erosion</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000517" MajorTopicYN="Y">prevention & control</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014089" MajorTopicYN="N">Tooth Remineralization</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2009</Year><Month>7</Month><Day>25</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2009</Year><Month>7</Month><Day>25</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2009</Year><Month>11</Month><Day>3</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">19627355</ArticleId><ArticleId IdType="pii">EOS647</ArticleId><ArticleId IdType="doi">10.1111/j.1600-0722.2009.00647.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Allemagne</li></country></list><tree><noCountry><name sortKey="Engelmann, Frank" sort="Engelmann, Frank" uniqKey="Engelmann F" first="Frank" last="Engelmann">Frank Engelmann</name><name sortKey="Ganss, Carolina" sort="Ganss, Carolina" uniqKey="Ganss C" first="Carolina" last="Ganss">Carolina Ganss</name><name sortKey="Hardt, Martin" sort="Hardt, Martin" uniqKey="Hardt M" first="Martin" last="Hardt">Martin Hardt</name><name sortKey="Klimek, Joachim" sort="Klimek, Joachim" uniqKey="Klimek J" first="Joachim" last="Klimek">Joachim Klimek</name><name sortKey="Lussi, Adrian" sort="Lussi, Adrian" uniqKey="Lussi A" first="Adrian" last="Lussi">Adrian Lussi</name></noCountry><country name="Allemagne"><noRegion><name sortKey="Schlueter, Nadine" sort="Schlueter, Nadine" uniqKey="Schlueter N" first="Nadine" last="Schlueter">Nadine Schlueter</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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