Development of an Antifungal Denture Adhesive Film for Oral Candidiasis Utilizing Hot Melt Extrusion Technology
Identifieur interne : 002638 ( Pmc/Corpus ); précédent : 002637; suivant : 002639Development of an Antifungal Denture Adhesive Film for Oral Candidiasis Utilizing Hot Melt Extrusion Technology
Auteurs : Jun-Bom Park ; Suneela Prodduturi ; Joe Morott ; Vijay I. Kulkarni ; Melissa R. Jacob ; Shabana I. Khan ; Steven P. Stodghill ; Michael A. RepkaSource :
- Expert opinion on drug delivery [ 1742-5247 ] ; 2014.
Abstract
The overall goal of this research was to produce a stable hot-melt extruded “Antifungal Denture Adhesive film” (ADA) system for the treatment of oral candidiasis.
The ADA systems with hydroxypropyl cellulose (HPC) and/or polyethylene oxide (PEO) containing clotrimazole (10%) or nystatin (10%) were extruded utilizing a lab scale twin-screw hot-melt extruder. Rolls of the antifungal-containing films were collected and subsequently die-cut into shapes adapted for a maxillary (upper) and mandibular (lower) denture.
DSC and PXRD results indicated that the crystallinity of both APIs was changed to amorphous phase after hot-melt extrusion. The ADA system, containing blends of HPC and PEO, enhanced the effectiveness of the antimicrobials a maximum of 5-fold toward the inhibition of cell adherence of
Based on these findings, the ADA system may be used for primary, prophylaxis or adjunct treatment of oral or pharyngeal candidiasis via controlled-release of the antifungal agent from the polymer matrix.
Url:
DOI: 10.1517/17425247.2014.949235
PubMed: 25169007
PubMed Central: 5629914
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PMC:5629914Le document en format XML
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<author><name sortKey="Park, Jun Bom" sort="Park, Jun Bom" uniqKey="Park J" first="Jun-Bom" last="Park">Jun-Bom Park</name>
<affiliation><nlm:aff id="A1">Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, MS, USA</nlm:aff>
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<author><name sortKey="Prodduturi, Suneela" sort="Prodduturi, Suneela" uniqKey="Prodduturi S" first="Suneela" last="Prodduturi">Suneela Prodduturi</name>
<affiliation><nlm:aff id="A1">Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, MS, USA</nlm:aff>
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<author><name sortKey="Morott, Joe" sort="Morott, Joe" uniqKey="Morott J" first="Joe" last="Morott">Joe Morott</name>
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<author><name sortKey="Kulkarni, Vijay I" sort="Kulkarni, Vijay I" uniqKey="Kulkarni V" first="Vijay I." last="Kulkarni">Vijay I. Kulkarni</name>
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<author><name sortKey="Khan, Shabana I" sort="Khan, Shabana I" uniqKey="Khan S" first="Shabana I." last="Khan">Shabana I. Khan</name>
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<author><name sortKey="Stodghill, Steven P" sort="Stodghill, Steven P" uniqKey="Stodghill S" first="Steven P." last="Stodghill">Steven P. Stodghill</name>
<affiliation><nlm:aff id="A3">Department of Pharmaceutical, Social & Administrative Sciences, Belmont University College of Pharmacy, 1900 Belmont Boulevard, Nashville, TN, USA</nlm:aff>
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<author><name sortKey="Repka, Michael A" sort="Repka, Michael A" uniqKey="Repka M" first="Michael A." last="Repka">Michael A. Repka</name>
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<affiliation><nlm:aff id="A1">Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, MS, USA</nlm:aff>
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<author><name sortKey="Prodduturi, Suneela" sort="Prodduturi, Suneela" uniqKey="Prodduturi S" first="Suneela" last="Prodduturi">Suneela Prodduturi</name>
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<author><name sortKey="Morott, Joe" sort="Morott, Joe" uniqKey="Morott J" first="Joe" last="Morott">Joe Morott</name>
<affiliation><nlm:aff id="A1">Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, MS, USA</nlm:aff>
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<author><name sortKey="Kulkarni, Vijay I" sort="Kulkarni, Vijay I" uniqKey="Kulkarni V" first="Vijay I." last="Kulkarni">Vijay I. Kulkarni</name>
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</affiliation>
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<author><name sortKey="Jacob, Melissa R" sort="Jacob, Melissa R" uniqKey="Jacob M" first="Melissa R." last="Jacob">Melissa R. Jacob</name>
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</affiliation>
</author>
<author><name sortKey="Khan, Shabana I" sort="Khan, Shabana I" uniqKey="Khan S" first="Shabana I." last="Khan">Shabana I. Khan</name>
<affiliation><nlm:aff id="A2">National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS, USA</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Stodghill, Steven P" sort="Stodghill, Steven P" uniqKey="Stodghill S" first="Steven P." last="Stodghill">Steven P. Stodghill</name>
<affiliation><nlm:aff id="A3">Department of Pharmaceutical, Social & Administrative Sciences, Belmont University College of Pharmacy, 1900 Belmont Boulevard, Nashville, TN, USA</nlm:aff>
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<author><name sortKey="Repka, Michael A" sort="Repka, Michael A" uniqKey="Repka M" first="Michael A." last="Repka">Michael A. Repka</name>
<affiliation><nlm:aff id="A1">Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, MS, USA</nlm:aff>
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<series><title level="j">Expert opinion on drug delivery</title>
<idno type="ISSN">1742-5247</idno>
<idno type="eISSN">1744-7593</idno>
<imprint><date when="2014">2014</date>
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<front><div type="abstract" xml:lang="en"><sec id="S1"><title>Objectives</title>
<p id="P1">The overall goal of this research was to produce a stable hot-melt extruded “Antifungal Denture Adhesive film” (ADA) system for the treatment of oral candidiasis.</p>
</sec>
<sec id="S2"><title>Methods</title>
<p id="P2">The ADA systems with hydroxypropyl cellulose (HPC) and/or polyethylene oxide (PEO) containing clotrimazole (10%) or nystatin (10%) were extruded utilizing a lab scale twin-screw hot-melt extruder. Rolls of the antifungal-containing films were collected and subsequently die-cut into shapes adapted for a maxillary (upper) and mandibular (lower) denture.</p>
</sec>
<sec id="S3"><title>Results</title>
<p id="P3">DSC and PXRD results indicated that the crystallinity of both APIs was changed to amorphous phase after hot-melt extrusion. The ADA system, containing blends of HPC and PEO, enhanced the effectiveness of the antimicrobials a maximum of 5-fold toward the inhibition of cell adherence of <italic>C. albicans</italic>
to mammalian cells/Vero cells. Remarkably, a combination of the two polymers without drug also demonstrated a 38% decrease in cell adhesion to the fungi due to the viscosity and the flexibility of the polymers. Drug-release profiles indicated that both drug concentrations were above the minimum inhibitory concentration (MIC) for <italic>C. albicans</italic>
within 10 minutes and was maintained for over 10 hours. In addition, based on the IC<sub>50</sub>
and MIC values, it was observed that the antifungal activities of both drugs were increased significantly in the ADA systems.</p>
</sec>
<sec id="S4"><title>Conclusions</title>
<p id="P4">Based on these findings, the ADA system may be used for primary, prophylaxis or adjunct treatment of oral or pharyngeal candidiasis via controlled-release of the antifungal agent from the polymer matrix.</p>
</sec>
</div>
</front>
</TEI>
<pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-journal-id">101228421</journal-id>
<journal-id journal-id-type="pubmed-jr-id">32621</journal-id>
<journal-id journal-id-type="nlm-ta">Expert Opin Drug Deliv</journal-id>
<journal-id journal-id-type="iso-abbrev">Expert Opin Drug Deliv</journal-id>
<journal-title-group><journal-title>Expert opinion on drug delivery</journal-title>
</journal-title-group>
<issn pub-type="ppub">1742-5247</issn>
<issn pub-type="epub">1744-7593</issn>
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<article-meta><article-id pub-id-type="pmid">25169007</article-id>
<article-id pub-id-type="pmc">5629914</article-id>
<article-id pub-id-type="doi">10.1517/17425247.2014.949235</article-id>
<article-id pub-id-type="manuscript">NIHMS908193</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Development of an Antifungal Denture Adhesive Film for Oral Candidiasis Utilizing Hot Melt Extrusion Technology</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Park</surname>
<given-names>Jun-Bom</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Prodduturi</surname>
<given-names>Suneela</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Morott</surname>
<given-names>Joe</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Kulkarni</surname>
<given-names>Vijay I.</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Jacob</surname>
<given-names>Melissa R.</given-names>
</name>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Khan</surname>
<given-names>Shabana I.</given-names>
</name>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Stodghill</surname>
<given-names>Steven P.</given-names>
</name>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Repka</surname>
<given-names>Michael A.</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A4">4</xref>
<xref rid="FN1" ref-type="author-notes">*</xref>
</contrib>
</contrib-group>
<aff id="A1"><label>1</label>
Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, MS, USA</aff>
<aff id="A2"><label>2</label>
National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS, USA</aff>
<aff id="A3"><label>3</label>
Department of Pharmaceutical, Social & Administrative Sciences, Belmont University College of Pharmacy, 1900 Belmont Boulevard, Nashville, TN, USA</aff>
<aff id="A4"><label>4</label>
Pii Center for Pharmaceutical Technology, School of Pharmacy, The University of Mississippi, University, MS, USA</aff>
<author-notes><corresp id="FN1"><label>*</label>
Address for correspondence: Michael A. Repka, D.D.S., Ph.D., Professor and Chair, Department of Pharmaceutics, Director, Pii Center for Pharmaceutical Technology, School of Pharmacy, The University of Mississippi, University, MS 38677, Phone: 662-915-1155, Fax: 662-915-1177, <email>marepka@olemiss.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted"><day>26</day>
<month>9</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub"><day>29</day>
<month>8</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="ppub"><month>1</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>06</day>
<month>10</month>
<year>2017</year>
</pub-date>
<volume>12</volume>
<issue>1</issue>
<fpage>1</fpage>
<lpage>13</lpage>
<pmc-comment>elocation-id from pubmed: 10.1517/17425247.2014.949235</pmc-comment>
<abstract><sec id="S1"><title>Objectives</title>
<p id="P1">The overall goal of this research was to produce a stable hot-melt extruded “Antifungal Denture Adhesive film” (ADA) system for the treatment of oral candidiasis.</p>
</sec>
<sec id="S2"><title>Methods</title>
<p id="P2">The ADA systems with hydroxypropyl cellulose (HPC) and/or polyethylene oxide (PEO) containing clotrimazole (10%) or nystatin (10%) were extruded utilizing a lab scale twin-screw hot-melt extruder. Rolls of the antifungal-containing films were collected and subsequently die-cut into shapes adapted for a maxillary (upper) and mandibular (lower) denture.</p>
</sec>
<sec id="S3"><title>Results</title>
<p id="P3">DSC and PXRD results indicated that the crystallinity of both APIs was changed to amorphous phase after hot-melt extrusion. The ADA system, containing blends of HPC and PEO, enhanced the effectiveness of the antimicrobials a maximum of 5-fold toward the inhibition of cell adherence of <italic>C. albicans</italic>
to mammalian cells/Vero cells. Remarkably, a combination of the two polymers without drug also demonstrated a 38% decrease in cell adhesion to the fungi due to the viscosity and the flexibility of the polymers. Drug-release profiles indicated that both drug concentrations were above the minimum inhibitory concentration (MIC) for <italic>C. albicans</italic>
within 10 minutes and was maintained for over 10 hours. In addition, based on the IC<sub>50</sub>
and MIC values, it was observed that the antifungal activities of both drugs were increased significantly in the ADA systems.</p>
</sec>
<sec id="S4"><title>Conclusions</title>
<p id="P4">Based on these findings, the ADA system may be used for primary, prophylaxis or adjunct treatment of oral or pharyngeal candidiasis via controlled-release of the antifungal agent from the polymer matrix.</p>
</sec>
</abstract>
<kwd-group><kwd>Oral candidiasis</kwd>
<kwd>Hot-melt extrusion</kwd>
<kwd>Bioadhesive film</kwd>
<kwd>Hydroxypropyl cellulose</kwd>
<kwd>Polyethylene oxide</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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