Interaction of various pectin formulations with porcine colonic tissues

Pectins of low and high degrees of esterification, as well as pectin derivatives carrying primary amines, were investigate for gel forming ability with mucosal tissues. The combination of scanning electronic microscopy and small deformation dynamic mechanical studies revealed that pectins with highe...

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Veröffentlicht in:Biomaterials 2005-10, Vol.26 (29), p.5907-5916
Hauptverfasser: Liu, LinShu, Fishman, Marshall L., Hicks, Kevin B., Kende, Meir
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container_end_page 5916
container_issue 29
container_start_page 5907
container_title Biomaterials
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creator Liu, LinShu
Fishman, Marshall L.
Hicks, Kevin B.
Kende, Meir
description Pectins of low and high degrees of esterification, as well as pectin derivatives carrying primary amines, were investigate for gel forming ability with mucosal tissues. The combination of scanning electronic microscopy and small deformation dynamic mechanical studies revealed that pectins with higher net electrical charges are more bioadhesive than the less charged ones. Both the negatively charged pectin formulation, P-25, and the positively charged formulation, P-N, were able to synergize with the mucus to produce rheologically strengthened gels. The highly esterified pectin, P-94, also synergized with the mucosal glycoproteins to form a gel structure via coil entanglements. The ex vivo studies further confirmed the microstructures of mucus gel networks with adsorbed pectins. When incubated with porcine intestinal mucus membrane, P-94 gels were found generally bound to the lumen area, P-25 gels were able to penetrate deeply near the wall area, P-N gels interacted with mucins via electrostatic bonding and dispersed into the whole area from the lumen to the wall. Hence, both P-N and P-94, by enhancing the protective barrier properties of mucus systems, may be useful alternatives for the treatment of mucus related irritation and infection. In drug-delivery systems, P-N and P-25 would deliver incorporated drugs mainly by pectin dissolution, while a diffusion mechanism would release drugs from P-94 gels.
doi_str_mv 10.1016/j.biomaterials.2005.03.005
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The combination of scanning electronic microscopy and small deformation dynamic mechanical studies revealed that pectins with higher net electrical charges are more bioadhesive than the less charged ones. Both the negatively charged pectin formulation, P-25, and the positively charged formulation, P-N, were able to synergize with the mucus to produce rheologically strengthened gels. The highly esterified pectin, P-94, also synergized with the mucosal glycoproteins to form a gel structure via coil entanglements. The ex vivo studies further confirmed the microstructures of mucus gel networks with adsorbed pectins. When incubated with porcine intestinal mucus membrane, P-94 gels were found generally bound to the lumen area, P-25 gels were able to penetrate deeply near the wall area, P-N gels interacted with mucins via electrostatic bonding and dispersed into the whole area from the lumen to the wall. Hence, both P-N and P-94, by enhancing the protective barrier properties of mucus systems, may be useful alternatives for the treatment of mucus related irritation and infection. 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The combination of scanning electronic microscopy and small deformation dynamic mechanical studies revealed that pectins with higher net electrical charges are more bioadhesive than the less charged ones. Both the negatively charged pectin formulation, P-25, and the positively charged formulation, P-N, were able to synergize with the mucus to produce rheologically strengthened gels. The highly esterified pectin, P-94, also synergized with the mucosal glycoproteins to form a gel structure via coil entanglements. The ex vivo studies further confirmed the microstructures of mucus gel networks with adsorbed pectins. When incubated with porcine intestinal mucus membrane, P-94 gels were found generally bound to the lumen area, P-25 gels were able to penetrate deeply near the wall area, P-N gels interacted with mucins via electrostatic bonding and dispersed into the whole area from the lumen to the wall. Hence, both P-N and P-94, by enhancing the protective barrier properties of mucus systems, may be useful alternatives for the treatment of mucus related irritation and infection. In drug-delivery systems, P-N and P-25 would deliver incorporated drugs mainly by pectin dissolution, while a diffusion mechanism would release drugs from P-94 gels.</description><subject>Animals</subject><subject>Bioadhesiveness</subject><subject>Biocompatible Materials - chemistry</subject><subject>Colon - drug effects</subject><subject>Colon - metabolism</subject><subject>Diffusion</subject><subject>Drug delivery</subject><subject>Drug Delivery Systems</subject><subject>Gels</subject><subject>Hydrogen-Ion Concentration</subject><subject>Microscopy, Confocal</subject><subject>Microscopy, Electron, Scanning</subject><subject>Mucin</subject><subject>Mucins - chemistry</subject><subject>Pectin</subject><subject>Pectins - chemistry</subject><subject>Pectins - pharmacology</subject><subject>Protein Structure, Tertiary</subject><subject>Rheology</subject><subject>Swine</subject><subject>Thermodynamics</subject><subject>Time Factors</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS0EokvhK6CIA7ek43-xzQ0VaCtV4tKeLds7Fl4l8WJni_j2eLUrwa2cnmb8m3kjP0I-UBgo0PFqN_iUZ7diSW6qAwOQA_ChyQuyoVrpXhqQL8kGqGC9GSm7IG9q3UGrQbDX5IJKI4yU44bc3C1tjwtrykuXY_fkSsqH2u2xtZYu5jIfJnd8rd2vtP7o9rmEtGAX8pSXFLo11XrA-pa8iu0YfHfWS_L47evD9W1___3m7vrzfR-EgLXnISoJBqVWyLXXSsbIUTNgPnitUUgAzrlwiguJY_Bxq9AHpYMB713kl-Tjae--5J_Nd7VzqgGnyS3Y7rajMowzwZ8FmZaGUzDPglTxUdBRNvDTCQwl11ow2n1Jsyu_LQV7DMbu7L_B2GMwFrht0obfn10Ofsbt39FzEg34cgKw_d5TwmJrSLgE3KbSsrDbnP7H5w8Ob6cP</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Liu, LinShu</creator><creator>Fishman, Marshall L.</creator><creator>Hicks, Kevin B.</creator><creator>Kende, Meir</creator><general>Elsevier Ltd</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>F28</scope><scope>7X8</scope></search><sort><creationdate>20051001</creationdate><title>Interaction of various pectin formulations with porcine colonic tissues</title><author>Liu, LinShu ; Fishman, Marshall L. ; Hicks, Kevin B. ; Kende, Meir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-3cf7509e587e38b875ff3e8202bcb88e45003334a7345e6cbfd7ebc78c90bbaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Bioadhesiveness</topic><topic>Biocompatible Materials - chemistry</topic><topic>Colon - drug effects</topic><topic>Colon - metabolism</topic><topic>Diffusion</topic><topic>Drug delivery</topic><topic>Drug Delivery Systems</topic><topic>Gels</topic><topic>Hydrogen-Ion Concentration</topic><topic>Microscopy, Confocal</topic><topic>Microscopy, Electron, Scanning</topic><topic>Mucin</topic><topic>Mucins - chemistry</topic><topic>Pectin</topic><topic>Pectins - chemistry</topic><topic>Pectins - pharmacology</topic><topic>Protein Structure, Tertiary</topic><topic>Rheology</topic><topic>Swine</topic><topic>Thermodynamics</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, LinShu</creatorcontrib><creatorcontrib>Fishman, Marshall L.</creatorcontrib><creatorcontrib>Hicks, Kevin B.</creatorcontrib><creatorcontrib>Kende, Meir</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>MEDLINE - Academic</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, LinShu</au><au>Fishman, Marshall L.</au><au>Hicks, Kevin B.</au><au>Kende, Meir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interaction of various pectin formulations with porcine colonic tissues</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2005-10-01</date><risdate>2005</risdate><volume>26</volume><issue>29</issue><spage>5907</spage><epage>5916</epage><pages>5907-5916</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Pectins of low and high degrees of esterification, as well as pectin derivatives carrying primary amines, were investigate for gel forming ability with mucosal tissues. 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Hence, both P-N and P-94, by enhancing the protective barrier properties of mucus systems, may be useful alternatives for the treatment of mucus related irritation and infection. In drug-delivery systems, P-N and P-25 would deliver incorporated drugs mainly by pectin dissolution, while a diffusion mechanism would release drugs from P-94 gels.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>15949556</pmid><doi>10.1016/j.biomaterials.2005.03.005</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Bioadhesiveness
Biocompatible Materials - chemistry
Colon - drug effects
Colon - metabolism
Diffusion
Drug delivery
Drug Delivery Systems
Gels
Hydrogen-Ion Concentration
Microscopy, Confocal
Microscopy, Electron, Scanning
Mucin
Mucins - chemistry
Pectin
Pectins - chemistry
Pectins - pharmacology
Protein Structure, Tertiary
Rheology
Swine
Thermodynamics
Time Factors
title Interaction of various pectin formulations with porcine colonic tissues
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