Labrasol® and Salts of Medium-Chain Fatty Acids Can Be Combined in Low Concentrations to Increase the Permeability of a Macromolecule Marker Across Isolated Rat Intestinal Mucosae
In addition to their solubilizing properties, excipients used in lipid-based formulations can improve intestinal permeability of macromolecules. We determined whether admixing of medium-chain fatty acid (MCFA) permeation enhancers with a lipoidal excipient (Labrasol®) could potentiate transepithelia...
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Veröffentlicht in: | Journal of pharmaceutical sciences 2018-06, Vol.107 (6), p.1648-1655 |
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creator | Heade, Joanne Maher, Sam Bleiel, Sinead B. Brayden, David J. |
description | In addition to their solubilizing properties, excipients used in lipid-based formulations can improve intestinal permeability of macromolecules. We determined whether admixing of medium-chain fatty acid (MCFA) permeation enhancers with a lipoidal excipient (Labrasol®) could potentiate transepithelial flux of a poorly permeable macromolecule (fluorescein isothiocyanate dextran 4 kDa [FD4]) across rat intestinal mucosae mounted in Ussing chambers. Low concentrations of sodium caprate (C10), sodium undecylenate (C11:1), or sodium laurate (C12) combined with Labrasol® increased the apparent permeability coefficient (Papp) of FD4 to values typically seen with higher concentrations of MCFAs or Labrasol® alone. For example, combination of C11:1 (0.5 mg/mL) with Labrasol® (1 mg/mL) increased the Papp of FD4 by 10- and 11-fold over the respective individual agents at the same concentrations where no enhancement was evident. The increased enhancement ratios seen with the combinations were associated with some perturbation in intestinal histology and with attenuation of an epithelial functional measure, carbachol-stimulated inward short-circuit current. In conclusion, combining three MCFAs separately with Labrasol® increased the Papp of FD4 to values greater than those seen for MCFAs or Labrasol® alone. Ultimately, this may permit lower concentrations of MCFA to be used in combination with other excipients in oral formulations of poorly permeable molecules. |
doi_str_mv | 10.1016/j.xphs.2018.02.012 |
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We determined whether admixing of medium-chain fatty acid (MCFA) permeation enhancers with a lipoidal excipient (Labrasol®) could potentiate transepithelial flux of a poorly permeable macromolecule (fluorescein isothiocyanate dextran 4 kDa [FD4]) across rat intestinal mucosae mounted in Ussing chambers. Low concentrations of sodium caprate (C10), sodium undecylenate (C11:1), or sodium laurate (C12) combined with Labrasol® increased the apparent permeability coefficient (Papp) of FD4 to values typically seen with higher concentrations of MCFAs or Labrasol® alone. For example, combination of C11:1 (0.5 mg/mL) with Labrasol® (1 mg/mL) increased the Papp of FD4 by 10- and 11-fold over the respective individual agents at the same concentrations where no enhancement was evident. The increased enhancement ratios seen with the combinations were associated with some perturbation in intestinal histology and with attenuation of an epithelial functional measure, carbachol-stimulated inward short-circuit current. In conclusion, combining three MCFAs separately with Labrasol® increased the Papp of FD4 to values greater than those seen for MCFAs or Labrasol® alone. Ultimately, this may permit lower concentrations of MCFA to be used in combination with other excipients in oral formulations of poorly permeable molecules.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1016/j.xphs.2018.02.012</identifier><identifier>PMID: 29462634</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>epithelial delivery/permeability ; macromolecular drug delivery ; oral drug delivery ; peptide delivery ; permeation enhancer</subject><ispartof>Journal of pharmaceutical sciences, 2018-06, Vol.107 (6), p.1648-1655</ispartof><rights>2018 American Pharmacists Association</rights><rights>Copyright © 2018 American Pharmacists Association®. Published by Elsevier Inc. 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We determined whether admixing of medium-chain fatty acid (MCFA) permeation enhancers with a lipoidal excipient (Labrasol®) could potentiate transepithelial flux of a poorly permeable macromolecule (fluorescein isothiocyanate dextran 4 kDa [FD4]) across rat intestinal mucosae mounted in Ussing chambers. Low concentrations of sodium caprate (C10), sodium undecylenate (C11:1), or sodium laurate (C12) combined with Labrasol® increased the apparent permeability coefficient (Papp) of FD4 to values typically seen with higher concentrations of MCFAs or Labrasol® alone. For example, combination of C11:1 (0.5 mg/mL) with Labrasol® (1 mg/mL) increased the Papp of FD4 by 10- and 11-fold over the respective individual agents at the same concentrations where no enhancement was evident. The increased enhancement ratios seen with the combinations were associated with some perturbation in intestinal histology and with attenuation of an epithelial functional measure, carbachol-stimulated inward short-circuit current. In conclusion, combining three MCFAs separately with Labrasol® increased the Papp of FD4 to values greater than those seen for MCFAs or Labrasol® alone. Ultimately, this may permit lower concentrations of MCFA to be used in combination with other excipients in oral formulations of poorly permeable molecules.</description><subject>epithelial delivery/permeability</subject><subject>macromolecular drug delivery</subject><subject>oral drug delivery</subject><subject>peptide delivery</subject><subject>permeation enhancer</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kUuO1DAQhi0EYpqBC7BAXrJJKDuPTiQ2Q8RAS90C8VhbFbuidpPEje0MzKVYcQJOhpseWLIqleqvrx4_Y08F5AJE_eKQfz_uQy5BNDnIHIS8x1aikpDVINb32QpAyqyoyvaCPQrhAAA1VNVDdiHbspZ1Ua7Yzy32HoMbf_3gOBv-EccYuBv4joxdpqzbo535NcZ4y6-0NYF3OPNXxDs39XYmw1N5676lfNY0R4_Rujnw6Phm1p4wEI974u_JT4S9HW0CJTzyHWrvJjeSXkZKmf9CPo3wLgS-SQthTPAPGBMnUoh2xpHvFu0C0mP2YMAx0JO7eMk-X7_-1L3Ntu_ebLqrbaZLgJhJOVRYghBV0a_bZoBS1LXp-1JQM7S9qcy6JZTCUJN-ZAbRaNMMuixlP-hBFsUle37mHr37uqQl1GSDpnHEmdwSlARYCyEbqJJUnqV_DvA0qKO3E_pbJUCd3FIHdXJLndxSIFVyKzU9u-Mv_UTmX8tfe5Lg5VlA6cobS14FbSk92lhPOirj7P_4vwHcsqk3</recordid><startdate>201806</startdate><enddate>201806</enddate><creator>Heade, Joanne</creator><creator>Maher, Sam</creator><creator>Bleiel, Sinead B.</creator><creator>Brayden, David J.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201806</creationdate><title>Labrasol® and Salts of Medium-Chain Fatty Acids Can Be Combined in Low Concentrations to Increase the Permeability of a Macromolecule Marker Across Isolated Rat Intestinal Mucosae</title><author>Heade, Joanne ; Maher, Sam ; Bleiel, Sinead B. ; Brayden, David J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-22f5a401153b798f04166dbb41e8f9bd5d79ea21de8549df18cd8fc442bfcf233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>epithelial delivery/permeability</topic><topic>macromolecular drug delivery</topic><topic>oral drug delivery</topic><topic>peptide delivery</topic><topic>permeation enhancer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heade, Joanne</creatorcontrib><creatorcontrib>Maher, Sam</creatorcontrib><creatorcontrib>Bleiel, Sinead B.</creatorcontrib><creatorcontrib>Brayden, David J.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heade, Joanne</au><au>Maher, Sam</au><au>Bleiel, Sinead B.</au><au>Brayden, David J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Labrasol® and Salts of Medium-Chain Fatty Acids Can Be Combined in Low Concentrations to Increase the Permeability of a Macromolecule Marker Across Isolated Rat Intestinal Mucosae</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J Pharm Sci</addtitle><date>2018-06</date><risdate>2018</risdate><volume>107</volume><issue>6</issue><spage>1648</spage><epage>1655</epage><pages>1648-1655</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><abstract>In addition to their solubilizing properties, excipients used in lipid-based formulations can improve intestinal permeability of macromolecules. We determined whether admixing of medium-chain fatty acid (MCFA) permeation enhancers with a lipoidal excipient (Labrasol®) could potentiate transepithelial flux of a poorly permeable macromolecule (fluorescein isothiocyanate dextran 4 kDa [FD4]) across rat intestinal mucosae mounted in Ussing chambers. Low concentrations of sodium caprate (C10), sodium undecylenate (C11:1), or sodium laurate (C12) combined with Labrasol® increased the apparent permeability coefficient (Papp) of FD4 to values typically seen with higher concentrations of MCFAs or Labrasol® alone. For example, combination of C11:1 (0.5 mg/mL) with Labrasol® (1 mg/mL) increased the Papp of FD4 by 10- and 11-fold over the respective individual agents at the same concentrations where no enhancement was evident. 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subjects | epithelial delivery/permeability macromolecular drug delivery oral drug delivery peptide delivery permeation enhancer |
title | Labrasol® and Salts of Medium-Chain Fatty Acids Can Be Combined in Low Concentrations to Increase the Permeability of a Macromolecule Marker Across Isolated Rat Intestinal Mucosae |
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