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dc.contributor.authorSo, Yean Cho
dc.contributor.authorJong, Sik Kim
dc.contributor.authorLi, Hong
dc.contributor.authorShim, Changkoo
dc.contributor.authorLinhardt, Robert J.
dc.contributor.authorYeong, Shik Kim
dc.date2002
dc.date.accessioned2022-06-27T16:19:12Z
dc.date.available2022-06-27T16:19:12Z
dc.date.issued2002-02-28
dc.identifier.citationEnhancement of Paracellular Transport of Heparin Disaccharide Across Caco-2 Cell Monolayers, S. Y. Cho, J. S. Kim, H. Li, C. Shim, R. J. Linhardt, Y. S. Kim, Archives Pharmacal Research, 25, 86-92 2002.
dc.identifier.issn2536269
dc.identifier.issn2536269
dc.identifier.urihttps://doi.org/10.1007/bf02975268
dc.identifier.urihttps://hdl.handle.net/20.500.13015/5836
dc.descriptionArchives Pharmacal Research, 25, 86-92
dc.descriptionNote : if this item contains full text it may be a preprint, author manuscript, or a Gold OA copy that permits redistribution with a license such as CC BY. The final version is available through the publisher’s platform.
dc.description.abstractThe enhancement of paracellular transport of heparin disaccharide using several absorption enhancers across Caco-2 cell monolayers was tested. The cytotoxicity of these enhancers was also examined. The enhancing effects by Quillaja saponin, dipotassium glycyrrhizinate, 18beta-glycyrrhetinic acid, sodium caprate and taurine were determined by changes in transepithelial electrical resistance (TEER) and the amount of heparin disaccharide transported across Caco-2 cell monolayers. Among the absorption enhancers, 18beta-glycyrrhetinic acid and taurine decreased TEER and increased the permeability of heparin disaccharide in a dose-dependent and time-dependent manner with little or negligible cytotoxicity. Our results indicate that these absorption enhancers can widen the tight junction, which is a dominant paracellular absorption route of hydrophilic compounds. It is highly possible that these absorption enhancers can be applied as pharmaceutical excipients to improve the transport of macromolecules and hydrophilic drugs having difficulty in permeability across the intestinal epithelium.
dc.description.urihttps://login.libproxy.rpi.edu/login?url=https://doi.org/10.1007/bf02975268
dc.languageen_US
dc.language.isoENG
dc.relation.ispartofThe Linhardt Research Labs Online Collection
dc.relation.ispartofRensselaer Polytechnic Institute, Troy, NY
dc.relation.ispartofArchives of Pharmacal Research
dc.relation.urihttps://harc.rpi.edu/
dc.subjectBiology
dc.subjectChemistry and chemical biology
dc.subjectChemical and biological engineering
dc.subjectBiomedical engineering
dc.titleEnhancement of Paracellular Transport of Heparin Disaccharide Across Caco-2 Cell Monolayers
dc.typeArticle
dcterms.accessRightshttps://login.libproxy.rpi.edu/login?url=https://doi.org/10.1007/bf02975268
dcterms.isPartOfJournal
dcterms.isVersionOfhttps://doi.org/10.1007/bf02975268
dc.rights.holderIn Copyright : this Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s). https://rightsstatements.org/page/InC/1.0/
dc.creator.identifierhttps://orcid.org/0000-0003-2219-5833
dc.relation.departmentThe Linhardt Research Labs.
dc.relation.departmentThe Shirley Ann Jackson, Ph.D. Center for Biotechnology and Interdisciplinary Studies (CBIS)
rpi.description.pages86-92
rpi.description.volume25


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