Source:http://linkedlifedata.com/resource/pubmed/id/18057726
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2007-12-6
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pubmed:abstractText |
The purpose of this study was to investigate the continuous and real-time influence of ophthalmic ingredients on rabbit cornea by monitoring electrophysiological characteristics. The tight junctional permeabilities of FITC-dextran 4,400 (FD-4) was also determined through the cornea in the presence of ophthalmic ingredients. Intact cornea showed approximately one k-ohmxcm(2) of transepithelial electrical resistance (TEER) and extremely low permeability of FD-4. The ophthalmic ingredients used in the present study were benzalkonium chloride (BK; 0.002%, 0.01%, 0.05%), ethylenediaminetetraacetic acid (EDTA; 0.5%), capric acid (C10; 0.25%), saponin (SP; 0.1%), taurocholic acid (TA; 1.0%) and sodium dodecyl sulfate (SDS; 0.01%). They were previously reported to be effective on corneal penetrations of various drugs at those concentrations without severe toxicity. These ingredients decreased TEER and increased corneal permeability of FD-4. BK reduced TEER in a concentration-dependent manner. There was a significant correlation (gamma=0.860) between the permeability coefficient (Papp) of FD-4 and conductance (Gm), which is the reciprocal value of TEER. It was also indicated that Papp and Gm have a relationship with the corneal cytotoxicity of the ingredients. In conclusion, an electrophysiological method using isolated cornea was very useful to determine the continuous and real-time influence of ophthalmic ingredients on the cornea. In this method, electrophysiological conductance must be able to predict corneal tight junction permeability and the corneal cytotoxicity of ingredients.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0918-6158
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2360-4
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pubmed:meshHeading |
pubmed-meshheading:18057726-Absorption,
pubmed-meshheading:18057726-Animals,
pubmed-meshheading:18057726-Cell Membrane Permeability,
pubmed-meshheading:18057726-Cell Survival,
pubmed-meshheading:18057726-Cornea,
pubmed-meshheading:18057726-Data Interpretation, Statistical,
pubmed-meshheading:18057726-Dextrans,
pubmed-meshheading:18057726-Diffusion Chambers, Culture,
pubmed-meshheading:18057726-Electrophysiology,
pubmed-meshheading:18057726-Fluorescein-5-isothiocyanate,
pubmed-meshheading:18057726-Male,
pubmed-meshheading:18057726-Ophthalmic Solutions,
pubmed-meshheading:18057726-Rabbits,
pubmed-meshheading:18057726-Signal Transduction,
pubmed-meshheading:18057726-Tight Junctions
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pubmed:year |
2007
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pubmed:articleTitle |
Electrophysiological characterization of tight junctional pathway of rabbit cornea treated with ophthalmic ingredients.
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pubmed:affiliation |
Department of Hospital Pharmacy, Nagasaki University Hospital of Medicine and Dentistry, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan.
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pubmed:publicationType |
Journal Article,
In Vitro
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