PERMEABILITY OF GLYCOSIDES THROUGH HUMAN ERYTHROCYTE MEMBRANE

The permeability of glycosides (arbutin, salicin, glycyrritin, p-nitrophenyl-β-D-glucopyranoside, p-nitrophenyl-β-D-galactopyranoside, p-nitrophenyl-β-D-lactopyranoside, p-nitrophenyl-β-D-maltopyranoside) and their aglycons through human erythrocyte membrane was investigated. The glycosides permeate...

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Veröffentlicht in:Chemical & pharmaceutical bulletin 1991/05/25, Vol.39(5), pp.1346-1348
Hauptverfasser: MATSUMOTO, Yasuhiro, OHSAKO, Masahiko, SAKATA, Ritsu
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container_end_page 1348
container_issue 5
container_start_page 1346
container_title Chemical & pharmaceutical bulletin
container_volume 39
creator MATSUMOTO, Yasuhiro
OHSAKO, Masahiko
SAKATA, Ritsu
description The permeability of glycosides (arbutin, salicin, glycyrritin, p-nitrophenyl-β-D-glucopyranoside, p-nitrophenyl-β-D-galactopyranoside, p-nitrophenyl-β-D-lactopyranoside, p-nitrophenyl-β-D-maltopyranoside) and their aglycons through human erythrocyte membrane was investigated. The glycosides permeated slowly, compared with their aglycons. Glycoside having disaccharide did not permeate the erythrocyte membrane. This suggested that the introduction of disaccharide to a drug significantly depresses the permeability of glycoside through erythrocyte membrane. The drug entrapped in erythrocytes was not released into the outer medium.
doi_str_mv 10.1248/cpb.39.1346
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The glycosides permeated slowly, compared with their aglycons. Glycoside having disaccharide did not permeate the erythrocyte membrane. This suggested that the introduction of disaccharide to a drug significantly depresses the permeability of glycoside through erythrocyte membrane. 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Pharm. Bull.</addtitle><description>The permeability of glycosides (arbutin, salicin, glycyrritin, p-nitrophenyl-β-D-glucopyranoside, p-nitrophenyl-β-D-galactopyranoside, p-nitrophenyl-β-D-lactopyranoside, p-nitrophenyl-β-D-maltopyranoside) and their aglycons through human erythrocyte membrane was investigated. The glycosides permeated slowly, compared with their aglycons. Glycoside having disaccharide did not permeate the erythrocyte membrane. This suggested that the introduction of disaccharide to a drug significantly depresses the permeability of glycoside through erythrocyte membrane. The drug entrapped in erythrocytes was not released into the outer medium.</description><subject>aglycon</subject><subject>Biological and medical sciences</subject><subject>Cell Membrane Permeability</subject><subject>disaccharide</subject><subject>drug delivery system</subject><subject>Erythrocyte Membrane - metabolism</subject><subject>erythrocytes</subject><subject>General pharmacology</subject><subject>glycoside</subject><subject>Glycosides - blood</subject><subject>glycyrritin</subject><subject>human erythrocyte</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Medical sciences</subject><subject>p-nitrophenyl- beta -D-galactopyranoside</subject><subject>p-nitrophenyl- beta -D-glucopyranoside</subject><subject>p-nitrophenyl- beta -D-maltopyranoside</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. 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Drug treatments</topic><topic>salicin</topic><topic>targetting</topic><topic>transport</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MATSUMOTO, Yasuhiro</creatorcontrib><creatorcontrib>OHSAKO, Masahiko</creatorcontrib><creatorcontrib>SAKATA, Ritsu</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical &amp; pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MATSUMOTO, Yasuhiro</au><au>OHSAKO, Masahiko</au><au>SAKATA, Ritsu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PERMEABILITY OF GLYCOSIDES THROUGH HUMAN ERYTHROCYTE MEMBRANE</atitle><jtitle>Chemical &amp; pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1991</date><risdate>1991</risdate><volume>39</volume><issue>5</issue><spage>1346</spage><epage>1348</epage><pages>1346-1348</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><coden>CPBTAL</coden><abstract>The permeability of glycosides (arbutin, salicin, glycyrritin, p-nitrophenyl-β-D-glucopyranoside, p-nitrophenyl-β-D-galactopyranoside, p-nitrophenyl-β-D-lactopyranoside, p-nitrophenyl-β-D-maltopyranoside) and their aglycons through human erythrocyte membrane was investigated. The glycosides permeated slowly, compared with their aglycons. Glycoside having disaccharide did not permeate the erythrocyte membrane. This suggested that the introduction of disaccharide to a drug significantly depresses the permeability of glycoside through erythrocyte membrane. The drug entrapped in erythrocytes was not released into the outer medium.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>1914012</pmid><doi>10.1248/cpb.39.1346</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record>
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subjects aglycon
Biological and medical sciences
Cell Membrane Permeability
disaccharide
drug delivery system
Erythrocyte Membrane - metabolism
erythrocytes
General pharmacology
glycoside
Glycosides - blood
glycyrritin
human erythrocyte
Humans
In Vitro Techniques
Medical sciences
p-nitrophenyl- beta -D-galactopyranoside
p-nitrophenyl- beta -D-glucopyranoside
p-nitrophenyl- beta -D-maltopyranoside
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
salicin
targetting
transport
title PERMEABILITY OF GLYCOSIDES THROUGH HUMAN ERYTHROCYTE MEMBRANE
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