Surface immobilization of galactose onto aliphatic biodegradable polymers for hepatocyte culture
A novel surface modification method of biodegradable polymers was investigated for inducing the attachment of specific cells onto the polymer surface via ligand‐receptor interactions. Galactose, a targeting ligand specific to asialoglycoprotein receptors present on cell membrane of hepatocytes, was...
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description | A novel surface modification method of biodegradable polymers was investigated for inducing the attachment of specific cells onto the polymer surface via ligand‐receptor interactions. Galactose, a targeting ligand specific to asialoglycoprotein receptors present on cell membrane of hepatocytes, was introduced on the surface of poly(D,L‐lactic‐co‐glycolic acid) (PLGA) films. A terminal end group of carboxylic acid in PLGA was activated by dicyclohexylcarbodiimide and N‐hydroxysuccinimide for the direct conjugation of lactose by reductive amination reaction. Di‐block copolymers of PLGA‐b‐poly(ethylene glycol) (PEG) having a free terminal amine group were also synthesized and used for the conjugation of galactose for the introduction of a PEG spacer between PLGA and galactose. The presence of galactose moieties on the blend film surface was characterized by measuring water contact angle and X‐ray photon spectroscopy, and the amount of galactose was indirectly determined by a specific lectin‐binding assay. With increasing the galactose concentration on the blend film surface, the initial attachment as well as the cell viability of hepatocyates concomitantly increased. The introduction of PEG spacer reduced the cell attachment and viability. Albumin secretion rate from hepatocytes was enhanced for galactose modified surfaces, whereas it was reduced for the surfaces not having galactose moieties. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 78: 1–10, 2002; DOI 10.1002/bit.10239 |
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Galactose, a targeting ligand specific to asialoglycoprotein receptors present on cell membrane of hepatocytes, was introduced on the surface of poly(D,L‐lactic‐co‐glycolic acid) (PLGA) films. A terminal end group of carboxylic acid in PLGA was activated by dicyclohexylcarbodiimide and N‐hydroxysuccinimide for the direct conjugation of lactose by reductive amination reaction. Di‐block copolymers of PLGA‐b‐poly(ethylene glycol) (PEG) having a free terminal amine group were also synthesized and used for the conjugation of galactose for the introduction of a PEG spacer between PLGA and galactose. The presence of galactose moieties on the blend film surface was characterized by measuring water contact angle and X‐ray photon spectroscopy, and the amount of galactose was indirectly determined by a specific lectin‐binding assay. With increasing the galactose concentration on the blend film surface, the initial attachment as well as the cell viability of hepatocyates concomitantly increased. The introduction of PEG spacer reduced the cell attachment and viability. Albumin secretion rate from hepatocytes was enhanced for galactose modified surfaces, whereas it was reduced for the surfaces not having galactose moieties. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 78: 1–10, 2002; DOI 10.1002/bit.10239</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.10239</identifier><identifier>PMID: 11857274</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animal cells ; Animals ; Biocompatible Materials - chemistry ; biodegradable polymer ; Biodegradation, Environmental ; Biological and medical sciences ; Biotechnology ; Cell Adhesion - physiology ; Cells, Cultured ; Enzyme-Linked Immunosorbent Assay ; Eukaryotic cell cultures ; Fundamental and applied biological sciences. Psychology ; galactose ; Galactose - metabolism ; hepatocytes ; Hepatocytes - metabolism ; Hepatocytes - ultrastructure ; Lactic Acid - chemistry ; Lectins - metabolism ; Male ; Methods. Procedures. Technologies ; Miscellaneous ; Polyglycolic Acid - chemistry ; Polymers - chemistry ; Rats ; Rats, Sprague-Dawley ; Serum Albumin - secretion ; surface modification ; Surface Properties</subject><ispartof>Biotechnology and bioengineering, 2002-04, Vol.78 (1), p.1-10</ispartof><rights>Copyright © 2002 Wiley Periodicals, Inc.</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 78: 1-10, 2002; DOI 10.1002/bit.10239</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5279-413d02815c3b9d32008349ba0bb0f3a4ce5097a53f62fe8ef560c1f1eac3867d3</citedby><cites>FETCH-LOGICAL-c5279-413d02815c3b9d32008349ba0bb0f3a4ce5097a53f62fe8ef560c1f1eac3867d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbit.10239$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbit.10239$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13557037$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11857274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoon, Jun Jin</creatorcontrib><creatorcontrib>Nam, Yoon Sung</creatorcontrib><creatorcontrib>Kim, Jung Hoe</creatorcontrib><creatorcontrib>Park, Tae Gwan</creatorcontrib><title>Surface immobilization of galactose onto aliphatic biodegradable polymers for hepatocyte culture</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>A novel surface modification method of biodegradable polymers was investigated for inducing the attachment of specific cells onto the polymer surface via ligand‐receptor interactions. Galactose, a targeting ligand specific to asialoglycoprotein receptors present on cell membrane of hepatocytes, was introduced on the surface of poly(D,L‐lactic‐co‐glycolic acid) (PLGA) films. A terminal end group of carboxylic acid in PLGA was activated by dicyclohexylcarbodiimide and N‐hydroxysuccinimide for the direct conjugation of lactose by reductive amination reaction. Di‐block copolymers of PLGA‐b‐poly(ethylene glycol) (PEG) having a free terminal amine group were also synthesized and used for the conjugation of galactose for the introduction of a PEG spacer between PLGA and galactose. The presence of galactose moieties on the blend film surface was characterized by measuring water contact angle and X‐ray photon spectroscopy, and the amount of galactose was indirectly determined by a specific lectin‐binding assay. With increasing the galactose concentration on the blend film surface, the initial attachment as well as the cell viability of hepatocyates concomitantly increased. The introduction of PEG spacer reduced the cell attachment and viability. Albumin secretion rate from hepatocytes was enhanced for galactose modified surfaces, whereas it was reduced for the surfaces not having galactose moieties. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 78: 1–10, 2002; DOI 10.1002/bit.10239</description><subject>Animal cells</subject><subject>Animals</subject><subject>Biocompatible Materials - chemistry</subject><subject>biodegradable polymer</subject><subject>Biodegradation, Environmental</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell Adhesion - physiology</subject><subject>Cells, Cultured</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>galactose</subject><subject>Galactose - metabolism</subject><subject>hepatocytes</subject><subject>Hepatocytes - metabolism</subject><subject>Hepatocytes - ultrastructure</subject><subject>Lactic Acid - chemistry</subject><subject>Lectins - metabolism</subject><subject>Male</subject><subject>Methods. Procedures. Technologies</subject><subject>Miscellaneous</subject><subject>Polyglycolic Acid - chemistry</subject><subject>Polymers - chemistry</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Serum Albumin - secretion</subject><subject>surface modification</subject><subject>Surface Properties</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10E1v1DAQBmALUdGlcOAPIF9A4pDWH3GcHGkFS6WqHFrgaCbOuDU462AnguXX47ILPfVkW35mRvMS8oKzY86YOOn9XC5Cdo_IirNOV0x07DFZMcaaSqpOHJKnOX8rT902zRNyyHmrtND1iny9WpIDi9SPY-x98L9h9nFDo6M3EMDOMSONmzlSCH66LZ-W9j4OeJNggD4gnWLYjpgydTHRW5xgjnY7I7VLmJeEz8iBg5Dx-f48Ip_ev7s--1BdfFyfn729qKwSuqtqLgcmWq6s7LtBCsZaWXc9sL5nTkJtUZXFQEnXCIctOtUwyx1HsLJt9CCPyOtd3ynFHwvm2Yw-WwwBNhiXbO42lqruCnyzgzbFnBM6MyU_QtoazsxdnKbEaf7GWezLfdOlH3G4l_v8Cni1B5AtBJdgY32-d1IpzaQu7mTnfvqA24cnmtPz63-jq12FzzP--l8B6btptNTKfLlcm9O6Y_pq_dm08g8-VJwf</recordid><startdate>20020405</startdate><enddate>20020405</enddate><creator>Yoon, Jun Jin</creator><creator>Nam, Yoon Sung</creator><creator>Kim, Jung Hoe</creator><creator>Park, Tae Gwan</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><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></search><sort><creationdate>20020405</creationdate><title>Surface immobilization of galactose onto aliphatic biodegradable polymers for hepatocyte culture</title><author>Yoon, Jun Jin ; Nam, Yoon Sung ; Kim, Jung Hoe ; Park, Tae Gwan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5279-413d02815c3b9d32008349ba0bb0f3a4ce5097a53f62fe8ef560c1f1eac3867d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animal cells</topic><topic>Animals</topic><topic>Biocompatible Materials - chemistry</topic><topic>biodegradable polymer</topic><topic>Biodegradation, Environmental</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell Adhesion - physiology</topic><topic>Cells, Cultured</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Eukaryotic cell cultures</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>galactose</topic><topic>Galactose - metabolism</topic><topic>hepatocytes</topic><topic>Hepatocytes - metabolism</topic><topic>Hepatocytes - ultrastructure</topic><topic>Lactic Acid - chemistry</topic><topic>Lectins - metabolism</topic><topic>Male</topic><topic>Methods. Procedures. Technologies</topic><topic>Miscellaneous</topic><topic>Polyglycolic Acid - chemistry</topic><topic>Polymers - chemistry</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Serum Albumin - secretion</topic><topic>surface modification</topic><topic>Surface Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoon, Jun Jin</creatorcontrib><creatorcontrib>Nam, Yoon Sung</creatorcontrib><creatorcontrib>Kim, Jung Hoe</creatorcontrib><creatorcontrib>Park, Tae Gwan</creatorcontrib><collection>Istex</collection><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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoon, Jun Jin</au><au>Nam, Yoon Sung</au><au>Kim, Jung Hoe</au><au>Park, Tae Gwan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface immobilization of galactose onto aliphatic biodegradable polymers for hepatocyte culture</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>2002-04-05</date><risdate>2002</risdate><volume>78</volume><issue>1</issue><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>A novel surface modification method of biodegradable polymers was investigated for inducing the attachment of specific cells onto the polymer surface via ligand‐receptor interactions. Galactose, a targeting ligand specific to asialoglycoprotein receptors present on cell membrane of hepatocytes, was introduced on the surface of poly(D,L‐lactic‐co‐glycolic acid) (PLGA) films. A terminal end group of carboxylic acid in PLGA was activated by dicyclohexylcarbodiimide and N‐hydroxysuccinimide for the direct conjugation of lactose by reductive amination reaction. Di‐block copolymers of PLGA‐b‐poly(ethylene glycol) (PEG) having a free terminal amine group were also synthesized and used for the conjugation of galactose for the introduction of a PEG spacer between PLGA and galactose. The presence of galactose moieties on the blend film surface was characterized by measuring water contact angle and X‐ray photon spectroscopy, and the amount of galactose was indirectly determined by a specific lectin‐binding assay. With increasing the galactose concentration on the blend film surface, the initial attachment as well as the cell viability of hepatocyates concomitantly increased. The introduction of PEG spacer reduced the cell attachment and viability. Albumin secretion rate from hepatocytes was enhanced for galactose modified surfaces, whereas it was reduced for the surfaces not having galactose moieties. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 78: 1–10, 2002; DOI 10.1002/bit.10239</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>11857274</pmid><doi>10.1002/bit.10239</doi><tpages>10</tpages></addata></record> |
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subjects | Animal cells Animals Biocompatible Materials - chemistry biodegradable polymer Biodegradation, Environmental Biological and medical sciences Biotechnology Cell Adhesion - physiology Cells, Cultured Enzyme-Linked Immunosorbent Assay Eukaryotic cell cultures Fundamental and applied biological sciences. Psychology galactose Galactose - metabolism hepatocytes Hepatocytes - metabolism Hepatocytes - ultrastructure Lactic Acid - chemistry Lectins - metabolism Male Methods. Procedures. Technologies Miscellaneous Polyglycolic Acid - chemistry Polymers - chemistry Rats Rats, Sprague-Dawley Serum Albumin - secretion surface modification Surface Properties |
title | Surface immobilization of galactose onto aliphatic biodegradable polymers for hepatocyte culture |
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