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Water-soluble and low molecular weight chitosan-based plasmid DNA delivery
Chitosan, a natural cationic polysaccharide, is a candidate non-viral vector for gene delivery because of its high positive charges and low cytotoxicity. In this study, low molecular weight chitosan (LMWC, molecular weight of 22 kDa) was characterized and evaluated as a gene carrier. Plasmid/LMWC co...
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Published in: | Pharmaceutical research 2001-04, Vol.18 (4), p.427-431 |
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creator | MINHYUNG LEE NAH, Jae-Woon YOUNGMIN KWON JAE JOON KOH KYUNG SOO KO SUNG WAN KIM |
description | Chitosan, a natural cationic polysaccharide, is a candidate non-viral vector for gene delivery because of its high positive charges and low cytotoxicity. In this study, low molecular weight chitosan (LMWC, molecular weight of 22 kDa) was characterized and evaluated as a gene carrier.
Plasmid/LMWC complex was analyzed in 1% agarose gel electrophoresis. To confirm that the LMWC protected plasmids from nuclease. DNase I protection assays were performed. pSV-beta-galactosidase plasmid/LMWC complex was transfected into 293T cells and transfection efficiency was evaluated by beta-galactosidase assay. Cytotoxicity of LMWC was determined by MTT assay.
Unlike high molecular weight chitosan (HMWC), LMWC is highly water soluble, and can form complex with plasmids in physiological buffer. The plasmid DNA was completely retarded at a weight ratio of 1:2 (plasmid:LMWC) in 1% agarose gel. DNase I protection assay showed that plasmids were protected from DNase-I over 60 min. The most efficient transfection was obtained at a weight ratio of 1:3 (plasmid:LMWC). The transfection efficiency of LMWC was significantly higher than naked DNA and higher than poly-L-lysine (PLL). MTT assay showed that LMWC was less cytotoxic than PLL.
LMWC is non-toxic and has higher transfection efficiency than PLL. Therefore, LMWC will be useful in the development of safe gene carriers. |
doi_str_mv | 10.1023/A:1011037807261 |
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Plasmid/LMWC complex was analyzed in 1% agarose gel electrophoresis. To confirm that the LMWC protected plasmids from nuclease. DNase I protection assays were performed. pSV-beta-galactosidase plasmid/LMWC complex was transfected into 293T cells and transfection efficiency was evaluated by beta-galactosidase assay. Cytotoxicity of LMWC was determined by MTT assay.
Unlike high molecular weight chitosan (HMWC), LMWC is highly water soluble, and can form complex with plasmids in physiological buffer. The plasmid DNA was completely retarded at a weight ratio of 1:2 (plasmid:LMWC) in 1% agarose gel. DNase I protection assay showed that plasmids were protected from DNase-I over 60 min. The most efficient transfection was obtained at a weight ratio of 1:3 (plasmid:LMWC). The transfection efficiency of LMWC was significantly higher than naked DNA and higher than poly-L-lysine (PLL). MTT assay showed that LMWC was less cytotoxic than PLL.
LMWC is non-toxic and has higher transfection efficiency than PLL. Therefore, LMWC will be useful in the development of safe gene carriers.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1023/A:1011037807261</identifier><identifier>PMID: 11451027</identifier><identifier>CODEN: PHREEB</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>Antineoplastic Agents - administration & dosage ; Biological and medical sciences ; Cell Line ; Chitin - administration & dosage ; Chitin - analogs & derivatives ; Chitin - genetics ; Chitosan ; Cytotoxicity ; DNA - administration & dosage ; DNA - genetics ; Drug Delivery Systems - methods ; Efficiency ; Gene therapy ; General pharmacology ; Humans ; Medical sciences ; Molecular weight ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Physiology ; Plasmids ; Plasmids - administration & dosage ; Plasmids - genetics ; Polymers ; Toxicity ; Transfection - methods</subject><ispartof>Pharmaceutical research, 2001-04, Vol.18 (4), p.427-431</ispartof><rights>2001 INIST-CNRS</rights><rights>Copyright Kluwer Academic Publishers Apr 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c309t-3c509f2210d2c82e5b608e0a2a6a871db360e7de6ae26809686e7dd7bb9bfee33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1062850$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11451027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MINHYUNG LEE</creatorcontrib><creatorcontrib>NAH, Jae-Woon</creatorcontrib><creatorcontrib>YOUNGMIN KWON</creatorcontrib><creatorcontrib>JAE JOON KOH</creatorcontrib><creatorcontrib>KYUNG SOO KO</creatorcontrib><creatorcontrib>SUNG WAN KIM</creatorcontrib><title>Water-soluble and low molecular weight chitosan-based plasmid DNA delivery</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><description>Chitosan, a natural cationic polysaccharide, is a candidate non-viral vector for gene delivery because of its high positive charges and low cytotoxicity. In this study, low molecular weight chitosan (LMWC, molecular weight of 22 kDa) was characterized and evaluated as a gene carrier.
Plasmid/LMWC complex was analyzed in 1% agarose gel electrophoresis. To confirm that the LMWC protected plasmids from nuclease. DNase I protection assays were performed. pSV-beta-galactosidase plasmid/LMWC complex was transfected into 293T cells and transfection efficiency was evaluated by beta-galactosidase assay. Cytotoxicity of LMWC was determined by MTT assay.
Unlike high molecular weight chitosan (HMWC), LMWC is highly water soluble, and can form complex with plasmids in physiological buffer. The plasmid DNA was completely retarded at a weight ratio of 1:2 (plasmid:LMWC) in 1% agarose gel. DNase I protection assay showed that plasmids were protected from DNase-I over 60 min. The most efficient transfection was obtained at a weight ratio of 1:3 (plasmid:LMWC). The transfection efficiency of LMWC was significantly higher than naked DNA and higher than poly-L-lysine (PLL). MTT assay showed that LMWC was less cytotoxic than PLL.
LMWC is non-toxic and has higher transfection efficiency than PLL. Therefore, LMWC will be useful in the development of safe gene carriers.</description><subject>Antineoplastic Agents - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Chitin - administration & dosage</subject><subject>Chitin - analogs & derivatives</subject><subject>Chitin - genetics</subject><subject>Chitosan</subject><subject>Cytotoxicity</subject><subject>DNA - administration & dosage</subject><subject>DNA - genetics</subject><subject>Drug Delivery Systems - methods</subject><subject>Efficiency</subject><subject>Gene therapy</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Molecular weight</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Physiology</subject><subject>Plasmids</subject><subject>Plasmids - administration & dosage</subject><subject>Plasmids - genetics</subject><subject>Polymers</subject><subject>Toxicity</subject><subject>Transfection - methods</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpFz01PwzAMBuAIgdgYnLmhCnEtOEnzUW7T-NYEFxDcqqRxWad0HUnLtH9PJYY4WbYe23oJOaVwSYHxq-k1BUqBKw2KSbpHxlQonuaQfeyT8TDLUq0yOiJHMS4BQNM8OyQjSjMx7KsxeXo3HYY0tr63HhOzcolvN0nTeix7b0Kywfpz0SXlou7aaFapNRFdsvYmNrVLbp6niUNff2PYHpODyviIJ7s6IW93t6-zh3T-cv84m87TkkPepbwUkFeMUXCs1AyFlaARDDPSaEWd5RJQOZQGmdSQSy2H1ilrc1shcj4h579316H96jF2xbLtw2p4WTDGpOBC5AM626HeNuiKdagbE7bFX_IBXOyAiaXxVTCrso7_DiTTAvgPlJBmsA</recordid><startdate>20010401</startdate><enddate>20010401</enddate><creator>MINHYUNG LEE</creator><creator>NAH, Jae-Woon</creator><creator>YOUNGMIN KWON</creator><creator>JAE JOON KOH</creator><creator>KYUNG SOO KO</creator><creator>SUNG WAN KIM</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20010401</creationdate><title>Water-soluble and low molecular weight chitosan-based plasmid DNA delivery</title><author>MINHYUNG LEE ; NAH, Jae-Woon ; YOUNGMIN KWON ; JAE JOON KOH ; KYUNG SOO KO ; SUNG WAN KIM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-3c509f2210d2c82e5b608e0a2a6a871db360e7de6ae26809686e7dd7bb9bfee33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Antineoplastic Agents - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Chitin - administration & dosage</topic><topic>Chitin - analogs & derivatives</topic><topic>Chitin - genetics</topic><topic>Chitosan</topic><topic>Cytotoxicity</topic><topic>DNA - administration & dosage</topic><topic>DNA - genetics</topic><topic>Drug Delivery Systems - methods</topic><topic>Efficiency</topic><topic>Gene therapy</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Molecular weight</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Physiology</topic><topic>Plasmids</topic><topic>Plasmids - administration & dosage</topic><topic>Plasmids - genetics</topic><topic>Polymers</topic><topic>Toxicity</topic><topic>Transfection - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MINHYUNG LEE</creatorcontrib><creatorcontrib>NAH, Jae-Woon</creatorcontrib><creatorcontrib>YOUNGMIN KWON</creatorcontrib><creatorcontrib>JAE JOON KOH</creatorcontrib><creatorcontrib>KYUNG SOO KO</creatorcontrib><creatorcontrib>SUNG WAN KIM</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>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MINHYUNG LEE</au><au>NAH, Jae-Woon</au><au>YOUNGMIN KWON</au><au>JAE JOON KOH</au><au>KYUNG SOO KO</au><au>SUNG WAN KIM</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Water-soluble and low molecular weight chitosan-based plasmid DNA delivery</atitle><jtitle>Pharmaceutical research</jtitle><addtitle>Pharm Res</addtitle><date>2001-04-01</date><risdate>2001</risdate><volume>18</volume><issue>4</issue><spage>427</spage><epage>431</epage><pages>427-431</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><coden>PHREEB</coden><abstract>Chitosan, a natural cationic polysaccharide, is a candidate non-viral vector for gene delivery because of its high positive charges and low cytotoxicity. In this study, low molecular weight chitosan (LMWC, molecular weight of 22 kDa) was characterized and evaluated as a gene carrier.
Plasmid/LMWC complex was analyzed in 1% agarose gel electrophoresis. To confirm that the LMWC protected plasmids from nuclease. DNase I protection assays were performed. pSV-beta-galactosidase plasmid/LMWC complex was transfected into 293T cells and transfection efficiency was evaluated by beta-galactosidase assay. Cytotoxicity of LMWC was determined by MTT assay.
Unlike high molecular weight chitosan (HMWC), LMWC is highly water soluble, and can form complex with plasmids in physiological buffer. The plasmid DNA was completely retarded at a weight ratio of 1:2 (plasmid:LMWC) in 1% agarose gel. DNase I protection assay showed that plasmids were protected from DNase-I over 60 min. The most efficient transfection was obtained at a weight ratio of 1:3 (plasmid:LMWC). The transfection efficiency of LMWC was significantly higher than naked DNA and higher than poly-L-lysine (PLL). MTT assay showed that LMWC was less cytotoxic than PLL.
LMWC is non-toxic and has higher transfection efficiency than PLL. Therefore, LMWC will be useful in the development of safe gene carriers.</abstract><cop>New York, NY</cop><pub>Springer</pub><pmid>11451027</pmid><doi>10.1023/A:1011037807261</doi><tpages>5</tpages></addata></record> |
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subjects | Antineoplastic Agents - administration & dosage Biological and medical sciences Cell Line Chitin - administration & dosage Chitin - analogs & derivatives Chitin - genetics Chitosan Cytotoxicity DNA - administration & dosage DNA - genetics Drug Delivery Systems - methods Efficiency Gene therapy General pharmacology Humans Medical sciences Molecular weight Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Physiology Plasmids Plasmids - administration & dosage Plasmids - genetics Polymers Toxicity Transfection - methods |
title | Water-soluble and low molecular weight chitosan-based plasmid DNA delivery |
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