Loading…

Fabrication of a biodegradable drug delivery system with controlled release made of PLGA 5-FU hydroxyapatite

Purpose - Rapid prototyping (RP) technology has been widely applied in biomedical research. The purpose of this paper is to describe how a scaffold composite drug delivery system (DDS) was fabricated using a nano composite deposition system (NCDS).Design methodology approach - A biocompatible and bi...

Full description

Saved in:
Bibliographic Details
Published in:Rapid prototyping journal 2008-01, Vol.14 (5), p.293-299
Main Authors: Chu, Won-Shik, Jeong, Suk-Young, Kim, Sung-Geun, Ha, Won-Shik, Chi, Sang-Chul, Ahn, Sung-Hoon
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c450t-d50d41023abfac305afe8a070e97069526d60bff6ece9dc6c1e215697ed18e293
cites cdi_FETCH-LOGICAL-c450t-d50d41023abfac305afe8a070e97069526d60bff6ece9dc6c1e215697ed18e293
container_end_page 299
container_issue 5
container_start_page 293
container_title Rapid prototyping journal
container_volume 14
creator Chu, Won-Shik
Jeong, Suk-Young
Kim, Sung-Geun
Ha, Won-Shik
Chi, Sang-Chul
Ahn, Sung-Hoon
description Purpose - Rapid prototyping (RP) technology has been widely applied in biomedical research. The purpose of this paper is to describe how a scaffold composite drug delivery system (DDS) was fabricated using a nano composite deposition system (NCDS).Design methodology approach - A biocompatible and biodegradable thermoplastic polymer (poly(DL-lactide-co-glycolide acid)) was used as the matrix, and a mixture of anti-cancer drug (5-fluorouracil) and bio-ceramic (hydroxyapatite - HA) was added to the polymer to form a bio-composite material for the DDS. An in vitro drug release test showed that the release rate of the drug composite could be controlled by the amount of HA for 50 days.Findings - Faster release was observed for the DDS with higher weight percent of HA. The relationship between release rate and the amount of HA showed a bi-linear manner, and bi-linear drug release models were developed based on the experimental results.Originality value - Cylindrical scaffolds were fabricated with polymer drug additive using an NCDS. A series of in vitro drug release tests was performed to evaluate the effectiveness of the additive, HA. Drug release models were developed based on the experimental results.
doi_str_mv 10.1108/13552540810907965
format article
fullrecord <record><control><sourceid>proquest_emera</sourceid><recordid>TN_cdi_proquest_journals_2439157041</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2439157041</sourcerecordid><originalsourceid>FETCH-LOGICAL-c450t-d50d41023abfac305afe8a070e97069526d60bff6ece9dc6c1e215697ed18e293</originalsourceid><addsrcrecordid>eNp10V1L7DAQBuAiCn7-AO-CB7yyOtPmo70UOavCgl7odUmTqVbSzZ6k67H_3iwrCMpeZSDPOzMwWXaKcIkI1RWWQhSCQ4VQg6ql2MkOUIkqV1LBbqrTf56A3M8OY3wDwIILOMjcTLehN3rs_YL5jmnW9t7SS9BWt46YDasXZsn17xQmFqc40sD-9-MrM34xBu8cWRbIkY7EBm1p3eRxfnvNRD57Zq-TDf5j0ss0YKTjbK_TLtLJ13uUPc_-Pt3c5fOH2_ub63lu0k5jbgVYjlCUuu20KUHojioNCqhWIGtRSCuh7TpJhmprpEEqUMhakcWKiro8ys43fZfB_1tRHJuhj4ac0wvyq9gUwLmSpUjwzw_45ldhkXZrCl7WKBRwTOpsq0IOCLxaI9wgE3yMgbpmGfpBh6lBaNYnan6dKGUuNhkaKGhnvyM_abO0XeKwhW-d8AkYBJ5W</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>214010481</pqid></control><display><type>article</type><title>Fabrication of a biodegradable drug delivery system with controlled release made of PLGA 5-FU hydroxyapatite</title><source>ABI/INFORM Global</source><source>Emerald:Jisc Collections:Emerald Subject Collections HE and FE 2024-2026:Emerald Premier (reading list)</source><creator>Chu, Won-Shik ; Jeong, Suk-Young ; Kim, Sung-Geun ; Ha, Won-Shik ; Chi, Sang-Chul ; Ahn, Sung-Hoon</creator><creatorcontrib>Chu, Won-Shik ; Jeong, Suk-Young ; Kim, Sung-Geun ; Ha, Won-Shik ; Chi, Sang-Chul ; Ahn, Sung-Hoon</creatorcontrib><description>Purpose - Rapid prototyping (RP) technology has been widely applied in biomedical research. The purpose of this paper is to describe how a scaffold composite drug delivery system (DDS) was fabricated using a nano composite deposition system (NCDS).Design methodology approach - A biocompatible and biodegradable thermoplastic polymer (poly(DL-lactide-co-glycolide acid)) was used as the matrix, and a mixture of anti-cancer drug (5-fluorouracil) and bio-ceramic (hydroxyapatite - HA) was added to the polymer to form a bio-composite material for the DDS. An in vitro drug release test showed that the release rate of the drug composite could be controlled by the amount of HA for 50 days.Findings - Faster release was observed for the DDS with higher weight percent of HA. The relationship between release rate and the amount of HA showed a bi-linear manner, and bi-linear drug release models were developed based on the experimental results.Originality value - Cylindrical scaffolds were fabricated with polymer drug additive using an NCDS. A series of in vitro drug release tests was performed to evaluate the effectiveness of the additive, HA. Drug release models were developed based on the experimental results.</description><identifier>ISSN: 1355-2546</identifier><identifier>EISSN: 1758-7670</identifier><identifier>DOI: 10.1108/13552540810907965</identifier><identifier>CODEN: RPJOFC</identifier><language>eng</language><publisher>Bradford: Emerald Group Publishing Limited</publisher><subject>Additives ; Biocompatibility ; Biodegradability ; Biodegradable materials ; Biomedical materials ; Biomedical research ; Composite materials ; Controlled release ; Drug delivery systems ; Drugs ; Electron microscopes ; Experiments ; Hydroxyapatite ; In vitro methods and tests ; Performance evaluation ; Permeability ; Polylactic acid ; Polymer matrix composites ; Polymers ; Pore size ; Product development ; Rapid prototyping ; Scaffolds ; Studies</subject><ispartof>Rapid prototyping journal, 2008-01, Vol.14 (5), p.293-299</ispartof><rights>Emerald Group Publishing Limited</rights><rights>Copyright Emerald Group Publishing Limited 2008</rights><rights>Emerald Group Publishing Limited 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-d50d41023abfac305afe8a070e97069526d60bff6ece9dc6c1e215697ed18e293</citedby><cites>FETCH-LOGICAL-c450t-d50d41023abfac305afe8a070e97069526d60bff6ece9dc6c1e215697ed18e293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/214010481?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,11688,27924,27925,36060,36061,44363</link.rule.ids></links><search><creatorcontrib>Chu, Won-Shik</creatorcontrib><creatorcontrib>Jeong, Suk-Young</creatorcontrib><creatorcontrib>Kim, Sung-Geun</creatorcontrib><creatorcontrib>Ha, Won-Shik</creatorcontrib><creatorcontrib>Chi, Sang-Chul</creatorcontrib><creatorcontrib>Ahn, Sung-Hoon</creatorcontrib><title>Fabrication of a biodegradable drug delivery system with controlled release made of PLGA 5-FU hydroxyapatite</title><title>Rapid prototyping journal</title><description>Purpose - Rapid prototyping (RP) technology has been widely applied in biomedical research. The purpose of this paper is to describe how a scaffold composite drug delivery system (DDS) was fabricated using a nano composite deposition system (NCDS).Design methodology approach - A biocompatible and biodegradable thermoplastic polymer (poly(DL-lactide-co-glycolide acid)) was used as the matrix, and a mixture of anti-cancer drug (5-fluorouracil) and bio-ceramic (hydroxyapatite - HA) was added to the polymer to form a bio-composite material for the DDS. An in vitro drug release test showed that the release rate of the drug composite could be controlled by the amount of HA for 50 days.Findings - Faster release was observed for the DDS with higher weight percent of HA. The relationship between release rate and the amount of HA showed a bi-linear manner, and bi-linear drug release models were developed based on the experimental results.Originality value - Cylindrical scaffolds were fabricated with polymer drug additive using an NCDS. A series of in vitro drug release tests was performed to evaluate the effectiveness of the additive, HA. Drug release models were developed based on the experimental results.</description><subject>Additives</subject><subject>Biocompatibility</subject><subject>Biodegradability</subject><subject>Biodegradable materials</subject><subject>Biomedical materials</subject><subject>Biomedical research</subject><subject>Composite materials</subject><subject>Controlled release</subject><subject>Drug delivery systems</subject><subject>Drugs</subject><subject>Electron microscopes</subject><subject>Experiments</subject><subject>Hydroxyapatite</subject><subject>In vitro methods and tests</subject><subject>Performance evaluation</subject><subject>Permeability</subject><subject>Polylactic acid</subject><subject>Polymer matrix composites</subject><subject>Polymers</subject><subject>Pore size</subject><subject>Product development</subject><subject>Rapid prototyping</subject><subject>Scaffolds</subject><subject>Studies</subject><issn>1355-2546</issn><issn>1758-7670</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>M0C</sourceid><recordid>eNp10V1L7DAQBuAiCn7-AO-CB7yyOtPmo70UOavCgl7odUmTqVbSzZ6k67H_3iwrCMpeZSDPOzMwWXaKcIkI1RWWQhSCQ4VQg6ql2MkOUIkqV1LBbqrTf56A3M8OY3wDwIILOMjcTLehN3rs_YL5jmnW9t7SS9BWt46YDasXZsn17xQmFqc40sD-9-MrM34xBu8cWRbIkY7EBm1p3eRxfnvNRD57Zq-TDf5j0ss0YKTjbK_TLtLJ13uUPc_-Pt3c5fOH2_ub63lu0k5jbgVYjlCUuu20KUHojioNCqhWIGtRSCuh7TpJhmprpEEqUMhakcWKiro8ys43fZfB_1tRHJuhj4ac0wvyq9gUwLmSpUjwzw_45ldhkXZrCl7WKBRwTOpsq0IOCLxaI9wgE3yMgbpmGfpBh6lBaNYnan6dKGUuNhkaKGhnvyM_abO0XeKwhW-d8AkYBJ5W</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Chu, Won-Shik</creator><creator>Jeong, Suk-Young</creator><creator>Kim, Sung-Geun</creator><creator>Ha, Won-Shik</creator><creator>Chi, Sang-Chul</creator><creator>Ahn, Sung-Hoon</creator><general>Emerald Group Publishing Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>0U~</scope><scope>1-H</scope><scope>7TB</scope><scope>7WY</scope><scope>7WZ</scope><scope>7XB</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>F~G</scope><scope>HCIFZ</scope><scope>K6~</scope><scope>L.-</scope><scope>L.0</scope><scope>L6V</scope><scope>M0C</scope><scope>M7S</scope><scope>PQBIZ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>S0W</scope><scope>PRINS</scope><scope>7QO</scope><scope>P64</scope></search><sort><creationdate>20080101</creationdate><title>Fabrication of a biodegradable drug delivery system with controlled release made of PLGA 5-FU hydroxyapatite</title><author>Chu, Won-Shik ; Jeong, Suk-Young ; Kim, Sung-Geun ; Ha, Won-Shik ; Chi, Sang-Chul ; Ahn, Sung-Hoon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-d50d41023abfac305afe8a070e97069526d60bff6ece9dc6c1e215697ed18e293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Additives</topic><topic>Biocompatibility</topic><topic>Biodegradability</topic><topic>Biodegradable materials</topic><topic>Biomedical materials</topic><topic>Biomedical research</topic><topic>Composite materials</topic><topic>Controlled release</topic><topic>Drug delivery systems</topic><topic>Drugs</topic><topic>Electron microscopes</topic><topic>Experiments</topic><topic>Hydroxyapatite</topic><topic>In vitro methods and tests</topic><topic>Performance evaluation</topic><topic>Permeability</topic><topic>Polylactic acid</topic><topic>Polymer matrix composites</topic><topic>Polymers</topic><topic>Pore size</topic><topic>Product development</topic><topic>Rapid prototyping</topic><topic>Scaffolds</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chu, Won-Shik</creatorcontrib><creatorcontrib>Jeong, Suk-Young</creatorcontrib><creatorcontrib>Kim, Sung-Geun</creatorcontrib><creatorcontrib>Ha, Won-Shik</creatorcontrib><creatorcontrib>Chi, Sang-Chul</creatorcontrib><creatorcontrib>Ahn, Sung-Hoon</creatorcontrib><collection>CrossRef</collection><collection>Global News &amp; ABI/Inform Professional</collection><collection>Trade PRO</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>ABI/INFORM Collection</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest Business Premium Collection</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ABI/INFORM Global (Corporate)</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Business Collection</collection><collection>ABI/INFORM Professional Advanced</collection><collection>ABI/INFORM Professional Standard</collection><collection>ProQuest Engineering Collection</collection><collection>ABI/INFORM Global</collection><collection>Engineering Database</collection><collection>One Business</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>DELNET Engineering &amp; Technology Collection</collection><collection>ProQuest Central China</collection><collection>Biotechnology Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Rapid prototyping journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chu, Won-Shik</au><au>Jeong, Suk-Young</au><au>Kim, Sung-Geun</au><au>Ha, Won-Shik</au><au>Chi, Sang-Chul</au><au>Ahn, Sung-Hoon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fabrication of a biodegradable drug delivery system with controlled release made of PLGA 5-FU hydroxyapatite</atitle><jtitle>Rapid prototyping journal</jtitle><date>2008-01-01</date><risdate>2008</risdate><volume>14</volume><issue>5</issue><spage>293</spage><epage>299</epage><pages>293-299</pages><issn>1355-2546</issn><eissn>1758-7670</eissn><coden>RPJOFC</coden><abstract>Purpose - Rapid prototyping (RP) technology has been widely applied in biomedical research. The purpose of this paper is to describe how a scaffold composite drug delivery system (DDS) was fabricated using a nano composite deposition system (NCDS).Design methodology approach - A biocompatible and biodegradable thermoplastic polymer (poly(DL-lactide-co-glycolide acid)) was used as the matrix, and a mixture of anti-cancer drug (5-fluorouracil) and bio-ceramic (hydroxyapatite - HA) was added to the polymer to form a bio-composite material for the DDS. An in vitro drug release test showed that the release rate of the drug composite could be controlled by the amount of HA for 50 days.Findings - Faster release was observed for the DDS with higher weight percent of HA. The relationship between release rate and the amount of HA showed a bi-linear manner, and bi-linear drug release models were developed based on the experimental results.Originality value - Cylindrical scaffolds were fabricated with polymer drug additive using an NCDS. A series of in vitro drug release tests was performed to evaluate the effectiveness of the additive, HA. Drug release models were developed based on the experimental results.</abstract><cop>Bradford</cop><pub>Emerald Group Publishing Limited</pub><doi>10.1108/13552540810907965</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1355-2546
ispartof Rapid prototyping journal, 2008-01, Vol.14 (5), p.293-299
issn 1355-2546
1758-7670
language eng
recordid cdi_proquest_journals_2439157041
source ABI/INFORM Global; Emerald:Jisc Collections:Emerald Subject Collections HE and FE 2024-2026:Emerald Premier (reading list)
subjects Additives
Biocompatibility
Biodegradability
Biodegradable materials
Biomedical materials
Biomedical research
Composite materials
Controlled release
Drug delivery systems
Drugs
Electron microscopes
Experiments
Hydroxyapatite
In vitro methods and tests
Performance evaluation
Permeability
Polylactic acid
Polymer matrix composites
Polymers
Pore size
Product development
Rapid prototyping
Scaffolds
Studies
title Fabrication of a biodegradable drug delivery system with controlled release made of PLGA 5-FU hydroxyapatite
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T06%3A43%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_emera&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Fabrication%20of%20a%20biodegradable%20drug%20delivery%20system%20with%20controlled%20release%20made%20of%20PLGA%205-FU%20hydroxyapatite&rft.jtitle=Rapid%20prototyping%20journal&rft.au=Chu,%20Won-Shik&rft.date=2008-01-01&rft.volume=14&rft.issue=5&rft.spage=293&rft.epage=299&rft.pages=293-299&rft.issn=1355-2546&rft.eissn=1758-7670&rft.coden=RPJOFC&rft_id=info:doi/10.1108/13552540810907965&rft_dat=%3Cproquest_emera%3E2439157041%3C/proquest_emera%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c450t-d50d41023abfac305afe8a070e97069526d60bff6ece9dc6c1e215697ed18e293%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=214010481&rft_id=info:pmid/&rfr_iscdi=true