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pH‐Responsive Starch‐Citrate Nanoparticles for Controlled Release of Paracetamol
Starch‐citrate samples with degrees of substitution (DS) ranging from 0.11 to 0.90 are synthesized by a green esterification reaction between citric acid and native sago starch (Metroxylon sagu) in an aqueous medium. Starch‐citrate nanoparticles with mean diameter of 105 nm are subsequently obtained...
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Published in: | Starch - Stärke 2019-09, Vol.71 (9-10), p.n/a |
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creator | Chin, Suk Fun Romainor, Ain N. B. Pang, Suh Cem Lee, Boon Kiat Hwang, Siaw San |
description | Starch‐citrate samples with degrees of substitution (DS) ranging from 0.11 to 0.90 are synthesized by a green esterification reaction between citric acid and native sago starch (Metroxylon sagu) in an aqueous medium. Starch‐citrate nanoparticles with mean diameter of 105 nm are subsequently obtained by controlled precipitation through drop‐wise addition of dissolved starch‐citrate solution into excess absolute ethanol. These nanoparticles are observed to exhibit pH‐responsive release profiles within the physiological pH range of 1.2–8.6. The release profile of a model drug (paracetamol) is observed to obey the zero‐order kinetics, with the release mechanism based on the diffusion and swelling model. The cytotoxicity study in HaCaT cell lines (human skin cells) shows that starch‐citrate nanoparticles are non‐toxic and hence are suitable for biomedical applications as pH‐responsive drug carriers.
pH responsive starch‐citrate nanoparticles are prepared. The nanoparticles can be used to control the release of drugs such as paracetamol. |
doi_str_mv | 10.1002/star.201800336 |
format | article |
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pH responsive starch‐citrate nanoparticles are prepared. The nanoparticles can be used to control the release of drugs such as paracetamol.</description><identifier>ISSN: 0038-9056</identifier><identifier>EISSN: 1521-379X</identifier><identifier>DOI: 10.1002/star.201800336</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Analgesics ; Aqueous solutions ; Biocompatibility ; Biomedical materials ; Cell lines ; Chemical precipitation ; Citric acid ; Controlled release ; Cytotoxicity ; Drug carriers ; Drug delivery ; drug release profiles ; Esterification ; Ethanol ; Kinetics ; Nanoparticles ; Paracetamol ; pH effects ; pH‐responsive ; Reaction kinetics ; Skin ; Starch ; starch‐citrate nanoparticles ; Substitution reactions ; Toxicity</subject><ispartof>Starch - Stärke, 2019-09, Vol.71 (9-10), p.n/a</ispartof><rights>2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3176-5793e8279a54b265b210c86b7293ba19da22a5819c6e081d7f6ea77c6ebd59c83</citedby><cites>FETCH-LOGICAL-c3176-5793e8279a54b265b210c86b7293ba19da22a5819c6e081d7f6ea77c6ebd59c83</cites><orcidid>0000-0002-4793-6813</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Chin, Suk Fun</creatorcontrib><creatorcontrib>Romainor, Ain N. B.</creatorcontrib><creatorcontrib>Pang, Suh Cem</creatorcontrib><creatorcontrib>Lee, Boon Kiat</creatorcontrib><creatorcontrib>Hwang, Siaw San</creatorcontrib><title>pH‐Responsive Starch‐Citrate Nanoparticles for Controlled Release of Paracetamol</title><title>Starch - Stärke</title><description>Starch‐citrate samples with degrees of substitution (DS) ranging from 0.11 to 0.90 are synthesized by a green esterification reaction between citric acid and native sago starch (Metroxylon sagu) in an aqueous medium. Starch‐citrate nanoparticles with mean diameter of 105 nm are subsequently obtained by controlled precipitation through drop‐wise addition of dissolved starch‐citrate solution into excess absolute ethanol. These nanoparticles are observed to exhibit pH‐responsive release profiles within the physiological pH range of 1.2–8.6. The release profile of a model drug (paracetamol) is observed to obey the zero‐order kinetics, with the release mechanism based on the diffusion and swelling model. The cytotoxicity study in HaCaT cell lines (human skin cells) shows that starch‐citrate nanoparticles are non‐toxic and hence are suitable for biomedical applications as pH‐responsive drug carriers.
pH responsive starch‐citrate nanoparticles are prepared. The nanoparticles can be used to control the release of drugs such as paracetamol.</description><subject>Analgesics</subject><subject>Aqueous solutions</subject><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Cell lines</subject><subject>Chemical precipitation</subject><subject>Citric acid</subject><subject>Controlled release</subject><subject>Cytotoxicity</subject><subject>Drug carriers</subject><subject>Drug delivery</subject><subject>drug release profiles</subject><subject>Esterification</subject><subject>Ethanol</subject><subject>Kinetics</subject><subject>Nanoparticles</subject><subject>Paracetamol</subject><subject>pH effects</subject><subject>pH‐responsive</subject><subject>Reaction kinetics</subject><subject>Skin</subject><subject>Starch</subject><subject>starch‐citrate nanoparticles</subject><subject>Substitution reactions</subject><subject>Toxicity</subject><issn>0038-9056</issn><issn>1521-379X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkM1Kw0AUhQdRsFa3rgOuU-en87csQa1QVNoK7obJ5AZT0kycSS3d-Qg-o09iSkWXri7n8J1z4SB0SfCIYEyvY2fDiGKiMGZMHKEB4ZSkTOqXYzToPZVqzMUpOotxhbHgckwGaNlOvz4-5xBb38TqHZJF3-Jeey-rumA7SB5s41sbusrVEJPShyTzTRd8XUORzKEGGyHxZfJkg3XQ2bWvz9FJaesIFz93iJ5vb5bZNJ093t1nk1nqGJEi5VIzUFRqy8c5FTynBDslckk1yy3RhaXUckW0E4AVKWQpwErZq7zg2ik2RFeH3jb4tw3Ezqz8JjT9S0OpYlIKrsc9NTpQLvgYA5SmDdXahp0h2OyXM_vlzO9yfUAfAtuqht0_tFksJ_O_7DdVXHS4</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Chin, Suk Fun</creator><creator>Romainor, Ain N. B.</creator><creator>Pang, Suh Cem</creator><creator>Lee, Boon Kiat</creator><creator>Hwang, Siaw San</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-4793-6813</orcidid></search><sort><creationdate>201909</creationdate><title>pH‐Responsive Starch‐Citrate Nanoparticles for Controlled Release of Paracetamol</title><author>Chin, Suk Fun ; Romainor, Ain N. B. ; Pang, Suh Cem ; Lee, Boon Kiat ; Hwang, Siaw San</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3176-5793e8279a54b265b210c86b7293ba19da22a5819c6e081d7f6ea77c6ebd59c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Analgesics</topic><topic>Aqueous solutions</topic><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>Cell lines</topic><topic>Chemical precipitation</topic><topic>Citric acid</topic><topic>Controlled release</topic><topic>Cytotoxicity</topic><topic>Drug carriers</topic><topic>Drug delivery</topic><topic>drug release profiles</topic><topic>Esterification</topic><topic>Ethanol</topic><topic>Kinetics</topic><topic>Nanoparticles</topic><topic>Paracetamol</topic><topic>pH effects</topic><topic>pH‐responsive</topic><topic>Reaction kinetics</topic><topic>Skin</topic><topic>Starch</topic><topic>starch‐citrate nanoparticles</topic><topic>Substitution reactions</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chin, Suk Fun</creatorcontrib><creatorcontrib>Romainor, Ain N. B.</creatorcontrib><creatorcontrib>Pang, Suh Cem</creatorcontrib><creatorcontrib>Lee, Boon Kiat</creatorcontrib><creatorcontrib>Hwang, Siaw San</creatorcontrib><collection>CrossRef</collection><jtitle>Starch - Stärke</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chin, Suk Fun</au><au>Romainor, Ain N. B.</au><au>Pang, Suh Cem</au><au>Lee, Boon Kiat</au><au>Hwang, Siaw San</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>pH‐Responsive Starch‐Citrate Nanoparticles for Controlled Release of Paracetamol</atitle><jtitle>Starch - Stärke</jtitle><date>2019-09</date><risdate>2019</risdate><volume>71</volume><issue>9-10</issue><epage>n/a</epage><issn>0038-9056</issn><eissn>1521-379X</eissn><abstract>Starch‐citrate samples with degrees of substitution (DS) ranging from 0.11 to 0.90 are synthesized by a green esterification reaction between citric acid and native sago starch (Metroxylon sagu) in an aqueous medium. Starch‐citrate nanoparticles with mean diameter of 105 nm are subsequently obtained by controlled precipitation through drop‐wise addition of dissolved starch‐citrate solution into excess absolute ethanol. These nanoparticles are observed to exhibit pH‐responsive release profiles within the physiological pH range of 1.2–8.6. The release profile of a model drug (paracetamol) is observed to obey the zero‐order kinetics, with the release mechanism based on the diffusion and swelling model. The cytotoxicity study in HaCaT cell lines (human skin cells) shows that starch‐citrate nanoparticles are non‐toxic and hence are suitable for biomedical applications as pH‐responsive drug carriers.
pH responsive starch‐citrate nanoparticles are prepared. The nanoparticles can be used to control the release of drugs such as paracetamol.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/star.201800336</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4793-6813</orcidid></addata></record> |
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subjects | Analgesics Aqueous solutions Biocompatibility Biomedical materials Cell lines Chemical precipitation Citric acid Controlled release Cytotoxicity Drug carriers Drug delivery drug release profiles Esterification Ethanol Kinetics Nanoparticles Paracetamol pH effects pH‐responsive Reaction kinetics Skin Starch starch‐citrate nanoparticles Substitution reactions Toxicity |
title | pH‐Responsive Starch‐Citrate Nanoparticles for Controlled Release of Paracetamol |
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