Development of a controlled release formulation based on a starch matrix system
Controlled release formulation (CRF) of the insecticide acetamiprid was made using tapioca starch, urea and sodium borate. The data show the recovery of this CRF process is >95.43%, there is no obvious difference with increase of sodium borate added, however, with the increase of urea in the mixt...
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Veröffentlicht in: | International journal of pharmaceutics 2005-07, Vol.298 (1), p.108-116 |
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creator | Cao, Yongsong Huang, Lu Chen, Jiuxin Liang, Ji Long, Shengyou Lu, Yitong |
description | Controlled release formulation (CRF) of the insecticide acetamiprid was made using tapioca starch, urea and sodium borate. The data show the recovery of this CRF process is >95.43%, there is no obvious difference with increase of sodium borate added, however, with the increase of urea in the mixture, the formulation has a decrease recovery. In stability test, the decomposition rate of acetamiprid CRF was less one tenth than that of the acetamiprid emulsifiable concentrate (EC) under UV radiation. The release kinetics of acetamiprid from granules with variation content of urea, sodium borate and granule sizes were evaluated in water under laboratory condition. The release data were fitted to the generalized model
M
t
/
M
z
=
kt
n
, where
M
t
/
M
z
is the percentage of insecticide released at time
t,
k and
n are constants, and
n is constant that indicates the mechanism of release. The results indicated that the release of acetamiprid was diffusion-controlled. The time taken for 50% of the active ingredient to be released into water,
T
50, was also calculated for the comparison of formulations. The results showed that the formulation with the increasing urea in formulation had the higher value of
T
50, which means a slower release of the active ingredient, while that the formulation with the increasing sodium borate in formulation had the lower value of
T
50, which means a faster release of the active ingredient. It was also found that as the size of this formulation decreased, the release of the active ingredient was faster. |
doi_str_mv | 10.1016/j.ijpharm.2005.04.005 |
format | Article |
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M
t
/
M
z
=
kt
n
, where
M
t
/
M
z
is the percentage of insecticide released at time
t,
k and
n are constants, and
n is constant that indicates the mechanism of release. The results indicated that the release of acetamiprid was diffusion-controlled. The time taken for 50% of the active ingredient to be released into water,
T
50, was also calculated for the comparison of formulations. The results showed that the formulation with the increasing urea in formulation had the higher value of
T
50, which means a slower release of the active ingredient, while that the formulation with the increasing sodium borate in formulation had the lower value of
T
50, which means a faster release of the active ingredient. It was also found that as the size of this formulation decreased, the release of the active ingredient was faster.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2005.04.005</identifier><identifier>PMID: 15905051</identifier><identifier>CODEN: IJPHDE</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Acetamiprid ; Biological and medical sciences ; Borates - administration & dosage ; Chemistry, Pharmaceutical ; Controlled release formulation ; Delayed-Action Preparations ; Drug Stability ; General pharmacology ; Kinetics ; Manihot ; Medical sciences ; Neonicotinoids ; Particle Size ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Pyridines - administration & dosage ; Pyridines - chemistry ; Stability ; Starch - administration & dosage ; Tapioca starch ; Urea - administration & dosage</subject><ispartof>International journal of pharmaceutics, 2005-07, Vol.298 (1), p.108-116</ispartof><rights>2005 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-aa84634f77e5ec594ecf4850f70746c833a3d6ed62826b7f686f0a10bed94be3</citedby><cites>FETCH-LOGICAL-c424t-aa84634f77e5ec594ecf4850f70746c833a3d6ed62826b7f686f0a10bed94be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijpharm.2005.04.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16926908$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15905051$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Yongsong</creatorcontrib><creatorcontrib>Huang, Lu</creatorcontrib><creatorcontrib>Chen, Jiuxin</creatorcontrib><creatorcontrib>Liang, Ji</creatorcontrib><creatorcontrib>Long, Shengyou</creatorcontrib><creatorcontrib>Lu, Yitong</creatorcontrib><title>Development of a controlled release formulation based on a starch matrix system</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>Controlled release formulation (CRF) of the insecticide acetamiprid was made using tapioca starch, urea and sodium borate. The data show the recovery of this CRF process is >95.43%, there is no obvious difference with increase of sodium borate added, however, with the increase of urea in the mixture, the formulation has a decrease recovery. In stability test, the decomposition rate of acetamiprid CRF was less one tenth than that of the acetamiprid emulsifiable concentrate (EC) under UV radiation. The release kinetics of acetamiprid from granules with variation content of urea, sodium borate and granule sizes were evaluated in water under laboratory condition. The release data were fitted to the generalized model
M
t
/
M
z
=
kt
n
, where
M
t
/
M
z
is the percentage of insecticide released at time
t,
k and
n are constants, and
n is constant that indicates the mechanism of release. The results indicated that the release of acetamiprid was diffusion-controlled. The time taken for 50% of the active ingredient to be released into water,
T
50, was also calculated for the comparison of formulations. The results showed that the formulation with the increasing urea in formulation had the higher value of
T
50, which means a slower release of the active ingredient, while that the formulation with the increasing sodium borate in formulation had the lower value of
T
50, which means a faster release of the active ingredient. It was also found that as the size of this formulation decreased, the release of the active ingredient was faster.</description><subject>Acetamiprid</subject><subject>Biological and medical sciences</subject><subject>Borates - administration & dosage</subject><subject>Chemistry, Pharmaceutical</subject><subject>Controlled release formulation</subject><subject>Delayed-Action Preparations</subject><subject>Drug Stability</subject><subject>General pharmacology</subject><subject>Kinetics</subject><subject>Manihot</subject><subject>Medical sciences</subject><subject>Neonicotinoids</subject><subject>Particle Size</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Pyridines - administration & dosage</subject><subject>Pyridines - chemistry</subject><subject>Stability</subject><subject>Starch - administration & dosage</subject><subject>Tapioca starch</subject><subject>Urea - administration & dosage</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1r3DAQhkVpaTZpf0KLLu3N7sj6sk-lpG1aCOSSu5DlEdEiW1vJG5p_Hy1ryDGndxDPjF4eQj4xaBkw9W3fhv3hwea57QBkC6Kt8YbsWK95w4VWb8kOuO4byTS_IJel7AFAdYy_JxdMDiBBsh25-4mPGNNhxmWlyVNLXVrWnGLEiWaMaAtSn_J8jHYNaaFjfZhoHSwtq83ugc52zeE_LU9lxfkDeedtLPhxyyty__vX_fWf5vbu5u_1j9vGiU6sjbW9UFx4rVGik4NA50UvwWvQQrmec8snhZPq-k6N2qteebAMRpwGMSK_Il_PZw85_TtiWc0cisMY7YLpWIzSg-RayVfBKkfVRn0F5Rl0OZWS0ZtDDrPNT4aBORk3e7MZNyfjBoSpUfc-bx8cxxmnl61NcQW-bIAtzkaf7eJCeeHU0KkBTgW-nzms2h4DZlNcwMXhFDK61UwpvFLlGb5Tods</recordid><startdate>20050714</startdate><enddate>20050714</enddate><creator>Cao, Yongsong</creator><creator>Huang, Lu</creator><creator>Chen, Jiuxin</creator><creator>Liang, Ji</creator><creator>Long, Shengyou</creator><creator>Lu, Yitong</creator><general>Elsevier B.V</general><general>Elsevier</general><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><scope>7X8</scope></search><sort><creationdate>20050714</creationdate><title>Development of a controlled release formulation based on a starch matrix system</title><author>Cao, Yongsong ; Huang, Lu ; Chen, Jiuxin ; Liang, Ji ; Long, Shengyou ; Lu, Yitong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-aa84634f77e5ec594ecf4850f70746c833a3d6ed62826b7f686f0a10bed94be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acetamiprid</topic><topic>Biological and medical sciences</topic><topic>Borates - administration & dosage</topic><topic>Chemistry, Pharmaceutical</topic><topic>Controlled release formulation</topic><topic>Delayed-Action Preparations</topic><topic>Drug Stability</topic><topic>General pharmacology</topic><topic>Kinetics</topic><topic>Manihot</topic><topic>Medical sciences</topic><topic>Neonicotinoids</topic><topic>Particle Size</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Pyridines - administration & dosage</topic><topic>Pyridines - chemistry</topic><topic>Stability</topic><topic>Starch - administration & dosage</topic><topic>Tapioca starch</topic><topic>Urea - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Yongsong</creatorcontrib><creatorcontrib>Huang, Lu</creatorcontrib><creatorcontrib>Chen, Jiuxin</creatorcontrib><creatorcontrib>Liang, Ji</creatorcontrib><creatorcontrib>Long, Shengyou</creatorcontrib><creatorcontrib>Lu, Yitong</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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Yongsong</au><au>Huang, Lu</au><au>Chen, Jiuxin</au><au>Liang, Ji</au><au>Long, Shengyou</au><au>Lu, Yitong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a controlled release formulation based on a starch matrix system</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2005-07-14</date><risdate>2005</risdate><volume>298</volume><issue>1</issue><spage>108</spage><epage>116</epage><pages>108-116</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><coden>IJPHDE</coden><abstract>Controlled release formulation (CRF) of the insecticide acetamiprid was made using tapioca starch, urea and sodium borate. The data show the recovery of this CRF process is >95.43%, there is no obvious difference with increase of sodium borate added, however, with the increase of urea in the mixture, the formulation has a decrease recovery. In stability test, the decomposition rate of acetamiprid CRF was less one tenth than that of the acetamiprid emulsifiable concentrate (EC) under UV radiation. The release kinetics of acetamiprid from granules with variation content of urea, sodium borate and granule sizes were evaluated in water under laboratory condition. The release data were fitted to the generalized model
M
t
/
M
z
=
kt
n
, where
M
t
/
M
z
is the percentage of insecticide released at time
t,
k and
n are constants, and
n is constant that indicates the mechanism of release. The results indicated that the release of acetamiprid was diffusion-controlled. The time taken for 50% of the active ingredient to be released into water,
T
50, was also calculated for the comparison of formulations. The results showed that the formulation with the increasing urea in formulation had the higher value of
T
50, which means a slower release of the active ingredient, while that the formulation with the increasing sodium borate in formulation had the lower value of
T
50, which means a faster release of the active ingredient. It was also found that as the size of this formulation decreased, the release of the active ingredient was faster.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15905051</pmid><doi>10.1016/j.ijpharm.2005.04.005</doi><tpages>9</tpages></addata></record> |
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language | eng |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Acetamiprid Biological and medical sciences Borates - administration & dosage Chemistry, Pharmaceutical Controlled release formulation Delayed-Action Preparations Drug Stability General pharmacology Kinetics Manihot Medical sciences Neonicotinoids Particle Size Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Pyridines - administration & dosage Pyridines - chemistry Stability Starch - administration & dosage Tapioca starch Urea - administration & dosage |
title | Development of a controlled release formulation based on a starch matrix system |
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