Controlled release of donepezil intercalated in smectite clays

The inorganic–organic hybrid for a drug delivery system was successfully realized by intercalating donepezil molecules into smectite clays (laponite XLG, saponite, and montmorillonite). According to the powder XRD patterns, TG profiles, and FT-IR spectra, it was confirmed that donepezil molecules we...

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Veröffentlicht in:International journal of pharmaceutics 2008-07, Vol.359 (1), p.198-204
Hauptverfasser: Park, Jin Kuen, Choy, Young Bin, Oh, Jae-Min, Kim, Ju Young, Hwang, Seong-Ju, Choy, Jin-Ho
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container_end_page 204
container_issue 1
container_start_page 198
container_title International journal of pharmaceutics
container_volume 359
creator Park, Jin Kuen
Choy, Young Bin
Oh, Jae-Min
Kim, Ju Young
Hwang, Seong-Ju
Choy, Jin-Ho
description The inorganic–organic hybrid for a drug delivery system was successfully realized by intercalating donepezil molecules into smectite clays (laponite XLG, saponite, and montmorillonite). According to the powder XRD patterns, TG profiles, and FT-IR spectra, it was confirmed that donepezil molecules were well stabilized in the interlayer space of clay via mono or double layer stacking. The adsorption amount and molecular structure of donepezil appeared to depend on the cation exchange capacity of the clay, which in turn, tailored the drug release patterns. Especially in the presence of a bulky cationic polymer (Eudragit ® E-100) in the release media, the release rate was found to be improved due to its effective replacement with intercalated donepezil molecules. Therefore, to formulate a complete drug delivery system, the hybrids were coated with Eudragit ® E-100 using a spray dryer, which also showed great enhancement in the release rate during a short period of time (180 min).
doi_str_mv 10.1016/j.ijpharm.2008.04.012
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Drug treatments</topic><topic>Piperidines - chemistry</topic><topic>Polymers - chemistry</topic><topic>Powder Diffraction</topic><topic>Silicates - chemistry</topic><topic>Smectite clay</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><topic>Thermogravimetry</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Jin Kuen</creatorcontrib><creatorcontrib>Choy, Young Bin</creatorcontrib><creatorcontrib>Oh, Jae-Min</creatorcontrib><creatorcontrib>Kim, Ju Young</creatorcontrib><creatorcontrib>Hwang, Seong-Ju</creatorcontrib><creatorcontrib>Choy, Jin-Ho</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>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Jin Kuen</au><au>Choy, Young Bin</au><au>Oh, Jae-Min</au><au>Kim, Ju Young</au><au>Hwang, Seong-Ju</au><au>Choy, Jin-Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Controlled release of donepezil intercalated in smectite clays</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2008-07-09</date><risdate>2008</risdate><volume>359</volume><issue>1</issue><spage>198</spage><epage>204</epage><pages>198-204</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><coden>IJPHDE</coden><abstract>The inorganic–organic hybrid for a drug delivery system was successfully realized by intercalating donepezil molecules into smectite clays (laponite XLG, saponite, and montmorillonite). According to the powder XRD patterns, TG profiles, and FT-IR spectra, it was confirmed that donepezil molecules were well stabilized in the interlayer space of clay via mono or double layer stacking. The adsorption amount and molecular structure of donepezil appeared to depend on the cation exchange capacity of the clay, which in turn, tailored the drug release patterns. Especially in the presence of a bulky cationic polymer (Eudragit ® E-100) in the release media, the release rate was found to be improved due to its effective replacement with intercalated donepezil molecules. Therefore, to formulate a complete drug delivery system, the hybrids were coated with Eudragit ® E-100 using a spray dryer, which also showed great enhancement in the release rate during a short period of time (180 min).</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>18502063</pmid><doi>10.1016/j.ijpharm.2008.04.012</doi><tpages>7</tpages></addata></record>
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subjects Acrylates - chemistry
Adsorption
Aluminum Silicates - chemistry
Bentonite - chemistry
Biological and medical sciences
Cholinesterase Inhibitors - chemistry
Controlled release
Delayed-Action Preparations
Donepezil
Drug Carriers - chemistry
Drug delivery system
Drug Delivery Systems
General pharmacology
Hybrid
Indans - chemistry
Medical sciences
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
Piperidines - chemistry
Polymers - chemistry
Powder Diffraction
Silicates - chemistry
Smectite clay
Spectroscopy, Fourier Transform Infrared
Thermogravimetry
Time Factors
title Controlled release of donepezil intercalated in smectite clays
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