Comparative Evaluation of Pellet Cushioning Agents by Various Imaging Techniques and Dissolution Studies
Most of the commercially available pharmaceutical products for oral administration route are marketed in the tablet dosage forms. However, compression of multiparticulate systems is a challenge for the pharmaceutical research and industry, especially if the individual unit is a coated particle, as t...
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creator | Sántha, Konrád Kállai-Szabó, Nikolett Fülöp, Viktor Jakab, Géza Gordon, Péter Kállai-Szabó, Barnabás Balogh, Emese Antal, István |
description | Most of the commercially available pharmaceutical products for oral administration route are marketed in the tablet dosage forms. However, compression of multiparticulate systems is a challenge for the pharmaceutical research and industry, especially if the individual unit is a coated particle, as the release of the active ingredient depends on the integrity of the coating. In the present study, polymer-coated pellets tableted with different types of excipients (powder, granules, pellets) then were investigated by various tablet-destructive (microscopic) and tablet non-destructive (microfocus X-ray; microCT) imaging methods. The information obtained from the independent evaluation of the
in vitro
drug release profiles model is confirmed by the results obtained by image analysis, regardless of whether X-ray or stereomicroscopic images of the coated, tableted pellets were used for image analysis. The results of this study show that the novel easy-to-use, fast, and non-destructive MFX method is a good alternative to the already used microscopic image analysis methods regarding the characterization of particulates, compressed into tablets. |
doi_str_mv | 10.1208/s12249-020-01902-x |
format | Article |
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in vitro
drug release profiles model is confirmed by the results obtained by image analysis, regardless of whether X-ray or stereomicroscopic images of the coated, tableted pellets were used for image analysis. The results of this study show that the novel easy-to-use, fast, and non-destructive MFX method is a good alternative to the already used microscopic image analysis methods regarding the characterization of particulates, compressed into tablets.</description><identifier>ISSN: 1530-9932</identifier><identifier>EISSN: 1530-9932</identifier><identifier>DOI: 10.1208/s12249-020-01902-x</identifier><identifier>PMID: 33377174</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Administration, Oral ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Biotechnology ; Chemistry, Pharmaceutical - methods ; Drug Implants ; Drug Liberation ; Excipients ; Pharmacology/Toxicology ; Pharmacy ; Polymers ; Powders ; Research Article ; Solubility ; Tablets</subject><ispartof>AAPS PharmSciTech, 2020-12, Vol.22 (1), p.14, Article 14</ispartof><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-8492a358be7823b3fc9bbfec803e55b9907c30f05a038456d8ac607ff4ddee703</citedby><cites>FETCH-LOGICAL-c446t-8492a358be7823b3fc9bbfec803e55b9907c30f05a038456d8ac607ff4ddee703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1208/s12249-020-01902-x$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1208/s12249-020-01902-x$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33377174$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sántha, Konrád</creatorcontrib><creatorcontrib>Kállai-Szabó, Nikolett</creatorcontrib><creatorcontrib>Fülöp, Viktor</creatorcontrib><creatorcontrib>Jakab, Géza</creatorcontrib><creatorcontrib>Gordon, Péter</creatorcontrib><creatorcontrib>Kállai-Szabó, Barnabás</creatorcontrib><creatorcontrib>Balogh, Emese</creatorcontrib><creatorcontrib>Antal, István</creatorcontrib><title>Comparative Evaluation of Pellet Cushioning Agents by Various Imaging Techniques and Dissolution Studies</title><title>AAPS PharmSciTech</title><addtitle>AAPS PharmSciTech</addtitle><addtitle>AAPS PharmSciTech</addtitle><description>Most of the commercially available pharmaceutical products for oral administration route are marketed in the tablet dosage forms. However, compression of multiparticulate systems is a challenge for the pharmaceutical research and industry, especially if the individual unit is a coated particle, as the release of the active ingredient depends on the integrity of the coating. In the present study, polymer-coated pellets tableted with different types of excipients (powder, granules, pellets) then were investigated by various tablet-destructive (microscopic) and tablet non-destructive (microfocus X-ray; microCT) imaging methods. The information obtained from the independent evaluation of the
in vitro
drug release profiles model is confirmed by the results obtained by image analysis, regardless of whether X-ray or stereomicroscopic images of the coated, tableted pellets were used for image analysis. The results of this study show that the novel easy-to-use, fast, and non-destructive MFX method is a good alternative to the already used microscopic image analysis methods regarding the characterization of particulates, compressed into tablets.</description><subject>Administration, Oral</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Chemistry, Pharmaceutical - methods</subject><subject>Drug Implants</subject><subject>Drug Liberation</subject><subject>Excipients</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Polymers</subject><subject>Powders</subject><subject>Research Article</subject><subject>Solubility</subject><subject>Tablets</subject><issn>1530-9932</issn><issn>1530-9932</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9kF1PwyAUhonROL_-gBeGP1A9QDvKjcky50dioonTW0Jb2rF0ZUK7bP9etqqZN15xwnveB_IgdEngmlBIbzyhNBYRUIiACKDR-gCdkIRBJASjh3vzAJ16PwegjAh2jAaMMc4Jj0_QbGwXS-VUa1YaT1aq7sJoG2xL_KrrWrd43PlZuDFNhUeVblqPsw3-UM7YzuOnhaq2yVTns8Z8dtpj1RT4znhv625Hemu7wmh_jo5KVXt98X2eoff7yXT8GD2_PDyNR89RHsfDNkpjQRVL0kzzlLKMlbnIslLnKTCdJJkQwHMGJSQKWBonwyJV-RB4WcZFoTUHdoZue-6yyxa6yMOPnarl0pmFchtplZF_k8bMZGVXknNOyZAGAO0BubPeO13-dgnIrXfZe5fBu9x5l-tQutp_9bfyIzossH7Bh6iptJNz27kmmPgP-wWh0pI4</recordid><startdate>20201229</startdate><enddate>20201229</enddate><creator>Sántha, Konrád</creator><creator>Kállai-Szabó, Nikolett</creator><creator>Fülöp, Viktor</creator><creator>Jakab, Géza</creator><creator>Gordon, Péter</creator><creator>Kállai-Szabó, Barnabás</creator><creator>Balogh, Emese</creator><creator>Antal, István</creator><general>Springer International Publishing</general><scope>C6C</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>5PM</scope></search><sort><creationdate>20201229</creationdate><title>Comparative Evaluation of Pellet Cushioning Agents by Various Imaging Techniques and Dissolution Studies</title><author>Sántha, Konrád ; Kállai-Szabó, Nikolett ; Fülöp, Viktor ; Jakab, Géza ; Gordon, Péter ; Kállai-Szabó, Barnabás ; Balogh, Emese ; Antal, István</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-8492a358be7823b3fc9bbfec803e55b9907c30f05a038456d8ac607ff4ddee703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Administration, Oral</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Chemistry, Pharmaceutical - methods</topic><topic>Drug Implants</topic><topic>Drug Liberation</topic><topic>Excipients</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Polymers</topic><topic>Powders</topic><topic>Research Article</topic><topic>Solubility</topic><topic>Tablets</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sántha, Konrád</creatorcontrib><creatorcontrib>Kállai-Szabó, Nikolett</creatorcontrib><creatorcontrib>Fülöp, Viktor</creatorcontrib><creatorcontrib>Jakab, Géza</creatorcontrib><creatorcontrib>Gordon, Péter</creatorcontrib><creatorcontrib>Kállai-Szabó, Barnabás</creatorcontrib><creatorcontrib>Balogh, Emese</creatorcontrib><creatorcontrib>Antal, István</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>AAPS PharmSciTech</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sántha, Konrád</au><au>Kállai-Szabó, Nikolett</au><au>Fülöp, Viktor</au><au>Jakab, Géza</au><au>Gordon, Péter</au><au>Kállai-Szabó, Barnabás</au><au>Balogh, Emese</au><au>Antal, István</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Evaluation of Pellet Cushioning Agents by Various Imaging Techniques and Dissolution Studies</atitle><jtitle>AAPS PharmSciTech</jtitle><stitle>AAPS PharmSciTech</stitle><addtitle>AAPS PharmSciTech</addtitle><date>2020-12-29</date><risdate>2020</risdate><volume>22</volume><issue>1</issue><spage>14</spage><pages>14-</pages><artnum>14</artnum><issn>1530-9932</issn><eissn>1530-9932</eissn><abstract>Most of the commercially available pharmaceutical products for oral administration route are marketed in the tablet dosage forms. However, compression of multiparticulate systems is a challenge for the pharmaceutical research and industry, especially if the individual unit is a coated particle, as the release of the active ingredient depends on the integrity of the coating. In the present study, polymer-coated pellets tableted with different types of excipients (powder, granules, pellets) then were investigated by various tablet-destructive (microscopic) and tablet non-destructive (microfocus X-ray; microCT) imaging methods. The information obtained from the independent evaluation of the
in vitro
drug release profiles model is confirmed by the results obtained by image analysis, regardless of whether X-ray or stereomicroscopic images of the coated, tableted pellets were used for image analysis. The results of this study show that the novel easy-to-use, fast, and non-destructive MFX method is a good alternative to the already used microscopic image analysis methods regarding the characterization of particulates, compressed into tablets.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>33377174</pmid><doi>10.1208/s12249-020-01902-x</doi><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Biochemistry Biomedical and Life Sciences Biomedicine Biotechnology Chemistry, Pharmaceutical - methods Drug Implants Drug Liberation Excipients Pharmacology/Toxicology Pharmacy Polymers Powders Research Article Solubility Tablets |
title | Comparative Evaluation of Pellet Cushioning Agents by Various Imaging Techniques and Dissolution Studies |
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