A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study
ABSTRACT: Objective: To evaluate and compare the particle and tableting properties of a new sorbitol (SOR) and anhydrous calcium diphosphate (ACD)composite with common excipients used for the preparation of tablets by direct compression such as polyvinylpyrrolidone (Ludipress®), lactose (Cellactose...
- Autores:
-
Echeverrri Pineda, Edward
Rojas Camargo, Jhon
Bedoya, Mauricio
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2016
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/32682
- Acceso en línea:
- https://hdl.handle.net/10495/32682
https://innovareacademics.in/journals/index.php/ijpps/article/view/8845/
- Palabra clave:
- Sorbitol
Pirofosfato de Calcio
Calcium Pyrophosphate
Aglomeración
Agglomeration
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by/4.0/
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A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study |
| title |
A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study |
| spellingShingle |
A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study Sorbitol Pirofosfato de Calcio Calcium Pyrophosphate Aglomeración Agglomeration |
| title_short |
A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study |
| title_full |
A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study |
| title_fullStr |
A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study |
| title_full_unstemmed |
A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study |
| title_sort |
A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study |
| dc.creator.fl_str_mv |
Echeverrri Pineda, Edward Rojas Camargo, Jhon Bedoya, Mauricio |
| dc.contributor.author.none.fl_str_mv |
Echeverrri Pineda, Edward Rojas Camargo, Jhon Bedoya, Mauricio |
| dc.contributor.researchgroup.spa.fl_str_mv |
Diseño y Formulación de Medicamentos Cosméticos y Afines |
| dc.subject.decs.none.fl_str_mv |
Sorbitol Pirofosfato de Calcio Calcium Pyrophosphate |
| topic |
Sorbitol Pirofosfato de Calcio Calcium Pyrophosphate Aglomeración Agglomeration |
| dc.subject.lemb.none.fl_str_mv |
Aglomeración Agglomeration |
| description |
ABSTRACT: Objective: To evaluate and compare the particle and tableting properties of a new sorbitol (SOR) and anhydrous calcium diphosphate (ACD)composite with common excipients used for the preparation of tablets by direct compression such as polyvinylpyrrolidone (Ludipress®), lactose (Cellactose 80®) and microcrystalline cellulose (Prosolv SMCC 90®). Methods: All materials were tested for lubricant sensitivity, ejection force, and elastic recovery, dilution potential and reworking ability. Further, compressibility and compactibility were determined using the Heckel and Leuenberger models, respectively.Results: This new excipient offered more benefits in terms of functionality than commercial direct compressive co-processed excipients andshowed better compressibility than other commercial excipients and its compactibility was ranked third after SOR and Prosolv SMCC 90®. However, this composite material was more susceptible to reprocessing than commercial products. Further, it showed a low lubricant sensitivity due to a combination of a plastic and brittle behavior. Moreover, the loading capacity of poorly compressible materials such as gemfibrozil was comparable to that of commercial direct compression excipients. It also showed the fastest in-vitro dissolution of gemfibrozil, whereas commercial products failed to fulfill the US pharmacopoeial requirements. Conclusion: This new composite material showed potential for use as a direct compression excipient. |
| publishDate |
2016 |
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2016 |
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2022-12-09T23:27:18Z |
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2022-12-09T23:27:18Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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Echeverri E, Rojas J, Bedoya M. A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study. Int J Pharm Pharm Sci [Internet]. 2016 Apr. 1 [cited 2022 Dec. 10];8(4):43-9. Available from: https://innovareacademics.in/journals/index.php/ijpps/article/view/8845 |
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0975-1491 |
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https://hdl.handle.net/10495/32682 |
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2656-0097 |
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https://innovareacademics.in/journals/index.php/ijpps/article/view/8845/ |
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Echeverri E, Rojas J, Bedoya M. A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study. Int J Pharm Pharm Sci [Internet]. 2016 Apr. 1 [cited 2022 Dec. 10];8(4):43-9. Available from: https://innovareacademics.in/journals/index.php/ijpps/article/view/8845 0975-1491 2656-0097 |
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eng |
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Int. J. Pharm. Pharm. Sci. |
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49 |
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4 |
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43 |
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8 |
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International Journal of Pharmacy and Pharmaceutical Sciences |
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Echeverrri Pineda, EdwardRojas Camargo, JhonBedoya, MauricioDiseño y Formulación de Medicamentos Cosméticos y Afines2022-12-09T23:27:18Z2022-12-09T23:27:18Z2016Echeverri E, Rojas J, Bedoya M. A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative Study. Int J Pharm Pharm Sci [Internet]. 2016 Apr. 1 [cited 2022 Dec. 10];8(4):43-9. Available from: https://innovareacademics.in/journals/index.php/ijpps/article/view/88450975-1491https://hdl.handle.net/10495/326822656-0097https://innovareacademics.in/journals/index.php/ijpps/article/view/8845/ABSTRACT: Objective: To evaluate and compare the particle and tableting properties of a new sorbitol (SOR) and anhydrous calcium diphosphate (ACD)composite with common excipients used for the preparation of tablets by direct compression such as polyvinylpyrrolidone (Ludipress®), lactose (Cellactose 80®) and microcrystalline cellulose (Prosolv SMCC 90®). Methods: All materials were tested for lubricant sensitivity, ejection force, and elastic recovery, dilution potential and reworking ability. Further, compressibility and compactibility were determined using the Heckel and Leuenberger models, respectively.Results: This new excipient offered more benefits in terms of functionality than commercial direct compressive co-processed excipients andshowed better compressibility than other commercial excipients and its compactibility was ranked third after SOR and Prosolv SMCC 90®. However, this composite material was more susceptible to reprocessing than commercial products. Further, it showed a low lubricant sensitivity due to a combination of a plastic and brittle behavior. Moreover, the loading capacity of poorly compressible materials such as gemfibrozil was comparable to that of commercial direct compression excipients. It also showed the fastest in-vitro dissolution of gemfibrozil, whereas commercial products failed to fulfill the US pharmacopoeial requirements. Conclusion: This new composite material showed potential for use as a direct compression excipient.COL00036237application/pdfengIJPPSBhopal, Indiahttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2A New Enhanced Sorbitol: Calcium Diphosphate Composite as A Direct Compression Excipient: A Comparative StudyArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionSorbitolPirofosfato de CalcioCalcium PyrophosphateAglomeraciónAgglomerationInt. J. Pharm. Pharm. 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