Comparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical Technology

Two processes have been developed for the enhancement of bioavailability of a poorly-soluble active substance, Eflucimibe by associating it with γ-CD (γ-cyclodextrin).In the first process (process a), Eflucimibe was added to an aqueous slurry of...

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Main Authors: Jacques Fages, Elisabeth Rodier, Alain Chamayou, Michel Baron
Format: Article
Language:English
Published: Hosokawa Powder Technology Foundation 2014-03-01
Series:KONA Powder and Particle Journal
Subjects:
Online Access:https://www.jstage.jst.go.jp/article/kona/25/0/25_2007019/_pdf/-char/en
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spelling doaj-89a36a49ca994338add94704e90b6b212021-02-03T01:02:42ZengHosokawa Powder Technology FoundationKONA Powder and Particle Journal0288-45342187-55372014-03-0125021722910.14356/kona.2007019konaComparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical TechnologyJacques Fages0Elisabeth Rodier1Alain Chamayou2Michel Baron3Ecole des Mines d’Albi, RAPSODEE Research CentreEcole des Mines d’Albi, RAPSODEE Research CentreEcole des Mines d’Albi, RAPSODEE Research CentreEcole des Mines d’Albi, RAPSODEE Research CentreTwo processes have been developed for the enhancement of bioavailability of a poorly-soluble active substance, Eflucimibe by associating it with γ-CD (γ-cyclodextrin).In the first process (process a), Eflucimibe was added to an aqueous slurry of CD, in a kneading device. The evolution of the transformation was followed by DSC, FTIR, Eflucimibe dissolution kinetics, as well as semi-solid state change of the mixture. An optimization of the process was performed and a prevision of the scaling-up was made using dimensionless numbers. This process is simple and robust. It can be compatible at the industrial scale with a good economy and appropriate control.In the second process (process b), Eflucimibe and CD are co-crystallized using an anti-solvent process, dimethylsulfoxide being the solvent and supercritical carbon dioxide being the anti-solvent. Then, the co-crystallized powder is held in a static mode under supercritical conditions for several hours. A final stripping step, is used to extract the residual solvent. The coupling of the first two steps brings about a significant synergistic effect to improve the dissolution rate of the drug.Both processes resulted in a strong acceleration of the in vitro dissolution rate of the drug. Finally, in an in vivo test, these two processes appeared to be very effective, process (a) and (b) giving respectively an 8-fold and 11-fold increase in bioavailability.https://www.jstage.jst.go.jp/article/kona/25/0/25_2007019/_pdf/-char/eneflucimibecyclodextrinkneadingsupercritical co2scale-upbioavailability
collection DOAJ
language English
format Article
sources DOAJ
author Jacques Fages
Elisabeth Rodier
Alain Chamayou
Michel Baron
spellingShingle Jacques Fages
Elisabeth Rodier
Alain Chamayou
Michel Baron
Comparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical Technology
KONA Powder and Particle Journal
eflucimibe
cyclodextrin
kneading
supercritical co2
scale-up
bioavailability
author_facet Jacques Fages
Elisabeth Rodier
Alain Chamayou
Michel Baron
author_sort Jacques Fages
title Comparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical Technology
title_short Comparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical Technology
title_full Comparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical Technology
title_fullStr Comparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical Technology
title_full_unstemmed Comparative Study of Two Processes to Improve the Bioavailability of an Active Pharmaceutical Ingredient: Kneading and Supercritical Technology
title_sort comparative study of two processes to improve the bioavailability of an active pharmaceutical ingredient: kneading and supercritical technology
publisher Hosokawa Powder Technology Foundation
series KONA Powder and Particle Journal
issn 0288-4534
2187-5537
publishDate 2014-03-01
description Two processes have been developed for the enhancement of bioavailability of a poorly-soluble active substance, Eflucimibe by associating it with γ-CD (γ-cyclodextrin).In the first process (process a), Eflucimibe was added to an aqueous slurry of CD, in a kneading device. The evolution of the transformation was followed by DSC, FTIR, Eflucimibe dissolution kinetics, as well as semi-solid state change of the mixture. An optimization of the process was performed and a prevision of the scaling-up was made using dimensionless numbers. This process is simple and robust. It can be compatible at the industrial scale with a good economy and appropriate control.In the second process (process b), Eflucimibe and CD are co-crystallized using an anti-solvent process, dimethylsulfoxide being the solvent and supercritical carbon dioxide being the anti-solvent. Then, the co-crystallized powder is held in a static mode under supercritical conditions for several hours. A final stripping step, is used to extract the residual solvent. The coupling of the first two steps brings about a significant synergistic effect to improve the dissolution rate of the drug.Both processes resulted in a strong acceleration of the in vitro dissolution rate of the drug. Finally, in an in vivo test, these two processes appeared to be very effective, process (a) and (b) giving respectively an 8-fold and 11-fold increase in bioavailability.
topic eflucimibe
cyclodextrin
kneading
supercritical co2
scale-up
bioavailability
url https://www.jstage.jst.go.jp/article/kona/25/0/25_2007019/_pdf/-char/en
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AT alainchamayou comparativestudyoftwoprocessestoimprovethebioavailabilityofanactivepharmaceuticalingredientkneadingandsupercriticaltechnology
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