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...
Main Authors: | , , , |
---|---|
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 |
id |
doaj-89a36a49ca994338add94704e90b6b21 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT jacquesfages comparativestudyoftwoprocessestoimprovethebioavailabilityofanactivepharmaceuticalingredientkneadingandsupercriticaltechnology AT elisabethrodier comparativestudyoftwoprocessestoimprovethebioavailabilityofanactivepharmaceuticalingredientkneadingandsupercriticaltechnology AT alainchamayou comparativestudyoftwoprocessestoimprovethebioavailabilityofanactivepharmaceuticalingredientkneadingandsupercriticaltechnology AT michelbaron comparativestudyoftwoprocessestoimprovethebioavailabilityofanactivepharmaceuticalingredientkneadingandsupercriticaltechnology |
_version_ |
1724289930213982208 |