Literature DB >> 16081259

A three step supercritical process to improve the dissolution rate of eflucimibe.

Elisabeth Rodier1, Hubert Lochard, Martial Sauceau, Jean-Jacques Letourneau, Bernard Freiss, Jacques Fages.   

Abstract

The aim of this study is to improve the dissolution properties of a poorly-soluble active substance, Eflucimibe by associating it with gamma-cyclodextrin. To achieve this objective, a new three-step process based on supercritical fluid technology has been proposed. First, Eflucimibe and cyclodextrin are co-crystallized using an anti-solvent process, dimethylsulfoxide being the solvent and supercritical carbon dioxide being the anti-solvent. Second, the co-crystallized powder is held in a static mode under supercritical conditions for several hours. This is the maturing step. Third, in a final stripping step, supercritical CO(2) is flowed through the matured powder 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. The nature of the entity obtained at the end of each step is discussed and some suggestions are made as to what happens in these operations. It is shown the co-crystallization ensures a good dispersion of both compounds and is rather insensitive to the operating parameters tested. The maturing step allows some dissolution-recrystallization to occur thus intensifying the intimate contact between the two compounds. Addition of water is necessary to make maturing effective as this is governed by the transfer properties of the medium. The stripping step allows extraction of the residual solvent but also removes some of the Eflucimibe which is the main drawback of this final stage.

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Year:  2005        PMID: 16081259     DOI: 10.1016/j.ejps.2005.05.011

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  7 in total

1.  Comparative physicochemical characterization of phospholipids complex of puerarin formulated by conventional and supercritical methods.

Authors:  Ying Li; Da-Jian Yang; Shi-Lin Chen; Si-Bao Chen; Albert Sun-Chi Chan
Journal:  Pharm Res       Date:  2007-09-08       Impact factor: 4.200

2.  Crystal structure changes of gamma-cyclodextrin after the SEDS process in supercritical carbon dioxide affect the dissolution rate of complexed budesonide.

Authors:  Tarja Toropainen; Teemu Heikkilä; Jukka Leppänen; Laura Matilainen; Sitaram Velaga; Pekka Jarho; Johan Carlfors; Vesa-Pekka Lehto; Tomi Järvinen; Kristiina Järvinen
Journal:  Pharm Res       Date:  2007-03-24       Impact factor: 4.580

3.  Dissolution enhancement of glibenclamide by solid dispersion: solvent evaporation versus a supercritical fluid-based solvent -antisolvent technique.

Authors:  M Tabbakhian; F Hasanzadeh; N Tavakoli; Z Jamshidian
Journal:  Res Pharm Sci       Date:  2014 Sep-Oct

Review 4.  Supercritical Fluid Technology: An Emphasis on Drug Delivery and Related Biomedical Applications.

Authors:  Ranjith Kumar Kankala; Yu Shrike Zhang; Shi-Bin Wang; Chia-Hung Lee; Ai-Zheng Chen
Journal:  Adv Healthc Mater       Date:  2017-07-28       Impact factor: 9.933

Review 5.  Supercritical Carbon Dioxide as a Green Alternative to Achieve Drug Complexation with Cyclodextrins.

Authors:  Mauro Banchero
Journal:  Pharmaceuticals (Basel)       Date:  2021-06-11

6.  An investigation on the solid dispersions of chlordiazepoxide.

Authors:  Ali Nokhodchi; Roya Talari; Hadi Valizadeh; Mohammad Barzegar Jalali
Journal:  Int J Biomed Sci       Date:  2007-09

7.  Preparation and Characterization of Fenofibrate Microparticles with Surface-Active Additives: Application of a Supercritical Fluid-Assisted Spray-Drying Process.

Authors:  Jeong-Soo Kim; Heejun Park; Eun-Sol Ha; Kyu-Tae Kang; Min-Soo Kim; Sung-Joo Hwang
Journal:  Pharmaceutics       Date:  2021-12-02       Impact factor: 6.321

  7 in total

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