Literature DB >> 23618964

Highly efficient miniaturized coprecipitation screening (MiCoS) for amorphous solid dispersion formulation development.

Qingyan Hu1, Duk Soon Choi, Hitesh Chokshi, Navnit Shah, Harpreet Sandhu.   

Abstract

Microprecipitated bulk powder (MBP) is a novel solid dispersion technology to manufacture amorphous formulations of poorly soluble compounds that cannot be processed by spray drying or melt extrusion. An efficient high-throughput screening method has been developed to aid the selection of polymer type, drug loading and antisolvent to solvent ratio for MBP formulation development. With a 96-well platform, the miniaturized coprecipitation screening (MiCoS) includes mixing of drug and polymer in dimethylacetamide, controlled precipitation to generate MBP, filtration/washing, drying and high throughput characterization. The integrated MiCoS approach has been demonstrated with a model compound, glybenclamide. Based on the solid state stability and kinetic solubility of the MBP, hydroxypropylmethylcellulose acetate succinate polymer with 40% or lower drug loading, and antisolvent (0.01 N HCl) to solvent (dimethylacetamide) ratio of 5:1 or higher were selected to make glybenclamide MBP. MiCoS can be applied to both early and late stage formulation processing. In early stage research programs, the system can be used to enable efficacy, pharmacokinetics or mini-toxicology studies for poorly water soluble molecules using minimal amount of drug substance (2-10mg). In late stage development programs, MiCoS can be used to optimize MBP formulation by expanding the experimental design space to include additional formulation variants.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23618964     DOI: 10.1016/j.ijpharm.2013.04.040

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  5 in total

1.  Stable amorphous solid dispersions of fenofibrate using hot melt extrusion technology: Effect of formulation and process parameters for a low glass transition temperature drug.

Authors:  Venkata Raman Kallakunta; Sandeep Sarabu; Suresh Bandari; Amol Batra; Vivian Bi; Thomas Durig; Michael A Repka
Journal:  J Drug Deliv Sci Technol       Date:  2019-11-18       Impact factor: 3.981

2.  Optimization of Spray-Drying Parameters for Formulation Development at Preclinical Scale.

Authors:  Marika Nespi; Robert Kuhn; Chun-Wan Yen; Joseph W Lubach; Dennis Leung
Journal:  AAPS PharmSciTech       Date:  2021-12-20       Impact factor: 3.246

3.  Physical Stability and Dissolution of Lumefantrine Amorphous Solid Dispersions Produced by Spray Anti-Solvent Precipitation.

Authors:  Sonal V Bhujbal; Vaibhav Pathak; Dmitry Y Zemlyanov; Lynne S Taylor; Qi Tony Zhou
Journal:  J Pharm Sci       Date:  2020-12-31       Impact factor: 3.534

Review 4.  The Need for Restructuring the Disordered Science of Amorphous Drug Formulations.

Authors:  Khadijah Edueng; Denny Mahlin; Christel A S Bergström
Journal:  Pharm Res       Date:  2017-05-18       Impact factor: 4.200

Review 5.  Insoluble Polymers in Solid Dispersions for Improving Bioavailability of Poorly Water-Soluble Drugs.

Authors:  Thao T D Tran; Phuong H L Tran
Journal:  Polymers (Basel)       Date:  2020-07-28       Impact factor: 4.329

  5 in total

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