Literature DB >> 19818402

Fusion production of solid dispersions containing a heat-sensitive active ingredient by hot melt extrusion and Kinetisol dispersing.

James C Dinunzio1, Chris Brough, Justin R Hughey, Dave A Miller, Robert O Williams, James W McGinity.   

Abstract

Many techniques for the production of solid dispersions rely on elevated temperatures and prolonged material residence times, which can result in decomposition of temperature-sensitive components. In this study, hydrocortisone was used as a model temperature-sensitive active ingredient to study the effect of formulation and processing techniques as well as to characterize the benefits of KinetiSol Dispersing for the production of solid dispersions. Preformulation studies were conducted using differential scanning calorimetry and hot stage microscopy to identify optimum carriers for the production of amorphous solid dispersions. After identification, solid dispersions were prepared by hot melt extrusion and KinetiSol Dispersing, with material characterized by X-ray diffraction, dissolution and potency testing to evaluate physicochemical properties. Results from the preformulation studies showed that vinylacetate:vinylpyrrolidone (PVPVA) copolymer allowed for hydrocortisone dissolution within the carrier at temperatures as low as 160 degrees C, while hydroxypropyl methylcellulose required temperatures upward of 180 degrees C to facilitate solubilization. Low substituted hydroxypropyl cellulose, a high glass transition temperature control, showed that the material was unable to solubilize hydrocortisone. Manufacturing process control studies using hot melt extruded compositions of hydrocortisone and PVPVA showed that increased temperatures and residence times negatively impacted product potency due to decomposition. Using KinetiSol Dispersing to reduce residence time and to facilitate lower temperature processing, it was possible to produce solid dispersions with improved product potency. This study clearly demonstrated the importance of carrier selection to facilitate lower temperature processing, as well as the effect of residence time on product potency. Furthermore, KinetiSol Dispersing provided significant advantages over hot melt extrusion due to the reduced residence times and lower required processing temperatures. This allowed for the production of solid dispersions with enhanced product potency. Copyright (c) 2009 Elsevier B.V. All rights reserved.

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Year:  2009        PMID: 19818402     DOI: 10.1016/j.ejpb.2009.09.007

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  19 in total

Review 1.  Challenges and Strategies in Thermal Processing of Amorphous Solid Dispersions: A Review.

Authors:  Justin S LaFountaine; James W McGinity; Robert O Williams
Journal:  AAPS PharmSciTech       Date:  2015-08-26       Impact factor: 3.246

2.  Improving the chemical stability of amorphous solid dispersion with cocrystal technique by hot melt extrusion.

Authors:  Xu Liu; Ming Lu; Zhefei Guo; Lin Huang; Xin Feng; Chuanbin Wu
Journal:  Pharm Res       Date:  2011-10-19       Impact factor: 4.200

3.  Development and characterization of solid dispersion for dissolution improvement of furosemide by cogrinding method.

Authors:  Mohammad Reza Siahi-Shadbad; Saeed Ghanbarzadeh; Mohammad Barzegar-Jalali; Hadi Valizadeh; Alireza Taherpoor; Ghobad Mohammadi; Azim Barzegar-Jalali; Khosro Adibkia
Journal:  Adv Pharm Bull       Date:  2014-08-10

4.  Dissolution enhancement of a drug exhibiting thermal and acidic decomposition characteristics by fusion processing: a comparative study of hot melt extrusion and KinetiSol dispersing.

Authors:  Justin R Hughey; James C DiNunzio; Ryan C Bennett; Chris Brough; Dave A Miller; Hua Ma; Robert O Williams; James W McGinity
Journal:  AAPS PharmSciTech       Date:  2010-05-05       Impact factor: 3.246

Review 5.  Hot-Melt Extrusion: a Roadmap for Product Development.

Authors:  Marta F Simões; Rui M A Pinto; Sérgio Simões
Journal:  AAPS PharmSciTech       Date:  2021-06-17       Impact factor: 3.246

6.  Thermal Processing of PVP- and HPMC-Based Amorphous Solid Dispersions.

Authors:  Justin S LaFountaine; Leena Kumari Prasad; Chris Brough; Dave A Miller; James W McGinity; Robert O Williams
Journal:  AAPS PharmSciTech       Date:  2015-10-13       Impact factor: 3.246

7.  Low-viscosity hydroxypropylcellulose (HPC) grades SL and SSL: versatile pharmaceutical polymers for dissolution enhancement, controlled release, and pharmaceutical processing.

Authors:  Ashish Sarode; Peng Wang; Catherine Cote; David R Worthen
Journal:  AAPS PharmSciTech       Date:  2012-12-19       Impact factor: 3.246

8.  Manufacturing strategies to develop amorphous solid dispersions: An overview.

Authors:  Nicole Mendonsa; Bjad Almutairy; Venkata Raman Kallakunta; Sandeep Sarabu; Priyanka Thipsay; Suresh Bandari; Michael A Repka
Journal:  J Drug Deliv Sci Technol       Date:  2019-12-11       Impact factor: 3.981

9.  Klucel™ EF and ELF polymers for immediate-release oral dosage forms prepared by melt extrusion technology.

Authors:  Noorullah Naqvi Mohammed; Soumyajit Majumdar; Abhilasha Singh; Weibin Deng; Narasimha S Murthy; Elanor Pinto; Divya Tewari; Thomas Durig; Michael A Repka
Journal:  AAPS PharmSciTech       Date:  2012-09-08       Impact factor: 3.246

10.  Influence of Molecular Weight of Carriers and Processing Parameters on the Extrudability, Drug Release, and Stability of Fenofibrate Formulations Processed by Hot-Melt Extrusion.

Authors:  Bader B Alsulays; Jun-Bom Park; Sultan M Alshehri; Joseph T Morott; Saad M Alshahrani; Roshan V Tiwari; Abdullah S Alshetaili; Soumyajit Majumdar; Nigel Langley; Karl Kolter; Andreas Gryczke; Michael A Repka
Journal:  J Drug Deliv Sci Technol       Date:  2015-10-01       Impact factor: 3.981

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