Literature DB >> 31605688

Impact of Hot-Melt Extrusion Processing Conditions on Physicochemical Properties of Amorphous Solid Dispersions Containing Thermally Labile Acrylic Copolymer.

Alex Mathers1, Fatima Hassouna2, Lenka Malinová3, Jan Merna3, Květoslav Růžička1, Michal Fulem4.   

Abstract

For successful formulation of amorphous solid dispersions (ASDs) using hot-melt extrusion, it is imperative to understand the effect that heat and shear rate has on the physicochemical properties of the excipient. In this study, we investigated the influence of hot-melt extrusion parameters on solvent-free binary ASDs of ibuprofen (IBU), a model active pharmaceutical ingredient, in methacrylic acid-ethyl acrylate copolymer type A, 1:1, EUDRAGIT® L100-55 (EUD). To evaluate the impact of barrel temperature, screw speed, and residence time on EUD mass average molar mass and IBU release profile, size-exclusion chromatography and dissolution testing were used, respectively. The optimal conditions were established for IBU loadings less than 40 wt. %. For ASD formulations prepared using the ideal variables, spectral and thermal analyses confirmed that, under dry conditions at a temperature of 25°C, IBU remained amorphous during an 18-month storage period. After 28 months, formulations with active pharmaceutical ingredient content above 30 wt. % started to recrystallize. A temperature-composition phase diagram, constructed using melting point depression and glass-transition temperature measurements of IBU-EUD mixtures, correlated well with the long-term physical stability. The effect that minor-to-moderate polymer degradation within the extrudates has on their long-term physical stability and dissolution characteristics is analyzed and discussed.
Copyright © 2020 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  amorphous solid dispersion(s) (ASD); bioavailability; extrusion, polymer chemical, degradation; formulation; glass transition(s); molecular weight; phase diagram(s); physical stability; solubility

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Substances:

Year:  2019        PMID: 31605688     DOI: 10.1016/j.xphs.2019.10.005

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  4 in total

1.  A Hot-Melt Extrusion Risk Assessment Classification System for Amorphous Solid Dispersion Formulation Development.

Authors:  Samuel O Kyeremateng; Kristin Voges; Stefanie Dohrn; Ekaterina Sobich; Ute Lander; Stefan Weber; David Gessner; Rachel C Evans; Matthias Degenhardt
Journal:  Pharmaceutics       Date:  2022-05-12       Impact factor: 6.525

Review 2.  Amorphous solid dispersions: An update for preparation, characterization, mechanism on bioavailability, stability, regulatory considerations and marketed products.

Authors:  Palpandi Pandi; Raviteja Bulusu; Nagavendra Kommineni; Wahid Khan; Mandip Singh
Journal:  Int J Pharm       Date:  2020-06-18       Impact factor: 5.875

3.  A Novel Approach to Optimize Hot Melt Impregnation in Terms of Amorphization Efficiency.

Authors:  Kamil Garbera; Krzesimir Ciura; Wiesław Sawicki
Journal:  Int J Mol Sci       Date:  2020-06-04       Impact factor: 5.923

Review 4.  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

  4 in total

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