Elucidation and visualization of solid-state transformation and mixing in a pharmaceutical mini hot melt extrusion process using in-line Raman spectroscopy

Int J Pharm. 2017 Jan 30;517(1-2):119-127. doi: 10.1016/j.ijpharm.2016.11.065. Epub 2016 Dec 1.

Abstract

Mixing of raw materials (drug+polymer) in the investigated mini pharma melt extruder is achieved by using co-rotating conical twin screws and an internal recirculation channel. In-line Raman spectroscopy was implemented in the barrels, allowing monitoring of the melt during processing. The aim of this study was twofold: to investigate (I) the influence of key process parameters (screw speed - barrel temperature) upon the product solid-state transformation during processing of a sustained release formulation in recirculation mode; (II) the influence of process parameters (screw speed - barrel temperature - recirculation time) upon mixing of a crystalline drug (tracer) in an amorphous polymer carrier by means of residence time distribution (RTD) measurements. The results indicated a faster mixing endpoint with increasing screw speed. Processing a high drug load formulation above the drug melting temperature resulted in the production of amorphous drug whereas processing below the drug melting point produced solid dispersions with partially amorphous/crystalline drug. Furthermore, increasing the screw speed resulted in lower drug crystallinity of the solid dispersion. RTD measurements elucidated the improved mixing capacity when using the recirculation channel. In-line Raman spectroscopy has shown to be an adequate PAT-tool for product solid-state monitoring and elucidation of the mixing behavior during processing in a mini extruder.

Keywords: Hot-melt extrusion; Mixing; Raman spectroscopy; Recirculation time; Residence time distribution; Solid-state transformation; Transport.

MeSH terms

  • Acrylates / chemistry
  • Calorimetry, Differential Scanning
  • Chemistry, Pharmaceutical / instrumentation
  • Chemistry, Pharmaceutical / methods*
  • Drug Compounding
  • Equipment Design
  • Hot Temperature*
  • Methylmethacrylate / chemistry
  • Metoprolol / chemistry*
  • Polymethacrylic Acids / chemistry
  • Spectrum Analysis, Raman
  • Technology, Pharmaceutical / instrumentation
  • Technology, Pharmaceutical / methods*

Substances

  • Acrylates
  • Eudragit RSPO
  • Polymethacrylic Acids
  • Methylmethacrylate
  • ethyl acrylate
  • Metoprolol