Evaluation of tableting performance of Poly (ethylene oxide) in abuse-deterrent formulations using compaction simulation studies

J Pharm Sci. 2021 Jul;110(7):2789-2799. doi: 10.1016/j.xphs.2021.03.008. Epub 2021 Mar 16.

Abstract

Poly (ethylene oxide) (PEO) has been widely used in abuse-deterrent formulations (ADFs) to increase tablet hardness. Previous studies have shown that formulation variables such as processing conditions and particle size of PEO can affect ADF performance in drug extraction efficiency. This work aims to understand the effect of PEO grades and sources on the compaction characteristics of model ADFs. PEOs from Dow Chemical and Sumitomo Chemical with different molecular weights were examined using a Styl'One compaction simulator at slow, medium, and fast tableting speeds. Particle-size distribution, thermal behavior, tabletability, compressibility using the Heckel model, compactibility, and elastic recovery were determined and compared between the neat PEOs and model ADFs. Multivariate linear regression was performed to understand the effect of compression conditions and PEO grades and sources. Our results show that neat PEOs with high molecular weight exhibit high tabletability. The source of neat PEOs contributes to the difference in tabletability, out-die compressibility, compactibility, and elastic recovery. However, the influence of the PEO source on tabletability and compactibility decreases after adding the model drug. In our model ADFs, tablets using PEOs with high molecular weight have high crushing strength, and tablets using PEOs from Dow Chemical display low elastic recovery.

Keywords: Abuse-deterrent formulation (ADF); Compactibility; Compaction simulator; Compressibility; Elastic recovery; Poly (ethylene oxide) (PEO); Tabletability.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Abuse-Deterrent Formulations*
  • Drug Compounding
  • Ethylene Oxide*
  • Particle Size
  • Polyethylene Glycols
  • Tablets
  • Tensile Strength

Substances

  • Abuse-Deterrent Formulations
  • Tablets
  • Polyethylene Glycols
  • Ethylene Oxide