High-Throughput Dissolution/Permeation Screening -A 96-Well Two-Compartment Microplate Approach

Ann-Christin Jacobsen, Anna Krupa, Martin Brandl, Annette Bauer-Brandl

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Abstract

Early formulation screening can alleviate development of advanced oral drug formulations, such as amorphous solid dispersions (ASDs). Traditionally, dissolution is used to predict ASD performance. Here, a high-throughput approach is described that simultaneously screens drug dissolution and permeation employing a two-compartment 96-well plate. Freeze-drying from hydro-alcoholic solutions was used to prepare amorphous formulations. The screening approach was tested on amorphous and crystalline tadalafil formulations with and without Soluplus®. The workflow consisted of: 1) dispersion of the formulations; 2) incubation within the two-compartment plate, where a dialysis membrane separated donor (dispersed formulation) and acceptor; 3) sampling (donor and acceptor), where donor samples were centrifuged to remove non-dissolved material; and 4) quantification by UHPLC-UV. To identify optimal screening conditions, the following parameters were varied: dispersion medium (buffer / biomimetic media), acceptor medium (buffer / surfactant solutions), and incubation time (1, 3, and 6 h). Surfactants (acceptor) increased tadalafil permeation. Biomimetic medium (donor) enhanced dissolution, but not permeation, except for freeze-dried tadalafil, for which the permeated amount increased. The predictiveness was evaluated by comparing dissolution-/permeation-results with in vivo bioavailability. In general, both dissolution and permeation reflected bioavailability, whereof the latter was a better predictor. High-throughput dissolution/permeation is regarded promising for formulation screening.

Original languageEnglish
JournalPharmaceutics
Volume11
Issue number5
Pages (from-to)227
ISSN1999-4923
DOIs
Publication statusPublished - 10. May 2019

Keywords

  • Amorphous solid dispersions
  • Biomimetic
  • Dissolution
  • High-throughput screening
  • Permeability
  • Sink
  • Solubility
  • Solubilization
  • Supersaturation

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