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Startseite » News » Development of indomethacin amorphous solid dispersion by applying acid-base supersolubilization (ABS) principle to enhance solubility and enable low-temperature hot melt extrusion

Development of indomethacin amorphous solid dispersion by applying acid-base supersolubilization (ABS) principle to enhance solubility and enable low-temperature hot melt extrusion

8. January 2026
Development of indomethacin amorphous solid dispersion by applying acid-base supersolubilization

Development of indomethacin amorphous solid dispersion by applying acid-base supersolubilization

This study explores a novel acid-base supersolubilization (ABS) principle for enhancing the solubility and dissolution rate of indomethacin, a poorly water-soluble and weakly acidic drug, by interaction with the weak base tromethamine. The reported aqueous solubilities of indomethacin are 1.5 and 105.2 µg/mL at pH 1.2 and 7.4, respectively.

However, in the present investigation, they were increased to 2.5 mg/mL at pH 7.3 and greater than 240 mg/mL at pH ∼ 8.0 by interaction with tromethamine. Such an acid-base interaction also occurred in the solid state, which reduced the melting temperature of indomethacin. An amorphous solid dispersion (ASD) could be prepared using the indomethacin-tromethamine mixture at a 1:2 M ratio, along with poloxamer 407 as surfactant and Kollidon® VA64 as polymeric matrix, by hot melt extrusion (HME) at 80 °C.

The lowering of processing temperature prevented any degradation of indomethacin during HME. The amorphous nature of indomethacin in ASDs was confirmed by DSC and PXRD analysis. In vitro dissolution studies at pH ∼ 1, pH 6.8, and when pH was changed stepwise from 1 to 6.8, demonstrated that the ASD with tromethamine achieved and maintained rapid and high (>80 %) indomethacin release at pH ∼ 1 and complete release (100 %) at pH 6.8. This improvement in dissolution performance, along with the ability to perform HME at lower temperatures, demonstrates the potential of the ABS principle to overcome longstanding challenges in developing ASDs for poorly water-soluble drugs.

Highlights

  • Acid-base supersolubilization increased indomethacin’s solubility to over 240 mg/mL with tromethamine, without salt formation.
  • Acid-base supersolubilization enabled the processing of indomethacin by hot-melt extrusion at 80 °C, instead of 140 °C.
  • Amorphous solid dispersion with tromethamine and poloxamer 407 achieved over 80% release at pH ~1 and 100% release at pH 6.8.
  • Acid-base supersolubilization improved solubility and processability for amorphous solid dispersion formulation.

Read more on Development of indomethacin amorphous solid dispersion by applying acid-base supersolubilization 

Materials

Indomethacin was purchased from TCI Chemicals (Philadelphia, PA, USA), tromethamine was purchased from J. T. Baker® (Radnor, PA, USA), and the samples of polyvinylpyrrolidone-vinyl acetate copolymer (Kollidon® VA64) and Poloxamer 407 (Kolliphor® P407; P407) were donated by BASF (Tarrytown, NY, USA). Chemical structures of indomethacin, tromethamine, and Kollidon® VA64 are shown in Fig. 1

Vishvesh Raje, Ida Lu, Raya S. Keir, Abu T.M. Serajuddin,
Development of indomethacin amorphous solid dispersion by applying acid-base supersolubilization (ABS) principle to enhance solubility and enable low-temperature hot melt extrusion,
International Journal of Pharmaceutics, Volume 687, 2026, 126405, ISSN 0378-5173,
https://doi.org/10.1016/j.ijpharm.2025.126405.

Tags: excipientsformulation

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