# Investigation of a simple suspension method for orexin receptor antagonist tablets

**Authors:** Kazuhiro Hada, Daichi Inoue, Kouyou Ohishi, Toshiya Yasunaga, Kayoko Ozeki, Hiromitsu Yamamoto, Nobuhiko Nakamura

PMC · DOI: 10.1186/s40780-026-00553-7 · Journal of Pharmaceutical Health Care and Sciences · 2026-02-14

## TL;DR

This study evaluates how well three orexin receptor antagonist tablets can be administered using a simple suspension method for patients who have difficulty swallowing.

## Contribution

The study provides the first detailed evaluation of suspension and catheter passage properties of three specific orexin receptor antagonist tablets.

## Key findings

- Belsomra® 20 mg tablets did not disintegrate or suspend properly.
- Dayvigo® 10 mg and Quviviq® 50 mg tablets showed good disintegration and suspension, with high drug recovery after catheter passage.
- Belsomra® is unsuitable for the simple suspension method, while Dayvigo® and Quviviq® may be suitable.

## Abstract

A simple suspension method is used in medical practice to administer several orexin receptor antagonists for patients with dysphagia; however, detailed suspension and passage through catheter evaluations have not been performed. Therefore, to safely administer orexin receptor antagonists using the simple suspension method in patients with dysphagia, this study evaluated the disintegration, suspension, passage through the catheter, and drug recovery after passage of Belsomra® 20 mg (suvorexant), Dayvigo® 10 mg (lemborexant), and Quviviq® 50 mg (daridorexant) tablets through a catheter.

Disintegration and suspension of Belsomra® 20 mg, Dayvigo® 10 mg, and Quviviq® 50 mg tablets, and passage through the catheter were visually confirmed. Drug recovery after passage through the catheter was quantified using liquid chromatography-mass spectrometry.

In this study, there was no disintegration and suspension of Belsomra® 20 mg tablets. However, Dayvigo® 10 mg and Quviviq® 50 mg tablets demonstrated disintegration and suspension, including passage through the catheter after rapid and complete disintegration. Drug recovery after catheter passage was >80% for Dayvigo® 10 mg without flushing and for Quviviq® 50 mg after two flushes.

As the disintegration and suspension properties of Belsomra® 20 mg tablet could not be confirmed, the conventional simple suspension method is not suitable for this product. However, Dayvigo® 10 mg and Quviviq® 50 mg tablets showed potential suitability for the simple suspension method.

The online version contains supplementary material available at 10.1186/s40780-026-00553-7.

## Full-text entities

- **Genes:** CCS (copper chaperone for superoxide dismutase) [NCBI Gene 9973], AFA1 (Alopecia, androgenetic) [NCBI Gene 100188784] {aka MPB}, HCRT (hypocretin neuropeptide precursor) [NCBI Gene 3060] {aka NRCLP1, OX, PPOX}
- **Diseases:** Dysphagia (MESH:D003680), L-HPC (MESH:C537243), insomnia (MESH:D007319), sleep disorders (MESH:D012893), cognitive impairment (MESH:D003072), trauma (MESH:D014947), stroke (MESH:D020521)
- **Chemicals:** Dayvigo (MESH:C000634104), formic acid (MESH:C030544), water (MESH:D014867), Barbiturates (MESH:D001463), cellulose (MESH:D002482), Bis[2-ethylhexyl] phthalate (MESH:D004051), polyvinyl chloride (MESH:D011143), acetonitrile (MESH:C032159), daridorexant (MESH:C000634383), D-mannitol (MESH:D008353), Copovidone (MESH:C402301), hydroxypropyl cellulose (MESH:C008079), povidone (MESH:D011205), Croscarmellose sodium (MESH:D002266), L-HPC (-), Belsomra (MESH:C551624)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13011777/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC13011777/full.md

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Source: https://tomesphere.com/paper/PMC13011777