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

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Kazuhiro Hada, Daichi Inoue, Kouyou Ohishi, Toshiya Yasunaga, Kayoko Ozeki, Hiromitsu Yamamoto, Nobuhiko Nakamura
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引用次数: 0

Abstract

BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSION: 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.

食欲素受体拮抗剂片的简易悬液法研究。
背景:在医疗实践中,一种简单的悬浮液方法用于给吞咽困难患者施用几种食欲素受体拮抗剂;然而,尚未进行详细的悬浮和导管通过评估。因此,为了在吞咽困难患者中使用简单悬液法安全地给药食欲素受体拮抗剂,本研究评估了Belsomra®20mg (suvorexant)、Dayvigo®10mg (lemborexant)和Quviviq®50mg (daridorexant)片剂通过导管后的崩解、悬浮、通过导管和药物恢复情况。方法:目测Belsomra®20mg、Dayvigo®10mg、Quviviq®50mg片崩解、悬浮,并通过导管。通过导管后的药物回收率采用液相色谱-质谱法定量。结果:在本研究中,Belsomra®20mg片无崩解和悬浮现象。然而,Dayvigo®10mg和Quviviq®50mg片剂表现出崩解和悬浮,包括在快速完全崩解后通过导管。Dayvigo®10 mg不冲洗,Quviviq®50 mg两次冲洗后,导管通过后药物回收率为80%。结论:由于无法确定Belsomra®20mg片剂的崩解和悬浮性能,常规的简单悬液法不适合该产品。然而,Dayvigo®10 mg和Quviviq®50 mg片剂显示出简单悬浮法的潜在适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
29
审稿时长
8 weeks
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