沙美特罗昔萘酸盐与环索奈德共无定形物及其制备方法和应用

By preparing co-amorphous and nano-co-amorphous compounds of salmeterol roxonaphthyl acid salt and cyclosonepine, the problems of poor water solubility and dispersibility were solved, resulting in better solubility and stability, and enhanced drug synergy. This method is suitable for preparing drugs for the prevention or treatment of obstructive airway diseases.

CN119751542BActive Publication Date: 2026-07-17EAST CHINA UNIV OF SCI & TECH

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
EAST CHINA UNIV OF SCI & TECH
Filing Date
2024-12-27
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

The combination of salmeterol roxonaphthyl acid salt and ccyclosone is difficult to manufacture due to its extremely low water solubility and dispersibility, making it hard to achieve effective synergistic anti-inflammatory and bronchodilator effects.

Method used

Amorphous and nano-amorphous compounds of salmeterol roxenamate and cyclosonepine were prepared. The amorphous compounds were formed by rotary evaporation or grinding, and the nano-amorphous compounds were prepared by freeze-drying with emulsified solvents to improve their solubility and stability.

Benefits of technology

It significantly improved the solubility and dissolution rate of salmeterol roxonaphthyl salt and ccyclosone, achieving simultaneous release of the two components and enhancing the synergistic anti-inflammatory and bronchodilatory effects, making it suitable as an API for combination therapy.

✦ Generated by Eureka AI based on patent content.

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Abstract

本发明提供了一种沙美特罗昔萘酸盐与环索奈德共无定形物及其制备方法和应用。具体的,提供了一种沙美特罗昔萘酸盐 / 环索奈德共无定形物,所述共无定形物为沙美特罗昔萘酸盐与环索奈德以摩尔比为1:(0.4‑4.1)形成的无定形物,并进一步提供了其纳米化的共无定形物。本发明的无定形物具有比沙美特罗昔萘酸盐与环索奈德更优的溶解性、稳定性和药动学药效学性能,可以增强沙美特罗昔萘酸盐与环索奈德的协同效果,非常适合作为沙美特罗昔萘酸盐与环索奈德联合用药的API。
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