Suppr超能文献

通过单次鼻腔给药实现抗病毒药物的靶向粉末制剂,可定制鼻腔和肺部沉积分布。

Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration.

机构信息

Department of Pharmacology and Pharmacy, LKS Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR.

State Key Laboratory of Emerging Infectious Diseases, Caro Yu Centre for Infection, Department of Microbiology, LKS Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR; Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science Park, New Territories, Hong Kong SAR.

出版信息

Int J Pharm. 2022 May 10;619:121704. doi: 10.1016/j.ijpharm.2022.121704. Epub 2022 Mar 28.

Abstract

Unpredictable outbreaks due to respiratory viral infections emphasize the need for new drug delivery strategies to the entire respiratory tract. As viral attack is not limited to a specific anatomic region, antiviral therapy that targets both the upper and lower respiratory tract would be most effective. This study aimed to formulate tamibarotene, a retinoid derivative previously reported to display broad-spectrum antiviral activity against influenza and severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), as a novel dual particle size powder formulation that targets both the nasal cavity and the lung by a single route of intranasal administration. Spray freeze drying (SFD) and spray drying (SD) techniques were employed to prepare tamibarotene powder formulations, and cyclodextrin was used as the sole excipient to enhance drug solubility. With the employment of appropriate atomizing nozzles, particles of size above 10 μm and below 5 μm could be produced for nasal and lung deposition, respectively. The aerosol performance of the powder was evaluated using Next Generation Impactor (NGI) coupled with a glass expansion chamber and the powder was dispersed with a nasal powder device. By blending powder of two different particle sizes, a single powder formulation with dual aerosol deposition characteristic in both the nasal and pulmonary regions was produced. The aerosol deposition fractions in the nasal cavity and pulmonary region could be modulated by varying the powder mixing ratio. All dry powder formulations exhibited spherical structures, amorphous characteristics and improved dissolution profile as compared to the unformulated tamibarotene. Overall, a novel dual targeting powder formulation of tamibarotene exhibiting customizable aerosol deposition profile was developed. This exceptional formulation strategy can be adopted to deliver other antimicrobial agents to the upper and lower airways for the prevention and treatment of human respiratory infections.

摘要

由于呼吸道病毒感染而导致的不可预测的爆发,强调了需要新的药物输送策略来覆盖整个呼吸道。由于病毒攻击并不局限于特定的解剖区域,因此针对上呼吸道和下呼吸道的抗病毒疗法将是最有效的。本研究旨在将先前报道具有广谱抗流感和严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)活性的维甲酸衍生物他米巴罗汀制成一种新型的双粒径粉末制剂,通过鼻腔给药单一途径靶向鼻腔和肺部。喷雾冷冻干燥(SFD)和喷雾干燥(SD)技术被用于制备他米巴罗汀粉末制剂,并且仅使用环糊精作为赋形剂来提高药物溶解度。通过使用适当的雾化喷嘴,可以分别生产出粒径大于 10μm 和小于 5μm 的颗粒,用于鼻腔和肺部沉积。使用下一代撞击器(NGI)与玻璃扩展室耦合评估粉末的气溶胶性能,并使用鼻粉装置分散粉末。通过混合两种不同粒径的粉末,可以产生具有鼻腔和肺部双重气溶胶沉积特性的单一粉末制剂。通过改变粉末混合比,可以调节鼻腔和肺部的气溶胶沉积分数。与未成型的他米巴罗汀相比,所有干粉制剂均表现出球形结构、无定形特征和改善的溶解曲线。总之,开发了一种具有可定制气溶胶沉积特性的新型双靶向他米巴罗汀粉末制剂。这种特殊的制剂策略可以用于将其他抗菌剂递送到上呼吸道和下呼吸道,以预防和治疗人类呼吸道感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87e4/8958263/0916c08840ef/ga1_lrg.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验