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用于小鼠模型中肺炎鼠疫治疗的庆大霉素喷雾干燥可吸入粉末制剂。

Spray-Dried Inhalable Powder Formulations of Gentamicin Designed for Pneumonic Plague Therapy in a Mouse Model.

作者信息

Zhu Menghuan, Zhang Dongna, Zhang Lili, Zhao Liangliang, Xu Likun, Wang Baogang, Zhang Xinyu, Chen Jinwei, Bei Zhuchun, Wang Hong, Zhou Dongsheng, Yang Wenhui, Song Yabin

机构信息

School of Public Health and Health Management, Gannan Medical University, Ganzhou 341000, China.

State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China.

出版信息

Pharmaceutics. 2022 Nov 29;14(12):2646. doi: 10.3390/pharmaceutics14122646.

Abstract

Infection with Yersinia pestis () may cause pneumonic plague, which is inevitably fatal without treatment. Gentamicin (GM), an aminoglycoside antibiotic, is a drug commonly used in the treatment of plague. However, it requires repeated intramuscular or intravenous administration. Pulmonary drug delivery is noninvasive, with the advantages of local targeting and reduced risk of systemic toxicity. In this study, GM powders were prepared using spray-drying technology. The powders displayed good physical and chemical properties and met the requirements for human pulmonary inhalation. The formulation of the powders was optimized using a 3 full factorial design. A formulation of 15% () of L-leucine was prepared, and the spray-drying process parameters using an inlet temperature of 120°C and a 15% pump rate were determined to produce the best powder. In addition, the optimized GM spray-dried powders were characterized in terms of morphology, crystallinity, powder fluidity, and aerodynamic particle size distribution analysis. In a mouse model of pneumonic plague, we compared the therapeutic effects among three administration routes, including subcutaneous injection, liquid atomization, and dry powder atomization. In conclusion, our data suggest that inhalation therapy with GM spray-dried powders is an effective treatment for pneumonic plague.

摘要

感染鼠疫耶尔森菌()可能会引发肺鼠疫,若不治疗必然致命。庆大霉素(GM)作为一种氨基糖苷类抗生素,是治疗鼠疫常用的药物。然而,它需要反复进行肌肉注射或静脉注射。肺部给药是非侵入性的,具有局部靶向性和降低全身毒性风险的优点。在本研究中,采用喷雾干燥技术制备了GM粉末。这些粉末展现出良好的物理和化学性质,符合人类肺部吸入的要求。使用三因素全因子设计对粉末的配方进行了优化。制备了含15%()L - 亮氨酸的配方,并确定使用120°C的进口温度和15%的泵速的喷雾干燥工艺参数以生产出最佳粉末。此外,对优化后的GM喷雾干燥粉末进行了形态、结晶度、粉末流动性和空气动力学粒径分布分析等表征。在肺鼠疫小鼠模型中,我们比较了皮下注射、液体雾化和干粉雾化三种给药途径的治疗效果。总之,我们的数据表明,GM喷雾干燥粉末吸入疗法是治疗肺鼠疫的一种有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aba9/9782578/46d6f6a32190/pharmaceutics-14-02646-g001.jpg

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