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基于丝素蛋白的粗糙可吸入盐酸环丙沙星微球用于非囊性纤维化支气管扩张症治疗,具有良好的生物相容性。

The rough inhalable ciprofloxacin hydrochloride microparticles based on silk fibroin for non-cystic fibrosis bronchiectasis therapy with good biocompatibility.

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.

College of Pharmacy, Jinan University, Guangzhou 510632, China.

出版信息

Int J Pharm. 2021 Sep 25;607:120974. doi: 10.1016/j.ijpharm.2021.120974. Epub 2021 Aug 4.

Abstract

Non-cystic fibrosis bronchiectasis (NCFB) is a chronic respiratory disease, and the thick and viscous mucus covering on respiratory epithelia can entrap the inhaled drugs, resulting in compromised therapeutic efficiency. In order to solve this problem, the inhalable ciprofloxacin hydrochloride microparticles (CMs) based on silk fibroin (SF) and mannitol (MAN) were designed and developed. SF was applied to increase the loading efficiency of ciprofloxacin hydrochloride by strong electrostatic interactions. MAN could facilitate the penetration of drugs through mucus, which ensured the drugs could reach their targets before clearance. Furthermore, the aerodynamic performance of the inhalable microparticles could be tuned by changing the surface roughness to achieve a high fine particle fraction value (45.04%). The antibacterial effects of CMs were also confirmed by measuring the minimum inhibitory concentration against four different bacteria strains. Moreover, a series of experiments both in vitro and in vivo showed that CMs would not affect the lung function and induce the secretion of inflammatory cytokines in lungs, demonstrating their excellent biocompatibility and biosafety. Therefore, CMs might be a promising pulmonary drug delivery system for the treatment of NCFB.

摘要

非囊性纤维化支气管扩张症(NCFB)是一种慢性呼吸道疾病,覆盖在呼吸道上皮的厚而粘稠的黏液会困住吸入的药物,从而降低治疗效果。为了解决这个问题,设计并开发了基于丝素蛋白(SF)和甘露醇(MAN)的盐酸环丙沙星吸入微球(CMs)。SF 被用来通过强静电相互作用来增加盐酸环丙沙星的载药量。MAN 可以促进药物穿透黏液,确保药物在清除之前到达靶点。此外,通过改变表面粗糙度来调整可吸入微球的空气动力学性能,以实现高微细颗粒分数值(45.04%)。通过测量对四种不同细菌株的最小抑菌浓度来确认 CMs 的抗菌效果。此外,一系列体外和体内实验表明,CMs 不会影响肺功能,也不会引起肺部炎症细胞因子的分泌,表明其具有良好的生物相容性和生物安全性。因此,CMs 可能是治疗 NCFB 的一种有前途的肺部药物递送系统。

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