Wang Zimeng, Gupta Sweta K, Meenach Samantha A
University of Rhode Island, College of Engineering, Department of Chemical Engineering, Kingston, RI 02881, USA.
University of Rhode Island, College of Engineering, Department of Chemical Engineering, Kingston, RI 02881, USA; University of Rhode Island, College of Pharmacy, Department of Biomedical and Pharmaceutical Sciences, Kingston, RI 02881, USA.
Int J Pharm. 2017 Jun 15;525(1):264-274. doi: 10.1016/j.ijpharm.2017.04.052. Epub 2017 Apr 24.
Biocompatible, biodegradable polymers are commonly used as excipients to improve the drug delivery properties of aerosol formulations, in which acetalated dextran (Ac-Dex) exhibits promising potential as a polymer in various therapeutic applications. Despite this promise, there is no comprehensive study on the use of Ac-Dex as an excipient for dry powder aerosol formulations. In this study, we developed and characterized pulmonary drug delivery aerosol microparticle systems based on spray-dried Ac-Dex with capabilities of (1) delivering therapeutics to the deep lung, (2) targeting the particles to a desired location within the lungs, and (3) releasing the therapeutics in a controlled fashion. Two types of Ac-Dex, with either rapid or slow degradation rates, were synthesized. Nanocomposite microparticle (nCmP) and microparticle (MP) systems were successfully formulated using both kinds of Ac-Dex as excipients and curcumin as a model drug. The resulting MP were collapsed spheres approximately 1μm in diameter, while the nCmP were similar in size with wrinkled surfaces, and these systems dissociated into 200nm nanoparticles upon reconstitution in water. The drug release rates of the Ac-Dex particles were tuned by modifying the particle size and ratio of fast to slow degrading Ac-Dex. The pH of the environment was also a significant factor that influenced the drug release rate. All nCmP and MP systems exhibited desirable aerodynamic diameters that are suitable for deep lung delivery (e.g. below 5μm). Overall, the engineered Ac-Dex aerosol particle systems have the potential to provide targeted and effective delivery of therapeutics into the deep lung.
生物相容性、可生物降解的聚合物通常用作辅料,以改善气雾剂配方的药物递送性能,其中乙酰化葡聚糖(Ac-Dex)在各种治疗应用中作为聚合物展现出了有前景的潜力。尽管有此前景,但尚未有关于将Ac-Dex用作干粉气雾剂配方辅料的全面研究。在本研究中,我们开发并表征了基于喷雾干燥的Ac-Dex的肺部药物递送气雾剂微粒系统,该系统具有以下能力:(1)将治疗药物递送至肺深部,(2)将颗粒靶向至肺内的期望位置,以及(3)以可控方式释放治疗药物。合成了两种降解速率分别为快速和缓慢的Ac-Dex。使用这两种Ac-Dex作为辅料以及姜黄素作为模型药物,成功制备了纳米复合微粒(nCmP)和微粒(MP)系统。所得的MP是直径约1μm的塌陷球体,而nCmP尺寸相似但表面有褶皱,并且这些系统在水中重构后会解离成200nm的纳米颗粒。通过改变快速和缓慢降解的Ac-Dex的粒径和比例来调节Ac-Dex颗粒的药物释放速率。环境的pH值也是影响药物释放速率的一个重要因素。所有nCmP和MP系统均表现出适合肺深部递送的理想空气动力学直径(例如低于5μm)。总体而言,工程化的Ac-Dex气雾剂颗粒系统有潜力实现治疗药物向肺深部的靶向且有效递送。