Benke Edit, Farkas Árpád, Szabó-Révész Piroska, Ambrus Rita
Institute of Pharmaceutical Technology and Regulatory Affairs, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary.
Centre for Energy Research, Hungarian Academy of Sciences, 1121 Budapest, Hungary.
Pharmaceutics. 2020 Jun 10;12(6):535. doi: 10.3390/pharmaceutics12060535.
Most of the marketed dry powder inhalation (DPI) products are traditional, carrier-based formulations with low drug concentrations deposited in the lung. However, due to their advantageous properties, their development has become justified. In our present work, we developed an innovative, carrier-based DPI system, which is an interactive physical blend of a surface-modified carrier and a spray-dried drug with suitable shape and size for pulmonary application. Meloxicam potassium, a nonsteroidal anti-inflammatory drug (NSAID), was used as an active ingredient due to its local anti-inflammatory effect and ability to decrease the progression of cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD). The results of the in vitro and in silico investigations showed high lung deposition in the case of this new formulation, confirming that the interparticle interactions were changed favorably.
大多数市售的干粉吸入剂(DPI)产品都是传统的、基于载体的制剂,药物在肺部的沉积浓度较低。然而,由于其具有优势特性,其开发已变得合理。在我们目前的工作中,我们开发了一种创新的、基于载体的DPI系统,它是表面改性载体与喷雾干燥药物的交互式物理混合物,具有适合肺部应用的形状和尺寸。美洛昔康钾是一种非甾体抗炎药(NSAID),因其局部抗炎作用以及降低囊性纤维化(CF)和慢性阻塞性肺疾病(COPD)进展的能力而被用作活性成分。体外和计算机模拟研究结果表明,这种新制剂在肺部的沉积率很高,证实颗粒间相互作用发生了有利变化。