Rodrigues Susana, da Costa Ana M Rosa, Flórez-Fernández Noelia, Torres María Dolores, Faleiro Maria Leonor, Buttini Francesca, Grenha Ana
Centre for Marine Sciences, Faculdade de Ciências e Tecnologia, Universidade do Algarve, 8005-139 Faro, Portugal.
Centre for Biomedical Research, Universidade do Algarve, 8005-139 Faro, Portugal.
Polymers (Basel). 2020 Feb 12;12(2):425. doi: 10.3390/polym12020425.
Spray-drying stands as one of the most used techniques to produce inhalable microparticles, but several parameters from both the process and the used materials affect the properties of the resulting microparticles. In this work, we describe the production of drug-loaded chondroitin sulphate microparticles by spray-drying, testing the effect of using different solvents during the process. Full characterisation of the polymer and of the aerodynamic properties of the obtained microparticles are provided envisaging an application in inhalable tuberculosis therapy. The spray-dried microparticles successfully associated two first-line antitubercular drugs (isoniazid and rifabutin) with satisfactory production yield (up to 85%) and drug association efficiency (60%-95%). Ethanol and HCl were tested as co-solvents to aid the solubilisation of rifabutin and microparticles produced with the former generally revealed the best features, presenting a better ability to sustainably release rifabutin. Moreover, these presented aerodynamic properties compatible with deep lung deposition, with an aerodynamic diameter around 4 μm and fine particle fraction of approximately 44%. Finally, it was further demonstrated that the antitubercular activity of the drugs remained unchanged after encapsulation independently of the used solvent.
喷雾干燥是生产可吸入微粒最常用的技术之一,但该工艺和所用材料的几个参数会影响最终微粒的性质。在这项工作中,我们描述了通过喷雾干燥生产载药硫酸软骨素微粒的过程,测试了在该过程中使用不同溶剂的效果。对聚合物以及所得微粒的空气动力学性质进行了全面表征,以期用于可吸入性结核病治疗。喷雾干燥的微粒成功地将两种一线抗结核药物(异烟肼和利福布汀)结合在一起,具有令人满意的产率(高达85%)和药物结合效率(60%-95%)。测试了乙醇和盐酸作为助溶剂以帮助利福布汀溶解,用前者生产的微粒通常表现出最佳特性,具有更好的可持续释放利福布汀的能力。此外,这些微粒具有与深部肺沉积相匹配的空气动力学性质,空气动力学直径约为4μm,细颗粒分数约为44%。最后,进一步证明了药物的抗结核活性在包封后保持不变,与所用溶剂无关。