Department of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, Saarland University, Campus A4 1, 66123 Saarbrücken, Germany.
Department of Functional Materials, Saarland University, Campus D3 3, 66123 Saarbrücken, Germany.
Eur J Pharm Sci. 2017 Jun 15;104:171-179. doi: 10.1016/j.ejps.2017.04.003. Epub 2017 Apr 5.
Nano-embedded microparticles represent a promising approach to deliver nanoparticles to the lungs. Microparticles with an appropriate aerodynamic diameter enable an application by dry powder inhaler and the transport of nanoparticles into the airways. By disintegration after deposition, nanoparticles can be released to exhibit their advantages such as a sustained drug release and delivery of the drug across the mucus barrier. The use of an appropriate matrix excipient to embed the nanoparticles is essential for the necessary disintegration and release of nanoparticles. In this context we investigated the influence of mannitol on the morphology, aerodynamic properties and disintegration behavior of nano-embedded microparticles. PLGA nanoparticles and mannitol were spray dried each as sole component and in combination in three different ratios. An influence of the mannitol content on the morphology was observed. Pure mannitol microparticles were solid and spherical, while the addition of nanoparticles resulted in raisin-shaped hollow particles. The different morphologies can be explained by diffusion processes of the compounds described by the Péclet-number. All powders showed suitable aerodynamic properties. By dispersion of the powders in simulated lung fluid, initial nanoparticle sizes could be recovered for samples containing mannitol. The fraction of redispersed nanoparticles was increased with increasing mannitol content. To evaluate the disintegration under conditions with higher comparability to the in vivo situation, spray-dried powders were exposed to >90% relative humidity. The disintegration behavior was monitored by analyzing roughness values by white light interferometry and supporting SEM imaging. The exposure to high relative humidity was shown to be sufficient for disintegration of the microparticles containing mannitol, releasing morphologically unchanged nanoparticles. With increasing mannitol content, the disintegration occurred faster and to a higher degree. Under these conditions, microparticles only composed of nanoparticles did not disintegrate. By enabling the release of nanoparticles from nano-embedded microparticles, mannitol was shown to be an ideal excipient to convert nanoparticles by spray drying into an inhalable dry power formulation.
纳米嵌入微球代表了一种有前途的方法,可以将纳米颗粒递送到肺部。具有适当空气动力学直径的微球能够通过干粉吸入器进行应用,并将纳米颗粒输送到气道中。通过沉积后的崩解,可以释放纳米颗粒以发挥其优势,例如药物的持续释放和穿过黏液屏障的药物输送。嵌入纳米颗粒的合适基质赋形剂的使用对于纳米颗粒的必要崩解和释放是必不可少的。在这方面,我们研究了甘露醇对纳米嵌入微球的形态、空气动力学性质和崩解行为的影响。PLGA 纳米颗粒和甘露醇各自作为单独成分,以及在三种不同比例下组合进行喷雾干燥。观察到甘露醇含量对形态的影响。纯甘露醇微球为固体和球形,而添加纳米颗粒则导致葡萄干状的空心颗粒。不同的形态可以通过描述扩散过程的 Peclet 数来解释。所有粉末都显示出合适的空气动力学性质。通过将粉末分散在模拟肺液中,可以回收含有甘露醇的样品中纳米颗粒的初始粒径。随着甘露醇含量的增加,重新分散的纳米颗粒的分数增加。为了评估在与体内情况更具可比性的条件下的崩解情况,将喷雾干燥的粉末暴露于相对湿度>90%的条件下。通过白光干涉测量法分析粗糙度值并支持 SEM 成像来监测崩解行为。结果表明,暴露于高相对湿度足以使含有甘露醇的微球崩解,释放形态未改变的纳米颗粒。随着甘露醇含量的增加,崩解发生得更快,程度更高。在这些条件下,仅由纳米颗粒组成的微球不会崩解。通过使纳米嵌入微球中的纳米颗粒释放,甘露醇被证明是一种理想的赋形剂,可以通过喷雾干燥将纳米颗粒转化为可吸入的干粉制剂。