Šimek Michal, Grünwaldová Veronika, Kratochvíl Bohumil
a Department of Solid State Chemistry , University of Chemistry and Technology Prague , Prague , Czech Republic and.
b Zentiva k.s. , Prague , Czech Republic.
Pharm Dev Technol. 2016 Aug;21(5):583-9. doi: 10.3109/10837450.2015.1026608. Epub 2015 May 21.
Although the fragmentation of the active pharmaceutical ingredient (API) is a phenomenon that is mentioned in many literature sources, no well-suited analytical tools for its investigation are currently known. We used the hot-stage microscopy method, already presented in our previous work, and studied the real fragmentation of the tadalafil particles in model tablets which were prepared under different compaction pressures. The morphology, spectral imaging and evaluation of plastic and elastic energies were also analyzed to support the hot-stage method. The prepared blend of tadalafil and excipients was compacted under a several forces from 5 to 35 kN to reveal the trend of fragmentation. The exact fragmentation of tadalafil with increased compaction pressure was revealed by the hot-stage microscopic method and it was in good agreement with plastic and elastic energies. Conversely, spectral imaging, which is being used for this analysis, was considered to be inaccurate methodology as mainly agglomerates, not individual particles, were measured. The availability of the hot-stage microscopic method equips pharmaceutical scientists with an in vitro assessment technique that will more reliably determine the fragmentation of the API in finished tablets and the behavior of the particles when compacted.
尽管活性药物成分(API)的破碎是许多文献中提到的一种现象,但目前尚无适用于其研究的分析工具。我们采用了在之前工作中已经介绍过的热台显微镜法,研究了在不同压制压力下制备的模型片剂中他达拉非颗粒的实际破碎情况。还对形态、光谱成像以及塑性和弹性能量进行了分析,以支持热台法。将制备好的他达拉非与辅料混合物在5至35 kN的几种压力下进行压制,以揭示破碎趋势。热台显微镜法揭示了随着压制压力增加他达拉非的确切破碎情况,并且与塑性及弹性能量结果吻合良好。相反,用于该分析的光谱成像被认为是不准确的方法,因为测量的主要是团聚体,而非单个颗粒。热台显微镜法的可用性为药物科学家提供了一种体外评估技术,该技术将更可靠地确定成品片剂中API的破碎情况以及颗粒在压制时的行为。