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Powder bed packing and API content homogeneity of granules in single drop granule formation

机译:单滴颗粒形成中颗粒的粉床包装和API含量均匀性

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Single drop granule formation on a static powder bed of pharmaceutical mixtures was studied to investigate the effects of hydrophobicity and primary particle size distribution on the powder bed packing structure and the content homogeneity of active pharmaceutical ingredient (API) in granules formed. The granule formation mechanisms, drop penetration time, granule morphology and internal structure have been previously investigated in a mixture of coarse microcrystalline cellulose (MCC) and line acetaminophen (APAP). When the APAP amount increased (decreasing particle size and increasing hydrophobicity), drop penetration time increased, formation mechanisms transitioned from Spreading to Tunneling, the granules became smaller in size, and the internal porosity of the granules decreased (Gao et al., 2018). In the current study, single drop granulation on mixtures of MCC and APAP with different particle sizes were investigated for formation mechanisms and granule morphology. Additionally, the powder bed packing structure was characterized by X-ray micro-CT and the API content uniformity was measured by UV-vis spectrometry. It was found that in the mixture made from coarse MCC and fine APAP, the internal structure became heterogeneous and there were dense aggregate regions in both the powder bed and granules from 25% APAP proportion, where the transition from Spreading to Tunneling occurs. The content uniformities of granules from fine powder beds are much more compromised (indicating a discrepancy between the actual value and theoretical value) than those from coarse powder beds. This content discrepancy becomes much larger when the APAP proportion in the powder bed is higher (above 50%). This was previously observed by other researchers (Nguyen et al., 2010) and was attributed to the preferential wetting of the ingredients. It is believed that the primary particle size of the powder bed is more significant than the hydrophobicity in affecting the formation mechanism, granule internal structure, and content uniformity. (C) 2020 Elsevier B.V. All rights reserved.
机译:研究了在药物混合物的静态粉末床上的单滴颗粒形成,研究了液体粒度和初级粒度分布对所形成的颗粒中活性药物成分(API)的粉末填料结构和均匀性均匀性的影响。先前已经在粗体微晶纤维素(MCC)和线乙酰氨基酚(APAP)的混合物中研究了颗粒形成机制,降渗时间,颗粒形态和内部结构。当APAP量增加(减小粒度和增加疏水性)时,降低渗透时间增加,从蔓延到隧道的形成机制,颗粒的尺寸较小,颗粒的内部孔隙率下降(Gao等,2018) 。在目前的研究中,针对形成机制和颗粒形态研究了对MCC和APAP混合物的单滴造粒。另外,粉末填充结构的特征在于X射线微型CT,通过UV-Vis光谱法测量API含量均匀性。发现,在由粗MCC和细APAP制成的混合物中,内部结构变得异质,粉末床和颗粒中的致密聚集区,25%APAP比例,其中发生从扩散到隧道的过渡发生。来自细粉床的颗粒的含量均匀性更大(表明实际值与理论值之间的差异),而不是来自粗粉床的那些。当粉末床中的APAP比例更高时,这种内容差异变得更大(高于50%)。这是由其他研究人员观察到的(Nguyen等,2010)并且归因于成分的优先润湿。据信粉末床的初级粒度比影响形成机制,颗粒内部结构和含量均匀性的疏水性更大。 (c)2020 Elsevier B.V.保留所有权利。

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