Laboratory of Pharmaceutical Technology, Ghent University, Belgium.
Laboratory of Pharmaceutical Process Analytical Technology, Ghent University, Belgium.
Int J Pharm. 2016 Jun 15;506(1-2):13-24. doi: 10.1016/j.ijpharm.2016.04.025. Epub 2016 Apr 16.
In most formulations processed via continuous twin screw granulation microcrystalline cellulose (MCC) and/or lactose are used as excipients, but mannitol is also a preferred excipient for wet granulation and tableting due to its non-hygroscopicity and inertness. Therefore, the aim of the current study was to investigate the influence of process parameters on critical quality attributes of granules (moisture content, solid state, morphology, size distribution, specific surface area, friability, flowability and hygroscopicity) and tablets (tensile strength and friability) after twin screw granulation of δ-mannitol. The δ-polymorph was selected since a moisture-induced transformation to β-mannitol was observed during batch wet granulation, which exhibited a unique morphology with a large surface area and improved tabletability. A full factorial experimental design was performed, varying screw speed (400-900rpm), granulation temperature (25-40°C), number of kneading elements (6 or 12) and liquid-to-solid (L/S) ratio, on the granulation unit of a ConsiGma™-25 line (a continuous powder-to-tablet manufacturing system). After tray drying the granules were milled and tableted. The results showed that the polymorphic transition from δ- to β-mannitol also occurred during twin screw granulation, although the residence time and L/S ratios were much lower in continuous twin screw granulation compared to batch processing. However, the polymorphic transition was not complete in all experiments and depended on the L/S ratio, screw speed and number of kneading elements. Nevertheless all granules exhibited the unique morphology linked to the polymorphic transition and had a superior tabletability compared to granules produced with β-mannitol as starting material. This was attributed to enhanced plastic deformation of the granules manufactured using δ-mannitol as starting material. In addition, it was concluded that mannitol was granulated via a different mechanism than other, less-soluble, excipients (e.g. lactose, microcrystalline cellulose) due to its high solubility and dissolution rate as the influence of process parameters on the mannitol granule characteristics was different.
在大多数通过连续双螺杆造粒工艺加工的配方中,使用微晶纤维素(MCC)和/或乳糖作为赋形剂,但甘露醇由于其非吸湿性和惰性,也是湿法制粒和压片的首选赋形剂。因此,本研究的目的是研究工艺参数对颗粒(水分含量、固体状态、形态、粒径分布、比表面积、脆性、流动性和吸湿性)和片剂(拉伸强度和脆性)的关键质量属性的影响,这些颗粒和片剂是通过 δ-甘露醇的双螺杆造粒得到的。选择 δ-多晶型是因为在批处理湿法制粒过程中观察到 δ-甘露醇向 β-甘露醇的水分诱导转变,β-甘露醇具有独特的形态,比表面积大,可压性提高。在 ConsiGma™-25 线(一种连续粉末到片剂制造系统)的造粒单元上进行完全因子实验设计,改变螺杆速度(400-900rpm)、造粒温度(25-40°C)、捏合元件数量(6 或 12)和固液比(L/S)。颗粒在托盘干燥后进行研磨和压片。结果表明,尽管连续双螺杆造粒中的停留时间和 L/S 比远低于批处理,但在双螺杆造粒过程中也会发生从 δ-到 β-甘露醇的多晶型转变。然而,多晶型转变并非在所有实验中都完全发生,且取决于 L/S 比、螺杆速度和捏合元件数量。尽管如此,所有颗粒都表现出与多晶型转变相关的独特形态,并且与以 β-甘露醇为起始原料生产的颗粒相比,可压性更好。这归因于使用 δ-甘露醇作为起始原料制造的颗粒具有增强的塑性变形。此外,由于甘露醇具有高溶解度和溶解速率,与其他溶解度较低的赋形剂(如乳糖、微晶纤维素)相比,其造粒机制不同,因此得出结论,工艺参数对甘露醇颗粒特性的影响也不同。