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Development of a controlled release formulation by continuous twin screw granulation: Influence of process and formulation parameters

机译:连续双螺杆造粒研制控制释放配方:工艺和配方参数的影响

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The aim of this study was to evaluate the potential of twin screw granulation for the continuous production of controlled release formulations with hydroxypropylmethylcellulose as hydrophilic matrix former. Metoprolol tartrate was included in the formulation as very water soluble model drug. A premix of metoprolol tartrate, hydroxypropylmethylcellulose and filler (ratio 20/20/60, wow) was granulated with demineralized water via twin screw granulation. After oven drying and milling, tablets were produced on a rotary Modul (TM) P tablet press. A D-optimal design (29 experiments) was used to assess the influence of process (screw speed, throughput, barrel temperature and screw design) and formulation parameters (starch content of the filler) on the process (torque), granule (size distribution, shape, friability, density) and tablet (hardness, friability and dissolution) critical quality attributes. The torque was dominated by the number of kneading elements and throughput, whereas screw speed and filling degree only showed a minor influence on torque. Addition of screw mixing elements after a block of kneading elements improved the yield of the process before milling as it resulted in less oversized granules and also after milling as less fines were present. Temperature was also an important parameter to optimize as a higher temperature yielded less fines and positively influenced the aspect ratio. The shape of hydroxypropylmethylcellulose granules was comparable to that of immediate release formulations. Tensile strength and friability of tablets were not dependent on the process parameters. The use of starch as filler was not beneficial with regard to granule and tablet properties. Complete drug release was obtained after 16-20 h and was independent of the design's parameters. (C) 2016 Elsevier B.V. All rights reserved.
机译:本研究的目的是评估双螺杆颗粒的潜力,用于连续生产与羟丙基甲基纤维素作为亲水基质前代的控释制剂。富含托洛尔酒酒石酸酯作为非常水溶性模型药物包含在制剂中。通过双螺杆造粒造粒,通过双螺杆造粒造粒与甲状腺滤醇,羟丙基甲基甲基纤维素和填料(比例20/20/60,哇)造粒。在烘箱干燥和研磨后,在旋转MODUL(TM)P压片机上产生片剂。 D-OPTEMAL设计(29实验)用于评估过程(螺杆速度,吞吐量,桶温和螺杆设计)和配方参数(填料的淀粉含量)对工艺(扭矩),颗粒(尺寸分布)的影响,形状,脆弱,密度)和平板电脑(硬度,脆性和溶解)关键质量属性。扭矩由捏合元件和产量的数量主导,而螺杆速度和填充程度仅对扭矩表示微小的影响。在捏合元件块之后添加螺杆混合元件在研磨前提高了该方法的产率,因为它导致较少的超大颗粒并且在铣削之后存在,因此存在较少的细粒。温度也是优化的重要参数,因为较高的温度产生的细粒少,并且积极影响纵横比。羟丙基甲基纤维素颗粒的形状与立即释放制剂的形状相当。片剂的拉伸强度和脆性不依赖于工艺参数。在颗粒和片剂性质方面,使用淀粉作为填料无益。在16-20小时后获得完整的药物释放,并且与设计的参数无关。 (c)2016 Elsevier B.v.保留所有权利。

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