Ghent University, Laboratory of Pharmaceutical Process Analytical Technology, Ottergemsesteenweg 460, 9000 Ghent, Belgium.
Pfizer Inc., Worldwide Research and Development, ARD, Eastern Point Road, Groton, CT 06340, USA.
Int J Pharm. 2022 Jan 5;611:121328. doi: 10.1016/j.ijpharm.2021.121328. Epub 2021 Nov 28.
The influence of different tableting process parameters on lead-lag was studied by collecting in-line near-infrared (NIR) spectra in the filling chamber of the tablet press feed frame and off-line NIR tablet data. Lead-lag is defined as the difference in time and API concentration between the measured in-line feed frame NIR response and the off-line NIR tablet data. Lead-lag results from the product formulation blend undergoing additional mixing after passing the NIR probe inside the feed frame, before being filled into the dies of the tablet press. A design of experiments (DoE) was performed to evaluate the effect of the tableting process factors paddle speed, turret speed, overfill level, paddle speed ratio and feed frame type upon lead-lag. Paddle speed and turret speed were identified as the only tableting parameters affecting lead-lag. Lead-lag decreased with increasing paddle speed or turret speed and became negligible at high paddle speed and high turret speed. Overfill level, paddle speed ratio and feed frame type did not affect lead-lag, suggesting that the amount and the trajectory of the recirculating powder in the feed frame did not significantly vary and hence influence the lead-lag within the examined process factor ranges. Finally, a methodology was developed using the in-line feed frame NIR measurements for the continuous monitoring and control of blend potency and tablet content uniformity. Tablet diversion should start when the in-line feed frame monitored blend potency exceeds the predefined control limits and can discontinue when this blend potency is again within the control limits for a duration equal to the lead-lag time. A combination of continuous blend potency monitoring inside the feed frame and in-process tablet weight control allows real-time tablet content uniformity assurance. Although the findings of this study are restricted to the specific equipment, tableting parameter ranges and product formulation used, the suggested approach for lead-lag determination and continuous tablet content uniformity monitoring can be applied to any rotary tablet press and product formulation.
研究了不同压片工艺参数对滞后的影响,方法是在压片机料斗的填充室内采集在线近红外(NIR)光谱和离线 NIR 片剂数据。滞后定义为测量的在线料斗 NIR 响应与离线 NIR 片剂数据之间的时间和 API 浓度差异。滞后是由于产品配方混合物在通过 NIR 探头后在料斗内部进行额外混合,然后再填充到压片机的冲模中,从而导致的。通过设计实验(DoE)来评估压片工艺因素桨叶速度、转塔速度、过量填充水平、桨叶速度比和料斗类型对滞后的影响。桨叶速度和转塔速度被确定为唯一影响滞后的压片参数。随着桨叶速度或转塔速度的增加,滞后减小,在高桨叶速度和高转塔速度下,滞后变得可以忽略不计。过量填充水平、桨叶速度比和料斗类型不影响滞后,这表明料斗中循环粉末的量和轨迹没有明显变化,因此在考察的工艺参数范围内不会显著影响滞后。最后,开发了一种使用在线料斗 NIR 测量进行混合强度和片剂含量均匀性连续监测和控制的方法。当在线料斗监测的混合强度超过预设控制限时,应开始片剂分流,并在混合强度再次在控制限内持续一段时间(等于滞后时间)时停止。在料斗内连续监测混合强度和过程中控制片剂重量的组合允许实时保证片剂含量均匀性。尽管本研究的结果仅限于特定设备、压片参数范围和使用的产品配方,但建议的用于确定滞后和连续片剂含量均匀性监测的方法可应用于任何旋转压片机和产品配方。