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In-Line UV-Vis Spectroscopy as a Fast-Working Process Analytical Technology (PAT) during Early Phase Product Development Using Hot Melt Extrusion (HME)

机译:在线紫外-可见光谱技术是使用热熔挤出(HME)进行早期产品开发过程中的快速工作过程分析技术(PAT)。

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摘要

This paper displays the potential of an in-line PAT system for early phase product development during pharmaceutical continuous manufacturing following a Quality by Design (QbD) framework. Hot melt extrusion (HME) is used as continuous manufacturing process and UV–Vis spectroscopy as an in-line monitoring system. A sequential design of experiments (DoE) (screening, optimisation and verification) was used to gain process understanding for the manufacture of piroxicam (PRX)/Kollidon® VA64 amorphous solid dispersions. The influence of die temperature, screw speed, solid feed rate and PRX concentration on the critical quality attributes (CQAs) absorbance and lightness of color (L*) of the extrudates was investigated using multivariate tools. Statistical analysis results show interaction effects between concentration and temperature on absorbance and L* values. Solid feed rate has a significant effect on absorbance only and screw speed showed least impact on both responses for the screening design. The optimum HME process conditions were confirmed by 4 independent studies to be 20% w/w of PRX, temperature 140 °C, screw speed 200 rpm and feed rate 6 g/min. The in-line UV-Vis system was used to assess the solubility of PRX in Kollidon® VA64 by measuring absorbance and L* values from 230 to 700 nm. Oversaturation was observed for PRX concentrations higher than 20% w/w. Oversaturation can be readily identified as it causes scattering in the visible range. This is observed by a shift of the baseline in the visible part of the spectrum. Extrudate samples were analyzed for degradation using off-line High-Performance Liquid Chromatography (HPLC) standard methods. Results from off-line experiments using differential scanning calorimetry (DSC), and X-ray diffraction (XRD) are also presented.
机译:本文展示了一种在线PAT系统的潜力,该系统遵循质量设计(QbD)框架在药品连续生产过程中进行早期产品开发。热熔挤出(HME)被用作连续生产过程,而UV-Vis光谱则被用作在线监测系统。通过序贯的实验设计(DoE)(筛选,优化和验证)来了解吡罗昔康(PRX)/ Kollidon ® VA64非晶态固体分散体的生产过程。使用多变量工具研究了模头温度,螺杆速度,固体进料速度和PRX浓度对挤出物的关键质量属性(CQA)吸光度和颜色亮度(L *)的影响。统计分析结果显示浓度和温度之间的相互作用对吸光度和L *值的影响。固体进料速率仅对吸光度有显着影响,而螺杆速度对筛分设计的两种响应均影响最小。通过四项独立研究确认,最佳HME工艺条件为PRX的20%w / w,温度140°C,螺杆速度200 rpm和进料速度6 g / min。在线UV-Vis系统用于通过测量230至700nm的吸光度和L *值来评估PRX在Kollidon s VA64中的溶解度。对于高于20%w / w的PRX浓度,观察到过饱和。过饱和很容易识别,因为它会导致可见光范围内的散射。通过基线在光谱可见部分中的移动可以观察到这一点。使用离线高效液相色谱(HPLC)标准方法分析挤出物样品的降解情况。还介绍了使用差示扫描量热法(DSC)和X射线衍射(XRD)进行的离线实验的结果。

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