TY - JOUR
T1 - Assessment of blend uniformity in a continuous tablet manufacturing process
AU - Sierra-Vega, Nobel O.
AU - Román-Ospino, Andrés
AU - Scicolone, James
AU - Muzzio, Fernando J.
AU - Romañach, Rodolfo J.
AU - Méndez, Rafael
N1 - Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/4/5
Y1 - 2019/4/5
N2 - Blend uniformity was monitored throughout a continuous manufacturing (CM) process by near infrared (NIR) spectroscopic measurements of flowing blends and compared to the drug concentration in the tablets. The NIR spectra were obtained through the chute after the blender and within the feed frame, while transmission spectra were obtained for the tablets. The CM process was performed with semi-fine acetaminophen blends at 10.0% (w/w). The blender was operated at 250 RPM, for best performance, and 106 and 495 rpm where a lower mixing efficiency was expected. The variation in blender RPM increased the variation in drug concentration at the chute but not at the feed frame. Statistical results show that the drug concentration of tablets can be predicted, with great accuracy, from blends within the feed frame. This study demonstrated a mixing effect within the feed frame, which contribute to a 60% decrease in the relative standard deviation of the drug concentration, when compared to the chute. Variographic analysis showed that the minimum sampling and analytical error was five times less in the feed frame than the chute. This study demonstrates that the feed frame is an ideal location for monitoring the drug concentration of powder blends for CM processes.
AB - Blend uniformity was monitored throughout a continuous manufacturing (CM) process by near infrared (NIR) spectroscopic measurements of flowing blends and compared to the drug concentration in the tablets. The NIR spectra were obtained through the chute after the blender and within the feed frame, while transmission spectra were obtained for the tablets. The CM process was performed with semi-fine acetaminophen blends at 10.0% (w/w). The blender was operated at 250 RPM, for best performance, and 106 and 495 rpm where a lower mixing efficiency was expected. The variation in blender RPM increased the variation in drug concentration at the chute but not at the feed frame. Statistical results show that the drug concentration of tablets can be predicted, with great accuracy, from blends within the feed frame. This study demonstrated a mixing effect within the feed frame, which contribute to a 60% decrease in the relative standard deviation of the drug concentration, when compared to the chute. Variographic analysis showed that the minimum sampling and analytical error was five times less in the feed frame than the chute. This study demonstrates that the feed frame is an ideal location for monitoring the drug concentration of powder blends for CM processes.
KW - Content uniformity
KW - Continuous tablet manufacturing
KW - Feed frame
KW - Powder blend uniformity
KW - Process Analytical Technology
KW - Transitional chute
UR - http://www.scopus.com/inward/record.url?scp=85061989764&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85061989764&partnerID=8YFLogxK
U2 - 10.1016/j.ijpharm.2019.01.073
DO - 10.1016/j.ijpharm.2019.01.073
M3 - Article
C2 - 30763679
AN - SCOPUS:85061989764
SN - 0378-5173
VL - 560
SP - 322
EP - 333
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
ER -