TY - JOUR
T1 - Improvement of flow and bulk density of pharmaceutical powders using surface modification
AU - Jallo, Laila J.
AU - Ghoroi, Chinmay
AU - Gurumurthy, Lakxmi
AU - Patel, Utsav
AU - Davé, Rajesh N.
N1 - Funding Information:
This work has been funded in part by the National Science Foundation (NSF) through the ERC award, EEC-0540855 . Additional funding from NSF awards, EEC-0552587 , DMI-0506722 , DGE-0504497 , and EEC-0908889 is also acknowledged. Special thanks to Aveka, Inc., Woodbury, MN, for providing the use of the MAIC and Sympatec GmbH, for providing the use of the RODOS/HELOS system. Thanks are also due to Nancy Farlow for her editorial contributions, in particular about the graphical abstract.
PY - 2012/2/28
Y1 - 2012/2/28
N2 - Improvement in flow and bulk density, the two most important properties that determine the ease with which pharmaceutical powders can be handled, stored and processed, is done through surface modification. A limited design of experiment was conducted to establish a standardized dry coating procedure that limits the extent of powder attrition, while providing the most consistent improvement in angle of repose (AOR). The magnetically assisted impaction coating (MAIC) was considered as a model dry-coater for pharmaceutical powders; ibuprofen, acetaminophen, and ascorbic acid. Dry coated drug powders were characterized by AOR, particle size as a function of dispersion pressure, particle size distribution, conditioned bulk density (CBD), Carr index (CI), flow function coefficient (FFC), cohesion coefficient using different instruments, including a shear cell in the Freeman FT4 powder rheometer, and Hansen flowability index. Substantial improvement was observed in all the measured properties after dry coating relative to the uncoated powders, such that each powder moved from a poorer to a better flow classification and showed improved dispersion. The material intrinsic property such as cohesion, plotted as a function of particle size, gave a trend similar to those of bulk flow properties, AOR and CI. Property improvement is also illustrated in a phase map of inverse cohesion (or FFC) as a function of bulk density, which also indicated a significant positive shift due to dry coating. It is hoped that such phase maps are useful in manufacturing decisions regarding the need for dry coating, which will allow moving from wet granulation to roller compaction or to direct compression based formulations.
AB - Improvement in flow and bulk density, the two most important properties that determine the ease with which pharmaceutical powders can be handled, stored and processed, is done through surface modification. A limited design of experiment was conducted to establish a standardized dry coating procedure that limits the extent of powder attrition, while providing the most consistent improvement in angle of repose (AOR). The magnetically assisted impaction coating (MAIC) was considered as a model dry-coater for pharmaceutical powders; ibuprofen, acetaminophen, and ascorbic acid. Dry coated drug powders were characterized by AOR, particle size as a function of dispersion pressure, particle size distribution, conditioned bulk density (CBD), Carr index (CI), flow function coefficient (FFC), cohesion coefficient using different instruments, including a shear cell in the Freeman FT4 powder rheometer, and Hansen flowability index. Substantial improvement was observed in all the measured properties after dry coating relative to the uncoated powders, such that each powder moved from a poorer to a better flow classification and showed improved dispersion. The material intrinsic property such as cohesion, plotted as a function of particle size, gave a trend similar to those of bulk flow properties, AOR and CI. Property improvement is also illustrated in a phase map of inverse cohesion (or FFC) as a function of bulk density, which also indicated a significant positive shift due to dry coating. It is hoped that such phase maps are useful in manufacturing decisions regarding the need for dry coating, which will allow moving from wet granulation to roller compaction or to direct compression based formulations.
KW - Cohesion
KW - Design of experiment
KW - Dry coating
KW - Flow properties
KW - Pharmaceutical powders
UR - http://www.scopus.com/inward/record.url?scp=84856535966&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84856535966&partnerID=8YFLogxK
U2 - 10.1016/j.ijpharm.2011.12.012
DO - 10.1016/j.ijpharm.2011.12.012
M3 - Article
C2 - 22197769
AN - SCOPUS:84856535966
SN - 0378-5173
VL - 423
SP - 213
EP - 225
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
IS - 2
ER -