TY - JOUR
T1 - Particle engineering for pulmonary drug delivery
AU - Chow, Albert H.L.
AU - Tong, Henry H.Y.
AU - Chattopadhyay, Pratibhash
AU - Shekunov, Boris Y.
N1 - Funding Information:
One of the authors (Henry H. Y. Tong) would like to acknowledge the financial support of Macao Polytechnic Institute (Project no.: RP/ESS-7/2005).
PY - 2007/3
Y1 - 2007/3
N2 - With the rapidly growing popularity and sophistication of inhalation therapy, there is an increasing demand for tailor-made inhalable drug particles capable of affording the most efficient delivery to the lungs and the most optimal therapeutic outcomes. To cope with this formulation demand, a wide variety of novel particle technologies have emerged over the past decade. The present review is intended to provide a critical account of the current goals and technologies of particle engineering for the development of pulmonary drug delivery systems. These technologies cover traditional micronization and powder blending, controlled solvent crystallization, spray drying, spray freeze drying, particle formation from liquid dispersion systems, supercritical fluid processing and particle coating. The merits and limitations of these technologies are discussed with reference to their applications to specific drug and/or excipient materials. The regulatory requirements applicable to particulate inhalation products are also reviewed briefly.
AB - With the rapidly growing popularity and sophistication of inhalation therapy, there is an increasing demand for tailor-made inhalable drug particles capable of affording the most efficient delivery to the lungs and the most optimal therapeutic outcomes. To cope with this formulation demand, a wide variety of novel particle technologies have emerged over the past decade. The present review is intended to provide a critical account of the current goals and technologies of particle engineering for the development of pulmonary drug delivery systems. These technologies cover traditional micronization and powder blending, controlled solvent crystallization, spray drying, spray freeze drying, particle formation from liquid dispersion systems, supercritical fluid processing and particle coating. The merits and limitations of these technologies are discussed with reference to their applications to specific drug and/or excipient materials. The regulatory requirements applicable to particulate inhalation products are also reviewed briefly.
KW - Aerosols
KW - Crystalline and amorphous solids
KW - Inhalers
KW - Micro- and nanoparticles
KW - Micronization
KW - Particle size
KW - Respiratory drug delivery
KW - Spray drying
KW - Spray freeze drying
KW - Supercritical fluids
UR - http://www.scopus.com/inward/record.url?scp=33847127477&partnerID=8YFLogxK
U2 - 10.1007/s11095-006-9174-3
DO - 10.1007/s11095-006-9174-3
M3 - Review article
C2 - 17245651
AN - SCOPUS:33847127477
SN - 0724-8741
VL - 24
SP - 411
EP - 437
JO - Pharmaceutical Research
JF - Pharmaceutical Research
IS - 3
ER -