Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2487139 | Journal of Pharmaceutical Sciences | 2009 | 11 Pages |
Abstract
This work was aimed at investigating the feasibility of fluidâbed coating as a new method to prepare cyclodextrin inclusion complex. The inclusion complex of the model drug piroxicam (PIX) and 2âhydroxypropylâβâcyclodextrin (HPCD) in aqueous ethanol solution was sprayed and deposited onto the surface of the pellet substrate upon removal of the solvent. The coating process was fluent with high coating efficiency. Scanning electron microscopy revealed a coarse pellet surface, and a loosely packed coating structure. Significantly enhanced dissolution, over 90% at 5 min, was observed at stoichiometric PIX/HPCD molar ratio (1/1) and at a ratio with excessive HPCD (1/2). Differential scanning calorimetry and powder Xâray diffractometry confirmed absence of crystallinity of PIX at PIX/HPCD molar ratio of 1/1 and 1/2. Fourier transformâinfrared spectrometry and Raman spectrometry revealed interaction between PIX and HPCD adding evidence on inclusion of PIX moieties into HPCD cavities. Solidâstate 13C NMR spectrometry indicated possible inclusion of PIX through the pyridine ring. It is concluded that fluidâbed coating has potential to be used as a new technique to prepare cyclodextrin inclusion complex. © 2008 WileyâLiss, Inc. and the American Pharmacists Association J Pharm Sci 98:665-675, 2009
Keywords
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Pharmacology, Toxicology and Pharmaceutical Science
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Authors
Xingwang Zhang, Danni Wu, Jie Lai, Yi Lu, Zongning Yin, Wei Wu,