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Preparation and characterization of genistein containing poly(ethylene glycol) microparticles
Author(s) -
Motlekar Nusrat,
Khan Mansoor A.,
Youan BiBotti C.
Publication year - 2006
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.23827
Subject(s) - dissolution , ethylene glycol , differential scanning calorimetry , materials science , solubility , chemical engineering , polymer , dissolution testing , fourier transform infrared spectroscopy , solvent , genistein , peg ratio , nuclear chemistry , chemistry , organic chemistry , biopharmaceutics classification system , composite material , medicine , physics , finance , engineering , economics , thermodynamics
The purpose of this study was to prepare, characterize, and evaluate genistein‐containing microparticles with enhanced dissolution profile using poly(ethylene glycol) (PEG) as polymer matrix. Genistein loaded microparticles were prepared by a solvent evaporation process and their surface, thermal, chemical, and dissolution properties were analyzed by microscopy, differential scanning calorimetry, ATR‐FTIR spectroscopy, and USP dissolution apparatus II, respectively. The wettability index was also determined. Genistein exhibited an elongated crystal habit. However, the drug containing PEG microparticles were discrete and quasispherical. The ATR‐FTIR studies performed on the formulation suggested hydrogen bonding between the drug and the polymer matrix. Thermal analysis indicated a conversion of the crystalline form of the drug to an amorphous form. Genistein, exhibiting low solubility and high permeability, is a Class II drug of the Biopharmaceutical Classification Scheme. However, there was a ∼9‐fold increase in the rate of dissolution of genistein in the case of all formulations as compared to native genistein. This study showed that genistein could be effectively encapsulated into PEG microparticles using an emulsion‐solvent evaporation technique, therefore avoiding the potential disadvantages of other solid dispersion techniques. This approach provided a significant enhancement in the drug dissolution profile. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2070–2078, 2006