DEVELOPMENT AND EVALUATION OF SUSTAINED-RELEASE IBUPROFEN-WAX MICROSPHERES .2. IN-VITRO DISSOLUTION

Adeyeye, CM; Price, JC

HERO ID

4936540

Reference Type

Journal Article

Year

1994

HERO ID 4936540
In Press No
Year 1994
Title DEVELOPMENT AND EVALUATION OF SUSTAINED-RELEASE IBUPROFEN-WAX MICROSPHERES .2. IN-VITRO DISSOLUTION
Authors Adeyeye, CM; Price, JC
Journal Pharmaceutical Research
Volume 11
Issue 4
Page Numbers 575-579
Abstract A modified USP paddle method using minibaskets was used to study the effects of various formulations on in vitro dissolution of ibuprofen microspheres. Formulations containing waxes such as paraffin or ceresine wax without modifiers exhibited very slow dissolution profiles and incomplete release, which did not improve with increased drug loading or the preparation of smaller microspheres. The addition of modifiers such as stearyl alcohol and glyceryl monostearate greatly increased the dissolution rate, with 20% (w/w) near the optimum for predictable dissolution. Higher drug loading and decreased microsphere size increased the dissolution rate from microspheres containing modifier. Optimum formulations contained ceresine wax or microcrystalline wax and stearyl alcohol as a modifier, with a drug content of 17%. An increase in the encapsulation dispersant concentration had little effect on the dissolution profiles. The dissolution data from narrow size fractions of microspheres indicated spherical matrix drug release kinetics; the 50% dissolution time decreased with the square of the microsphere diameter. With appropriate modifiers, wax microsphere formulations of drugs with solubility characteristics similar to those of ibuprofen can offer a starting basis for predictable sustained release dosage forms.
Doi 10.1023/A:1018931002991
Wosid WOS:A1994NF63300020
Is Certified Translation No
Dupe Override No
Is Public Yes
Keyword IBUPROFEN; MICROSPHERES; DISSOLUTION; MATRIX DRUG RELEASE