期刊
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS
卷 69, 期 3, 页码 1114-1120出版社
ELSEVIER
DOI: 10.1016/j.ejpb.2008.02.007
关键词
ternary solid dispersion; MDSC; powder x-ray diffraction; dissolution; GC-MS; itraconazole; PEG 6000; PVPVA 64
资金
- university research council [OT 03/60]
The good compatibility between Itraconazole and polyvidone-vinylacetate 64 (PVPVA 64) was pointed out previously. However, the dissolution properties of these systems left room for improvement. Therefore polyethylene glycol 6000 (PEG 6000). known for its solubilizing and wetting properties. was added to the PVPVA 64 matrix. Physicochemical analysis showed that LIP to 10%, of PEG 6000 Could be mixed with PVPVA 64. Addition of 10%, 20% or 40% of Itraconazole rendered amorphous solid dispersions consisting of a ternary mixed phase and a PVPVA 64 rich amorphous phase. If the PEG 6000 fraction was elevated LIP to 25% of the carrier, the PEG 6000 crystallinity degree was around 73 +/- 0.6%. Up to 20%, of' Itraconazole Could be Molecularly dispersed in the 25/75 w/w polymer blend. An Itraconazole Filching peak Could be detected for the sample containing 40% of drug. Dissolution experiments showed that no benefit was obtained by adding PEG 6000 to the PVPVA 64 matrix for samples containing tip to 20% of Itraconazole. The dissolution of the ternary dispersions with 40% of Itraconazole oil the other hand showed improvement compared to binary Itraconazole/PVPVA 64 dispersions. (C) 2008 Elsevier B.V. All rights reserved.
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