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Formulacija krute disperzije×Faktor sličnosti otapanja f1/f2×
PodručjeFarmakologijaFarmakologija
ObiteljProcess / pipelineProcess / pipeline
Godina nastanka19711996
TvoracWilliam Chiou and Solomon RiegelmanJames Moore and Hector Flanner
Vrstasolubility enhancementsimilarity testing
Temeljni izvorChiou, W. L., Riegelman, S. (1971). Pharmaceutical applications of solid dispersions. Journal of Pharmaceutical Sciences, 60(9), 1281-1302. link ↗Moore, J. W., & Flanner, H. H. (1996). Mathematical comparison of dissolution profiles. Pharmaceutical Technology, 20(6), 64-74. link ↗
Drugi nazivisolid solution, amorphous dispersion, polymer-based formulationf1, f2, similarity factor
Srodne33
SažetakSolid dispersion is a formulation technique where a poorly soluble drug is molecularly dispersed in a hydrophilic polymer matrix, improving aqueous solubility and bioavailability. Introduced by Chiou and Riegelman in 1971, solid dispersions remain a key strategy for overcoming solubility-limited absorption.The f1 and f2 factors are dimensionless statistical measures developed by Moore and Flanner to quantify the similarity between two dissolution profiles. Adopted by regulatory agencies (FDA, EMA) as the gold standard for comparing dissolution curves, these factors enable rapid assessment of whether formulation changes significantly impact drug release.
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ScholarGateUsporedite metode: Solid Dispersion · Dissolution f1/f2 Similarity. Preuzeto 2026-06-18 s https://scholargate.app/hr/compare