השוואת שיטות
סקרו את השיטות שבחרתם זו לצד זו; שורות שבהן יש הבדל מודגשות.
| פורמולציית דיספרסיה מוצקה× | גורם דמיון f1/f2 (Dissolution f1/f2 Similarity Factor)× | אספקת תרופות ליפוזומלית× | |
|---|---|---|---|
| תחום | פרמקולוגיה | פרמקולוגיה | פרמקולוגיה |
| משפחה | Process / pipeline | Process / pipeline | Process / pipeline |
| שנת המקור≠ | 1971 | 1996 | 1965 |
| הוגה השיטה≠ | William Chiou and Solomon Riegelman | James Moore and Hector Flanner | Alec Bangham |
| סוג≠ | solubility enhancement | similarity testing | formulation technology |
| מקור מכונן≠ | Chiou, 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 ↗ | Bangham, A. D., Standish, M. M., & Watkins, J. C. (1965). Diffusion of univalent ions across the lamellae of swollen phospholipid films and the determination of membrane potential. Journal of Molecular Biology, 13(1), 238-252. DOI ↗ |
| כינויים | solid solution, amorphous dispersion, polymer-based formulation | f1, f2, similarity factor | liposomal formulation, vesicular delivery, lipid nanoparticles |
| קשורות | 3 | 3 | 3 |
| תקציר≠ | Solid 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. | Liposomal encapsulation is a formulation technique using lipid bilayer vesicles (liposomes) to enclose drugs, improving bioavailability, reducing toxicity, and enabling targeted delivery. Developed by Alec Bangham in 1965, liposomes are now standard in pharmaceutical development, with several FDA-approved liposomal drugs on the market. |
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