Võrdle meetodeid
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| Liposoomne ravimikandja× | Tahke dispersioon (Solid Dispersion Formulation)× | |
|---|---|---|
| Valdkond | Farmakoloogia | Farmakoloogia |
| Perekond | Process / pipeline | Process / pipeline |
| Tekkeaasta≠ | 1965 | 1971 |
| Looja≠ | Alec Bangham | William Chiou and Solomon Riegelman |
| Tüüp≠ | formulation technology | solubility enhancement |
| Algallikas≠ | 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 ↗ | Chiou, W. L., Riegelman, S. (1971). Pharmaceutical applications of solid dispersions. Journal of Pharmaceutical Sciences, 60(9), 1281-1302. link ↗ |
| Rööpnimetused | liposomal formulation, vesicular delivery, lipid nanoparticles | solid solution, amorphous dispersion, polymer-based formulation |
| Seotud | 3 | 3 |
| Kokkuvõte≠ | 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. | 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. |
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