ScholarGate
Assistente

Comparar métodos

Examine os métodos selecionados lado a lado; as linhas que diferem ficam destacadas.

Formulação de Dispersão Sólida×Fator de Similaridade f1/f2 para Dissolução×Entrega de Fármacos Lipossomais×
ÁreaFarmacologiaFarmacologiaFarmacologia
FamíliaProcess / pipelineProcess / pipelineProcess / pipeline
Ano de origem197119961965
Autor originalWilliam Chiou and Solomon RiegelmanJames Moore and Hector FlannerAlec Bangham
Tiposolubility enhancementsimilarity testingformulation technology
Fonte seminalChiou, 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 ↗
Outros nomessolid solution, amorphous dispersion, polymer-based formulationf1, f2, similarity factorliposomal formulation, vesicular delivery, lipid nanoparticles
Relacionados333
ResumoSolid 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.
ScholarGateConjunto de dados
  1. v1
  2. 2 Fontes
  3. PUBLISHED
  1. v1
  2. 2 Fontes
  3. PUBLISHED
  1. v1
  2. 2 Fontes
  3. PUBLISHED

Ir para a pesquisa Baixar slides

ScholarGateComparar métodos: Solid Dispersion · Dissolution f1/f2 Similarity · Liposome Encapsulation. Recuperado em 2026-06-19 de https://scholargate.app/pt/compare