ScholarGate
Pembantu

Bandingkan kaedah

Semak kaedah pilihan anda secara bersebelahan; baris yang berbeza akan diserlahkan.

Formulasi Dispersi Pepejal×Faktor Keserupaan f1/f2 Pembubaran×Penghantaran Ubat Liposom×
BidangFarmakologiFarmakologiFarmakologi
KeluargaProcess / pipelineProcess / pipelineProcess / pipeline
Tahun asal197119961965
PengasasWilliam Chiou and Solomon RiegelmanJames Moore and Hector FlannerAlec Bangham
Jenissolubility enhancementsimilarity testingformulation technology
Sumber perintisChiou, 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 ↗
Aliassolid solution, amorphous dispersion, polymer-based formulationf1, f2, similarity factorliposomal formulation, vesicular delivery, lipid nanoparticles
Berkaitan333
RingkasanSolid 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.
ScholarGateSet data
  1. v1
  2. 2 Sumber
  3. PUBLISHED
  1. v1
  2. 2 Sumber
  3. PUBLISHED
  1. v1
  2. 2 Sumber
  3. PUBLISHED

Pergi ke carian Muat turun slaid

ScholarGateBandingkan kaedah: Solid Dispersion · Dissolution f1/f2 Similarity · Liposome Encapsulation. Dicapai 2026-06-19 daripada https://scholargate.app/ms/compare