Indomethacin-loaded solid lipid nanoparticles for ocular delivery: development, characterization, and in vitro evaluation.

作者: Ketan Hippalgaonkar , Goutham R. Adelli , Kanchan Hippalgaonkar , Michael A. Repka , Soumyajit Majumdar

DOI: 10.1089/JOP.2012.0069

关键词: Particle sizePartition coefficientPulmonary surfactantSolubilityDispersityPoloxamerNanoparticleChemistrySolid lipid nanoparticleChromatography

摘要: Abstract Purpose: The goal of this study was to develop and characterize indomethacin-loaded solid lipid nanoparticles (IN-SLNs; 0.1% w/v) for ocular delivery. Methods: Various lipids, homogenization pressures/cycles, Tween 80 fraction in the mixture surfactants (Poloxamer 188 80; total surfactant concentration at 1% w/v), pH were investigated preparation IN-SLNs. Compritol® 888 ATO selected as phase IN-SLNs, indomethacin exhibited a highest distribution coefficient solubility phase. Results: Homogenization 15,000 psi 6 cycles resulted smallest particle size. Increase Poloxamer decrease entrapment efficiency (EE). mean size, polydispersity index, zeta-potential, EE optimized formulation 140 nm, 0.16, −21 mV, 72.0%, respectively. IN-SLNs physically stable post-sterilization on storage period 1 month (last timepoint tested). A dramatic in...

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