Supersaturated polymeric micelles for oral cyclosporine A delivery

H Yu, D Xia, Q Zhu, C Zhu, D Chen, Y Gan - European Journal of …, 2013 - Elsevier
Polymeric micelles provide a promising platform for improving oral absorption of poorly
soluble drugs. However, improved understanding of how drug retention within the …

Evaluation of oral bioaccessibility of aged citrus peel extracts encapsulated in different lipid-based systems: A comparison study using different in vitro digestion …

X Lu, H Zhang, T Zheng, Q Liu, J Zhu… - Journal of agricultural …, 2019 - ACS Publications
The oral delivery efficiency of aged citrus peel extract containing polymethoxyflavones and 5-
demethylated polymethoxyflavones (PMFs) in three different systems, including a pure oil …

'Stealth'lipid-based formulations: Poly (ethylene glycol)-mediated digestion inhibition improves oral bioavailability of a model poorly water soluble drug

OM Feeney, HD Williams, CW Pouton… - Journal of Controlled …, 2014 - Elsevier
For over 20 years, stealth drug delivery has been synonymous with nanoparticulate
formulations and intravenous dosing. The putative determinants of stealth in these …

The precipitation behavior of poorly water-soluble drugs with an emphasis on the digestion of lipid based formulations

J Khan, T Rades, B Boyd - Pharmaceutical research, 2016 - Springer
An increasing number of newly discovered drugs are poorly water-soluble and the use of
natural and synthetic lipids to improve the oral bioavailability of these drugs by utilizing the …

Impact of drug physicochemical properties on lipolysis-triggered drug supersaturation and precipitation from lipid-based formulations

LC Alskär, J Keemink, J Johannesson… - Molecular …, 2018 - ACS Publications
In this study we investigated lipolysis-triggered supersaturation and precipitation of a set of
model compounds formulated in lipid-based formulations (LBFs). The purpose was to …

Characterising lipid lipolysis and its implication in lipid-based formulation development

N Thomas, R Holm, T Rades, A Müllertz - The AAPS journal, 2012 - Springer
Facing the increasing number of poorly water-soluble drugs, pharmaceutical scientists are
required to break new grounds for the delivery of these pharmaceutically problematic drugs …

Ultra-fine self nanoemulsifying drug delivery system for transdermal delivery of meloxicam: dependency on the type of surfactants

MM Badran, EI Taha, MM Tayel… - Journal of Molecular …, 2014 - Elsevier
The aim of this study was to develop and evaluate ultra-fine selfnanoemulsifying drug
delivery system (UF-SNEDDS) of meloxicam (MLX) to enhance its transdermal delivery. The …

Anticancer activity of 5-fluorouracil-loaded nanoemulsions containing Fe3O4/Au core-shell nanoparticles

Z Izadiyan, K Shameli, SY Teow, M Yusefi, P Kia… - Journal of Molecular …, 2021 - Elsevier
Nanoemulsions (NEs) as multi-compartmentalized systems are extensively considered as
versatile drug delivery systems, due to their multifunctional and tuneable physicochemical …

An oral malaria therapy: curcumin-loaded lipid-based drug delivery systems combined with β-arteether

PB Memvanga, R Coco, V Préat - Journal of controlled release, 2013 - Elsevier
Curcumin (CC), a potential antimalarial drug, has poor water solubility, stability and oral
bioavailability. To circumvent these pitfalls, lipid-based drug delivery systems (LBDDSs) with …

Zeta potential changing self-emulsifying drug delivery systems: A promising strategy to sequentially overcome mucus and epithelial barrier

I Nazir, A Fürst, N Lupo, A Hupfauf, R Gust… - European Journal of …, 2019 - Elsevier
Aim The aim of the present study was to develop zeta potential changing self-emulsifying
drug delivery systems (SEDDS) via a flip-flop mechanism in order to improve their mucus …