[HTML][HTML] An update on oral drug delivery via intestinal lymphatic transport

Z Zhang, Y Lu, J Qi, W Wu - Acta Pharmaceutica Sinica B, 2021 - Elsevier
Orally administered drug entities have to survive the harsh gastrointestinal environment,
penetrate the enteric epithelia and circumvent hepatic metabolism before reaching the …

Electrospun self-emulsifying core-shell nanofibers for effective delivery of paclitaxel

R Ge, Y Ji, Y Ding, C Huang, H He… - Frontiers in Bioengineering …, 2023 - frontiersin.org
The poor solubility of numerous drugs pose a long-existing challenge to the researchers in
the fields of pharmaceutics, bioengineering and biotechnology. Many “top-down” and …

Preparation of 2-methoxyestradiol self-emulsified drug delivery system and the effect on combination therapy with doxorubicin against MCF-7/ADM cells

C Yu, C Li, H Pan, T Li, S He - AAPS PharmSciTech, 2022 - Springer
Due to the poor solubility and bioavailability of 2-methoxyestradiol (2-ME), 2-ME emulsified
drug delivery system (2-ME-SEDDS) was designed and characterized. After dilution with 5 …

Multi-strategic approaches for enhancing active transportation using self-emulsifying drug delivery system

S Poudwal, P Shende - Journal of Drug Targeting, 2022 - Taylor & Francis
Oral delivery is the most desired route of drug administration and it can be more beneficial
for patients suffering from chronic diseases wherein frequent parenteral administration of …

[HTML][HTML] Preparation of Sorafenib tosylate self-emulsified drug delivery system and the effect on combination therapy with Bosutinib against HCT116/SW1417 cells

S Bhattacharya, D Pawde, RL Dumpala - Results in Chemistry, 2022 - Elsevier
The Sorafenib tosylate (ST) emulsified drug delivery system (ST-SEDDS) was designed and
characterized in response to the poor solubility and bioavailability of ST. ST-SEDDS formed …

Bile acids for probucol formulations applications in drug induced ototoxicity

CM Ionescu - 2024 - espace.curtin.edu.au
Within this thesis, probucol's otoprotective application is assessed in vitro on House Ear
Institute-Organ of Corti 1 (HEI-OC1) using three different formulation methods; 1) spray …

[PDF][PDF] MD simulation study on drug release from HPMCAS-based amorphous solid dispersions upon reaching cell membrane

R Hasani - 2022 - diva-portal.org
The amorphous solid dispersion (ASD) formulation improves the bioavailability of
pharmaceutical compounds by enhancing the drug's apparent solubility which facilitates the …

[PDF][PDF] Results in Chemistry

S Bhattacharya, D Pawde, RL Dumpala - researchgate.net
The need for novel approaches to the treatment of colon cancer, a common and deadly
disease, is universal. In this compilation, we look at how polymeric nanoparticles (Polymeric …