[HTML][HTML] Oral drug delivery strategies for development of poorly water soluble drugs in paediatric patient population

S Salunke, F O'Brien, DCT Tan, D Harris… - Advanced Drug Delivery …, 2022 - Elsevier
Selecting the appropriate formulation and solubility-enabling technology for poorly water
soluble drugs is an essential element in the development of formulations for paediatric …

[HTML][HTML] Nanosuspensions technology as a master key for nature products drug delivery and in vivo fate

Y Ma, Z Cong, P Gao, Y Wang - European Journal of Pharmaceutical …, 2023 - Elsevier
The drug nanosuspensions is a universal formulation approach for improved drug delivery
of hydrophobic drugs and one the most promising approaches for increasing the …

Pharmaceutical amorphous nanoparticles

R Jog, DJ Burgess - Journal of pharmaceutical sciences, 2017 - Elsevier
There has been a tremendous revolution in the field of nanotechnology, resulting in the
advent of novel drug delivery systems known as nanomedicines for diagnosis and therapy …

The need for restructuring the disordered science of amorphous drug formulations

K Edueng, D Mahlin, CAS Bergström - Pharmaceutical research, 2017 - Springer
The alarming numbers of poorly soluble discovery compounds have centered the efforts
towards finding strategies to improve the solubility. One of the attractive approaches to …

Soluplus micelles for improving the oral bioavailability of scopoletin and their hypouricemic effect in vivo

Y Zeng, S Li, C Liu, T Gong, X Sun, Y Fu… - Acta Pharmacologica …, 2017 - nature.com
Scopoletin is an active coumarin possessing a variety of pharmacological activities,
including anti-hyperuricemic effect, but with poor solubility. To improve its oral bioavailability …

Development of sorafenib loaded nanoparticles to improve oral bioavailability using a quality by design approach

SY Park, Z Kang, P Thapa, YS Jin, JW Park… - International journal of …, 2019 - Elsevier
Sorafenib, a potent anticancer drug, has low absorption in the gastrointestinal tract due to its
poor aqueous solubility. The main purpose of this investigation was to design sorafenib …

Impact of Eudragit EPO and hydroxypropyl methylcellulose on drug release rate, supersaturation, precipitation outcome and redissolution rate of indomethacin …

T Xie, W Gao, LS Taylor - International journal of pharmaceutics, 2017 - Elsevier
The purpose of this work was to evaluate the impact of polymer (s) on the dissolution rate,
supersaturation and precipitation of indomethacin amorphous solid dispersions (ASD), and …

Fabrication of solid lipid nanoparticles of lurasidone HCl for oral delivery: optimization, in vitro characterization, cell line studies and in vivo efficacy in schizophrenia

MH Patel, VP Mundada, KK Sawant - Drug development and …, 2019 - Taylor & Francis
Objective: The aim of the present investigation was to investigate the efficacy of solid lipid
nanoparticles (SLNs) to enhance the absorption and bioavailability of lurasidone …

A retrospective biopharmaceutical analysis of> 800 approved oral drug products: are drug properties of solid dispersions and lipid-based formulations distinctive?

H Bennett-Lenane, JP O'Shea, CM O'Driscoll… - Journal of …, 2020 - Elsevier
Increasing numbers of poorly water soluble drugs in development has intensified need for
bio-enabling formulations including Lipid-Based Formulations (LBF) and Solid Dispersions …

[HTML][HTML] Computational and experimental approaches for development of methotrexate nanosuspensions by bottom-up nanoprecipitation

AM Dos Santos, FC Carvalho, DA Teixeira… - International Journal of …, 2017 - Elsevier
Abstract Development of nanosuspensions offers a promising tool for formulations involving
poorly water-soluble drugs. In this study, methotrexate (MTX) nanosuspensions were …