[HTML][HTML] Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability

P Khadka, J Ro, H Kim, I Kim, JT Kim, H Kim… - Asian journal of …, 2014 - Elsevier
Pharmaceutical particle technology is employed to improve poor aqueous solubility of drug
compounds that limits in vivo bioavailability owing to their low dissolution rate in the …

Solubility and dissolution enhancement strategies: current understanding and recent trends

S Jain, N Patel, S Lin - Drug development and industrial pharmacy, 2015 - Taylor & Francis
Identification of lead compounds with higher molecular weight and lower aqueous solubility
has become increasingly prevalent with the advent of high throughput screening. Poor …

From 'fixed dose combinations' to 'a dynamic dose combiner': 3D printed bi-layer antihypertensive tablets

M Sadia, A Isreb, I Abbadi, M Isreb, D Aziz… - European Journal of …, 2018 - Elsevier
There is an increased evidence for treating hypertension by a combination of two or more
drugs. Increasing the number of daily intake of tablets has been reported to negatively affect …

Tranilast-matrine co-amorphous system: Strong intermolecular interactions, improved solubility, and physiochemical stability

D Hu, X Chen, D Li, H Zhang, Y Duan… - International Journal of …, 2023 - Elsevier
There is a great interest to develop co-amorphous drug delivery systems to enhance the
solubility of biopharmaceutics classification system (BCS) class II and IV drugs. However …

Mechanochemical synthesis of pharmaceutical cocrystal suspensions via hot melt extrusion: feasibility studies and physicochemical characterization

S Li, T Yu, Y Tian, CP McCoy, DS Jones… - Molecular …, 2016 - ACS Publications
Engineered cocrystals offer an alternative solid drug form with tailored physicochemical
properties. Interestingly, although cocrystals provide many new possibilities, they also …

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 …

Development and evaluation of gastroretentive raft forming systems incorporating curcumin-Eudragit® EPO solid dispersions for gastric ulcer treatment

N Kerdsakundee, S Mahattanadul… - European Journal of …, 2015 - Elsevier
Novel raft forming systems incorporating curcumin-Eudragit® EPO solid dispersions were
developed to prolong the gastric residence time and provide for a controlled release therapy …

[HTML][HTML] Directly compressed rosuvastatin calcium tablets that offer hydrotropic and micellar solubilization for improved dissolution rate and extent of drug release

S Butt, SMF Hasan, MM Hassan, KM Alkharfy… - Saudi Pharmaceutical …, 2019 - Elsevier
The objective was to use caffeine and Soluplus® to improve the dissolution rate and to
maintain a concentration of BCS Class II rosuvastatin calcium that exceeds its solubility …

Physiologically based pharmacokinetic models predicting renal and hepatic concentrations of industrial chemicals after virtual oral doses in rats

Y Kamiya, S Otsuka, T Miura… - Chemical research in …, 2020 - ACS Publications
Recently developed high-throughput in vitro assays in combination with computational
models could provide alternatives to animal testing. The purpose of the present study was to …

Co-amorphous formation induced by combination of tranilast and diphenhydramine hydrochloride

H Ueda, K Kadota, M Imono, T Ito, A Kunita… - Journal of …, 2017 - Elsevier
In this study, we investigated the formation of a co-amorphous system of tranilast (TRL) and
diphenhydramine hydrochloride (DPH), which are drugs used for treating allergies and …