Overview of the manufacturing methods of solid dispersion technology for improving the solubility of poorly water-soluble drugs and application to anticancer drugs
P Tran, YC Pyo, DH Kim, SE Lee, JK Kim, JS Park - Pharmaceutics, 2019 - mdpi.com
Approximately 40% of new chemical entities (NCEs), including anticancer drugs, have been
reported as poorly water-soluble compounds. Anticancer drugs are classified into biologic …
reported as poorly water-soluble compounds. Anticancer drugs are classified into biologic …
Application of supercritical fluid technology for solid dispersion to enhance solubility and bioavailability of poorly water-soluble drugs
P Tran, JS Park - International Journal of Pharmaceutics, 2021 - Elsevier
Many new chemical entities (NCEs) have been discovered with the development of the
pharmaceutical industry. However, the main disadvantage of these drugs is their low …
pharmaceutical industry. However, the main disadvantage of these drugs is their low …
The use of zein in the controlled release of poorly water-soluble drugs
Although zein is a natural protein derived from corn, it has attracted much interest in
pharmaceutical and biomedical sciences. Recent remarkable investigations on the use of …
pharmaceutical and biomedical sciences. Recent remarkable investigations on the use of …
Theoretical modeling study on preparation of nanosized drugs using supercritical-based processing: Determination of solubility of Chlorothiazide in supercritical …
Y Li, AA Alameri, ZA Farhan, ME Alosaimi… - Journal of Molecular …, 2023 - Elsevier
Preparation of drug nanoparticles has been studied and evaluated in this study based on
supercritical-based processing as green technology. Computational works have been …
supercritical-based processing as green technology. Computational works have been …
Solid dispersion technology as a formulation strategy for the fabrication of modified release dosage forms: A comprehensive review
Solubility limited bioavailability is one of the crucial parameters that affect the formulation
development of the new chemical entities. Thus the major constraint in the pharmaceutical …
development of the new chemical entities. Thus the major constraint in the pharmaceutical …
Dosage form designs for the controlled drug release of solid dispersions
PHL Tran, TTD Tran - International journal of pharmaceutics, 2020 - Elsevier
Although solid dispersions have been reported as an efficient drug delivery system, the
design of specific dosage forms for pharmaceutical therapy is necessary to improve the …
design of specific dosage forms for pharmaceutical therapy is necessary to improve the …
Role of surfactant micellization for enhanced dissolution of poorly water-soluble cilostazol using poloxamer 407-based solid dispersion via the anti-solvent method
This study aimed to investigate the role of micellization of sodium lauryl sulfate (SLS) in
poloxamer 407 (POX)-based solid dispersions (POX-based SDs) using the anti-solvent …
poloxamer 407 (POX)-based solid dispersions (POX-based SDs) using the anti-solvent …
[HTML][HTML] A novel in vitro approach to investigate the effect of food intake on release profile of valsartan in solid dispersion-floating gel in-situ delivery system
Valsartan (VAL) is a BCS class II drug with low solubility and high permeability and, thus, its
formulations often encounter low bioavailability problems. Its low bioavailability can be …
formulations often encounter low bioavailability problems. Its low bioavailability can be …
Modulation of drug crystallization and molecular interactions by additives in solid dispersions for improving drug bioavailability
Background: An increase in poorly water-soluble drugs makes the design of drug delivery
systems challenging. Methods: Currently, a number of prospective solid dispersions have …
systems challenging. Methods: Currently, a number of prospective solid dispersions have …
Miscibility and solubility of caffeine and theophylline in hydroxypropyl methylcellulose
E Leyk, M Wesolowski - Pharmaceutics, 2021 - mdpi.com
As amorphization may improve the solubility and bioavailability of a drug substance, the aim
of this work was to assess to what extent the crystallinity of caffeine (CAF) and theophylline …
of this work was to assess to what extent the crystallinity of caffeine (CAF) and theophylline …