Novel strategies for the formulation and processing of poorly water-soluble drugs

K Göke, T Lorenz, A Repanas, F Schneider… - European Journal of …, 2018 - Elsevier
Low aqueous solubility of active pharmaceutical ingredients presents a serious challenge in
the development process of new drug products. This article provides an overview on some …

Solubility and dissolution profile assessment in drug discovery

K Sugano, A Okazaki, S Sugimoto… - Drug metabolism and …, 2007 - jstage.jst.go.jp
The purposes of the review are to: a) Provide a comprehensible introduction of the-state-
ofthe-art sciences of solubility and dissolution, b) introduce typical technologies to assess …

Impact of emulsion-based drug delivery systems on intestinal permeability and drug release kinetics

F Buyukozturk, JC Benneyan, RL Carrier - Journal of controlled release, 2010 - Elsevier
Lipid based drug delivery systems, and in particular self-emulsifying drug delivery systems
(SEDDS), show great potential for enhancing oral bioavailability but have not been broadly …

Biowaiver monographs for immediate release solid oral dosage forms: Diclofenac sodium and diclofenac potassium

B Chuasuwan, V Binjesoh, JE Polli, H Zhang… - Journal of …, 2009 - Elsevier
Literature data are reviewed regarding the scientific advisability of allowing a waiver of in
vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage …

Selection of In Vivo Predictive Dissolution Media Using Drug Substance and Physiological Properties

DM Mudie, N Samiei, DJ Marshall, GE Amidon… - The AAPS journal, 2020 - Springer
The rate and extent of drug dissolution in the gastrointestinal (GI) tract are highly dependent
upon drug physicochemical properties and GI fluid properties. Biorelevant dissolution media …

Role of surfactant and pH on dissolution properties of fenofibrate and glipizide—a technical note

S Jamzad, R Fassihi - Aaps Pharmscitech, 2006 - Springer
Summary and Conclusions Depending on the dose size and solubility characteristics of low
solubility drugs, a meaningful and discriminatory power of dissolution rate testing can be …

Pulmonary drug delivery for acute respiratory distress syndrome

Q Fei, I Bentley, SN Ghadiali, JA Englert - Pulmonary Pharmacology & …, 2023 - Elsevier
The acute respiratory distress syndrome (ARDS) is a life-threatening condition that causes
respiratory failure. Despite numerous clinical trials, there are no molecularly targeted …

Design of multifunctional nanostructured lipid carriers enriched with α-tocopherol using vegetable oils

F Pinto, DPC de Barros, LP Fonseca - Industrial Crops and Products, 2018 - Elsevier
Vegetable oils are commonly used as components in many cosmetic products intended for
daily care due to their high beneficial and multifunctional effect on skin. The general …

Enhancement of dissolution rate and bioavailability of aceclofenac: a chitosan-based solvent change approach

S Mutalik, P Anju, K Manoj, AN Usha - International journal of …, 2008 - Elsevier
In this study the significant effect of chitosan on improving the dissolution rate and
bioavailability of aceclofenac has been demonstrated by simple solvent change method …

A brief literature and patent review of nanosuspensions to a final drug product

WWL Chin, J Parmentier, M Widzinski, EH Tan… - Journal of …, 2014 - Elsevier
Particle size reduction can be used for enhancing the dissolution of poorly water-soluble
drugs in order to enhance bioavailability. In nanosuspensions, the particle size of the drug is …