The cosolvency models frequently used in solubility data modeling of drugs in mixed
solvents were reviewed and their accuracies for calculating the solubility of solutes were …

Background Use of skin personal care products on a regular basis is nearly ubiquitous, but
their effects on molecular and microbial diversity of the skin are unknown. We evaluated the …

Drug development is a time‐consuming and costly process. It is usually divided into four
phases, although it is not always possible to draw a sharp line between the various stages …

Micellar solubilization is a great method for increasing drugs solubility in aqueous
environments. At concentrations above the critical micelle concentration (CMC), micelles are …

The development of accurate models to predict the solvation, solubility, and partitioning of
nonpolar and amphiphilic compounds in aqueous environments remains an important …

The aim of this study is to develop general models based on Abraham solvation parameters
and Hansen solubility parameters for the prediction of paracetamol solubility in cosolvency …

The solubility of sulfapyridine (SP) in propylene glycol+ water mixtures was determined at
temperatures from 293.15 K to 313.15 K. The solubility was maximal in pure propylene …

Computational modeling is of great importance in solvent selection for new active
pharmaceutical ingredients (APIs), with the Perturbed-Chain Statistical Associating Fluid …

This work reports the aqueous solubility of acetaminophen (ACP), a most traditionally used
analgesics and antipyretic drug, in betaine/propylene glycol deep eutectic solvent (Bet/PG …

Solubility of drugs in binary and ternary solvent mixtures composed of water and
pharmaceutical cosolvents at different temperatures were predicted using the Jouyban …