Silicon Dioxide

The use of physiologically based biopharmaceutics modeling (PBBM) and bioequivalence safe space is increasingly common for immediate-release drug products. However,...

This exploratory study investigated the minimum required Raman mapping area for predicting sustained-release tablet dissolution profiles based on intra-tablet homogeneity....

Abstract Risk control for nitrosamine impurities in drug products is currently a major challenge in the industry. Nitrosamines can form...

Unveiling Neusilin US2´s Prowess Neusilin® US2 by Fuji Chemical Industries is a synthetic, amorphous form of Magnesium Aluminometasilicate with a...

Hydrochlorothiazide (HTZ) and Valsartan (VAL) are poorly soluble drugs in BCS classes IV and II. This study aimed to develop...

Abstract We designed a bioequivalent tablet form of solifenacin succinate (SOL) with an improved storage stability using a direct compression...

1. Introduction The introduction of continuous manufacturing of tablets has been gaining momentum, because it offers reductions in development and...

The aim of the present study was to design and optimize the oral tablet formulation of Merremia tridentata extract (MSE) with...

This study describes the first implementation of Raman spectrometer in a stream sampler for the in-line monitoring of low drug...

The purpose of this study is to derive an optimal drug release formulation with human clinical bioequivalence in developing a...