Studies of active drug/excipient compatibility represent an important phase in the
preformulation stage of the development of all dosage forms. The potential physical and …

Pharmaceutical research, whether industrial or academic, has attempted to adopt
approaches most efficient for the development of innovations. With the abundance of …

Purpose The purpose of this paper is to discuss the pharmaceutical Quality by Design (QbD)
and describe how it can be used to ensure pharmaceutical quality. Materials and Methods …

Chitosan (Ch)-coated nanostructured lipid carriers (NLCs) have great potential for
transdermal delivery with high localization of chemotherapeutics in breast cancer. This study …

Practically all medications contain excipients, which are added for the purpose of production
enhancement, patient acceptability, improving stability, controlling release etc. Typically …

The purpose of this study was to explore the feasibility of combining fused deposition
modeling (FDM) 3D printing technology with hot melt extrusion (HME) to fabricate a novel …

Vaginal candidiasis is considered a frequent opportunistic mucosal infection and the second
most common cause of vaginitis after bacterial vaginosis. In this work, different vaginal films …

The aim of this study was to develop self emulsifying drug delivery systems (SEDDS) of
glipizide and to convert it into solid SEDDS (S-SEDDS) using Syloid® 244 FP as adsorbent …

Experiments were done to assess the compatibility of nateglinide (NTG) with selected
excipients in the development of immediate release tablets of NTG by thermal and …

Drug-excipient compatibility study is the essential basis for excipient selection at the pre-
formulation stage. According to the pharmaceutical Quality by Design (QbD) principles, a …