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 …

Estimation of drug–excipient interactions is a crucial step in preformulation studies of drug
development to achieve consistent stability, bioavailability and manufacturability of solid …

Lubrication plays a key role in successful manufacturing of pharmaceutical solid dosage
forms; lubricants are essential ingredients in robust formulations to achieve this. Although …

In this paper we review cucurbit [n] urils (CB [n]), a relatively new family of macrocycles that
has shown potential in improving drug delivery. Encapsulation of drugs within the …

Gellan gum/pectin beads were prepared by ionotropic gelation, using Al 3+ as crosslinker.
High yield (92.76%) and entrapment efficiency (52.22–88.78%) were reached. Beads …

The choice of excipients constitutes a major part of preformulation and formulation studies
during the preparation of pharmaceutical dosage forms. The physical, mechanical, and …

In order to investigate the effects of solid carriers on the crystalline properties, dissolution
and bioavailability of flurbiprofen in a solid self-nanoemulsifying drug delivery system (solid …

The present work reports the study of different ketoprofen: excipient formulations, in order to
determine the effect of the polymer substitution and type of diluent on the drug-release …

In order to compare the effects of hydrophilic and hydrophobic solid carrier on the formation
of solid self-microemulsifying drug delivery system (SMEDDS), two solid SMEDDS …

For the development of extended release formulations of glipizide, techniques of thermal
and isothermal stress testing (IST) were used to assess the compatibility of glipizide with …