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Nanoemulsions have been developed for the oral delivery of poorly bioavailable phenolic compounds that are sensitive to… Expand The main objective of this study was to prepare a solid form of lipid-based self-emulsifying drug delivery system (SEDDS) by… Expand Labrasol is a lipid-based self-emulsifying excipient used in the preparation of lipophilic drugs intended for oral delivery. It… Expand The aim of this study was to investigate the effect of two novel self-microemulsifying drug delivery systems (SMEDDS) containing… Expand A review of commercially available oral and injectable solution formulations reveals that the solubilizing excipients include… Expand The efflux transporter, P-glycoprotein (P-gp), located in the apical membranes of intestinal absorptive cells, can reduce the… Expand Piroxicam is a non-steroidal anti-inflammatory drug that is characterized by low solubility and high permeability. The purpose of… Expand The goals of our investigations are to develop and characterize self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10… Expand A transdermal preparation containing ketoprofen was developed using O/W microemulsion system. Of the oils tested, oleic acid was… Expand The purpose of this study was to investigate the influence of structure and composition of microemulsions (Labrasol/Plurol… Expand