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Labrasol

National Institutes of Health

Papers overview

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2015
2015
Nanoemulsions have been developed for the oral delivery of poorly bioavailable phenolic compounds that are sensitive to… Expand
Highly Cited
2009
Highly Cited
2009
The main objective of this study was to prepare a solid form of lipid-based self-emulsifying drug delivery system (SEDDS) by… Expand
Highly Cited
2007
Highly Cited
2007
Labrasol is a lipid-based self-emulsifying excipient used in the preparation of lipophilic drugs intended for oral delivery. It… Expand
Highly Cited
2005
Highly Cited
2005
The aim of this study was to investigate the effect of two novel self-microemulsifying drug delivery systems (SMEDDS) containing… Expand
Review
2004
Review
2004
A review of commercially available oral and injectable solution formulations reveals that the solubilizing excipients include… Expand
Highly Cited
2004
Highly Cited
2004
The efflux transporter, P-glycoprotein (P-gp), located in the apical membranes of intestinal absorptive cells, can reduce the… Expand
Highly Cited
2003
Highly Cited
2003
Piroxicam is a non-steroidal anti-inflammatory drug that is characterized by low solubility and high permeability. The purpose of… Expand
Highly Cited
2001
Highly Cited
2001
The goals of our investigations are to develop and characterize self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10… Expand
Highly Cited
2001
Highly Cited
2001
A transdermal preparation containing ketoprofen was developed using O/W microemulsion system. Of the oils tested, oleic acid was… Expand
Highly Cited
2000
Highly Cited
2000
The purpose of this study was to investigate the influence of structure and composition of microemulsions (Labrasol/Plurol… Expand