Enzymatic characterization of lipid-based drug delivery systems.

Abstract:

:The present work introduces a simple and robust in vitro method for enzymatic characterisation of surface properties of lipid dispersions in aqueous media. The initial lipolysis rate in biorelevant media, using pancreatic lipase and a self-microemulsifying formulation (SMEDDS) containing digestible lipids as substrate, was determined. The impact of incorporating two sparingly water soluble model drugs, probucol and halofantrine, into the SMEDDS was studied. It was found that both model drugs reduced the initial rate of lipolysis compared with the vehicle, probucol having a larger effect than halofantrine. The reduction of initial lipolysis rate indicates that probucol and halofantrine are bound in the water/emulsion interface limiting the substrate availability.

journal_name

Int J Pharm

authors

Ljusberg-Wahren H,Seier Nielsen F,Brogård M,Troedsson E,Müllertz A

doi

10.1016/j.ijpharm.2005.02.038

keywords:

subject

Has Abstract

pub_date

2005-07-25 00:00:00

pages

328-32

issue

2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(05)00241-3

journal_volume

298

pub_type

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