Comparative study on digestive lipase activities on the self emulsifying excipient Labrasol®, medium chain glycerides and PEG esters

被引:100
作者
Fernandez, Sylvie
Jannin, Vincent
Rodier, Jean-David
Ritter, Nicolas
Mahler, Bruno
Carriere, Frederic
机构
[1] CNRS, Lab Enzymol Interfaciale & Physiol Lipolyse, UPR 9025, F-13402 Marseille 20, France
[2] Gattefosse SAS, F-69804 St Priest, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2007年 / 1771卷 / 05期
关键词
digestive enzyme; lipase; lipid excipient; lipolysis; oral drug delivery;
D O I
10.1016/j.bbalip.2007.02.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Labrasol (R) is a lipid-based self-emulsifying excipient used in the preparation of lipophilic drugs intended for oral delivery. It is mainly composed of PEG esters and glycerides with medium acyl chains, which are potential substrates for digestive lipases. The hydrolysis of Labrasol (R) by porcine pancreatic extracts, human pancreatic juice and several purified digestive lipases was investigated in the present study. Classical human pancreatic lipase (HPL) and porcine pancreatic lipase, which are the main lipases involved in the digestion of dietary triglycerides, showed very low levels of activity on the entire Labrasol (R) excipient as well as on separated fractions of glycerides and PEG esters. On the other hand, gastric lipase, pancreatic lipase-related protein 2 (PLRP2) and carboxyl ester hydrolase (CEH) showed high specific activities on Labrasol (R)). These lipases were found to hydrolyze the main components of Labrasol (R) (PEG esters and monoglycerides) used as individual substrates, whereas these esters were found to be poor substrates for HPL. The lipolytic activity of pancreatic extracts and human pancreatic juice on Labrasol (R) is therefore mainly due to the combined action of CEH and PLRP2. These two pancreatic enzymes, together with gastric lipase, are probably the main enzymes involved in the in vivo lipolysis of Labrasol (R) taken orally. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:633 / 640
页数:8
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