A new standardized lipolysis approach for characterization of emulsions and dispersions

被引:21
作者
Brogard, M.
Troedsson, E.
Thuresson, K.
Ljusberg-Wahren, H.
机构
[1] Camurus AB, SE-22370 Lund, Sweden
[2] Lund Univ, Div Food Technol, SE-22100 Lund, Sweden
[3] Lund Univ, Ctr Chem & Chem Engn, SE-22100 Lund, Sweden
关键词
structured lipids; lamellar; lipid-based drug delivery; lipid digestion; lipolysis; self-emulsifying drug delivery systems (SEDDS); triglyceride; dispersion; emulsion;
D O I
10.1016/j.jcis.2006.12.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new standardized lipolysis approach is presented where the focus is on the initial rate of lipolysis. An advantage is that data obtained in this way reflect degradation before growing amounts of lipolysis products retard the process. The method can be used to rank different lipase substrates. In particular, the method can be used to obtain information about the susceptibility to degradation of various emulsions and dispersions that are used in technical applications. We present how the method is standardized to facilitate comparison of various substrates. This involves (i) lipase substrate in excess, i.e., the amount of lipase is rate limiting, and (ii) expressing rate of degradation relative to that of a reference substrate, tributyrin. Under such conditions, with the amount of lipase substrate held constant, an increase in enzymatic activity will generate a proportional increase in the lipolysis rate. This enables comparison of results obtained from different enzyme batches and corrects for day-to-day variability. Examples illustrating the potential of the method to discriminate and rank different lipase substrates with regard to enzymatic degradation are presented. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:500 / 507
页数:8
相关论文
共 32 条
[1]   Self-assembled lipid superstructures: Beyond vesicles and liposomes [J].
Barauskas, J ;
Johnsson, M ;
Tiberg, F .
NANO LETTERS, 2005, 5 (08) :1615-1619
[2]  
Beisson F, 2000, EUR J LIPID SCI TECH, V102, P133, DOI 10.1002/(SICI)1438-9312(200002)102:2<133::AID-EJLT133>3.3.CO
[3]  
2-O
[4]   Effect of lipase on monoolein-based cubic phase dispersion (cubosomes) and vesicles [J].
Borné, J ;
Nylander, T ;
Khan, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (40) :10492-10500
[5]   LIPID MICROEMULSIONS FOR IMPROVING DRUG DISSOLUTION AND ORAL ABSORPTION - PHYSICAL AND BIOPHARMACEUTICAL ASPECTS [J].
CONSTANTINIDES, PP .
PHARMACEUTICAL RESEARCH, 1995, 12 (11) :1561-1572
[6]   In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs [J].
Dressman, JB ;
Reppas, C .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 11 :S73-S80
[7]   Surfactant self-assembly objects as novel drug delivery vehicles [J].
Drummond, CJ ;
Fong, C .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 1999, 4 (06) :449-456
[8]  
GARGOURI Y, 1983, J LIPID RES, V24, P1336
[9]   Techniques to measure lipase and esterase activity in vitro [J].
Gilham, D ;
Lehner, R .
METHODS, 2005, 36 (02) :139-147
[10]   PHYSICAL-CHEMICAL BEHAVIOR OF DIETARY AND BILIARY LIPIDS DURING INTESTINAL DIGESTION AND ABSORPTION .2. PHASE-ANALYSIS AND AGGREGATION STATES OF LUMINAL LIPIDS DURING DUODENAL FAT DIGESTION IN HEALTHY ADULT HUMAN-BEINGS [J].
HERNELL, O ;
STAGGERS, JE ;
CAREY, MC .
BIOCHEMISTRY, 1990, 29 (08) :2041-2056