Effect of microencapsulation of dietary oil on postprandial lipemia

被引:3
作者
Tuomasjukka, S [1 ]
Kallio, H
Forssell, P
机构
[1] Univ Turku, Dept Biochem & Food Chem, FI-20014 Turku, Finland
[2] VTT Biotechnol, FI-02044 Espoo, Finland
关键词
blackcurrant seed oil; microencapsulation; postprandial lipemia; sea buckthorn oil;
D O I
10.1111/j.1365-2621.2006.tb15645.x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Microencapsulation is increasingly applied to dietary oils, but only limited information is available about the effect on bioavailability. The aim of the present study was to evaluate the bioavailability of microencapsulated vegetable oil from a liquid food product in a clinical trial. Another aim was to compare the suitability of sodium octenyl succinate starch (SOSS) and oat starch aggregate (OSA) in sustained release of a vegetable oil. Twenty-four healthy young men were recruited and randomly allocated into 1 of 3 groups (A, B, C). All subjects consumed 2 liquid test meals, which differed only with respect to microencapsulation. Groups A and B consumed berry juice or fermented oat drink, respectively, containing either non-encapsulated or SOSS-encapsulated blackcurrant seed oil (BCO). Group C received sea buckthorn oil (SBO) encapsulated with SOSS or OSA. Blood samples were collected at 0, 30,60,90,180,270, and 360 min after the meal, and chylomicron-rich (CM-rich) fraction was separated for subsequent triacylglycerol (TAG) analysis. Microencapsulation increased the glycemic response. SOSS-encapsulated BCO resulted in a similar CM-rich TAG response as non-encapsulated BCO, indicating that the SOSS-encapsulated oil was fully bioavailable. OSA-encapsulation had a similar bioavailability. The lipemic response of subjects who consumed the oil mixed in the fermented oat drink was higher than that of other subjects. This most likely resulted from the slightly higher fat and energy content of the fermented oat drink compared with berry juice. Contrary to expectations, the use of OSA in microencapsulation did not result in sustained release.
引用
收藏
页码:S225 / S230
页数:6
相关论文
共 30 条
  • [1] Postprandial lipemic response is modified by the polymorphism at codon 54 of the fatty acid-binding protein 2 gene
    Ågren, JJ
    Valve, R
    Vidgren, H
    Laakso, M
    Uusitupa, M
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (10) : 1606 - 1610
  • [2] BAKAN JA, 1973, FOOD TECHNOL-CHICAGO, V27, P34
  • [3] EFFECTS OF OAT BRAN, RICE BRAN, WHEAT FIBER, AND WHEAT-GERM ON POSTPRANDIAL LIPEMIA IN HEALTHY-ADULTS
    CARA, L
    DUBOIS, C
    BOREL, P
    ARMAND, M
    SENFT, M
    PORTUGAL, H
    PAULI, AM
    BERNARD, PM
    LAIRON, D
    [J]. AMERICAN JOURNAL OF CLINICAL NUTRITION, 1992, 55 (01) : 81 - 88
  • [4] LIPID DIGESTION AND ABSORPTION
    CAREY, MC
    SMALL, DM
    BLISS, CM
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1983, 45 : 651 - 677
  • [5] REASSESSING THE EFFECTS OF SIMPLE CARBOHYDRATES ON THE SERUM TRIGLYCERIDE RESPONSES TO FAT MEALS
    COHEN, JC
    SCHALL, R
    [J]. AMERICAN JOURNAL OF CLINICAL NUTRITION, 1988, 48 (04) : 1031 - 1034
  • [6] COHEN JC, 1990, J LIPID RES, V31, P597
  • [7] Connor WE, 2000, AM J CLIN NUTR, V71, p171S, DOI 10.1093/ajcn/71.1.171S
  • [8] A formula to estimate the approximate surface area if height and weight be known
    Du Bois, D
    Du Bois, EF
    [J]. ARCHIVES OF INTERNAL MEDICINE, 1916, 17 (06) : 863 - 871
  • [9] Soluble non-starch polysaccharides derived from complex food matrices do not increase average lipid droplet size during gastric lipid emulsification in rats
    FilleryTravis, AJ
    Gee, JM
    Waldron, KW
    Robins, MM
    Johnson, IT
    [J]. JOURNAL OF NUTRITION, 1997, 127 (11) : 2246 - 2252
  • [10] Plant- and marine-derived n-3 polyunsaturated fatty acids have differential effects on fasting and postprandial blood lipid concentrations and on the susceptibility of LDL to oxidative modification in moderately hyperlipidemic subjects
    Finnegan, YE
    Minihane, AM
    Leigh-Firbank, EC
    Kew, K
    Meijer, GW
    Muggli, R
    Calder, PC
    Williams, CM
    [J]. AMERICAN JOURNAL OF CLINICAL NUTRITION, 2003, 77 (04) : 783 - 795