TY - JOUR
T1 - Preparation and characterization of crystalline complexes between amylose and C18 fatty acids
AU - Seo, Tae Rang
AU - Kim, Jong Yea
AU - Lim, Seung Taik
N1 - Funding Information:
This work was suprted by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (No. 2014R1A2A2A01007996 ).
Publisher Copyright:
© 2015 Elsevier Ltd. All rights reserved.
PY - 2015
Y1 - 2015
N2 - Inclusion complexes were prepared by using high amylose maize starch and C18 fatty acids including stearic, oleic, linoleic, and α-linolenic acids, under reaction conditions varied in temperature (50, 70, and 90 °C), pH (5, 6, 7, and 8), and reaction time (3, 6, 24, and 48 h). Among the four C18 fatty acids tested, stearic acid was most effective and linoleic acid was least effective in the complex formation. The reaction at 90 °C for 24 h provided the maximum recovery (about 75%) in the complex formation using stearic and oleic acids. Linolenic acid, however, could reach its maximum recovery (>70%) when reacted for a shorter period (6 h, 90 °C). Under DSC analyses, the polymorphs formed by linolenic acid appeared more uniform compared to those by other FAs. All the complexes exhibited V type crystalline structures under X-ray diffraction analyses, consisting of type I and type II polymorphs in DSC thermograms when recovered from the reaction mixtures.
AB - Inclusion complexes were prepared by using high amylose maize starch and C18 fatty acids including stearic, oleic, linoleic, and α-linolenic acids, under reaction conditions varied in temperature (50, 70, and 90 °C), pH (5, 6, 7, and 8), and reaction time (3, 6, 24, and 48 h). Among the four C18 fatty acids tested, stearic acid was most effective and linoleic acid was least effective in the complex formation. The reaction at 90 °C for 24 h provided the maximum recovery (about 75%) in the complex formation using stearic and oleic acids. Linolenic acid, however, could reach its maximum recovery (>70%) when reacted for a shorter period (6 h, 90 °C). Under DSC analyses, the polymorphs formed by linolenic acid appeared more uniform compared to those by other FAs. All the complexes exhibited V type crystalline structures under X-ray diffraction analyses, consisting of type I and type II polymorphs in DSC thermograms when recovered from the reaction mixtures.
KW - Amylose
KW - Fatty acids
KW - Linolenic acid
KW - V-amylose complex
UR - http://www.scopus.com/inward/record.url?scp=84944907012&partnerID=8YFLogxK
U2 - 10.1016/j.lwt.2015.06.021
DO - 10.1016/j.lwt.2015.06.021
M3 - Article
AN - SCOPUS:84944907012
SN - 0023-6438
VL - 64
SP - 889
EP - 897
JO - LWT - Food Science and Technology
JF - LWT - Food Science and Technology
IS - 2
ER -