2011
DOI: 10.1016/j.carbpol.2010.10.055
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Formation of inclusion complexes of starch with fatty acid esters of bioactive compounds

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Cited by 122 publications
(26 citation statements)
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“…(12,141,142) However, in case of impossible or limited inclusion due to an unsuitable bioactive ligand structures, complex formation could be initiated by converting them to fatty acid esters. (143) Use of amylose through V-amylose has advantages of ready availability, relatively low cost, nontoxicity, biodegradability, and capacity for targeted delivery at particular GIT locations. (144) This targeted delivery allows for application of reduced active ingredient dosages because the included ligand is released only where its needed or absorbed.…”
Section: Encapsulation Of Flavor and Bioactive Substancesmentioning
confidence: 99%
“…(12,141,142) However, in case of impossible or limited inclusion due to an unsuitable bioactive ligand structures, complex formation could be initiated by converting them to fatty acid esters. (143) Use of amylose through V-amylose has advantages of ready availability, relatively low cost, nontoxicity, biodegradability, and capacity for targeted delivery at particular GIT locations. (144) This targeted delivery allows for application of reduced active ingredient dosages because the included ligand is released only where its needed or absorbed.…”
Section: Encapsulation Of Flavor and Bioactive Substancesmentioning
confidence: 99%
“…Starch‐inclusion complexes have been proposed to function as carriers for delivering and protecting bioactive molecules from degradation and for stabilizing volatile compounds . Inclusion complexes involving starch and various molecules such as lipids , flavors , and bioactive compounds have been investigated. The formation of inclusion complexes between amylose and fatty acids has been reported to be affected by many factors, such as amylose degree of polymerization (DP) , lipid structure and chain length , reaction temperature , reaction pH , and complexing solvent .…”
Section: Introductionmentioning
confidence: 99%
“…In general, the relative crystallinity can be affected by various factors such as crystal size, amount of crystalline regions, orientation of the double helices within the crystalline domains, extent of interaction between double helices (Miao, Jiang, & Zhang, 2009), and the ability of individual complexed helices to pack into a crystallite (Ma et al, 2011). The relative crystallinity in NC complexes increased in the order of NC (11.2%) <NC/M (19.4%) <NC/P (22.4%).…”
Section: X-ray Diffraction Pattern and Relative Crystallinitymentioning
confidence: 99%
“…Therefore, comparing the thermal transition parameters of ASWC/M and ASWC/P, it seems that the ability to disrupt the pre-existing crystalline organization of the complexes with palmitic acid is greater than that of the complexes with myristic acid. Generally, the relative crystallinity of starches could be affected by various factors such as crystal size, amount of crystalline regions, orientation of the double helices within the crystalline domains, extent of interaction between double helices (Miao et al, 2009), and the ability of individual complexed helices to pack into a crystallite (Ma et al, 2011). The factors listed above could also affect the thermal transition properties of starches, with regard to crystalline property.…”
Section: Thermal Transition Propertiesmentioning
confidence: 99%
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