2014
DOI: 10.1016/j.jff.2014.03.032
|View full text |Cite
|
Sign up to set email alerts
|

Beta-glucan complexes with selected nutraceuticals: Synthesis, characterization, and stability

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

4
13
0
1

Year Published

2017
2017
2024
2024

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 48 publications
(19 citation statements)
references
References 33 publications
4
13
0
1
Order By: Relevance
“…All the samples showed a broad diffraction peak at an angle around 20° (2θ) except for HFO‐114 cv. Veverka et al () described a diffractogram pattern in commercial oat β‐glucan (93% purity) sample similar to that observed in our study. These workers also observed broad peaks for β‐glucans which is typically of noncrystalline structure.…”
Section: Resultssupporting
confidence: 89%
“…All the samples showed a broad diffraction peak at an angle around 20° (2θ) except for HFO‐114 cv. Veverka et al () described a diffractogram pattern in commercial oat β‐glucan (93% purity) sample similar to that observed in our study. These workers also observed broad peaks for β‐glucans which is typically of noncrystalline structure.…”
Section: Resultssupporting
confidence: 89%
“…Generally, these small changes imply that no substantial hydrogen‐bonding interaction exists between polysaccharide and CLA, suggesting that a “hydrophobic” binding mechanism is the most probable. It has been reported that for BG matrices that material retention is primarily a surface phenomenon due to hydrophobic interaction . The FTIR spectra of the physical mixtures did not differ from those obtained from the individual components.…”
Section: Resultsmentioning
confidence: 73%
“…Thus, only a fraction of CLA is located inside the helical inclusion complex and the rest is adsorbed outside, covering the polysaccharide matrix surface; however, the system maintains its improved oxidative stability. On the basis of our previous work on polysaccharide complexes with structurally diverse nutraceuticals we suggest that the key interactions responsible for the CLA complexation are non‐covalent bond formation and hydrophobic interactions. The complexes exhibit up to 3–5 times higher oxidation stability compared to free CLA.…”
Section: Discussionmentioning
confidence: 89%
“…5, X-ray diffraction analysis of samples of LAS-N and LAS-C indicated diffraction patterns with broad peaks, which are common to β-glucans due to their polymeric structure (Veverka et al, 2014). Broad peaks indicate structures that are different from conventional crystalline structures (Kagimura et al, 2015a).…”
Section: Discussionmentioning
confidence: 97%