Polysaccharide with antioxidant, α-amylase inhibitory and ACE inhibitory activities from Momordica charantia
International Journal of Biological Macromolecules, ISSN: 0141-8130, Vol: 85, Page: 487-496
2016
- 105Citations
- 114Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations105
- Citation Indexes105
- 105
- CrossRef74
- Captures114
- Readers114
- 114
Article Description
Functional polysaccharide was isolated from Momordica charantia, with a yield of 36% (w/w). M. charantia bioactive polysaccharide (MCBP) was an acidic and branched heteropolysaccharide with a molecular weight of 92 kDa. Fourier transform infrared spectroscopic analysis indicated that MCBP was a pectin-like polysaccharide with an esterification degree of 53% and it contains numerous monosaccharides, predominantly glucose, galactose, and galaturonic acid. The results also showed that MCBP exhibited free radical scavenging activity (31.9%), ferric reducing antioxidant power (0.95 mM), α-amylase inhibition (89.1%), and angiotensin-converting enzyme inhibition (94.1%). In the terms of functionality, MCBP showed a lower water-holding capacity but higher in oil-holding capacity, emulsifying activity and foaming capacity compared to citrus pectin. Scanning electron microscopy images demonstrated that MCBP formed gels with a porous structure, and flow analysis showed that the gel solution exhibited pseudoplastic shear-thinning behavior. These findings indicated that MCBP is a promising functional macromolecular carbohydrate for the food and nutraceutical industries.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0141813016300241; http://dx.doi.org/10.1016/j.ijbiomac.2016.01.023; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84954304581&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/26778156; https://linkinghub.elsevier.com/retrieve/pii/S0141813016300241; https://dx.doi.org/10.1016/j.ijbiomac.2016.01.023
Elsevier BV
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