Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase

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Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase. / Zaharudin, Nazikussabah Binti; Asunción Salmeán, Armando; Dragsted, Lars Ove.

In: Food Chemistry, Vol. 245, 15.04.2018, p. 1196-1203.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Zaharudin, NB, Asunción Salmeán, A & Dragsted, LO 2018, 'Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase', Food Chemistry, vol. 245, pp. 1196-1203. https://doi.org/10.1016/j.foodchem.2017.11.027

APA

Zaharudin, N. B., Asunción Salmeán, A., & Dragsted, L. O. (2018). Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase. Food Chemistry, 245, 1196-1203. https://doi.org/10.1016/j.foodchem.2017.11.027

Vancouver

Zaharudin NB, Asunción Salmeán A, Dragsted LO. Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase. Food Chemistry. 2018 Apr 15;245:1196-1203. https://doi.org/10.1016/j.foodchem.2017.11.027

Author

Zaharudin, Nazikussabah Binti ; Asunción Salmeán, Armando ; Dragsted, Lars Ove. / Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase. In: Food Chemistry. 2018 ; Vol. 245. pp. 1196-1203.

Bibtex

@article{7f712ea647284a01b442c2b422621f89,
title = "Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase",
abstract = "Edible seaweeds are valuable because of their organoleptic properties and complex polysaccharide content. A study was conducted to investigate the potential of dried edible seaweed extracts, its potential phenolic compoundsand alginates for α-amylase inhibitory effects. The kinetics of inhibition was assessed in comparison with acarbose. The methanol extract of Laminaria digitata and the acetone extract of Undaria pinnatifida showed inhibitory activity against α-amylase, IC50 0.74 ± 0.02 mg/ml and 0.81 ± 0.03 mg/ml, respectively; both showed mixed-type inhibition. Phenolic compound, 2,5-dihydroxybenzoic acid was found to be a potent inhibitor of α-amylase with an IC50 value of 0.046 ± 0.004 mg/ml. Alginates found in brown seaweeds appeared to be potent inhibitors of α-amylase activity with an IC50 of (0.075 ± 0.010–0.103 ± 0.017) mg/ml, also a mixed-type inhibition. Overall, the findings provide information that crude extracts of brown edible seaweeds, phenolic compounds and alginates are potent α-amylase inhibitors, thereby potentially retarding glucose liberation from starches and alleviation of postprandial hyperglycaemia.",
keywords = "Faculty of Science, Seaweed, Glucose liberation, α-Amylase, Phenolic compound, Alginate, Inhibitor, Hyperglycaemia",
author = "Zaharudin, {Nazikussabah Binti} and {Asunci{\'o}n Salme{\'a}n}, Armando and Dragsted, {Lars Ove}",
note = "CURIS 2018 NEXS 006",
year = "2018",
month = apr,
day = "15",
doi = "10.1016/j.foodchem.2017.11.027",
language = "English",
volume = "245",
pages = "1196--1203",
journal = "Food Chemistry",
issn = "0308-8146",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Inhibitory effects of edible seaweeds, polyphenolics and alginates on the activities of porcine pancreatic α-amylase

AU - Zaharudin, Nazikussabah Binti

AU - Asunción Salmeán, Armando

AU - Dragsted, Lars Ove

N1 - CURIS 2018 NEXS 006

PY - 2018/4/15

Y1 - 2018/4/15

N2 - Edible seaweeds are valuable because of their organoleptic properties and complex polysaccharide content. A study was conducted to investigate the potential of dried edible seaweed extracts, its potential phenolic compoundsand alginates for α-amylase inhibitory effects. The kinetics of inhibition was assessed in comparison with acarbose. The methanol extract of Laminaria digitata and the acetone extract of Undaria pinnatifida showed inhibitory activity against α-amylase, IC50 0.74 ± 0.02 mg/ml and 0.81 ± 0.03 mg/ml, respectively; both showed mixed-type inhibition. Phenolic compound, 2,5-dihydroxybenzoic acid was found to be a potent inhibitor of α-amylase with an IC50 value of 0.046 ± 0.004 mg/ml. Alginates found in brown seaweeds appeared to be potent inhibitors of α-amylase activity with an IC50 of (0.075 ± 0.010–0.103 ± 0.017) mg/ml, also a mixed-type inhibition. Overall, the findings provide information that crude extracts of brown edible seaweeds, phenolic compounds and alginates are potent α-amylase inhibitors, thereby potentially retarding glucose liberation from starches and alleviation of postprandial hyperglycaemia.

AB - Edible seaweeds are valuable because of their organoleptic properties and complex polysaccharide content. A study was conducted to investigate the potential of dried edible seaweed extracts, its potential phenolic compoundsand alginates for α-amylase inhibitory effects. The kinetics of inhibition was assessed in comparison with acarbose. The methanol extract of Laminaria digitata and the acetone extract of Undaria pinnatifida showed inhibitory activity against α-amylase, IC50 0.74 ± 0.02 mg/ml and 0.81 ± 0.03 mg/ml, respectively; both showed mixed-type inhibition. Phenolic compound, 2,5-dihydroxybenzoic acid was found to be a potent inhibitor of α-amylase with an IC50 value of 0.046 ± 0.004 mg/ml. Alginates found in brown seaweeds appeared to be potent inhibitors of α-amylase activity with an IC50 of (0.075 ± 0.010–0.103 ± 0.017) mg/ml, also a mixed-type inhibition. Overall, the findings provide information that crude extracts of brown edible seaweeds, phenolic compounds and alginates are potent α-amylase inhibitors, thereby potentially retarding glucose liberation from starches and alleviation of postprandial hyperglycaemia.

KW - Faculty of Science

KW - Seaweed

KW - Glucose liberation

KW - α-Amylase

KW - Phenolic compound

KW - Alginate

KW - Inhibitor

KW - Hyperglycaemia

U2 - 10.1016/j.foodchem.2017.11.027

DO - 10.1016/j.foodchem.2017.11.027

M3 - Journal article

C2 - 29287342

VL - 245

SP - 1196

EP - 1203

JO - Food Chemistry

JF - Food Chemistry

SN - 0308-8146

ER -

ID: 186906090