Generic placeholder image

Current Nutraceuticals

Editor-in-Chief

ISSN (Print): 2665-9786
ISSN (Online): 2665-9794

Research Article

Preliminary Study on Major Phenolic Groups, Antioxidant and Cytotoxic Capacity of Tuckeroo (Cupaniopsis Anacardioides) Fruit Extracts

Author(s): Ngoc M.Q. Pham*, Quan V. Vuong, Jennette A. Sakoff, Michael C. Bowyer and Christopher J. Scarlett*

Volume 2, Issue 4, 2021

Published on: 09 July, 2021

Article ID: e090721194661 Pages: 9

DOI: 10.2174/2665978602666210709110427

Abstract

Background: Tuckeroo (Cupaniopsis anacardioides) is one of eleven species that belongs to the Sapindaceae family, which is native to Australia.

Objective: This study screened major phenolic groups from fresh or dried whole fruits, or just their skin.

Methods: Using optimal ultrasound assisted extraction conditions with either acetone (50%) or methanol (50%) as extraction solvents. This study further tested their antioxidant capacity and cytotoxic activity against a panel of ten cancer cell lines for their potential health benefits.

Results: The results showed that levels of major phenolic groups were significantly different with solvents used or types of materials (whole fruit or skin). The extract from dried skin fruit using acetone 50 % (SD-A50) had the highest level of total phenolic content(112.47 mg GAE/g) and total flavonoid content (101.89 mg CAE/g); however, the extract from fresh skin (SF-A50) had the greatest proanthocyanidin content (124.22 mg CAE/g). This SF-A50 extract also showed the strongest antioxidant activity and had the highest growth inhibition and the lower dose response (GI50 values of 20-145 μg/mL) against the HT29 (colon); U87, SJ-G2 (glioblastoma); MCF-7 (Breast); A2780 (ovarian); H460 (lung); A431 (skin); Du145 (prostate); BE2-C (neuroblastoma); and MIA PaCa-2 (pancreas) cancer cell line, revealing its therapeutic potential.

Conclusion: Fourteen major compounds, including catechin were detected from the Tuckeroo fruit extract; future studies are recommended to further isolate, identify and test the health potentials from group and individual compounds of the Tuckeroo fruit extract.

Keywords: Tuckeroo, fruits, phytochemical, phenolics, extract, antioxidant, anti-cancer activities.

Graphical Abstract
[1]
Floyd, A.G. Rainforest trees of mainland south-eastern Australia., 1989, 420.
[2]
Pham, N.M.Q. Characterising the Physical, Phytochemical and Antioxidant Properties of the Tuckeroo (Cupaniopsis anacardioides) Fruit. Technologies (Basel), 2017, 5(3), 57.
[3]
Hidalgo, M. Pancreatic cancer. N. Engl. J. Med., 2010, 362(17), 1605-1617.
[4]
Neoptolemos, J.P. A randomized trial of chemoradiotherapy and chemotherapy after resection of pancreatic cancer. N. Engl. J. Med., 2004, 350(12), 1200-1210.
[5]
Duell, E. Pancreatitis and pancreatic cancer risk: A pooled analysis in the international pancreatic cancer case-control consortium (PanC4). Ann. Oncol., 2012, 23(11), 2964-2970.
[6]
Scarlett, C.J.; Vuong, Q.V. Plant bioactive compounds for prevention and treatment pancreatic cancer; , 2015, Vol. 1., .
[7]
Balick, M.J. Medicinal plants used by Latino healers for women’s health conditions in New York City. Econ. Bot., 2000, 54(3), 344-357.
[8]
Ballabh, B.; Chaurasia, O. Traditional medicinal plants of cold desert Ladakh-used in treatment of cold, cough and fever. J. Ethnopharmacol., 2007, 112(2), 341-349.
[9]
Bhuyan, D.J. Exploring the least studied Australian eucalypt genera: Corymbia and Angophora for phytochemicals with anticancer activity against pancreatic malignancies. Chem. Biodivers., 2017, 14(3), 1600291.
[10]
Cragg, G.M.; Newman, D.J. Plants as a source of anti-cancer agents. J. Ethnopharmacol., 2005, 100(1), 72-79.
[11]
Tabor, R. Wild about herbs. Read. Dig., 2002.
[12]
Balandrin, M.F. Natural plant chemicals: sources of industrial and medicinal materials. Science, 1985, 228(4704), 1154-1160.
[13]
Vuong, Q. Physicochemical composition, antioxidant and anti-proliferative capacity of a lilly pilly (Syzygium paniculatum) extract. J. Herb. Med., 2014, 4(3), 134-140.
[14]
Pham, N.M.Q. Optimization of ultrasound-assisted extraction conditions for phenolic compounds and antioxidant capacity from Tuckeroo (Cupaniopsis anacardioides) fruit. Sep. Sci. Technol., 2019, 1-10.
[15]
Škerget, M. Phenols, proanthocyanidins, flavones and flavonols in some plant materials and their antioxidant activities. Food Chem., 2005, 89(2), 191-198.
[16]
Arnao, M.B.; Cano, A.; Acosta, M. The hydrophilic and lipophilic contribution to total antioxidant activity. Food Chem., 2001, 73(2), 239-244.
[17]
Arnao, M.B.; Cano, A.; Acosta, M. Methods to measure the antioxidant activity in plant material. A comparative discussion. 1999.
[18]
Brand-Williams, W.; Cuvelier, M-E.; Berset, C. Use of a free radical method to evaluate antioxidant activity. Lebensm. Wiss. Technol., 1995, 28(1), 25-30.
[19]
Thaipong, K. Comparison of ABTS, DPPH, FRAP, and ORAC assays for estimating antioxidant activity from guava fruit extracts. J. Food Compos. Anal., 2006, 19(6-7), 669-675.
[20]
Benzie, I.F.; Strain, J.J. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal. Biochem., 1996, 239(1), 70-76.
[21]
Apak, R. Novel total antioxidant capacity index for dietary polyphenols and vitamins C and E, using their cupric ion reducing capability in the presence of neocuproine: CUPRAC method. J. Agric. Food Chem., 2004, 52(26), 7970-7981.
[22]
Vuong, Q.V. Physicochemical, antioxidant and anti-cancer activity of a Eucalyptus robusta (Sm.) leaf aqueous extract. Ind. Crops Prod., 2015, 64, 167-174.
[23]
Bhuyan, D.J. In vitro anticancer properties of selected Eucalyptus species. In Vitro Cell. Dev. Biol. Anim., 2017, 53(7), 604-615.

© 2024 Bentham Science Publishers | Privacy Policy