EVALUATION OF BIOACTIVITY OF JAGGERY PREPARED USING PLANT MUCILAGE AS CLARIFICANT
DOI:
https://doi.org/10.22159/ajpcr.2018.v11i11.22764Keywords:
Jaggery, Plant mucilage, Clarificants, Total phenols, Antihelmintic activityAbstract
Objective: The aim of the study was to prepare the jaggery using plant mucilage as clarificants and to evaluate the bioactivity of jaggery by determining total phenols, total flavonoids, reducing power, antibacterial activity, and antihelmintic activity.
Methods: Jaggery was prepared from sugarcane variety Co-80632 using five plant mucilage as clarificants, namely Aloe vera, flax seeds, fenugreek, purslane, and malabar spinach at three different concentrations, i.e., 0.1%, 0.2%, and 0.4% of raw sugarcane juice. The characteristic bioactivities such as total phenol content by Folin–Ciocalteu method, flavonoids content by spectrophotometer method, reducing power assay by measuring the absorbance at 700 nm, antibacterial activity by well-diffusion method, and antihelmintic activity by in vitro were determined.
Results: The highest total phenolic content was observed in jaggery prepared using plant mucilage clarificant of A. vera (JAV4 [3.68±0.02]) and Fenugreek seeds (JFG4 [3.61±0.02]) at 0.4% followed by them at 0.2% and 0.1% concentration, respectively. Similarly, a significant amount of total flavonoids content was elevated only in 0.4% plant mucilage clarificants of Aloe vera-treated experimental group jaggery (0.73±0.01) compared to control (0.61±0.02). Further, the antioxidant activity of jaggery was evaluated by reducing power. The increased absorbance at 700 nm indicated the presence of reducing power. At 10 mg/ml concentration, an absorbance unit of 1.93 and 1.80 was observed for jaggery prepared using 0.4% concentration of A. vera and fenugreek seed mucilage clarificants. Antihelmintic activity of jaggery showed dosage depended on the pattern where with the increase in the concentration of mucilage, the antihelmintic activity enhanced. A. vera mucilage showed maximum antihelmintic activity at 0.4% concentration with paralytic time (28.6 min) and death time (39.6 min).
Conclusion: Jaggery prepared using plants mucilaginous clarificants is the richest source of polyphenols such as phenolic acids and flavonoids, thereby contributed to the enhancement of bioactivity such as antioxidant, antibacterial, and antihelmintic activity. Thus, jaggery prepared using plant mucilage as clarificants is a novel nutraceutical product which can supplement the nutrients along with various medicinal properties through antioxidant, antibacterial, and antihelmintic activity.
Downloads
References
Roy SC. Monograph of the Gur Industry in India. Kanpur: India Institute of Sugar Technop; 1951. p. 55-64, 74-9.
Rao PV, Madhusweta D, Das SK. Jaggery a traditional Indians sweetener. Indian J Tradit Know 2007;6:95-102.
Jaffe RW. Health effects of non-centrifugal sugar (NCS): A review. Sugar Tech 2012;14:87-94.
Sahu AP, Saxena AK. Enhanced translocation of particles from lungs by jaggery. Environ Health Perspect 1994;102 Suppl 5:211-4.
Singh N, Kumar D, Raisuddin S, Sahu AP. Genotoxic effects of arsenic: Prevention by functional food-jaggery. Cancer Lett 2008;268:325-30.
Okabe, Toda TT, Inafuku M, Wada K, Iwasaki H, Oku H. Anti-atherosclerotic functions of Kokuto, Okinawan non centrifuged cane sugar. J Agr Food Chem 2009;57:69-75.
Nayaka H, Sathisha UV, Manohar MP, Chandrashekar KB, Dharmesh SM. Cytoprotective and antioxidant activity studies of jaggery sugar. Food Chem 2009;115:113-8.
El-Abasy M, Motobu M, Shimura K, Na KJ, Kang CB, Koge K, et al. Immunostimulating and growth-promoting effects of sugar cane extract (SCE) in chickens. J Vet Med Sci 2002;64:1061-3.
Molina V, Noa M, Arruzazabala L, Carbajal D, Más R. Effect of D-003, a mixture of very-long-chain aliphatic acids purified from sugarcane wax, on cerebral ischemia in Mongolian gerbils. J Med Food 2005;8:482-7.
Ledón N, Casacó A, RodrÃguez V, Cruz J, González R, Tolón Z, et al. Anti-inflammatory and analgesic effects of a mixture of fatty acids isolated and purified from sugar cane wax oil. Planta Med 2003;69:367 9.
MaurÃcio Duarte-Almeida J, Novoa AV, Linares AF, Lajolo FM, Inés Genovese M. Antioxidant activity of phenolics compounds from sugar cane (Saccharum officinarum L.) juice. Plant Foods Hum Nutr 2006;61:187-92.
Prasad P, Kumar PP, Satyavathi K, Prabhakar MC. Comparatives studies on anthelmintic activity of natural sweeteners. Res J Pharma Bio Chem Sci 2010;1:510-14.
Vinutha C, Sudarshan S, Pradeep S, Nayaka MA. Antioxidant activity of sugarcane jaggery with neem (Azadirachta indica) leaf extract. Int J Recent Sci Res 2014;1:99-101.
Nayaka MA, Vinuta C, Sudarshan S, Manohar MP. Physico-chemical, antioxidant and sensory attributes of ginger (Zingiber officinale) enriched jaggery of different sugarcane varieties. Sugar Tech 2015;17:305-13.
Repetto MG, Llesuy SF. Antioxidant properties of natural compounds used in popular medicine for gastric ulcers. Braz J Med Biol Res 2002;35:523-34.
Sachidanandam K, Fagan SC, Ergul A. Oxidative stress and cardiovascular disease: Antioxidants and unresolved issues. Cardiovasc Drug Rev 2005;23:115-32.
Halliwell B. Oxidative stress and cancer: Have we moved forward? Biochem J 2007;401:1-1.
Shah SV, Baliga R, Rajapurkar M, Fonseca VA. Oxidants in chronic kidney disease. J Am Soc Nephrol 2007;18:16-28.
Scalbert A, Johnson IT, Saltmarsh M. Polyphenols: Antioxidants and beyond. Am J Clin Nutr 2005;81:215S-217S.
Shankunthala VA. Proceeding of National Seminar on Jaggery Manufacture and Storage; 1985. P. 90-3.
Baboo B. Nutritive sweeteners from sugar crops: Development of jiggery. J Agr Eng 1991;1:252-63.
Mungare TS, Jadhav HD, Patil JP, Hasure IL, Jadhav BS, Jaswant S. Clarification technique for production of quality jaggery. Co op. Sugar 2000;32:283-5.
Ragavan T, Thirumurugan A, Sathiya K, Vadana SS. A case study: Studies on quality jaggery (gur) production with organic clarificants. Int J For Crop Improv 2011;2:207-10.
Kharwade RS, More SM, Mahajan UN. Formulation and evaluation of gastroretentive floating tablet using Hibiscus rosa-Sinensis mucilage. Asian J Pharm Clin Res 2017;10:444-8.
Chikkappaiah L, Nayaka HM, Manohar MP, Santhosh C, Properties of liquid jaggery prepared using plant mucilage as clarificant. Int J Recent Sci Res 2017;8:19590-5.
Shafi N, Khan L, Khan GA. Commercial extraction of gel from Aloe vera (L) leaves. J Chem Soc Pak 2000;22:47-9.
Inamdar M, Abhang P, Momin M. Isolation and evaluation of fenugreek, flaxseed mucilages and its use as a pharmaceutical binder. Int J Pharm Technol 2012;4:4766-77.
Chattoraj S, Bandyopadhyay AK. Development and evaluation of donut matrix tablets of bracofen using mucilaginous polymer from Portulaca oleracea Linn. Pharm Ind 2010;72:11.
Hameed AM, Hamied RS, Shnain ZY. Drag-reducing agent for aqueous liquid flowing in turbulent mode through pipelines. Al-Khwarizmi Eng J 2014;10:15-22.
Kulkarni GT, Gowthamarajan K, Brahmajirao G, Suresh B. Evaluation of binding properties of selected natural mucilages. J Sci Ind Res 2002;61:529-32.
Chang CM, Yang H, Chern JW. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal 2002;10:178-82.
Chikkappaiah L, Nayaka MA, Mahadevaiah H, Kumar GM. Preparation of plant mucilage clarificants and their effect on jaggery processing of sugarcane variety Co 86032. Int J Pharm Pharm Sci 2017;9:32-6.
McDonald S, Prenzler PD, Autolovich M, Robards K. Phenolic content and antioxidant activity of olive extracts. Food Chem 2001;73:73-84.
Yen GC, Chen HY. Antioxidant activity of various tea extracts in relation to their ant mutagenicity. J Agr Food Chem 1995;43:27-32.
National Committee for Clinical Laboratory Standards. Performance standards for Antimicrobial Susceptibility Testing, 9th Informational Supplement. Approved standard M100-S9. Wayne, Pa: National Committee for Clinical Laboratory Standards; 1999.
Aiyegoro OA, Okoh AI. Preliminary phytochemical screening and in vitro antioxidant activities of the aqueous extract of Helichrysum longifolium DC. BMC Complement Altern Med 2010;10:21.
Meir S, Kanner J, Akiri B, Hadas SP. Determination and involvement of aqueous reducing compounds in oxidative defense systems of various senescing leaves. J Agr Food Chem 1995;43:1813-7.
Harborne JB, Williams CA. Advances in flavonoid research since 1992. Phytochemistry 2000;55:481-504.
Payet B, Shum Cheong Sing A, Smadja J. Assessment of antioxidant activity of cane brown sugars by ABTS and DPPH radical scavenging assays: Determination of their polyphenolic and volatile constituents. J Agric Food Chem 2005;53:10074-9.
Takara K, Matsui D, Wada K, Ichiba T, Nakasone Y. New antioxidative phenolic glycosides isolated from Kokuto non-centrifuged cane sugar. Biosci Biotechnol Biochem 2002;66:29-35.
Dittrich R, El-Massry F, Kunz K, Rinaldi F, Peich CC, Beckmann MW, et al. Maillard reaction products inhibit oxidation of human low-density lipoproteins in vitro. J Agr Food Chem 2003;51:3900-4.
Paton NH, Duong M. Sugar-cane phenolics and 1st expressed juice color role of chlorogenic acid and flavonoids in enzymatic browning of cane juice. Int Sugar Journal 1992;94:170-6.
McGhie TK. Analysis of sugarcane flavonoids by capillary zone electrophoresis. J Chromatrography 1993;634:107-12.
Rice-Evans CA, Miller NJ, Paganga G. Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radic Biol Med 1996;20:933-56.
Noa M, Mendoza S, Más R, Mendoza N. Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on CL4C-induced liver acute injury in rats. Drugs Exp Clin Res 2002;28:177-83.
EFSA. Scientific opinion on the substantiation of health claims related to various food(s)/food constituents and protection of cells from premature aging, antioxidant activity, antioxidant content and antioxidative properties, and protection of DNA, proteins, and lipids from oxidative damage pursuant to Article 13(1) of Regulation (EC) No. 1924/2006. EFSA J 2010;8:1489.
Yoko N, Takara K, Wada K, Tanaka J, Yogi S, Nakatani NN. Antioxidative compounds isolated from Kokuto, non-centrifugal cane sugar. Biosci Biotechnol Biochem 1996;60:1714-6.
Sies H. Antioxidant in Disease, Mechanism and Therapy. New York: Academic Press; 1996.
Shan B, Cai YZ, Sun M, Corke H. Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. J Agric Food Chem 2005;53:7749-59.
Gibbs HC. Epidemiology, Diagnosis and Control of Gastrointestinal parasitism. Kenya: ILARD; 1986. p. 121.
Gasbarre CL, Stout LW, Leighton AE. Gastrointestinal nematodes of cattle in the North Eastern US: Results of a producer survey. Vet Parasitol 2001;101:29-44.
Saeed M, Iqbal Z, Jabbar A. Oxfendazole resistance in gastro-intestinal nematode of beetal goats at livestock farms of Punjab (Pakistan). Acta Veterinaria Brno 2007;76:79-85.
Bate-smith EC. The phenolic constituents of plants and their taxonomic significance I Dicotyledons. J Linn Soc (Bot) 1962;58:95-173.
Martin RJ. Mode of action of antihelmintic drugs. Vet J 1997;154:11 34.
Thomson DP, Geary TG. The structure and function of helminth surface. In: Marr JJ, editor. Biochemistry and Molecular Biology of Parasite. 1st ed. New York: Academic Press; 1995. p. 203-32.
Pessoa LM, Morais SM, Bevilaqua CM, Luciano JH. Anthelmintic activity of essential oil of Ocimum gratissimum Linn. And eugenol against Haemonchus contortus. Vet Parasitol 2002;109:59-63.
Lahlou M. Potential of Origanum compactum as a cercaricide in morocco. Ann Trop Med Parasitol 2002;96:587-93.
Published
How to Cite
Issue
Section
The publication is licensed under CC By and is open access. Copyright is with author and allowed to retain publishing rights without restrictions.