Refine your search
Collections
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Srinivasan, Krishnapura
- Weight Reducing Potential of Dietary Tender Cluster Beans (Cyamopsis tetragonoloba) in High-Fat Fed Rats
Abstract Views :210 |
PDF Views:0
Authors
Affiliations
1 Department of Biochemistry and Nutrition, Central Food Technological Research Institute, Mysore – 570 020, IN
1 Department of Biochemistry and Nutrition, Central Food Technological Research Institute, Mysore – 570 020, IN
Source
The Indian Journal of Nutrition and Dietetics, Vol 51, No 3 (2014), Pagination: 236-251Abstract
Soluble dietary fibre-rich tender cluster beans (Cyamopsis tetragonoloba) were explored for its potential in weight management in rats maintained on high-fat diet (HFD). The impact of three dietary levels of cluster beans was examined in terms of body weight gain, absorption and elimination of dietary fat, accumulation of fat in adipose and influence on lipogenic and lipolytic enzymes. The results indicated the potential of dietary cluster beans as useful in weight management by lowering fat absorption, enhanced lipolysis through increased activity of hormone sensitive lipase causing decreased adipose weight and increased mobilization of accumulated fat. All these contributed to a reduction in weight gain in animals maintained on HFD by inclusion of tender cluster beans in the diet. A dietary dose of 15 per cent cluster bean powder produced the maximum effect with respect to body weight management, and further increase in the dietary dose did not bring any significantly higher benefit.Keywords
Adipose Fat, Fat Absorption, High-Fat Fed Rats, Lipogenic Enzymes, Tender Cluster Beans, Weight Management.- Bioaccessibility of Polyphenols from Onion (Allium cepa) as Influenced by Domestic Heat Processing and Food Acidulants
Abstract Views :274 |
PDF Views:2
Authors
Affiliations
1 Department of Biochemistry and Nutrition, CSIR – Central Food Technological Research Institute, Mysore – 570 020, IN
1 Department of Biochemistry and Nutrition, CSIR – Central Food Technological Research Institute, Mysore – 570 020, IN
Source
The Indian Journal of Nutrition and Dietetics, Vol 53, No 4 (2016), Pagination: 391-404Abstract
Polyphenols are gaining importance in view of their health beneficial influences. Onion (Allium cepa) was analyzed for total polyphenol and flavonoid contents and their bioaccessibility as influenced by heat processing and food acidulants. Total polyphenols in raw onion (2.17 mg/g) were increased by 50% upon roasting. Total flavonoids in onion (0.27 mg/g) remained unchanged in heat processing. Bio accessible polyphenols and flavonoids from onion were 0.96 and 0.02 mg/g respectively and open-pan boiling increased the bio accessible polyphenols from onion. Addition of food acidulants to onion altered the composition and concentration of phenolic compounds. Total bio accessible polyphenols of onion decreased by 15% in presence of lime juice, while the same increased from microwave heated onions by 21% in presence of amchur. Presence of lime juice decreased bio accessible polyphenols in native and pressure-cooked onion, while the same increased by 37% in roasted onion in presence of amchur. Bioaccessibility of quercetin from onion increased 6-fold in presence of amchur, while a few polyphenols viz., protocatechuic acid, syringic acid, rutin and myricetin became bio accessible in presence of these food acidulants. Amchur enhanced the bio accessible polyphenols from onion more than lime juice. Concentration of bio accessible polyphenols was higher upon open-pan boiling of onion. There was a qualitative as well as quantitative change in the phenolic composition on addition of the food acidulants. Since amchur enhances the concentration of bio accessible polyphenols more than lime juice, its use in food preparations could be a strategy to maximize bioavailability of polyphenols, especially flavonoids from onion.Keywords
Food Acidulants, Heat Processing, Onion, Polyphenol Content, Polyphenol Bioaccessibility.References
- Lee, J. and Mitchell, A.E. Quercetin and isorhamnetin glycosides in onion (Allium cepa L.): Varietal comparison, physical distribution, coproduct evaluation, and long-term storage stability. J. Agric. Fd. Chem., 2011, 59, 857–863.
- Srinivasan, K. Plant foods in the management of diabetes mellitus: Spices as potential antidiabetic agents. Int. J. Fd. Sci. Nutr., 2005, 56, 399–414.
- Vidyavati, H.G., Manjunatha, H., Hemavathy, J. and Srinivasan, K. Hypolipidemic and antioxidant efficacy of dehydrated onion in experimental rats. J. Fd. Sci. Tech., 2010, 47, 55–60.
- Annapurna, A., Reddy, C.S., Akondi, R.B. and Rao, S.R. Cardio protective actions of two bioflavonoids, quercetin and rutin, in experimental myocardial infarction in both normal and streptozotocin-induced type I diabetic rats. J. Pharm. Pharmacol., 2009, 6, 1365–1374.
- Chopra, K. and Singh, M. Involvement of oxygen free radicals in cardioprotective effect of rutin–a naturally occurring flavonoid. Indian J. Pharmacol., 1994, 26, 13–18.
- Kawamoto, E., Sakai, Y., Okamura, Y. and Yamamoto, Y. Effects of boiling on the antihypertensive and antioxidant activities of onion. J. Nutr. Sci. Vitaminol., 2004, 50, 171–176.
- Faller, A.L.K. and Fialho, E. The antioxidant capacity and polyphenol content of organic and conventional retail vegetables after domestic cooking. Fd. Res. Int. 2009, 42, 210–215.
- Gorinstein, S., Jastrzebski, Z., Leontowicz, H., Leontowicz, M., Namiesnik, J. et al. Comparative control of the bio activity of some frequently consumed vegetables subjected to different processing conditions. Fd. Control., 2009, 20, 407–413.
- Hansen, E.A., Folts, J.D. and Goldman, I.L. Steam-cooking rapidly destroys and reverses onion-induced antiplatelet activity. Nutr. J., 2012, 11, 76.
- Hemalatha, S., Platel, K. and Srinivasan, K. Influence of food acidulants on bioaccessibility of zinc and iron from selected food grains. Mol. Nutr. Fd. Res., 2005, 49, 950–956.
- Veda, S., Platel, K. and Srinivasan, K. Influence of food acidulants and antioxidant spices on bioaccessibility of â-carotene from selected vegetables. J. Agric. Fd. Chem., 2008, 56, 8714–8719.
- Chetan, S. and Malleshi, N.G. Finger millet polyphenols: Optimization of extraction and the effect of pH on their stability. Fd. Chem., 2007, 105, 860-870.
- Singleton, V.L. and Rossi, J.A. Colorimetry of total phenolics with phosphomolybdicphosphotungstic acid reagents. Am. J. Enol. Vitic., 1965, 16, 144–158.
- Zhishen, J., Mengcheng, T. and Jianming, W. The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Fd. Chem., 1999, 64, 555–559.
- Sreerama, Y.N., Sashikala, V.B. and Pratape, V.M. Variability in the distribution of phenolic compounds in milled fractions of chickpea and horse gram: Evaluation of their antioxidant properties. J. Agric. Fd. Chem., 2010, 58, 8322–8330.
- Luten, J., Crews, H., Flynn, A., Van Dael, P., et al. Inter-laboratory trial on the determination of the in vitro iron dialyzability from food. J. Sci. Fd. Agric., 1996, 72, 415-424.
- Hithamani, G. and Srinivasan, K. Effect of domestic processing on the polyphenol content and bioaccessibility in finger millet (Eleusine coracana) and pearl millet (Pennisetum glaucum). Fd. Chem., 2014, 164, 55–62.
- Hithamani, G. and Srinivasan, K. Bioaccessibility of polyphenols from wheat (Triticum aestivum), sorghum (Sorghum bicolor), green gram (Vigna radiata), and chickpea (Cicer arietinum) as influenced by domestic food processing. J. Agric. Fd. Chem., 2014, 62, 11170-11179.
- Im, M.H., Park, Y.S., Ham, K.S., Kang, S.G., Heo, B.G. et al. Effects of cooking on the bio activity of lotus ischolar_mains and white onions. Int. J. Fd. Prop., 2012, 15, 49–59.
- Crozier, A., Lean, M.E.J., McDonald, M.S. and Black, C. Quantitative analysis of the flavonoid content of commercial tomatoes, onions, lettuce and celery. J. Agric. Fd. Chem., 1997, 45, 590–595.
- Makris, D.P. and Rossiter, J.T. Domestic processing of onion bulbs (Allium cepa) and Asparagus spears (Asparagus officinalis): effect on flavonol content and antioxidant status. J. Agric. Fd. Chem., 2001, 49, 3216–3222.
- Lombarda, K., Peffley, E., Geoffriau, E., Thompson, L. and Herringe, A. Quercetin in onion (Allium cepa L.) after heat-treatment simulating home preparation. J. Fd. Compos. Anal., 2005, 18, 571–578.
- Bentz, A.B. A review of quercetin: chemistry, antioxidant properties, and bioavailability. J. Young Investig., http://www.jyi.org/issue/a-review-of-quercetin-chemistry-antioxidant-propertiesand-bioavailability, 2009.
- Price, K.R., Bacon, J.R. and Rhodes, M.J.C. Effect of storage and domestic processing on the content and composition of flavonol glucosides in onion (Allium cepa). J. Agric. Fd. Chem., 1997, 45, 938–942.
- Chan, S.T., Yang, N.C., Huang, C.S., Liao, J.W. and Yeh, S.L. Quercetin enhances the antitumor activity of trichostatin a through upregulation of p53 protein expression in vitro and in vivo. PLoS One, 2013, 8, e54255.
- Nair, M.P.N., Saiyed, Z.M., Gandhi, N.H. and Ramchand, C.N. The flavonoid quercetin inhibits HIV-1 infection in normal peripheral blood mononuclear cells. Am. J. Infect. Dis., 2009, 5, 135–141.
- Boots, A.W., Wilms, L.C., Swennen, E.L., Kleinjans, J.C., Bast, A. and Haenen, G.R. In vitro and ex vivo anti-inflammatory activity of quercetin in healthy volunteers. Nutr., 2008, 24, 703–710.
- Gupta, R., Singh, M. and Sharma, A.A. Neuroprotective effect of antioxidants on ischaemia and reperfusion-induced cerebral injury. Pharmacol. Res., 2003, 48, 209–215.
- Shim, S.M., Yi, H.L. and Kim, Y.S. Bioaccessibility of flavonoids and total phenolic content in onions and its relationship with antioxidant activity. Int. J. Fd. Sci. Nutr., 2011, 62, 835–838.
- Zhu, Q.Y., Huang, Y. and Chen, Z.Y. Interaction between flavonoids and tocopherol in human low density lipoprotein. J. Nutr. Biochem., 2000, 11, 14–21.
- Onyeagba, R.A., Ugbogu, O.C., Okeke, C.U. and Iroakasi, O. Studies on the antimicrobial effects of garlic (Allium sativum Linn), ginger (Zingiber officinale Roscoe) and lime (Citrus aurantifolia Linn). Afr. J. Biotech., 2004, 10, 552–554.
- Wang, L., Kim, D. and Park, J. Various anti-browning agents and green tea extract during processing and storage. J. Fd. Process. Preserv., 2003, 27, 213–225.
- Gautam, S., Platel, K. and Srinivasan, K. Influence of combinations of promoter and inhibitor on the bioaccessibility of iron and zinc from food grains. Int. J. Fd. Sci. Nutr., 2011, 62, 826– 834.
- Shim, S.M., Yoo, S.H., Ra, C.S., Kim, Y.K., Chung, J.O. and Lee, S.J. Digestive stability and absorption of green tea polyphenols: Influence of acid and xylitol addition. Fd. Res. Int., 2012, 45, 204–210.
- Hithamani, G. and Srinivasan, K. Bioaccessibility of polyphenols from selected cereal grains and legumes as influenced by food acidulants. J. Sci. Food Agric., 2016, Published online, DOI 10.1002/jsfa.7776.
- Accelerated Attenuation of Pre-Formed Cholesterol Gallstones by Dietary Tender Cluster Beans (Cyamopsis tetragonoloba) in Mice
Abstract Views :266 |
PDF Views:2
Authors
Affiliations
1 Department of Biochemistry and Nutrition, CSIR - Central Food Technological Research Institute, Mysore - 570 020, IN
1 Department of Biochemistry and Nutrition, CSIR - Central Food Technological Research Institute, Mysore - 570 020, IN
Source
The Indian Journal of Nutrition and Dietetics, Vol 54, No 2 (2017), Pagination: 127-148Abstract
Dietary soluble fibre-rich tender cluster beans (Cyamopsis tetragonoloba) (CB) is previously shown to reduce the susceptibility for cholesterol gallstone (CGS) formation in experimental mice. The present study evaluated if dietary CB could also accelerate dissolution of pre-formed CGS in mice. The possible additive influence of dietary fibre-rich CB and sulfur compounds-rich garlic in dissolving CGS was also evaluated. CGS was induced with a high-cholesterol diet for ten weeks. CB (10%) and garlic (1%) were included individually and in combination in the diet of gallstoneinduced mice for another ten weeks. CB, garlic, and CB+garlic reduced the preestablished CGS by 61, 50, and 72%, respectively, in 10 weeks as compared to 27% regression observed with the control diet. There was a reduction in cholesterol saturation index and ratios of cholesterol: bile acid and cholesterol: phospholipid in the bile, facilitating the desaturation of cholesterol. mRNA expression of CYP7A was up-regulated in CB-fed animals. CB+garlic produced a higher up-regulation of mRNA expression of CYP7A and CYP27. These results corroborate with the observed increase in the bile acid pool as a result of these dietary interventions. Acceleration of the regression of preformed CGS is complimentary to the previously reported CGSpreventive influence of dietary CB.Keywords
Cholesterol Gallstones, Cholelithiasic Effect, Cholesterol Saturation Index, Tender Cluster Beans, Garlic.References
- Berr, F., Holl, J., Jungst, D., Fischer, S., Richter, W.O., et al. Dietary n-3 polyunsaturated fatty acids decrease biliary cholesterol saturation in gallstone disease. Hepatol., 1992, 16, 960-967.
- Misciagna, G., Centonze, S., Leoci, C., Guerra, V., Cisternino, A.M., Ceo, R. and Trevisan, M. Diet, physical activity and gallstones – a population, case-control study in southern Italy. Am. J. Clin. Nutr., 1999, 69, 120-126.
- Samarghandian, S., Hadjzadeh, M., Davari, A.S. and Abachi, M. Reduction of serum cholesterol in hypercholesterolemic rats by guar gum. Afr. J. Physiol., 2011, 1, 36-42.
- James, S.L., Muir, J.G., Curtis, S.L. and Gibson, P.R. Dietary fiber: a roughage guide. Int. Med. J., 2003, 33, 291-296.
- Tomolin, J., Taylor, J.S. and Read, N.W. The effect of mixed fecal bacteria on a selection of viscous polysaccharide in vitro. Nutr. Rep. Int., 1989, 39, 121-135.
- Raghavendra, C.K. and Srinivasan, K. Anti-cholelithogenic potential of dietary tender cluster beans (Cyamopsis tetragonoloba) during experimental formation of cholesterol gallstone in mice. Appl. Physiol. Nutr. Metab., 2014, 39, 152-157.
- Pande, S. and Srinivasan, K. Potentiation of the hypolipidemic influence of dietaty tender cluster bean (Cyamopsis tetragonoloba) by garlic in cholesterol-fed rats. Fd. Chem., 2012, 133, 798-805.
- Vidyashankar, S., Sambaiah, K. and Srinivasan, K. Regression of pre-established cholesterol gallstones by dietary garlic and onion in experimental mice. Metabol., 2010, 59, 1402-1412.
- Kannar, D., Wattanapenpaiboon, N., Savige, G.S. and Wahlqvist, M.L. Hypocholesterolemic effect of an enteric-coated garlic supplement. J. Am. Coll. Nutr., 2001, 20, 225-231.
- Akiyoshi, T., Uchida, K., Takase, H., Nomura, Y. and Takeuchi, N. Cholesterol gallstones in alloxan-diabetic mice. J. Lipid Res., 1986, 27, 915-924.
- Bligh, E.G. and Dyer, W.J. A rapid method of total lipid extraction and purification, Can. J. Biochem. Physiol., 1959, 37, 911-917.
- Turley, S.D. and Dietschy, J.M. Re-evaluation of 3α-hydroxysteroid dehydrogenase assay for total bile acids. J. Lipid Res., 1970, 19, 924-928.
- Folch, J., Lees, M. and Sloane-Stanley, G.H. A simple method for the isolation and purification of total lipids from animal tissue. J. Biol. Chem., 1957, 226, 497-509.
- Warnick, G.R. and Albers, J.J. A comprehensive evaluation of the heparin-manganese precipitation procedure for estimating high density lipoprotein cholesterol. J. Lipid Res., 1978, 19, 65-76.
- Searcy, R.L. and Bergquist, L.M. A new colour reaction for the quantification of serum cholesterol. Clin. Chim. Acta, 1960, 5, 192-199.
- Stewart, J.C.M. Colorimetric estimation of phospholipids with ammonium ferro thiocyanate. Anal. Biochem., 1980, 104, 10-14.
- Fletcher, M.J. A colorimetric method for estimating serum triglycerides. Clin. Chim. Acta, 1968, 22, 303-307.
- Ohkawa, H., Ohishi, N. and Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem., 1979, 95, 351-358.
- Omaye, S.T., Turnbull, J.D. and Sauberlich, H.E. Selected methods for the determinations of the ascorbic acid in animal cells, tissues and fluids. Methods Enzymol., 1973, 62, 3-11.
- Warholm, W., Guthenberg, C., Bahr, C.V. and Mannervik, B. Glutathione transferase from human liver. Methods Enzymol., 1985, 113, 499-504.
- Carlberg, I. and Mannervik, B. Glutathione reductase. Methods Enzymol., 1985, 113, 484-490.
- Flohe, L. and Gunzler, W.A. Assays of glutathione peroxidase. Methods Enzymol., 1984, 105, 114-121.
- Aebi, H. Catalase in vitro. Methods Enzymol., 1984, 105, 121-126.
- Flohe, L. and Otting, F. Superoxide dismutase assays. Methods Enzymol., 1984, 105, 93-104.
- Bergmeyer, H.U. and Bernt, E. LDH – UV assay with pyruvate and NADH. In: Bergmeyer, H.U. (ed). Methods of Enzymatic Analysis, Vol. 2. Academic Press, New York, 1974, 574-579.
- Lowry, O.H., Rosebrough, N.J., Farr, A.L. and Randall, R.J. Protein measurement with the Folin phenol reagent. J. Biol. Chem., 1951, 193, 265-275.
- Petrack, B. and Latario, B.J. Synthesis of 27-hydroxycholesterol in rat liver mitochondria: HPLC assay and marked activation by exogenous cholesterol. J. Lipid Res., 1993, 34, 643-649.
- Hulcher, F.H. and Oleson, W.H. Simplified spectrophotometric assay for microsomal 3-hydroxy-3-methyl glutaryl CoA reductase by measurement of coenzyme-A. J. Lipid Res., 1973, 14, 625-631.
- Roslyn, I.T., Binns, G.S. and Mughes, B.F. Open cholecystectomy. A contemporary analysis of 42,474 patients. Ann. Surgery, 1993, 218, 129-137.
- Bouchier, A.D. New drugs for gallstones. Br. Med. J., 1990, 300, 5927-5931.
- Frias, A.D. and Sgarbieri, V.C. Guar gum effects on food intake, blood serum lipids and glucose levels of Wistar rats. Plant Fd. Hum. Nutr., 1998, 53, 15-28.
- Ramirez, M.I., Karaoglu, D., Haro, D., Barillas, T.C., Bashirzadeh, R. and Gil, G. Cholesterol and bile acids regulate cholesterol-7α-hydroxylase expression at the transcriptional level in culture and in transgenic mice. Mol. Cell. Biochem., 1994, 14, 2809-2821.
- Chen, W.J., Anderson, J.W. and Jennings, D. Propionate may mediate the hypocholesterolemic effects of certain soluble fibre in cholesterol-fed rats. Proc. Soc. Exp. Biol. Med., 1984, 175, 215-218.
- Chi, M.S., Koh, E.T. and Steward, T.J. Effects of garlic on lipid metabolism in rats fed cholesterol or lard. J. Nutr., 1982, 12, 241-248.
- Qureshi, A.A., Crenshaw, T.D., Abuirmeileh, N., Peterson, D.M. and Elson, C.E. Influence of minor plant constituents on porcine hepatic lipid metabolism: Impact on serum lipid. Atherosclerosis, 1983, 64, 109-115.
- Eder, M.I., Miquel, J.F., Jungst, D., Paumgartner, G. and Von Ritter, C. Reactive oxygen metabolites promote cholesterol crystal formation in model bile: role of lipid peroxidation. Free Radic. Biol. Med., 1996, 20, 743-749.
- Eder, M.I., Jungst, D., Meyer, G., Paumgartner, C. and Von Ritter, C. Lipid peroxidation products are increased in lithogenic human gallbladder bile. Gastroenterol., 1995, 114, 548-552.
- Holan, K.R., Holzbach, R.T, Hermann, R.E., Cooperman, A.M. and Claffey, W.J. Nucleation time; a key factor in the pathogenesis of cholesterol gallstone disease. Gastroenterol., 1979, 77, 611-617.
- Gallinger, S., Taylor, R.D., Harvey, P.R., Petrunka, C.N. and Strasberg, S.M. Effect of mucous glycoprotein on nucleation time of human bile. Gastroenterol., 1985, 89, 648-658.
- Groen, A.K, Stout, J.P., Draper, J.A., Hoek, F.J., Grijm, R. and Tygat, G.N. Effect of cholesterol nucleation. promoting activity on cholesterol solubilisation in model bile. Hepatol, 1988, 8, 347-352.
- Raghavendra, C.K. and Srinivasan, K. Influence of dietary tender cluster beans (Cyamopsis tetragonoloba) on biliary proteins, bile acid synthesis and cholesterol crystal growth in rat bile. Steroids, 2015, 94, 21-30.
- Nutritional Profile of Chekurmanis (Sauropus androgynus), a Less Explored Green Leafy Vegetable
Abstract Views :406 |
PDF Views:4
Authors
Affiliations
1 Department of Biochemistry, CSIR - Central Food Technological Research Institute, Mysore – 570 020, IN
1 Department of Biochemistry, CSIR - Central Food Technological Research Institute, Mysore – 570 020, IN
Source
The Indian Journal of Nutrition and Dietetics, Vol 54, No 3 (2017), Pagination: 243-252Abstract
Chekurmanis (Sauropus androgynus) belonging to Euphorbiaceae, is a perennial shrub, growing wildly in Southeast Asia. The leaves of chekurmanis are highly nutritious, being a very rich source of micronutrients and protein. In this study, chekurmanis leaves were evaluated for protein and micronutrient content at different stages of maturity. Maturity of the leaves did not alter the rich content of protein which remained around 22.0 g/100 g. Total dietary fibre content of the leaves ranged between 34 and 36% at different stages of maturity. Fully matured leaves contained a significantly higher amount of calcium, as compared to the tender leaves. The iron content of these leaves ranged from 3.89 to 4.50 mg/100 g, while the zinc content of the same was between 1.26 and 1.48 mg/100 g. The bioaccessibility of iron and zinc was significantly higher in the tender leaves. The tender and partially mature leaves of chekurmanis contained 74 and 69 mg/100 g of niacin, respectively. The β-carotene content of the leaves ranged from 7400 to 9250 μg/100 g, while that of vitamin E ranged between 17.6 to 15.6 mg/100 g. Chekurmanis leaves contain an alkaloid, the content of which was significantly higher in mature leaves (1740 mg/100 g) as compared to tender leaves (1439 mg/100 g). The alkaloid content of chekurmanis leaves was significantly reduced upon pressure cooking. This is the first report on the nutrient content of chekurmanis leaves at different stages of maturity, as also on the bioaccessibility of minerals.Keywords
Chekurmanis Leaves, Nutritional Profile, Stages of Maturity, Bioaccessibility Of Minerals, Alkaloid Content.References
- Petrus, A.J.A. Sauropus androgynus (L.) Merrill-A potentially nutritive functional leafy-vegetable. Asian J. Chem., 2013, 25, 9425–9433.
- Sheela, K., Nath, K.G., Vijayalakshmi, D., Yankanchi, G.M. and Patil, R.B. Proximate composition of underutilized green leafy vegetables in Southern Karnataka. J. Hum. Ecol., 2004, 15, 227–229.
- Nahak, G. and Sahu, R.K. Free radical scavenging activity of multi-vitamin plant (Sauropus androgynus L. Merr) Researcher, 2010, 2, 6–14.
- Ching, L.S. and Mohamed, S. Alpha tocopherol content in 62 edible tropical plants. J. Agric. Fd. Chem., 2001, 49, 3101–3105.
- Padmavathi, P. and Rao, M.P. Nutritive value of Sauropus androgynus leaves. Plant Fds Hum. Nutri., 1990, 40, 107–113.
- Luten, J., Crews, H., Flynn, A., Dael, P.V., Kastenmayer, P., Hurrel, R., et al. Inter-laboratory trial on the determination of the in vitro iron dialyzability from food. J. Sci. Fd. Agric., 1996, 72, 415–424.
- AOAC Official methods of analysis. Estimation of thiamine in foods by fluorometry. Method No. 942.23, Chapter 45,17th Edition, AOAC Int., 2000.
- AOAC Official methods of analysis. Riboflavin in foods and vitamin preparations. Method No. 970.65; Chapter 45, 18th Edition, AOAC Int., 2006.
- Tyler, T.A. and Gonzale, J.A. Liquid chromatographic determination of total niacin in beef, semolina and cottage cheese. J. AOAC Int., 1990, 73, 467–469.
- Veda, S., Kamath, A., Platel, K., Begum, K. and Srinivasan, K. Determination of bioaccessible β-carotene from green leafy and yellow-orange vegetables by in vitro procedures. Mol. Nutr. Fd. Res. 2006, 50, 1047–1052.
- Zaspel, B.J. and Csallany, A.S. Determination of α-tocopherol in tissues and plasma by HPLC. Anal. Biochem. 1983, 130, 146–150.
- Narasimhan, S. and Shanta, M. Spectrophotometric method for estimation of alkaloids precipitable with Dragendorff’s reagent in plant materials. J. AOAC Int., 2003, 86, 1124–1127.
- Gopalan, C., Rama Sastri, B.V. and Balasubramanian, S.C. Nutritive value of Indian foods. National Institute of Nutrition, Indian Council of Medical Research, Hyderabad, 2012.