Development and Validation of an UV-Visible Method for the Determination of β-Carotene in the Leafy Vegetables in Thailand

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Abstract:

Determination of β-carotene content in four types of leafy vegetables, water morning glory, kale, lettuce and Chinese cabbage by using a simple, rapid and low cost of UV-Visible method. This study was in the concentration range of 0.5 to 12 mg/L, and showed the linear regression equation y = 0.0764x - 0.0008, and an excellent linearity with correlation coefficient (R2) was 0.9999. The accuracy of the method analysis was reported by percentage recovery of about 80-106%. The precision was reported by percent of relative standard deviation and varies for intra-day 3.92% and inter-day 3.99%. The limits of detection and limit of quantification were 0.004 and 0.013 mg/L, respectively. Acetone is the most suitable for extraction, ratio of weight of samples to solvent, and extraction time was 1:3 g/mL and 10 min. Moreover, the most appropriate storage temperature for leafy vegetable samples is 4°C. Evaluation of β-carotene content under the suitable conditions in the kale, Chinese cabbage, lettuce and water morning glory was found to be 27.96 ± 2.99, 19.35 ± 1.92, 18.78 ± 0.88 and 18.48 ± 1.86 mg/100 g, respectively.

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Advanced Materials Research (Volumes 1033-1034)

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652-657

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October 2014

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] M. Kimura and D.B. Rodriguez-Amaya: Food Chemistry Vol. 78 (2002), pp.389-398.

Google Scholar

[2] A.I.O. Barba, M.C. Hurtado, M.C.S. Mata, V.F. Ruiz and M.L.S. Tejada: Food Chemistry Vol. 95 (2006), pp.328-336.

Google Scholar

[3] M. N. Ahamad, M. Saleemullah, H.U. Shah, I.A. Khalil and A.U.R. Saljoqi: Sarhad J. Agric Vol. 23 (2007), pp.767-770.

Google Scholar

[4] P. Karnjanawipagul, W. Nittayanuntawech, P. Rojsanga and L. Suntornsuk: Mahidol University Journal of Pharmaceutical Science Vol. 37 (2010), pp.8-16.

Google Scholar

[5] S. Gautam, K. Platel and K. Srinivasan: Food Chemistry Vol. 122 (2010), pp.668-672.

Google Scholar

[6] R. Martinez-Tomas, F. Perez-Llamas, M. Sanchez-Campillo, D. Genzalez-Silvera, A.I. Cascales, M. Garcia-Fernandez, J.A. Lopez-Jimenez, S.Z. Navarro, M.I. Burgos, F. Lopez-Azorin, A. Wellner, F.A. Plaza, L. Bialek, M. Alminger and E. Larque: Food Chemistry Vol. 134 (2012).

Google Scholar

[7] M.G. Dias, M. Filomena, G.F.C. Camoes and L. Oliveira: Food Chemistry Vol. 156 (2014), pp.37-41.

Google Scholar

[8] M.G. Dias, M. Filomena, G.F.C. Camoes and L. Oliveira: Food Chemistry Vol. 113 (2009), pp.808-815.

Google Scholar

[9] M.G. Dias, L. Oliveira, M. Filomena, G.F.C. Camoes, B. Nunes, P. Versloot and P.J.M. Hulshof: Journal of Chromatography A Vol. 1217 (2010), pp.3494-3502.

Google Scholar

[10] E. Dauqan, H.A. Sani, A. Abdullah, H. Muhamad and Ab.G. Md. Top: American Journal of Applied Sciences Vol. 8(5) (2011), pp.407-412.

Google Scholar

[11] D. Tatraaljai, L. Major, E. Foldes, B. Pukanszky: Polymer Degradation and Stability Vol. 102 (2014), pp.33-40.

Google Scholar

[12] I. Cantuti-Castelvetri, B. Shukitt-Hale and J.A. Joseph Tatraaljai: International Journal of Developmental Neuroscience Vol. 18(4-5) (2000), pp.367-381.

DOI: 10.1016/s0736-5748(00)00008-3

Google Scholar

[13] H.S. Lee, J.J. In, Y. Hee-Kang, F. Khachik and J.H.Y. Park: Journal of Korean Society of Food Science and Nutrition Vol. 32(3) (2003), pp.437-443.

Google Scholar

[14] S. Dey and V.K. Rathod: Ultrasonics Sonochemistry Vol. 20 (2013), pp.271-276.

Google Scholar

[15] S. C. Chua, C.P. Tan, H. Mirhosseini, O.M. Lai, K. Long, B.S. Baharin: J. Food Eng Vol. 92 (2009), pp.403-409.

Google Scholar

[16] W. Vongsangnak, J. Gua, S. Chauvatcharin, J.J. Zhong: Biochem. Eng. J. Vol. 18 (2004), pp.115-120.

Google Scholar