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Title: | Screening natural content of water soluble b vitamins in fish: enzymatic extraction, HILIC separation and tandem mass spectrometric determination |
Other Titles: | Not Available |
Authors: | Chatterjee, N.S. Ashok Kumar, K. Ajeeshkumar, K.K. Remya Kumari, K.R. Vishnu, K.V. Anandan, R. Suseela Mathew Ravishankar, C.N. |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | ICAR::Central Institute of Fisheries Technology |
Published/ Complete Date: | 2017-05-01 |
Project Code: | Not Available |
Keywords: | Not available |
Publisher: | AOAC International |
Citation: | Chatterjee, N.S., Ashok Kumar, K., Ajeeshkumar, K.K., Remyakumari, K.R., Vishnu, K.V., Anandan, R., Suseela Mathew and Ravishankar, C.N. (2017) - Screening natural content of water soluble B vitamins in fsh: Enzymatic extraction, HILIC separation and Tandem Mass Spectrometric Determination.J. AOAC Int. 100(3): 579-585 |
Series/Report no.: | Not Available; |
Abstract/Description: | Despite the potential of LC with tandem MS (MS/MS) in improving sensitivity and selectivity, analytical methods are scarce for the determination of protein-bound and phosphorylated forms of B vitamins in food. This prompted us to develop a method for LC-MS/MS determination of naturally occurring nicotinamide, nicotinic acid, thiamine, pyridoxine, riboflavin, pantothenic acid, biotin, folic acid, and cyanocobalamin in fish. Baseline separation of the vitamins was achieved in a hydrophilic interaction LC condition. An ultrasonication-assisted enzymatic extraction protocol for sample preparation was optimized and validated. The time required for extraction was significantly reduced (to 4 h), while maintaining good extraction efficiency. Acetonitrile content (80%, v/v) in the prepared sample was found to be optimum for excellent peak shape and sensitivity. The dynamic linear range of the vitamins ranged from 2.5 to 500 ng/g, and the regression coefficient values were greater than 0.99. LOQ values ranged from 0.4 to 50 ng/g for the different vitamins. The spike recovery values at 50 and 100 ng/g ranged from 87.5 to 97.5%. The intra- and interday precision values were satisfactory. Accuracy of the developed method was determined by analysis of a Certified Reference Material. The method could also be used for unambiguous determination of the natural content of the target vitamins in fish. |
Description: | Not Available |
ISSN: | Not Available |
Type(s) of content: | Research Paper |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | Journal of Association of Official Analytical Chemists - JAOAC Int |
NAAS Rating: | 7.51 |
Volume No.: | 100(3) |
Page Number: | 579-585 |
Name of the Division/Regional Station: | Not Available |
Source, DOI or any other URL: | 10.5740/jaoacint.17-0056 |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/15003 |
Appears in Collections: | FS-CIFT-Publication |
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