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Title: | Development and validation of a method for direct analysis of aflatoxins in animal feeds by ultra-high performance liquid chromatography with fluorescence detection |
Other Titles: | Not Available |
Authors: | Kumar A., Dhanshetty M., Banerjee Kaushik |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | ICAR::National Research Centre for Grapes ICAR::Indian Grassland and Fodder Research Institute |
Published/ Complete Date: | 2020-03-12 |
Project Code: | Not Available |
Keywords: | Aflatoxins Feed Ultra-High-Performance Liquid Chromatography with Fluorescence Detection |
Publisher: | Oxford University Press |
Citation: | Kumar A., Dhanshetty M., Banerjee Kaushik (2020). Development and validation of a method for direct analysis of aflatoxins in animal feeds by ultra-high performance liquid chromatography with fluorescence detection. Journal of AOAC International https://doi.org/10.1093/jaoacint/qsz037 |
Series/Report no.: | Not Available; |
Abstract/Description: | Background and Objective Aflatoxin (AF) contamination is one of the major regulatory concerns for animal feed. As feed is a complex analytical matrix, validated methods on AFs in feed are scanty. The available methods involve a derivatization step before AF analysis by high-performance liquid chromatography (HPLC) with fluorescence detection (FLD). The aim of this study was thus to develop and validate a simple and rapid method for direct analysis of AFs (AFB1, AFB2, AFG1, AFG2) in a range of animal feed matrices. Methods Feed samples were extracted with 80% methanol, followed by dilution with water and immmunoaffinity column cleanup. AFs were estimated using an ultra-high performance liquid chromatography (UHPLC) instrument. Use of a large volume flow cell in FLD allowed direct analysis of all AFs with high sensitivity. The method was thoroughly validated in a range of feed matrices. Results This sample preparation workflow minimized co-extractives, along with matrix interferences. In pigeon pea husk feed, the method provided a limit of quantification (LOQ) of 0.5 ng/g for each AF with recoveries of AF- B1, B2, G1, and G2 as 71.5, 75.6, 82.4, and 78.2%, respectively. The precision (relative standard deviation, RSD) was below 5%. A similar method performance was also recorded in other matrices, including wheat bran feed and poultry feed. Conclusions The optimized method is suitable for regulatory testing because it is simple, robust, cost-effective, and high throughput in nature, with high sensitivity and selectivity. |
Description: | Not Available |
Type(s) of content: | Journal |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | Journal of AOAC International |
Volume No.: | 103 (4) |
Page Number: | 940-945 |
Name of the Division/Regional Station: | National Reference Laboratory |
Source, DOI or any other URL: | https://doi.org/10.1093/jaoacint/qsz037 |
URI: | https://doi.org/10.1093/jaoacint/qsz037 http://krishi.icar.gov.in/jspui/handle/123456789/38640 |
Appears in Collections: | HS-NRCG-Publication |
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