4.6 Article

Immunochromatographic strip development for ultrasensitive analysis of aflatoxin M1

期刊

ANALYTICAL METHODS
卷 5, 期 23, 页码 6567-6571

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ay41498a

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资金

  1. National Natural Science Foundation of China [21101079, 21175034, 21371081, 21301073]
  2. MOST [2012BAC01B07, 2012AA06A303, 2012BAD29B04, 2012 BAK11B01, 2011BAK10B07, 2011BAK10B01, 2010AA06Z302, 2010DFB3047, 2013ZX08012-001, 2012BAK17B10, 2012BAK08B01, 2012YQ090194, 2012BAD29B05, 2013AA065501]
  3. MOE [NCET-12-0879, BE2011626, BE2013613, BE2013611, 201310128, 201210127, 201210036, 201310135, 311002, JUSRP51308A]
  4. Jiangsu Province
  5. MOF

向作者/读者索取更多资源

A specific monoclonal antibody against aflatoxin (AF) M1 was prepared by a duo-immunogen immunization strategy. After two immunizations of Balb/c mice with AFB1 keyhole limpet hemocyanin (KLH) conjugates and followed by five subsequent immunizations of AFM-KLH, the mice secreting antibody against AFM1 were selected for cell fusion and a 7C6-H1 cell line was obtained to produce the antibody. The 50% inhibition rate of the prepared antibody was calculated as 0.034 +/- 0.002 mu g L-1. The anti-AFM1 antibody was characterized with high affinity to AFM1 (1.28 x 10(9) mol L-1) and low cross-reactivity to related AFs (<5%). With a competitive format, an immunochromatographic strip was developed using AFB1-bovine serum albumin as the immobilized antigen and anti-AFM1 antibody labeled with gold nanoparticles as tracers. Without any sample preparation, the strip could be directly applied to detect AFM1 contamination in liquid milk. The minimum cut-off concentrations were 0.2 mu g L-1 and 1.6 mu g kg(-1) in liquid milk and powdered milk, respectively, by assessment with the naked eye. Detection of real samples and spiked milk samples indicated the potential of this strip in routine AFM1 monitoring.

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