Liposomes loaded with quantum dots for ultrasensitive on-site determination of aflatoxin M1 in milk products

被引:34
作者
Beloglazova, N. V. [1 ]
Shmelin, P. S. [2 ]
Goryacheva, I. Yu [3 ]
De Saeger, S. [1 ]
机构
[1] Univ Ghent, Fac Pharmaceut Sci, Lab Food Anal, B-9000 Ghent, Belgium
[2] OJSC CSRIT Technomash, Neuronet Dept, Moscow 121108, Russia
[3] Saratov NG Chernyshevskii State Univ, Inst Chem, Dept Gen & Inorgan Chem, Saratov 410012, Russia
关键词
Liposomes; Quantum dots; Immunoassay; On-site method; Fluorescence-labeled immunoassay; Aflatoxin M1; IMMUNOASSAY; ASSAY; M-1; CONTAMINATION; TESTS;
D O I
10.1007/s00216-013-7096-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A quantitative fluorescence-labeled immunosorbent assay and qualitative on-site column tests were developed for the determination of aflatoxin M1 in milk products. The use of liposomes loaded with quantum dots as a label significantly increased the assay sensitivity by encapsulating multiple quantum dots in a single liposome and, therefore, amplifying the analytical signal. Two different techniques were compared to obtain aflatoxin-protein conjugates, used for further coupling with the liposomes. The influence of nonspecific interactions of the liposome-labeled conjugates obtained with the surface of microtiter plates and column cartridges was evaluated and discussed. The limit of detection for fluorescence-labeled immunosorbent assay was 0.014 mu g kg(-1). For qualitative on-site tests, the cutoff was set at 0.05 mu g kg(-1), taking into account the EU maximum level for aflatoxin M1 in raw milk, heat-treated milk, and milk for the manufacture of milk-based products. The direct addition of labeled conjugate to the milk samples resulted in an additional decrease of analysis time. An intralaboratory validation was performed with sterilized milk and cream samples artificially spiked with aflatoxin M1 at concentrations less than, equal to and greater than the cutoff level. It is shown that milk products can be analyzed without any sample preparation, just diluted with the buffer. The rates for false-positive and false-negative results were below 5 % (2.6 % and 3.3 %, respectively).
引用
收藏
页码:7795 / 7802
页数:8
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