Single Laboratory Validation of a Surface Plasmon Resonance Biosensor Screening method for Paralytic Shellfish Poisoning Toxins

被引:54
作者
Campbell, Katrina [1 ]
Haughey, Simon A. [1 ]
van den Top, Hester [2 ]
van Egmond, Hans [2 ]
Vilarino, Natalia [3 ]
Botana, Luis M. [3 ]
Elliott, Christopher T. [1 ]
机构
[1] Queens Univ Belfast, Sch Biol Sci, IAFLU, Belfast BT9 5AG, Antrim, North Ireland
[2] RIKILT, Inst Food Safety, NL-6708 WB Wageningen, Netherlands
[3] Univ Santiago de Compostela, Fac Vet, Dept Farmacol, Lugo 27002, Spain
关键词
LINKED-IMMUNOSORBENT-ASSAY; PRECHROMATOGRAPHIC OXIDATION; QUANTITATIVE-DETERMINATION; LIQUID-CHROMATOGRAPHY; FLUORESCENCE DETECTION; ENZYME-IMMUNOASSAY; SAXITOXIN; ANTIBODIES;
D O I
10.1021/ac1000338
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A research element of the European Union (EU) sixth Framework project BioCop focused on the development of a surface plasmon resonance (SPR) biosensor assay for the detection of paralytic shellfish poisoning (PSP) toxins in shellfish as an alternative to the increasingly ethically unacceptable mouse bioassay. A biosensor assay was developed using both a saxitoxin binding protein and chip surface in tandem with a highly efficient simple extraction procedure. The present report describes the single laboratory validation of this immunological screening method, for this complex group of toxins with differing toxicities, according to the European Decision 2002/657/EC in conjunction with IUPAC and AOAC single laboratory validation guidelines. The different performance characteristics (detection capability CC beta, specificity/selectivity, repeatability, reproducibility, stability, and applicability) were determined in relation to the EU regulatory limit of 800 mu g of saxitoxin equivalents (STX eq) per kg of shellfish meat. The detection capability CC beta was calculated to be 120 mu g/kg. Intra-assay repeatability was found to be between 2.5 and 12.3% and interassay reproducibility was between 6.1 and 15.2% for different shellfish matrices. Natural samples were also evaluated and the resultant data displayed overall agreements of 96 and 92% with that of the existing AOAC approved methods of mouse bioassay (MBA) and high performance liquid chromatography (HPLC), respectively.
引用
收藏
页码:2977 / 2988
页数:12
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