首页> 外文会议>Genetically Engineered and Optical Probes for Biomedical Applications III; Progress in Biomedical Optics and Imaging; vol.6, no.19 >Chemiluminescence and fluorescence spectrum methods for determination of Aflatoxin B1 mediated by 'FCLA + BSA'
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Chemiluminescence and fluorescence spectrum methods for determination of Aflatoxin B1 mediated by 'FCLA + BSA'

机译:化学发光和荧光光谱法测定'FCLA + BSA'介导的黄曲霉毒素B1

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BSA (Bovine Serum Albumin) can enlarge the CL intensity of FCLA(3,7-dihydro-6-{4-{2-(N'-(5-fluoresceinyl) thioureido)ethoxy}phenyl}-2-methylimi-dazo{1,2-a}pyrazin-3-one dosium salt) to 763%. This report presents novel methods for determination of Aflatoxin B1 (AfB1) mediated by FCLA+BSA. The concentration of AFB1 showed an obvious positive correlation with the chemiluminescence (CL) intensity mediated by FCLA+BSA, correlative coefficient R ≈ 0.94. This method could measure accurately ng/ml of AfBl concentration. 365nm as excitated wavelength, 440nm and 520nm-two fluorescence peaks of FCLA+BSA+AfB1 were found. The fluorescence intensity of peak at 440nm showed an obvious positive correlation with the concentration of AFB1, R ≈ 0.97; the fluorescence intensity of peak at 520nm showed a positive correlation with the concentration of AFB1, R ≈ 0.90. Comparing the peak of FCLA, FCLA+BSA and FCLA+BSA+AfB1 had a 6nm Einstein shift (red shift). The study suggested that CL and fluorescence spectrum methods mediated by FCLA+BSA might be applicable to the determination of AfBl concentration.
机译:牛血清白蛋白(BSA)可以增强FCLA(3,7-二氢-6- {4- {2-(N'-(5-氟乙烯基)硫脲基)乙氧基}苯基}苯基} -2-甲基咪唑{ 1,2-a}吡嗪-3-一one盐)至763%。本报告介绍了测定由FCLA + BSA介导的黄曲霉毒素B1(AfB1)的新方法。 AFB1的浓度与FCLA + BSA介导的化学发光(CL)强度呈明显的正相关,相关系数R≈0.94。该方法可以准确测量ng / ml的AfB1浓度。激发波长为365nm,在440nm和520nm处发现了两个FCLA + BSA + AfB1的荧光峰。 440nm处的荧光峰强度与AFB1浓度呈明显的正相关,R≈0.97。 520nm处的荧光峰强度与AFB1浓度呈正相关,R≈0.90。比较FCLA,FCLA + BSA和FCLA + BSA + AfB1的峰有6nm的爱因斯坦位移(红移)。研究表明,由FCLA + BSA介导的CL和荧光光谱方法可能适用于AfB1浓度的测定。

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