Analysis of aflatoxins and ochratoxin a in chilli powder using ultrahigh performance liquid chromatography with fluorescence detection and tandem mass spectrometry

被引:18
作者
Dhanshetty, Manisha [1 ]
Shinde, Raviraj [1 ]
Goon, Arnab [1 ]
Oulkar, Dasharath [1 ]
Elliott, Christopher T. [2 ]
Banerjee, Kaushik [1 ]
机构
[1] ICAR Natl Res Ctr Grapes, Natl Reference Lab, PO Manjri Farm, Pune 412307, Maharashtra, India
[2] Queens Univ Belfast, Sch Biol Sci, Inst Global Food Secur, Belfast, Antrim, North Ireland
关键词
Aflatoxins; Ochratoxin A; Chilli powder; UHPLC-fluorescence; LC-MS/MS; Method validation; NATURAL OCCURRENCE; MYCOTOXINS; COOCCURRENCE;
D O I
10.1007/s12550-022-00460-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chilli powder, a popular spice, is predominantly contaminated with aflatoxins (AFs) and ochratoxin A (OTA), posing a menace to public health. As no validated method exists for the simultaneous and direct analysis of AFs and OTA in chilli powder, it was imperative to develop one to ensure their effective monitoring and promote trade. In this research, we developed and validated a multi-mycotoxin analysis method that allows the simultaneous determination of AFs (AFB(1), AFB(2), AFG(1) and AFG(2)) and OTA in chilli powder with high sensitivity, accuracy and precision. The optimised sample preparation workflow started with the extraction of chilli powder (25 g) with methanol-water (100 mL, 80:20). An aliquot (3 mL) was cleaned on a multi-mycotoxin, immunoaffinity column (AFLAOCHRA PREP (R)) and analysed using ultrahigh performance liquid chromatography with fluorescence (UHPLC-FLD) and tandem mass spectrometric (LC-MS/MS) detection in a single chromatographic run. The method performance was evaluated through intra- and inter-laboratory validation (ILV) studies, and also by analysing a certified reference material. A direct analysis using UHPLC-FLD (without derivatisation) provided the limits of quantification (LOQ) of 0.25 and 1 ng/g for AFs and OTA, respectively, while the LOQ for all these mycotoxins in LC-MS/MS was 0.5 ng/g. These LOQs are much lower than the maximum levels (MLs) specified by the European Commission. The recoveries of these analytes at LOQ and higher levels were above 75% (RSDr < 12%). The ILV study demonstrated satisfactory method-reproducibility (RSDR <25%). The analysis of the certified reference material provided accuracies of AFs and OTA in the range of 83-101%. The analysis by UHPLC-FLD and LC-MS/MS provided very similar results. The incurred levels of B1 in market samples were estimated with a precision-RSD of < 6%. Considering its efficiency and alignment with the regulatory requirements, this method can be implemented for the routine analysis of AFs and OTA in chilli powder.
引用
收藏
页码:193 / 203
页数:11
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