State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
NMPA Key Laboratory of Quality Control of Chinese Medicine (HuBei), Wuhan 430075, China.
Anal Chem. 2024 Sep 24;96(38):15322-15329. doi: 10.1021/acs.analchem.4c02934. Epub 2024 Sep 6.
A multiplex assay of mycotoxins in food and medicine is urgently needed and challenging due to synergistic hazards of trace mycotoxins and a lack of sensitive and user-friendly detection approaches. Herein, a cobalt DNA-inorganic hybrid superstructure (Co@DS) was developed through isothermal rolling circle amplification (RCA) for an ultrasensitive chemiluminescence (CL) imaging assay of multiple mycotoxins. Cobalt ions were enriched in the RCA product, endowing the Co@DS with a high CL catalytic property. Experimental studies elucidated the formation and CL catalytic mechanism of Co@DS. Co@DS was facilely integrated with biotinylated DNA to function as a universal platform and combined with a disposable immunosensor array chip. After a competitive immunoassay and biotin-avidin recognition, the CL signals of luminol and hydrogen peroxide, catalyzed by Co@DS captured on each testing zone of the array chip, were imaged simultaneously. Target mycotoxins can be quantitated by CL intensities. To validate the concept, the CL imaging approach was employed for joint determination of aflatoxin B, ochratoxins A, and zearalenone. Under optimal conditions, it showed advantages including simple sample pretreatment, acceptable throughput, high accuracy, minimal sample consumption, broad linear ranges, and detection limits as low as 0.75, 0.62, and 0.61 pg mL, respectively. Furthermore, the approach was applied in analyzing real coix seed samples, showcasing excellent performance in effectively distinguishing qualified and contaminated medicine, revealing the great potential in managing the complex issue of mycotoxins cocontamination in food and medicine.
由于痕量真菌毒素的协同危害以及缺乏敏感和易用的检测方法,食品和药品中真菌毒素的多重分析检测非常紧迫且具有挑战性。在此,通过等温滚环扩增(RCA)开发了一种钴 DNA-无机杂化超结构(Co@DS),用于痕量多真菌毒素的超灵敏化学发光(CL)成像分析。钴离子在 RCA 产物中富集,赋予 Co@DS 高 CL 催化性能。实验研究阐明了 Co@DS 的形成和 CL 催化机制。Co@DS 与生物素化 DNA 简便地集成,用作通用平台,并与一次性免疫传感器阵列芯片结合。在竞争性免疫测定和生物素-亲和素识别后,通过 Co@DS 催化的每个测试区域的发光氨和过氧化氢的 CL 信号被同时成像。通过 CL 强度可以定量目标真菌毒素。为了验证该概念,使用 CL 成像方法联合测定黄曲霉毒素 B、赭曲霉毒素 A 和玉米赤霉烯酮。在最佳条件下,该方法具有简单的样品预处理、可接受的通量、高准确性、最小的样品消耗、宽线性范围和检测限低至 0.75、0.62 和 0.61 pg mL 的优点。此外,该方法还应用于分析真实的薏苡仁样品,在有效区分合格和污染药物方面表现出优异的性能,表明在管理食品和药品中真菌毒素共存的复杂问题方面具有巨大潜力。