Key Laboratory of Functional Small Organic Molecule, Ministry of Education, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, PR China.
Key Laboratory of Functional Small Organic Molecule, Ministry of Education, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, PR China.
Biosens Bioelectron. 2016 May 15;79:508-14. doi: 10.1016/j.bios.2015.12.097. Epub 2015 Dec 29.
Methods based on surfactant-responsive controlled release systems of cargoes from nanocontainers have been developed for bioanalytical applications, but most were utilized for drug delivery and a few reports were focused on immunoassays. Herein we design an in situ amplified immunoassay protocol for high-efficient detection of aflatoxins (aflatoxin B1, AFB1 used in this case) based on surfactant-responsive cargo release from glucose-encapsulated liposome nanocarriers with sensitivity enhancement. Initially, biotinylated liposome nanocarrier encapsulated with glucose was synthesized using a reverse-phase evaporation method. Thereafter, the nanocarrier was utilized as the signal-generation tag on capture antibody-coating microplate through classical biotin-avidin linkage after reaction with biotinylated detection antibody. Upon addition of buffered surfactant (1X PBS-Tween 20 buffer) into the medium, the surfactant immediately hydrolyzed the conjugated liposome, and released the encapsulated glucose from the nanocarriers, which could be quantitatively determined by using a low-cost personal glucometer (PGM). The detectable signal increased with the increment of target analyte. Under the optimal conditions, the assay could allow PGM detection toward target AFB1 as low as 0.6 pg mL(-1) (0.6 ppt). Moreover, the methodology also showed good reproducibility and high specificity toward target AFB1 against other mycotoxins and proteins, and was applicable for quantitatively monitoring target AFB1 in the complex systems, e.g., naturally contaminated/spiked peanut samples and serum specimens, with the acceptable results. Taking these advantages of simplification, low cost, universality and sensitivity, our design provides a new horizon for development of advanced immunoassays in future point-of-care testing.
基于纳米容器中货物的表面活性剂响应控制释放系统的方法已被开发用于生物分析应用,但大多数方法用于药物输送,只有少数报道集中于免疫分析。在此,我们设计了一种基于葡萄糖包封脂质体纳米载体中货物的表面活性剂响应释放的原位放大免疫分析方案,用于高效检测黄曲霉毒素(本案例中使用黄曲霉毒素 B1,AFB1),具有灵敏度增强作用。最初,使用反相蒸发法合成了用葡萄糖包封的生物素化脂质体纳米载体。此后,通过经典的生物素-亲和素键合,将纳米载体与生物素化检测抗体反应后,用作捕获抗体包被微孔板上的信号产生标记物。在缓冲表面活性剂(1X PBS-Tween 20 缓冲液)加入到介质中后,表面活性剂立即水解共轭脂质体,并从纳米载体中释放出包裹的葡萄糖,可使用低成本的个人血糖仪(PGM)进行定量测定。检测信号随目标分析物的增加而增加。在最佳条件下,该测定法可以允许 PGM 检测低至 0.6 pg mL(-1)(0.6 ppt)的目标 AFB1。此外,该方法还表现出对其他真菌毒素和蛋白质的良好重现性和高特异性,适用于定量监测复杂系统中的目标 AFB1,例如天然污染/添加的花生样品和血清标本,结果可接受。利用这种简化、低成本、通用性和灵敏度的优势,我们的设计为未来即时检测中先进免疫分析的发展提供了新的前景。