Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University, 35516, Mansoura, Egypt.
Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University, 35516, Mansoura, Egypt.
Anal Chim Acta. 2024 Sep 22;1323:343061. doi: 10.1016/j.aca.2024.343061. Epub 2024 Aug 5.
Nitroxinil has been used extensively to treat parasitic worms, mainly Fasciola, in food-producing cattle and sheep. The reported methods for nitroxinil analysis included expensive instrumentation, the need for skilled operators, and tedious procedures. Fluorimetry is one of the fastest and simplest methods widely used; hence, we aimed to develop a simple, cost-effective, and convenient fluorometric approach for the estimation of nitroxinil in various matrices. Compared with other detection methods, self-ratiometric fluorescent probes are considered a promising approach for the detection of analytes as their detection accuracy overcomes traditional fluorescence sensing probe in that it is not affected by the probe concentration, solution polarity, instrument parameters, and other factors. In this research, room temperature instantaneously synthesized carbon dots were used as a sensitive and selective self-ratiometric probe for the determination of the veterinary medicine nitroxinil in various matrices.
A room-temperature synthesized quinone-ethanolamine carbon dots (RTQECDs) was fabricated using the instantaneous reaction of sodium 1,2-naphthoquinone-4-sulfonate (Folin's) with ethanolamine, without any energy/catalyzing reagents, for the first time. The prepared carbon dots show green-blue fluorescence at 450 nm upon exposure to UV light at 365 nm with a quantum yield of 26.6 %. Upon interaction with nitroxinil, the fluorescence intensity of RTQECDs at 450 nm is quenched and shifted to a longer wavelength at 475 nm. Meanwhile, the fluorescence of RTQECDs at 400 nm (absorbance maxima of nitroxinil) was more extremely quenched under the same conditions. Taking this in hand, a new RTQECDs self-ratiometric probe was developed for the determination of nitroxinil using the decrease in peaks at 450 nm and 400 nm and the shift of the fluorescence maxima to 475 nm as built-in reference peaks. The probe showed a quantitative increase in signal output of F/F in the range of 0.10-30.0 μg/mL nitroxinil with a limit of detection of 30.0 ppb. The nitroxinil-sensing mechanism using RTQECDs is mainly ascribed to the partial secondary blue-type inner filter effect (IFE). The designed study was applied for the estimation of nitroxinil in veterinary dosage forms (recoveries; 99.78 %-100.35 %), river water (recoveries; 98.55 %-101.53 %), and food products, including meat, liver, kidney, and milk (recoveries; 97.60 %-104.25 %).
The novelty of our work includes the immediate synthesis of the sensing probe at room temperature, as well as its use as a self-ratiometric fluorescence probe for the determination of nitroxinil in veterinary samples, river water, and food products with excellent sensitivity down to 30.0 ppb. RTQECDs own the highest response and selectivity to nitroxinil compared with cations, anions, as well as other co-administered drugs, including cefotaxime and ivermectin.
硝碘酚腈被广泛用于治疗食品生产牛和羊中的寄生蠕虫,主要是片形吸虫。硝碘酚腈的分析方法包括昂贵的仪器、需要熟练的操作人员和繁琐的程序。荧光法是广泛使用的最快和最简单的方法之一;因此,我们旨在开发一种简单、经济高效且方便的荧光方法,用于各种基质中硝碘酚腈的估计。与其他检测方法相比,自比荧光探针被认为是一种很有前途的分析物检测方法,因为它的检测精度克服了传统荧光传感探针的缺点,不受探针浓度、溶液极性、仪器参数和其他因素的影响。在这项研究中,室温即时合成的碳点被用作一种灵敏和选择性的自比荧光探针,用于检测各种基质中的兽药硝碘酚腈。
首次使用瞬时反应,即用乙醇胺与 1,2-萘醌-4-磺酸钠(福林)合成了室温合成的醌-乙醇胺碳点(RTQECDs),无需任何能量/催化试剂。制备的碳点在暴露于 365nm 的紫外光下时在 450nm 处显示出绿色-蓝色荧光,量子产率为 26.6%。与硝碘酚腈相互作用后,RTQECDs 在 450nm 处的荧光强度被猝灭,并移至 475nm 的较长波长处。同时,在相同条件下,RTQECDs 在 400nm(硝碘酚腈的吸收最大值)处的荧光被更极端地猝灭。在此基础上,利用 450nm 和 400nm 处峰的降低以及荧光最大值向 475nm 的位移作为内置参考峰,开发了一种新的 RTQECDs 自比荧光探针,用于检测硝碘酚腈。探针在 0.10-30.0μg/mL 硝碘酚腈范围内显示出信号输出的定量增加,检出限为 30.0ppb。使用 RTQECDs 的硝碘酚腈传感机制主要归因于部分二级蓝型内滤效应(IFE)。该设计研究用于估计兽医剂型(回收率;99.78%-100.35%)、河水(回收率;98.55%-101.53%)和食品中的硝碘酚腈,包括肉、肝、肾和奶(回收率;97.60%-104.25%)。
我们工作的新颖之处包括在室温下即时合成传感探针,以及将其用作自比荧光探针,用于检测兽医样品、河水和食品中的硝碘酚腈,灵敏度高达 30.0ppb。与阳离子、阴离子以及其他同时给药的药物(包括头孢噻肟和伊维菌素)相比,RTQECDs 对硝碘酚腈的响应和选择性最高。