Department of Pharmaceutical Chemistry, H. R. Patel Institute of Pharmaceutical Education and Research, Shirpur, MS, 425405, India.
Department of Pharmaceutics, Krishna Institute of Pharmacy, Malkapur, Karad, MS, 415539, India.
Anal Sci. 2024 Jun;40(6):1177-1191. doi: 10.1007/s44211-024-00548-0. Epub 2024 Mar 30.
Despite the high medicinal value of tiopronin, there are substantial adverse effects such as yellow skin, yellow eyes, muscle aches, etc. Therefore, there is a huge necessity to identify tiopronin using advanced sensors in provided samples. Recently, the preference for graphene quantum dots (GQDs) and inorganic nanomaterial-based fluorescent sensors for the detection of pharmaceuticals has been extensively documented due to their plentiful advantages. Therefore, in this work, the cobalt-doped GQDs decorated vanadium pentoxide nanosheet-based fluorescence switch 'Off-On' sensor (Co-GQDs@VO-NS) was designed for highly sensitive and selective detection of tiopronin. Briefly, the green synthesis of highly fluorescent Co-GQDs was carried out using a hydrothermal method. Meanwhile, the synthesis of VO-NS was synthesized using the liquid exfoliation method. The synthesis of Co-GQDs@VO-NS was accomplished wherein Co-GQDs adsorbed on the surface of VO-NS that offered the quenching of fluorescence of Co-GQDs. Afterward, the addition of tiopronin into the quenched probe disclosed the proportional recovery of fluorescence of Co-GQDs. Here, the addition of tiopronin provides the decomposition of VO-NS and conversion into the V that aids in releasing the quenched fluorescence of Co-GQDs. The limit of detection and linearity range for tiopronin was found to be 1.43 ng/mL and 10-700 ng/mL, respectively. Moreover, it demonstrated high selectivity, good stability at experimental conditions, and practicality in analyzing tiopronin in spiked sample analysis. Hence, the designed Co-GQDs@VO-NS nanosized sensor enables high sensitivity, selectivity, simplicity, label-free, and eco-friendly tiopronin recognition. In the future, the utility of Co-GQDs@VO-NS can open a new door for sensing tiopronin in provided samples.
尽管硫普罗宁具有很高的药用价值,但它也有很大的副作用,如皮肤发黄、眼睛发黄、肌肉疼痛等。因此,需要在提供的样本中使用先进的传感器来识别硫普罗宁。由于具有丰富的优点,最近,人们越来越倾向于使用石墨烯量子点(GQDs)和基于无机纳米材料的荧光传感器来检测药物。因此,在这项工作中,设计了基于钴掺杂 GQDs 修饰的五氧化二钒纳米片的荧光开关“关-开”传感器(Co-GQDs@VO-NS),用于对硫普罗宁进行高灵敏度和选择性检测。简而言之,使用水热法进行了高度荧光 Co-GQDs 的绿色合成。同时,使用液体剥离法合成了 VO-NS。Co-GQDs@VO-NS 的合成是通过 Co-GQDs 吸附在 VO-NS 表面完成的,这提供了 Co-GQDs 荧光的猝灭。随后,将硫普罗宁加入到猝灭探针中,发现 Co-GQDs 的荧光恢复呈比例关系。在这里,加入硫普罗宁会导致 VO-NS 的分解并转化为 V,从而有助于释放 Co-GQDs 的猝灭荧光。硫普罗宁的检测限和线性范围分别为 1.43ng/mL 和 10-700ng/mL。此外,它表现出高选择性、在实验条件下良好的稳定性以及在分析加标样品中的实用性。因此,设计的 Co-GQDs@VO-NS 纳米传感器能够实现对硫普罗宁的高灵敏度、选择性、简单性、无标记和环保识别。在未来,Co-GQDs@VO-NS 的应用将为提供样本中硫普罗宁的检测开辟新的途径。