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氮掺杂碳点:用于选择性诺氟沙星检测和生物成像的新型生物传感平台。

Nitrogen-doped carbon dots: a novel biosensing platform for selective norfloxacin detection and bioimaging.

机构信息

Division of Biophotonics and Imaging, Department of Biomaterial Sciences and Technology, Biomedical Technology Wing, Sree Chitra Tirunal Institute for Medical Sciences and Technology (SCTIMST), Trivandrum 695012, India.

出版信息

J Mater Chem B. 2024 Aug 7;12(31):7635-7645. doi: 10.1039/d4tb01006j.

Abstract

Incomplete metabolism and non-biodegradable nature of norfloxacin (NORx) lead to its persistent residues in the environment and food, potentially fostering the emergence of antibiotic resistance and posing a significant threat to public health. Hence, we developed a norfloxacin sensor employing hydrothermally synthesized N-doped carbon dots (N-Ch-CQDs) from chitosan and PEI demonstrated high sensitivity and specificity towards the antibiotic detection. The quantum yield of excitation-dependent emission of N-Ch-CQDs was effectively tuned from 4.6 to 21.5% by varying the concentration of PEI (5-15%). With the enhanced fluorescence in the presence of norfloxacin, N-Ch-CQDs exhibited a linear detection range of 20-1400 nM with a limit of detection (LoD) of 9.3 nM. The high biocompatibility of N-Ch-CQDs was confirmed in the and model and showed the environment-friendly nature of the sensor. Detailed study elucidated the formation of strong hydrogen bonds between N-Ch-CQDs and NORx, leading to fluorescence enhancement. The developed sensor's capability to detect NORx was evaluated in water and milk samples. The recovery rate ranged from 98.5% to 103.5%, demonstrating the sensor's practical applicability. Further, the bioimaging potential of N-Ch-CQDs was demonstrated in both the (L929 cells) and model (). The synergistic influence of the defecation pattern and functioning of intestinal barrier mitigates the translocation of N-Ch-CQDs into the reproductive organ of nematodes. This study revealed the bioimaging and fluorescent sensing ability of N-Ch-CQDs, which holds significant promise for extensive application in the biomedical field.

摘要

氟哌酸(NORx)的不完全代谢和不可生物降解性导致其在环境和食品中持续残留,有可能助长抗生素耐药性的出现,对公众健康构成重大威胁。因此,我们开发了一种基于壳聚糖和聚乙烯亚胺水热合成的氮掺杂碳点(N-Ch-CQDs)的氟哌酸传感器,该传感器对抗生素检测具有高灵敏度和特异性。通过改变聚乙烯亚胺(5-15%)的浓度,可以有效地将 N-Ch-CQDs 的激发依赖性发射量子产率从 4.6%调谐至 21.5%。在存在氟哌酸的情况下,N-Ch-CQDs 的荧光增强,对氟哌酸的检测范围为 20-1400 nM,检测限(LoD)为 9.3 nM。在 和 模型中证实了 N-Ch-CQDs 的高生物相容性,并显示了传感器的环境友好性。详细研究阐明了 N-Ch-CQDs 与 NORx 之间形成的强氢键导致荧光增强。在水样和奶样中评估了开发的传感器检测 NORx 的能力。回收率范围为 98.5%至 103.5%,表明传感器具有实际应用的潜力。此外,还在 和 模型()中证明了 N-Ch-CQDs 的生物成像潜力。排便模式和肠道屏障功能的协同影响减轻了 N-Ch-CQDs 向线虫生殖器官的易位。这项研究揭示了 N-Ch-CQDs 的生物成像和荧光传感能力,这为其在生物医学领域的广泛应用提供了巨大的潜力。

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