journal article·2023-12-22

Nanoporous Pyrene-Based Metal–Organic Frameworks for Fluorescence Screening and Discrimination of Sulfonamide Antibiotics

Zhengshuang Yang, Jiaqing Tang, Beining Chen, Xiaolei Qu, Heyun Fu

ACS Applied Nano Materials· Volume 6· Issue 24
Publisher page

Abstract

The presence of antibiotics in aquatic environments has recently raised significant concerns due to their toxic effects as well as the propagation of antibiotic resistances. Thus, efforts are devoted to developing facile screening methods for sulfonamide antibiotics in waters. In this study, we designed a fluorescent array comprising three structurally different pyrene-based luminescent metal–organic framework (LMOF) sensors and applied it in the simultaneous screening of multiple sulfonamides. The pyrene-based LMOFs produced fluorescence quenching responses to sulfonamides via the static quenching mechanism and/or inner filter effect. The array was able to effectively sense and discriminate five structurally similar sulfonamides (sulfamethoxazole, sulfadiazine, sulfapyridine, sulfamerazine, and sulfamethazine), individual sulfonamide at different concentrations, and mixtures of two sulfonamides with various molar ratios. The detection limit of the pyrene-based MOF array for individual sulfonamide was lower than most previously reported fluorescent sensors. It also afforded a fast sulfonamide response (response equilibrium <2 min) owing to the open and uniform nanoporous structures of the LMOF array elements, which allowed a screening speed as fast as approximately 20 min/100 samples. The constructed array exhibited good performance in the discrimination of sulfonamides in real water samples, validating its practicability. This study provides a convenient strategy for the rapid screening of sulfonamide antibiotics in aquatic environments. It also validates the application potential of LMOF array in fluorescence sensing fields.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · Metal-Organic Frameworks: Synthesis and Applications · Molecular Sensors and Ion Detection

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Pollution Control and Resource Reuse/School of the Environment, Nanjing University, Nanjing, Jiangsu 210046, China

Funding

National Key Research and Development Program of China · National Natural Science Foundation of China

References (59)

Show source-provided references
1. 10.1016/j.chemosphere.2006.03.02610.1016/j.chemosphere.2006.03.026 ↗
2. 10.1021/acs.est.8b0653510.1021/acs.est.8b06535 ↗
3. 10.1002/etc.562019101110.1002/etc.5620191011 ↗
4. 10.1016/j.jhazmat.2011.08.08210.1016/j.jhazmat.2011.08.082 ↗
5. 10.1021/es060737+10.1021/es060737+ ↗
6. 10.1016/j.envint.2013.06.01210.1016/j.envint.2013.06.012 ↗
7. 10.1016/j.envint.2018.04.01110.1016/j.envint.2018.04.011 ↗
8. 10.1016/j.scitotenv.2022.15317810.1016/j.scitotenv.2022.153178 ↗
9. US Environmental Protection Agency. Method 1694: Pharmaceuticals and Personal Care Products in Water, Soil, Sediment, and Biosolids by HPLC/MS/MS. EPA 821/R-08/002. 2007.
10. 10.1021/ac060972a10.1021/ac060972a ↗
11. 10.1016/j.aca.2014.08.02310.1016/j.aca.2014.08.023 ↗
12. 10.1021/cr500552410.1021/cr5005524 ↗
13. 10.1039/b802352m10.1039/b802352m ↗
14. 10.1021/acsami.7b0391410.1021/acsami.7b03914 ↗
15. 10.1021/acsanm.2c0262810.1021/acsanm.2c02628 ↗
16. 10.1039/D0CS00955E10.1039/D0CS00955E ↗
17. 10.1021/acsanm.0c0272710.1021/acsanm.0c02727 ↗
18. 10.1039/D2TC01610A10.1039/D2TC01610A ↗
19. 10.1021/acs.inorgchem.0c0262910.1021/acs.inorgchem.0c02629 ↗
20. 10.1016/j.cclet.2023.10822710.1016/j.cclet.2023.108227 ↗
21. 10.1021/acs.inorgchem.7b0247110.1021/acs.inorgchem.7b02471 ↗
22. 10.1016/j.talanta.2021.12292010.1016/j.talanta.2021.122920 ↗
23. 10.1039/C9CC07869J10.1039/C9CC07869J ↗
24. 10.1021/acs.chemrev.8b0022610.1021/acs.chemrev.8b00226 ↗
25. 10.1039/c3cs60136f10.1039/c3cs60136f ↗
26. 10.1021/acsanm.2c0414210.1021/acsanm.2c04142 ↗
27. 10.1021/acsanm.1c0181710.1021/acsanm.1c01817 ↗
28. 10.1021/acs.chemrev.8b0022610.1021/acs.chemrev.8b00226 ↗
29. 10.1021/acs.accounts.0c0067110.1021/acs.accounts.0c00671 ↗
30. 10.1021/ja507905r10.1021/ja507905r ↗
31. 10.1002/anie.20180960710.1002/anie.201809607 ↗
32. 10.1039/D0CC01156H10.1039/D0CC01156H ↗
33. 10.1039/D0CC01489C10.1039/D0CC01489C ↗
34. 10.1039/D0CC05749E10.1039/D0CC05749E ↗
35. 10.1021/acsami.1c1552810.1021/acsami.1c15528 ↗
36. 10.1038/s41557-021-00647-910.1038/s41557-021-00647-9 ↗
37. 10.1002/anie.20220519310.1002/anie.202205193 ↗
38. 10.1039/D2SC05685B10.1039/D2SC05685B ↗
39. 10.1016/j.talanta.2021.12236610.1016/j.talanta.2021.122366 ↗
40. 10.1021/jacs.7b0218810.1021/jacs.7b02188 ↗
41. 10.1021/ja405082810.1021/ja4050828 ↗
42. 10.1002/adma.20180340110.1002/adma.201803401 ↗
43. 10.1021/acs.chemmater.7b0162410.1021/acs.chemmater.7b01624 ↗
44. 10.1039/C9DT00492K10.1039/C9DT00492K ↗
45. 10.1021/acs.jpcc.5b0606510.1021/acs.jpcc.5b06065 ↗
46. 10.1021/ja070039510.1021/ja0700395 ↗
47. 10.1039/c4cs00003j10.1039/c4cs00003j ↗
48. 10.1021/jacs.8b0498010.1021/jacs.8b04980 ↗
49. 10.1021/jacs.7b0218810.1021/jacs.7b02188 ↗
50. 10.1021/acs.jpcc.1c0642710.1021/acs.jpcc.1c06427 ↗
51. 10.1021/ac403536a10.1021/ac403536a ↗
52. 10.1021/acs.analchem.9b0584110.1021/acs.analchem.9b05841 ↗
53. 10.1016/j.aca.2017.10.02610.1016/j.aca.2017.10.026 ↗
54. 10.1021/la036285l10.1021/la036285l ↗
55. 10.1002/aenm.20190328910.1002/aenm.201903289 ↗
56. 10.1021/la901583810.1021/la9015838 ↗
57. 10.1016/j.cej.2019.12342310.1016/j.cej.2019.123423 ↗
58. 10.1016/j.chemosphere.2010.11.06710.1016/j.chemosphere.2010.11.067 ↗
59. 10.1021/es00005a03910.1021/es00005a039 ↗