journal article·2025-01-10

Machine Learning-Empowered Multicolor Detection and Discrimination of Dopaminergic Agents: Utilizing Gold Nanorods for Generating Rainbow Signals

Zahra Hozhabr, Afsaneh Orouji, Mohammad Reza Hormozi-Nezhad

ACS Applied Nano Materials· Volume 8· Issue 1
Publisher page

Abstract

The demand for rapid and sensitive multianalyte detection of dopaminergic agents in assessing the progression of Parkinson’s disease (PD) has attracted recurring interest in recent years. In this study, a multicolor sensor was devised to multiplex detection and discrimination of levodopa ( l -DOPA), carbidopa (Carbi), and benserazide (Benz)─key dopaminergic compounds. Notably, the presence of dopaminergic agents inhibits the etching of gold nanorods (AuNRs) by N -bromosuccinimide (NBS), with varying degrees of inhibition depending on the concentration and properties of the analytes. This interaction induces alterations in the size and aspect ratio of the AuNRs, resulting in a red shift within the plasmonic band. Remarkably, this shift in the plasmonic band of AuNRs corresponds to color variations akin to a rainbow in the solution, providing a valuable opportunity for precise visual detection. Statistical analysis of the collected data set was performed using two machine learning techniques: linear discriminant analysis (LDA) for pattern recognition and partial least-squares regression (PLSR) for regression analysis. LDA effectively discriminated dopaminergic agents and their binary and ternary mixtures with 100% accuracy, while PLSR enabled quantitative analysis over a wide concentration range: 1.17–25.0, 2.63–25.0, and 1.18–25.0 μmol L –1, with detection limits of 0.93, 0.88, and 0.39 μmol L –1, for l -DOPA, Carbi, and Benz, respectively. Furthermore, we validated the practical applicability of the sensor assay by identifying and quantifying dopaminergic agent in medicines tablets containing mixtures of these compounds, affirming its utility and reliability for on-site medicines quality control.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrochemical sensors and biosensors · Spectroscopy and Chemometric Analyses

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

Affiliations

Department of Chemistry

Sharif University of Technology

Center for Nanoscience and Nanotechnology

Institute for Convergence Science & Technology, Sharif University of Technology

Funding

Sharif University of Technology

References (51)

Show source-provided references
1. 10.1021/acschemneuro.7b0028310.1021/acschemneuro.7b00283 ↗
2. 10.1021/acsmeasuresciau.2c0007110.1021/acsmeasuresciau.2c00071 ↗
3. 10.1021/acs.chemrev.3c0047910.1021/acs.chemrev.3c00479 ↗
4. 10.1021/acsomega.0c0337510.1021/acsomega.0c03375 ↗
5. 10.1021/acssensors.9b0112710.1021/acssensors.9b01127 ↗
6. 10.1039/D2NA00524G10.1039/D2NA00524G ↗
7. 10.1039/d1fo00007a10.1039/d1fo00007a ↗
8. 10.1021/jacs.0c0939010.1021/jacs.0c09390 ↗
9. 10.1016/j.microc.2020.10510610.1016/j.microc.2020.105106 ↗
10. 10.1021/acs.bioconjchem.8b0089410.1021/acs.bioconjchem.8b00894 ↗
11. 10.1007/s40262-017-0511-y10.1007/s40262-017-0511-y ↗
12. 10.1021/cn500175910.1021/cn5001759 ↗
13. 10.1021/acschemneuro.1c0069310.1021/acschemneuro.1c00693 ↗
14. 10.1021/acsbiomaterials.4c0104210.1021/acsbiomaterials.4c01042 ↗
15. 10.1021/acssensors.4c0064910.1021/acssensors.4c00649 ↗
16. 10.1007/s40120-024-00635-410.1007/s40120-024-00635-4 ↗
17. 10.1021/acssensors.4c0060210.1021/acssensors.4c00602 ↗
18. 10.18433/J3K92310.18433/J3K923 ↗
19. 10.1016/j.talanta.2010.05.07110.1016/j.talanta.2010.05.071 ↗
20. 10.1002/elan.20050344510.1002/elan.200503445 ↗
21. 10.1002/1522-2683(20000701)21:12<2432::AID-ELPS2432>3.0.CO;2-E10.1002/1522-2683(20000701)21:12<2432::AID-ELPS2432>3.0.CO;2-E ↗
22. 10.1021/acsami.2c1551610.1021/acsami.2c15516 ↗
23. 10.1021/acsomega.3c0179510.1021/acsomega.3c01795 ↗
24. 10.1021/acsanm.3c0458710.1021/acsanm.3c04587 ↗
25. 10.1039/D2AY01797K10.1039/D2AY01797K ↗
26. 10.1039/c2an35101c10.1039/c2an35101c ↗
27. 10.1039/D0AN02171G10.1039/D0AN02171G ↗
28. 10.1039/D0EN00449A10.1039/D0EN00449A ↗
29. 10.1039/D0NA00961J10.1039/D0NA00961J ↗
30. 10.1039/C2CS35367A10.1039/C2CS35367A ↗
31. 10.1021/ja312327m10.1021/ja312327m ↗
32. 10.1039/c3an02164e10.1039/c3an02164e ↗
33. 10.1016/j.ccr.2021.21393410.1016/j.ccr.2021.213934 ↗
34. 10.1039/C9TC00757A10.1039/C9TC00757A ↗
35. 10.1021/acsanm.1c0181710.1021/acsanm.1c01817 ↗
36. 10.1021/jp208106610.1021/jp2081066 ↗
37. 10.1021/acsanm.0c0064110.1021/acsanm.0c00641 ↗
38. 10.1021/acs.analchem.9b0113910.1021/acs.analchem.9b01139 ↗
39. 10.1021/acs.analchem.2c0223610.1021/acs.analchem.2c02236 ↗
40. 10.1039/C7NR03311G10.1039/C7NR03311G ↗
41. Brereton, R. G. Multivariate Pattern Recognition in Chemometrics: Illustrated by Case Studies, 1st ed. Elsevier, 1992; Vol. 9, pp 46.10.1016/S0922-3487(08)70200-4 ↗
42. 10.1039/D4CS00328D10.1039/D4CS00328D ↗
43. 10.1021/acs.analchem.3c0310610.1021/acs.analchem.3c03106 ↗
44. 10.1016/j.aca.2013.03.05610.1016/j.aca.2013.03.056 ↗
45. 10.38212/2224-6614.233010.38212/2224-6614.2330 ↗
46. 10.2169/internalmedicine.8940-2110.2169/internalmedicine.8940-21 ↗
47. 10.1080/00032719.2010.52039510.1080/00032719.2010.520395 ↗
48. 10.1021/bc500366v10.1021/bc500366v ↗
49. 10.3390/s2322914210.3390/s23229142 ↗
50. 10.1021/acs.analchem.3c0190410.1021/acs.analchem.3c01904 ↗
51. 10.1039/C5RA25375F10.1039/C5RA25375F ↗