journal article·2026-03-10

A Dual-Hue Recognizable Lateral Flow Immunoassay Corresponding to Distinct Sensitivity Ranges for Timely and Quantitative Diagnosis of Prostate Cancer

Rong Hu, Xueqiang Zhang, Liang Huang, Jun Hu, Jing Wang

ACS Nano· Volume 20· Issue 9
Publisher page

Abstract

Early cancer screening is pivotal for reducing mortality yet remains constrained by the trade-off between analytical accuracy and operational simplicity. Here, we present a dual-hue recognizable lateral flow immunoassay (DHLFIA) that enables rapid, quantitative, and user-friendly detection of prostate cancer biomarkers. The platform integrates dual-ratiometric fluorescence transitions, establishing two hue recognition pathways (green-to-red and blue-to-red) with distinct sensitivities for the precise quantification of total (t-PSA) and free (f-PSA) prostate-specific antigens. The differentiated color responsiveness of the two ratio system, governed by the inner filter effect, was elucidated both theoretically and experimentally. This dual-hue strategy enables semiquantitative visual discrimination of the clinically significant "gray zone" (t-PSA: 4-10 ng/mL) by the naked eyes, while smartphone-based tonal analysis of the f-PSA/t-PSA ratio (cutoff = 0.16) allows accurate risk stratification within this range. Validated with clinical serum samples, the DHLFIA achieved a diagnostic accuracy of 96.7%, comparable to chemiluminescent assays, yet offered markedly improved speed and ease of operation. By coupling a modular design with dual-ratiometric readout principles, this work establishes a generalizable framework for multiplexed, point-of-care diagnostics of noncommunicable diseases.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Biosensors and Analytical Detection · Advanced biosensing and bioanalysis techniques · Innovative Microfluidic and Catalytic Techniques Innovation

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

Affiliations

State Key Laboratory of Green Chemical Synthesis and Conversion, College of Chemical Engineering

Zhejiang University of Technology

ZJUT Yinhu Research Institute of Innovation and Entrepreneurship Fuyang District, Zhejiang Key Laboratory of Minimal-Perception Technology and Passive Navigation

Analytical & Testing Center

Funding

National Natural Science Foundation of China

References (65)

Show source-provided references
1. 10.1039/C5RA20313A10.1039/C5RA20313A ↗
2. 10.3322/caac.2166010.3322/caac.21660 ↗
3. 10.1186/s12916-015-0296-510.1186/s12916-015-0296-5 ↗
4. 10.1309/JYBPMFNUF6EYY9TB10.1309/JYBPMFNUF6EYY9TB ↗
5. 10.1007/s11255-023-03692-010.1007/s11255-023-03692-0 ↗
6. 10.1016/j.juro.2016.03.01110.1016/j.juro.2016.03.011 ↗
7. 10.1001/jama.279.19.154210.1001/jama.279.19.1542 ↗
8. 10.1016/S0090-4295(99)80192-710.1016/S0090-4295(99)80192-7 ↗
9. 10.1021/acsami.4c0678810.1021/acsami.4c06788 ↗
10. 10.1002/bio.335810.1002/bio.3358 ↗
11. 10.1021/acsnano.5c0156410.1021/acsnano.5c01564 ↗
12. 10.1021/acs.analchem.1c0449110.1021/acs.analchem.1c04491 ↗
13. 10.1002/anie.20171329810.1002/anie.201713298 ↗
14. 10.1021/acs.analchem.8b0497310.1021/acs.analchem.8b04973 ↗
15. 10.1016/j.trac.2025.11849410.1016/j.trac.2025.118494 ↗
16. 10.1002/anie.20200900010.1002/anie.202009000 ↗
17. 10.1002/anie.20181091710.1002/anie.201810917 ↗
18. 10.1016/j.cclet.2024.10983410.1016/j.cclet.2024.109834 ↗
19. 10.1016/j.talanta.2023.12501710.1016/j.talanta.2023.125017 ↗
20. 10.1021/acs.analchem.8b0154310.1021/acs.analchem.8b01543 ↗
21. 10.1021/acs.analchem.4c0578110.1021/acs.analchem.4c05781 ↗
22. 10.1002/smll.20170178210.1002/smll.201701782 ↗
23. 10.1002/smll.20190386110.1002/smll.201903861 ↗
24. 10.1021/acs.analchem.7b0222210.1021/acs.analchem.7b02222 ↗
25. 10.1016/j.bios.2022.11485410.1016/j.bios.2022.114854 ↗
26. 10.1021/acsnano.2c0000810.1021/acsnano.2c00008 ↗
27. 10.1002/smll.20231021210.1002/smll.202310212 ↗
28. 10.1021/acsnano.4c0182410.1021/acsnano.4c01824 ↗
29. 10.1021/acsami.9b0020410.1021/acsami.9b00204 ↗
30. 10.1002/anie.20231324310.1002/anie.202313243 ↗
31. 10.1016/j.bios.2020.11252410.1016/j.bios.2020.112524 ↗
32. 10.1016/j.bios.2018.08.01510.1016/j.bios.2018.08.015 ↗
33. 10.1021/acsnano.7b0153610.1021/acsnano.7b01536 ↗
34. 10.1021/acs.analchem.5b0101110.1021/acs.analchem.5b01011 ↗
35. 10.1021/acsnano.5c0043010.1021/acsnano.5c00430 ↗
36. 10.1021/acs.analchem.4c0086210.1021/acs.analchem.4c00862 ↗
37. 10.1039/D2SC00928E10.1039/D2SC00928E ↗
38. 10.1002/anie.20210345810.1002/anie.202103458 ↗
39. 10.1021/acs.analchem.2c0202010.1021/acs.analchem.2c02020 ↗
40. 10.1021/acs.analchem.3c0375310.1021/acs.analchem.3c03753 ↗
41. 10.1021/acs.analchem.2c0083810.1021/acs.analchem.2c00838 ↗
42. 10.1002/agt2.7003310.1002/agt2.70033 ↗
43. 10.1021/acsanm.2c0369510.1021/acsanm.2c03695 ↗
44. 10.1002/adfm.20231614710.1002/adfm.202316147 ↗
45. 10.1016/j.nantod.2024.10245210.1016/j.nantod.2024.102452 ↗
46. 10.1016/j.aca.2025.34446610.1016/j.aca.2025.344466 ↗
47. 10.1021/acs.nanolett.5c0101210.1021/acs.nanolett.5c01012 ↗
48. 10.1002/admt.20210145010.1002/admt.202101450 ↗
49. 10.1021/acs.analchem.4c0641410.1021/acs.analchem.4c06414 ↗
50. 10.1021/acs.analchem.2c0254410.1021/acs.analchem.2c02544 ↗
51. 10.1016/j.bios.2019.11171910.1016/j.bios.2019.111719 ↗
52. 10.1021/acsami.2c2104210.1021/acsami.2c21042 ↗
53. 10.1021/acs.chemmater.5b0396310.1021/acs.chemmater.5b03963 ↗
54. 10.1021/ja311687310.1021/ja3116873 ↗
55. 10.1002/adfm.20170538010.1002/adfm.201705380 ↗
56. 10.1016/0021-9797(68)90272-510.1016/0021-9797(68)90272-5 ↗
57. 10.1039/D0DT00678E10.1039/D0DT00678E ↗
58. 10.1021/ja058366510.1021/ja0583665 ↗
59. 10.1002/anie.20251080110.1002/anie.202510801 ↗
60. 10.1016/j.trac.2019.11574810.1016/j.trac.2019.115748 ↗
61. 10.1039/D2CC06178C10.1039/D2CC06178C ↗
62. 10.1016/j.trac.2018.11.00210.1016/j.trac.2018.11.002 ↗
63. 10.1021/acs.analchem.3c0370410.1021/acs.analchem.3c03704 ↗
64. 10.1093/clinchem/45.4.48610.1093/clinchem/45.4.486 ↗
65. 10.1155/2004/91387010.1155/2004/913870 ↗