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Exogenous-Label-Free Colorimetric/SERS Dual-Mode Immunosensing Platform Driven by Au NCs@Pt Nanozyme for Ultrasensitive and Rapid Detection of the Pancreatic Cancer Biomarker CA19-9.

Analytical chemistry 2026 Vol.98(7) p. 5715-5724

Qi QJ, Xu Z, Yu YF, Guan PC, Lin JS, Zhou JW, Wu Y, Zheng S, Zhang YJ, Li JF

📝 환자 설명용 한 줄

Early diagnosis of pancreatic cancer is critical for improving survival rates, yet conventional CA19-9 immunoassays and labeled surface-enhanced Raman scattering (SERS) methods are often limited by sl

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 연구 설계 cohort study

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BibTeX ↓ RIS ↓
APA Qi QJ, Xu Z, et al. (2026). Exogenous-Label-Free Colorimetric/SERS Dual-Mode Immunosensing Platform Driven by Au NCs@Pt Nanozyme for Ultrasensitive and Rapid Detection of the Pancreatic Cancer Biomarker CA19-9.. Analytical chemistry, 98(7), 5715-5724. https://doi.org/10.1021/acs.analchem.5c08069
MLA Qi QJ, et al.. "Exogenous-Label-Free Colorimetric/SERS Dual-Mode Immunosensing Platform Driven by Au NCs@Pt Nanozyme for Ultrasensitive and Rapid Detection of the Pancreatic Cancer Biomarker CA19-9.." Analytical chemistry, vol. 98, no. 7, 2026, pp. 5715-5724.
PMID 41668424

Abstract

Early diagnosis of pancreatic cancer is critical for improving survival rates, yet conventional CA19-9 immunoassays and labeled surface-enhanced Raman scattering (SERS) methods are often limited by slow processing, complex fabrication, or instability. Herein, we report a rapid, exogenous-label-free colorimetric/SERS dual-mode sandwich immunoassay utilizing coral-like gold nanocores decorated with platinum clusters (Au NCs@Pt). This unique nanozyme architecture synergistically integrates high-density electromagnetic hotspots with efficient peroxidase-like activity to catalyze the oxidation of TMB. The resulting oxidized product (oxTMB) acts as an intrinsic Raman reporter, eliminating the need for exogenous labels and enabling catalysis-amplified signal reporting. The proposed platform achieves quantitative CA19-9 detection within 15 min, featuring a linear range of 1-200 IU/mL and an ultralow limit of detection (LOD) of 0.16 IU/mL. Clinical validation using 60 serum samples demonstrated 100% diagnostic accuracy (AUC = 1.00 in this cohort study). This strategy successfully overcomes the limitations of traditional SERS tags, offering a robust, ultrasensitive tool for the point-of-care screening of digestive system malignancies.

MeSH Terms

Gold; Humans; Pancreatic Neoplasms; Colorimetry; Biomarkers, Tumor; Platinum; Immunoassay; Metal Nanoparticles; Spectrum Analysis, Raman; CA-19-9 Antigen; Limit of Detection