Abstract

MicroRNAs (miRNAs) play an important regulatory role in tumor progression and have been emerging as promising biomarkers for early diagnosis of breast cancer. Herein, we developed a dual-signal surface-enhanced Raman scattering (SERS) biosensor for the quantitative detection of miRNA 21 (miR-21) by utilizing a tightly ordered spindle-shaped gold (SAu) array with 5, 5′-dithio-bis-(2-nitrobenzoic acid) (DTNB) molecule as an internal standard. Meanwhile, 6-carboxyl-Xrhodamine (ROX) labeled hairpin DNA H1 was linked to the SAu array by Au–S bonds generating another SERS signal. In the presence of miR-21, H1 was turned on with a decrease in SERS signal of ROX, while the SERS signal of DTNB remained stable. The SAu array as substrate provides a large area of hot spots, and the dual-signal can avoid background interference and achieve signal self-calibration. By the dual-signal SERS biosensor, target miR-21 could be detected over a broad linear range (0.1 −105 pM) with a low detection limit (0.046 pM) without signal amplification strategy. Thanks to the SAu array and dual-signal output, the sensor showed high sensitivity, good signal reproducibility, excellent specificity, and high detection accuracy. When this sensor was applied to the miR-21 assay in human serum samples, its performance was comparable to quantitative reverse transcription polymerase chain reaction (qRT-PCR), indicating promising applications of the developed sensor for cancer diagnostics.

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