PCA-TLNN-based SERS analysis platform for label-free detection and identification of cisplatin-treated gastric cancer

被引:13
作者
Cao, Dawei [1 ]
Lin, Hechuan [1 ]
Liu, Ziyang [1 ]
Qiu, Jiaji [1 ]
Ge, Shengjie [2 ]
Hua, Weiwei [2 ]
Cao, Xiaowei [2 ]
Qian, Yayun [2 ]
Xu, Huiying [1 ]
Zhu, Xinzhong [1 ]
机构
[1] Zhejiang Normal Univ, Coll Math & Comp Sci, Jinhua 321004, Peoples R China
[2] Yangzhou Univ, Inst Translat Med, Med Coll, Yangzhou 225001, Peoples R China
关键词
Surface -enhanced Raman scattering; Gastric cancer; Au nano -hexagons; Principal component analysis; Two -layer nearest neighbour; ENHANCED RAMAN-SPECTROSCOPY; CLASSIFICATION;
D O I
10.1016/j.snb.2022.132903
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Serum analysis is crucial for favourable prognosis of gastric cancer (GC) and for improving patient survival rates. However, it remains a challenge to develop an effective strategy to accurately identify differences in gastric cancer before and after treatment to guide efficacy evaluation. In this study, we combined surface-enhanced Raman scattering (SERS) with principal component analysis (PCA)-two-layer nearest neighbour (TLNN) to propose a promising serum analytical platform for label-free detection of cisplatin-treated GC mice. A microarray chip fabricated from Au nano-hexagon (AuNH) substrates was employed to measure the SERS spectra of the serum of GC mice at different treatment stages, and then a model for recognition of SERS spectra was constructed using a PCA-TLNN algorithm. The results revealed that the microarray chip exhibited superior portability, SERS activity, stability, and uniformity. Through PCA-TLNN, the GC mice at different treatment stages were successfully segregated, and several key spectral features for distinguishing different treatment stages were captured. The established PCA-TLNN model achieved satisfactory results, with an accuracy of over 97.5%, a sensitivity of over 90%, and a specificity of over 96.7%. Label-free serum SERS in combination with multivariate analysis could serve as a potential technique for the clinical diagnosis and staging of treatments.
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页数:8
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