Rapid Identification of Drug Mechanisms with Deep Learning-Based Multichannel Surface-Enhanced Raman Spectroscopy

被引:0
|
作者
Sun, Jiajia [1 ]
Lai, Wei [2 ]
Zhao, Jiayan [1 ]
Xue, Jinhong [1 ]
Zhu, Tong [1 ]
Xiao, Mingshu [1 ]
Man, Tiantian [3 ]
Wan, Ying [3 ]
Pei, Hao [1 ]
Li, Li [1 ]
机构
[1] East China Normal Univ, Shanghai Frontiers Sci Ctr Genome Editing & Cell T, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200241, Peoples R China
[2] Hubei Univ Automot Technol, Sch Math Phys & Optoelect Engn, Hubei Key Lab Energy Storage & Power Battery, Shiyan 442002, Peoples R China
[3] Nanjing Univ Sci & Technol, Sch Mech Engn, Nanjing 210094, Peoples R China
来源
ACS SENSORS | 2024年 / 9卷 / 08期
关键词
SERS; drug mechanisms; artificial nose; self-assembled monolayers; convolutional neural network; EXPRESSION SIGNATURES; METASTATIC CELLS; GOLD; SCATTERING; SERS; DIFFERENTIATION; CLASSIFICATION; PHENOTYPE; PROTEIN; FILMS;
D O I
10.1021/acssensors.4c01205
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rapid identification of drug mechanisms is vital to the development and effective use of chemotherapeutics. Herein, we develop a multichannel surface-enhanced Raman scattering (SERS) sensor array and apply deep learning approaches to realize the rapid identification of the mechanisms of various chemotherapeutic drugs. By implementing a series of self-assembled monolayers (SAMs) with varied molecular characteristics to promote heterogeneous physicochemical interactions at the interfaces, the sensor can generate diversified SERS signatures for directly high-dimensionality fingerprinting drug-induced molecular changes in cells. We further train the convolutional neural network model on the multidimensional SAM-modulated SERS data set and achieve a discriminatory accuracy toward 99%. We expect that such a platform will contribute to expanding the toolbox for drug screening and characterization and facilitate the drug development process.
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页码:4227 / 4235
页数:9
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