Quantitative detection of a1-acid glycoprotein (AGP) level in blood plasma using SERS and CNN transfer learning approach; Sensors and Actuators B: Chemical; Vol. 367

التفاصيل البيبلوغرافية
Parent link:Sensors and Actuators B: Chemical
Vol. 367.— 2022.— [132057, 8 p.]
مؤلف مشترك: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
مؤلفون آخرون: Erzina M. Mariia, Trelin A., Guselnikova O. A. Olga Andreevna, Skvortsova A., Strnadova K., Svorcik V., Lyutakov O. Oleksy
الملخص:Title screen
Surface-enhanced Raman spectroscopy (SERS) is a highly sensitive tool in medical diagnostics and bioanalysis fields, aimed at the qualitative detection of relevant biomolecules. However, quantitative SERS analysis of complex (bio)samples is a more challenging and, in many cases, almost impossible task, requiring functional SERS substrates or advanced spectral data analysis. In this work, we propose the combination of a functional SERS substrate, capable of trapping target biomolecules, with CNN transfer learning for quantitative detection of the relevant a1-acid glycoprotein (AGP, also known as orosomucoid) in human serum. As a SERS substrate, the plasmonic gold grating was functionalized with boronic acid moieties to entrap target AGP. The functionality of the substrate was tested on two model solutions: a solution containing saccharides as competing molecules and human serum with added AGP, which is close to real samples. The convolution neural network (CNN) was previously trained on a huge number of (bio)samples. Then CNN transfer learning was used to quantify AGP concentration in model samples, as well as in human serum. Developed strategy is able to identify the alarming increase of AGP concentration in an express and medically decentralized way, on short time and under lack of spectral data. Generally, the proposed combination of SERS and machine transfer learning could be expanded to a range of alternative cases, where the collection of real samples is restricted and can be substituted by the measurements of similar model systems, without loss of analysis reliability.
اللغة:الإنجليزية
منشور في: 2022
الموضوعات:
الوصول للمادة أونلاين:https://doi.org/10.1016/j.snb.2022.132057
التنسيق: الكتروني فصل الكتاب
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=668625

MARC

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200 1 |a Quantitative detection of a1-acid glycoprotein (AGP) level in blood plasma using SERS and CNN transfer learning approach  |f M. Erzina, A. Trelin, O. A. Guselnikova [et al.] 
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330 |a Surface-enhanced Raman spectroscopy (SERS) is a highly sensitive tool in medical diagnostics and bioanalysis fields, aimed at the qualitative detection of relevant biomolecules. However, quantitative SERS analysis of complex (bio)samples is a more challenging and, in many cases, almost impossible task, requiring functional SERS substrates or advanced spectral data analysis. In this work, we propose the combination of a functional SERS substrate, capable of trapping target biomolecules, with CNN transfer learning for quantitative detection of the relevant a1-acid glycoprotein (AGP, also known as orosomucoid) in human serum. As a SERS substrate, the plasmonic gold grating was functionalized with boronic acid moieties to entrap target AGP. The functionality of the substrate was tested on two model solutions: a solution containing saccharides as competing molecules and human serum with added AGP, which is close to real samples. The convolution neural network (CNN) was previously trained on a huge number of (bio)samples. Then CNN transfer learning was used to quantify AGP concentration in model samples, as well as in human serum. Developed strategy is able to identify the alarming increase of AGP concentration in an express and medically decentralized way, on short time and under lack of spectral data. Generally, the proposed combination of SERS and machine transfer learning could be expanded to a range of alternative cases, where the collection of real samples is restricted and can be substituted by the measurements of similar model systems, without loss of analysis reliability. 
338 |b Российский научный фонд  |d 19-73-00238 
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610 1 |a serum 
610 1 |a CNN transfer learning 
701 1 |a Erzina  |b M.  |g Mariia 
701 1 |a Trelin  |b A. 
701 1 |a Guselnikova  |b O. A.  |c chemist  |c Researcher at Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1992-  |g Olga Andreevna  |3 (RuTPU)RU\TPU\pers\34478  |9 17861 
701 1 |a Skvortsova  |b A. 
701 1 |a Strnadova  |b K. 
701 1 |a Svorcik  |b V. 
701 1 |a Lyutakov  |b O.  |c chemist-technologist  |c Associate Scientist of Tomsk Polytechnic University  |f 1982-  |g Oleksy  |3 (RuTPU)RU\TPU\pers\36875 
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