SERS-Spectroscopy for Biosensing

A special issue of Biosensors (ISSN 2079-6374).

Deadline for manuscript submissions: closed (31 March 2020) | Viewed by 11924

Special Issue Editors


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Guest Editor
Head of Laboratory of Applied Plasmonics, Micro- and Nanoelectronics Department, Belarusian State University of Informatics and Radioelectronics, 220013 Minsk, Belarus
Interests: raman spectroscopy; SERS; biomedical analysis; plasmonic and luminescent nanomaterials; wet chemical and electrochemical processing
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Guest Editor
Department of Chemistry and Institute for Lasers, Photonics and Biophotonics, University at Buffalo, State University of New York, Buffalo, NY, USA
Interests: laser physics; nonlinear optics; photonics and biophotonics; biomedical optics; Raman and CARS spectroscopy and imaging
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Over the past fifteen years, we have been observing a drastic increase in the number of research papers on biosensing. Despite the fact that various principles (electrochemical, piezoelectric, thermal, magnetic, micromechanical, etc.) have been used to design biosensing systems, this tendency has been mostly caused by a contribution from works devoted to optical techniques of analysis combined with the unique capabilities of nanostructured materials. As of today, publications on the surface enhanced Raman scattering (SERS) spectroscopy dominate the other optical methods. SERS-based biosensoring combines all of the benefits of ordinary Raman spectroscopy and significant sensitivity. It answers “Yes” or “No” to the question of whether there is a trace amount of target biomolecules in the analyte substance. This technique is able to reveal molecular fingerprints, i.e., to disclose molecular composition and structural changes. A pronounced SERS-effect takes place when the molecules of analyte are arranged near nanoparticles of metals. Considering the biosensing area of interest, SERS-spectroscopy has been subjected to reasonable doubt due to difficulties in catching target molecules in complex substances, the denaturation of proteomic analytes on nanostructures of coinage metals, molecule changes in ‘hot’ spots, the different orientation of macromolecules near the SERS-active surface, and the cytotoxicity of metallic nanoparticles for living cells.. This Special Issue aims to collect the state-of-the-art papers on the recent progress regarding how to overcome the above-mentioned hurdles of SERS-spectroscopy for biosensing. Emphasis should be placed on but not limited to breakthroughs in adaptation of SERS-active substrates for reliable in vivo and in vitro detection, identification, and the qualitative and quantitative study of diverse biologically substantial components. All novel aspects of the fabrication and characterization of SERS-active substrates, the non-conventional handling of SERS principles that allow reliable biosensing, new reports on the detection of any molecules via the combination of the SERS-active substrates, and biological compounds are most welcome. We encourage the preparation of not only research papers but also of review articles summarizing the application of SERS spectroscopy for biosensing in medical diagnosis/therapy, ecology, pharmaceutics, forensic science, and other spheres of human life. We would like to demonstrate that the SERS-technique comes closer to practical biomedical applications for ultrasensitive analysis and, therefore, to the analytical and life science instrumentation industry market.

Dr. Hanna Bandarenka
Dr. Andrey Kuzmin
Guest Editors

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Keywords

  • Surface-enhanced Raman scattering;
  • Fabrication and characterization of SERS-active substrates;
  • Ultrasensitive detection;
  • Functionalization;
  • Microfluidics;
  • Label-free detection;
  • Limit of detection;
  • Biomolecules;
  • Nucleic acids;
  • Proteins and peptides;
  • Enzymes;
  • Lipids;
  • Physiological fluids;
  • Living cells;
  • Medical diagnosis/therapy;
  • Ecology, pharmaceutics;
  • Forensic science.

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Published Papers (2 papers)

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Research

13 pages, 3683 KiB  
Article
Silver SERS Adenine Sensors with a Very Low Detection Limit
by Yonhua Tzeng and Bo-Yi Lin
Biosensors 2020, 10(5), 53; https://doi.org/10.3390/bios10050053 - 15 May 2020
Cited by 26 | Viewed by 5067
Abstract
The detection of adenine molecules at very low concentrations is important for biological and medical research and applications. This paper reports a silver-based surface-enhanced Raman scattering (SERS) sensor with a very low detection limit for adenine molecules. Clusters of closely packed silver nanoparticles [...] Read more.
The detection of adenine molecules at very low concentrations is important for biological and medical research and applications. This paper reports a silver-based surface-enhanced Raman scattering (SERS) sensor with a very low detection limit for adenine molecules. Clusters of closely packed silver nanoparticles on surfaces of discrete ball-like copper bumps partially covered with graphene are deposited by immersion in silver nitrate. These clusters of silver nanoparticles exhibit abundant nanogaps between nanoparticles, where plasmonic coupling induces very high local electromagnetic fields. Silver nanoparticles growing perpendicularly on ball-like copper bumps exhibit surfaces of large curvature, where electromagnetic field enhancement is high. Between discrete ball-like copper bumps, the local electromagnetic field is low. Silver is not deposited on the low-field surface area. Adenine molecules interact with silver by both electrostatic and functional groups and exhibit low surface diffusivity on silver surface. Adenine molecules are less likely to adsorb on low-field sensor surface without silver. Therefore, adenine molecules have a high probability of adsorbing on silver surface of high local electric fields and contribute to the measured Raman scattering signal strength. We demonstrated SERS sensors made of clusters of silver nanoparticles deposited on discrete ball-like copper bumps with very a low detection limit for detecting adenine water solution of a concentration as low as 10−11 M. Full article
(This article belongs to the Special Issue SERS-Spectroscopy for Biosensing)
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12 pages, 1533 KiB  
Article
Application of Aluminum Hydroxide for Improvement of Label-Free SERS Detection of Some Cephalosporin Antibiotics in Urine
by Natalia E. Markina and Alexey V. Markin
Biosensors 2019, 9(3), 91; https://doi.org/10.3390/bios9030091 - 23 Jul 2019
Cited by 23 | Viewed by 6318
Abstract
This report is dedicated to development of surface-enhanced Raman spectroscopy (SERS) based analysis protocol for detection of antibiotics in urine. The key step of the protocol is the pretreatment of urine before the detection to minimize background signal. The pretreatment includes extraction of [...] Read more.
This report is dedicated to development of surface-enhanced Raman spectroscopy (SERS) based analysis protocol for detection of antibiotics in urine. The key step of the protocol is the pretreatment of urine before the detection to minimize background signal. The pretreatment includes extraction of intrinsic urine components using aluminum hydroxide gel (AHG) and further pH adjusting of the purified sample. The protocol was tested by detection of a single antibiotic in artificially spiked samples of real urine. Five antibiotics of cephalosporin class (cefazolin, cefoperazone, cefotaxime, ceftriaxone, and cefuroxime) were used for testing. SERS measurements were performed using a portable Raman spectrometer with 638 nm excitation wavelength and silver nanoparticles as SERS substrate. The calibration curves of four antibiotics (cefuroxime is the exception) cover the concentrations required for detection in patient’s urine during therapy (25/100‒500 μg/mL). Random error of the analysis (RSD < 20%) and limits of quantification (20‒90 μg/mL) for these antibiotics demonstrate the applicability of the protocol for reliable quantitative detection during therapeutic drug monitoring. The detection of cefuroxime using the protocol is not sensitive enough, allowing only for qualitative detection. Additionally, time stability and batch-to-batch reproducibility of AHG were studied and negative influence of the pretreatment protocol and its limitations were estimated and discussed. Full article
(This article belongs to the Special Issue SERS-Spectroscopy for Biosensing)
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