Optical Biosensors and Their Biomedical Applications

A special issue of Micromachines (ISSN 2072-666X). This special issue belongs to the section "B:Biology and Biomedicine".

Deadline for manuscript submissions: closed (30 April 2026) | Viewed by 1191

Special Issue Editor


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Guest Editor
Department of Electronic Engineering, Pukyong National University, Busan 48513, Republic of Korea
Interests: nanoplasmonics; surface-enhanced Raman spectroscopy; nano-bio interface; biosensors; machine learning

Special Issue Information

Dear Colleagues,

This Special Issue, titled “Optical Biosensors and Their Biomedical Applications”, spotlights the rapid advances and transformative potential of micro- and nanoscale photonic platforms that are reshaping biosensing and cellular analysis. Cutting-edge devices—spanning plasmonic nanoantennas, metamaterial substrates, photonic crystals, and other engineered nanostructures—now deliver sensitivities and specificities once attainable only with bulky laboratory equipment, while providing extreme miniaturization suitable for lab-on-a-chip, fiber, or wearable formats. Featured papers delve into design and fabrication strategies, including surface functionalization, signal-amplifying architectures, and seamless optofluidic or semiconductor integration. Techniques such as surface-enhanced Raman spectroscopy (SERS) figure prominently for label-free molecular fingerprinting at ultra-low levels, even within complex biological matrices. This Special Issue highlights how these sensors enable early disease diagnosis, real-time therapeutic monitoring, high-throughput drug screening, and targeted drug delivery by precisely detecting and manipulating biomolecules, cells, and biomarkers. Alongside fundamental studies that unravel light–matter interactions at the nanoscale, authors present demonstrations in clinically relevant contexts, underscoring pathways toward point-of-care testing and personalized medicine. Collectively, the contributions chart the future of biomedical optics, where compact, high-performance sensors promise to improve healthcare outcomes across scales—from single-cell interrogation to systemic monitoring in vivo.

Dr. Wonil Nam
Guest Editor

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Keywords

  • surface-enhanced Raman spectroscopy (SERS)
  • plasmonic nanoantenna
  • microfluidic biosensor
  • lab-on-a-chip
  • photonic crystal sensor
  • whispering-gallery-mode microresonator
  • optical microfiber
  • optofluidics
  • fluorescence lifetime imaging
  • intracellular sensing
  • optoporation
  • wearable optical sensor
  • point-of-care diagnostics
  • nanoplasmonics
  • single-molecule detection

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Published Papers (2 papers)

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Research

11 pages, 4036 KB  
Article
Label-Free Malignancy Phenotyping of Living Cancer Cells by High-Performance Surface-Enhanced Raman Spectroscopy Substrates
by Jiwon Yun, Hyeim Yu, Youngho Yun and Wonil Nam
Micromachines 2026, 17(4), 461; https://doi.org/10.3390/mi17040461 - 9 Apr 2026
Viewed by 377
Abstract
Surface-enhanced Raman spectroscopy (SERS) amplifies Raman scattering by placing molecules in the near-field of plasmonic nanostructures, enabling label-free molecular fingerprinting. While attractive for living cell phenotyping, many cellular SERS works rely on internalized colloidal nanoparticles, leading to variable uptake/localization, aggregation-driven hotspot fluctuations, and [...] Read more.
Surface-enhanced Raman spectroscopy (SERS) amplifies Raman scattering by placing molecules in the near-field of plasmonic nanostructures, enabling label-free molecular fingerprinting. While attractive for living cell phenotyping, many cellular SERS works rely on internalized colloidal nanoparticles, leading to variable uptake/localization, aggregation-driven hotspot fluctuations, and potential cellular perturbation. Here, we report a chip-like Au/SiO2 nanolaminate SERS substrate that supports direct culture and label-free measurements of living cells on spatially defined hotspots without nanoparticle uptake. The periodic nanolaminate forms dense nanogaps and is engineered for 785 nm excitation, providing uniform enhancement over a large, culture-compatible area with high hotspot uniformity. By engineering the cell–substrate nano–bio interface, the platform enables reproducible acquisition of intrinsic cellular vibrational fingerprints under physiological conditions without Raman tags. Using MCF-7 and MDA-MB-231 breast cancer cells, we collected hundreds of spectra per line, and MDA-MB-231 exhibited broader spectral variations, indicating greater heterogeneity. Principal component analysis and linear discriminant analysis achieved 99% classification accuracy for MCF-7 and MDA-MB-231, and bright-field imaging confirmed preserved adhesion and canonical morphologies. This chip-based, label-free living cell SERS platform enables scalable, nonperturbative phenotyping and may support rapid malignancy classification and treatment response screening across subtle cancer states. Full article
(This article belongs to the Special Issue Optical Biosensors and Their Biomedical Applications)
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15 pages, 2752 KB  
Article
Development of a Highly Sensitive SPR Biosensor for BCR–ABL Gene Sequence Detection Using a Novel Gold Nanoparticle–Enhanced Sandwich Assay Format
by Maksym S. Sobolevskyi, Andrii M. Lopatynskyi, Anton V. Samoylov, Glib V. Dorozinsky, Oleksandr M. Lyapin, Roman V. Khrystosenko, Volodymyr I. Chegel, Viktoriya M. Pyeshkova, Abdelhamid Errachid, Sergei V. Dzyadevych and Oleksandr O. Soldatkin
Micromachines 2026, 17(4), 426; https://doi.org/10.3390/mi17040426 - 30 Mar 2026
Viewed by 513
Abstract
SPR (surface plasmon resonance) biosensor–based analytical methods enable rapid, straightforward, and cost-effective detection of DNA oligonucleotides. However, the detection limits of currently available SPR biosensors for BCR–ABL gene oligonucleotides remain too high to reliably detect sub-nanomolar concentrations. This study presents a new signal-enhancement [...] Read more.
SPR (surface plasmon resonance) biosensor–based analytical methods enable rapid, straightforward, and cost-effective detection of DNA oligonucleotides. However, the detection limits of currently available SPR biosensors for BCR–ABL gene oligonucleotides remain too high to reliably detect sub-nanomolar concentrations. This study presents a new signal-enhancement approach for SPR DNA biosensors based on a gold nanoparticle (AuNP) sandwich assay. In this work, we demonstrated that AuNP-modified oligonucleotides can serve as labels that significantly amplify the SPR biosensor response in a sandwich-type SPR DNA biosensor. The analytical characteristics of the developed AuNP-labeled biosensor for detection of BCR–ABL fusion gene oligonucleotides were studied. The AuNP-labeled biosensor exhibited a detection limit of 80 pM, which is significantly lower than that of a traditional label-free SPR biosensor (50 nM). The measurement error for BCR–ABL target detection was significantly lower with the AuNP-labeled biosensor than with the label-free SPR biosensor. The conditions of synthesis of AuNPs by citrate reduction of AuCl3 that allow the monodisperse size distribution and absence of AuNP aggregation were established as well. Based on the obtained data, we conclude that a sandwich assay employing AuNP-modified oligonucleotides as labels is a promising approach for the highly sensitive detection of genetic markers. The developed AuNP-labeled DNA biosensing approach can be adapted to enhance the signal in other DNA hybridization-based SPR biosensors. Full article
(This article belongs to the Special Issue Optical Biosensors and Their Biomedical Applications)
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