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Chapter 17:
Diagnostic Sensing of Specific Proteins in Breast Cancer Cells Using Hollow- Core Photonic Crystal Fiber
Editor(s): E. Y. K. Ng; U. Rajendra Acharya; Rangaraj M. Rangayyan; Jasjit S. Suri
Author(s): Shinoj, Vengalathunadakal Kuttinarayanan, Nanyang Technological Univ.; Murukeshan, Vadakke Matham, Nanyang Technological Univ.; Padmanabhan, Saraswathi, Nanyang Technological Univ.; Padmanabhan, Parasuraman, Singapore BioImaging Consortium
Abstract
The recent drive in biomedical research has been mainly focused on detection, diagnosis, treatment, and prevention of diseases in order to ultimately foster better health. Detection of cancerous tissue or relevant cancer-causing entities using an extremely low sample volume and at an early stage is another targeted objective of researchers in the recent past. From that perspective, ultrasensitive detection and imaging methods are treated as enablers for the advancement of diagnostic methodologies to the next level. The steady progress in biology, engineering, and medicine toward diagnostics based on molecular markers leads to the exploration of high-throughput methods for the detection of biomolecules and their interactions in a biological system. Fluorescence-based bioassays are novel diagnostic tools available to clinicians for deciding on further treatment and to researchers for monitoring biological functions that lead to novel investigations. Protein microarrays are an essential tool in proteomics research and are also used in biomedical applications to determine the presence and/or amount of proteins in a biological sample.1 In recent years, fluorescence assay technologies have played a pivotal role in the high-throughput analysis of proteins and protein interactions. The precise measurement of a fluorescence signal is a prime parameter in analyzing the functional responses of the biological samples. Diagnostics or detection at the molecular level using reporter assays or expression studies are led by improved techniques using fluorescent proteins as biomarkers.
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CHAPTER 17
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