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spelling todo:paper_00214922_v50_n1PART3_p_Chathirat2023-10-03T14:20:48Z A micrograting sensor for DNA hybridization and antibody human serum Albumin-Antigen human serum albumin interaction experiments Chathirat, N. Atthi, N. Hruanun, C. Poyai, A. Leasen, S. Osotchan, T. Hodak, J.H. Amine functional groups Antibody-antigen interactions Antigen-antibody binding Bovine serum albumins Deep reactive ion etching Detection sensitivity DNA hybridization DNA molecules DNA sensing Fiberoptic probes Grating structures Grating surface Human serum albumins Micro gratings Normal incidence Oligonucleotide probes Reflectance spectrum Reflected light Refractive index changes Sensing devices Small spots Spin-on-glass Wavelength shift White light Antibodies Antigens Biosensors Body fluids DNA Experiments Functional groups Oligonucleotides Probes Reactive ion etching Refractive index Silicon nitride Spin glass Spinning (fibers) Surfaces Nucleic acids A biosensor structure comprising silicon nitride (Si3N 4) micrograting arrays coated with a spin-on-glass (SOG) material was investigated. This grating structure was located on a silicon groove, which was etched by a deep reactive ion etching (DRIE) process. The biosensor was used as a specific detector of DNA molecules and antibody-antigen interactions. In our DNA sensing experiments, the first step was the activation of the grating surface with amine functional groups, followed by attachment of a 23-base oligonucleotide probe layer for hybridization with a complementary target DNA. The sensing device was tested for detecting specific antigen/antibody interactions for human serum albumin (HSA) and antigen bovine serum albumin (BSA). The readout system consisted of a white light lamp that illuminated a small spot on the grating surface at normal incidence through a fiber optic probe with a spectrometer used to collect the reflected light through a second fiber. We show that these sensing devices have the capability to detect DNA as well as antigen-antibody binding for HSA. The detection sensitivity for HSA was better than that for DNA mainly owing to the larger size and concomitant refractive index changes upon binding to the sensor. We show that it is possible to quantify the amount of biomolecules bound to the grating surface by measuring the wavelength shift of the reflectance spectra upon exposure to the samples. © 2011 The Japan Society of Applied Physics. Fil:Hodak, J.H. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00214922_v50_n1PART3_p_Chathirat
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Amine functional groups
Antibody-antigen interactions
Antigen-antibody binding
Bovine serum albumins
Deep reactive ion etching
Detection sensitivity
DNA hybridization
DNA molecules
DNA sensing
Fiberoptic probes
Grating structures
Grating surface
Human serum albumins
Micro gratings
Normal incidence
Oligonucleotide probes
Reflectance spectrum
Reflected light
Refractive index changes
Sensing devices
Small spots
Spin-on-glass
Wavelength shift
White light
Antibodies
Antigens
Biosensors
Body fluids
DNA
Experiments
Functional groups
Oligonucleotides
Probes
Reactive ion etching
Refractive index
Silicon nitride
Spin glass
Spinning (fibers)
Surfaces
Nucleic acids
spellingShingle Amine functional groups
Antibody-antigen interactions
Antigen-antibody binding
Bovine serum albumins
Deep reactive ion etching
Detection sensitivity
DNA hybridization
DNA molecules
DNA sensing
Fiberoptic probes
Grating structures
Grating surface
Human serum albumins
Micro gratings
Normal incidence
Oligonucleotide probes
Reflectance spectrum
Reflected light
Refractive index changes
Sensing devices
Small spots
Spin-on-glass
Wavelength shift
White light
Antibodies
Antigens
Biosensors
Body fluids
DNA
Experiments
Functional groups
Oligonucleotides
Probes
Reactive ion etching
Refractive index
Silicon nitride
Spin glass
Spinning (fibers)
Surfaces
Nucleic acids
Chathirat, N.
Atthi, N.
Hruanun, C.
Poyai, A.
Leasen, S.
Osotchan, T.
Hodak, J.H.
A micrograting sensor for DNA hybridization and antibody human serum Albumin-Antigen human serum albumin interaction experiments
topic_facet Amine functional groups
Antibody-antigen interactions
Antigen-antibody binding
Bovine serum albumins
Deep reactive ion etching
Detection sensitivity
DNA hybridization
DNA molecules
DNA sensing
Fiberoptic probes
Grating structures
Grating surface
Human serum albumins
Micro gratings
Normal incidence
Oligonucleotide probes
Reflectance spectrum
Reflected light
Refractive index changes
Sensing devices
Small spots
Spin-on-glass
Wavelength shift
White light
Antibodies
Antigens
Biosensors
Body fluids
DNA
Experiments
Functional groups
Oligonucleotides
Probes
Reactive ion etching
Refractive index
Silicon nitride
Spin glass
Spinning (fibers)
Surfaces
Nucleic acids
description A biosensor structure comprising silicon nitride (Si3N 4) micrograting arrays coated with a spin-on-glass (SOG) material was investigated. This grating structure was located on a silicon groove, which was etched by a deep reactive ion etching (DRIE) process. The biosensor was used as a specific detector of DNA molecules and antibody-antigen interactions. In our DNA sensing experiments, the first step was the activation of the grating surface with amine functional groups, followed by attachment of a 23-base oligonucleotide probe layer for hybridization with a complementary target DNA. The sensing device was tested for detecting specific antigen/antibody interactions for human serum albumin (HSA) and antigen bovine serum albumin (BSA). The readout system consisted of a white light lamp that illuminated a small spot on the grating surface at normal incidence through a fiber optic probe with a spectrometer used to collect the reflected light through a second fiber. We show that these sensing devices have the capability to detect DNA as well as antigen-antibody binding for HSA. The detection sensitivity for HSA was better than that for DNA mainly owing to the larger size and concomitant refractive index changes upon binding to the sensor. We show that it is possible to quantify the amount of biomolecules bound to the grating surface by measuring the wavelength shift of the reflectance spectra upon exposure to the samples. © 2011 The Japan Society of Applied Physics.
format JOUR
author Chathirat, N.
Atthi, N.
Hruanun, C.
Poyai, A.
Leasen, S.
Osotchan, T.
Hodak, J.H.
author_facet Chathirat, N.
Atthi, N.
Hruanun, C.
Poyai, A.
Leasen, S.
Osotchan, T.
Hodak, J.H.
author_sort Chathirat, N.
title A micrograting sensor for DNA hybridization and antibody human serum Albumin-Antigen human serum albumin interaction experiments
title_short A micrograting sensor for DNA hybridization and antibody human serum Albumin-Antigen human serum albumin interaction experiments
title_full A micrograting sensor for DNA hybridization and antibody human serum Albumin-Antigen human serum albumin interaction experiments
title_fullStr A micrograting sensor for DNA hybridization and antibody human serum Albumin-Antigen human serum albumin interaction experiments
title_full_unstemmed A micrograting sensor for DNA hybridization and antibody human serum Albumin-Antigen human serum albumin interaction experiments
title_sort micrograting sensor for dna hybridization and antibody human serum albumin-antigen human serum albumin interaction experiments
url http://hdl.handle.net/20.500.12110/paper_00214922_v50_n1PART3_p_Chathirat
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