Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells
Attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy has been used widely for probing the molecular properties of materials. Coupling a synchrotron infrared (IR) beam to an ATR element using a high numerical aperture (NA) microscope objective enhances the spatial resolution...
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sg-ntu-dr.10356-1442952020-10-29T20:12:28Z Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells Vongsvivut, Jitraporn (Pimm) Pérez-Guaita, D. Wood, B. R. Heraud, P. Khambatta, K. Hartnell, D. Hackett, M. J. Tobin, M. J. Asian Spectroscopy Conference 2020 Institute of Advanced Studies Science::Chemistry Synchrotron Infrared ATR FTIR Attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy has been used widely for probing the molecular properties of materials. Coupling a synchrotron infrared (IR) beam to an ATR element using a high numerical aperture (NA) microscope objective enhances the spatial resolution, relative to transmission or transflectance microspectroscopy, by a factor proportional to the refractive index (n) of the ATR element. This work presents the development of the synchrotron macro ATR-FTIR microspectroscopy at Australian Synchrotron Infrared Microspectroscopy (IRM) Beamline, and demonstrates that high quality FTIR chemical maps of single cells and tissues can be achieved at an enhanced spatial resolution [1]. Published version 2020-10-27T05:19:54Z 2020-10-27T05:19:54Z 2020 Conference Paper Vongsvivut, J., Pérez-Guaita, D., Wood, B. R., Heraud, P., Khambatta, K., Hartnell, D., ... Tobin, M. J. (2020). Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells. Proc. Of the 7th Asian Spectroscopy Conference (ASC 2020). doi:10.32655/ASC_8-10_Dec2020.43 https://hdl.handle.net/10356/144295 10.32655/ASC_8-10_Dec2020.43 en © 2020 Nanyang Technological University. application/pdf |
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Science::Chemistry Synchrotron Infrared ATR FTIR Vongsvivut, Jitraporn (Pimm) Pérez-Guaita, D. Wood, B. R. Heraud, P. Khambatta, K. Hartnell, D. Hackett, M. J. Tobin, M. J. Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells |
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Attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy has been used widely for probing the molecular properties of materials. Coupling a synchrotron infrared (IR) beam to an ATR element using a high numerical aperture (NA) microscope objective enhances the spatial resolution, relative to transmission or transflectance microspectroscopy, by a factor proportional to the refractive index (n) of the ATR element. This work presents the development of the synchrotron macro ATR-FTIR microspectroscopy at Australian Synchrotron Infrared Microspectroscopy (IRM) Beamline, and demonstrates that high quality FTIR chemical maps of single cells and tissues can be achieved at an enhanced spatial resolution [1]. |
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Asian Spectroscopy Conference 2020 |
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Asian Spectroscopy Conference 2020 Vongsvivut, Jitraporn (Pimm) Pérez-Guaita, D. Wood, B. R. Heraud, P. Khambatta, K. Hartnell, D. Hackett, M. J. Tobin, M. J. |
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Conference or Workshop Item |
author |
Vongsvivut, Jitraporn (Pimm) Pérez-Guaita, D. Wood, B. R. Heraud, P. Khambatta, K. Hartnell, D. Hackett, M. J. Tobin, M. J. |
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Vongsvivut, Jitraporn (Pimm) |
title |
Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells |
title_short |
Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells |
title_full |
Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells |
title_fullStr |
Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells |
title_full_unstemmed |
Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells |
title_sort |
synchrotron macro atr-ftir microspectroscopy for high-resolution chemical mapping of single cells |
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2020 |
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https://hdl.handle.net/10356/144295 |
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