Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy

The transverse and longitudinal plasmon resonance in gold nanorods can be exploited to localize the photothermal therapy and influence the fluorescence to monitor the treatment outcome at the same time. While the longitudinal plasmon peak contributes to the photothermal effect, the transverse peak c...

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Main Authors: Kannadorai, Ravi Kumar, Chiew, Geraldine Giap Ying, Luo, Kathy Qian, Liu, Quan
Other Authors: Brown, J. Quincy
Format: Article
Language:English
Published: 2015
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Online Access:https://hdl.handle.net/10356/81179
http://hdl.handle.net/10220/39192
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-811792023-12-29T06:51:32Z Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy Kannadorai, Ravi Kumar Chiew, Geraldine Giap Ying Luo, Kathy Qian Liu, Quan Brown, J. Quincy Deckert, Volker School of Chemical and Biomedical Engineering European Conferences on Biomedical Optics Hyperthermia Autofluorescence Photothermal therapy Fluorescence enhancement Cell viability The transverse and longitudinal plasmon resonance in gold nanorods can be exploited to localize the photothermal therapy and influence the fluorescence to monitor the treatment outcome at the same time. While the longitudinal plasmon peak contributes to the photothermal effect, the transverse peak can enhance fluorescence. After cells take in PEGylated nanorods through endocytosis, autofluorescence from endogenous fluorophores such as nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FAD) in the mitochondria is enhanced two times, which is a good indicator of the respiratory status of the cell. When cells are illuminated continuously with near infrared laser, the temperature reaches the hyperthermic region within the first four minutes, which demonstrates the efficiency of gold nanorods in photothermal therapy. The cell viability test and autofluorescence intensity show good correlation indicating the progress of cell death over time. Published version 2015-12-21T07:12:45Z 2019-12-06T14:23:04Z 2015-12-21T07:12:45Z 2019-12-06T14:23:04Z 2015 Journal Article Kannadorai, R. K., Chiew, G. G. Y., Luo, K. Q., & Liu, Q. (2015). Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy. Proc. SPIE 9537, Clinical and Biomedical Spectroscopy and Imaging IV, 9537, 95371B-. 1605-7422 https://hdl.handle.net/10356/81179 http://hdl.handle.net/10220/39192 10.1117/12.2183581 en Proc. SPIE 9537, Clinical and Biomedical Spectroscopy and Imaging IV © 2015 Society of Photo-optical Instrumentation Engineers. This paper was published in Proc. SPIE 9537, Clinical and Biomedical Spectroscopy and Imaging IV and is made available as an electronic reprint (preprint) with permission of Society of Photo-optical Instrumentation Engineers. The published version is available at: [http://dx.doi.org/10.1117/12.2183581]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. 6 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Hyperthermia
Autofluorescence
Photothermal therapy
Fluorescence enhancement
Cell viability
spellingShingle Hyperthermia
Autofluorescence
Photothermal therapy
Fluorescence enhancement
Cell viability
Kannadorai, Ravi Kumar
Chiew, Geraldine Giap Ying
Luo, Kathy Qian
Liu, Quan
Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy
description The transverse and longitudinal plasmon resonance in gold nanorods can be exploited to localize the photothermal therapy and influence the fluorescence to monitor the treatment outcome at the same time. While the longitudinal plasmon peak contributes to the photothermal effect, the transverse peak can enhance fluorescence. After cells take in PEGylated nanorods through endocytosis, autofluorescence from endogenous fluorophores such as nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FAD) in the mitochondria is enhanced two times, which is a good indicator of the respiratory status of the cell. When cells are illuminated continuously with near infrared laser, the temperature reaches the hyperthermic region within the first four minutes, which demonstrates the efficiency of gold nanorods in photothermal therapy. The cell viability test and autofluorescence intensity show good correlation indicating the progress of cell death over time.
author2 Brown, J. Quincy
author_facet Brown, J. Quincy
Kannadorai, Ravi Kumar
Chiew, Geraldine Giap Ying
Luo, Kathy Qian
Liu, Quan
format Article
author Kannadorai, Ravi Kumar
Chiew, Geraldine Giap Ying
Luo, Kathy Qian
Liu, Quan
author_sort Kannadorai, Ravi Kumar
title Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy
title_short Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy
title_full Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy
title_fullStr Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy
title_full_unstemmed Gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy
title_sort gold nanorods as photothermal agents and autofluorescence enhancer to track cell death during plasmonic photothermal therapy
publishDate 2015
url https://hdl.handle.net/10356/81179
http://hdl.handle.net/10220/39192
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