Published February 25, 2010 | Version Published
Book Section - Chapter Open

Molecular photoacoustic imaging using gold nanoparticles as a contrast agent

  • 1. ROR icon Washington University in St. Louis
  • 2. ROR icon The University of Texas Southwestern Medical Center

Abstract

Gold nanoparticles have received much attention due to their potential diagnostic and therapeutic applications. Gold nanoparticles are attractive in many biomedical applications because of their biocompatibility, easily modifiable surfaces for targeting, lack of heavy metal toxicity, wide range of sizes (35-100 nm), tunable plasmonic resonance peak, encapsulated site-specific drug delivery, and strong optical absorption in the near-infrared regime. Specifically, due to their strong optical absorption, gold nanoparticles have been used as a contrast agent for molecular photoacoustic (PA) imaging of tumor. The plasmonic resonance peak of the gold nanocages (AuNCs) was tuned to the near-infrared region, and the ratio of the absorption cross-section to the extinction cross-section was approximately ~70%, as measured by PA sensing. We used PEGylated gold nanocages (PEG-AuNCs) as a passive targeting contrast agent on melanomas. After 6-h intravenous injection of PEG-AuNCs, PA amplitude was increased by ~14 %. These results strongly suggest PA imaging paired with AuNCs is a promising diagnostic tool for early cancer detection.

Additional Information

© 2010 Society of Photo-Optical Instrumentation Engineers (SPIE). This work was supported in part by grants from National Institutes of Health (R01 EB000712, R01 EB008085, and U54 CA136398 -- the Network for Translational Research -- to L.V.W.). L.V.W. has a financial interest in Microphotoacoustics, Inc. and Endra, Inc., which, however, did not support this work. Y.X. thanks the National Institutes of Health for a 2006 Director's Pioneer Award (DP1 OD000798-04). E.C.C. was also partially supported by a fellowship award from the Korea Research Foundation (KRF-2007-357-D00070) funded by the Korean Government. J.C. was supported by a Pilot Grant from Washington University Molecular Imaging Center.

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Identifiers

Eprint ID
89711
Resolver ID
CaltechAUTHORS:20180918-140708286

Funding

NIH
R01 EB000712
NIH
R01 EB008085
NIH
U54 CA136398
NIH
DP1 OD000798-04
National Research Foundation of Korea
KRF-2007-357-D00070
Washington University

Dates

Created
2018-09-19
Created from EPrint's datestamp field
Updated
2021-11-16
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Caltech Custom Metadata

Series Name
Proceedings of SPIE
Series Volume or Issue Number
7564