TY - GEN
T1 - Near-infrared fluorophore capped gold nanostars for enhanced detection of choroidal neovascularization in living rabbits using multimodal photoacoustic microscopy, optical coherence tomography, and fluorescence microscopy
AU - Nguyen, Van Phuc
AU - Li, Yanxiu
AU - Henry, Jeßica
AU - Aaberg, Michael
AU - Jones, Sydney
AU - Qian, Thomas
AU - Zhang, Wei
AU - Wang, Xueding
AU - Paulus, Yannis M.
N1 - Publisher Copyright:
© COPYRIGHT SPIE. Downloading of the abstract is permitted for personal use only.
PY - 2020
Y1 - 2020
N2 - Enhanced visualization of choroidal neovascularization (CNV) is critical to the precise diagnosis and treatment for patients with neovascular eye diseases such as wet macular degeneration. Currently, eye clinics lack an imaging modality that can precisely detect and visualize the position and margins of CNV in three-dimensions. This study shows that a unique multimodal photoacoustic microscopy, optical coherence tomography, and florescence microscopy system can accurately identify CNV in living rabbits with high resolution and image contrast at a sub-10-micron scale. In addition, to better visualize CNV and distinguish it from normal blood veßels, the peptide RGD targeting neovascularization was conjugated with gold nanostars (GNS) capped with photostable near-infrared (NIR) fluorophore alexa fluor 790 (AF790). Four New Zealand white rabbits with laser-induced CNV were intravenously administered with 400μL of GNS at a concentration of 5 mg/mL. The accumulation of GNS at CNV was monitored by multimodal OCT, PAM, color fundus photographs, fluorescein angiography (FA), and indocyanine green angiography (ICGA) at various time points: 1 h, 2 h, 4 h, 8 h, 24 h, 48 h, 72 h, day 4, day 7, day 9, day 11, and day 14. The experimental results show that GNS accumulation occurs in the region of CNV. The GNS were detected by all three imaging modalities both in vitro and in living rabbits. The PA signal was increased 19-fold 24 h post-injection. In addition, fluorescence signal gradually decreased over time. Histological analysis and TUNEL aßay show no toxicity in the rabbit at the administered concentrations. Therefore, GNS-aßisted multimodal imaging has the poßibility to improve microvasculature imaging.
AB - Enhanced visualization of choroidal neovascularization (CNV) is critical to the precise diagnosis and treatment for patients with neovascular eye diseases such as wet macular degeneration. Currently, eye clinics lack an imaging modality that can precisely detect and visualize the position and margins of CNV in three-dimensions. This study shows that a unique multimodal photoacoustic microscopy, optical coherence tomography, and florescence microscopy system can accurately identify CNV in living rabbits with high resolution and image contrast at a sub-10-micron scale. In addition, to better visualize CNV and distinguish it from normal blood veßels, the peptide RGD targeting neovascularization was conjugated with gold nanostars (GNS) capped with photostable near-infrared (NIR) fluorophore alexa fluor 790 (AF790). Four New Zealand white rabbits with laser-induced CNV were intravenously administered with 400μL of GNS at a concentration of 5 mg/mL. The accumulation of GNS at CNV was monitored by multimodal OCT, PAM, color fundus photographs, fluorescein angiography (FA), and indocyanine green angiography (ICGA) at various time points: 1 h, 2 h, 4 h, 8 h, 24 h, 48 h, 72 h, day 4, day 7, day 9, day 11, and day 14. The experimental results show that GNS accumulation occurs in the region of CNV. The GNS were detected by all three imaging modalities both in vitro and in living rabbits. The PA signal was increased 19-fold 24 h post-injection. In addition, fluorescence signal gradually decreased over time. Histological analysis and TUNEL aßay show no toxicity in the rabbit at the administered concentrations. Therefore, GNS-aßisted multimodal imaging has the poßibility to improve microvasculature imaging.
KW - Choroidal neovascularization (CNV)
KW - Fluorescence microscopy
KW - Gold nanostars (GNS)
KW - Optical coherence tomography
KW - Organic fluorophore
KW - Photoacoustic microscopy
KW - Retinal imaging contrast agents
UR - https://www.scopus.com/pages/publications/85082751506
UR - https://www.scopus.com/pages/publications/85082751506#tab=citedBy
U2 - 10.1117/12.2543214
DO - 10.1117/12.2543214
M3 - Conference contribution
AN - SCOPUS:85082751506
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Multimodal Biomedical Imaging XV
A2 - Azar, Fred S.
A2 - Intes, Xavier
A2 - Fang, Qianqian
PB - SPIE
T2 - Multimodal Biomedical Imaging XV 2020
Y2 - 1 February 2020
ER -