Contrast Agent Enhanced Multimodal Photoacoustic Microscopy and Optical Coherence Tomography for Imaging of Rabbit Choroidal and Retinal Vessels in vivo

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作者
Van Phuc Nguyen
Yanxiu Li
Wei Qian
Bing Liu
Chao Tian
Wei Zhang
Ziyi Huang
Arjun Ponduri
Madison Tarnowski
Xueding Wang
Yannis M. Paulus
机构
[1] University of Michigan,Department of Ophthalmology and Visual Sciences
[2] University of Michigan,Department of Biomedical Engineering
[3] University of Michigan,Department of Electrical Engineering and Computer Science
[4] IMRA America Inc,Department of Radiology
[5] University of Michigan,Department of Ophthalmology, Xiangya Hospital
[6] Central South University,NTT
[7] Nguyen Tat Thanh University,Hitech Insitute
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Scientific Reports | / 9卷
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摘要
Multimodal imaging with photoacoustic microscopy (PAM) and optical coherence tomography (OCT) can be an effective method to evaluate the choroidal and retinal microvasculature. To improve the efficiency for visualizing capillaries, colloidal gold nanoparticles (AuNPs) have been applied as a multimodal contrast agent for both OCT and PAM imaging by taking advantage of the strong optical scattering and the strong optical absorption of AuNPs due to their surface plasmon resonance. Ultra-pure AuNPs were fabricated by femtosecond laser ablation, capped with polyethylene glycol (PEG), and administered to 13 New Zealand white rabbits and 3 Dutch Belted pigmented rabbits. The synthesized PEG-AuNPs (20.0 ± 1.5 nm) were demonstrated to be excellent contrast agents for PAM and OCT, and do not demonstrate cytotoxicity to bovine retinal endothelial cells in cell studies. The image signal from the retinal and choroidal vessels in living rabbits was enhanced by up to 82% for PAM and up to 45% for OCT, respectively, by the administered PEG-AuNPs, which enables detection of individual blood vessels by both imaging modalities. The biodistribution study demonstrated the AuNP accumulated primarily in the liver and spleen. Histology and TUNEL staining did not indicate cell injury or death in the lung, liver, kidney, spleen, heart, or eyes up to seven days after AuNP administration. PEG-AuNPs offer an efficient and safe contrast agent for multimodal ocular imaging to achieve improved characterization of microvasculature.
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