Indocyanine green-enhanced multimodal photoacoustic microscopy and optical coherence tomography molecular imaging of choroidal neovascularization

被引:12
作者
Van Phuc Nguyen [1 ,2 ]
Folz, Jeff [3 ]
Li, Yanxiu [1 ]
Henry, Jessica [1 ]
Zhang, Wei [4 ]
Qian, Thomas [1 ]
Wang, Xueding [4 ]
Paulus, Yannis M. [1 ,4 ]
机构
[1] Univ Michigan, Dept Ophthalmol & Visual Sci, 1000 Wall St, Ann Arbor, MI 48105 USA
[2] Nguyen Tat Thanh Univ, NTT Hi Tech Inst, Ho Chi Minh, Vietnam
[3] Univ Michigan, Biophys Program, Ann Arbor, MI 48105 USA
[4] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48105 USA
关键词
choroidal neovascularization; contrast agent; indocyanine green; multimodal imaging modality; optical coherence tomography; photoacoustic microscopy;
D O I
10.1002/jbio.202000458
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Photoacoustic microscopy (PAM) has great potential for visualization of the microvasculature with high spatial resolution and contrast. Early detection and differentiation of newly developed blood vessels named choroidal neovascularization (CNV) from normal vasculature remains a challenge in ophthalmology. Exogenous contrast agents can assist with improving PAM sensitivity, leading to differentiation of CNV. Here, an FDA-approved indocyanine green (ICG) was utilized as a PAM contrast agent. ICG was conjugated with RGD peptides, allowing the ICG to bind to the integrin expressed in CNV. Molecular PAM imaging showed that ICG-RGD can target CNV for up to 5 days post intravenous administration in living rabbits with a model of CNV. The PAM image sensitivity and image contrast were significantly enhanced by 15-fold at 24 h post-injection. Overall, the presented approach demonstrates the possibility of targeted ICG to be employed in PAM molecular imaging, allowing more precise evaluation of neovascularization.
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页数:17
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