Affiliation:
1. Department of Chemistry Stanford University 380 Roth Way Stanford CA 94305‐5080 USA
2. Veterans Affairs Palo Alto Health Care System 3801 Miranda Avenue Palo Alto CA 94304 USA
3. Department of Pediatrics Stanford University 318 Campus Drive West Stanford CA 94305 USA
4. Department of Cardiothoracic Surgery and Cardiovascular Institute Stanford University 300 Pasteur Drive Stanford CA 94305‐5407 USA
Abstract
AbstractReal‐time optical imaging is a promising approach for visualizing in vivo hemodynamics and vascular structure in mice with experimentally induced peripheral arterial disease (PAD). The application of a novel fluorescence‐based all‐optical imaging approach in the near‐infrared IIb (NIR‐IIb, 1500–1700 nm emission) window, for imaging hindlimb microvasculature and blood perfusion in a mouse model of PAD is reported. In phantom studies, lead sulfide/cadmium sulfide (PbS/CdS) quantum dots show better retention of image clarity, in comparison with single‐walled nanotube (SWNT) NIR‐IIa (1000–1400 nm) dye, at varying depths of penetration. When systemically injected to mice, PbS/CdS demonstrates improved clarity of the vasculature, compared to SWNTs, as well as higher spatial resolution than in vivo microscopic computed tomography. In a mouse model of PAD, NIR‐IIb imaging of the ischemic hindlimb vasculature shows significant improvement in blood perfusion over the course of 10 days (P < 0.05), as well as a significant increase in microvascular density over the first 7 days after induction of PAD. In conclusion, NIR‐IIb imaging of PbS/CdS vascular contrast agent is a useful multifunctional imaging approach for high spatial resolution imaging of the microvasculature and quantification of blood perfusion recovery.
Funder
National Institutes of Health
Cited by
124 articles.
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