(a) A dual-port optical imager, which can be positioned
percutaneously by using a guiding needle, has an input to deliver excitation
light into the target and an output to detect emission light from the target.
(b) With real-time ultrasonographic (US) imaging guidance, the
optical imager (arrowheads) is percutaneously inserted to image a target artery
(arrow) that received gene transfer for expressing green fluorescent protein.
(c, d) Direct views from percutaneous optical imaging show that
the emission light is brighter in (d) the green fluorescent
protein–treated artery than in (c) the saline-treated
control artery. (e, f) Results of fluorescent microscopy confirm
higher green fluorescence from both the intima (arrows in f) and
media (M) of (f) the green fluorescent
protein–treated artery compared with (e) the
autofluorescence from the internal elastic lamina (arrows) of the
saline-treated control artery. (Reprinted, with permission, from reference 4.)