DocumentCode
2182688
Title
Design of minimally invasive optical imaging probes to track vascular gene expression: a Monte Carlo simulation analysis
Author
Kumar, Ananda ; Chen, Hunter H. ; Long, Erin ; Yang, Xiaoming
Author_Institution
Departments of Radiol. & Biomed. Eng., Johns Hopkins Univ. Sch. of Med., Baltimore, MD, USA
fYear
2002
fDate
2002
Firstpage
285
Lastpage
288
Abstract
A Monte Carlo simulation analysis of optical probe design for minimally invasive tracking of gene expression in the vasculature was performed. The simulations based on efficient light delivery for excitation of green fluorescent protein (GFP) marker revealed the possibility of using percutaneous probes and intravascular probes to detect gene expression in the vessel walls. A percutaneous probe of 5 mm diameter and an intravascular probe of 2 mm diameter produced identical fluence distribution in the media-intima interface of a diseased aorta for optimal excitation of GFP. But there was a seven-fold increase in the fluence rate in the normal aorta by the intravascular probe.
Keywords
Monte Carlo methods; bio-optics; biomedical optical imaging; blood vessels; cardiovascular system; diseases; fluorescence; genetics; proteins; 2 mm; 5 mm; Monte Carlo simulation analysis; atherosclerotic cardiovascular disease; deep-seated arteries; diseased aorta; efficient light delivery; fluence distribution; fluence rate; gene expression; green fluorescent protein marker; intravascular probes; light propagation; media-intima interface; minimally invasive optical imaging probes; minimally invasive tracking; normal aorta; optical probe design; optimal excitation; percutaneous probes; vascular gene expression; vessel surface; vessel walls; Biomedical optical imaging; Fluorescence; Gene expression; Minimally invasive surgery; Monte Carlo methods; Optical attenuators; Optical design; Optical imaging; Optical scattering; Probes;
fLanguage
English
Publisher
ieee
Conference_Titel
Biomedical Imaging, 2002. Proceedings. 2002 IEEE International Symposium on
Print_ISBN
0-7803-7584-X
Type
conf
DOI
10.1109/ISBI.2002.1029249
Filename
1029249
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