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SU‐FF‐I‐119: Novel MicroCT Imaging Techniques for In Vivo Quantification of Vascular Volume in Murine Tumor Models
Author(s) -
Nyflot M,
Grudzinski J,
Jeraj R
Publication year - 2007
Publication title -
medical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 180
eISSN - 2473-4209
pISSN - 0094-2405
DOI - 10.1118/1.2760495
Subject(s) - in vivo , angiogenesis , medicine , blood volume , nuclear medicine , prostate , pathology , volume (thermodynamics) , biomedical engineering , cancer , cancer research , biology , physics , microbiology and biotechnology , quantum mechanics
Purpose: Growing interest in angiogenesis and anti‐angiogenic tumor therapy has created a demand for vascular imaging techniques. This work describes a method for in vivo quantification of vasculature in murine tumor models using contrast enhanced μCT. Method and Materials: Mice from a prostate tumor line were imaged over a span of three weeks to measure growth, and SCC xenograft mice undergoing anti‐angiogenic therapy with Avastin™ were imaged over eleven days to monitor tumor response. Mice were injected with 0.4 mL of a μCT blood pool contrast agent and scanned using a Siemens Inveon μCT/PET scanner. CT images were manually segmented into tumor and vascular volume in a commercial software package (Amira 4.0, Mercury Computer Systems) and tumor volume was compared to vascular volume. Results: Over the span of three weeks, the prostate model increased in tumor volume by a factor of four and the vascular volume increased by a factor of 15. The ratio of vascular volume to tumor volume increased from 1.5% to 6%. In the xenograft models, a measurable decrease in tumor and vascular volume was seen in both mice, but the ratio of vascular volume to tumor volume stayed relatively constant (approximately 4% in the 400 mm 3 tumor and 17% in the 100 mm 3 tumor). Conclusion: This work demonstrates the capability for in vivo quantification of tumor vasculature with a minimally invasive procedure. In particular, the technique was sufficiently sensitive to monitor vascular growth and to determine a therapeutic effect from molecular therapy over the span of eleven days. This technique may be useful as a tool to better understand the process of tumor‐induced angiogenesis and evaluate the efficacy of targeted molecular therapies.

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