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. Author manuscript; available in PMC: 2013 Nov 1.
Published in final edited form as: Nucl Med Biol. 2012 Jun 30;39(8):1105–1116. doi: 10.1016/j.nucmedbio.2012.05.011

Figure 5.

Figure 5

Biodistribution of 8β-(2-[18F]Fluoroethyl)estradiol [18F]6in Immature Female Sprague Dawley Rats with Letrozole and PMSG treatments.The organ most rich in ERα is the uterus, and the organs most rich in ERβ are the ovaries. Uptake of [18F]6 in these organs was low and was not effectively blocked by estradiol (would block uptake by both ERα and ERβ), by DPN (an ERβ-selective ligand that would block uptake by ERβ) and PPT (an ERα-selective ligand that would block uptake by ERα).