PERFLUOROCARBON DISTRIBUTION TO LIVER, LUNG AND SPLEEN OF EMULSIONS OF PERFLUOROTRIBUTYLAMINE (FTBA) IN PIGS AND RATS AND PERFLUOROOCTYL BROMIDE (PFOB) IN RATS AND DOGS BY F-19 NMR-SPECTROSCOPY
Aj. Mcgoron et al., PERFLUOROCARBON DISTRIBUTION TO LIVER, LUNG AND SPLEEN OF EMULSIONS OF PERFLUOROTRIBUTYLAMINE (FTBA) IN PIGS AND RATS AND PERFLUOROOCTYL BROMIDE (PFOB) IN RATS AND DOGS BY F-19 NMR-SPECTROSCOPY, Artificial cells, blood substitutes, and immobilization biotechnology, 22(4), 1994, pp. 1243-1250
Perfluorocarbon emulsion (FCE) particles are reported to be taken up b
y the reticuloendothelial system (RES) and ultimately eliminated by th
e lung. This distribution provides an opportunity to measure oxygen pa
rtial pressure in vivo with fluorine -19 magnetic resonance imaging (F
-19 MRI). Since the MR image signal-to-noise ratio is directly proport
ional to the fluorine concentration in the tissue, a greater concentra
tion of perfluorocarbon (PFC) in the tissue will result in a greater c
onfidence in the oxygen image and reduce measurement time. it was post
ulated that the biodistribution of PFC administered in emulsion form m
ay depend on species RES or FCE composition. The distribution of an em
ulsion (Oxypherol(TM)-E.T.) containing perfluorotributylamine (FTBA) 5
days after administration to pigs (11 g FTBA/kg body weight i.p.) and
rats (19 g FTBA/kg i.p.) and an emulsion (Oxygent(TM)) containing per
fluorooctyl bromide (PFOB) 7 days after administration to dogs (11 g P
FOB/kg i.v.) and 5 days after administrations to rats (19 g PFOB/kg i.
p.) was analyzed by F-19 NMR spectroscopy of tissue samples. PFC conce
ntrations in spleen are 2 to 3 times those in liver. This pattern appe
ars to be independent of PFC emulsion or species. In contrast, lung PF
C content was less than that in the liver and showed a dependence upon
both species and PFC emulsion.