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Vol. 286, Issue 1, 447-458, July 1998
Isis Pharmaceuticals, Inc., Carlbad Research Center, Carlsbad,
California
In the rat, the liver represents a major site of phosphorothioate
oligodeoxynucleotide deposition after i.v. administration. For this
reason, we examined the intracellular fate of ISIS 1082, a 21-base
heterosequence phosphorothioate oligodeoxynucleotide, isolated from
parenchymal and nonparenchymal cell types after systemic dosing using
established perfusion and separation techniques followed by CGE.
Isolated cells were further fractionated into nuclear, cytosolic and
membrane constituents to assess the intracellular localization,
distribution and metabolic profiles as a function of time and dose.
After a 10-mg/kg i.v. bolus, intracellular drug levels where maximal
after 8 hr and diminished significantly thereafter, suggesting an
active efflux mechanism or metabolism. Nonparenchymal (i.e., Kupffer and endothelial) cells contained
approximately 80% of the total organ cellular dose, and this was
equivalently distributed between the two cell types, while the
remaining 20% was associated with hepatocytes. Nonparenchymal cells
contained abundant nuclear, cytosolic and membrane drug levels over a
wide dose range. In contrast, at doses of less than 25 mg/kg,
hepatocytes contained significantly less drug with no detectable
nuclear-association. Doses at or above 25 mg/kg appeared to saturate
nonparenchymal cell types, whereas hepatocytes continued to accumulate
drug in all cellular compartments, including the nucleus. Our results suggest that although pharmacokinetic parameters vary as a function of
hepatic cell type, significant intracellular delivery can be readily
achieved in the liver after systemic administration.
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