PURPOSE: To compare the pharmacokinetics and bioavailability of an oligonucleotide delivered in a free form or using cationic or anionic synthetic carrier systems. METHODS: Whole body dynamic quantitative imaging and metabolism of a HIV antisense oligonucleotide intravenously administered either free or incorporated into synthetic carriers were compared in baboons. using non invasive positron emission tomography and an enzyme-based competitive hybridization assay, respectively. RESULTS: In its free form, the oligonucleotide showed high liver and kidney concentration, rapid plasmatic degradation and elimination from the body. Use of a cationic vector slightly protected the oligonucleotide against degradation and enhanced uptake by the reticulo-endothelial system. In contrast, the anionic vector dramatically enhanced the uptake in several organs, including the lungs, spleen and brain, with a prolonged accumulation of radioactivity in the brain. Using this vector, intact oligonucleotide was detected in plasma for up to two hours after injection. and the T 1/2beta and distribution volume increased by 4- and 7-fold, respectively. No evidence of toxicity was found after a single dose administration. CONCLUSIONS: The anionic vector improves significantly the bioavailability and the pharmacokinetics of the oligonucleotide, and is a promising delivery system for in vivo administration of therapeutic nucleic acids.
PURPOSE: To compare the pharmacokinetics and bioavailability of an oligonucleotide delivered in a free form or using cationic or anionic synthetic carrier systems. METHODS: Whole body dynamic quantitative imaging and metabolism of a HIV antisense oligonucleotide intravenously administered either free or incorporated into synthetic carriers were compared in baboons. using non invasive positron emission tomography and an enzyme-based competitive hybridization assay, respectively. RESULTS: In its free form, the oligonucleotide showed high liver and kidney concentration, rapid plasmatic degradation and elimination from the body. Use of a cationic vector slightly protected the oligonucleotide against degradation and enhanced uptake by the reticulo-endothelial system. In contrast, the anionic vector dramatically enhanced the uptake in several organs, including the lungs, spleen and brain, with a prolonged accumulation of radioactivity in the brain. Using this vector, intact oligonucleotide was detected in plasma for up to two hours after injection. and the T 1/2beta and distribution volume increased by 4- and 7-fold, respectively. No evidence of toxicity was found after a single dose administration. CONCLUSIONS: The anionic vector improves significantly the bioavailability and the pharmacokinetics of the oligonucleotide, and is a promising delivery system for in vivo administration of therapeutic nucleic acids.
Authors: F I Raynaud; R M Orr; P M Goddard; H A Lacey; H Lancashire; I R Judson; T Beck; B Bryan; F E Cotter Journal: J Pharmacol Exp Ther Date: 1997-04 Impact factor: 4.030
Authors: P L Felgner; Y Barenholz; J P Behr; S H Cheng; P Cullis; L Huang; J A Jessee; L Seymour; F Szoka; A R Thierry; E Wagner; G Wu Journal: Hum Gene Ther Date: 1997-03-20 Impact factor: 5.695
Authors: R K DeLong; A Nolting; M Fisher; Q Chen; E Wickstrom; M Kligshteyn; S Demirdji; M Caruthers; R L Juliano Journal: Antisense Nucleic Acid Drug Dev Date: 1997-04
Authors: A R Thierry; Y Lunardi-Iskandar; J L Bryant; P Rabinovich; R C Gallo; L C Mahan Journal: Proc Natl Acad Sci U S A Date: 1995-10-10 Impact factor: 11.205