Safety, Pharmacokinetics, and Tissue Distribution of Liposomal P-Ethoxy Antisense Oligonucleotides Targeted to Bcl-2

Antisense oligonucleotides (oligos) have the ability to selectively block disease-causing genes, thereby inhibiting production of disease-associated proteins. However, their effectiveness has been limited by their low intracellular delivery. We had previously demonstrated that liposomes could increa...

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Bibliographic Details
Published in:The Journal of pharmacology and experimental therapeutics 1999-11, Vol.291 (2), p.865
Main Authors: Gutiérrez-Puente, Y, Tari, A M, Stephens, C, Rosenblum, M, Guerra, R T, Lopez-Berestein, G
Format: Article
Language:English
Subjects:
Animals
Genes, bcl-2 - physiology
Kidney - drug effects
Kidney - pathology
Liposomes - administration & dosage
Liposomes - adverse effects
Liposomes - metabolism
Liver - drug effects
Liver - pathology
Mice
Mice, Inbred ICR
Rats
Rats, Inbred Lew
Spleen - pathology
Tissue Distribution
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Summary:Antisense oligonucleotides (oligos) have the ability to selectively block disease-causing genes, thereby inhibiting production of disease-associated proteins. However, their effectiveness has been limited by their low intracellular delivery. We had previously demonstrated that liposomes could increase the intracellular uptake of P-ethoxy oligos, hydrophobic analogs of phosphodiesters, and that liposomal Bcl-2 P-ethoxy antisense oligos (L-Bcl-2) could selectively inhibit Bcl-2 protein production, thereby inducing growth inhibition in Follicular Lymphoma cell lines. To understand the in vivo behavior of L-Bcl-2, we conducted a series of studies to evaluate the safety, pharmacokinetics, and tissue distribution of i.v. injections of L-Bcl-2 in normal rodents. Daily administration of 20 mg of L-Bcl-2/kg of body weight in 5 consecutive days had no adverse effects on renal or hepatic functions, nor on hematological parameters. Histopathology also did not reveal any significant changes in the morphology of the organs studied. In rats, the area under the curve of L-Bcl-2 reflects a two-compartment model of distribution with a biphasic plasma clearance. The T ½α and T ½β were approximately 8 min and 4.2 h, respectively, and the V d was 79 ml, indicating a broad body distribution. The highest concentrations of L-Bcl-2 were found in spleen > liver > kidneys. These studies showed that in the schedules studied no significant toxicity associated with L-Bcl-2 was observed over 6 weeks, and that L-Bcl-2 could be widely distributed in the body.
ISSN:0022-3565
1521-0103