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Improved oral bioavailability of anti-HIV agent N'-[2-(2-thiophene)ethyl]-N'-[2-(5-bromopyridyl)]-thiourea (HI-443) in a novel lipophilic formulation.
- Source :
-
Arzneimittel-Forschung [Arzneimittelforschung] 2007; Vol. 57 (3), pp. 164-70. - Publication Year :
- 2007
-
Abstract
- N'-[2-(2-Thiophene)ethyl]-N'-[2-(5-bromopyridyl)]-thiourea (CAS 258340-15-7, HI-443) is a rationally designed non-nucleoside reverse transcriptase inhibitor (NNRTI) with potent anti-HIV activity at nanomolar concentrations but poor oral bioavailability. Here the identification of a novel oleic acid containing lead formulation of HI-443 is described which resulted in a approximately 10-fold improvement of its oral bioavailability yielding 10-fold higher systemic exposure levels in mice. Formulated HI-443 exhibited a favorable pharmacokinetics and toxicity profile in mice.
- Subjects :
- Animals
Area Under Curve
Biological Availability
Blood Cell Count
Chemistry, Pharmaceutical
Excipients
Female
Mice
Mice, Inbred BALB C
Pyridines toxicity
Reverse Transcriptase Inhibitors toxicity
Thiourea administration & dosage
Thiourea pharmacokinetics
Thiourea toxicity
Pyridines administration & dosage
Pyridines pharmacokinetics
Reverse Transcriptase Inhibitors administration & dosage
Reverse Transcriptase Inhibitors pharmacokinetics
Thiourea analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 0004-4172
- Volume :
- 57
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Arzneimittel-Forschung
- Publication Type :
- Academic Journal
- Accession number :
- 17469651
- Full Text :
- https://doi.org/10.1055/s-0031-1296600