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Improved brain delivery of AZT using a glycosyl phosphotriester prodrug.

作者信息

Namane A, Gouyette C, Fillion M P, Fillion G, Huynh-Dinh T

机构信息

Unité de Chimie Organique, URA CNRS 487, Institut Pasteur, Paris, France.

出版信息

J Med Chem. 1992 Aug 7;35(16):3039-44. doi: 10.1021/jm00094a018.

DOI:10.1021/jm00094a018
PMID:1501232
Abstract

The concentration of AZT in mice plasma and brain was measured using HPLC after an ingestion of 20 mg/kg of AZT or the molar equivalent of hexadecyl 2-(alpha-D-mannopyranosidyl)ethyl 3'-azido-3'-deoxy-5'-thymidinyl phosphate 3. The results demonstrated the promising qualities of the prodrug 3 which gave AZT-5'-phosphate as the main metabolite: the total concentration of AZT derivatives detected in brain presented a peak of 156 nmol/g (5 nmol/g for AZT) at 1 h; the half-life was about 24 h (1 h for AZT) with an AUC of 4366 nmol h/g as compared to 4 nmol h/g for AZT. The lipophilic properties of 3 were confirmed by its in vitro transport of inside synaptosomes. The derivative 2-(alpha-D-mannopyranosidyl)ethyl 3'-azido-3'-deoxy-5'-thymidinyl phosphate (2) provided also a good delivery of AZT to the central nervous system, with values intermediate between those of AZT and 3.

摘要

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