PT - JOURNAL ARTICLE AU - Philip L. Lorenzi AU - Christopher P. Landowski AU - Xueqin Song AU - Katherine Z. Borysko AU - Julie M. Breitenbach AU - Jae Seung Kim AU - John M. Hilfinger AU - Leroy B. Townsend AU - John C. Drach AU - Gordon L. Amidon TI - Amino Acid Ester Prodrugs of 2-Bromo-5,6-dichloro-1-(β-<span class="sc">d</span>-ribofuranosyl)benzimidazole Enhance Metabolic Stability in Vitro and in Vivo AID - 10.1124/jpet.104.082412 DP - 2005 Aug 01 TA - Journal of Pharmacology and Experimental Therapeutics PG - 883--890 VI - 314 IP - 2 4099 - http://jpet.aspetjournals.org/content/314/2/883.short 4100 - http://jpet.aspetjournals.org/content/314/2/883.full SO - J Pharmacol Exp Ther2005 Aug 01; 314 AB - 2-Bromo-5,6-dichloro-1-(β-d-ribofuranosyl)benzimidazole (BDCRB) is a potent and selective inhibitor of human cytomegalovirus (HCMV), but it lacks clinical utility due to rapid in vivo metabolism. We hypothesized that amino acid ester prodrugs of BDCRB may enhance both in vitro potency and systemic exposure of BDCRB through evasion of BDCRB-metabolizing enzymes. To this end, eight different amino acid prodrugs of BDCRB were tested for N-glycosidic bond stability, ester bond stability, Caco-2 cell uptake, antiviral activity, and cytotoxicity. The prodrugs were resistant to metabolism by BDCRB-metabolizing enzymes, and ester bond cleavage was rate-limiting in metabolite formation from prodrug. Thus, BDCRB metabolism could be controlled by the selection of promoiety. In HCMV plaque-formation assays, l-Asp-BDCRB exhibited 3-fold greater selectivity than BDCRB for inhibition of HCMV replication. This potent and selective antiviral activity in addition to favorable stability profile made l-Asp-BDCRB an excellent candidate for in vivo assessment and pharmacokinetic comparison with BDCRB. In addition to rapid absorption and sufficient prodrug activation after oral administration to mice, l-Asp-BDCRB exhibited a 5-fold greater half-life than BDCRB. Furthermore, the sum of area under the concentration-time profile (AUC)BDCRB and AUCprodrug after l-Asp-BDCRB administration was roughly 3-fold greater than AUCBDCRB after BDCRB administration, suggesting that a reservoir of prodrug was delivered in addition to parent drug. Overall, these findings demonstrate that amino acid prodrugs of BDCRB exhibit evasion of metabolizing enzymes (i.e., bioevasion) in vitro and provide a modular approach for translating this in vitro stability into enhanced in vivo delivery of BDCRB. The American Society for Pharmacology and Experimental Therapeutics