Octadecyloxyethyl benzyl tenofovir: A novel tenofovir diester provides sustained intracellular levels of tenofovir diphosphate

• Published in: Antiviral research 2019-11, Vol.171, p.104614-104614, Article 104614
• Main Authors: Beadle, James R., Aldern, Kathy A., Zhang, Xing-Quan, Valiaeva, Nadejda, Hostetler, Karl Y., Schooley, Robert T.
• Format: Article
• Language: English
• Subjects: Adherence; HIV-1 prophylaxis; Long-acting antiretroviral; Tenofovir
• ISSN: 0166-3542; 1872-9096
• DOI: 10.1016/j.antiviral.2019.104614

Pre-exposure prophylaxis (PrEP) with topically or systemically administered antiretroviral agents can prevent acquisition of human immunodeficiency virus type 1 (HIV-1) infection. However, in clinical trials using tenofovir-containing agents, HIV-1 acquisition is reduced but not eliminated. Incomplete adherence remains the major contributor to failure. Sustained release or long-acting antiretroviral agents may provide better HIV-1 protection by reducing the clinical impact of incomplete adherence. To reduce dosing frequency, we synthesized a novel tenofovir prodrug, octadecyloxyethyl benzyl tenofovir (ODE-Bn-TFV), that is designed to release TFV slowly in tissues, and showed potent anti-HIV activity in vitro (EC50 = 1.7 nM). In cells exposed to 14C labeled TFV, ODE-Bn-TFV or the quickly activated monoester ODE-TFV, rapid cellular uptake for both lipophilic analogs was noted, achieving 50-fold higher levels than unmodified TFV after 48 h. Following exposure to ODE-[8–14C]TFV, the intracellular diphosphate levels were approximately four-fold higher than with ODE-Bn-TFV. However, intracellular TFVpp drug levels fell rapidly yielding a half-life of about two days. TFVpp levels in ODE-Bn-TFV treated cells decreased much more slowly and reached half-maximal levels in about seven days. These results suggest early accumulation of ODE-Bn-TFV followed by sustained intracellular release following cleavage of the ester bonds linking the ODE and benzyl moieties to the active molecular precursor, thereby potentially allowing for less frequent administration than with more rapidly activated forms of tenofovir. •Synthesis of octadecyloxyethyl benzyl tenofovir (ODE-Bn-TFV) is described.•ODE-Bn-TFV inhibits HIV-1 replication in PBMCs, EC50 = 1.7 nM.•ODE-Bn-TFV provided sustained intracellular levels of tenofovir diphosphate.