Lee William A, Martin John C
Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404, USA.
Antiviral Res. 2006 Sep;71(2-3):254-9. doi: 10.1016/j.antiviral.2006.05.020. Epub 2006 Jun 19.
The development of Viread (tenofovir disoproxil) for HIV and Hepsera (adefovir dipivoxil) for HBV presented many unique challenges. Unlike nucleosides and most conventional drugs, the parent acyclic nucleotide analogs are charged at physiologic pH and not suitable for oral administration which is highly desired in chronic therapies. Physicochemical properties, cellular permeation, renal toxicity, and bioavailability all had to be addressed during the development of these compounds. As a class, the acyclic nucleotides have long intracellular half-lives, allowing once-daily dosing, which provided the initial rationale for treatment of chronic viral diseases such as HIV and HBV. Prodrugs originally designed to deliver the parent acyclic nucleotide analog to the systemic circulation, also function to increase the tissue distribution and intracellular concentrations of the acyclic nucleotide diphosphate inside cells.
替诺福韦酯(Viread)用于治疗艾滋病病毒(HIV)以及阿德福韦酯(Hepsera)用于治疗乙型肝炎病毒(HBV)的研发面临诸多独特挑战。与核苷及大多数传统药物不同,无环核苷酸母体类似物在生理pH值下带电荷,不适合口服给药,而口服给药在慢性治疗中是非常理想的。在这些化合物的研发过程中,必须解决物理化学性质、细胞渗透、肾毒性和生物利用度等问题。作为一类药物,无环核苷酸在细胞内具有较长的半衰期,允许每日给药一次,这为治疗诸如HIV和HBV等慢性病毒性疾病提供了最初的理论依据。最初设计用于将无环核苷酸母体类似物输送至体循环的前药,还起到增加无环核苷酸二磷酸在细胞内的组织分布和细胞内浓度的作用。