In vitro protein-binding characteristics of delavirdine and its N-dealkylated metabolite

被引:12
作者
Chaput, AJ
DAmbrosio, R
Morse, GD
机构
[1] SUNY BUFFALO,DEPT PHARM PRACTICE,LAB ANTIVIRAL RES,BUFFALO,NY 14260
[2] SUNY BUFFALO,DEPT MED,BUFFALO,NY 14260
关键词
delavirdine; protein binding; HIV; reverse transcriptase inhibitor; pharmacokinetics; bisheteroarylpiperazine;
D O I
10.1016/0166-3542(95)00984-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study was performed to determine delavirdine protein-binding characteristics as well as those of its N-dealkylated metabolite (N-DLV). Initial studies of 36 mu M delavirdine and 30 mu M N-DLV in solutions of plasma, albumin 4 g%, alpha-1-acid glycoprotein (AAG) 100 mg% or immune globulin (IVIG) 5 g% were conducted. Delavirdine (12, 36 and 73 mu M) and N-DLV (10, 30 and 60 mu M) were then studied alone and in combination in plasma and various concentrations of albumin. Studies were done in triplicate using equilibrium dialysis. The mean delavirdine fraction unbound (f(u)) in plasma, albumin, IVIG and AAG was 0.013, 0.033, 0.752 and 0.912 while the mean f(u) of N-DLV in these same protein solutions was 0.139, 0.195, 0.329 and 0.359. In plasma and albumin, a greater f(u) was observed at higher delavirdine concentrations and no significant changes in f(u) were noted with the addition of N-DLV. An increase in delavirdine f(u) was noted as the albumin concentrations decreased. The f(u) of N-DLV increased significantly as the concentration of albumin decreased as well as with decreasing N-DLV concentration. The potential implications of extensive delavirdine binding to plasma proteins, primarily albumin, are discussed.
引用
收藏
页码:81 / 89
页数:9
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