Gulati Abhishek, Boudinot F Douglas, Gerk Phillip M
Department of Pharmaceutics, Virginia Commonwealth University, MCV Campus, 410 N. 12th Street, Richmond, VA, USA.
Drug Metab Dispos. 2009 Aug;37(8):1572-5. doi: 10.1124/dmd.109.026708. Epub 2009 May 13.
HIV protease inhibitors are an important component of highly active antiretroviral therapy used to treat pregnant women infected with HIV. They have a low placental transfer and are highly plasma protein bound. This study was carried out to determine the unbound fraction of lopinavir in cord blood, and to characterize the binding of lopinavir to alpha(1)-acid glycoprotein (AAG) and human serum albumin (HSA), and displacement by ritonavir. Serum was obtained from cord blood from placentas obtained after cesarean section of healthy, non-HIV-infected women (n = 4). The unbound fraction of lopinavir in serum obtained from this cord blood was 0.022 +/- 0.011%. The unbound fraction of lopinavir in separately obtained maternal serum samples (n = 4) was 0.89 +/- 0.12%, which was not significantly different from that observed with cord serum samples. Varying concentrations of lopinavir, AAG, and HSA in buffer solutions were then used to characterize the lopinavir binding. The data were fit to obtain the number of binding sites (N) and equilibrium dissociation constant (K(D)). Binding of lopinavir to AAG (7-23 microM) was saturable with K(D) of 5.0 +/- 1.1 microM and N of 1.2 +/- 0.2. At low HSA concentrations (15-152 microM), lopinavir binding K(D) was 24.3 +/- 8.7 microM and N was 1.1 +/- 0.4; however, at 758 microM, lopinavir binding was essentially unsaturable. Lopinavir binding to AAG and HSA was not sensitive to ritonavir, and, thus, efforts to enhance fetal exposure to lopinavir should be focused on other issues such as efflux transporters.
HIV蛋白酶抑制剂是用于治疗感染HIV的孕妇的高效抗逆转录病毒疗法的重要组成部分。它们的胎盘转运率低,且与血浆蛋白高度结合。本研究旨在测定洛匹那韦在脐血中的游离分数,表征洛匹那韦与α1-酸性糖蛋白(AAG)和人血清白蛋白(HSA)的结合情况,以及利托那韦对其的置换作用。血清取自健康、未感染HIV的妇女剖宫产术后胎盘的脐血(n = 4)。从该脐血获得的血清中洛匹那韦的游离分数为0.022±0.011%。在单独获得的母体血清样本(n = 4)中,洛匹那韦的游离分数为0.89±0.12%,与脐血血清样本中观察到的结果无显著差异。然后使用缓冲溶液中不同浓度的洛匹那韦、AAG和HSA来表征洛匹那韦的结合情况。对数据进行拟合以获得结合位点数量(N)和平衡解离常数(KD)。洛匹那韦与AAG(7 - 23 microM)的结合具有饱和性,KD为5.0±1.1 microM,N为1.2±0.2。在低HSA浓度(15 - 152 microM)下,洛匹那韦结合KD为24.3±8.7 microM,N为1.1±0.4;然而,在758 microM时,洛匹那韦结合基本不饱和。洛匹那韦与AAG和HSA的结合对利托那韦不敏感,因此,提高胎儿对洛匹那韦暴露的努力应集中在其他问题上,如外排转运体。