Majumdar Soumyajit, Hippalgaonkar Ketan, Srirangam Ramesh
Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, MS 38677, USA.
Drug Metab Dispos. 2009 Aug;37(8):1718-25. doi: 10.1124/dmd.108.026450. Epub 2009 Apr 30.
The purpose of this study was to investigate whether topically administered P-glycoprotein (P-gp) substrates/modulators can alter vitreal kinetics of intravitreally administered quinidine. Male New Zealand rabbits were used under anesthesia. Vitreal kinetics of intravitreally administered quinidine (0.75-microg dose) was determined alone and in the presence of verapamil (coadministered topically/intravitreally) or prednisolone hemisuccinate sodium (PHS) (coadministered topically). In the presence of topically instilled verapamil (1% w/v), elimination half-life (t(1/2)) (176 +/- 7 min), apparent elimination rate constant (lambda(z)) (0.0039 +/- 0.0001 min(-1)), and mean retention time (MRT) (143 +/- 30 min) of intravitreally administered quinidine were significantly different from those of the control (105 +/- 11 min, 0.0066 +/- 0.0007 min(-1), and 83 +/- 13 min, respectively). A 2-fold increase in the t(1/2) with a corresponding decrease in lambda(z) and a 1.5-fold increase in the MRT of quinidine were observed in the presence of topically coadministered 2% w/v PHS. Intravitreal coadministration of quinidine and verapamil resulted in a significant increase in t(1/2) (159 +/- 9 min) and a decrease in lambda(z) (0.0043 +/- 0.0002 min(-1)) of quinidine. The vitreal pharmacokinetic parameters of sodium fluorescein, alone or in the presence of topically instilled verapamil, did not show any statistically significant difference, indicating that ocular barrier integrity was not affected by topical verapamil administration. Results from this study suggest that topically applied P-gp substrates/modulators can alter vitreal pharmacokinetics of intravitreally administered P-gp substrates, possibly through the inhibition of P-gp expressed on the basolateral membrane of the retinal pigmented epithelium.
本研究的目的是调查局部应用的P-糖蛋白(P-gp)底物/调节剂是否能改变玻璃体内注射奎尼丁的玻璃体动力学。在麻醉状态下使用雄性新西兰兔。单独测定玻璃体内注射奎尼丁(剂量为0.75微克)的玻璃体动力学,并在维拉帕米(局部/玻璃体内联合给药)或琥珀酸氢化泼尼松钠(PHS)(局部联合给药)存在的情况下进行测定。在局部滴注1%(w/v)维拉帕米的情况下,玻璃体内注射奎尼丁的消除半衰期(t(1/2))(176±7分钟)、表观消除速率常数(lambda(z))(0.0039±0.0001分钟(-1))和平均滞留时间(MRT)(143±30分钟)与对照组(分别为105±11分钟、0.0066±0.0007分钟(-1)和83±13分钟)有显著差异。在局部联合给予2%(w/v)PHS的情况下,观察到奎尼丁的t(1/2)增加了2倍,lambda(z)相应降低,MRT增加了1.5倍。玻璃体内联合注射奎尼丁和维拉帕米导致奎尼丁的t(1/2)显著增加(159±9分钟),lambda(z)降低(0.0043±0.0002分钟(-1))。单独或在局部滴注维拉帕米存在的情况下,荧光素钠的玻璃体药代动力学参数均未显示出任何统计学上的显著差异,表明局部应用维拉帕米不会影响眼屏障的完整性。本研究结果表明,局部应用的P-gp底物/调节剂可能通过抑制视网膜色素上皮基底外侧膜上表达的P-gp来改变玻璃体内注射的P-gp底物的玻璃体药代动力学。