Makoid M C, Robinson J R
J Pharm Sci. 1979 Apr;68(4):435-43. doi: 10.1002/jps.2600680411.
The temporal and spatial pattern of [3H]-pilocarpine nitrate distribution in the albino rabbit eye following topical administration was determined. A four-compartment caternary chain model describing this disposition corresponds to the precorneal area, the cornea, the aqueous humor, and the lens and vitreous. Simultaneous computer fitting of data from tissue corresponding to some compartments in the model supported the proposed model. Additional support was provided by the excellent correlation between predicted and observed values in multiple-dosing studies. Several important aspects of ocular drug disposition are evident from the model. The extensive parallel elimination at the absorption site gives rise to an apparent absorption rate constant that is one to two orders of magnitude larger than the true absorption rate constant. In addition, aqueous flow accounts for most of the drug removal. Thus, major effects on absorption and elimination, independent of the drug structure, suggest the possibility of similar pharmacokinetics for vastly different drugs.
测定了局部给药后白化兔眼中[3H]-硝酸毛果芸香碱分布的时空模式。描述这种处置的四室链状模型对应于角膜前区域、角膜、房水以及晶状体和玻璃体。对模型中某些隔室相应组织的数据进行同时计算机拟合,支持了所提出的模型。多次给药研究中预测值与观测值之间的良好相关性提供了额外支持。从该模型可以明显看出眼内药物处置的几个重要方面。吸收部位的广泛平行消除导致表观吸收速率常数比真实吸收速率常数大1至2个数量级。此外,房水流动占药物清除的大部分。因此,与药物结构无关的对吸收和消除的主要影响表明,差异极大的药物可能具有相似的药代动力学。