Owada E, Behl C R, Hwang S S, Suhardja L, Flynn G L
J Pharm Sci. 1977 Feb;66(2):216-9. doi: 10.1002/jps.2600660221.
Earlier reports from these laboratories described a procedure for determining vaginal drug absorption in the rabbit based upon a perfusion system, and data on the vaginal absorption of the straight-chain aliphatic alcohols and carboxylic acids were given. These studies have been extended to the rhesus monkey. Rib-cage-type cells were designed for intravaginal insertion through the vulval orifice and to fit the specific dimensions of the monkey vagina. The general design of the cell was similar to that used in the rabbit vaginal absorption studies. The persusion system was checked by using 3H-polyethylene glycol 4000, and no significant leaks from the cell were found. The absorption of the alcohols followed first-order kinetics. The computed apparent permeability coefficients for the alcohols were of comparable magnitude to those previously reported for the rabbit vaginal membrane.
这些实验室早期的报告描述了一种基于灌注系统测定家兔阴道药物吸收的方法,并给出了直链脂肪醇和羧酸阴道吸收的数据。这些研究已扩展到恒河猴。设计了肋骨笼式细胞,用于通过外阴口插入阴道内,并适配猴阴道的特定尺寸。细胞的总体设计与家兔阴道吸收研究中使用的类似。通过使用3H-聚乙二醇4000检查灌注系统,未发现细胞有明显渗漏。醇类的吸收遵循一级动力学。计算得到的醇类表观渗透系数与先前报道的家兔阴道膜的表观渗透系数大小相当。