Vidmar V, Jalsenjak I
J Pharm Pharmacol. 1983 Aug;35(8):482-5. doi: 10.1111/j.2042-7158.1983.tb04814.x.
The permeation of barbitone sodium, benzoic acid, and salicylic acid from microcapsules into aqueous medium has been examined at different pH values. The apparent diffusion coefficients of drugs were linearly proportional to the ethyl cellulose/water partition coefficient of drugs, and the straight line parameters were dependent upon volume fractions of water-filled pores (i.e. capsule size), testifying to a previously proposed mechanism of drug permeation. The rate of drug permeation was also a function of the pH-value of the surrounding sink solution; the period of zero order release was longer at low pH because of the change of drug partition or solubility or both.
已在不同pH值下研究了巴比妥钠、苯甲酸和水杨酸从微胶囊向水性介质的渗透情况。药物的表观扩散系数与药物的乙基纤维素/水分配系数呈线性比例关系,且直线参数取决于充水孔隙的体积分数(即胶囊大小),这证实了先前提出的药物渗透机制。药物渗透速率也是周围接收溶液pH值的函数;在低pH值下零级释放期更长,这是由于药物分配或溶解度或两者的变化所致。