Fantini Sebastien, Clohessy Jason, Gorgy Karine, Fusalba Florence, Johans Christoffer, Kontturi Kyösti, Cunnane Vincent J
Materials Surface Sciences Institute, Department of Chemical and Environmental Sciences, University of Limerick, Limerick, Ireland.
Eur J Pharm Sci. 2003 Mar;18(3-4):251-7. doi: 10.1016/s0928-0987(03)00018-6.
The transfer of ionic species of three beta-blockers (propranolol, sotalol and timolol) has been studied by cyclic voltammetry at a macroscopic water 1,2-dichloroethane (1,2-DCE) interface. The aqueous solution has been gellified in order to study the effect of the gel on the transport properties of the drugs. The gelling agent also stabilizes the interface overcoming mechanical instability. The standard potential and standard Gibbs energy of transfer across the interface, the partition coefficient and the diffusion coefficient of each drug were determined in the presence of a gelled interface. The diffusion coefficients were shifted relative to those obtained at normal water 1,2-DCE interfaces (free of gel).
通过循环伏安法在宏观水-1,2-二氯乙烷(1,2-DCE)界面研究了三种β受体阻滞剂(普萘洛尔、索他洛尔和噻吗洛尔)离子物种的转移。为了研究凝胶对药物传输性质的影响,已将水溶液凝胶化。凝胶剂还克服了机械不稳定性,稳定了界面。在存在凝胶化界面的情况下,测定了每种药物跨界面转移的标准电位和标准吉布斯自由能、分配系数和扩散系数。相对于在正常水-1,2-DCE界面(无凝胶)获得的扩散系数,这些扩散系数发生了偏移。