Seki Toshinobu, Wang Aiping, Yuan Dan, Saso Yuko, Hosoya Osamu, Chono Sumio, Morimoto Kazuhiro
Hokkaido College of Pharmacy, 7-1 Katsuraoka-cho, Otaru, Hokkaido 047-0264, Japan.
J Control Release. 2004 Nov 24;100(2):181-9. doi: 10.1016/j.jconrel.2004.08.016.
Microdialysis is useful as a method to evaluate the disposition of drugs in the skin to design improved transdermal delivery systems (TDDSs). In this study, quantitative microdialysis methods were validated in excised porcine skin experimental systems in vitro. Flurbiprofen (FP), used as a model drug, showed high affinity for the skin tissues in equilibrium states between the medium and skin. The membrane clearances of FP for permeation through the membrane of a dialysis fiber placed in the skin (CL(m in S)) were lower than that in the medium. The adsorption of components in the skin to the membrane surface of the dialysis fiber and accumulation of FP near the dialysis fiber are the most likely reasons for this. When CL(m in S) was used to predict the extracellular FP concentration in skin (C(T)), the value obtained was lower than that expected from the FP concentration in the medium on the dermis side, which should be equal to C(T) at equilibrium. In the zero net flux (ZNF) method, in which the concentration difference of perfusate (DeltaC) between the inflow and outflow were used to obtain C(T), the predicted C(T) was similar to the expected value. In an in vitro skin permeation experiment, the ZNF method was used for the prediction of C(T) near the dialysis fiber. The predicted C(T) was over 10 times higher than the FP concentration in the medium on the dermis side, suggesting a concentration gradient in the dermis. Although the ZNF method is good for predicting the C(T) in skin, the mass balance has to be considered for the quantitative evaluation of the skin permeation of drugs. In this study, the effect of the mass transfer of FP from the perfusate to the skin on the cumulative amount of FP passing through the skin was relatively low because of the use of suitable solutions as perfusate. The perfusion conditions and schedules should be designed carefully for quantitative evaluations using the ZNF method. These results provide useful information for the in vivo application of quantitative microdialysis to evaluate TDDS.
微透析作为一种评估药物在皮肤中处置情况的方法,对于设计改进的透皮给药系统(TDDS)很有用。在本研究中,定量微透析方法在体外切除的猪皮实验系统中得到了验证。作为模型药物的氟比洛芬(FP)在介质与皮肤之间的平衡状态下对皮肤组织表现出高亲和力。FP通过置于皮肤中的透析纤维膜的渗透膜清除率(CL(m in S))低于在介质中的清除率。皮肤中的成分吸附到透析纤维的膜表面以及FP在透析纤维附近的积累是最可能的原因。当使用CL(m in S)预测皮肤中细胞外FP浓度(C(T))时,得到的值低于真皮侧介质中FP浓度预期的值,而在平衡时该值应等于C(T)。在零净通量(ZNF)方法中,使用灌注液流入和流出之间的浓度差(DeltaC)来获得C(T),预测的C(T)与预期值相似。在体外皮肤渗透实验中,ZNF方法用于预测透析纤维附近的C(T)。预测的C(T)比真皮侧介质中FP浓度高出10倍以上,表明真皮中存在浓度梯度。尽管ZNF方法有利于预测皮肤中的C(T),但在药物皮肤渗透的定量评估中必须考虑质量平衡。在本研究中,由于使用了合适的溶液作为灌注液,FP从灌注液向皮肤的传质对通过皮肤的FP累积量的影响相对较小。使用ZNF方法进行定量评估时,应仔细设计灌注条件和方案。这些结果为定量微透析在体内评估TDDS的应用提供了有用信息。