Padula Cristina, Nicoli Sara, Colombo Paolo, Santi Patrizia
Department of Pharmacy, University of Parma, Parma, Italy.
Eur J Pharm Biopharm. 2007 Jun;66(3):422-8. doi: 10.1016/j.ejpb.2006.11.014. Epub 2006 Nov 29.
We have recently described an innovative drug delivery system, a water-based and vapor permeable film intended for dermal and/or transdermal delivery. The aim of this work was to modulate the delivery of the model drug lidocaine hydrochloride from the transdermal film across rabbit ear skin. The effect of drug loading, of film-forming polymer type and content, of adhesive and plasticizer on lidocaine transport across the skin was evaluated. Additional objective was to evaluate the effect of occlusion on the kinetics of lidocaine transport, by applying an occlusive backing on the surface of the transdermal film. From the data obtained it can be concluded that the transdermal film acts as a matrix controlling drug delivery. The film-forming polymer molecular weight had a negligible effect on drug penetration, while its content was more effective. The choice of the adhesive seems to be the most important variable governing drug transport. In particular, the presence of lauric acid combined with a basic drug, such as lidocaine, can produce a relevant improvement in permeation, because of the formation of an ion pair. Concerning the kinetics, drug depletion is responsible for the declining permeation rates observed in the late times of permeation.
我们最近描述了一种创新的药物递送系统,即一种用于皮肤和/或透皮递送的水基且可透水蒸气的薄膜。这项工作的目的是调节模型药物盐酸利多卡因从透皮薄膜穿过兔耳皮肤的递送。评估了药物负载量、成膜聚合物类型和含量、粘合剂和增塑剂对利多卡因透过皮肤转运的影响。另一个目标是通过在透皮薄膜表面施加封闭背衬来评估封闭对利多卡因转运动力学的影响。从获得的数据可以得出结论,透皮薄膜起到控制药物递送的基质作用。成膜聚合物分子量对药物渗透的影响可忽略不计,而其含量的影响更显著。粘合剂的选择似乎是控制药物转运的最重要变量。特别是,月桂酸与碱性药物(如利多卡因)结合,由于形成离子对,可使渗透有显著改善。关于动力学,药物耗尽是渗透后期观察到的渗透率下降的原因。