Cho Cheong-Weon, Choi Jun-Shik, Kim Seong-Jin, Shin Sang-Chul
Chungnam National University, Daejeon, South Korea.
Drug Deliv. 2009 May;16(4):230-5. doi: 10.1080/10717540902872264.
Various enhancers, such as fatty acids (saturated, unsaturated), glycerides, propylene glycols, and non-ionic surfactants, have been incorporated in the loratadine-EVA matrix to increase the rate of skin permeation of loratadine from an EVA matrix. The enhancing effects of these enhancers on the skin permeation of loratadine were evaluated using a modified Keshary-Chien cell fitted with intact excised rat skin. The penetration enhancers showed a higher flux, probably due to the enhancing effect on the skin barrier, the stratum corneum. Among the enhancers used, such as the fatty acids, glycols, propylene glycols, and non-ionic surfactants, linoleic acid showed the best enhancement. For the enhanced transdermal delivery of loratadine, application of an EVA matrix containing a permeation enhancer might be useful in the development of a transdermal drug delivery system.
已将各种促渗剂,如脂肪酸(饱和、不饱和)、甘油酯、丙二醇和非离子表面活性剂,加入氯雷他定 - EVA 基质中,以提高氯雷他定从 EVA 基质中的皮肤渗透速率。使用装有完整切除大鼠皮肤的改良 Keshary - Chien 细胞评估了这些促渗剂对氯雷他定皮肤渗透的增强作用。渗透促进剂显示出更高的通量,这可能是由于其对皮肤屏障即角质层的增强作用。在所使用的促渗剂中,如脂肪酸、二醇、丙二醇和非离子表面活性剂,亚油酸显示出最佳的增强效果。对于氯雷他定的增强透皮给药,含有渗透促进剂的 EVA 基质的应用可能有助于透皮给药系统的开发。