Faergemann J, Zehender H, Jones T, Maibach I
Department of Dermatology, Sahlgrenska Hospital, Göteborg, Sweden.
Acta Derm Venereol. 1991;71(4):322-6.
We determined terbinafine levels in serum, stratum corneum, dermis-epidermis (without stratum corneum), hair, sebum and eccrine sweat before, during and after 250 mg doses orally to volunteers once daily. Terbinafine is concentrated rapidly in stratum corneum (up to 9.1 micrograms/g of tissue) primarily by diffusion from the vascular system through the dermisepidermis. It also reaches high concentration in sebum (up to 45.1 micrograms/ml) after several days and continue to concentrate in sebum for up to two days after discontinuation of drug. Hair concentration reach levels of 2.6 micrograms/g of tissue indicating high drug levels in and around the hair follicle. It is not found in sweat. Plasma levels range between 0.1 and 1.0 micrograms/ml. There is a tenfold accumulation of drug in stratum corneum by day 2. Elimination of drug from tissue occurs with a half-life of 4 to 5 days and with the potential for drug levels above fungicidal concentrations for dermatophytes for more than 3 weeks. The tissue pharmacokinetic profile of terbinafine is similar to that of another lipophilic drug, itraconazole, but is very different from ketoconazole and griseofulvin. Higher levels of terbinafine are achieved than of either of the imidazoles and remain longer than griseofulvin.
我们测定了志愿者每日口服250毫克剂量药物前、服药期间及停药后的血清、角质层、真皮-表皮(不含角质层)、毛发、皮脂和外泌汗腺汗液中的特比萘芬水平。特比萘芬主要通过从血管系统经真皮-表皮扩散,迅速在角质层中富集(最高可达9.1微克/克组织)。服药数天后,其在皮脂中也达到高浓度(最高可达45.1微克/毫升),停药后在皮脂中持续富集长达两天。毛发中的浓度达到2.6微克/克组织,表明毛囊及其周围药物浓度较高。汗液中未检测到该药物。血浆水平在0.1至1.0微克/毫升之间。到第2天时,角质层中的药物蓄积量增加了10倍。药物从组织中的消除半衰期为4至5天,且在超过3周的时间内,药物水平可能高于皮肤癣菌的杀菌浓度。特比萘芬的组织药代动力学特征与另一种亲脂性药物伊曲康唑相似,但与酮康唑和灰黄霉素非常不同。特比萘芬达到的水平高于任何一种咪唑类药物,且比灰黄霉素持续时间更长。