皮密莫司
体内
角质层
药理学
人体皮肤
钙调神经磷酸酶
化学
皮肤病科
吸收(声学)
真皮
体外
医学
生物
移植
病理
内科学
生物化学
生物技术
物理
遗传学
声学
作者
Hans‐Peter Gschwind,Felix Waldmeier,Markus Zollinger,A. Schweitzer,Maximilian A. Grassberger
标识
DOI:10.1016/j.ejps.2007.09.004
摘要
The dermal disposition of pimecrolimus, a non-steroid, anti-inflammatory calcineurin inhibitor used for the treatment of atopic dermatitis, was evaluated in minipigs in vivo and in human skin in vitro using tritium-radiolabeled compound, and in dermal toxicokinetic investigations in minipigs using unlabeled compound. Following topical application of pimecrolimus 1% market form (MF) cream to minipig skin, approximately 2% of the dose penetrated into the stratum corneum and part of it into deeper skin layers. The remainder of the dose was recovered non-absorbed on the skin surface. The total systemic absorption was ≤0.8% of dose. Highest pimecrolimus blood concentrations (0.44 ng/mL) were reached between 2 and 6 h post-end of topical application. Most of the absorbed drug was excreted as metabolites with feces. In human skin treated in vitro with pimecrolimus 1% MF cream for 24 h, ≥94% of dose remained non-absorbed, 3.1% was found in the epidermis (including stratum corneum) and 2.9% in the dermis. There was no indication of metabolism of pimecrolimus in human skin in vitro or minipig skin in vivo. No drug accumulation was observed in minipig skin after up to 13 weeks of once daily topical application of 0.1% or 0.3% pimecrolimus cream.
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