Hatanaka T, Manabe E, Ohtsuki T, Okuyama K, Mori M, Okada H, Katayama K, Koizumi T
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Japan.
Biol Pharm Bull. 2000 Jul;23(7):860-5. doi: 10.1248/bpb.23.860.
A physiological pharmacokinetic model describing the absorption and disposition of topically applied drugs was proposed, and the effect of various pharmacokinetic and physiological parameters on the drug delivery into the targeted muscle was simulated. The proposed model consists of vehicle, and stratum corneum, viable epidermis and muscle below the application and reference sites, and plasma, each joined with transfer clearance and plasma flow. Indomethacin concentrations in tissues and plasma after topical application to rats could be explained by the model. Most indomethacin delivered into the underlying muscle was via direct penetration. The model simulation showed that the increase in plasma clearance and clearance between viable skin and muscle, and the decrease in application area and plasma flow rate into viable skin and muscle would promote the targeting efficacy of topically applied drugs to the underlying muscle.
提出了一种描述局部应用药物吸收和处置的生理药代动力学模型,并模拟了各种药代动力学和生理参数对药物递送至目标肌肉的影响。所提出的模型包括载体、角质层、给药部位和参考部位下方的活表皮和肌肉,以及血浆,各部分通过转运清除率和血浆流量相连。该模型可以解释大鼠局部应用吲哚美辛后组织和血浆中的浓度。大部分递送至下层肌肉的吲哚美辛是通过直接渗透。模型模拟表明,血浆清除率以及活皮肤与肌肉之间清除率的增加,以及给药面积和进入活皮肤与肌肉的血浆流速的降低,将促进局部应用药物对下层肌肉的靶向效果。