Leopold C S, Lippold B C
Department of Pharmaceutical Technology, Heinrich-Heine-University, Düsseldorf, Germany.
J Pharm Sci. 1995 Feb;84(2):195-8. doi: 10.1002/jps.2600840214.
Vehicle effects may be caused by thermodynamic effects and by specific (penetration enhancing) effects. To investigate the effects of various lipophilic vehicles on drug penetration, an in vivo permeability study was conducted with methyl nicotinate as the model drug. The drug was dissolved in the respective vehicles at concentrations that provide equal drug escaping tendencies. Drug solutions were applied to the upper arms of volunteers with a glass chamber system. To avoid drug depletion effects, drug disappearance rates were measured under steady-state conditions by the difference method. Enhancement factors were calculated from the steady-state flux values (i.e., drug disappearance rates per area unit) and compared with results from non-steady-state experiments. Significant enhancing effects (p < 0.01) were observed with dibutyl adipate, caprylic/capric acid triglycerides containing 5% phospholipids, isopropyl myristate, and mineral oil. Caprylic/capric acid triglycerides, cetearyl isooctanoate, and the standard vehicle dimethicone 100 were without effect on drug penetration. The explanation for the observed enhancing effects may be an interaction of the lipophilic liquids with the lipid bilayers of the stratum corneum that leads to a decrease of the barrier resistance.
载体效应可能由热力学效应和特定的(促渗透)效应引起。为了研究各种亲脂性载体对药物渗透的影响,以烟酸甲酯为模型药物进行了体内渗透性研究。将药物以提供相等药物逸出趋势的浓度溶解在各自的载体中。用玻璃腔室系统将药物溶液涂抹于志愿者的上臂。为避免药物耗竭效应,通过差值法在稳态条件下测量药物消失率。根据稳态通量值(即每单位面积的药物消失率)计算增强因子,并与非稳态实验结果进行比较。己二酸二丁酯、含5%磷脂的辛酸/癸酸甘油三酯、肉豆蔻酸异丙酯和矿物油观察到显著的增强效应(p < 0.01)。辛酸/癸酸甘油三酯、异壬酸鲸蜡硬脂醇酯和标准载体聚二甲基硅氧烷100对药物渗透没有影响。观察到的增强效应的解释可能是亲脂性液体与角质层脂质双层相互作用导致屏障阻力降低。