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Skin Disposition of Drugs after Topical Application in Hairless Rats

机译:在无毛大鼠中局部应用药物后的皮肤处置

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摘要

Drug fraction transported from a topical formulation on skin to subsutaneous tissues or muscles is dependent on the physicochemical properties of the entrapped drug. Cutaneous disposition of model drugs, antipyrine(ANP), lidocaine (LC) and piroxicam (PXC) as well as flurbiprofen (FP) was thus evaluated in hairless rats in which an agar gel disc was subcutaneously inserted into abdominal region as a drug receptor and a drug donor cell was placed above it. Time courses of plasma level and agar gel amount were measured after topical application of 50% ANP, 3% LC, 1% PXC and 1% FP in hydroxypropylcellulose gel. Percutaneous absorption clearance of unionized from, CL*ab was proportional to true octanol/water distribution coefficient and the order of FP>PXC>LC>ANP, suggesting that permeation of the drug was determined mainly by its distribution from the formulation to the skin barrier. PXC, however, had a relatively low flux compared to the other three drugs, probably due to its high molecular weight and meltiong point. Migration clearance of unionized form from systemic cirsulation to the subcutaneous agar gel, CL*g was also influenced by the lipophilicity of drugs. On the other hand, fraction from the formulation to the systemic circulation was in the order of PXC>FP>ANP>LC.This fraction was much higher than the direct migration fraction from the formulation to the subcutaneous agar gel. Factors determining for these fractions are still unclear. A drug having a low lipophilicity and a low prorein binding, however, had a tendency to have a great targeting ability to the subcutaneous agar gel. In addition, most of the drug in the agar gel was contributed by the direct flow from formulation, not from the systemic circulation. The present in situ experimental method is a useful tool to evaluate skin disposition of drugs. Detailed understanding of the skin disposition of drugs from several formulations will enable the finding of a good drug and formulation candidates.
机译:从皮肤上的局部制剂运输到皮下组织或肌肉的药物部分取决于所包埋的药物的物理化学性质。因此,在无毛大鼠中评估了模型药物,安替比林(ANP),利多卡因(LC)和吡罗昔康(PXC)以及氟比洛芬(FP)的皮肤处置,其中将琼脂凝胶盘作为药物受体皮下插入腹部区域,将药物供体细胞置于其上方。在羟丙基纤维素凝胶中局部应用50%ANP,3%LC,1%PXC和1%FP后,测量血浆水平和琼脂凝胶量的时程。联合的CL * ab的经皮吸收清除率与真实的辛醇/水分配系数成正比,并且FP> PXC> LC> ANP的顺序高,这表明药物的渗透主要取决于其从制剂到皮肤屏障的分布。但是,与其他三种药物相比,PXC的通量相对较低,这可能是由于其高分子量和高熔点。工会形式从全身性运动到皮下琼脂的迁移清除率CL * g也受药物亲脂性的影响。另一方面,从制剂到体循环的比例为PXC> FP> ANP> LC的顺序,该比例远高于从制剂到皮下琼脂凝胶的直接迁移比例。确定这些分数的因素仍不清楚。然而,具有低亲脂性和低蛋白原结合的药物倾向于对皮下琼脂凝胶具有很大的靶向能力。另外,琼脂凝胶中的大多数药物是来自制剂而不是全身循环的直接流动。本原位实验方法是评估药物皮肤处置的有用工具。对几种配方中药物在皮肤上的处置方式的详细了解将使人们能够找到一种好的药物和配方候选物。

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