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吡罗昔康凝胶局部应用后的血浆和皮肤药物水平:一项在健康志愿者中的研究。

Plasma and cutaneous drug levels after topical application of piroxicam gel: a study in healthy volunteers.

作者信息

Marks R, Dykes P

机构信息

University of Wales College of Medicine, Cardiff, UK.

出版信息

Skin Pharmacol. 1994;7(6):340-4. doi: 10.1159/000211316.

Abstract

Two studies in healthy male and female volunteers (aged 18-65 years) were undertaken to determine plasma and cutaneous levels of drug following topical application of piroxicam gel. Twelve subjects applied piroxicam gel to the knee (1 g of 0.5% Feldene gel) at baseline and then after 6, 12 and 24 h. Plasma was collected after 1, 2, 4, 6, 14, 24, 28 and 48 h and piroxicam content determined by high-pressure liquid chromatography (HPLC). For the majority of samples collected, piroxicam levels were below the limit of detection (LOD) of the assay and the maximum recorded plasma level in any subject at any time point was 75.4 ng/ml. A single application of gel was administered to the forearms of four groups each of 6 subjects, and biopsy samples of the stratum corneum (skin surface biopsy, SBB) and epidermis/dermis were taken after 0.5, 1, 2 and 4 h. The levels of piroxicam were again measured in each sample by HPLC. The highest levels of piroxicam were found in the superficial skin surface biopsy with the lowest levels recorded in the skin surface biopsies nearest the viable epidermis. The mean tissue concentrations ranged from 160 to 640 ng per sample (calculated to be 80-320 micrograms/g of tissue). The mean levels of piroxicam in a 4-mm punch biopsy showed an increase with time after application, rising from 60.3 to 94.6 ng per biopsy (calculated to be 2.4 to 3.8 micrograms/g of tissue). It may be concluded that piroxicam rapidly permeates through the stratum corneum into the epidermis/dermis after application of the gel. Low and often undetectable plasma levels of drug were observed after topical application of piroxicam gel in a manner comparable to clinical usage.

摘要

开展了两项针对健康男性和女性志愿者(年龄在18 - 65岁)的研究,以确定局部应用吡罗昔康凝胶后药物在血浆和皮肤中的水平。12名受试者在基线时以及6、12和24小时后,将吡罗昔康凝胶涂抹于膝盖(1克0.5%的吡罗昔康凝胶)。在1、2、4、6、14、24、28和48小时后采集血浆,并通过高压液相色谱法(HPLC)测定吡罗昔康含量。对于采集的大多数样本,吡罗昔康水平低于该检测方法的检测限(LOD),任何受试者在任何时间点记录的最高血浆水平为75.4纳克/毫升。将凝胶单次应用于每组6名受试者的四组前臂,并在0.5、1、2和4小时后采集角质层(皮肤表面活检,SBB)和表皮/真皮的活检样本。通过HPLC再次测定每个样本中的吡罗昔康水平。在浅表皮肤表面活检中发现吡罗昔康水平最高,而在最接近活表皮的皮肤表面活检中记录的水平最低。每个样本的平均组织浓度范围为160至640纳克(计算为80 - 320微克/克组织)。4毫米打孔活检中吡罗昔康的平均水平显示在应用后随时间增加,从每次活检60.3纳克升至94.6纳克(计算为2.4至3.8微克/克组织)。可以得出结论,应用凝胶后吡罗昔康迅速透过角质层进入表皮/真皮。以与临床使用相当的方式局部应用吡罗昔康凝胶后,观察到药物的血浆水平较低且常常无法检测到。

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