Greive Kerryn A, Barnes Tanya M
Ego Pharmaceuticals, Braeside, Victoria, Australia.
Australas J Dermatol. 2015 May;56(2):e30-4. doi: 10.1111/ajd.12128. Epub 2013 Dec 23.
BACKGROUND/OBJECTIVES: The aim of this study was to compare vasoconstrictor activity and, by inference, the clinical anti-inflammatory effectiveness of hydrocortisone in two different formulations: 1% dissolved hydrocortisone cream and 1% dispersed hydrocortisone cream. Moisturising capacity and safety were also determined.
Both topical preparations were applied without occlusion on forearms twice daily for 5 days. An assessment of vasoconstriction was performed in a double-blinded manner pretreatment and then thrice daily for 6 days and once 7 days post-application, using an objective rating scale. For the dissolved preparation only, moisturising capacity was determined by measurement of transepidermal water loss (TEWL) at 0, 2, 4, 6 and 24 h, and also by the measurement of water content at 0 and 24 h. Safety was assessed by repeat insult patch tests (RIPT).
In all, 10 volunteers completed the vasoconstrictor and moisturising studies, while 52 completed the RIPT. For 1% dissolved hydrocortisone cream and 1% dispersed hydrocortisone cream, respectively, areas under the blanching curves were 1240 and 295; total scores were 129.0 and 31.5; summed % total possible scores were 161.3 and 39.4; Tm/10 mean values were 3.47 and 1.64. The 1% dissolved hydrocortisone cream was found to be statistically more potent than the 1% dispersed hydrocortisone cream. Furthermore, the 1% dissolved hydrocortisone cream was found to be moisturising compared to no treatment. No adverse events were observed.
A cream containing 1% dissolved hydrocortisone exhibits greater vasoconstrictor activity than a cream containing 1% dispersed hydrocortisone.
背景/目的:本研究旨在比较氢化可的松两种不同制剂(1%氢化可的松溶解乳膏和1%氢化可的松分散乳膏)的血管收缩活性,并由此推断其临床抗炎效果。同时还测定了保湿能力和安全性。
两种外用制剂均不封包,每天两次涂抹于前臂,共5天。采用客观评分量表,在预处理时进行双盲血管收缩评估,然后在用药后每天三次,共6天,以及用药后7天进行一次评估。仅对溶解制剂,通过在0、2、4、6和24小时测量经表皮水分流失(TEWL)以及在0和24小时测量水分含量来测定保湿能力。通过重复刺激斑贴试验(RIPT)评估安全性。
共有10名志愿者完成了血管收缩和保湿研究,52名完成了RIPT。1%氢化可的松溶解乳膏和1%氢化可的松分散乳膏的变白曲线下面积分别为1240和295;总分分别为129.0和31.5;总可能得分的总和百分比分别为161.3和39.4;Tm/10平均值分别为3.47和1.64。发现1%氢化可的松溶解乳膏在统计学上比1%氢化可的松分散乳膏更有效。此外,与未治疗相比,1%氢化可的松溶解乳膏具有保湿作用。未观察到不良事件。
含1%溶解氢化可的松的乳膏比含1%分散氢化可的松的乳膏表现出更强的血管收缩活性。