卵磷脂微乳凝胶和卵磷脂脂质体的人体皮肤刺激性研究。

F Dreher, P Walde, P L Luisi, P Elsner
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引用次数: 81

摘要

大豆卵磷脂微乳液凝胶可用作透皮治疗系统的基质,具有良好的前景。为了评估凝胶对皮肤的潜在刺激性,我们使用单酰胺大豆卵磷脂脂质体制剂和溶剂棕榈酸异丙酯(IPP)作为对比,对人体进行了体内急性和累积性刺激试验。对 151 名志愿者进行了 48 小时的急性刺激性贴片试验,对 20 名志愿者进行了 21 天的人体重复刺激性贴片试验,评估了累积刺激性。在急性刺激试验中,凝胶对 2 名受试者(1.3%)、脂质体对 3 名受试者(2.0%)、IPP 对 2 名受试者(1.3%)产生了离散性刺激(仅红斑)。为了评估累积刺激性,计算了 IT50(50% 受试者的刺激时间)。凝胶的 IT50 为 13 天,脂质体为 14 天,IPP 为 17 天。这项研究表明,大豆卵磷脂微乳液凝胶的急性刺激性和累积刺激性都很低,因此在毒理学方面也可作为透皮治疗系统的候选基质。
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Human skin irritation studies of a lecithin microemulsion gel and of lecithin liposomes.

Soybean lecithin microemulsion gels offer promising features for the possible use as matrices in transdermal therapeutic systems. In order to assess the skin irritancy potential of the gel, acute and cumulative irriation tests were performed in human subjects in vivo using as comparison an unilamellar soybean lecithin liposome preparation and the solvent isopropyl palmitate (IPP). Acute irritation was tested in 151 volunteers in a 48-hour patch test, whereas cumulative irritation was assessed in a 21-day human repeated insult patch test in 20 volunteers. In the acute irritation test, discrete irritation (erythema only) developed with the gel in 2 subjects (1.3%), with the liposomes in 3 subjects (2.0%), and with IPP in 2 subjects (1.3%). For the assessment of cumulative irritation, the IT50 (irritation time of 50% of the test population) was calculated. IT50 was 13 days for the gel, 14 days for the liposomes and 17 days for IPP. This study shows a very low acute and a low cumulative irritancy potential for the soybean lecithin microemulsion gel making it a candidate matrix for transdermal therapeutic systems also under toxicological aspects.

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