新型穿透增强剂1-[2-(癸基硫)乙基]氮杂环戊烷-2- 1 (HPE-101)的评价。

T Yano, N Higo, K Furukawa, M Tsuji, K Noda, M Otagiri
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引用次数: 16

摘要

合成了新化合物1-[2-(癸基硫)乙酯]氮杂环戊烷-2- 1 (HPE-101),并以14c -吲哚美辛为渗透剂考察了其促皮肤渗透活性。将HPE-101和吲哚美辛溶液涂在布垫上,贴在胶带上,制成HPE-101贴片,贴于无毛小鼠皮肤。应用24 h后,通过测定尿中放射量测定经皮吸收吲哚美辛的量。1)以丙二醇-乙醇(9:1 v/v)混合物为溶剂时,氮酮和十二甲基亚砜显著增强吲哚美辛的经皮吸收。2)在吲哚美辛溶液中溶解的多种促渗剂中,HPE-101的促渗活性最显著。3) HPE-101含量大于3% (w/w)的溶剂具有平台型的促渗活性。4)每日应用1% (w/w) HPE-101或Azone溶液可显著提高吲哚美辛日排泄量,高于前一天水平。然而,每天重复使用超过3天,吲哚美辛的排泄状态稳定。5)小鼠皮肤第1天分别用3% (w/w)的HPE-101或Azone溶液预处理24 h,第3天和第7天分别用吲哚美辛溶液预处理24 h,观察皮肤屏障功能恢复情况。第3天吲哚美辛的排泄仍有增加,但第7天未见增加。
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Evaluation of a new penetration enhancer 1-[2-(decylthio)ethyl]azacyclopentan-2-one (HPE-101).

A new compound, 1-[2-(decylthio)ethyl]azacyclopentan-2-one (HPE-101) was synthesized, and its skin penetration enhancing activity was examined by using 14C-indomethacin as a penetrant. A solution of HPE-101 and indomethacin was applied to a cloth pad affixed onto an adhesive tape to give a HPE-101 patch, and the patch was applied to hairless mouse skin. The amount of percutaneously absorbed indomethacin was determined by measuring the radioactivity excreted in urine for 24 h after application. 1) Azone and decylmethyl sulfoxide, enhanced markedly the percutaneous absorption of indomethacin when the propylene glycol-ethanol (9:1 v/v) mixture was used as the solvent. 2) Among various penetration enhancers dissolved in the indomethacin solutions and applied to screen for penetration enhancing activity, HPE-101 was found to be the most prominent. 3) Solvents containing more than 3% (w/w) of HPE-101 produced a plateau level of the penetration enhancing activity. 4) Daily application of 1% (w/w) solutions of HPE-101 or Azone increased the daily excretion of indomethacin significantly above the level excreted on the previous day. However, repeated daily application beyond 3 d gave a steady state excretion of indomethacin. 5) The mouse skin was pretreated with 3% (w/w) solutions of HPE-101 or Azone for 24 h on the 1st day, and the indomethacin solution was applied for 24 h on the 3rd day and 7th day to examine the recovery of skin barrier function. Enhanced excretion of indomethacin was still noted on the 3rd day, but enhancement was not observed on the 7th day.

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