Yano T, Higo N, Furukawa K, Tsuji M, Noda K, Otagiri M
Research Laboratories, Hisamitsu Pharmaceutical Co., Inc., Saga, Japan.
J Pharmacobiodyn. 1992 Sep;15(9):527-33. doi: 10.1248/bpb1978.15.527.
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.
合成了一种新化合物1-[2-(癸硫基)乙基]氮杂环戊烷-2-酮(HPE-101),并以14C-吲哚美辛为渗透剂检测其皮肤渗透促进活性。将HPE-101和吲哚美辛的溶液涂覆在粘贴于胶带上的布垫上制成HPE-101贴剂,然后将该贴剂贴于无毛小鼠皮肤上。通过测量给药后24小时尿液中排出的放射性来确定经皮吸收的吲哚美辛量。1)当使用丙二醇-乙醇(9:1 v/v)混合物作为溶剂时,氮酮和癸基甲基亚砜显著增强了吲哚美辛的经皮吸收。2)在溶解于吲哚美辛溶液中并用于筛选渗透促进活性的各种渗透促进剂中,发现HPE-101最为突出。3)含有超过3%(w/w)HPE-101的溶剂产生了稳定的渗透促进活性水平。4)每天应用1%(w/w)的HPE-101或氮酮溶液,吲哚美辛的每日排泄量显著高于前一天的排泄水平。然而,连续每日应用超过3天会使吲哚美辛的排泄达到稳态。5)在第1天用3%(w/w)的HPE-101或氮酮溶液预处理小鼠皮肤24小时,在第3天和第7天应用吲哚美辛溶液24小时以检查皮肤屏障功能的恢复情况。在第3天仍观察到吲哚美辛排泄增加,但在第7天未观察到增强作用。