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硝酸益康唑在兔皮肤和阴道给药后的吸收与分布。

Absorption and disposition of econazole nitrate after application to the skins and vaginas of rabbits.

作者信息

Cameron B D, Chasseaud L F, Conway B, Fox N, Taylor T

出版信息

Arzneimittelforschung. 1976;26(11):2054-9.

PMID:1037247
Abstract
  1. The absorption and tissue distribution of radioactivity has been studied in rabbits after application of a cream containing 10 mg of the 3H-labelled 1-(2,4-dichloro-beta-[(p-chlorobenzyl)oxy]phenethyl) imidazole nitrate (econazole nitrate, Pevaryl) to the normal or abraded skins of rabbits. 2. Approximately one-third of the dose was absorbed through the occluded normal skins of rabbits during 8 days, mainly during 7 to 24 h. In the same time interval, slightly more of the dose was absorbed through the occluded abraded skins of rabbits at slightly greater rates. Co-formulation of triamcinolone acetonide in the cream reduced and delayed the peak rates of absorption through normal and abraded skin, but the extent of absorption during 8 days was similar in the presence or absence of triamcinolone acetonide. 3. After application to normal skin or abraded skin, the peak of mean concentrations in the plasma of 220 ng/ml (range 132-276 ng/ml) or 307 ng/ml (range 270-321 ng/ml), respectively, occurred at 24 h. Tissue distribution of radioactivity was similar after application to normal or abraded skin, and concentrations were highest in the liver, kidneys and gastrointestinal tract (which are the organs of biotransformation and excretion) and also in the adrenals and to a lesser extent in the uterus, ovaries and untreated skin. 4. After application of a cream containing 5 mg of 3H-econazole nitrate to the vaginas of rabbits, approximately one-third of the dose was absorbed during 8-24 h, and rates of excretion were higher through the more permeable vaginal membrane. 5. After vaginal doses of 5 mg, a peak concentration of 209 ng/ml occurred at 6 h in the plasma. Tissue concentrations of radioactivity after vaginal doses were highest in liver, kidneys, gastrointestinal tract, adrenals and ovaries, and the tissue distribution was similar to that observed after cutaneous doses.
摘要
  1. 将含有10毫克3H标记的1-(2,4-二氯-β-[(对氯苄基)氧基]苯乙基)咪唑硝酸盐(硝酸益康唑,派瑞松)的乳膏涂抹于兔的正常皮肤或破损皮肤上后,研究了兔体内放射性的吸收和组织分布情况。2. 在8天内,约三分之一的剂量通过兔的封闭正常皮肤吸收,主要在7至24小时内。在相同时间间隔内,通过兔的封闭破损皮肤吸收的剂量略多,且速率稍快。乳膏中曲安奈德的共同配方降低并延迟了通过正常皮肤和破损皮肤的吸收峰值速率,但在有或没有曲安奈德的情况下,8天内的吸收程度相似。3. 涂抹于正常皮肤或破损皮肤后,血浆中平均浓度的峰值分别在24小时时出现,正常皮肤为220纳克/毫升(范围132 - 276纳克/毫升),破损皮肤为307纳克/毫升(范围270 - 321纳克/毫升)。涂抹于正常皮肤或破损皮肤后,放射性的组织分布相似,浓度在肝脏、肾脏和胃肠道(生物转化和排泄器官)中最高,在肾上腺中也较高,在子宫、卵巢和未处理的皮肤中浓度较低。4. 将含有5毫克3H - 硝酸益康唑的乳膏涂抹于兔阴道后,约三分之一的剂量在8 - 24小时内被吸收,且通过更易渗透的阴道黏膜排泄速率更高。5. 阴道给予5毫克剂量后,血浆中在6小时时出现峰值浓度209纳克/毫升。阴道给药后放射性的组织浓度在肝脏、肾脏、胃肠道、肾上腺和卵巢中最高,且组织分布与皮肤给药后观察到的相似。

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引用本文的文献

1
Econazole: a review of its antifungal activity and therapeutic efficacy.益康唑:其抗真菌活性与治疗效果综述
Drugs. 1978 Sep;16(3):177-201. doi: 10.2165/00003495-197816030-00001.