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阴道栓剂中酮康唑的全身吸收。

Systemic absorption of ketoconazole from vaginal pessaries.

作者信息

Ene M D, Williamson P J, Daneshmend T K, Blatchford N R

出版信息

Br J Clin Pharmacol. 1984 Feb;17(2):173-5. doi: 10.1111/j.1365-2125.1984.tb02334.x.

Abstract

Eight healthy female subjects were each given (a) ketoconazole 400 mg orally, (b) ketoconazole 400 mg as a single vaginal pessary, (c) ketoconazole 800 mg as two vaginal pessaries, and (d) ketoconazole 1200 mg as three vaginal pessaries. The area under the plasma concentration time curve (AUC) after the oral dose was 51.41 +/- 10.99 mg l-1 h (mean +/- s.d.) and the half-life of ketoconazole was 2.98 +/- 1.41 h. The AUCs after vaginal administration were 0.27 +/- 0.14, 0.52 +/- 0.25, and 0.43 +/- 0.22 mg-1 l h following the 400, 800 and 1200 mg pessaries respectively. Systemic absorption of single doses of vaginally administered ketoconazole appears to be negligible in the absence of vaginal infection. There were no local or systemic side effects related to ketoconazole in these healthy volunteers.

摘要

八名健康女性受试者分别接受了以下治疗

(a)口服400毫克酮康唑;(b)单次阴道栓剂给药400毫克酮康唑;(c)两次阴道栓剂给药800毫克酮康唑;(d)三次阴道栓剂给药1200毫克酮康唑。口服给药后血浆浓度-时间曲线下面积(AUC)为51.41±10.99毫克·升⁻¹·小时(平均值±标准差),酮康唑的半衰期为2.98±1.41小时。阴道给药后,400毫克、800毫克和1200毫克栓剂的AUC分别为0.27±0.14、0.52±0.25和0.43±0.22毫克⁻¹·升·小时。在无阴道感染的情况下,单次阴道给药酮康唑的全身吸收似乎可忽略不计。这些健康志愿者中未出现与酮康唑相关的局部或全身副作用。

相似文献

1
Systemic absorption of ketoconazole from vaginal pessaries.阴道栓剂中酮康唑的全身吸收。
Br J Clin Pharmacol. 1984 Feb;17(2):173-5. doi: 10.1111/j.1365-2125.1984.tb02334.x.
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Oral versus local treatment of vaginal candidosis.阴道念珠菌病的口服治疗与局部治疗
Int J Gynaecol Obstet. 1989 Sep;30(1):57-62. doi: 10.1016/0020-7292(89)90216-6.
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Influence of food on the pharmacokinetics of ketoconazole.食物对酮康唑药代动力学的影响。
Antimicrob Agents Chemother. 1984 Jan;25(1):1-3. doi: 10.1128/AAC.25.1.1.

引用本文的文献

1
Clinical pharmacokinetics of ketoconazole.酮康唑的临床药代动力学
Clin Pharmacokinet. 1988 Jan;14(1):13-34. doi: 10.2165/00003088-198814010-00002.

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