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经阴道给予雌三醇乳膏后,雌三醇的血清浓度差异很大。

Serum concentrations of estriol vary widely after application of vaginal oestriol cream.

机构信息

Department of Urogynaecology, St George Hospital, School of Women's and Children's Health, University of NSW, Sydney, Australia.

Department of Clinical Pharmacology and Toxicology, St. Vincent's Hospital, Sydney, Australia.

出版信息

Br J Clin Pharmacol. 2021 May;87(5):2354-2360. doi: 10.1111/bcp.14635. Epub 2020 Dec 19.

Abstract

AIMS

The aim of this study was to establish the pharmacokinetic profile of serum oestriol (E ) concentrations over 24 h following application of vaginal E in chronic users (>12 weeks of E use). The interindividual and intraindividual differences before and after E were examined.

METHODS

Ten women participated. Vaginal cream was omitted for ≥36 h prior to the study days. Blood sampling was performed for E , oestradiol and oestrone concentrations prior to cream application and at 1, 2, 3, 5, 8, 10, 12 and 24 h afterwards. In five women, all samples were repeated on a separate day.

RESULTS

E was absorbed rapidly in most women. Peak serum E concentration occurred around 2 h (range 1-5 h). The decline in E concentrations was also rapid: falling <100 pmol L in six out of ten women within 8 h and returning to ≤ 10 pmol L at 24 h in nine out of the ten patients. Interindividual variability for peak concentrations was considerable (mean 546 pmol L ; 95% CI 349-743). Area under the concentration-time curve (AUC) values over a dosage interval also varied widely: mean 2145 pmol.h L ; 95% CI 1422-3233. However, repeated measurements in the same woman were highly (peaks: ρ = 0.94) or moderately (AUC: P = 0.74) correlated.

CONCLUSIONS

Postmenopausal E concentrations are negligible. Serum E concentrations of chronic users of E cream varied greatly; however, concentrations declined rapidly within 8 h, generally reaching 'postmenopausal' levels by 24 h. The basis for the variation between subjects needs further elucidation. Additional research is required to establish the safety of topical E .

摘要

目的

本研究旨在建立慢性使用者(>12 周使用 E)阴道 E 给药后 24 小时内血清雌三醇(E)浓度的药代动力学特征。检测 E 给药前后个体内和个体间的差异。

方法

10 名女性参与。在研究日之前,阴道乳膏已停用≥36 小时。在乳膏应用前和应用后 1、2、3、5、8、10、12 和 24 小时,进行 E、雌二醇和雌酮浓度的血样采集。在 5 名女性中,所有样本均在另一天重复采集。

结果

E 在大多数女性中被迅速吸收。血清 E 浓度峰值出现在 2 小时左右(范围 1-5 小时)。E 浓度的下降也很快:在 10 名女性中有 6 名在 8 小时内下降到<100 pmol/L,在 10 名女性中有 9 名在 24 小时内降至≤10 pmol/L。峰浓度的个体间变异性很大(平均 546 pmol/L;95%CI 349-743)。剂量间隔内的浓度-时间曲线下面积(AUC)值也差异很大:平均 2145 pmol.h/L;95%CI 1422-3233。然而,同一名女性的重复测量高度(峰:ρ=0.94)或中度(AUC:P=0.74)相关。

结论

绝经后 E 浓度可忽略不计。E 乳膏慢性使用者的血清 E 浓度差异很大;然而,E 浓度在 8 小时内迅速下降,通常在 24 小时内达到“绝经后”水平。需要进一步阐明受试者之间差异的基础。需要进一步研究来确定局部 E 的安全性。

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