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中国临床药理学与治疗学 ›› 1998, Vol. 3 ›› Issue (2): 81-84.

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长期口服复方左旋炔诺孕酮长效避孕片的临床药代动力学及体内蓄积

周晓飞, 邵庆翔, 韩学军1, 翁梨驹1, 经小萍1, 桑国卫   

  1. 浙江省医学科学院, 杭州 310013;
    1北京朝阳医院
  • 收稿日期:1998-04-15 出版日期:1998-06-26 发布日期:2020-12-01
  • 作者简介:周晓飞, 女, 27岁, 助理研究员。主要研究方向:甾体药代动力学。桑国卫, 男, 56岁, 研究员, 临床药理学专家, 国家卫生部进口药品审评委员会委员。

Clinical pharmacokinetic study on levonorgestrel and possible accumulation after long-term treatment of themonthly combined oral contraceptive

ZHOU Xiao-Fei, SHAO Qing-Xiang, HAN Xue-Jun1, WENG Li-Ju1, JING Xiao-Ping1, SANG Guo-Wei   

  1. Zhejiang Academy of Medical Sciences, Hangzhou 310013;
    1Beijing Chaoyang Hospital
  • Received:1998-04-15 Online:1998-06-26 Published:2020-12-01

摘要: 目的 比较中国妇女单剂及连续口服复方左旋炔诺孕酮长效避孕片后体内左旋炔诺酮(LNG)的药代动力学变化,为长期应用该长效避孕片的安全性提供依据。方法 9例健康育龄妇女于月经第5天口服复方左旋炔诺孕酮长效片(左旋炔诺孕酮6mg+炔雌醚3mg),每月1片,连续服用1年。于第1和第12次给药前及给药后不同时间取血,放射免疫法测定血清LNG浓度,并采用自身对照比较单剂和长期给药后LNG的药代动力学特征。结果 首次单剂给药后LNG药-时曲线呈二室开放模型,分布半衰期(αT1/2)为2.86±1.60小时,消除半衰期(βT1/2)为1.52±0.35天。血清LNG于2.56±1.13小时达峰浓度;血药峰值水平(Cmax)存在明显的个体差异,平均为141.36±70.20nmol/L。服用第12片后LNG平均Cmax为314.83±128.55nmol/L,显示连续给药后血LNG峰浓度显著升高。第1和第12次用药后AUC0~∞分别为182.42±135.85nmol/L·d-1和601.60±320.99nmol/L·d-1,两者亦有显著的统计学差异。第12次服药后Tmax为2.11±0.78小时,与单次给药相比无显著变化。第12次服药后LNG平均βT1/2为1.67±0.48天,与单剂给药相比亦无统计学差异,表明多次给药后药物的代谢速率并未发生明显改变,且21天体内LNG血浓度已降至0.058±0.069nmol/L(<100pg/ml)。结论 长期应用该复方口服避孕片并不引起受试者体内LNG的明显蓄积。

关键词: 左旋炔诺孕酮, 药代动力学, 复方口服避孕片

Abstract: Aim With comparison of pharmacokinetic profiles of levonor gestrel after single and mul tiple administration of thecombined oral contraceptive, this study would provide pharmacokinetic data for safety evaluation on proloned treatment of this monthly long-acting oral contraceptive.Methods Nine healthy fertile women received themonthly combined oral contraceptive (containing LNG 6 mg and quinestrol 3 mg) for up to 1 year.Blood samples werecollectedimmediately prior to drug intake and at consecutive timepoints after oral administration for determination of serum LNG by RIA.Intraindividual comparison was appliedin this long itudinal study.Results Serum LNG concentration-t imecurve showed an open two compartment model after single dose administration, with 2.86±1.60 hours for αT1/2 and 1.52±0.35 days for βT1/2.Cmax of LNG was observed after 2.56±1.13 h in the1sttreatment cycle.Mean Cmax was 141.36±70.20 nmol/L with signif icant interindividual variation.C m ax in 12 th treatment cyclereached to 314.83±128.55 nmol/L, which was much higher than that in the1st cycle. AUC0~28 were 182.42±135.85 and 533.96±319.31 nmol/L·d-1, respectively, also showingstatistically significant difference.There was no meaning ful di fference on Tmax after sing le and mul tiple do sing.Themean value of βT1/2 in the12th dosing was 1.67±0.48 days, which showed no ma rked changes, sugg esting that multiple do sing did no t influence thevelocity of drug metabolism.Cd21 declined below 100 pg/ml.Conclusion There was no obvious accumulation of LNG afterrepeated dosing of this monthly long-acting combined oral contreceptive.

Key words: levonorgestrel, pharmacokinetics, combined oral contraceptive

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