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两种市售左甲状腺素钠制剂在甲状腺功能减退患者中的生物等效性。

Bioequivalence of two commercially available levothyroxine-Na preparations in athyreotic patients.

作者信息

Gottwald R, Lorkowski G, Petersen G, Schnitzler M, Lücker P W

机构信息

Arbeitskreis klinische Arzneimittelprüfungen (AKP), Institut für klinische Pharmakologie Bobenheim, Grünstadt, Germany.

出版信息

Methods Find Exp Clin Pharmacol. 1994 Nov;16(9):645-50.

PMID:7746026
Abstract

The thyroid hormones levothyroxine and levotriiodothyronine are vital for normal growth and development and play an important role in energy metabolism. The bioequivalence of levothyroxine following administration of the test preparation (Eferox 100 tablets, Wyeth Pharma GmbH, Münster, Germany) and a reference preparation (each containing 100 micrograms levothyroxine-Na, the sodium salt of the natural thyroxine isomer) was investigated in 24 male and female patients with a lack of basal thyroid hormone secretion after an ablative thyroidectomy and postoperative radiotherapy. In a randomized, multicentric, open 3-factorial Latin-square (2 x 2 x 2) crossover study the subjects received two pharmaceutical units of the formulations once daily in the morning 30 min before breakfast during two periods of 35-42 consecutive days each. Serum concentrations of total thyroxine and total triiodothyronine were determined on screening day (basal concentrations), on the last 3 days of administration at predose to verify steady-state conditions, and on the last day of administration at 9 predetermined time points up to 24 h postadministration to obtain 24-h hormone profiles. The two formulations proved to be bioequivalent for levothyroxine regarding rate and extent of absorption. The bioequivalence decision was based on CSS,max and AUD0-24h.

摘要

甲状腺激素左甲状腺素和左三碘甲状腺原氨酸对正常生长发育至关重要,在能量代谢中发挥重要作用。在24例因甲状腺切除术后消融及术后放疗导致基础甲状腺激素分泌不足的男性和女性患者中,研究了受试制剂(Eferox 100片,德国明斯特惠氏制药有限公司)和参比制剂(均含100微克左甲状腺素钠,天然甲状腺素异构体的钠盐)给药后左甲状腺素的生物等效性。在一项随机、多中心、开放的3因素拉丁方(2×2×2)交叉研究中,受试者在两个连续35 - 42天的周期内,每天早晨早餐前30分钟服用两个制剂单位。在筛选日(基础浓度)、给药最后3天的给药前测定总甲状腺素和总三碘甲状腺原氨酸的血清浓度以验证稳态情况,并在给药最后一天的9个预定时间点直至给药后24小时测定以获得24小时激素谱。两种制剂在左甲状腺素的吸收速率和程度方面被证明具有生物等效性。生物等效性判定基于CSS,max和AUD0 - 24h。

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